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低浓度亚甲蓝维持能量产生并显著提高法国加拿大 Leigh 综合征皮肤成纤维细胞的存活率。

Low-concentration methylene blue maintains energy production and strongly improves survival of Leigh syndrome French Canadian skin fibroblasts.

机构信息

Department of Fundamental Sciences, Université du Québec à Chicoutimi, 555 Boulevard de l'Université, Chicoutimi, Québec, Canada.

出版信息

J Pharm Pharm Sci. 2011;14(3):438-49. doi: 10.18433/j3m01x.

Abstract

Leigh syndrome French Canadian (LSFC) is a recessive disease caused by mutations in the LRPPRC gene (leucine-rich pentatricopeptide repeat containing protein). These mutations induce a cytochrome c oxidase (COX) deficiency resulting in episodes of acute acidotic crisis that will often lead to death. There is no effective treatment. Methylene blue (MB) is a redox dye that increases COX content and activity in vitro and in vivo suggesting that MB could prevent and treat LSFC. In this study, the protective effect of low-concentration MB was tested on two LSFC cell lines, including LSFC-F1, homozygous for the mutation A354V, and LSFC-F2 a compound heterozygous for the mutations A354V and C12775STOP. MB effect on metabolic activity was assessed on both LSFC cells in stable and acidotic conditions. For LSFC-F1, results showed that metabolic activity drastically decline after 96 hours in both conditions but not LSFC-F2 and normal cells. MB completely prevents the decrease of metabolic activity in LSFC-F1. Intracellular ATP content was also measured in both culture media. After 96 hours in acidotic medium, ATP content was almost completely depleted for both LSFC cells. Interestingly, MB completely restores ATP content in LSFC-F1 and LSFC-F2 cells. Finally, MB strongly improves the survival of both LSFC cells.

摘要

Leigh 综合征法国裔(LSFC)是一种由 LRPPRC 基因突变引起的隐性疾病(leucine-rich pentatricopeptide repeat containing protein)。这些突变诱导细胞色素 c 氧化酶(COX)缺乏,导致急性酸中毒危象发作,常导致死亡。目前尚无有效治疗方法。亚甲蓝(MB)是一种氧化还原染料,可增加 COX 含量和体外及体内活性,表明 MB 可能预防和治疗 LSFC。在这项研究中,低浓度 MB 的保护作用在两种 LSFC 细胞系中进行了测试,包括 LSFC-F1,纯合突变 A354V,以及 LSFC-F2 复合杂合突变 A354V 和 C12775STOP。MB 对两种 LSFC 细胞在稳定和酸中毒条件下的代谢活性的影响进行了评估。对于 LSFC-F1,结果表明,在两种条件下,代谢活性在 96 小时后急剧下降,但 LSFC-F2 和正常细胞没有下降。MB 完全阻止了 LSFC-F1 代谢活性的下降。还测量了两种培养基中的细胞内 ATP 含量。在酸性培养基中培养 96 小时后,LSFC 细胞的 ATP 含量几乎完全耗尽。有趣的是,MB 完全恢复了 LSFC-F1 和 LSFC-F2 细胞中的 ATP 含量。最后,MB 显著提高了两种 LSFC 细胞的存活率。

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