Pioglitazone alleviates the mitochondrial apoptotic pathway and mito-oxidative damage in the d-galactose-induced mouse model

被引:41
作者
Prakash, Atish [1 ,2 ]
Kumar, Anil [2 ]
机构
[1] Univ Melbourne, Mental Hlth Res Inst, Melbourne, Vic, Australia
[2] Panjab Univ, Div Pharmacol, Univ Inst Pharmaceut Sci, UGC Ctr Adv Study, Chandigarh 160014, India
关键词
caspase-3; d-galactose; mitochondria; neuroprotection; senescence; PROLIFERATOR-ACTIVATED-RECEPTOR; PPAR-GAMMA AGONISTS; BRAIN MITOCHONDRIA; ADVANCED GLYCATION; HIPPOCAMPUS; MECHANISMS; STRESS; DYSFUNCTION; PROTECTION; INJECTION;
D O I
10.1111/1440-1681.12144
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
1. Chronic injection of D-galactose can cause gradual deterioration in learning and memory capacity, and activates oxidative stress, mitochondrial dysfunction and apoptotic cell death in the brain of mice. Thus, it serves as an animal model of ageing. Recent evidence has shown that mild cognitive impairment in humans might be alleviated by treatment with piogliatzone (peroxisome proliferator-activated receptor gamma (PPARc) agonists). To continue exploring the effects of piogliatzone in this model, we focused on behavioural alteration, oxidative damage, mitochondrial dysfunction and apoptosis in D-galactose-induced mice. 2. The ageing model was established by administration of D-galactose (100 mg/kg) for 6 weeks. Pioglitazone (10 and 30 mg/kg) and bisphenol A diglycidyl ether (15 mg/kg) were given daily to D-galactose-induced senescent mice. The cognitive behaviour of mice was monitored using the Morris water maze. The anti-oxidant status and apoptotic activity in the ageing mice was measured by determining mito-oxidative parameters and caspase-3 activity in brain tissue. 3. Systemic administration of D-galactose significantly increased behavioural alterations, biochemical parameters, mitochondrial enzymes, and activations of caspase-3 and acetylcholinesterase enzyme activity as compared with the control group. Piogliatzone treatment significantly improved behavioural abnormalities, biochemical, cellular alterations, and attenuated the caspase-3 and acetylcholinesterase enzyme activity as compared with the control. Furthermore, pretreatment of BADGE (PPARc antagonist) with pioglitazone reversed the protective effect of pioglitazone in D-galactose- induced mice. 4. The present study highlights the protective effects of pioglitzone against D-galactose-induced memory dysfunction, mito-oxidative damage and apoptosis through activation of PPARc receptors. These findings suggest that pioglitazone might be helpful for the prevention or alleviation of ageing.
引用
收藏
页码:644 / 651
页数:8
相关论文
共 45 条
[1]  
Alleva DG, 2002, J LEUKOCYTE BIOL, V71, P677
[2]   The mechanisms of action of PPARs [J].
Berger, J ;
Moller, DE .
ANNUAL REVIEW OF MEDICINE, 2002, 53 :409-435
[3]   Dopamine oxidation alters mitochondrial respiration and induces permeability transition in brain mitochondria: Implications for Parkinson's disease [J].
Berman, SB ;
Hastings, TG .
JOURNAL OF NEUROCHEMISTRY, 1999, 73 (03) :1127-1137
[4]   PPAR-γ agonists as regulators of microglial activation and brain inflammation [J].
Bernardo, A ;
Minghetti, L .
CURRENT PHARMACEUTICAL DESIGN, 2006, 12 (01) :93-109
[5]   Mechanisms of caspase activation [J].
Boatright, KM ;
Salvesen, GS .
CURRENT OPINION IN CELL BIOLOGY, 2003, 15 (06) :725-731
[6]   Active glycation in neurofibrillary pathology of Alzheimer disease:: Nε-(carboxymethyl) lysine and hexitol-lysine [J].
Castellani, RJ ;
Harris, PLR ;
Sayre, LM ;
Fujii, J ;
Taniguchi, N ;
Vitek, MP ;
Founds, H ;
Atwood, CS ;
Perry, G ;
Smith, MA .
FREE RADICAL BIOLOGY AND MEDICINE, 2001, 31 (02) :175-180
[7]   Age-related changes in neutral sphingomyelin-specific phospholipase C activity in striatum, hippocampus, and frontal cortex: Implication for sensitivity to stress and inflammation [J].
Crivello, NA ;
Rosenberg, IH ;
Dallal, GE ;
Bielinski, D ;
Joseph, JA .
NEUROCHEMISTRY INTERNATIONAL, 2005, 47 (08) :573-579
[8]   Mitochondrial intermembrane junctional complexes and their role in cell death [J].
Crompton, M .
JOURNAL OF PHYSIOLOGY-LONDON, 2000, 529 (01) :11-21
[9]   Chronic systemic D-galactose exposure induces memory loss, neuro degeneration, and oxidative damage in mice:: Protective effects of R-α-lipoic acid [J].
Cui, Xu ;
Zuo, Pingping ;
Zhang, Qing ;
Li, Xuekun ;
Hu, Yazhuo ;
Long, Jiangang ;
Packer, Lester ;
Liu, Jiankang .
JOURNAL OF NEUROSCIENCE RESEARCH, 2006, 84 (03) :647-654
[10]   PPAR-γ:: therapeutic target for ischemic stroke [J].
Culman, Juraj ;
Zhao, Yi ;
Gohlke, Peter ;
Herdegen, Thomas .
TRENDS IN PHARMACOLOGICAL SCIENCES, 2007, 28 (05) :244-249