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丹曲林钠和辅酶 Q10 作为一种联合治疗建议用于高脂肪饮食诱导的他汀类药物诱导的肌病大鼠:一种可能与 ROS/TGF-β/Smad4 信号通路的干扰。

Dantrolene and coenzyme Q10 as a suggested combination therapy to statin-induced myopathy in high fat diet rats: A possible interference with ROS/ TGF-β / Smad4 signaling pathway.

机构信息

Department of Pharmacology and Toxicology, Faculty of Pharmacy, Kafrelsheikh University, Kafrelsheikh 33516, Egypt.

Department of Pharmacology and Toxicology, Faculty of Pharmacy, Kafrelsheikh University, Kafrelsheikh 33516, Egypt; Department of Pharmacology and Toxicology, Massey Cancer Center, Virginia Commonwealth University, 401 College St., Richmond, VA 23298, USA.

出版信息

Toxicol Appl Pharmacol. 2024 Apr;485:116900. doi: 10.1016/j.taap.2024.116900. Epub 2024 Mar 18.

Abstract

One of the major hitches for statins' utilization is the development of myotoxicity. Versatile studies reported that the underlining molecular mechanisms including coenzyme Q10 (CoQ10)/ubiquinone depletion, as well as the disturbance in the cytoplasmic Ca homeostasis. Therefore, we investigated the consequences of supplementing CoQ10 and dantrolene, a cytoplasmic Ca reducing agent, in combination with simvastatin. This adjuvant therapy normalized the simvastatin-mediated elevation in serum ALT, AST, CK-MM, as well as tissue Ca content, in addition to suppressing the simvastatin-mediated oxidative stress in simvastatin-treated rats, while having no effect upon statin-induced antihyperlipidemic effect. Additionally, the combination inhibited the simvastatin-induced TGF-β/ Smad4 pathway activation. Collectively, the current study emphasizes on the potential utilization of dantrolene and CoQ10 as an adjuvant therapy to statins treatment for improving their side effect profile.

摘要

他汀类药物应用的主要障碍之一是肌毒性的发展。多项研究报道,潜在的分子机制包括辅酶 Q10(CoQ10)/泛醌耗竭,以及细胞质 Ca 稳态的紊乱。因此,我们研究了补充 CoQ10 和细胞质 Ca 减少剂丹曲林与辛伐他汀联合应用的后果。这种辅助治疗使辛伐他汀介导的血清 ALT、AST、CK-MM 升高以及组织 Ca 含量恢复正常,同时抑制了辛伐他汀处理大鼠中辛伐他汀介导的氧化应激,而对他汀类药物诱导的降血脂作用没有影响。此外,该联合治疗抑制了辛伐他汀诱导的 TGF-β/Smad4 通路的激活。总之,本研究强调了丹曲林和 CoQ10 作为他汀类药物治疗的辅助治疗的潜在应用,以改善其副作用。

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