Antidepressant-like effects of neferine in the forced swimming test involve the serotonin1A (5-HT1A) receptor in mice

被引:48
作者
Sugimoto, Yumi [1 ]
Furutani, Sachiko [2 ]
Nishimura, Katsumi [3 ]
Itoh, Atsuko [3 ]
Tanahashi, Takao [3 ]
Nakajima, Hiroshi [4 ]
Oshiro, Hideo [5 ]
Sun, Shujian [5 ]
Yamada, Jun [1 ]
机构
[1] Yokohama Coll Pharm, Pharmacol Lab, Dept Clin Pharm, Totsuka Ku, Yokohama, Kanagawa 2450066, Japan
[2] Kobe Pharmaceut Univ, Dept Pharmacol, Higashianda Ku, Kobe, Hyogo 6588558, Japan
[3] Kobe Pharmaceut Univ, Dept Organ Chem, Higashinada Ku, Kobe, Hyogo 6588558, Japan
[4] Osaka City Univ, Res Ctr Ind Innovat, Sumiyoshi Ku, Osaka 5588585, Japan
[5] Shanghai Univ Tradit Chinese Med, Kita Ku, Osaka 530004, Japan
关键词
Neferine; Nelumbo nucifera Gaertner; Forced swimming test; Antidepressant-like effect; Serotonin receptor; (Mouse); REUPTAKE INHIBITORS; IMMOBILITY; ANTAGONISTS; MECHANISMS; DISORDERS; ANXIETY;
D O I
10.1016/j.ejphar.2010.02.016
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The effects of neferine, an alkaloid of Nelumbo nucifera Gaertner embryos, on immobility in the forced swimming test, which is used to evaluate antidepressants, were investigated in mice. The administration of neferine from 25 to 100 mg/kg i.p. elicited anti-immobility effects in mice. The molecular dose effects of neferine in the forced swimming test were almost equal to those of the typical antidepressants maprotiline and imipramine. The involvement of the 5-HT receptor subtypes was also studied using 5-HT receptor antagonists. Anti-immobility effects of neferine are antagonized by the serotonin(1A) (5-HT1A) receptor antagonist, N-[2-[4-(2-methoxyphenyl)-1-piperaziny]ethyl]-N-(2-pyridinyl)cyclohexanecarboxamide (WAY 100635). However, the 5-HT1B receptor antagonist, 3-[3-(dimethylamino)propyl]-4-hydroxy-N-[4-(4-pyridinyl)phenyl] benzamide dihydrochloride (GR 55562), the 5-HT2 receptor antagonist, 6-methyl-1-(methylethyl)-ergoline-8-beta carboxylic acid 2-hydroxy-1-methylpropyl ester (LY 53857), the 5-HT3 receptor antagonist, ondansetron and the 5-HT4 receptor antagonist, 4-amino-5-chloro-2-methoxy-benzoic acid 2-(diethylamino)ethyl ester (SDZ 205,557) did not affect the anti-immobility effects of neferine. The anti-immobility effect of the selective 5-HT1A receptor agonist, 8-hydroxy-2-(di-n-propylamino)tetaralin (8-OH-DPAT) was also antagonized by WAY 100635. Furthermore, co-administration of subactive doses of neferine (10 mg/kg) and 8-OH-DPAT (0.1 mg/kg) produced synergistic antidepressant-like effects. These results suggest that neferine shows antidepressant-like effects in mice similar to typical antidepressants and that these effects are mediated by the 5-HT1A receptor. Therefore, the central effects of neferine are likely to be linked to serotonergic neurotransmission. (C) 2010 Elsevier B.V. All rights reserved.
引用
收藏
页码:62 / 67
页数:6
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