» Articles » PMID: 16254070

Removal of Ovarian Hormones from Mature Mice Detrimentally Affects Muscle Contractile Function and Myosin Structural Distribution

Overview
Date 2005 Oct 29
PMID 16254070
Citations 48
Authors
Affiliations
Soon will be listed here.
Abstract

The purposes of this study were to determine the effects of ovarian hormone removal on force-generating capacities and contractile proteins in soleus and extensor digitorum longus (EDL) muscles of mature female mice. Six-month-old female C57BL/6 mice were randomly assigned to either an ovariectomized (OVX; n = 13) or a sham-operated (sham; n = 13) group. In vitro contractile function of soleus and EDL muscles were determined 60 days postsurgery. Total protein and contractile protein contents were quantified, and electron paramagnetic resonance (EPR) spectroscopy was used to determine myosin structural distribution during contraction. OVX mice weighed 15% more than sham mice 60 days postsurgery, and soleus and EDL muscle masses were 19 and 15% greater in OVX mice, respectively (P < or = 0.032). Soleus and EDL muscles from OVX mice generated less maximal isometric force than did those from sham mice [soleus: 0.27 (SD 0.04) vs. 0.22 N.cm.mg(-1) (SD 0.04); EDL: 0.33 (SD 0.04) vs. 0.27 N.cm.mg(-1) (SD 0.04); P < or = 0.006]. Total and contractile protein contents of soleus and EDL muscles were not different between OVX and sham mice (P > or = 0.242), indicating that the quantity of contractile machinery was not affected by removing ovarian hormones. EPR spectroscopy showed that the fraction of strong-binding myosin during contraction was 15% lower in EDL muscles from OVX mice compared with shams [0.277 (SD 0.039) vs. 0.325 (SD 0.020); P = 0.004]. These results indicate that the loss of ovarian hormones has detrimental effects on skeletal muscle force-generating capacities that can be explained by altered actin-myosin interactions.

Citing Articles

The association between reproductive factors and frailty risk: a population-based analysis from the UK biobank.

Chang T, Zhao Z, Liu X, Liu X, Zhang Y, Lu M BMC Public Health. 2025; 25(1):762.

PMID: 39994608 PMC: 11853312. DOI: 10.1186/s12889-025-22012-y.


Shatavari supplementation during eight weeks of resistance training increases training load, enhances skeletal muscle contractility and alters the skeletal muscle proteome in older women.

Greed E, Pritchard J, Struszczak L, Bozbas E, Ek G, Acheson J Front Nutr. 2025; 11():1498674.

PMID: 39834460 PMC: 11743497. DOI: 10.3389/fnut.2024.1498674.


Estrogen deficiency reduces maximal running capacity and affects serotonin levels differently in the hippocampus and nucleus accumbens in response to acute exercise.

Lee E, Nissinen T, Yla-Outinen L, Jalkanen A, Karppinen J, Vieira-Potter V Front Neurosci. 2024; 18:1399229.

PMID: 38983274 PMC: 11231437. DOI: 10.3389/fnins.2024.1399229.


Reduced cardiac antioxidant defenses mediate increased susceptibility to workload-induced myocardial injury in males with genetic cardiomyopathy.

Vetter T, Parthiban P, Stevens J, Revelo X, Kohr M, Townsend D J Mol Cell Cardiol. 2024; 190:24-34.

PMID: 38527667 PMC: 11060907. DOI: 10.1016/j.yjmcc.2024.03.004.


Time course changes in in vivo muscle mechanical function and Ca regulation of force following experimentally induced gradual ovarian failure in mice.

Hinks A, Dalton B, Mashouri P, Flewwelling L, Pyle W, Cheng A Exp Physiol. 2024; 109(5):711-728.

PMID: 38500268 PMC: 11061627. DOI: 10.1113/EP091735.