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辛伐他汀与肌肉:斑马鱼和鸡的研究表明,其益处抵不过损害。

Simvastatin and Muscle: Zebrafish and Chicken Show that the Benefits are not Worth the Damage.

作者信息

Campos Laise M, Guapyassu Livia, Gomes Cyro, Midlej Victor, Benchimol Marlene, Mermelstein Claudia, Costa Manoel Luis

机构信息

Instituto de Ciências da Saúde, Universidade Federal da Bahia, Salvador, Brazil.

Instituto de Ciências Biomédicas, Universidade Federal do Rio de Janeiro, Rio de Janeiro, Brazil.

出版信息

Front Cell Dev Biol. 2022 Mar 14;10:778901. doi: 10.3389/fcell.2022.778901. eCollection 2022.

DOI:10.3389/fcell.2022.778901
PMID:35359432
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8964290/
Abstract

Simvastatin is one of the most common medicines prescribed to treat human hypercholesterolemia. Simvastatin acts through the inhibition of cholesterol synthesis. Unfortunately, simvastatin causes unwanted side effects on muscles, such as soreness, tiredness, or weakness. Therefore, to understand the mechanism of action of simvastatin, it is important to study its physiological and structural impacts on muscle in varied animal models. Here we report on the effects of simvastatin on two biological models: zebrafish embryos and chicken muscle culture. In the last years, our group and others showed that simvastatin treatment in zebrafish embryos reduces fish movements and induces major structural alterations in skeletal muscles. We also showed that simvastatin and membrane cholesterol depletion induce major changes in proliferation and differentiation of muscle cells in chick muscle cultures. Here, we review and discuss these observations considering reported data on the use of simvastatin as a potential therapy for Duchenne muscular dystrophy.

摘要

辛伐他汀是治疗人类高胆固醇血症最常用的药物之一。辛伐他汀通过抑制胆固醇合成发挥作用。不幸的是,辛伐他汀会对肌肉产生不良副作用,如酸痛、疲劳或无力。因此,为了解辛伐他汀的作用机制,在不同动物模型中研究其对肌肉的生理和结构影响很重要。在此,我们报告辛伐他汀对两种生物学模型的影响:斑马鱼胚胎和鸡肌肉培养物。在过去几年中,我们团队和其他研究表明,在斑马鱼胚胎中使用辛伐他汀会减少鱼的活动,并导致骨骼肌出现重大结构改变。我们还表明,辛伐他汀和膜胆固醇耗竭会引起鸡肌肉培养物中肌肉细胞增殖和分化的重大变化。在此,我们结合已报道的关于辛伐他汀作为杜氏肌营养不良潜在治疗方法的数据,对这些观察结果进行综述和讨论。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e937/8964290/6c1fcaceac8f/fcell-10-778901-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e937/8964290/77446baee352/fcell-10-778901-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e937/8964290/6c1fcaceac8f/fcell-10-778901-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e937/8964290/77446baee352/fcell-10-778901-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e937/8964290/6c1fcaceac8f/fcell-10-778901-g002.jpg

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本文引用的文献

1
Rebuttal to: Simvastatin Treatment Does Not Ameliorate Muscle Pathophysiology in a Mouse Model for Duchenne Muscular Dystrophy, Verhaart et al. 2020.对《辛伐他汀治疗不能改善杜氏肌营养不良小鼠模型的肌肉病理生理学》的反驳,Verhaart等人,2020年。
J Neuromuscul Dis. 2021;8(5):865-866. doi: 10.3233/JND-219005.
2
Author's Response to: Rebuttal to: Simvastatin Treatment Does Not Ameliorate Muscle Pathophysiology in a Mouse Model for Duchenne Muscular Dystrophy, Verhaart et al. 2020.作者对以下内容的回应:对《辛伐他汀治疗不能改善杜氏肌营养不良小鼠模型的肌肉病理生理学》的反驳,Verhaart等人,2020年。
J Neuromuscul Dis. 2021;8(5):867-868. doi: 10.3233/JND-219004.
3
Simvastatin does not alleviate muscle pathology in a mouse model of Duchenne muscular dystrophy.
辛伐他汀不能缓解杜氏肌营养不良症小鼠模型的肌肉病理。
Skelet Muscle. 2021 Sep 3;11(1):21. doi: 10.1186/s13395-021-00276-3.
4
The Role of Embryonic Chick Muscle Cell Culture in the Study of Skeletal Myogenesis.胚胎鸡肌肉细胞培养在骨骼肌生成研究中的作用
Front Physiol. 2021 May 20;12:668600. doi: 10.3389/fphys.2021.668600. eCollection 2021.
5
Simvastatin Treatment Does Not Ameliorate Muscle Pathophysiology in a Mouse Model for Duchenne Muscular Dystrophy.辛伐他汀治疗不能改善杜氏肌营养不良症小鼠模型的肌肉病理生理学。
J Neuromuscul Dis. 2021;8(5):845-863. doi: 10.3233/JND-200524.
6
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Expert Opin Drug Saf. 2020 May;19(5):601-615. doi: 10.1080/14740338.2020.1747431. Epub 2020 Apr 13.
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Making Waves: New Developments in Toxicology With the Zebrafish.掀起波澜:斑马鱼在毒理学中的新发展。
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