40 results on '"Cumbo S"'
Search Results
2. Combined high-fat-resveratrol diet and RIP140 knockout mice reveal a novel relationship between elevated bone mitochondrial content and compromised bone microarchitecture, bone mineral mass, and bone strength in the tibia.
- Author
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Miotto, PM, Frendo-Cumbo, S, Sacco, SM, Wright, DC, Ward, WE, Holloway, GP, Miotto, PM, Frendo-Cumbo, S, Sacco, SM, Wright, DC, Ward, WE, and Holloway, GP
- Abstract
SCOPE: While resveratrol (RSV) is associated with the prevention of high-fat (HF) diet-induced insulin resistance, the effects on bone health combined with an HF-diet is unknown. Therefore, we determined the effect of RSV on bone microarchitecture in the presence of an HF-diet, while also elucidating molecular adaptations within bone that could contribute to bone health status. METHODS AND RESULTS: Male C57BL6 mice were provided control (10% fat) or HF-diet (60% fat) in the presence or absence of RSV for 12 weeks. While RSV prevented HF diet-induced glucose intolerance, HF-RSV compromised tibial microarchitecture, mineral mass, and strength. The compromised outcomes following HF-RSV corresponded with higher markers of osteoclast-activation and bone-resorption (decreased OPG/RANKL ratio; increased cathepsin K), as well as higher markers of tibial mitochondrial content. A molecular model of elevated mitochondrial content (RIP140 knock out (KO) mice) was utilized to determine proof-of-principle that increasing mitochondrial content coincides with decrements in bone health. RIP140 KO mice displayed higher markers of mitochondrial content, and similar to HF-RSV, had compromised bone microarchitecture, lower BMD/strength, and higher markers of osteoclast-activation/bone-resorption. CONCLUSION: These data show that in the presence of an HF-diet, RSV negatively alters bone health, a process associated with increased mitochondrial content and markers of bone resorption.
- Published
- 2016
3. Volume-To-Creatinine Clearance Ratio In Patients Undergoing Coronary Angiography With or Without Percutaneous Coronary Intervention: Implications Of Varying Definitions Of Contrast-Induced Nephropathy
- Author
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Capodanno, DAVIDE FRANCESCO MARIA, Ministeri, M, Cumbo, S, Dalessandro, V, and Tamburino, Corrado
- Published
- 2014
4. Aging-Associated Reductions in Lipolytic and Mitochondrial Proteins in Mouse Adipose Tissue Are Not Rescued by Metformin Treatment
- Author
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Mennes, E., primary, Dungan, C. M., additional, Frendo-Cumbo, S., additional, Williamson, D. L., additional, and Wright, D. C., additional
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- 2013
- Full Text
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5. Risk prediction of contrast-induced nephropathy by ACEF score in patients undergoing coronary catheterization
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Corrado Tamburino, Margherita Ministeri, Davide Capodanno, Giuseppe Gargiulo, Silvia Cumbo, Fabio Dipasqua, Veronica Dalessandro, Capodanno, D., Ministeri, M., Dipasqua, F., Dalessandro, V., Cumbo, S., Gargiulo, G., and Tamburino, C.
- Subjects
Male ,renal failure ,Cardiac Catheterization ,Percutaneous ,Kidney Disease ,medicine.medical_treatment ,Contrast Media ,Predictive Value of Test ,030204 cardiovascular system & hematology ,Coronary Angiography ,Severity of Illness Index ,risk prediction ,0302 clinical medicine ,Risk Factors ,Odds Ratio ,Medicine ,030212 general & internal medicine ,Multivariate Analysi ,Aged, 80 and over ,Incidence (epidemiology) ,Incidence ,General Medicine ,coronary catheterisation ,Middle Aged ,Italy ,Predictive value of tests ,Creatinine ,Cardiology ,Female ,Kidney Diseases ,Cardiology and Cardiovascular Medicine ,contrast-induced neuropathy ,Human ,medicine.medical_specialty ,ACEF score ,Logistic Model ,Contrast-induced nephropathy ,Nephropathy ,03 medical and health sciences ,Percutaneous Coronary Intervention ,Predictive Value of Tests ,Internal medicine ,Severity of illness ,Humans ,Aged ,business.industry ,Risk Factor ,Percutaneous coronary intervention ,Odds ratio ,medicine.disease ,Logistic Models ,ROC Curve ,Multivariate Analysis ,business - Abstract
Aims: To explore the ability of the ACEF score to predict the incidence of contrast-induced nephropathy (CIN) in patients undergoing coronary angiography with or without percutaneous coronary intervention. Methods: A total of 706 patients undergoing coronary angiography ± percutaneous coronary intervention (PCI) between March 2011 and October 2011 were analyzed. CIN using different definitions was termed as CINnarrow (rise in serum creatinine ≥0.5 mg/dl) and CINbroad (rise in serum creatinine ≥0.5 mg/dl and/or ≥25% increase in baseline serum creatinine). Results: The mean ACEF score was 1.5 ± 0.6. Overall incidences of CINnarrow and CINbroad were 5.5% and 13.6%, respectively. There was a significant gradient in the incidence of CINnarrow (2.9%, 3.9%, 10.6% in the I, II, and III tertiles, respectively, P < 0.001) and CINbroad (9.1%, 14.2%, 17.9% in the I, II, and III tertiles, respectively, P = 0.021) across increasing ACEF tertiles. The ACEF score was independently associated with the risk of CINnarrow (adjusted odds ratio [OR] 1.6, 95% confidence interval [CI] 1.0-2.7; P = 0.047). Discrimination was more satisfactory when using the ACEF as a predictor of CINnarrow (c-statistic 0.71, 95% 0.63-0.79). Conclusion: The ACEF score is an independent and potentially useful predictor of CIN defined as rise in serum creatinine ≥0.5 mg/dl.
- Published
- 2014
6. Reduced adipocyte glutaminase activity promotes energy expenditure and metabolic health.
- Author
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Lecoutre S, Maqdasy S, Rizo-Roca D, Renzi G, Vlassakev I, Alaeddine LM, Higos R, Jalkanen J, Zhong J, Zareifi DS, Frendo-Cumbo S, Massier L, Hodek O, Juvany M, Moritz T, de Castro Barbosa T, Omar-Hmeadi M, López-Yus M, Merabtene F, Abatan JB, Marcelin G, El Hachem EJ, Rouault C, Bergo MO, Petrus P, Zierath JR, Clément K, Krook A, Mejhert N, and Rydén M
- Subjects
- Animals, Mice, Humans, Male, Female, Obesity metabolism, Insulin Resistance, Glutamine metabolism, Diet, High-Fat, Glycolysis, Energy Metabolism, Glutaminase metabolism, Adipocytes metabolism, Mice, Knockout
- Abstract
Glutamine and glutamate are interconverted by several enzymes and alterations in this metabolic cycle are linked to cardiometabolic traits. Herein, we show that obesity-associated insulin resistance is characterized by decreased plasma and white adipose tissue glutamine-to-glutamate ratios. We couple these stoichiometric changes to perturbed fat cell glutaminase and glutamine synthase messenger RNA and protein abundance, which together promote glutaminolysis. In human white adipocytes, reductions in glutaminase activity promote aerobic glycolysis and mitochondrial oxidative capacity via increases in hypoxia-inducible factor 1α abundance, lactate levels and p38 mitogen-activated protein kinase signalling. Systemic glutaminase inhibition in male and female mice, or genetically in adipocytes of male mice, triggers the activation of thermogenic gene programs in inguinal adipocytes. Consequently, the knockout mice display higher energy expenditure and improved glucose tolerance compared to control littermates, even under high-fat diet conditions. Altogether, our findings highlight white adipocyte glutamine turnover as an important determinant of energy expenditure and metabolic health., (© 2024. The Author(s).)
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- 2024
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7. Iterative Development of an Interactive Website to Support Shared Decision-Making in Metastatic Breast Cancer.
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Conley CC, Cumbo S, Chavez Ochoa J, Boles A, Rodriguez JD, Schwab N, Farrell D, Abduljawad S, Isaacs C, and O'Neill SC
- Abstract
Recent treatment advances have resulted in significantly increased survival times following metastatic breast cancer (MBC) diagnosis. Novel treatment approaches-and their related side effects-have changed the landscape of MBC treatment decision-making. We developed a prototype of an online educational tool to prepare patients with MBC for shared decision-making with their oncologists. We describe the five phases of tool development: (1) in-depth, semi-structured qualitative interviews and (2) feedback on storyboards of initial content with patients with MBC and oncology providers. This was followed by three phases of iterative feedback with patients in which they responded to (3) initial, non-navigable website content and (4) a beta version of the full website. In the final phase (5), patients newly diagnosed with MBC (N = 6) used the website prototype for 1 week and completed surveys assessing acceptability, feasibility, treatment knowledge, preparation for decision-making, and self-efficacy for decision-making. Participants in Phase 1 characterized a cyclical process of MBC treatment decision-making and identified key information needs. Website content and structure was iteratively developed in Phases 2-4. Most participants in Phase 5 (n = 4) accessed the website 2-5 times. All participants who accessed the website at least once (n = 5) felt they learned new information from the website prototype and would recommend it to others newly-diagnosed with MBC. After using the website prototype, participants reported high preparation and self-efficacy for decision-making. This multiphase, iterative process resulted in a prototype intervention designed to support decision-making for MBC patients., (© 2024. The Author(s) under exclusive licence to American Association for Cancer Education.)
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- 2024
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8. A spatiotemporal proteomic map of human adipogenesis.
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Klingelhuber F, Frendo-Cumbo S, Omar-Hmeadi M, Massier L, Kakimoto P, Taylor AJ, Couchet M, Ribicic S, Wabitsch M, Messias AC, Iuso A, Müller TD, Rydén M, Mejhert N, and Krahmer N
- Subjects
- Humans, Lipid Metabolism, Mitochondria metabolism, Lipid Droplets metabolism, Proteome metabolism, Adipocytes metabolism, Cell Differentiation, Adipogenesis, Proteomics methods
- Abstract
White adipocytes function as major energy reservoirs in humans by storing substantial amounts of triglycerides, and their dysfunction is associated with metabolic disorders; however, the mechanisms underlying cellular specialization during adipogenesis remain unknown. Here, we generate a spatiotemporal proteomic atlas of human adipogenesis, which elucidates cellular remodelling as well as the spatial reorganization of metabolic pathways to optimize cells for lipid accumulation and highlights the coordinated regulation of protein localization and abundance during adipocyte formation. We identify compartment-specific regulation of protein levels and localization changes of metabolic enzymes to reprogramme branched-chain amino acids and one-carbon metabolism to provide building blocks and reduction equivalents. Additionally, we identify C19orf12 as a differentiation-induced adipocyte lipid droplet protein that interacts with the translocase of the outer membrane complex of lipid droplet-associated mitochondria and regulates adipocyte lipid storage by determining the capacity of mitochondria to metabolize fatty acids. Overall, our study provides a comprehensive resource for understanding human adipogenesis and for future discoveries in the field., (© 2024. The Author(s).)
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- 2024
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9. Exercise-induced crosstalk between immune cells and adipocytes in humans: Role of oncostatin-M.
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Dollet L, Lundell LS, Chibalin AV, Pendergrast LA, Pillon NJ, Lansbury EL, Elmastas M, Frendo-Cumbo S, Jalkanen J, de Castro Barbosa T, Cervone DT, Caidahl K, Dmytriyeva O, Deshmukh AS, Barrès R, Rydén M, Wallberg-Henriksson H, Zierath JR, and Krook A
- Subjects
- Female, Humans, Male, Adipocytes metabolism, Adipose Tissue metabolism, Cells, Cultured, Lipolysis, Diabetes Mellitus, Type 2 metabolism
- Abstract
The discovery of exercise-regulated circulatory factors has fueled interest in organ crosstalk, especially between skeletal muscle and adipose tissue, and the role in mediating beneficial effects of exercise. We studied the adipose tissue transcriptome in men and women with normal glucose tolerance or type 2 diabetes following an acute exercise bout, revealing substantial exercise- and time-dependent changes, with sustained increase in inflammatory genes in type 2 diabetes. We identify oncostatin-M as one of the most upregulated adipose-tissue-secreted factors post-exercise. In cultured human adipocytes, oncostatin-M enhances MAPK signaling and regulates lipolysis. Oncostatin-M expression arises predominantly from adipose tissue immune cell fractions, while the corresponding receptors are expressed in adipocytes. Oncostatin-M expression increases in cultured human Thp1 macrophages following exercise-like stimuli. Our results suggest that immune cells, via secreted factors such as oncostatin-M, mediate a crosstalk between skeletal muscle and adipose tissue during exercise to regulate adipocyte metabolism and adaptation., Competing Interests: Declaration of interests J.R.Z. serves on the advisory boards for Cell and Cell Metabolism., (Copyright © 2024 The Authors. Published by Elsevier Inc. All rights reserved.)
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- 2024
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10. CRISPR/Cas9-mediated deletion of adipocyte genes associated with NAFLD alters adipocyte lipid handling and reduces steatosis in hepatocytes in vitro.
- Author
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Lopez-Yus M, Frendo-Cumbo S, Del Moral-Bergos R, Garcia-Sobreviela MP, Bernal-Monterde V, Rydén M, Lorente-Cebrian S, and Arbones-Mainar JM
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- Humans, Lipogenesis genetics, Protein Serine-Threonine Kinases metabolism, Protein Serine-Threonine Kinases genetics, Suppressor of Cytokine Signaling 3 Protein genetics, Suppressor of Cytokine Signaling 3 Protein metabolism, Hep G2 Cells, Gene Editing methods, Cells, Cultured, Adipogenesis genetics, CRISPR-Cas Systems, Non-alcoholic Fatty Liver Disease genetics, Non-alcoholic Fatty Liver Disease metabolism, Non-alcoholic Fatty Liver Disease pathology, Hepatocytes metabolism, Hepatocytes pathology, Mesenchymal Stem Cells metabolism, Adipocytes metabolism, Adipocytes pathology, Dual Specificity Phosphatase 1 genetics, Dual Specificity Phosphatase 1 metabolism, Lipid Metabolism genetics
- Abstract
Obesity is a major risk factor for the development of nonalcoholic fatty liver disease (NAFLD), and the subcutaneous white adipose tissue (scWAT) is the primary lipid storage depot and regulates lipid fluxes to other organs. Our previous work identified genes upregulated in scWAT of patients with NAFLD: SOCS3 , DUSP1 , and SIK1 . Herein, we knocked down (KD) their expression in human adipose-derived mesenchymal stem cells (hADMSCs) using clustered regularly interspaced short palindromic repeats (CRISPR)/Cas9 technology and characterized their phenotype. We found that SOCS3 , DUSP1 , and SIK1 expression in hADMSC-derived adipocytes was not critical for adipogenesis. However, the metabolic characterization of the cells suggested that the genes played important roles in lipid metabolism. Reduction of SIK1 expression significantly increased both de novo lipogenesis (DNL) and palmitate-induced lipogenesis (PIL). Editing out SOCS3 reduced DNL while increasing isoproterenol-induced lipolysis and insulin-induced palmitate accumulation. Conversely, DUSP1 reduced PIL and DNL. Moreover, RNA-sequencing analysis of edited cells showed that these genes not only altered lipid metabolism but also other biological pathways related to inflammatory processes, in the case of DUSP1 , extracellular matrix remodeling for SOCS3 , or cellular transport for SIK1 . Finally, to evaluate a possible adipocyte-hepatocyte axis, human hepatoma HepG2 cells were cocultured with edited hADMSCs-derived adipocytes in the presence of [3H]-palmitate. All HepG2 cells cultured with DUSP1-, SIK1-, or SOCS3-KD adipocytes decreased [3H]-palmitate accumulation compared with control adipocytes. These results support our hypotheses that SOCS3 , DUSP1 , and SIK1 regulate multiple aspects of adipocyte function, which may play a role in the progression of obesity-associated comorbidities, such as NAFLD. NEW & NOTEWORTHY Clustered regularly interspaced short palindromic repeats (CRISPR)/Cas9 technology successfully edited genomic DNA of human adipose-derived mesenchymal stem cells (hADMSC). SOCS3 , SIK1 , and DUSP1 regulate adipocyte lipid handling. Silencing SOCS3 , SIK1 , and DUSP1 expression in hADMSC-derived adipocytes reduces hepatocyte lipid storage in vitro.
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- 2023
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11. Monitoring anesthesia depth with patient state index during pediatric surgery.
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Ricci Z, Robino C, Rufini P, Cumbo S, Cavallini S, Gobbi L, Brocchi A, Serio P, and Romagnoli S
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- Humans, Child, Prospective Studies, Anesthesia, Intravenous, Electroencephalography, Anesthesia, General, Emergence Delirium
- Abstract
Background: Monitoring anesthesia depth in children is challenging. Pediatric anesthesiologists estimate general anesthesia depth using indirect methods such as pharmacokinetic models and neurovegetative reflexes. The application of processed electroencephalography may help to identify the correct anesthesia depth (i.e., patient state index between 25 and 50)., Aims: To determine the median values of patient state index and spectral edge frequency 95% in children undergoing general anesthesia conducted according to indirect evaluation of depth. The relationships between patient state index and spectral edge frequency 95% and indirect monitoring of anesthesia depth, type of anesthesia, age subgroups, and postoperative delirium were also assessed., Methods: A prospective observational study on children (aged 1-18 years) undergoing surgery longer than 60 min. The SedLine monitor and the novel SedLine pediatric sensors (Masimo Inc., Irvine California) were applied. Patient state index levels were recorded for the duration of the anesthesia until the discharge to the ward at predefined time points., Results: In the 111 enrolled children, median patient state index level at the end of anesthesia induction was 25 (22-32) and ranged from 26 (23-34) to 28 (25-36) in the maintenance phase. Patient state index at extubation was 48 (35-60) and 69 (62-75) at discharge from the operatory room. Median right/left spectral edge frequency 95% values at the end of induction were 10 (6-14)/9 (5-14) Hz and median right/left spectral edge frequency 95% values in the maintenance phase ranged from 10 (6-14) to 12 (11-15) Hz in both hemispheres. At extubation, right/left spectral edge frequency 95% levels were 18 (15-21)/17 (15-21) Hz. We observed 39 episodes of burst suppression in 20 patients (19%). Median patient state index levels were not different between patients undergoing inhalational and intravenous anesthesia and between those undergoing general anesthesia and general anesthesia added to locoregional anesthesia. Children <2 years displayed significantly higher patient state index levels than older patients (p = .0004). The presence of a burst suppression episode was not associated with PAED levels (OR 1.58, 95% CI 0.14-16.74, p` = .18)., Conclusions: NonpEEG-guided anesthesia in children led to median patient state index levels at the low range of recommended unconsciousness values with frequent episodes of burst suppression. Patient state index levels were generally higher in children below 2 years., (© 2023 The Authors. Pediatric Anesthesia published by John Wiley & Sons Ltd.)
- Published
- 2023
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12. Erector spinae plane block for thoraco-abdominal surgery in an infant with palliated tetralogy of Fallot and pentalogy of Cantrell.
- Author
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Cumbo S, Rufini P, and Ricci Z
- Subjects
- Humans, Infant, Paraspinal Muscles, Pain, Postoperative, Tetralogy of Fallot surgery, Pentalogy of Cantrell surgery, Nerve Block
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- 2023
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13. An integrated single cell and spatial transcriptomic map of human white adipose tissue.
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Massier L, Jalkanen J, Elmastas M, Zhong J, Wang T, Nono Nankam PA, Frendo-Cumbo S, Bäckdahl J, Subramanian N, Sekine T, Kerr AG, Tseng BTP, Laurencikiene J, Buggert M, Lourda M, Kublickiene K, Bhalla N, Andersson A, Valsesia A, Astrup A, Blaak EE, Ståhl PL, Viguerie N, Langin D, Wolfrum C, Blüher M, Rydén M, and Mejhert N
- Subjects
- Humans, Adipocytes metabolism, Gene Expression Profiling, Adipogenesis genetics, Adipose Tissue, Transcriptome genetics, Adipose Tissue, White metabolism
- Abstract
To date, single-cell studies of human white adipose tissue (WAT) have been based on small cohort sizes and no cellular consensus nomenclature exists. Herein, we performed a comprehensive meta-analysis of publicly available and newly generated single-cell, single-nucleus, and spatial transcriptomic results from human subcutaneous, omental, and perivascular WAT. Our high-resolution map is built on data from ten studies and allowed us to robustly identify >60 subpopulations of adipocytes, fibroblast and adipogenic progenitors, vascular, and immune cells. Using these results, we deconvolved spatial and bulk transcriptomic data from nine additional cohorts to provide spatial and clinical dimensions to the map. This identified cell-cell interactions as well as relationships between specific cell subtypes and insulin resistance, dyslipidemia, adipocyte volume, and lipolysis upon long-term weight changes. Altogether, our meta-map provides a rich resource defining the cellular and microarchitectural landscape of human WAT and describes the associations between specific cell types and metabolic states., (© 2023. The Author(s).)
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- 2023
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14. Erratum: DCAF7 regulates cell proliferation through IRS1-FOXO1 signaling.
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Frendo-Cumbo S, Li T, Ammendolia DA, Coyaud E, Laurent EMN, Liu Y, Bilan PJ, Polevoy G, Raught B, Brill JA, Klip A, and Brumell JH
- Abstract
[This corrects the article DOI: 10.1016/j.isci.2022.105188.]., (© 2022 The Author(s).)
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- 2022
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15. DCAF7 regulates cell proliferation through IRS1-FOXO1 signaling.
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Frendo-Cumbo S, Li T, Ammendolia DA, Coyaud E, Laurent EMN, Liu Y, Bilan PJ, Polevoy G, Raught B, Brill JA, Klip A, and Brumell JH
- Abstract
Cell proliferation is dependent on growth factors insulin and IGF1. We sought to identify interactors of IRS1, the most proximal mediator of insulin/IGF1 signaling, that regulate cell proliferation. Using proximity-dependent biotin identification (BioID), we detected 40 proteins displaying proximal interactions with IRS1, including DCAF7 and its interacting partners DYRK1A and DYRK1B. In HepG2 cells, DCAF7 knockdown attenuated cell proliferation by inducing cell cycle arrest at G2. DCAF7 expression was required for insulin-stimulated AKT phosphorylation, and its absence promoted nuclear localization of the transcription factor FOXO1. DCAF7 knockdown induced expression of FOXO1-target genes implicated in G2 cell cycle inhibition, correlating with G2 cell cycle arrest. In Drosophila melanogaster , wing-specific knockdown of DCAF7/ wap caused smaller wing size and lower wing cell number; the latter recovered upon double knockdown of wap and dfoxo . We propose that DCAF7 regulates cell proliferation and cell cycle via IRS1-FOXO1 signaling, of relevance to whole organism growth., Competing Interests: The authors declare no competing interests., (© 2022 The Author(s).)
- Published
- 2022
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16. Reversed ultrasound-guided dorsal penile nerve block in children: A retrospective study.
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Rufini P, Cumbo S, Caccavale AR, Azzari C, Germini F, L'Erario M, and Ricci Z
- Subjects
- Anesthesia, Conduction, Child, Humans, Male, Pain, Postoperative, Retrospective Studies, Ultrasonography, Interventional, Circumcision, Male, Nerve Block, Pudendal Nerve diagnostic imaging
- Published
- 2022
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17. Multisystem Inflammatory Syndrome in Children and Acute Kidney Injury: Retrospective Study of Five Italian PICUs.
- Author
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Ricci Z, Colosimo D, Cumbo S, L'Erario M, Duchini P, Rufini P, Perrotta D, De Sanctis F, Di Nardo M, Amigoni A, and Pulitanò S
- Subjects
- Adolescent, COVID-19 complications, Child, Humans, Intensive Care Units, Pediatric, Prospective Studies, Retrospective Studies, Systemic Inflammatory Response Syndrome, Acute Kidney Injury diagnosis, Acute Kidney Injury epidemiology, Acute Kidney Injury etiology
- Abstract
Objectives: Multisystem inflammatory syndrome in children (MIS-C) manifests with heart dysfunction and respiratory failure some weeks after a severe acute respiratory syndrome coronavirus disease 2 infection. The aim of our study was to explore the prevalence, severity, timing, and duration of acute kidney injury (AKI) in MIS-C patients. Furthermore, we evaluated which clinical variables and outcomes are associated with AKI., Design: Multicenter retrospective study., Setting: Five tertiary hospital PICUs in Italy. Data were collected in the first 7 days of PICU admission and renal function was followed throughout the hospital stay., Patients: Patients less than 18 years old admitted to the PICU for greater than 24 hours with MIS-C., Interventions: None., Measurements and Main Results: We collected the following data, including: demographic information, inflammatory biomarkers, lactate levels, Pa o2 /F io2 , ejection fraction, N-terminal pro-B-type natriuretic peptide (NT-proBNP), renal function (serum creatinine, urinary output, fluid balance, and percentage fluid accumulation), Vasoactive-Inotropic Score (VIS), pediatric Sequential Organ Failure Assessment (pSOFA), and Pediatric Index of Mortality 3. AKI was diagnosed in eight of 38 patients (21%) and severe AKI was present in four of eight patients. In all cases, AKI was present at PICU admission and its median (interquartile range) duration was 3.5 days (1.5-5.7 d). We did not identify differences between AKI and no-AKI patients when not making correction for multiple comparisons, for example, in weight, ejection fraction, pSOFA, Pa o2 /F io2 , and lactates. We failed to identify any difference in these groups in urine output and fluid balance. Exploratory analyses of serial data between no-AKI and AKI patients showed significant differences on lymphocyte count, NT-proBNP value, ejection fraction, pSOFA, Pa o2 /F io2 , and VIS., Conclusions: In this multicenter Italian PICU experience, MIS-C is associated with AKI in one-in-five cases. In general, AKI is characterized by an associated reduction in glomerular filtration rate with a self-limiting time course., Competing Interests: The authors have disclosed that they do not have any potential conflicts of interest., (Copyright © 2022 by the Society of Critical Care Medicine and the World Federation of Pediatric Intensive and Critical Care Societies.)
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- 2022
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18. The Lipid Droplet Knowledge Portal: A resource for systematic analyses of lipid droplet biology.
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Mejhert N, Gabriel KR, Frendo-Cumbo S, Krahmer N, Song J, Kuruvilla L, Chitraju C, Boland S, Jang DK, von Grotthuss M, Costanzo MC, Rydén M, Olzmann JA, Flannick J, Burtt NP, Farese RV Jr, and Walther TC
- Subjects
- Animals, Cholesterol Esters metabolism, Data Mining, Genome, Humans, Inflammation pathology, Lipid Metabolism, Liver metabolism, Male, Mice, Inbred C57BL, Phenotype, Phosphorylation, RNA Interference, Mice, Databases as Topic, Lipid Droplets metabolism
- Abstract
Lipid droplets (LDs) are organelles of cellular lipid storage with fundamental roles in energy metabolism and cell membrane homeostasis. There has been an explosion of research into the biology of LDs, in part due to their relevance in diseases of lipid storage, such as atherosclerosis, obesity, type 2 diabetes, and hepatic steatosis. Consequently, there is an increasing need for a resource that combines datasets from systematic analyses of LD biology. Here, we integrate high-confidence, systematically generated human, mouse, and fly data from studies on LDs in the framework of an online platform named the "Lipid Droplet Knowledge Portal" (https://lipiddroplet.org/). This scalable and interactive portal includes comprehensive datasets, across a variety of cell types, for LD biology, including transcriptional profiles of induced lipid storage, organellar proteomics, genome-wide screen phenotypes, and ties to human genetics. This resource is a powerful platform that can be utilized to identify determinants of lipid storage., Competing Interests: Declaration of interests The authors declare no competing interests., (Copyright © 2022 The Authors. Published by Elsevier Inc. All rights reserved.)
- Published
- 2022
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19. Impaired phosphocreatine metabolism in white adipocytes promotes inflammation.
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Maqdasy S, Lecoutre S, Renzi G, Frendo-Cumbo S, Rizo-Roca D, Moritz T, Juvany M, Hodek O, Gao H, Couchet M, Witting M, Kerr A, Bergo MO, Choudhury RP, Aouadi M, Zierath JR, Krook A, Mejhert N, and Rydén M
- Subjects
- Animals, Humans, Inflammation metabolism, Mice, Obesity metabolism, Phosphocreatine, Adipocytes, White metabolism, Creatine
- Abstract
The mechanisms promoting disturbed white adipocyte function in obesity remain largely unclear. Herein, we integrate white adipose tissue (WAT) metabolomic and transcriptomic data from clinical cohorts and find that the WAT phosphocreatine/creatine ratio is increased and creatine kinase-B expression and activity is decreased in the obese state. In human in vitro and murine in vivo models, we demonstrate that decreased phosphocreatine metabolism in white adipocytes alters adenosine monophosphate-activated protein kinase activity via effects on adenosine triphosphate/adenosine diphosphate levels, independently of WAT beigeing. This disturbance promotes a pro-inflammatory profile characterized, in part, by increased chemokine (C-C motif) ligand 2 (CCL2) production. These data suggest that the phosphocreatine/creatine system links cellular energy shuttling with pro-inflammatory responses in human and murine white adipocytes. Our findings provide unexpected perspectives on the mechanisms driving WAT inflammation in obesity and may present avenues to target adipocyte dysfunction., (© 2022. The Author(s).)
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- 2022
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20. Communication Between Autophagy and Insulin Action: At the Crux of Insulin Action-Insulin Resistance?
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Frendo-Cumbo S, Tokarz VL, Bilan PJ, Brumell JH, and Klip A
- Abstract
Insulin is a paramount anabolic hormone that promotes energy-storage in adipose tissue, skeletal muscle and liver, and these responses are significantly attenuated in insulin resistance leading to type 2 diabetes. Contrasting with insulin's function, macroautophagy/autophagy is a physiological mechanism geared to the degradation of intracellular components for the purpose of energy production, building-block recycling or tissue remodeling. Given that both insulin action and autophagy are dynamic phenomena susceptible to the influence of nutrient availability, it is perhaps not surprising that there is significant interaction between these two major regulatory mechanisms. This review examines the crosstalk between autophagy and insulin action, with specific focus on dysregulated autophagy as a cause or consequence of insulin resistance., Competing Interests: The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest., (Copyright © 2021 Frendo-Cumbo, Tokarz, Bilan, Brumell and Klip.)
- Published
- 2021
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21. Complexin-2 redistributes to the membrane of muscle cells in response to insulin and contributes to GLUT4 translocation.
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Pavarotti MA, Tokarz V, Frendo-Cumbo S, Bilan PJ, Liu Z, Zanni-Ruiz E, Mayorga LS, and Klip A
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- Adaptor Proteins, Vesicular Transport genetics, Animals, Cell Membrane drug effects, Cell Membrane metabolism, Cells, Cultured, Glucose Transporter Type 4 genetics, Insulin genetics, Insulin metabolism, Muscle, Skeletal cytology, Myoblasts drug effects, Nerve Tissue Proteins genetics, Protein Transport drug effects, Proto-Oncogene Proteins c-akt metabolism, Rats, Signal Transduction, rac1 GTP-Binding Protein metabolism, Adaptor Proteins, Vesicular Transport metabolism, Glucose Transporter Type 4 metabolism, Insulin pharmacology, Myoblasts metabolism, Nerve Tissue Proteins metabolism
- Abstract
Insulin stimulates glucose uptake in muscle cells by rapidly redistributing vesicles containing GLUT4 glucose transporters from intracellular compartments to the plasma membrane (PM). GLUT4 vesicle fusion requires the formation of SNARE complexes between vesicular VAMP and PM syntaxin4 and SNAP23. SNARE accessory proteins usually regulate vesicle fusion processes. Complexins aide in neuro-secretory vesicle-membrane fusion by stabilizing trans-SNARE complexes but their participation in GLUT4 vesicle fusion is unknown. We report that complexin-2 is expressed and homogeneously distributed in L6 rat skeletal muscle cells. Upon insulin stimulation, a cohort of complexin-2 redistributes to the PM. Complexin-2 knockdown markedly inhibited GLUT4 translocation without affecting proximal insulin signalling of Akt/PKB phosphorylation and actin fiber remodelling. Similarly, complexin-2 overexpression decreased maximal GLUT4 translocation suggesting that the concentration of complexin-2 is finely tuned to vesicle fusion. These findings reveal an insulin-dependent regulation of GLUT4 insertion into the PM involving complexin-2., (© 2021 The Author(s). Published by Portland Press Limited on behalf of the Biochemical Society.)
- Published
- 2021
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22. Deficiency of the autophagy gene ATG16L1 induces insulin resistance through KLHL9/KLHL13/CUL3-mediated IRS1 degradation.
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Frendo-Cumbo S, Jaldin-Fincati JR, Coyaud E, Laurent EMN, Townsend LK, Tan JMJ, Xavier RJ, Pillon NJ, Raught B, Wright DC, Brumell JH, and Klip A
- Subjects
- Animals, Autophagy physiology, Autophagy-Related Proteins genetics, Autophagy-Related Proteins metabolism, Cullin Proteins metabolism, Fibroblasts metabolism, Genes, Regulator, HEK293 Cells, Humans, Insulin metabolism, Male, Mice, Mice, Inbred C57BL, Proteins metabolism, Signal Transduction, Ubiquitin-Protein Ligase Complexes metabolism, Autophagy-Related Proteins deficiency, Insulin Receptor Substrate Proteins metabolism, Insulin Resistance
- Abstract
Connections between deficient autophagy and insulin resistance have emerged, however, the mechanism through which reduced autophagy impairs insulin-signaling remains unknown. We examined mouse embryonic fibroblasts lacking Atg16l1 (ATG16L1 KO mouse embryonic fibroblasts (MEFs)), an essential autophagy gene, and observed deficient insulin and insulin-like growth factor-1 signaling. ATG16L1 KO MEFs displayed reduced protein content of insulin receptor substrate-1 (IRS1), pivotal to insulin signaling, whereas IRS1myc overexpression recovered downstream insulin signaling. Endogenous IRS1 protein content and insulin signaling were restored in ATG16L1 KO mouse embryonic fibroblasts (MEF) upon proteasome inhibition. Through proximity-dependent biotin identification (BioID) and co-immunoprecipitation, we found that Kelch-like proteins KLHL9 and KLHL13, which together form an E3 ubiquitin (Ub) ligase complex with cullin 3 (CUL3), are novel IRS1 interactors. Expression of Klhl9 and Klhl13 was elevated in ATG16L1 KO MEFs and siRNA-mediated knockdown of Klhl9 , Klhl13 , or Cul3 recovered IRS1 expression. Moreover, Klhl13 and Cul3 knockdown increased insulin signaling. Notably, adipose tissue of high-fat fed mice displayed lower Atg16l1 mRNA expression and IRS1 protein content, and adipose tissue KLHL13 and CUL3 expression positively correlated to body mass index in humans. We propose that ATG16L1 deficiency evokes insulin resistance through induction of Klhl9 and Klhl13 , which, in complex with Cul3 , promote proteasomal IRS1 degradation., (© 2019 Frendo-Cumbo et al.)
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- 2019
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23. Regulation of Hepatic Follistatin Expression at Rest and during Exercise in Mice.
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Peppler WT, Castellani LN, Root-McCaig J, Townsend LK, Sutton CD, Frendo-Cumbo S, Medak KD, Macpherson REK, Charron MJ, and Wright DC
- Subjects
- Adrenergic beta-Antagonists pharmacology, Animals, Epinephrine administration & dosage, Epinephrine antagonists & inhibitors, Female, Gene Expression, Glucagon administration & dosage, Injections, Male, Mice, Inbred C57BL, Mice, Knockout, Phosphorylation, Propranolol pharmacology, Proto-Oncogene Proteins c-akt metabolism, RNA, Messenger genetics, RNA, Messenger metabolism, Smad2 Protein metabolism, Smad3 Protein metabolism, Epinephrine physiology, Follistatin metabolism, Glucagon physiology, Liver metabolism, Physical Conditioning, Animal, Rest
- Abstract
Introduction: Follistatin (FST) is a protein with numerous biological roles and was recently identified as an exercise-inducible hepatokine; however, the signals that regulate this are not well understood. The purpose of this study was to delineate potential endocrine factors that may regulate hepatic FST at rest and during exercise., Methods: This study used four experiments. First, male and female C57BL/6J mice remained sedentary or were subjected to a single bout of exercise at moderate or exhaustive intensity with liver collected immediately post. Second, mice were injected with glucagon (1 mg·kg, 60 min), epinephrine (2 mg·kg, 30 min), glucagon then epinephrine, or saline. Third, mice were pretreated with propranolol (20-60 mg·kg, 30 min) before epinephrine injection. Fourth, glucagon receptor wild type (Gcgr) or knockout (Gcgr) mice were pretreated with saline or propranolol (20 mg·kg, 30 min) and were subjected to a single bout of exhaustive exercise with liver collected immediately post or after 2 h recovery. In all experiments liver FST mRNA expression was measured, and in experiment four FST protein content was measured., Results: A single bout of treadmill exercise performed at an exhaustive but not moderate-intensity increased FST expression, as did injection of glucagon or epinephrine alone and when combined. Pretreatment of mice with propranolol attenuated the epinephrine-induced increase in FST expression. The exercise-induced increase in FST expression was attenuated in Gcgr mice, with no effect of propranolol. Gcgr mice had higher protein content of FST, but there was no effect of exercise or propranolol., Conclusions: These data suggest that both glucagon and epinephrine regulate hepatic FST expression at rest; however, only glucagon is required for the exercise-induced increase.
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- 2019
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24. Resveratrol and Metformin Recover Prefrontal Cortex AMPK Activation in Diet-Induced Obese Mice but Reduce BDNF and Synaptophysin Protein Content.
- Author
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Yang AJT, Frendo-Cumbo S, and MacPherson REK
- Subjects
- Animals, Autophagy drug effects, Blood Glucose metabolism, Brain-Derived Neurotrophic Factor biosynthesis, Diet, High-Fat, Enzyme Activation drug effects, Insulin Resistance, Male, Mice, Mice, Inbred C57BL, Obesity metabolism, Synaptophysin biosynthesis, TOR Serine-Threonine Kinases biosynthesis, TOR Serine-Threonine Kinases genetics, AMP-Activated Protein Kinases metabolism, Antioxidants pharmacology, Hypoglycemic Agents pharmacology, Metformin pharmacology, Obesity enzymology, Prefrontal Cortex enzymology, Resveratrol pharmacology
- Abstract
Background: Obesity, insulin resistance, and type 2 diabetes are established risk factors for the development of Alzheimer's disease (AD). Given this connection, two drugs, metformin (MET) and resveratrol (RESV), are considered for the clearance of amyloid-β peptides through AMPK-mediated activation of autophagy. However, overactivation of AMPK observed in late-stage AD brains and relationships between AMPK and neurogenesis (through mTORC1 inhibition), questions treatment with these drugs., Objective: To examine if MET and/or RESV supplementation activates brain AMPK, regulates markers of autophagy, and affects markers of neuronal health/neurogenesis., Methods: 8-week-old male C57BL/6J mice were fed a low (N = 12; 10% kcal fat; LFD) or high fat diet (N = 40; 60% kcal fat; HFD) for 9 weeks to induce insulin resistance and obesity. HFD mice were then treated with/without MET (250 mg/kg/day), RESV (100 mg/kg/day), or COMBO (MET: 250 mg/kg/day, RESV: 100 mg/kg/day) for 5 weeks. Hippocampus and prefrontal cortex were extracted for western blotting analysis., Results: Cortex AMPK (T172) and raptor (S792, the regulatory subunit of mTORC1) phosphorylation were upregulated following RESV, COMBO treatments. mTOR (S2448) and ULK1 (S555) activation was seen following MET, COMBO and RESV, COMBO treatments, respectively, in the cortex and hippocampus. p62 content was decreased following RESV, COMBO, with LC3 content being increased following RESV treatment in the cortex. Brain derived neurotropic factor (BDNF) was significantly decreased following RESV, COMBO, and synaptophysin following all treatment in the cortex., Conclusion: These results demonstrate that while treatments upregulated markers of autophagy in the prefrontal cortex, reductions in neuronal health markers question the efficacy of AMPK as a therapy for AD.
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- 2019
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25. Sphingolipid changes do not underlie fatty acid-evoked GLUT4 insulin resistance nor inflammation signals in muscle cells.
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Pillon NJ, Frendo-Cumbo S, Jacobson MR, Liu Z, Milligan PL, Hoang Bui H, Zierath JR, Bilan PJ, Brozinick JT, and Klip A
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- Animals, Inflammation metabolism, Inflammation pathology, Muscle Fibers, Skeletal drug effects, Muscle Fibers, Skeletal metabolism, Muscle Fibers, Skeletal pathology, NF-kappa B metabolism, Palmitic Acid pharmacology, Protein Transport drug effects, Rats, Fatty Acids metabolism, Glucose Transporter Type 4 metabolism, Insulin Resistance, Muscles metabolism, Muscles pathology, Signal Transduction drug effects, Sphingolipids metabolism
- Abstract
Ceramides contribute to obesity-linked insulin resistance and inflammation in vivo, but whether this is a cell-autonomous phenomenon is debated, particularly in muscle, which dictates whole-body glucose uptake. We comprehensively analyzed lipid species produced in response to fatty acids and examined the consequence to insulin resistance and pro-inflammatory pathways. L6 myotubes were incubated with BSA-adsorbed palmitate or palmitoleate in the presence of myriocin, fenretinide, or fumonisin B1. Lipid species were determined by lipidomic analysis. Insulin sensitivity was scored by Akt phosphorylation and glucose transporter 4 (GLUT4) translocation, while pro-inflammatory indices were estimated by IκBα degradation and cytokine expression. Palmitate, but not palmitoleate, had mild effects on Akt phosphorylation but significantly inhibited insulin-stimulated GLUT4 translocation and increased expression of pro-inflammatory cytokines Il6 and Ccl2 Ceramides, hexosylceramides, and sphingosine-1-phosphate significantly heightened by palmitate correlated negatively with insulin sensitivity and positively with pro-inflammatory indices. Inhibition of sphingolipid pathways led to marked changes in cellular lipids, but did not prevent palmitate-induced impairment of insulin-stimulated GLUT4 translocation, suggesting that palmitate-induced accumulation of deleterious lipids and insulin resistance are correlated but independent events in myotubes. We propose that muscle cell-endogenous ceramide production does not evoke insulin resistance and that deleterious effects of ceramides in vivo may arise through ancillary cell communication., (Copyright © 2018 by the American Society for Biochemistry and Molecular Biology, Inc.)
- Published
- 2018
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26. Update on GLUT4 Vesicle Traffic: A Cornerstone of Insulin Action.
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Jaldin-Fincati JR, Pavarotti M, Frendo-Cumbo S, Bilan PJ, and Klip A
- Subjects
- Animals, Cytoplasmic Vesicles drug effects, Humans, Insulin pharmacology, Mice, Protein Transport drug effects, Cytoplasmic Vesicles metabolism, Glucose Transporter Type 4 metabolism, Insulin physiology
- Abstract
Glucose transport is rate limiting for dietary glucose utilization by muscle and fat. The glucose transporter GLUT4 is dynamically sorted and retained intracellularly and redistributes to the plasma membrane (PM) by insulin-regulated vesicular traffic, or 'GLUT4 translocation'. Here we emphasize recent findings in GLUT4 translocation research. The application of total internal reflection fluorescence microscopy (TIRFM) has increased our understanding of insulin-regulated events beneath the PM, such as vesicle tethering and membrane fusion. We describe recent findings on Akt-targeted Rab GTPase-activating proteins (GAPs) (TBC1D1, TBC1D4, TBC1D13) and downstream Rab GTPases (Rab8a, Rab10, Rab13, Rab14, and their effectors) along with the input of Rac1 and actin filaments, molecular motors [myosinVa (MyoVa), myosin1c (Myo1c), myosinIIA (MyoIIA)], and membrane fusion regulators (syntaxin4, munc18c, Doc2b). Collectively these findings reveal novel events in insulin-regulated GLUT4 traffic., (Copyright © 2017 Elsevier Ltd. All rights reserved.)
- Published
- 2017
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27. Searching for and Sharing Research in the Information Age: A Trainee's Perspective.
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Frendo-Cumbo S and Chan KL
- Subjects
- Humans, Information Dissemination, Research, Science in Literature, Social Media
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- 2017
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28. Combined high-fat-resveratrol diet and RIP140 knockout mice reveal a novel relationship between elevated bone mitochondrial content and compromised bone microarchitecture, bone mineral mass, and bone strength in the tibia.
- Author
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Miotto PM, Frendo-Cumbo S, Sacco SM, Wright DC, Ward WE, and Holloway GP
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- Adaptor Proteins, Signal Transducing genetics, Animals, Body Weight drug effects, Bone Density drug effects, Bone Resorption drug therapy, Male, Mice, Inbred C57BL, Mice, Knockout, Mitochondria metabolism, Nuclear Proteins genetics, Nuclear Receptor Interacting Protein 1, Osteoclasts drug effects, Osteoclasts metabolism, RANK Ligand metabolism, Resveratrol, Tibia physiology, Tibia ultrastructure, Diet, High-Fat adverse effects, Mitochondria drug effects, Stilbenes pharmacology, Tibia drug effects
- Abstract
Scope: While resveratrol (RSV) is associated with the prevention of high-fat (HF) diet-induced insulin resistance, the effects on bone health combined with an HF-diet is unknown. Therefore, we determined the effect of RSV on bone microarchitecture in the presence of an HF-diet, while also elucidating molecular adaptations within bone that could contribute to bone health status., Methods and Results: Male C57BL6 mice were provided control (10% fat) or HF-diet (60% fat) in the presence or absence of RSV for 12 weeks. While RSV prevented HF diet-induced glucose intolerance, HF-RSV compromised tibial microarchitecture, mineral mass, and strength. The compromised outcomes following HF-RSV corresponded with higher markers of osteoclast-activation and bone-resorption (decreased OPG/RANKL ratio; increased cathepsin K), as well as higher markers of tibial mitochondrial content. A molecular model of elevated mitochondrial content (RIP140 knock out (KO) mice) was utilized to determine proof-of-principle that increasing mitochondrial content coincides with decrements in bone health. RIP140 KO mice displayed higher markers of mitochondrial content, and similar to HF-RSV, had compromised bone microarchitecture, lower BMD/strength, and higher markers of osteoclast-activation/bone-resorption., Conclusion: These data show that in the presence of an HF-diet, RSV negatively alters bone health, a process associated with increased mitochondrial content and markers of bone resorption., (© 2016 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.)
- Published
- 2016
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29. Beneficial effects of combined resveratrol and metformin therapy in treating diet-induced insulin resistance.
- Author
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Frendo-Cumbo S, MacPherson RE, and Wright DC
- Subjects
- Adiposity, Animals, Blood Glucose metabolism, Drug Therapy, Combination, Inflammation Mediators metabolism, Male, Mice, Mice, Inbred C57BL, Oncogene Protein v-akt metabolism, Organ Specificity, Resveratrol, Diet, High-Fat adverse effects, Insulin Resistance, Metformin administration & dosage, Stilbenes administration & dosage
- Abstract
The polyphenol compound resveratrol (RSV) has attracted attention due to its reputed beneficial effects on insulin sensitivity. Our lab has previously identified protective effects of RSV against the development of type 2 diabetes in rats. These effects occurred in a manner similar to thiazolidinedione's (TZDs), a class of insulin sensitizing drugs. TZDs are commonly prescribed in combination with metformin (MET) and thus we sought to examine the combined effects of RSV and MET in treating insulin resistance. Male C57BL6 mice were fed a low- (LFD; 10% Kcal from fat) or high-fat diet (HFD; 60% Kcal from fat) for 9 weeks to induce glucose and insulin intolerance. HFD mice were then assigned to control (HFD), MET (231.28 ± 12.24 mg/kg/day), RSV (93.68 ± 3.51 mg/kg/day), or combined (COM; MET 232.01 ± 17.12 mg/kg/day and RSV 92.77 ± 6.92 mg/kg/day) treatment groups. Changes in glucose and insulin tolerance and tissue-specific insulin signaling were measured 4 weeks post-treatment. RSV or MET alone did not have beneficial effects on glucose tolerance, although MET significantly improved insulin tolerance compared to HFD Glucose and insulin tolerance were significantly improved in COM compared to HFD and this was mirrored by enhanced insulin-stimulated AKT phosphorylation in triceps muscle and inguinal subcutaneous adipose tissue in COM compared to HFD mice. Improvements with COM treatment were not explained by differences in body weight, adiposity, or markers of adipose tissue inflammation. In summary, this study provides evidence of beneficial effects of combined RSV and MET therapy in treating impairments in glucose homeostasis., (© 2016 The Authors. Physiological Reports published by Wiley Periodicals, Inc. on behalf of the American Physiological Society and The Physiological Society.)
- Published
- 2016
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30. Prior exercise training blunts short-term high-fat diet-induced weight gain.
- Author
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Snook LA, MacPherson RE, Monaco CM, Frendo-Cumbo S, Castellani L, Peppler WT, Anderson ZG, Buzelle SL, LeBlanc PJ, Holloway GP, and Wright DC
- Subjects
- Animals, Glucose pharmacokinetics, Glucose Tolerance Test, Male, Mice, Mice, Inbred C57BL, Diet, High-Fat methods, Dietary Fats pharmacokinetics, Energy Metabolism physiology, Physical Conditioning, Animal methods, Weight Gain physiology
- Abstract
High-fat diets rapidly cause weight gain and glucose intolerance. We sought to determine whether these changes could be mitigated with prior exercise training. Male C57BL/6J mice were exercise-trained by treadmill running (1 h/day, 5 days/wk) for 4 wk. Twenty-four hours after the final bout of exercise, mice were provided with a high-fat diet (HFD; 60% kcal from lard) for 4 days, with no further exercise. In mice fed the HFD prior to exercise training, the results were blunted weight gain, reduced fat mass, and a slight attenuation in glucose intolerance that was mirrored by greater insulin-induced Akt phosphorylation in skeletal muscle compared with sedentary mice fed the HFD. When ad libitum-fed sedentary mice were compared with sedentary high-fat fed mice that were calorie restricted (-30%) to match the weight gain of the previously trained high-fat fed mice, the same attenuated impairments in glucose tolerance were found. Blunted weight gain was associated with a greater capacity to increase energy expenditure in trained compared with sedentary mice when challenged with a HFD. Although mitochondrial enzymes in white adipose tissue and UCP-1 protein content in brown adipose tissue were increased in previously exercised compared with sedentary mice fed a HFD, ex vivo mitochondrial respiration was not increased in either tissue. Our data suggest that prior exercise training attenuates high-fat diet-induced weight gain and glucose intolerance and is associated with a greater ability to increase energy expenditure in response to a high-fat diet., (Copyright © 2016 the American Physiological Society.)
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- 2016
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31. Reduced ATGL-mediated lipolysis attenuates β-adrenergic-induced AMPK signaling, but not the induction of PKA-targeted genes, in adipocytes and adipose tissue.
- Author
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MacPherson RE, Dragos SM, Ramos S, Sutton C, Frendo-Cumbo S, Castellani L, Watt MJ, Perry CG, Mutch DM, and Wright DC
- Subjects
- 3T3-L1 Cells, Adipocytes drug effects, Adipose Tissue drug effects, Adrenergic Agents pharmacology, Adrenergic beta-Agonists pharmacology, Animals, Cell Line, Fatty Acids metabolism, Lipolysis drug effects, Male, Mice, Mice, Inbred C57BL, Mice, Knockout, Phosphorylation drug effects, Phosphorylation physiology, Signal Transduction drug effects, Signal Transduction physiology, AMP-Activated Protein Kinases metabolism, Adipocytes metabolism, Adipose Tissue metabolism, Cyclic AMP-Dependent Protein Kinases metabolism, Lipase metabolism, Lipolysis physiology
- Abstract
5'-AMP-activated protein kinase (AMPK) is activated as a consequence of lipolysis and has been shown to play a role in regulation of adipose tissue mitochondrial content. Conversely, the inhibition of lipolysis has been reported to potentiate the induction of protein kinase A (PKA)-targeted genes involved in the regulation of oxidative metabolism. The purpose of the current study was to address these apparent discrepancies and to more fully examine the relationship between lipolysis, AMPK, and the β-adrenergic-mediated regulation of gene expression. In 3T3-L1 adipocytes, the adipose tissue triglyceride lipase (ATGL) inhibitor ATGListatin attenuated the Thr(172) phosphorylation of AMPK by a β3-adrenergic agonist (CL 316,243) independent of changes in PKA signaling. Similarly, CL 316,243-induced increases in the Thr(172) phosphorylation of AMPK were reduced in adipose tissue from whole body ATGL-deficient mice. Despite reductions in the activation of AMPK, the induction of PKA-targeted genes was intact or, in some cases, increased. Similarly, markers of mitochondrial content and respiration were increased in adipose tissue from ATGL knockout mice independent of changes in the Thr(172) phosphorylation of AMPK. Taken together, our data provide evidence that AMPK is not required for the regulation of adipose tissue oxidative capacity in conditions of reduced fatty acid release., (Copyright © 2016 the American Physiological Society.)
- Published
- 2016
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32. Sarcolipin knockout mice fed a high-fat diet exhibit altered indices of adipose tissue inflammation and remodeling.
- Author
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MacPherson RE, Gamu D, Frendo-Cumbo S, Castellani L, Kwon F, Tupling AR, and Wright DC
- Subjects
- Animals, Epinephrine metabolism, Fatty Acids, Nonesterified metabolism, Glucose Intolerance etiology, Glucose Intolerance physiopathology, Inflammation pathology, Interleukin-1beta metabolism, Interleukin-6 metabolism, Macrophages physiology, Male, Mice, Mice, Inbred C57BL, Mice, Knockout, Obesity etiology, Obesity physiopathology, Suppressor of Cytokine Signaling 3 Protein metabolism, Thermogenesis, Tumor Necrosis Factor-alpha metabolism, Adipose Tissue pathology, Diet, High-Fat adverse effects, Muscle Proteins physiology, Obesity pathology, Proteolipids physiology
- Abstract
Objective: To investigate indices of adipose tissue inflammation and remodeling in high-fat diet (HFD) sarcolipin-knockout (SLN(-) (/-) ) mice. SLN regulates muscle-based nonshivering thermogenesis and is up-regulated with HFD. SLN(-) (/-) mice develop greater diet-induced obesity and glucose intolerance. This is accompanied by increases in circulating catecholamines and fatty acids. Catecholamines and fatty acids play a role in the pathology of adipose tissue inflammation., Methods: Male mice (wild type and SLN(-) (/-) ) were fed a HFD (42% kcal from fat) for 8 weeks., Results: SLN(-) (/-) mice displayed greater obesity and glucose intolerance. This was accompanied by higher circulating epinephrine and nonesterified fatty acids. Epididymal but not inguinal subcutaneous adipose tissue from SLN(-) (/-) mice displayed higher interleukin-6, suppressor of cytokine signaling 3, interleukin-1β, and tumor necrosis factor-α mRNA expression, and this was associated with increased markers of macrophage infiltration (F4/80 expression and crown-like structures) and M1 polarization (higher CD11c expression and CD11c/MGL1). Interestingly, this occurred despite SLN(-) (/-) mice having smaller adipocytes., Conclusions: In conditions of nutrient excess, SLN(-) (/-) mice display depot-specific increases in indices of adipose tissue inflammation and remodeling. This could be a compensatory response to reductions in muscle-based thermogenesis., (© 2016 The Obesity Society.)
- Published
- 2016
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33. Risk prediction of contrast-induced nephropathy by ACEF score in patients undergoing coronary catheterization.
- Author
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Capodanno D, Ministeri M, Dipasqua F, Dalessandro V, Cumbo S, Gargiulo G, and Tamburino C
- Subjects
- Aged, Aged, 80 and over, Creatinine blood, Female, Humans, Incidence, Italy, Logistic Models, Male, Middle Aged, Multivariate Analysis, Odds Ratio, Percutaneous Coronary Intervention, Predictive Value of Tests, ROC Curve, Risk Factors, Severity of Illness Index, Cardiac Catheterization adverse effects, Contrast Media adverse effects, Coronary Angiography adverse effects, Kidney Diseases chemically induced, Kidney Diseases epidemiology
- Abstract
Aims: To explore the ability of the ACEF score to predict the incidence of contrast-induced nephropathy (CIN) in patients undergoing coronary angiography with or without percutaneous coronary intervention., Methods: A total of 706 patients undergoing coronary angiography ± percutaneous coronary intervention (PCI) between March 2011 and October 2011 were analyzed. CIN using different definitions was termed as CINnarrow (rise in serum creatinine ≥0.5 mg/dl) and CINbroad (rise in serum creatinine ≥0.5 mg/dl and/or ≥25% increase in baseline serum creatinine)., Results: The mean ACEF score was 1.5 ± 0.6. Overall incidences of CINnarrow and CINbroad were 5.5% and 13.6%, respectively. There was a significant gradient in the incidence of CINnarrow (2.9%, 3.9%, 10.6% in the I, II, and III tertiles, respectively, P < 0.001) and CINbroad (9.1%, 14.2%, 17.9% in the I, II, and III tertiles, respectively, P = 0.021) across increasing ACEF tertiles. The ACEF score was independently associated with the risk of CINnarrow (adjusted odds ratio [OR] 1.6, 95% confidence interval [CI] 1.0-2.7; P = 0.047). Discrimination was more satisfactory when using the ACEF as a predictor of CINnarrow (c-statistic 0.71, 95% 0.63-0.79)., Conclusion: The ACEF score is an independent and potentially useful predictor of CIN defined as rise in serum creatinine ≥0.5 mg/dl.
- Published
- 2016
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34. Adipose Tissue Insulin Action and IL-6 Signaling after Exercise in Obese Mice.
- Author
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Macpherson RE, Huber JS, Frendo-Cumbo S, Simpson JA, and Wright DC
- Subjects
- Animals, Body Mass Index, Diet, Fat-Restricted, Diet, High-Fat, Insulin Resistance, Interleukin-10 metabolism, MAP Kinase Signaling System physiology, Macrophages metabolism, Male, Mice, Inbred C57BL, Mice, Obese, Running physiology, Adipose Tissue metabolism, Insulin metabolism, Interleukin-6 metabolism, Physical Conditioning, Animal physiology
- Abstract
Introduction: Adipose tissue insulin action is impaired in obesity and is associated with inflammation, macrophage infiltration, and polarization toward a proinflammatory phenotype. Acute exercise can reduce markers of adipose inflammation, including interleukin (IL) 6, in parallel with improvements in insulin action; however, others have provided evidence that IL-6 has anti-inflammatory properties., Purpose: This study aimed to examine the relation between IL-6 signaling, macrophage infiltration, and polarization and insulin action in inguinal fat after acute exercise in obese, insulin-resistant mice., Methods: Male C57BL/6 mice were fed a low-fat diet (10% kcal lard) or a high-fat diet (HFD, 60% kcal lard) for 7 wk and then underwent an acute bout of exercise (2-h treadmill running: 15 m·min, 5% incline)., Results: The HFD resulted in increased body mass, glucose intolerance, and attenuated insulin-induced AKT Thr308 phosphorylation in inguinal fat. This was accompanied by increases in indices of macrophage infiltration (F4/80, CD68, and monocyte chemoattractant protein-1 expression) and polarization toward an M1 phenotype (increased expression of CD11c, CD11c/galactose-type C-type lectin 1, and inducible nitric oxide synthase). Immunofluorescence imaging demonstrated increased F4/80- and CD11c-positive cells with the HFD. Two hours after exercise, the insulin-induced activation of AKT Th308 phosphorylation was recovered in HFD mice. This was accompanied by an upregulation of IL-6 and IL-10 signaling, as demonstrated by increased expression of IL-6, IL-10, and SOCS3 as well as STAT3 phosphorylation. Furthermore, acute exercise resulted in a shift toward reduction in M1 polarization indicated by a decrease in the ratio of CD11c to galactose-type C-type lectin 1 mRNA as well as a decline in F4/80- and CD11c-positive cells., Conclusions: The results suggest a link between exercise-induced increases in IL-6, reductions in indices of M1 macrophages, and increased IL-10, a reputed anti-inflammatory cytokine with insulin-sensitizing properties.
- Published
- 2015
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35. A maternal high fat diet has long-lasting effects on skeletal muscle lipid and PLIN protein content in rat offspring at young adulthood.
- Author
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MacPherson RE, Castelli LM, Miotto PM, Frendo-Cumbo S, Milburn A, Roy BD, LeBlanc PJ, Ward WE, and Peters SJ
- Subjects
- Animals, Female, Lipids analysis, Male, Perilipin-5, Pregnancy, Proteins analysis, Rats metabolism, Triglycerides analysis, Triglycerides metabolism, Diet, High-Fat adverse effects, Lipid Metabolism, Muscle, Skeletal metabolism, Prenatal Exposure Delayed Effects metabolism, Proteins metabolism, Rats growth & development
- Abstract
A maternal high fat diet (HFD) can have adverse effects on skeletal muscle development. Skeletal muscle PLIN proteins (PLIN2, 3 and 5) are thought to play critical roles in lipid metabolism, however effects of HFD on PLIN and lipases (HSL, ATGL, CGI-58) in mothers as well as their offspring have yet to be investigated. The primary objective of this study was to determine whether maternal HFD would influence skeletal muscle lipase and PLIN protein content in offspring at weaning (19 d) and young adulthood (3 mo). Female rats (28 d old, n = 9/group) were fed control (CON, AIN93G, 7% soybean oil) or HFD (AIN93G, 20% lard) for 10 weeks prior to mating and throughout pregnancy and lactation. All offspring were weaned to CON [n = 18/group, 1 female and 1 male pup per litter were studied at weaning (19 d) and 3 mo of age]. There was no effect of sex for the main outcomes measured in plantaris, therefore male and female data was combined. Maternal HFD resulted in higher triacylglycerol content in pups at 3 mo (p < 0.05), as well as in the dams (p = 0.015). Maternal HFD resulted in higher PLIN5 content in pups at weaning and 3 mo (p = 0.05). PLIN2 and PLIN5 content decreased at 3 mo versus weaning (p < 0.001). HFD dams had a higher PLIN3 content (p = 0.016). Diet had no effect on ATGL, CGI-58, or HSL content. In conclusion, exposure to a maternal HFD resulted in higher skeletal muscle lipid and PLIN5 content in plantaris of offspring through to young adulthood.
- Published
- 2015
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36. Aging-associated reductions in lipolytic and mitochondrial proteins in mouse adipose tissue are not rescued by metformin treatment.
- Author
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Mennes E, Dungan CM, Frendo-Cumbo S, Williamson DL, and Wright DC
- Subjects
- AMP-Activated Protein Kinases analysis, Adenosine Monophosphate physiology, Adipose Tissue enzymology, Animals, Blotting, Western, Down-Regulation drug effects, Fatty Acids, Nonesterified blood, Glucose metabolism, Glycerol blood, Homeostasis physiology, Lipase analysis, Male, Mice, Phosphoenolpyruvate Carboxykinase (ATP) analysis, Protein Kinases analysis, Proteins analysis, Sterol Esterase analysis, p38 Mitogen-Activated Protein Kinases analysis, Adipose Tissue chemistry, Aging physiology, Hypoglycemic Agents pharmacology, Metformin pharmacology, Mitochondrial Proteins analysis
- Abstract
Mitochondrial enzyme expression is reduced in adipose tissue from old mice, yet little is known regarding mechanisms that could be mediating, or interventions that could be used, to reverse these changes. The purpose of this study was to examine the relationship between lipolytic and fatty acid reesterification enzymes, 5' adenosine monophosphate-activated protein kinase and mitochondrial proteins in adipose tissue from young versus old mice. A second aim was to determine whether metformin treatment could rescue the age-associated decline in adipose tissue mitochondrial proteins. Approximately 22-month-old male C57BL/6 mice were fed a diet with or without 0.5% metformin for 8 weeks. Compared with young mice (~11 wk of age), the protein content/phosphorylation of hormone-sensitive lipase, adipose tissue triglyceride lipase, and phosphoenolpyruvate carboxykinase were reduced in old mice. This was paralleled by increases in the plasma nonesterified fatty acid:glycerol ratio and reductions in adipose tissue 5' adenosine monophosphate-activated protein kinase activity and select mitochondrial proteins in old mice. There were no differences in these variables when comparing adipose tissue from young and 6-month-old mice. While metformin improved glucose homeostasis, it did not increase 5' adenosine monophosphate-activated protein kinase phosphorylation or mitochondrial enzymes. Our findings demonstrate a co-ordinated down regulation of lipolytic, reesterification, and mitochondrial enzymes in adipose tissue with aging that is unresponsive to metformin treatment., (© The Author 2013. Published by Oxford University Press on behalf of The Gerontological Society of America. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com.)
- Published
- 2014
- Full Text
- View/download PDF
37. Exercise training protects against an acute inflammatory insult in mouse epididymal adipose tissue.
- Author
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Castellani L, Root-Mccaig J, Frendo-Cumbo S, Beaudoin MS, and Wright DC
- Subjects
- Acute Disease, Adiposity immunology, Animals, Humans, Immunologic Factors immunology, Male, Mice, Mice, Inbred C57BL, Treatment Outcome, Adipose Tissue immunology, Cytokines immunology, Epididymitis immunology, Exercise Therapy methods, Panniculitis immunology, Panniculitis prevention & control, Physical Conditioning, Animal methods
- Abstract
Exercise training reduces systemic and adipose tissue inflammation. However, these beneficial effects seem to be largely tied to reductions in adipose tissue mass. The purpose of the present study was to determine if exercise training confers a protective effect against an acute inflammatory challenge. We hypothesized that the induction of inflammatory markers, such as interleukin 6 (IL-6), suppressor of cytokine signaling 3 (SOCS3), and TNF-α by the beta-3 adrenergic agonist CL 316,243 would be reduced in adipose tissue from trained mice and this would be associated with reductions in transient receptor potential cation channel 4 (TRPV4), a protein recently shown to regulate the expression of proinflammatory cytokines. Exercise training (4 wk of treadmill running, 1 h/day, 5 days/wk) increased markers of skeletal muscle mitochondrial content and the induction of PPAR-gamma coactivator 1 alpha in epididymal adipose tissue. The mRNA expression of IL-6, SOCS3, and TNFα were not different in subcutaneous and epididymal adipose tissue from sedentary and trained mice; however, the CL 316,243-mediated induction of these genes was attenuated ∼50% in epididymal adipose tissue from trained mice as were increases in plasma IL-6. The effects of training were not explained by reductions in lipolytic responsiveness, but were associated with decreases in TRPV4 protein content. These results highlight a previously unappreciated anti-inflammatory effect of exercise training on adipose tissue immunometabolism and underscores the value of assessing adipose tissue inflammation in the presence of an inflammatory insult., (Copyright © 2014 the American Physiological Society.)
- Published
- 2014
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38. Volume-to-creatinine clearance ratio in patients undergoing coronary angiography with or without percutaneous coronary intervention: implications of varying definitions of contrast-induced nephropathy.
- Author
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Capodanno D, Ministeri M, Cumbo S, Dalessandro V, and Tamburino C
- Subjects
- Aged, Aged, 80 and over, Biomarkers blood, Coronary Artery Disease blood, Female, Humans, Kidney Diseases blood, Kidney Diseases diagnosis, Logistic Models, Male, Middle Aged, Multivariate Analysis, Odds Ratio, Predictive Value of Tests, Risk Factors, Time Factors, Treatment Outcome, Up-Regulation, Contrast Media adverse effects, Coronary Angiography adverse effects, Coronary Artery Disease diagnostic imaging, Coronary Artery Disease therapy, Coronary Vessels diagnostic imaging, Creatinine blood, Kidney Diseases chemically induced, Percutaneous Coronary Intervention adverse effects, Terminology as Topic
- Abstract
Objectives: Whether predicting the risk of early serum creatinine rise using the ratio of the volume of contrast media administered to the estimated creatinine clearance (V/CrCl) is applicable to the broader definition of contrast-induced nephropathy (CIN) (≥0.5 mg/dL absolute and/or 25% relative increase from baseline serum creatinine) is unknown., Background: A V/CrCl ≥4 has been proven to predict the risk of ≥0.5 mg/dL postprocedural absolute rise in serum creatinine., Methods: A total of 722 patients undergoing coronary angiography ± percutaneous coronary intervention (PCI) between March 2011 and October 2011 with paired serum creatinine determinations at preprocedure and within 72-hr postprocedure were analyzed. The V/CrCl ratio was calculated by dividing the volume of contrast received by the patient's creatinine clearance. CIN using different definitions was termed as CINnarrow (rise in serum creatinine ≥0.5 mg/dL) and CINbroad (rise in serum creatinine ≥0.5 mg/dL and/or ≥25% increase in baseline serum creatinine)., Results: The mean age was 66 ± 11 years and the mean baseline serum creatinine was 1.1 ± 0.8 mg/dL. Patients with V/CrCl ≥4 were significantly older and more frequently underwent ad hoc PCI compared with those with V/CrCl <4. CINnarrow and CINbroad were observed in 13 versus 3% (P < 0.001) and 23 versus 11% (P < 0.001) of patients with or without V/CrCl ≥4, respectively. After statistical adjustment, a V/CrCl ratio ≥4 remained significantly associated with the risk of both CINnarrow [adjusted OR 3.5, 95% confidence intervals (95% CI) 1.7-7.3; P < 0.001] and CINbroad (adjusted OR 2.5, 95% 1.6-3.9; P < 0.001)., Conclusions: A volume-to-creatinine clearance ratio ≥4 significantly predicts the risk of early postprocedural rise in serum creatinine regardless of the CIN definition adopted., (Copyright © 2013 Wiley Periodicals, Inc.)
- Published
- 2014
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39. IL-6 and epinephrine have divergent fiber type effects on intramuscular lipolysis.
- Author
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Macdonald TL, Wan Z, Frendo-Cumbo S, Dyck DJ, and Wright DC
- Subjects
- 1-Acylglycerol-3-Phosphate O-Acyltransferase metabolism, AMP-Activated Protein Kinases metabolism, Animals, Glycerol metabolism, Glycolysis, Interleukin-6 deficiency, Interleukin-6 genetics, Interleukin-6 pharmacology, Lipase metabolism, Male, Mice, Mice, Inbred C57BL, Mice, Knockout, Muscle Fibers, Skeletal metabolism, Oxidation-Reduction, Phenotype, Phosphorylation, Recombinant Proteins pharmacology, STAT3 Transcription Factor metabolism, Signal Transduction drug effects, Time Factors, Epinephrine pharmacology, Interleukin-6 metabolism, Lipolysis drug effects, Muscle Fibers, Skeletal drug effects
- Abstract
IL-6 is an exercise-regulated myokine that has been suggested to increase lipolysis in fast-twitch skeletal muscle. However, it is not known if a similar effect is present in slow-twitch muscle. Furthermore, epinephrine increases IL-6 secretion from skeletal muscle, suggesting that IL-6 could play a role in mediating the lipolytic effects of catecholamines. The purpose of this study was to determine whether IL-6 stimulates skeletal muscle lipolysis in a fiber type dependent manner and is required for epinephrine-stimulated lipolysis in murine skeletal muscle. Soleus and extensor digitorum longus (EDL) muscles from male C57BL/6J wild-type and IL-6(-/-) mice were incubated with 1 μM (183 ng/ml) epinephrine or 75 ng/ml recombinant IL-6 (rIL-6) for 60 min. IL-6 treatment increased 5'-AMP-activated protein kinase and signal transducer and activator of transcription 3 phosphorylation and glycerol release in isolated EDL but not soleus muscles from C57BL/6J mice. Conversely, epinephrine increased glycerol release in soleus but not EDL muscles from C57BL/6J mice. Basal lipolysis was elevated in soleus muscle from IL-6(-/-) mice, and this was associated with increases in adipose triglyceride lipase (ATGL) and its coactivator comparative gene identification-58 (CGI-58). The increase in ATGL content does not appear to be due to a loss of IL-6's direct effects, because ex vivo treatment with IL-6 failed to alter the expression of ATGL mRNA in soleus muscle. In summary, IL-6 stimulates lipolysis in glycolytic but not oxidative muscle, whereas the opposite fiber type effect is seen with epinephrine. The absence of IL-6 indirectly upregulates lipolysis, and this is associated with increases in ATGL and its coactivator CGI-58.
- Published
- 2013
- Full Text
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40. [Cystic lymphangioma of the mediastinum. A case complicated by chylothorax and diagnosed by lymphography (author's transl)].
- Author
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Pedicelli G, Daddi G, Cumbo S, Alessi G, and Ingianna O
- Subjects
- Adult, Humans, Lymphangioma complications, Lymphography, Male, Mediastinal Neoplasms complications, Chylothorax etiology, Lymphangioma diagnostic imaging, Mediastinal Neoplasms diagnostic imaging
- Published
- 1980
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