Ursolic acid ameliorates hypobaric hypoxia‐induced skeletal muscle protein loss via upregulating Akt pathway: An experimental study using rat model. Issue 2 (24th December 2020)

• Record Type: Journal Article
• Authors: Rathor, Richa; Agrawal, Akanksha; Kumar, Ravi; Suryakumar, Geetha; Singh, Som Nath
• Is Part Of: IUBMB life. Volume 73:Issue 2(2021)
• Page Start: 375
• Page End: 389
• Publication Date: 2020-12-24
• Subjects: anti‐inflammatory -- antioxidant -- muscle atrophy -- protein synthesis -- ursolic acid; Biochemistry -- Periodicals; Molecular biology -- Periodicals; 572.8
• DOI: 10.1002/iub.2435
• Languages: English
• ISSNs: 1521-6543

Abstract

Abstract: Hypobaric hypoxic stress leads to oxidative stress, inflammation, and disturbance in protein turnover rate. Aggregately, this imbalance in redox homeostasis is responsible for skeletal muscle protein loss and a decline in physical performance. Hence, an urgent medical need is required to ameliorate skeletal muscle protein loss. The present study investigated the efficacy of ursolic acid (UA), a pentacyclic triterpene acid to ameliorate hypobaric hypoxia (HH)‐induced muscle protein loss. UA is a naturally occurring pentacyclic triterpene acid present in several edible herbs and fruits such as apples. It contains skeletal muscle hypertrophy activity; still its potential against HH‐induced muscle protein loss is unexplored. To address this issue, an in vivo study was planned to examine the beneficial effect of UA supplementation on HH‐induced skeletal muscle loss. Male Sprague Dawley rats were exposed to HH with and without UA supplementation (20 mg/kg; oral) for 3 continuous days. The results described the beneficial role of UA as supplementation of UA with HH exposure attenuated reactive oxygen species production and oxidative protein damage, which indicate the potent antioxidant activity. Furthermore, UA supplementation enhanced Akt, pAkt, and p70S6kinase activity (Akt pathway) and lowered the pro‐inflammatory cytokines in HH exposed rats. UA has potent antioxidant and anti‐inflammatory activity, and it enhanced the protein content via upregulation of Akt pathway‐related proteins against HH exposure. These three biological activities of UA make it a novel candidate for amelioration of HH‐induced skeletal muscle damage and protein loss.