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6. No evidence of brown adipose tissue activation after 24 weeks of supervised exercise training in young sedentary adults in the ACTIBATE randomized controlled trial

Author

Martinez-Tellez, Borja, Sanchez-Delgado, Guillermo, Acosta, Francisco M., Alcantara, Juan M. A., Amaro-Gahete, Francisco J., Martinez-Avila, Wendy D., Merchan-Ramirez, Elisa, Muñoz-Hernandez, Victoria, Osuna-Prieto, Francisco J., Jurado-Fasoli, Lucas, Xu, Huiwen, Ortiz-Alvarez, Lourdes, Arias-Tellez, María J., Mendez-Gutierrez, Andrea, Labayen, Idoia, Ortega, Francisco B., Schönke, Milena, Rensen, Patrick C. N., Aguilera, Concepción M., Llamas-Elvira, José M., Gil, Ángel, and Ruiz, Jonatan R.

Published
2022
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9. Microglia-specific knock-down of Bmal1 improves memory and protects mice from high fat diet-induced obesity

Author

Wang, Xiao-Lan, Kooijman, Sander, Gao, Yuanqing, Tzeplaeff, Laura, Cosquer, Brigitte, Milanova, Irina, Wolff, Samantha E. C., Korpel, Nikita, Champy, Marie-France, Petit-Demoulière, Benoit, Goncalves Da Cruz, Isabelle, Sorg-Guss, Tania, Rensen, Patrick C. N., Cassel, Jean-Christophe, Kalsbeek, Andries, Boutillier, Anne-Laurence, and Yi, Chun-Xia

Published
2021
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12. Immunoproteasomal Inhibition With ONX-0914 Attenuates Atherosclerosis and Reduces White Adipose Tissue Mass and Metabolic Syndrome in Mice.

Author

Schaftenaar, Frank H., van Dam, Andrea D., de Bruin, Gerjan, Depuydt, Marie A. C., de Mol, Jill, Amersfoort, Jacob, Douna, Hidde, Meijer, Menno, Kröner, Mara J., van Santbrink, Peter J., Bernabé Kleijn, Mireia N. A., van Puijvelde, Gijs H. M., Florea, Bogdan I., Slütter, Bram, Foks, Amanda C., Bot, Ilze, Rensen, Patrick C. N., and Kuiper, Johan

Published
2024
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13. Higher Plasma Levels of Endocannabinoids and Analogues Correlate With a Worse Cardiometabolic Profile in Young Adults.

Author

Di, Xinyu, Martinez-Tellez, Borja, Krekels, Elke H J, Jurado-Fasoli, Lucas, Osuna-Prieto, Francisco J, Ortiz-Alvarez, Lourdes, Hankemeier, Thomas, Rensen, Patrick C N, Ruiz, Jonatan R, and Kohler, Isabelle

Subjects
HEART metabolism disorders, CANNABINOIDS, BODY composition
Abstract

Context The endocannabinoid system (ECS) is a signaling system composed of endocannabinoids (eCBs), their receptors, and the enzymes involved in their synthesis and metabolism. Alterations in the ECS are linked to the development of cardiometabolic diseases. Objective Here, we investigated the relationship between plasma levels of eCBs and their analogues with body composition and cardiometabolic risk factors. Methods The study included 133 young adults (age 22.1 ± 2.2 years, 67% women). Fasting plasma levels of eCBs and their analogues were measured using liquid chromatography-tandem mass spectrometry. Body composition, brown adipose tissue (BAT) volume, glucose uptake, and traditional cardiometabolic risk factors were measured. Results Plasma levels of eCBs and several eCB analogues were positively correlated with adiposity and traditional cardiometabolic risk factors (eg, serum insulin and triacylglyceride levels, all r ≥ 0.17 and P ≤.045). Plasma levels of 2-arachidonoyl glycerol and N-pentadecenoylethanolamine were negatively correlated with BAT volume and glucose uptake (all r ≤ −0.17 and P ≤.047). We observed that the plasma levels of eCBs and their analogues were higher in metabolically unhealthy overweight–obese participants than in metabolically healthy overweight–obese participants. Conclusion Our findings show that the plasma levels of eCBs and their analogues are related to higher levels of adiposity and worse cardiometabolic profile. [ABSTRACT FROM AUTHOR]

Published
2024
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14. Fasting mimicking diet in diabetic mice partially preserves glomerular endothelial glycocalyx coverage, without changing the diabetic metabolic environment.

Author

van der Velden, Anouk I. M., Koudijs, Angela, Kooijman, Sander, Rietjens, Rosalie G. J., Sol, Wendy M. P. J., Avramut, M. Cristina, Gangqi Wang, Rensen, Patrick C. N., Rabelink, Ton J., van der Vlag, Johan, and van den Berg, Bernard M.

Subjects
GLYCOCALYX, LEAN body mass, FATTY acid oxidation, INTERMITTENT fasting, ADIPOSE tissues
Abstract

Intermittent fasting has become of interest for its possible metabolic benefits and reduction of inflammation and oxidative damage, all of which play a role in the pathophysiology of diabetic nephropathy. We tested in a streptozotocin (60 mg/kg)-induced diabetic apolipoprotein E knockout mouse model whether repeated fasting mimicking diet (FMD) prevents glomerular damage. Diabetic mice received 5 FMD cycles in 10 wk, and during cycles 1 and 5 caloric measurements were performed. After 10 wk, glomerular endothelial morphology was determined together with albuminuria, urinary heparanase-1 activity, and spatial mass spectrometry imaging to identify specific glomerular metabolic dysregulation. During FMD cycles, blood glucose levels dropped while a temporal metabolic switch was observed to increase fatty acid oxidation. Overall body weight at the end of the study was reduced together with albuminuria, although urine production was dramatically increased without affecting urinary heparanase-1 activity. Weight loss was found to be due to lean mass and water, not fat mass. Although capillary loop morphology and endothelial glycocalyx heparan sulfate contents were preserved, hyaluronan surface expression was reduced together with the presence of UDP-glucuronic acid. Mass spectrometry imaging further revealed reduced protein catabolic breakdown products and increased oxidative stress, not different from diabetic mice. In conclusion, although FMD preserves partially glomerular endothelial glycocalyx, loss of lean mass and increased glomerular oxidative stress argue whether such diet regimes are safe in patients with diabetes. [ABSTRACT FROM AUTHOR]

Published
2024
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15. Ethnic Disparities in Lipid Metabolism and Clinical Outcomes between Dutch South Asians and Dutch White Caucasians with Type 2 Diabetes Mellitus

Author

Yuan, Lushun, primary, Verhoeven, Aswin, additional, Blomberg, Niek, additional, van Eyk, Huub J., additional, Bizino, Maurice B., additional, Rensen, Patrick C. N., additional, Jazet, Ingrid M., additional, Lamb, Hildo J., additional, Rabelink, Ton J., additional, Giera, Martin, additional, and van den Berg, Bernard M., additional

Published
2024
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19. Elevated plasma succinate levels are linked to higher cardiovascular disease risk factors in young adults

Author

Osuna-Prieto, Francisco J., Martinez-Tellez, Borja, Ortiz-Alvarez, Lourdes, Di, Xinyu, Jurado-Fasoli, Lucas, Xu, Huiwen, Ceperuelo-Mallafré, Victoria, Núñez-Roa, Catalina, Kohler, Isabelle, Segura-Carretero, Antonio, García-Lario, José V., Gil, Angel, Aguilera, Concepción M., Llamas-Elvira, Jose M., Rensen, Patrick C. N., Vendrell, Joan, Ruiz, Jonatan R., and Fernández-Veledo, Sonia

Published
2021
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20. Investigating the relationships between unfavourable habitual sleep and metabolomic traits: evidence from multi-cohort multivariable regression and Mendelian randomization analyses

Author

Bos, Maxime M., Goulding, Neil J., Lee, Matthew A., Hofman, Amy, Bot, Mariska, Pool, René, Vijfhuizen, Lisanne S., Zhang, Xiang, Li, Chihua, Mustafa, Rima, Neville, Matt J., Li-Gao, Ruifang, Trompet, Stella, Beekman, Marian, Biermasz, Nienke R., Boomsma, Dorret I., de Boer, Irene, Christodoulides, Constantinos, Dehghan, Abbas, van Dijk, Ko Willems, Ford, Ian, Ghanbari, Mohsen, Heijmans, Bastiaan T., Ikram, M. Arfan, Jukema, J. Wouter, Mook-Kanamori, Dennis O., Karpe, Fredrik, Luik, Annemarie I., Lumey, L. H., van den Maagdenberg, Arn M. J. M., Mooijaart, Simon P., de Mutsert, Renée, Penninx, Brenda W. J. H., Rensen, Patrick C. N., Richmond, Rebecca C., Rosendaal, Frits R., Sattar, Naveed, Schoevers, Robert A., Slagboom, P. Eline, Terwindt, Gisela M., Thesing, Carisha S., Wade, Kaitlin H., Wijsman, Carolien A., Willemsen, Gonneke, Zwinderman, Aeilko H., van Heemst, Diana, Noordam, Raymond, and Lawlor, Deborah A.

Published
2021
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26. Effect of sitagliptin on energy metabolism and brown adipose tissue in overweight individuals with prediabetes: a randomised placebo-controlled trial

Author

Nahon, Kimberly J., Doornink, Fleur, Straat, Maaike E., Botani, Kani, Martinez-Tellez, Borja, Abreu-Vieira, Gustavo, van Klinken, Jan B., Voortman, Gardi J., Friesema, Edith C. H., Ruiz, Jonatan R., van Velden, Floris H. P., de Geus-Oei, Lioe-Fee, Smit, Frits, Pereira Arias-Bouda, Lenka M., Berbée, Jimmy F. P., Jazet, Ingrid M., Boon, Mariëtte R., and Rensen, Patrick C. N.

Published
2018
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27. Inhibition of DHCR24 activates LXRα to ameliorate hepatic steatosis and inflammation

Author

Zhou, Enchen, primary, Ge, Xiaoke, additional, Nakashima, Hiroyuki, additional, Li, Rumei, additional, van der Zande, Hendrik J P, additional, Liu, Cong, additional, Li, Zhuang, additional, Müller, Christoph, additional, Bracher, Franz, additional, Mohammed, Yassene, additional, de Boer, Jan Freark, additional, Kuipers, Folkert, additional, Guigas, Bruno, additional, Glass, Christopher K, additional, Rensen, Patrick C N, additional, Giera, Martin, additional, and Wang, Yanan, additional

Published
2023
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28. Altered high‐density lipoprotein composition is associated with risk for complications in type 2 diabetes mellitus in South Asian descendants: A cross‐sectional, case‐control study on lipoprotein subclass profiling

Author

Yuan, Lushun, primary, Li‐Gao, Ruifang, additional, Verhoeven, Aswin, additional, van Eyk, Huub J., additional, Bizino, Maurice B., additional, Rensen, Patrick C. N., additional, Giera, Martin, additional, Jazet, Ingrid M., additional, Lamb, Hildo J., additional, Rabelink, Ton J., additional, and van den Berg, Bernard M., additional

Published
2023
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30. Multi-ancestry sleep-by-SNP interaction analysis in 126,926 individuals reveals lipid loci stratified by sleep duration

Author

Noordam, Raymond, Bos, Maxime M., Wang, Heming, Winkler, Thomas W., Bentley, Amy R., Kilpeläinen, Tuomas O., de Vries, Paul S., Sung, Yun Ju, Schwander, Karen, Cade, Brian E., Manning, Alisa, Aschard, Hugues, Brown, Michael R., Chen, Han, Franceschini, Nora, Musani, Solomon K., Richard, Melissa, Vojinovic, Dina, Aslibekyan, Stella, Bartz, Traci M., de las Fuentes, Lisa, Feitosa, Mary, Horimoto, Andrea R., Ilkov, Marjan, Kho, Minjung, Kraja, Aldi, Li, Changwei, Lim, Elise, Liu, Yongmei, Mook-Kanamori, Dennis O., Rankinen, Tuomo, Tajuddin, Salman M., van der Spek, Ashley, Wang, Zhe, Marten, Jonathan, Laville, Vincent, Alver, Maris, Evangelou, Evangelos, Graff, Maria E., He, Meian, Kühnel, Brigitte, Lyytikäinen, Leo-Pekka, Marques-Vidal, Pedro, Nolte, Ilja M., Palmer, Nicholette D., Rauramaa, Rainer, Shu, Xiao-Ou, Snieder, Harold, Weiss, Stefan, Wen, Wanqing, Yanek, Lisa R., Adolfo, Correa, Ballantyne, Christie, Bielak, Larry, Biermasz, Nienke R., Boerwinkle, Eric, Dimou, Niki, Eiriksdottir, Gudny, Gao, Chuan, Gharib, Sina A., Gottlieb, Daniel J., Haba-Rubio, José, Harris, Tamara B., Heikkinen, Sami, Heinzer, Raphaël, Hixson, James E., Homuth, Georg, Ikram, M. Arfan, Komulainen, Pirjo, Krieger, Jose E., Lee, Jiwon, Liu, Jingmin, Lohman, Kurt K., Luik, Annemarie I., Mägi, Reedik, Martin, Lisa W., Meitinger, Thomas, Metspalu, Andres, Milaneschi, Yuri, Nalls, Mike A., O’Connell, Jeff, Peters, Annette, Peyser, Patricia, Raitakari, Olli T., Reiner, Alex P., Rensen, Patrick C. N., Rice, Treva K., Rich, Stephen S., Roenneberg, Till, Rotter, Jerome I., Schreiner, Pamela J., Shikany, James, Sidney, Stephen S., Sims, Mario, Sitlani, Colleen M., Sofer, Tamar, Strauch, Konstantin, Swertz, Morris A., Taylor, Kent D., Uitterlinden, André G., van Duijn, Cornelia M., Völzke, Henry, Waldenberger, Melanie, Wallance, Robert B., van Dijk, Ko Willems, Yu, Caizheng, Zonderman, Alan B., Becker, Diane M., Elliott, Paul, Esko, Tõnu, Gieger, Christian, Grabe, Hans J., Lakka, Timo A., Lehtimäki, Terho, North, Kari E., Penninx, Brenda W. J. H., Vollenweider, Peter, Wagenknecht, Lynne E., Wu, Tangchun, Xiang, Yong-Bing, Zheng, Wei, Arnett, Donna K., Bouchard, Claude, Evans, Michele K., Gudnason, Vilmundur, Kardia, Sharon, Kelly, Tanika N., Kritchevsky, Stephen B., Loos, Ruth J. F., Pereira, Alexandre C., Province, Mike, Psaty, Bruce M., Rotimi, Charles, Zhu, Xiaofeng, Amin, Najaf, Cupples, L. Adrienne, Fornage, Myriam, Fox, Ervin F., Guo, Xiuqing, Gauderman, W. James, Rice, Kenneth, Kooperberg, Charles, Munroe, Patricia B., Liu, Ching-Ti, Morrison, Alanna C., Rao, Dabeeru C., van Heemst, Diana, and Redline, Susan

Published
2019
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31. Glucocorticoid Receptor Antagonism Improves Glucose Metabolism in a Mouse Model of Polycystic Ovary Syndrome.

Author

Li, Sheng, Ying, Zhixiong, Gentenaar, Max, Rensen, Patrick C N, Kooijman, Sander, Visser, Jenny A, Meijer, Onno C, and Kroon, Jan

Subjects
POLYCYSTIC ovary syndrome, GLUCOCORTICOID receptors, GLUCOSE metabolism, METABOLIC models, ANDROGEN receptors, HYPERGLYCEMIA
Abstract

Context Polycystic ovary syndrome (PCOS) is a complex metabolic disorder associated with obesity, insulin resistance, and dyslipidemia. Hyperandrogenism is a major characteristic of PCOS. Increased androgen exposure is believed to deregulate metabolic processes in various tissues as part of the PCOS pathogenesis, predominantly through the androgen receptor (AR). Notably, various metabolic features in PCOS are similar to those observed after excess glucocorticoid exposure. Objective We hypothesized that glucocorticoid receptor (GR) signaling is involved in the metabolic symptoms of PCOS. Methods In a PCOS model of chronic dihydrotestosterone (DHT) exposure in female mice, we investigated whether GR signaling machinery was (de)regulated, and if treatment with a selective GR antagonist alleviated the metabolic symptoms. Results We observed an upregulation of GR messenger RNA expression in the liver after DHT exposure. In white adipose tissues and liver we found that DHT upregulated Hsd11b1 , which encodes for the enzyme that converts inactive into active glucocorticoids. We found that preventive but not therapeutic administration of a GR antagonist alleviated DHT-induced hyperglycemia and restored glucose tolerance. We did not observe strong effects of GR antagonism in DHT-exposed mice on other features like total fat mass and lipid accumulation in various tissues. Conclusion We conclude that GR activation may play a role in glucose metabolism in DHT-exposed mice. [ABSTRACT FROM AUTHOR]

Published
2024
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33. Adipocytes control hematopoiesis and inflammation through CD40 signaling

Author

Reiche, Myrthe E., Poels, Kikkie, Bosmans, Laura A., Vos, Winnie G., van Tiel, Claudia M., Gijbels, Marion J. J., Aarts, Suzanne A. B. M., den Toom, Myrthe, Beckers, Linda, Weber, Christian, Atzler, Dorothee, Rensen, Patrick C. N., Kooijman, Sander, Lutgens, Esther, Reiche, Myrthe E., Poels, Kikkie, Bosmans, Laura A., Vos, Winnie G., van Tiel, Claudia M., Gijbels, Marion J. J., Aarts, Suzanne A. B. M., den Toom, Myrthe, Beckers, Linda, Weber, Christian, Atzler, Dorothee, Rensen, Patrick C. N., Kooijman, Sander, and Lutgens, Esther

Abstract

The co-stimulatory CD40-CD40L dyad plays an important role in chronic inflammatory diseases associated with aging. Although CD40 is mainly expressed by immune cells, CD40 is also present on adipocytes. We aimed to delineate the role of adipocyte CD40 in the aging hematopoietic system and evaluated the effects of adipocyte CD40 deficiency on cardiometabolic diseases. Adult adipocyte CD40-deficient mice (AdiCD40KO) mice had a decrease in bone marrow hematopoietic stem cells (Lin-Sca+cKit+, LSK) and common lymphoid progenitors, which was associated with increased bone marrow adiposity and T-cell activation, along with elevated plasma corticosterone levels, a phenotype that became more pronounced with age. Atherosclerotic AdiCD40koApoE-/- (CD40AKO) mice also displayed changes in the LSK population, showing increased myeloid and lymphoid multipotent progenitors, and augmented corticosterone levels. Increased T-cell activation could be observed in bone marrow, spleen, and adipose tissue, while the numbers of B cells were decreased. Although atherosclerosis was reduced in CD40AKO mice, plaques contained more activated T cells and larger necrotic cores. Analysis of peripheral adipose tissue in a diet-induced model of obesity revealed that obese AdiCD40KO mice had increased T-cell activation in adipose tissue and lymphoid organs, but decreased weight gain and improved insulin sensitivity, along with increased fat oxidation. In conclusion, adipocyte CD40 plays an important role in maintaining immune cell homeostasis in bone marrow during aging and chronic inflammatory diseases, particularly of the lymphoid populations. Although adipocyte CD40 deficiency reduces atherosclerosis burden and ameliorates diet-induced obesity, the accompanying T-cell activation may eventually aggravate cardiometabolic diseases.

Published
2023
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39. A bout of endurance and resistance exercise transiently decreases plasma levels of bile acids in young, sedentary adults.

Author

Osuna‐Prieto, Francisco J., Jurado‐Fasoli, Lucas, Plaza‐Florido, Abel, Yang, Wei, Kohler, Isabelle, Di, Xinyu, Rubio‐López, José, Sanchez‐Delgado, Guillermo, Rensen, Patrick C. N., Ruiz, Jonatan R., and Martinez‐Tellez, Borja

Subjects
RESISTANCE training, SEDENTARY lifestyles, GRIP strength, HOMEOSTASIS, ENDURANCE sports training, CARDIOPULMONARY fitness, GROWTH factors, LIQUID chromatography, GENETIC disorders, PHYSICAL fitness, BILE acids, EXERCISE, RESEARCH funding, MASS spectrometry, DESCRIPTIVE statistics, GLUCOSE, LIPID metabolism disorders, ADULTS
Abstract

Circulating bile acids (BA) are signaling molecules that control glucose and lipid metabolism. However, the effects of acute exercise on plasma levels of BA in humans remain poorly understood. Here, we evaluate the effects of a bout of maximal endurance exercise (EE) and resistance exercise (RE) on plasma levels of BA in young, sedentary adults. Concentration of eight plasma BA was measured by liquid chromatography–tandem mass spectrometry before and 3, 30, 60, and 120 min after each exercise bout. Cardiorespiratory fitness (CRF) was assessed in 14 young adults (21.8 ± 2.5 yo, 12 women); muscle strength was assessed in 17 young adults (22.4 ± 2.5 yo, 11 women). EE transiently decreased plasma levels of total, primary, and secondary BA at 3 and 30 min after exercise. RE exerted a prolonged reduction in plasma levels of secondary BA (p < 0.001) that lasted until 120 min. Primary BA levels of cholic acid (CA) and chenodeoxycholic acid (CDCA) were different across individuals with low/high CRF levels after EE (p ≤ 0.044); CA levels were different across individuals with low/high handgrip strength levels. High CRF individuals presented higher levels of CA and CDCA 120 min after exercise vs baseline (+77% and +65%) vs the low CRF group (−5% and −39%). High handgrip strength levels individuals presented higher levels of CA 120 min after exercise versus baseline (+63%) versus the low handgrip strength group (+6%). The study findings indicate that an individual's level of physical fitness can influence how circulating BA respond to both endurance and resistance exercise. Additionally, the study suggests that changes in plasma BA levels after exercising could be related to the control of glucose homeostasis in humans. [ABSTRACT FROM AUTHOR]

Published
2023
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40. Circadian disruption impairs glucose homeostasis in male but not in female mice and is dependent on gonadal sex hormones

Author

In het Panhuis, Wietse, primary, Schönke, Milena, additional, Siebeler, Ricky, additional, Banen, Dorien, additional, Pronk, Amanda C. M., additional, Streefland, Trea C. M., additional, Afkir, Salwa, additional, Sips, Hetty C. M., additional, Kroon, Jan, additional, Rensen, Patrick C. N., additional, and Kooijman, Sander, additional

Published
2023
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41. Time to run: Late rather than early exercise training in mice remodels the gut microbiome and reduces atherosclerosis development

Author

Schönke, Milena, primary, Ying, Zhixiong, additional, Kovynev, Artemiy, additional, In het Panhuis, Wietse, additional, Binnendijk, Anne, additional, van der Poel, Sabine, additional, Pronk, Amanda C. M., additional, Streefland, Trea C. M., additional, Hoekstra, Menno, additional, Kooijman, Sander, additional, and Rensen, Patrick C. N., additional

Published
2022
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42. Plasma Levels of Omega-3 and Omega-6 Derived Oxylipins Are Associated with Fecal Microbiota Composition in Young Adults

Author

Xu, Huiwen, primary, Jurado-Fasoli, Lucas, additional, Ortiz-Alvarez, Lourdes, additional, Osuna-Prieto, Francisco J., additional, Kohler, Isabelle, additional, Di, Xinyu, additional, Vilchez-Vargas, Ramiro, additional, Link, Alexander, additional, Plaza-Díaz, Julio, additional, Gil, Angel, additional, Rensen, Patrick C. N., additional, Ruiz, Jonatan R., additional, and Martinez-Tellez, Borja, additional

Published
2022
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43. A Systems Analysis of Phenotype Heterogeneity in APOE*3Leiden.CETP Mice Induced by Long-Term High-Fat High-Cholesterol Diet Feeding

Author

Paalvast, Yared, primary, Zhou, Enchen, additional, Rozendaal, Yvonne J. W., additional, Wang, Yanan, additional, Gerding, Albert, additional, van Dijk, Theo H., additional, de Boer, Jan Freark, additional, Rensen, Patrick C. N., additional, Dijk, Ko Willems van, additional, Kuivenhoven, Jan A., additional, Bakker, Barbara M., additional, van Riel, Natal A. W., additional, and Groen, Albert K., additional

Published
2022
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46. Differences in Inflammatory Pathways Between Dutch South Asians vs Dutch Europids With Type 2 Diabetes

Author

Straat, Maaike E, primary, Martinez-Tellez, Borja, additional, van Eyk, Huub J, additional, Bizino, Maurice B, additional, van Veen, Suzanne, additional, Vianello, Eleonora, additional, Stienstra, Rinke, additional, Ottenhoff, Tom H M, additional, Lamb, Hildo J, additional, Smit, Johannes W A, additional, Jazet, Ingrid M, additional, Rensen, Patrick C N, additional, and Boon, Mariëtte R, additional

Published
2022
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47. Castration of Male Mice Induces Metabolic Remodeling of the Heart

Author

Svedlund Eriksson, Elin, primary, Johansson, Inger, additional, Mårtensson, Anna K F, additional, Lantero Rodriguez, Marta, additional, Schilperoort, Maaike, additional, Kroon, Jan, additional, Kooijman, Sander, additional, Omerovic, Elmir, additional, Andersson, Linda, additional, Levin, Malin C, additional, Rensen, Patrick C N, additional, and Tivesten, Åsa, additional

Published
2022
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49. Dexamethasone-associated metabolic effects in male mice are partially caused by depletion of endogenous corticosterone

Author

Koorneef, Lisa L., primary, van der Meulen, Merel, additional, Kooijman, Sander, additional, Sánchez-López, Elena, additional, Scheerstra, Jari F., additional, Voorhoeve, Maaike C., additional, Ramesh, Ajith N. Nadamuni, additional, Rensen, Patrick C. N., additional, Giera, Martin, additional, Kroon, Jan, additional, and Meijer, Onno C., additional

Published
2022
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