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首页> 外文期刊>Canadian Journal of Physiology and Pharmacology >Protective efficacy of carnosic acid against hydrogen peroxide induced oxidative injury in HepG2 cells through the SIRT1 pathway
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Protective efficacy of carnosic acid against hydrogen peroxide induced oxidative injury in HepG2 cells through the SIRT1 pathway

机译:肌苷酸通过SIRT1途径对HepG2细胞中过氧化氢诱导的氧化损伤的保护作用

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摘要

Carnosic acid (CA), found in rosemary, has been reported to have antioxidant and antiadipogenic properties. Here, we investigate the molecular mechanism by which CA inhibits hydrogen peroxide (H2O2)-induced injury in HepG2 cells. Cells were pretreated with 2.5-10 mu mol/L CA for 2 h and then exposed to 3 mmol/L H2O2 for an additional 4 h. CA dose-dependently increased cell viability and decreased lactate dehydrogenase activities. Pretreatment with CA completely attenuated the inhibited expression of manganese superoxide dismutase (MnSOD) and the B-cell lymphoma-extra large (Bcl-xL), and reduced glutathione activity caused by H2O2, whereas it reversed reactive oxygen species accumulation and the increase in cleaved caspase-3. Importantly, sirtuin 1 (SIRT1), a NAD(+)-dependent deacetylase, was significantly increased by CA. Considering the above results, we hypothesized that SIRT1 may play important roles in the protective effects of CA in injury induced by H2O2. As expected, SIRT1 suppression by Ex527 (6-chloro-2,3,4,9-tetrahydro-1H-carbazole-1-carboxamide) and siRNA-mediated SIRT1 silencing (si-SIRT1) significantly aggravated the H2O2-induced increased level of cleaved caspase-3 but greatly reduced the decreased expression of MnSOD and Bcl-xL. Furthermore, the positive regulatory effect of CA was inhibited by si-SIRT1. Collectively, the present study indicated that CA can alleviate H2O2-induced hepatocyte damage through the SIRT1 pathway.
机译:迷迭香中发现的肌酸(CA)具有抗氧化和抗脂肪形成的特性。在这里,我们调查CA抑制HepG2细胞中过氧化氢(H2O2)诱导的损伤的分子机制。将细胞用2.5-10μmol/ L CA预处理2 h,然后再暴露于3 mmol / L H2O2中4 h。 CA剂量依赖性地增加细胞活力,并降低乳酸脱氢酶活性。 CA预处理完全减弱了锰超氧化物歧化酶(MnSOD)和超大型B细胞淋巴瘤(Bcl-xL)的抑制表达,并降低了H2O2引起的谷胱甘肽活性,而它逆转了活性氧的积累和裂解的增加。 caspase-3。重要的是,sirtuin 1(SIRT1),一种NAD(+)依赖性脱乙酰基酶,被CA显着增加。考虑到以上结果,我们假设SIRT1可能在CA对H2O2引起的损伤的保护作用中起重要作用。不出所料,Ex527(6-氯-2,3,4,9-四氢-1H-咔唑-1-羧酰胺)对SIRT1的抑制作用和siRNA介导的SIRT1沉默(si-SIRT1)显着加重了H2O2诱导的SIRT1升高水平。裂解caspase-3,但大大降低了MnSOD和Bcl-xL表达的降低。此外,si-SIRT1抑制了CA的积极调节作用。总体而言,本研究表明,CA可以通过SIRT1途径减轻H2O2诱导的肝细胞损伤。

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