We have developed a mathematical description of the equilibrium (Donnan) distribution of mobile ions between two phases containing fixed charges. This differs from the classical Donnan derivation by including mobile polyvalent ions such as those present in intact muscle fibers and in solutions used with skinned muscle fibers. Given the average concentrations of ionic species present in intact frog muscle, we calculate that the myofibrillar fixed charge density (-42 meq/liter cytoplasmic fluid) is in close agreement with estimates from amino acid analysis of myofibrillar proteins. As expected, with negative fixed charges in the myofibril, anions are excluded from the myofibrillar space while cations are concentrated in this space; the ratio between the average intra- and extramyofibrillar concentrations for an ion of valence n is (1.11)n. This model allowed us to design a bathing solution for skinned muscle fibers in which the intramyofibrillar ion concentrations closely approximate those found in intact frog muscle cells. Our model, applied to the A- and I-bands of the sarcomere, suggests that likely differences in fixed charge densities in these regions accounts for only a small fraction of the extreme concentration of phosphocreatine observed in the I-bands of intact frog muscle.
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http://dx.doi.org/10.1016/S0006-3495(89)82719-5 | DOI Listing |
J Cachexia Sarcopenia Muscle
February 2025
Department of International Agricultural Technology, Graduate School of International Agricultural Technology, Seoul National University, Seoul, Republic of Korea.
Background: Muscle diseases are serious challenges to human health. Prokineticin receptor 1 (PROKR1) has emerged as a potential target to improve muscle function through increasing oxidative muscle fibres, but there are no clinically applicable synthetic PROKR1 agonists.
Methods: Drugs with biological properties of prokineticin 2 (PK2) were discovered through connectivity map (CMap) analysis.
J Cachexia Sarcopenia Muscle
February 2025
Department of Biomedicine, Aarhus University, Aarhus, Denmark.
Background: Anti-Activin Receptor Type IIA and Type IIB antibody (αActRIIA/IIB ab) is a recently developed drug class that targets the activin receptor signalling pathway. Inhibition of receptor ligands (activins, myostatin, growth differentiation factor 11, etc.) can lead to skeletal muscle hypertrophy, bone formation, and increased haematopoiesis.
View Article and Find Full Text PDFMuscle Nerve
January 2025
Departments of Pediatrics and Neurology, Emory University School of Medicine, Atlanta, Georgia, USA.
Introduction/aims: Stimulated jitter analysis (stim-JA) involves analyzing the variation in time intervals between stimulations and action potentials, expressed as the mean consecutive difference (MCD). The MCD upper limits are derived from adult populations and warrant a re-evaluation in children to accurately diagnose neuromuscular junction (NMJ) defects.
Methods: A retrospective chart review was conducted which analyzed orbicularis oculi stim-JA studies performed on children between January 2014 and December 2021.
Vopr Pitan
January 2025
Ufa University of Science and Technology, 450076, Ufa, Russian Federation.
The most common mechanism of the development of cardiovascular diseases is atherosclerosis, caused by genetic predisposition, hyperlipidemia, inflammation and metabolic disorders. Statins used in medicine inhibit endogenous cholesterol synthesis, but are characterized by diabetogenic effect, development of intolerance in 9.1%, and muscle symptoms in 10-25% of patients.
View Article and Find Full Text PDFBackground: Previous studies have suggested that changes in the composition of the extracellular matrix (ECM) play a significant role in the development of ligamentum flavum hypertrophy (LFH) and the histological differences between the ventral and dorsal layers of the hypertrophied ligamentum flavum. Although LFH is associated with increased fibrosis in the dorsal layer, comprehensive research exploring the characteristics of the ECM and its mechanical properties in both regions is limited. Furthermore, the distribution of fibrosis-associated myofibroblasts within LFH remains poorly understood.
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