Objective: We investigated the effect of hypokinesia (diminished movement) on muscle calcium (Ca(2+)) content with and without Ca(2+) supplementation and Ca(2+) loss with different muscle Ca(2+) deficiency; muscle Ca(2+) content, plasma Ca(2+) level, and Ca(2+) loss were measured.
Methods: Studies were performed in 40 physically healthy male volunteers during a pre-experimental period of 30 d and an experimental period of 364 d. Subjects in equal numbers were assigned to one of four groups: unsupplemented active control subjects (UACSs), unsupplemented hypokinetic subjects (UHKSs), supplemented active control subjects (SACSs), and supplemented hypokinetic subjects (SHKSs). A daily supplementation of 0.7 mmol of calcium lactate per kilogram of body weight was given to SACSs and SHKSs.
Results: Muscle Ca(2+) content decreased, and plasma Ca(2+) concentration and Ca(2+) loss in urine and feces increased (P < 0.05) in the SHKS and UHKS groups compared with their pre-experimental values and the values in their respective active control groups (SACS and UACS). However, muscle Ca(2+) content decreased more, and plasma Ca(2+) concentration and Ca(2+) loss increased more (P < 0.05) in the SHKS group than in the UHKS group.
Conclusion: Muscle Ca(2+) deficiency is more evident when Ca(2+) intake is higher and Ca(2+) loss is more exacerbated with higher than with lower muscle Ca(2+) deficiency, indicating that muscle Ca(2+) deficiency during prolonged hypokinesia is due to an inability of the body to use Ca(2+) but not to a Ca(2+) shortage in the diet.
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http://dx.doi.org/10.1016/j.nut.2007.11.004 | DOI Listing |
FASEB J
January 2025
Key Laboratory of Biomechanics and Mechanobiology, Ministry of Education, Key Laboratory of Innovation and Transformation of Advanced Medical Devices, Ministry of Industry and Information Technology, National Medical Innovation Platform for Industry-Education Integration in Advanced Medical Devices (Interdiscipline of Medicine and Engineering), School of Biological Science and Medical Engineering, Beihang University, Beijing, China.
The smooth muscle cells (SMCs) located in the vascular media layer are continuously subjected to cyclic stretching perpendicular to the vessel wall and play a crucial role in vascular wall remodeling and blood pressure regulation. Mesenchymal stem cells (MSCs) are promising tools to differentiate into SMCs. Mechanical stretch loading offers an opportunity to guide the MSC-SMC differentiation and mechanical adaption for function regeneration of blood vessels.
View Article and Find Full Text PDFScand J Med Sci Sports
January 2025
Department of Sports Science and Clinical Biomechanics, University of Southern Denmark, Odense, Denmark.
While acute exercise affects sarcoplasmic reticulum (SR) function, the impact of resistance training remains unclear. The purpose of the present study was to investigate SR Ca handling plasticity in response to moderate- and high-volume strength training in elite rowers. Twenty elite male (n = 12) and female (n = 8) rowers performed three weekly strength training sessions for 8 weeks and were randomly allocated to either perform 3 sets (3-SET) or progressive increase from 5 to 10 sets (10-SET) of 10 repetitions during the training period.
View Article and Find Full Text PDFAm J Physiol Endocrinol Metab
January 2025
Brain Research Center and State Key Laboratory of Trauma, Burns, and Combined Injury, Third Military Medical University, Chongqing, China.
Parturition is a vital physiological process in the reproduction of female mammals, regulated by neurohumoral mechanisms coordinated by the central nervous system. The uterus is essential for this process; however, the neural pathways connecting the brain to the uterus remain poorly understood. In this study, we combined the pseudorabies virus (PRV) tracing tool with c-Fos immunofluorescence staining to identify brain regions that may regulate uterine muscle activity during parturition.
View Article and Find Full Text PDFBr J Pharmacol
January 2025
Department of Pharmacology, University of Oxford, Oxford, UK.
Background And Purpose: TMEM16A chloride channels constitute a depolarising mechanism in arterial smooth muscle cells (SMCs) and contractile cerebral pericytes. TMEM16A pharmacology is incompletely defined. We elucidated the mode of action and selectivity of a recently identified positive allosteric modulator of TMEM16A (PAM_16A) and of a range of TMEM16A inhibitors.
View Article and Find Full Text PDFAm J Physiol Cell Physiol
January 2025
Smooth Muscle Research Centre, Dundalk Institute of Technology, Dundalk, Ireland.
Adrenergic stimulation induces contractions in the corpus cavernosum smooth muscle (CCSM) that are important in maintaining penile flaccidity. The aim of this study was to investigate the role of K7 channels in regulating contractions and their underlying Ca signals in mouse CCSM. Quantitative PCR revealed transcriptional expression of KCNQ1 and KCNQ3-5 genes in whole CCSM, with KCNQ5 as the most highly transcribed K7 encoding gene.
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