Telmisartan, a partial agonist of peroxisome proliferator-activated receptor γ, improves impairment of spatial memory and hippocampal apoptosis in rats treated with repeated cerebral ischemia

被引:48
作者
Haraguchi, Tamami [1 ]
Iwasaki, Katsunori [1 ]
Takasaki, Kotaro [1 ]
Uchida, Kanako [1 ]
Naito, Tetsuya [1 ]
Nogami, Ai [1 ]
Kubota, Kaori [1 ]
Shindo, Taro [2 ]
Uchida, Naoki [2 ]
Katsurabayashi, Shutaro [1 ]
Mishima, Kenichi [1 ]
Nishimura, Ryoji [2 ]
Fujiwara, Michihiro [1 ]
机构
[1] Fukuoka Univ, Dept Neuropharmacol, Fac Pharmaceut Sci, Fukuoka 8140180, Japan
[2] Fukuoka Univ, Dept Psychiat, Fac Med, Fukuoka 8140180, Japan
关键词
Telmisartan; PPAR gamma; Cerebral ischemia; Dementia; Apoptosis; GW9662; TRANSIENT FOCAL ISCHEMIA; II TYPE-2 RECEPTOR; PPAR-GAMMA; 15D-PROSTAGLANDIN J(2); NEURONAL DEATH; EMBOLIC MODEL; EXPRESSION; BRAIN; ROSIGLITAZONE; INJURY;
D O I
10.1016/j.brainres.2010.07.017
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Telmisartan, an angiotensin type 1 receptor blocker (ARB), is used for hypertension to control blood pressure and has been shown to have a partial agonistic effect on peroxisome proliferator-activated receptor gamma (PPAR gamma). Recently, the ligand of PPAR gamma has been implicated in cerebroprotection due to its anti-inflammatory effect. In this study, we investigated whether telmisartan has a cerebroprotective effect on memory impairment and neuronal cell death induced by repeated cerebral ischemia. Repeated cerebral ischemia (RI: 10 min x 2) significantly induced impairment of spatial memory and hippocampal apoptosis in rats. Fourteen-day pre- and post-ischemic administration of telmisartan (0.3, 1, 3 mg/kg/day, p.o.) increased the number of correct choices and reduced the number of errors made in the eight-arm radial maze task in a dose-dependent manner in RI treated rats. TUNEL-positive cells in the hippocampus CA1 areas were also reduced following 14-day administration of telmisartan (3 mg/kg/day, p.o.). Seven-day post-ischemic administration of telmisartan improved spatial memory and reduced TUNEL-positive cells while 7-day pre-ischemic administration of telmisartan did not. These effects of telmisartan were inhibited by the PPAR gamma antagonist, GW9662. On further experiment, 7-day post-ischemic administration of telmisartan reduced the expression of caspase-3 in the hippocampus, and this effect was also inhibited by GW9662. These results suggest that telmisartan improves memory impairment and reduces neuronal apoptosis via a PPAR gamma-dependent caspase-3 inhibiting mechanism. Telmisartan, which has the unique character of having both ARB and PPAR gamma agonistic effect, will be useful for preventing memory impairment after cerebrovascular disease. (C) 2010 Elsevier B.V. All rights reserved.
引用
收藏
页码:125 / 132
页数:8
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