Effects of ovarian hormones and estrogen receptor α on physical activity and skeletal muscle fatigue in female mice
Autor: | Gengyun Le, Christine A. Cabelka, Nardina Nash, Espen E. Spangenburg, Cory W. Baumann, Angus Lindsay, Brittany C. Collins, Dawn A. Lowe |
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Rok vydání: | 2019 |
Předmět: |
0301 basic medicine
Aging Estrogen receptor Biochemistry Mice Random Allocation 0302 clinical medicine Endocrinology Tandem Mass Spectrometry Progesterone computer.programming_language Mice Knockout Estradiol sed Menopause medicine.anatomical_structure Muscle Fatigue Female hormones hormone substitutes and hormone antagonists Muscle Contraction medicine.medical_specialty Ovariectomy Article Contractility 03 medical and health sciences Physical Conditioning Animal Internal medicine Genetics medicine Animals Muscle Strength Muscle Skeletal Molecular Biology Soleus muscle business.industry Estrogen Receptor alpha Wild type Skeletal muscle Estrogens Cell Biology medicine.disease Mice Inbred C57BL 030104 developmental biology Torque Progestins business computer 030217 neurology & neurosurgery Chromatography Liquid Hormone |
Zdroj: | Experimental Gerontology. 115:155-164 |
ISSN: | 0531-5565 |
DOI: | 10.1016/j.exger.2018.11.003 |
Popis: | Menopause is associated with declines in physical activity and skeletal muscle strength. Physical activity is also reduced in rodents after ovariectomy (OVX) and whole-body estrogen receptor α (ERα) knockout. However, it is unclear if the effects are estradiol (E(2)) specific. Thus, the overall purpose of this study was to investigate the effects of the ovarian hormones, E(2) and progesterone (P4), and skeletal muscle ERα (skmERα) on physical activity and skeletal muscle contractility in female mice. METHODS: Study 1: Forty female C57Bl/6J mice were given free access to running wheels for 2 weeks to assess baseline running and randomized into 4 treatment groups: OVX, OVX+E(2), OVX+P4, OVX+E(2)+P4. All mice underwent OVX, returned to wheels for 2 weeks, received hormone pellet implants and returned to running wheels for 6 weeks, after which soleus muscle contractility testing was completed. Study 2: Thirty-two skeletal muscle specific ERα knock-out (skmERαKO) mice and wildtype (WT) littermates were randomized into 4 groups: skmERαKO-Run, skmERαWT-Run, skmERαKO-Sed, and skmERαWT-Sed. Run mice were given free access to wheels for 20 wk and sedentary (Sed) mice maintained normal cage activities. At the end point, muscle contractility was tested. RESULTS: Study 1: OVX+E(2)+P4 group ran greater distances than both the OVX and OVX+P4 groups (p≤0.009). After fatiguing contractions, soleus muscles of the OVX+E(2)+P4 group maintained greater submaximal force than those of other groups (p=0.023). Immediately after the fatiguing contractions, OVX+E(2)+P4 muscles had greater maximal force production than the OVX+E(2) group (p=0.027). Study 2: There were no differences in running distance between skmERαWT and skmERαKO mice (p=0.240). Soleus muscles of skmERαKO mice were more fatigable (p |
Databáze: | OpenAIRE |
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