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Maslinic Acid Enhances mTOR Signaling Activity After Acute Resistance Exercise in Mouse Skeletal Muscle

عنوان مقاله: Maslinic Acid Enhances mTOR Signaling Activity After Acute Resistance Exercise in Mouse Skeletal Muscle
شناسه ملی مقاله: JR_IJNS-7-3_006
منتشر شده در در سال 1401
مشخصات نویسندگان مقاله:

Kazuki Uemichi - Graduate School of Comprehensive Human Sciences, University of Tsukuba, Tnnoudai, Tsukuba, Ibaraki, Japan
Takanaga Shirai - Faculty of Health and Sport Sciences, University of Tsukuba, Tennodai, Tsukuba, Ibaraki, Japan
Hideto Hanakita - Kashima Gakuen High School, Kashima Gakuen School Corporation, Tanobe, Kashima, Ibaraki, Japan
Yuki Yamauchi - Tsukuba Life Science Innovation Program (T-LSI), University of Tsukuba, Tennodai, Tsukuba, Ibaraki ۳۰۵-۸۵۷۷, Japan
Tohru Takemasa - Faculty of Health and Sport Sciences, University of Tsukuba, Tennodai, Tsukuba, Ibaraki, Japan

خلاصه مقاله:
Background: Maslinic acid (MA) is an olive-derived extract with the structure of pentacyclic triterpenes, which potents anti-inflammatory effects. It has been reported that the combination of MA and resistance exercise increases skeletal muscle mass, but there are many unknowns regarding its detailed molecular mechanism. The present study aimed to clarify the effect of MA supplementation on muscle hypertrophic response to acute muscle contraction-induced resistance exercise using animal model.Methods: Seven-week-old ICR (Institute of Cancer Research) male mice fed a diet containing ۰.۲۷% MA during an acclimatization of ۱ week. After an overnight fast, the right gastrocnemius muscle was subjected to acute resistance exercise using percutaneous electrical stimulationinduced muscle contractions, while the left gastrocnemius muscle was saved as control. The muscle was excised at ۱, ۳, and ۶ hours after exercise and protein synthesis-related signaling expressions were examined.Results: MA was demonstrated to significantly activate the downstream targets of mammalian/mechanistic target of rapamycin (mTOR), phosphorylated ribosomal protein S۶ (rpS۶) at Ser۲۴۰/۲۴۴ site particularly, while Akt/glycogen synthase kinase-۳β (GSK-۳β) pathway and mitogenactivated protein kinase (MAPK) signaling were unaffected.Conclusion: Our results suggested that acute resistance exercise-induced muscle protein synthesis-promoting effect of MA is supported by the activation of downstream signaling of mTOR.

کلمات کلیدی:
Regulatory-associated protein of mTOR, Muscle proteins, Muscle Contraction, Resistance exercise, Mouse

صفحه اختصاصی مقاله و دریافت فایل کامل: https://civilica.com/doc/1551791/