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他汀类药物肌毒性机制的新研究:阿托伐他汀在低氧环境下对呼吸肌的影响。

A novel investigation of statins myotoxic mechanism: effect of atorvastatin on respiratory muscles in hypoxic environment.

机构信息

Department of Pharmacology and Toxicology, Faculty of Pharmacy, Pharos University in Alexandria, Alexandria, Egypt.

Department of Pharmacology and Toxicology, Faculty of Pharmacy, Alexandria University, Alexandria, Egypt.

出版信息

Toxicol Lett. 2019 May 1;305:58-64. doi: 10.1016/j.toxlet.2019.02.001. Epub 2019 Feb 5.

Abstract

Myopathy is a well-known adverse effect of statins, affecting a large sector of statins users. The reported experimental data emphasized on mechanistic study of statin myopathy on large muscles. Clinically, both large muscles and respiratory muscles are reported to be involved in the myotoxic profile of statins. However, the experimental data investigating the myopathic mechanism on respiratory muscles are still lacking. The present work aimed to study the effect of atorvastatin treatment on respiratory muscles using rat isolated hemidiaphragm in normoxic & hypoxic conditions. The contractile activity of isolated hemidiaphragm in rats treated with atorvastatin for 21 days was investigated using nerve stimulated technique. Muscle twitches, train of four and tetanic stimulation was measured in normoxic, hypoxic and reoxygenation conditions. Atorvastatin significantly increased the tetanic fade, a measure of muscle fatigability, in hypoxic conditions. Upon reoxygenation, rat hemidiaphragm regains its normal contractile profile. Co-treatment with coenzyme Q10 showed significant improvement in defective diaphragmatic contractility in hypoxic conditions. This work showed that atorvastatin treatment rapidly deteriorates diaphragmatic activity in low oxygen environment. The mitochondrial respiratory dysfunction is probably the mechanism behind such finding. This was supported by the improvement of muscle contractile activity following CoQ10 co-treatment.

摘要

他汀类药物的肌病是一种众所周知的不良反应,影响了很大一部分他汀类药物使用者。已报道的实验数据强调了他汀类药物肌病的机制研究。临床上,大肌群和呼吸肌均被报道与他汀类药物的肌肉毒性有关。然而,关于他汀类药物对呼吸肌的肌病机制的实验数据仍然缺乏。本研究旨在使用大鼠离体膈神经刺激技术,研究阿托伐他汀治疗对正常氧合和低氧条件下呼吸肌的影响。在正常氧合、低氧和再氧合条件下,测量了阿托伐他汀治疗 21 天后大鼠离体膈神经的收缩活性。在低氧条件下,阿托伐他汀显著增加了强直衰减,这是衡量肌肉疲劳的一个指标。再氧合后,大鼠膈神经恢复正常的收缩特性。辅酶 Q10 的共同治疗显示,在低氧条件下,膈肌无力的缺陷得到了显著改善。本研究表明,阿托伐他汀治疗可迅速恶化低氧环境下的膈神经活性。这种发现可能是由于线粒体呼吸功能障碍所致。辅酶 Q10 的共同治疗改善了肌肉收缩活性,支持了这一观点。

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