Ferulic Acid Exerts Anti-apoptotic Effects against Ischemic Injury by Activating HSP70/Bcl-2-and HSP70/Autophagy-Mediated Signaling after Permanent Focal Cerebral Ischemia in Rats

被引:33
|
作者
Cheng, Chin-Yi [1 ,5 ]
Kao, Shung-Te [2 ]
Lee, Yu-Chen [3 ,4 ,6 ]
机构
[1] China Med Univ, Coll Chinese Med, Sch Postbaccalaureate Chinese Med, Taichung 40402, Taiwan
[2] China Med Univ, Coll Chinese Med, Sch Chinese Med, Taichung 40402, Taiwan
[3] China Med Univ, Res Ctr Chinese Med & Acupuncture, Taichung 40402, Taiwan
[4] China Med Univ, Grad Inst Acupuncture Sci, 91 Hsueh Shih Rd, Taichung 40402, Taiwan
[5] Hui Sheng Hosp, Dept Chinese Med, Taichung 42056, Taiwan
[6] China Med Univ Hosp, Dept Chinese Med, Taichung 40447, Taiwan
来源
AMERICAN JOURNAL OF CHINESE MEDICINE | 2019年 / 47卷 / 01期
关键词
Cerebral Ischemia; Ferulic Acid; Apoptosis; Heat Shock Protein 70; Bcl-2; Autophagy; ISCHEMIA/REPERFUSION INJURY; AUTOPHAGY ACTIVATION; MOLECULAR CHAPERONES; NEURONAL INJURY; CYTOCHROME-C; CELL-DEATH; BRAIN; PROTECTS; HEAT-SHOCK-PROTEIN-70; NEUROPROTECTION;
D O I
10.1142/S0192415X19500034
中图分类号
R [医药、卫生];
学科分类号
10 ;
摘要
This study assessed the anti-apoptotic effects of the administration of ferulic acid (FrA) in rats 30 min before middle cerebral artery occlusion (MCAo) followed by 3 d of ischemia and the involvement of 70 kDa heat shock protein (HSP70)-mediated signaling in the penumbral cortex. Our results demonstrated that FrA pretreatment at doses of 80 mg/kg (FrA-80 mg) and 100 mg/kg (FrA-100 mg) effectively ameliorated neurological functions and reduced the numbers of cytochrome c-, cleaved caspase-3-, and terminal deoxynucleotidyl transferase dUTP nick-end labeling (TUNEL)-positive cells in the penumbral cortex 3 d after ischemia. Moreover, FrA-80 mg and FrA-100 mg pretreatment markedly upregulated cytosolic HSP70, Beclin-1, microtubule-associated protein 1 light chain 3 (LC3) A/B-II and autophagy-related protein 5 (Atg5) expression; cytosolic and mitochondrial X-linked inhibitor of apoptosis (XIAP) expression and the Bcl-2/Bax ratio. FrA pretreatment downregulated cytosolic cytochrome c, apoptosis-inducing factor (AIF), procathepsin B, and cathepsin B expression and mitochondrial and cytosolic second mitochondria-derived activator of caspase/direct inhibitor of apoptosis protein-binding protein with a low isoelectric point (Smac/DIABLO) expression in the penumbral cortex. Pretreatment with VER155008, a HSP70 family inhibitor, significantly inhibited the effects of FrA-100 mg on the expression of the aforementioned proteins expression in the penumbral cortex. FrA-80 mg and FrA-100 mg pretreatment exerts neuroprotective effects against caspase-dependent and -independent apoptosis through activating HSP70/Bcl-2- and HSP70/autophagy-induced signaling pathways. Furthermore, the HSP70/Bcl-2- and HSP70/autophagy-induced anti-apoptotic effects of FrA pretreatment can be attributed to the regulation of Bax/cytochrome c/Smac/DIABLO/XIAP/caspase-3- (or Bax/AIF-) and Beclin-1/LC3A/B-II/Atg5-mediated signaling, respectively, in the penumbral cortex 3 d after permanent MCAo.
引用
收藏
页码:39 / 61
页数:23
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