Tetrahydrocurcumin Ameliorates Homocysteinylated Cytochrome-c Mediated Autophagy in Hyperhomocysteinemia Mice after Cerebral Ischemia

被引:77
作者
Tyagi, Neetu [1 ]
Qipshidze, Natia [1 ]
Munjal, Charu [1 ]
Vacek, Jonathan C. [1 ]
Metreveli, Naira [1 ]
Givvimani, Srikanth [1 ]
Tyagi, Suresh C. [1 ]
机构
[1] Univ Louisville, Dept Physiol & Biophys, Sch Med, Hlth Sci Ctr, Louisville, KY 40202 USA
关键词
Stroke; Blood brain barrier; Redox stress; Methionine; Curcumin; BLOOD-BRAIN-BARRIER; CYSTATHIONINE BETA-SYNTHASE; GENE KNOCK-OUT; MATRIX METALLOPROTEINASES; OXIDATIVE STRESS; ARTERY OCCLUSION; ACTIVATED MATRIX-METALLOPROTEINASE-9; INTRACEREBRAL HEMORRHAGE; MITOCHONDRIAL MECHANISM; QUANTITATIVE-EVALUATION;
D O I
10.1007/s12031-011-9695-z
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
High levels of homocysteine (Hcy) known as hyperhomocysteinemia (HHcy), contribute to autophagy and ischemia/reperfusion injury (I/R). Previous studies have shown that I/R injury and HHcy cause increased cerebrovascular permeability; however, the associated mechanism remains obscure. Interestingly, during HHcy, cytochome-c becomes homocysteinylated (Hcy-cyto-c). Cytochrome-c (cyto-c) transports electrons and facilitates bioenergetics in the system. However, its role in autophagy during ischemia/reperfusion injury is unclear. Tetrahydrocurcumin (THC) is a major herbal antioxidant and anti-inflammatory agent. Therefore, the objective of this study was to determine whether THC ameliorates autophagy during ischemia/reperfusion injury by reducing homocysteinylation of cyto-c in hyperhomocysteinemia pathological condition. To test this hypothesis, we employed 8-10-week-old male cystathionine-beta-synthase heterozygote knockout (CBS+/-) mice (genetically hyperhomocystemic mice). Experimental group was: CBS+/-, CBS+/-aEuro parts per thousand+ THC (25 mg/kg in 0.1% DMSO dose); CBS (+/-)/I/R, and CBS (+/-)/I/R + THC (25 mg/kg in 0.1% DMSO dose). Ischemia was performed for 30 min and reperfusion for 72 h. THC was injected intra-peritoneally (I.P.) once daily for a period of 3 days after 30 min of ischemia. The infarct area was measured using 2,3,5-triphenyltetrazolium chloride staining. Permeability was determined by brain edema and Evans Blue extravasation. The brain tissues were analyzed for oxidative stress, matrix metalloproteinase-9 (MMP-9), damage-regulated autophagy modulator (DRAM), and microtubule-associated protein 1 light chain 3 (LC3) by Western blot. The mRNA levels of S-adenosyl-l-homocysteine hydrolases (SAHH) and methylenetetrahydrofolate reductase (MTHFR) genes were measured by quantitative real-time polymerase chain reaction. Co-immunoprecipitation was used to determine the homocysteinylation of cyto-c. We found that brain edema and Evans Blue leakage were reduced in I/R + THC-treated groups as compared to sham-operated groups along with reduced brain infarct size. THC also decreased oxidative damage and ameliorated the homocysteinylation of cyto-c in-part by MMP-9 activation which leads to autophagy in I/R groups as compared to sham-operated groups. This study suggests a potential therapeutic role of dietary THC in cerebral ischemia.
引用
收藏
页码:128 / 138
页数:11
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