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布洛芬不会损害心脏毒素诱导损伤后的骨骼肌再生。

Ibuprofen does not impair skeletal muscle regeneration upon cardiotoxin-induced injury.

机构信息

Exercise Physiology Research Group, Department of Movement Sciences, Faculty of Movement and Rehabilitation Sciences, Catholic University of Leuven, Leuven, Belgium.

出版信息

Physiol Res. 2020 Nov 16;69(5):847-859. doi: 10.33549/physiolres.934482. Epub 2020 Sep 9.

Abstract

Muscle regeneration is regulated through interaction between muscle and immune cells. Studies showed that treatment with supra-physiological doses of Non-Steroidal Anti-Inflammatory Drug (NSAID) abolished inflammatory signaling and impaired muscle recovery. The present study examines the effects of pharmacologically-relevant NSAID treatment on muscle regeneration. C57BL/6 mice were injected in the tibialis anterior (TA) with either PBS or cardiotoxin (CTX). CTX-injected mice received ibuprofen (CTX-IBU) or were untreated (CTX-PLAC). After 2 days, Il-1beta and Il-6 expression was upregulated in the TA of CTX-IBU and CTX-PL vs. PBS. However, Cox-2 expression and macrophage infiltration were higher in CTX-PL vs. PBS, but not in CTX-IBU. At the same time, anabolic markers were higher in CTX-IBU vs. PBS, but not in CTX-PL. Nevertheless, ibuprofen did not affect muscle mass or muscle fiber regeneration. In conclusion, mild ibuprofen doses did not worsen muscle regeneration. There were even signs of a transient improvement in anabolic signaling and attenuation of inflammatory signaling.

摘要

肌肉再生是通过肌肉和免疫细胞之间的相互作用来调节的。研究表明,超生理剂量的非甾体抗炎药(NSAID)治疗会消除炎症信号,并损害肌肉恢复。本研究检查了药理相关的 NSAID 治疗对肌肉再生的影响。C57BL/6 小鼠在前胫骨肌(TA)中注射 PBS 或心脏毒素(CTX)。CTX 注射的小鼠接受布洛芬(CTX-IBU)或未治疗(CTX-PLAC)。2 天后,CTX-IBU 和 CTX-PL 中的 IL-1beta 和 IL-6 表达在上皮 TA 中上调,而不是 PBS。然而,在 CTX-PL 中,cox-2 表达和巨噬细胞浸润高于 PBS,但在 CTX-IBU 中则没有。与此同时,CTX-IBU 中的合成代谢标记物高于 PBS,但在 CTX-PL 中则没有。然而,布洛芬并没有影响肌肉质量或肌纤维再生。总之,轻度布洛芬剂量不会加重肌肉再生。甚至有迹象表明,合成代谢信号的短暂改善和炎症信号的衰减。

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