22 results on '"*STRIATED muscle physiology"'
Search Results
2. Skeletal myosin binding protein-C: An increasingly important regulator of striated muscle physiology.
- Author
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McNamara, James W. and Sadayappan, Sakthivel
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CARDIOMYOPATHIES , *MYOSIN , *CARRIER proteins , *STRIATED muscle physiology , *MOLECULAR structure - Abstract
Abstract The Myosin Binding Protein-C (MyBP-C) family is a group of sarcomeric proteins important for striated muscle structure and function. Comprising approximately 2% of the myofilament mass, MyBP-C has important roles in both contraction and relaxation. Three paralogs of MyBP-C are encoded by separate genes with distinct expression profiles in striated muscle. In mammals, cardiac MyBP-C is limited to the heart, and it is the most extensively studied owing to its involvement in cardiomyopathies. However, the roles of two skeletal paralogs, slow and fast, in muscle biology remain poorly characterized. Nonetheless, both have been recently implicated in the development of skeletal myopathies. This calls for a better understanding of their function in the pathophysiology of distal arthrogryposis. This review characterizes MyBP-C as a whole and points out knowledge gaps that still remain with respect to skeletal MyBP-C. [ABSTRACT FROM AUTHOR]
- Published
- 2018
- Full Text
- View/download PDF
3. Editorial: Insights in striated muscle physiology: 2021.
- Author
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Reiser, Peter J. and Janssen, Paul M. L.
- Subjects
MUSCLE physiology ,STRIATED muscle ,CYTOLOGY ,CELL physiology ,CARDIAC hypertrophy - Published
- 2022
- Full Text
- View/download PDF
4. Coupling between myosin head conformation and the thick filament backbone structure.
- Author
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Hu, Zhongjun, Taylor, Dianne W., Edwards, Robert J., and Taylor, Kenneth A.
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MOLECULAR structure of myosin , *CONFORMATIONAL analysis , *STRIATED muscle physiology , *ELECTRON microscopy , *LETHOCERUS - Abstract
The recent high-resolution structure of the thick filament from Lethocerus asynchronous flight muscle shows aspects of thick filament structure never before revealed that may shed some light on how striated muscles function. The phenomenon of stretch activation underlies the function of asynchronous flight muscle. It is most highly developed in flight muscle, but is also observed in other striated muscles such as cardiac muscle. Although stretch activation is likely to be complex, involving more than a single structural aspect of striated muscle, the thick filament itself, would be a prime site for regulatory function because it must bear all of the tension produced by both its associated myosin motors and any externally applied force. Here we show the first structural evidence that the arrangement of myosin heads within the interacting heads motif is coupled to the structure of the thick filament backbone. We find that a change in helical angle of 0.16° disorders the blocked head preferentially within the Lethocerus interacting heads motif. This observation suggests a mechanism for how tension affects the dynamics of the myosin heads leading to a detailed hypothesis for stretch activation and shortening deactivation, in which the blocked head preferentially binds the thin filament followed by the free head when force production occurs. [ABSTRACT FROM AUTHOR]
- Published
- 2017
- Full Text
- View/download PDF
5. Dynamics of regeneration of striated muscles in rats with posttraumatic reflex contractures.
- Author
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Matolych, U. D., Pankevych, V. V., and Ushtan, S. V.
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STRIATED muscle regeneration , *POST-traumatic stress , *MYOBLASTS , *STRIATED muscle physiology , *CONNECTIVE tissues , *PHYSIOLOGY - Abstract
In the comparative aspect the regeneration processes of striated muscles of hind left leg were researched in rats with posttraumatic reflex contractures against the background of physiotherapeutic treatment. Macroscopic and microscopic evaluation of pathomorphological changes has been conducted in this work. A relative area of myogenic elements (striated muscle elements), connective-tissue elements and neovasculature in the muscular-connective tissue in the scar in percentage has been determined using the method of point counting (field method). Depending on the signs of pain behavior (behavioral changes, additional signs), the intensity of myogenic pain syndrome (low, moderate, high, very high) has been studied. It has been established that the use of magnetic-laser therapy led to the formation of muscular-connective tissue scar up to the 28th day with a predominance of a portion of striated muscle tissue of 90.74±0.17%. Behavioral and motor responses became normalized; no pain was observed in 56% of rats, pain intensity was low in 44%. In animals with the same trauma that were not treated, the portion of striated muscle tissue was 37.08±0.34%, and signs of pain of high and moderate intensity were observed. By the 28th day, the animals could brace against their hind limbs while moving, but due to a sharp restriction of the function of the left hind limb, they could not move freely. The obtained results are the basis for developing new approaches to improving the methods of remedial treatment of contractures using magnetic-laser therapy. [ABSTRACT FROM AUTHOR]
- Published
- 2017
- Full Text
- View/download PDF
6. Release of calcium into the myofibrillar space in response to active shortening of striated muscle.
- Author
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Edman, K. A. P. and Caputo, C.
- Subjects
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STRIATED muscle physiology , *MYOFIBRILS , *CALCIUM channels , *TIBIALIS anterior , *SARCOMERES - Abstract
Aim The study was undertaken to explore whether shortening of striated muscle during activity is associated with release of bound Ca2+ into the myofibrillar space as has previously been proposed in order to explain the depressant effect of active shortening. Methods The experiments were carried out on single muscle fibres isolated from the anterior tibialis muscle of Rana temporaria. The fibres were loaded with the calcium sensitive indicator Fluo-3. The fibres, stimulated to produce a partially fused isometric tetanus, were subjected to a shortening ramp or, alternatively, to a stretch ramp during activity while force, fibre length, sarcomere length and the Fluo-3 signal were recorded. Results A shortening ramp performed during a partially fused tetanus caused an increase in the myofibrillar free calcium concentration and produced, simultaneously, a decrease in active force. The isometric force recovered gradually after the shortening ramp, while the intracellular Ca2+ concentration stayed above the control level during the remainder of the stimulation period. A stretch ramp applied during a partially fused tetanus caused a considerably smaller change in the myofibrillar Ca2+ concentration. Conclusion The results provide evidence that the myosin cross-bridges interact with the calcium binding sites on the thin filaments during active shortening, causing sustained release of calcium and reduced contractile strength. [ABSTRACT FROM AUTHOR]
- Published
- 2017
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7. Seasonal changes in proteolytic activity of calpains in striated muscles of long-tailed ground squirrel Spermophilus undulatus.
- Author
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Popova, S., Vikhlyantsev, I., Zakharova, N., Podlubnaya, Z., and Fesenko, E.
- Subjects
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CALPAIN , *PROTEOLYTIC enzymes , *LONG-tailed souslik , *STRIATED muscle physiology , *CASEINS - Abstract
Seasonal changes in proteolytic activity and content of calpains in striated muscles of the longtailed ground squirrel Spermophilus undulatus were studied by casein zymography and Western blotting analysis. The results testify to hyperactivation of calpain proteases in the skeletal muscles of awakened animals during the 'winter' activity. The observed changes are discussed in the context of adaptation of skeletal muscles of long-tailed ground squirrels to hibernation. [ABSTRACT FROM AUTHOR]
- Published
- 2017
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8. The evolutionary origin of bilaterian smooth and striated myocytes.
- Author
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Brunet, Thibaut, Fischer, Antje H. L., Steinmetz, Patrick R. H., Lauri, Antonella, Bertucci, Paola, and Arendt, Detlev
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MUSCLE cells , *STRIATED muscle physiology , *MOLECULAR evolution , *ANNELIDA , *SMOOTH muscle physiology , *GENE expression profiling , *PHYSIOLOGY - Abstract
The dichotomy between smooth and striated myocytes is fundamental for bilaterian musculature, but its evolutionary origin is unsolved. In particular, interrelationships of visceral smooth muscles remain unclear. Absent in fly and nematode, they have not yet been characterized molecularly outside vertebrates. Here, we characterize expression profile, ultrastructure, contractility and innervation of the musculature in the marine annelid Platynereis dumerilii and identify smooth muscles around the midgut, hindgut and heart that resemble their vertebrate counterparts in molecular fingerprint, contraction speed and nervous control. Our data suggest that both visceral smooth and somatic striated myocytes were present in the protostome-deuterostome ancestor and that smooth myocytes later co-opted the striated contractile module repeatedly - for example, in vertebrate heart evolution. During these smooth-to-striated myocyte conversions, the core regulatory complex of transcription factors conveying myocyte identity remained unchanged, reflecting a general principle in cell type evolution. [ABSTRACT FROM AUTHOR]
- Published
- 2016
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9. Modelling Ca2+ bound Troponin in Excitation Contraction Coupling
- Author
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Henry G. Zot and Javier E. Hasbun
- Subjects
Excitation Contraction Coupling ,Troponin ,skeletal muscle ,Calcium regulation ,Models, Theoretical ,striated muscle physiology ,Physiology ,QP1-981 - Abstract
To explain disparate decay rates of cytosolic Ca2+ and structural changes in the thin filaments during a twitch, we model the time course of Ca2+ bound troponin (Tn) resulting from the free Ca2+ transient of fast skeletal muscle. In fibers stretched beyond overlap, the decay of Ca2+ as measured by a change in fluo 3 fluorescence is significantly slower than the intensity decay of the meridional 1/38.5 nm-1 reflection of Tn; this is not simply explained by considering only the Ca2+ binding properties of Tn alone (Matsuo, T., Iwamoto, H., and Yagi, N. (2010). Biophys. J. 99, 193-200). We apply a comprehensive model that includes the known Ca2+ binding properties of Tn in the context of the thin filament with and without cycling crossbridges. Calculations based on the model predict that the transient of Ca2+ bound Tn correlates with either the fluo 3 time course in muscle with overlapping thin and thick filaments or the intensity of the meridional 1/38.5 nm-1 reflection in overstretched muscle. Hence, cycling crossbridges delay the dissociation of Ca2+ from Tn. Correlation with the fluo 3 fluorescence change is not causal given that the transient of Ca2+ bound Tn depends on sarcomere length, whereas the fluo-3 fluorescence change does not. Transient positions of tropomyosin calculated from the time course of Ca2+ bound Tn are in reasonable agreement with the transient of measured perturbations of the Tn repeat in overlap and non-overlap muscle preparations.
- Published
- 2016
- Full Text
- View/download PDF
10. Mitochondria in the middle: exercise preconditioning protection of striated muscle.
- Author
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Lawler, John M., Rodriguez, Dinah A., and Hord, Jeffrey M.
- Subjects
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MITOCHONDRIAL physiology , *CELLULAR signal transduction , *STRIATED muscle physiology , *CELL communication , *GENE expression , *ANTIOXIDANTS - Abstract
Cellular and physiological adaptations to an atmosphere which became enriched in molecular oxygen spurred the development of a layered system of stress protection, including antioxidant and stress response proteins. At physiological levels reactive oxygen and nitrogen species regulate cell signalling as well as intracellular and intercellular communication. Exercise and physical activity confer a variety of stressors on skeletal muscle and the cardiovascular system: mechanical, metabolic, oxidative. Transient increases of stressors during acute bouts of exercise or exercise training stimulate enhancement of cellular stress protection against future insults of oxidative, metabolic and mechanical stressors that could induce injury or disease. This phenomenon has been termed both hormesis and exercise preconditioning (EPC). EPC stimulates transcription factors such as Nrf-1 and heat shock factor-1 and up-regulates gene expression of a cadre of cytosolic (e.g. glutathione peroxidase and heat shock proteins) and mitochondrial adaptive or stress proteins (e.g. manganese superoxide dismutase, mitochondrial KATP channels and peroxisome proliferator activated receptor γ coactivator-1 (PGC-1)). Stress response and antioxidant enzyme inducibility with exercise lead to protection against striated muscle damage, oxidative stress and injury. EPC may indeed provide significant clinical protection against ischaemia-reperfusion injury, Type II diabetes and ageing. New molecular mechanisms of protection, such as δ-opioid receptor regulation and mitophagy, reinforce the notion that mitochondrial adaptations (e.g. heat shock proteins, antioxidant enzymes and sirtuin-1/PGC-1 signalling) are central to the protective effects of exercise preconditioning. [ABSTRACT FROM AUTHOR]
- Published
- 2016
- Full Text
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11. Expression of Muscle-Specific Ribosomal Protein L3-Like Impairs Myotube Growth.
- Author
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Chaillou, Thomas, Zhang, Xiping, and McCarthy, John J.
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GENE expression profiling , *RIBOSOMAL proteins , *MYOGENESIS , *STRIATED muscle physiology , *STIMULUS & response (Biology) , *HETEROGENEITY - Abstract
The ribosome has historically been considered to have no cell-specific function but rather serve in a 'housekeeping' capacity. This view is being challenged by evidence showing that heterogeneity in the protein composition of the ribosome can lead to the functional specialization of the ribosome. Expression profiling of different tissues revealed that ribosomal protein large 3-like ( Rpl3l) is exclusively expressed in striated muscle. In response to a hypertrophic stimulus, Rpl3l expression in skeletal muscle was significantly decreased by 82% whereas expression of the ubiquitous paralog Rpl3 was significantly increased by ∼fivefold. Based on these findings, we developed the hypothesis that Rpl3l functions as a negative regulator of muscle growth. To test this hypothesis, we used the Tet-On system to express Rpl3l in myoblasts during myotube formation. In support of our hypothesis, RPL3L expression significantly impaired myotube growth as assessed by myotube diameter (-23%) and protein content (-14%). Further analysis showed that the basis of this impairment was caused by a significant decrease in myoblast fusion as the fusion index was significantly lower (-17%) with RPL3L expression. These findings are the first evidence to support the novel concept of ribosome specialization in skeletal muscle and its role in the regulation of skeletal muscle growth. J. Cell. Physiol. 231: 1894-1902, 2016. © 2015 Wiley Periodicals, Inc. [ABSTRACT FROM AUTHOR]
- Published
- 2016
- Full Text
- View/download PDF
12. Involvement of catecholaminergic neurons in motor innervation of striated muscle in the mouse esophagus.
- Author
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Keylen, Piet, Garreis, Fabian, Steigleder, Ruth, Sommer, Daniel, Neuhuber, Winfried, and Wörl, Jürgen
- Subjects
- *
CATECHOLAMINES , *STRIATED muscle physiology , *ESOPHAGEAL physiology , *INNERVATION , *MOTOR ability , *NEURONS , *LABORATORY mice - Abstract
Enteric co-innervation is a peculiar innervation pattern of striated esophageal musculature. Both anatomical and functional data on enteric co-innervation related to various transmitters have been collected in different species, although its function remains enigmatic. However, it is unclear whether catecholaminergic components are involved in such a co-innervation. Thus, we examined to identify catecholaminergic neuronal elements and clarify their relationship to other innervation components in the esophagus, using immunohistochemistry with antibodies against tyrosine hydroxylase (TH), vesicular acetylcholine transporter (VAChT), choline acetyltransferase (ChAT) and protein gene product 9.5 (PGP 9.5), α-bungarotoxin (α-BT) and PCR with primers for amplification of cDNA encoding TH and dopamine-β-hydroxylase (DBH). TH-positive nerve fibers were abundant throughout the myenteric plexus and localized on about 14 % of α-BT-labelled motor endplates differing from VAChT-positive vagal nerve terminals. TH-positive perikarya represented a subpopulation of only about 2.8 % of all PGP 9.5-positive myenteric neurons. Analysis of mRNA showed both TH and DBH transcripts in the mouse esophagus. As ChAT-positive neurons in the compact formation of the nucleus ambiguus were negative for TH, the TH-positive nerve varicosities on motor endplates are presumably of enteric origin, although a sympathetic origin cannot be excluded. In the medulla oblongata, the cholinergic ambiguus neurons were densely supplied with TH-positive varicosities. Thus, catecholamines may modulate vagal motor innervation of esophageal-striated muscles not only at the peripheral level via enteric co-innervation but also at the central level via projections to the nucleus ambiguus. As Parkinson's disease, with a loss of central dopaminergic neurons, also affects the enteric nervous system and dysphagia is prevalent in patients with this disease, investigation of intrinsic catecholamines in the esophagus may be worthwhile to understand such a symptom. [ABSTRACT FROM AUTHOR]
- Published
- 2016
- Full Text
- View/download PDF
13. Lessons from mammalian hibernators: molecular insights into striated muscle plasticity and remodeling.
- Author
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Tessier, Shannon N. and Storey, Kenneth B.
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STRIATED muscle physiology , *MAMMAL hibernation , *MUSCULAR atrophy , *HYPERTROPHY , *TISSUE remodeling , *ANTIOXIDANTS , *TRANSCRIPTION factors , *FORKHEAD transcription factors - Abstract
Striated muscle shows an amazing ability to adapt its structural apparatus based on contractile activity, loading conditions, fuel supply, or environmental factors. Studies with mammalian hibernators have identified a variety of molecular pathways which are strategically regulated and allow animals to endure multiple stresses associated with the hibernating season. Of particular interest is the observation that hibernators show little skeletal muscle atrophy despite the profound metabolic rate depression and mechanical unloading that they experience during long weeks of torpor. Additionally, the cardiac muscle of hibernators must adjust to low temperature and reduced perfusion, while the strength of contraction increases in order to pump cold, viscous blood. Consequently, hibernators hold a wealth of knowledge as it pertains to understanding the natural capacity of myocytes to alter structural, contractile and metabolic properties in response to environmental stimuli. The present review outlines the molecular and biochemical mechanisms which play a role in muscular atrophy, hypertrophy, and remodeling. In this capacity, four main networks are highlighted: (1) antioxidant defenses, (2) the regulation of structural, contractile and metabolic proteins, (3) ubiquitin proteosomal machinery, and (4) macroautophagy pathways. Subsequently, we discuss the role of transcription factors nuclear factor (erythroid-derived 2)-like 2 (Nrf2), Myocyte enhancer factor 2 (MEF2), and Forkhead box (FOXO) and their associated posttranslational modifications as it pertains to regulating each of these networks. Finally, we propose that comparing and contrasting these concepts to data collected from model organisms able to withstand dramatic changes in muscular function without injury will allow researchers to delineate physiological versus pathological responses. [ABSTRACT FROM AUTHOR]
- Published
- 2016
- Full Text
- View/download PDF
14. Bone and Muscle Endocrine Functions: Unexpected Paradigms of Inter-organ Communication.
- Author
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Karsenty, Gerard and Olson, Eric N.
- Subjects
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CELL communication , *BONE physiology , *ENDOCRINE system physiology , *STRIATED muscle physiology , *GENETICS , *LABORATORY mice - Abstract
Most physiological functions originate with the communication between organs. Mouse genetics has revived this holistic view of physiology through the identification of inter-organ communications that are unanticipated, functionally important, and would have been difficult to uncover otherwise. This Review highlights this point by showing how two tissues usually not seen as endocrine ones, bone and striated muscles, influence several physiological processes in a significant manner. [ABSTRACT FROM AUTHOR]
- Published
- 2016
- Full Text
- View/download PDF
15. The effect of striatal dopamine depletion on striatal and cortical glutamate: A mini-review.
- Author
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Caravaggio, Fernando, Nakajima, Shinichiro, Plitman, Eric, Gerretsen, Philip, Chung, Jun Ku, Iwata, Yusuke, and Graff-Guerrero, Ariel
- Subjects
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DOPAMINE , *GLUTAMIC acid , *STRIATED muscle physiology , *DRUG efficacy , *BASAL ganglia - Abstract
Understanding the interplay between the neurotransmitters dopamine and glutamate in the striatum has become the highlight of several theories of neuropsychiatric illnesses, such as schizophrenia. Using in vivo brain imaging in humans, alterations in dopamine and glutamate concentrations have been observed in several neuropsychiatric disorders. However, it is unclear a priori how alterations in striatal dopamine should modulate glutamate concentrations in the basal ganglia. In this selective mini-review, we examine the consequence of reducing striatal dopamine functioning on glutamate concentrations in the striatum and cortex; regions of interest heavily examined in the human brain imaging studies. We examine the predictions of the classical model of the basal ganglia, and contrast it with findings in humans and animals. The review concludes that chronic dopamine depletion (> 4 months) produces decreases in striatal glutamate levels which are consistent with the classical model of the basal ganglia. However, acute alterations in striatal dopamine functioning, specifically at the D 2 receptors, may produce opposite affects. This has important implications for models of the basal ganglia and theorizing about neurochemical alterations in neuropsychiatric diseases. Moreover, these findings may help guide a priori hypotheses for 1 H-MRS studies measuring glutamate changes given alterations in dopaminergic functioning in humans. [ABSTRACT FROM AUTHOR]
- Published
- 2016
- Full Text
- View/download PDF
16. Differential CaMKII regulation by voltage-gated calcium channels in the striatum.
- Author
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Pasek, Johanna G., Wang, Xiaohan, and Colbran, Roger J.
- Subjects
- *
SPINAL nerves , *CALCIUM-dependent protein kinase , *VOLTAGE-gated ion channels , *STRIATED muscle physiology , *CALCIUM channels , *NEUROPLASTICITY , *AUTOPHOSPHORYLATION - Abstract
Calcium signaling regulates synaptic plasticity and many other functions in striatal medium spiny neurons to modulate basal ganglia function. Ca 2 + /calmodulin-dependent protein kinase II (CaMKII) is a major calcium-dependent signaling protein that couples calcium entry to diverse cellular changes. CaMKII activation results in autophosphorylation at Thr286 and sustained calcium-independent CaMKII activity after calcium signals dissipate. However, little is known about the mechanisms regulating striatal CaMKII. To address this, mouse brain slices were treated with pharmacological modulators of calcium channels and punches of dorsal striatum were immunoblotted for CaMKII Thr286 autophosphorylation as an index of CaMKII activation. KCl depolarization increased levels of CaMKII autophosphorylation ~ 2-fold; this increase was blocked by an LTCC antagonist and was mimicked by treatment with pharmacological LTCC activators. The chelation of extracellular calcium robustly decreased basal CaMKII autophosphorylation within 5 min and increased levels of total CaMKII in cytosolic fractions, in addition to decreasing the phosphorylation of CaMKII sites in the GluN2B subunit of NMDA receptors and the GluA1 subunit of AMPA receptors. We also found that the maintenance of basal levels of CaMKII autophosphorylation requires low-voltage gated T-type calcium channels, but not LTCCs or R-type calcium channels. Our findings indicate that CaMKII activity is dynamically regulated by multiple calcium channels in the striatum thus coupling calcium entry to key downstream substrates. [ABSTRACT FROM AUTHOR]
- Published
- 2015
- Full Text
- View/download PDF
17. Normobaric hyperoxia treatment prevents early alteration in dopamine level in mice striatum after fluid percussion injury: a biochemical approach.
- Author
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Muthuraju, Sangu, Islam, Mohammad Rafiqul, Pati, Soumya, Jaafar, Hasnan, Abdullah, Jafri Malin, and Yusoff, Kamaruddin Mohd.
- Subjects
- *
HYPEROXIA , *DOPAMINE , *STRIATED muscle physiology , *PERCUSSION (Medicine) , *DOPAMINERGIC neurons , *LABORATORY mice , *THERAPEUTICS - Abstract
Dopamine (DA) is one of the key neurotransmitters in the striatum, which is functionally important for a variety of cognitive and motor behaviours. It is known that the striatum is vulnerable to damage from traumatic brain injury (TBI). However, a therapeutic approach has not yet been established to treat TBI. Hence, the present work aimed to evaluate the ability of Normobaric hyperoxia treatment (NBOT) to recover dopaminergic neurons following a fluid percussion injury (FPI) as a TBI experimental animal model. To examine this, mice were divided into four groups: (i) Control, (ii) Sham, (iii) FPI and (iv) FPI+NBOT. Mice were anesthetized and surgically prepared for FPI in the striatum and immediate exposure to NBOT at various time points (3, 6, 12 and 24 h). Dopamine levels were then estimated post injury by utilizing a commercially available ELISA method specific to DA. We found that DA levels were significantly reduced at 3 h, but there was no reduction at 6, 12 and 24 h in FPI groups when compared to the control and sham groups. Subjects receiving NBOT showed consistent increased DA levels at each time point when compared with Sham and FPI groups. These results suggest that FPI may alter DA levels at the early post-TBI stages but not in later stages. While DA levels increased in 6, 12 and 24 h in the FPI groups, NBOT could be used to accelerate the prevention of early dopaminergic neuronal damage following FPI injury and improve DA levels consistently. [ABSTRACT FROM PUBLISHER]
- Published
- 2015
- Full Text
- View/download PDF
18. Comparative Sensitivity Analysis of Muscle Activation Dynamics.
- Author
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Rockenfeller, Robert, Günther, Michael, Schmitt, Syn, and Götz, Thomas
- Subjects
- *
STRIATED muscle physiology , *SENSITIVITY analysis , *ORDINARY differential equations , *BIOLOGICAL mathematical modeling , *COMPARATIVE studies - Abstract
We mathematically compared two models of mammalian striated muscle activation dynamics proposed by Hatze and Zajac. Both models are representative for a broad variety of biomechanical models formulated as ordinary differential equations (ODEs). These models incorporate parameters that directly represent known physiological properties. Other parameters have been introduced to reproduce empirical observations. We used sensitivity analysis to investigate the influence of model parameters on the ODE solutions. In addition, we expanded an existing approach to treating initial conditions as parameters and to calculating second-order sensitivities. Furthermore, we used a global sensitivity analysis approach to include finite ranges of parameter values. Hence, a theoretician striving for model reduction could use the method for identifying particularly low sensitivities to detect superfluous parameters. An experimenter could use it for identifying particularly high sensitivities to improve parameter estimation. Hatze’s nonlinear model incorporates some parameters to which activation dynamics is clearly more sensitive than to any parameter in Zajac’s linear model. Other than Zajac’s model, Hatze’s model can, however, reproduce measured shifts in optimal muscle length with varied muscle activity. Accordingly we extracted a specific parameter set for Hatze’s model that combines best with a particular muscle force-length relation. [ABSTRACT FROM AUTHOR]
- Published
- 2015
- Full Text
- View/download PDF
19. Muscle LIM Protein: Master regulator of cardiac and skeletal muscle functions.
- Author
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Vafiadaki, Elizabeth, Arvanitis, Demetrios A., and Sanoudou, Despina
- Subjects
- *
MUSCLE proteins , *MYOCARDIUM physiology , *SKELETAL muscle physiology , *STRIATED muscle physiology , *PATHOLOGICAL physiology , *CYSTEINE , *GENETIC mutation - Abstract
Muscle LIM Protein (MLP) has emerged as a key regulator of striated muscle physiology and pathophysiology. Mutations in cysteine and glycine-rich protein 3 ( CSRP3 ), the gene encoding MLP, are causative of human cardiomyopathies, whereas altered expression patterns are observed in human failing heart and skeletal myopathies. In vitro and in vivo evidences reveal a complex and diverse functional role of MLP in striated muscle, which is determined by its multiple interacting partners and subcellular distribution. Experimental evidence suggests that MLP is implicated in both myogenic differentiation and myocyte cytoarchitecture, although the full spectrum of its intracellular roles still unfolds. [ABSTRACT FROM AUTHOR]
- Published
- 2015
- Full Text
- View/download PDF
20. Novel Presentation of Rosai-Dorfman Histiocytosis With a Prolonged Course of Cranial and Peripheral Neuropathies.
- Author
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Tripathi, Richa, Serajee, Fatema, Jiang, Huiyuan, and Huq, A.H.M. Mahbubul
- Subjects
- *
LANGERHANS-cell histiocytosis , *PERIPHERAL neuropathy , *NEUROPHYSIOLOGY , *STRIATED muscle physiology , *IMMUNOGLOBULINS , *BRAIN , *DIFFERENTIAL diagnosis , *MUSCLES , *HISTIOCYTOSIS , *SPINAL cord - Abstract
Background: Rosai-Dorfman disease is a form of histiocytosis affecting the systemic lymph nodes. Intracranial Rosai-Dorfman disease is rare and presents with extra-parenchymal or intraparenchymal proliferative mass lesions. Cranial neuropathy has not been reported in Rosai-Dorfman disease except when caused by mass effect by an adjacent lesion.Patient Description: We describe a girl with Rosai-Dorfman disease who presented with peripheral and multiple cranial neuropathies. Detailed clinical, immunologic, neurophysiology, imaging, and genetic studies were performed. She had a prolonged course but recovered fully after immune therapies. She had increased titers of striated muscle and smooth muscle antibodies. Imaging studies revealed contrast enhancement of cranial nerves and striated muscles. Demyelination was evident in the nerve twigs from muscle biopsy. Exome sequencing did not reveal a genetic mutation.Conclusions: Most patients with Rosai-Dorfman disease have a benign course, but severe neurological dysfunction due to bulbar involvement and cranial and peripheral neuropathies may occur. Treatment with immunoglobulin and steroids may be of benefit. [ABSTRACT FROM AUTHOR]- Published
- 2017
- Full Text
- View/download PDF
21. Modelling Ca2+ bound Troponin in Excitation Contraction Coupling
- Author
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Javier E. Hasbun and Henry G. Zot
- Subjects
0301 basic medicine ,muscle ,Physiology ,Sarcomere ,lcsh:Physiology ,03 medical and health sciences ,chemistry.chemical_compound ,Physiology (medical) ,Myosin ,medicine ,skeletal muscle ,Actin ,Excitation Contraction Coupling ,Fluo-3 ,calcium ,model ,biology ,lcsh:QP1-981 ,EC-coupling ,contraction ,excitation ,Skeletal muscle ,Anatomy ,Models, Theoretical ,Troponin ,Tropomyosin ,Fluorescence ,030104 developmental biology ,medicine.anatomical_structure ,chemistry ,kinetics ,striated muscle physiology ,biology.protein ,Biophysics ,Calcium regulation - Abstract
To explain disparate decay rates of cytosolic Ca2+ and structural changes in the thin filaments during a twitch, we model the time course of Ca2+ bound troponin (Tn) resulting from the free Ca2+ transient of fast skeletal muscle. In fibers stretched beyond overlap, the decay of Ca2+ as measured by a change in fluo 3 fluorescence is significantly slower than the intensity decay of the meridional 1/38.5 nm-1 reflection of Tn; this is not simply explained by considering only the Ca2+ binding properties of Tn alone (Matsuo, T., Iwamoto, H., and Yagi, N. (2010). Biophys. J. 99, 193-200). We apply a comprehensive model that includes the known Ca2+ binding properties of Tn in the context of the thin filament with and without cycling crossbridges. Calculations based on the model predict that the transient of Ca2+ bound Tn correlates with either the fluo 3 time course in muscle with overlapping thin and thick filaments or the intensity of the meridional 1/38.5 nm-1 reflection in overstretched muscle. Hence, cycling crossbridges delay the dissociation of Ca2+ from Tn. Correlation with the fluo 3 fluorescence change is not causal given that the transient of Ca2+ bound Tn depends on sarcomere length, whereas the fluo-3 fluorescence change does not. Transient positions of tropomyosin calculated from the time course of Ca2+ bound Tn are in reasonable agreement with the transient of measured perturbations of the Tn repeat in overlap and non-overlap muscle preparations.
- Published
- 2016
22. P.10 - A histologically diagnosed case with limb-girdle muscular dystrophy type 1A: The youngest case in the literature.
- Author
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Diniz, G., Edizer, S., Gurbuz, G., and Unalp, A.
- Subjects
- *
LIMB-girdle muscular dystrophy , *PROTEIN expression , *STRIATED muscle physiology , *FATIGUE (Physiology) , *HISTOLOGY , *DIAGNOSIS - Published
- 2016
- Full Text
- View/download PDF
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