The seed extract of Cassia obtusifolia ameliorates learning and memory impairments induced by scopolamine or transient cerebral hypoperfusion in mice

被引:98
作者
Kim, Dong Hyun
Yoon, Byung Hoon
Kim, Yong-Won
Lee, Seungjoo
Shin, Bum Young
Jung, Ji Wook
Kim, Hyoung Ja
Lee, Yong Sup
Choi, Jae Sue
Kim, Sun Yeou
Lee, Kyung-Tae
Ryu, Jong Hoon
机构
[1] Kyung Hee Univ, Dept Life & Nanopharmaceut Sci, Seoul, South Korea
[2] Kyung Hee Univ, Coll Pharm, Kyung Hee East West Pharmaceut Res Inst, Seoul 130701, South Korea
[3] Kyung Hee Univ, Dept Pharmaceut Sci, Seoul 130701, South Korea
[4] Kyung Hee Univ, Grad Sch East West Med Sci, Seoul 130701, South Korea
[5] Daegu Haany Univ, Coll Hlth & Welfare, Dept Herbal Med Resource, Gyongsan 712715, South Korea
[6] Pukyong Natl Univ, Fac Food Sci & Technol, Pusan 608737, South Korea
[7] Kyung Hee Univ, Dept Oriental Pharmaceut Sci, Seoul 130701, South Korea
关键词
Cassia obtusifolia; memory; scopolamine; common carotid artery occlusion; acetylcholinesterase;
D O I
10.1254/jphs.FP0061565
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
In the present study, we assessed the effect of the ethanolic extract of the seeds of Cassia obtusifolia (COE) on the learning and memory impairments induced by scopolamine or transient bilateral common carotid artery occlusion (2VO). In a study of the cholinergic dysfunction induced by scopolamine, single COE (25, 50, or 100 mg/kg, p.o.) administration significantly attenuated scopolamine-induced cognitive impairments as determined by the passive avoidance and Y-maze tasks (P<0.05) and also reduced escape-latency on the Morris water maze task (P<0.05). In the 2VO study, COE (50 mg/kg, p.o.) significantly reversed 2VO-induced cognitive impairments in mice by the passive avoidance and the Y-maze tasks (P<0.05). Moreover, COE (50 mg/kg, p.o.) also reduced escape-latency and prolonged swimming time in the target quadrant during a probe trial of the Morris water maze task (P<0.05). In an in vitro study, COE was found to inhibit acetylcholinesterase activity in a dose-dependent manner (IC50 value: 81.6 mu g/ml). Furthermore, COE also inhibited acetylcholinesterase activity in an ex vivo study. These results suggest that COE attenuates memory impairment induced by scopolamine or 2VO and that these effects are mediated by enhancing the cholinergic nervous system via acetylcholinesterase inhibition.
引用
收藏
页码:82 / 93
页数:12
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