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在大鼠心肌细胞中诱导锰超氧化物歧化酶可提高预处理后24小时对缺氧的耐受性。

Induction of manganese superoxide dismutase in rat cardiac myocytes increases tolerance to hypoxia 24 hours after preconditioning.

作者信息

Yamashita N, Nishida M, Hoshida S, Kuzuya T, Hori M, Taniguchi N, Kamada T, Tada M

机构信息

First Department of Medicine, Osaka University Medical School, Japan.

出版信息

J Clin Invest. 1994 Dec;94(6):2193-9. doi: 10.1172/JCI117580.

Abstract

Manganese superoxide dismutase (Mn-SOD) is induced in ischemic hearts 24 h after ischemic preconditioning, when tolerance to ischemia is acquired. We examined the relationship between Mn-SOD induction and the protective effect of preconditioning using cultured rat cardiac myocytes. Exposure of cardiac myocytes to brief hypoxia (1 h) decreased creatine kinase release induced by sustained hypoxia (3 h) that follows when the sustained hypoxia was applied 24 h after hypoxic preconditioning (57% of that in cells without preconditioning). The activity and content of Mn-SOD in cardiac myocytes were increased 24 h after hypoxic preconditioning (activity, 170%; content, 139% compared with cells without preconditioning) coincidentally with the acquisition of tolerance to hypoxia. Mn-SOD mRNA was also increased 20-40 min after preconditioning. Antisense oligodeoxyribonucleotides corresponding to the initiation site of Mn-SOD translation inhibited the increases in the Mn-SOD content and activity and abolished the expected decrease in creatine kinase release induced by sustained hypoxia after 24 h of hypoxic preconditioning. Sense oligodeoxyribonucleotides did not abolish either Mn-SOD induction or tolerance to hypoxia. These results suggest that the induction of Mn-SOD in myocytes by preconditioning plays a pivotal role in the acquisition of tolerance to ischemia at a later phase (24 h) of ischemic preconditioning.

摘要

锰超氧化物歧化酶(Mn-SOD)在缺血预处理24小时后的缺血心脏中被诱导产生,此时心脏获得了对缺血的耐受性。我们使用培养的大鼠心肌细胞研究了Mn-SOD的诱导与预处理保护作用之间的关系。将心肌细胞暴露于短暂缺氧(1小时)可降低随后持续缺氧(3小时)诱导的肌酸激酶释放,当在缺氧预处理24小时后施加持续缺氧时(与未预处理的细胞相比,降低至57%)。缺氧预处理24小时后,心肌细胞中Mn-SOD的活性和含量增加(活性为未预处理细胞的170%;含量为139%),同时获得了对缺氧的耐受性。预处理后20 - 40分钟,Mn-SOD mRNA也增加。与Mn-SOD翻译起始位点对应的反义寡脱氧核苷酸抑制了Mn-SOD含量和活性的增加,并消除了缺氧预处理24小时后持续缺氧诱导的肌酸激酶释放预期的降低。正义寡脱氧核苷酸既没有消除Mn-SOD的诱导,也没有消除对缺氧的耐受性。这些结果表明,预处理诱导心肌细胞中Mn-SOD的产生在缺血预处理后期(24小时)获得对缺血的耐受性中起关键作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf4d/330044/46026e6f5de3/jcinvest00490-0026-a.jpg

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