Department of Biology, Faculty of Chemistry, National Autonomous University of Mexico (UNAM), Mexico City, Mexico.
Department of Biociences and Engineering, CIIEMAD-IPN, Mexico City, Mexico.
Biofactors. 2016 Nov 12;42(6):686-702. doi: 10.1002/biof.1313. Epub 2016 Jul 13.
We have previously reported that the antioxidant curcumin exerts nephroprotection in maleate-induced renal damage, a model associated with oxidative stress. However, the mechanisms involved in curcumin protective effect were not explored, to assess this issue, curcumin was administered daily by gavage (150 mg/kg) five days before a single maleate (400 mg/kg)-injection. Curcumin prevented maleate-induced proteinuria, increased heat shock protein of 72 KDa (Hsp72) expression, and decreased plasma glutathione peroxidase activity. Maleate-induced oxidative stress by increasing the nicotinamide-adenine dinucleotide phosphate oxidase 4 (NOX4) and mitochondrial complex I-dependent superoxide anion (O • ) production, formation of malondialdehyde (MDA)- and 3-nitrotyrosine (3-NT)-protein adducts and protein carbonylation and decreased GSH/GSSG ratio. Curcumin treatment ameliorated all the above-described changes. The maleate-induced epithelial damage, evaluated by claudin-2 and occludin expressions, was ameliorated by curcumin. It was found that maleate-induced oxidative stress promoted mitochondrial fission, evaluated by dynamin-related protein (Drp) 1 and fission (Fis) 1 expressions and by electron-microscopy, and autophagy, evaluated by phospho-threonine 389 from p70 ribosomal protein S6 kinase (p-Thr 389 p70S6K), beclin 1, microtubule-associated protein 1A/1B-light chain 3 phosphatidylethanolamine conjugate (LC3-II), autophagy-related gene 5 and 12 (Atg5-Atg12) complex, p62, and lysosomal-associated membrane protein (LAMP)-2 expressions in isolated proximal tubules and by electron-microscopy and LC-3 immunolabelling. Curcumin treatment ameliorated these changes. Moreover, curcumin alone induced autophagy in proximal tubules. These data suggest that the nephroprotective effect exerted by curcumin in maleate-induced renal damage is associated with decreased mitochondrial fission and autophagy. © 2016 BioFactors, 42(6):686-702, 2016.
我们之前曾报道,抗氧化剂姜黄素可减轻马来酸诱导的肾损伤(一种与氧化应激相关的模型)中的肾损伤,但是,尚未探索姜黄素的保护作用机制,为了评估这一问题,我们通过灌胃(150mg/kg)每天给予姜黄素 5 天,然后单次给予马来酸(400mg/kg)注射。姜黄素可预防马来酸诱导的蛋白尿,增加热休克蛋白 72kDa(Hsp72)的表达,并降低血浆谷胱甘肽过氧化物酶的活性。通过增加烟酰胺腺嘌呤二核苷酸磷酸氧化酶 4(NOX4)和线粒体复合物 I 依赖性超氧阴离子(O • )的产生,马来酸诱导的氧化应激增加了丙二醛(MDA)和 3-硝基酪氨酸(3-NT)-蛋白质加合物的形成以及蛋白质羰基化和降低 GSH/GSSG 比值。姜黄素治疗改善了所有上述变化。姜黄素可改善马来酸诱导的上皮损伤,通过 Claudin-2 和 Occludin 的表达来评估。发现马来酸诱导的氧化应激通过二联蛋白相关蛋白 1(Drp1)和分裂(Fis)1 的表达以及电子显微镜评估促进线粒体分裂,以及自噬,通过磷酸化核糖体蛋白 S6 激酶的 Thr389 (p-Thr389 p70S6K),Beclin1,微管相关蛋白 1A/1B-轻链 3 磷酸乙醇胺结合物(LC3-II),自噬相关基因 5 和 12(Atg5-Atg12)复合物,p62 和溶酶体相关膜蛋白(LAMP)-2 的表达来评估在分离的近端肾小管中,并通过电子显微镜和 LC-3 免疫标记进行评估。姜黄素治疗可改善这些变化。此外,姜黄素本身可诱导近端肾小管中的自噬。这些数据表明,姜黄素在马来酸诱导的肾损伤中发挥的肾保护作用与减少线粒体分裂和自噬有关。