Effects of Chronic Akt/mTOR Inhibition by Rapamycin on Mechanical Overload-Induced Hypertrophy and Myosin Heavy Chain Transition in Masseter Muscle

To examine the effects of the Akt/mammalian target of rapamycin (mTOR) pathway on masseter muscle hypertrophy and myosin heavy chain (MHC) transition in response to mechanical overload, we analyzed the effects of bite-opening (BO) on the hypertrophy and MHC composition of masseter muscle of BO-rats...

Full description

Saved in:
Bibliographic Details
Main Authors: Daisuke Umeki (Author), Yoshiki Ohnuki (Author), Yasumasa Mototani (Author), Kouichi Shiozawa (Author), Takayuki Fujita (Author), Yoshiki Nakamura (Author), Yasutake Saeki (Author), Satoshi Okumura (Author)
Format: Book
Published: Elsevier, 2013-01-01T00:00:00Z.
Subjects:
Online Access:Connect to this object online.
Tags: Add Tag
No Tags, Be the first to tag this record!
Description
Summary:To examine the effects of the Akt/mammalian target of rapamycin (mTOR) pathway on masseter muscle hypertrophy and myosin heavy chain (MHC) transition in response to mechanical overload, we analyzed the effects of bite-opening (BO) on the hypertrophy and MHC composition of masseter muscle of BO-rats treated or not treated with rapamycin (RAPA), a selective mTOR inhibitor. The masseter muscle weight in BO-rats was significantly greater than that in controls, and this increase was attenuated by RAPA treatment. Expression of slow-twitch MHC isoforms was significantly increased in BO-rats with/without RAPA treatment, compared with controls, but the magnitude of the increase was much smaller in RAPA-treated BO-rats. Phosphorylation of p44/42 MAPK (ERK1/2), which preserves fast-twitch MHC isoforms in skeletal muscle, was significantly decreased in BO-rats, but the decrease was abrogated by RAPA treatment. Calcineurin signaling is known to be important for masseter muscle hypertrophy and fast-to-slow MHC isoform transition, but expression of known calcineurin activity modulators was unaffected by RAPA treatment. Taken together, these results indicate that the Akt/mTOR pathway is involved in both development of masseter muscle hypertrophy and fast-to-slow MHC isoform transition in response to mechanical overload with inhibition of the ERK1/2 pathway and operates independently of the calcineurin pathway. Keywords:: masseter muscle, Akt/mammalian target of rapamycin (mTOR) pathway, hypertrophy, myosin heavy chain, mechanical stress
Item Description:1347-8613
10.1254/jphs.12195FP