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血红素加氧酶-1通过激活血管平滑肌细胞中的p44/42丝裂原活化蛋白激酶来促进α-硫辛酸的细胞保护作用。

Heme oxygenase-1 contributes to the cytoprotection of alpha-lipoic acid via activation of p44/42 mitogen-activated protein kinase in vascular smooth muscle cells.

作者信息

Cheng Pao-Yun, Lee Yen-Mei, Shih Neng-Lang, Chen Yao-Chang, Yen Mao-Hsiung

机构信息

Graduate Institute of Life Sciences, National Defense Medical Center, Taipei, Taiwan.

出版信息

Free Radic Biol Med. 2006 Apr 15;40(8):1313-22. doi: 10.1016/j.freeradbiomed.2005.11.024. Epub 2006 Jan 6.

Abstract

Alpha-lipoic acid (ALA) is a natural antioxidant that scavenges reactive oxygen species (ROS) and regenerates or recycles endogenous antioxidants. ALA has recently been reported to protect against oxidative injury in various disease processes. The aim of this study was to investigate whether the antioxidant effect of ALA is mediated by the induction of heme oxygenase (HO)-1 in rat aortic smooth muscle cells (A10 cells). ALA significantly induced HO-1 expression accompanied by an increase in HO activity in A10 cells. Pretreatment with ALA increased the resistance of A10 cells to hydrogen-peroxide-induced oxidant stress. This protection of ALA was abrogated in the presence of the HO inhibitor zinc protoporphyrin IX. ALA significantly increased ROS, and this effect was blocked by N-acetyl-cysteine, which also inhibited ALA-induced activation of p44/42 mitogen-activated protein kinase (MAPK) and AP-1, HO-1 expression, and HO activity. These results suggest that ALA induces HO-1 expression through the production of ROS and subsequent activation of the p44/42 MAPK pathway and AP-1 in vascular smooth muscle cells. This study demonstrated that ALA increases the expression of HO-1, a critical cytoprotective molecule, and identified a novel pleiotropic effect of ALA on cardiovascular protection.

摘要

α-硫辛酸(ALA)是一种天然抗氧化剂,可清除活性氧(ROS)并使内源性抗氧化剂再生或循环利用。最近有报道称,ALA可在各种疾病过程中预防氧化损伤。本研究的目的是探讨ALA的抗氧化作用是否通过诱导大鼠主动脉平滑肌细胞(A10细胞)中的血红素加氧酶(HO)-1来介导。ALA显著诱导A10细胞中HO-1的表达,并伴随HO活性增加。用ALA预处理可增加A10细胞对过氧化氢诱导的氧化应激的抵抗力。在HO抑制剂锌原卟啉IX存在的情况下,ALA的这种保护作用被消除。ALA显著增加ROS,而N-乙酰半胱氨酸可阻断这种作用,N-乙酰半胱氨酸还可抑制ALA诱导的p44/42丝裂原活化蛋白激酶(MAPK)和AP-1的激活、HO-1的表达以及HO活性。这些结果表明,ALA通过产生ROS以及随后激活血管平滑肌细胞中的p44/42 MAPK途径和AP-1来诱导HO-1的表达。本研究表明,ALA可增加关键细胞保护分子HO-1的表达,并确定了ALA在心血管保护方面的一种新的多效性作用。

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