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四氢氨基吖啶和树眼镜蛇毒素对血清素抑制的[3H]乙酰胆碱释放的衰减作用:与米那普明结合位点的相互作用。

Attenuation of serotonin-suppressed [3H]acetylcholine release by tetrahydroaminoacridine and dendrotoxin: interaction with minaprine binding site.

作者信息

Muramatsu M, Chaki S, Usuki-ito C, Otomo S

机构信息

Department of Pharmacology, Taisho Pharmaceutical Co., Ltd., Saitama, Japan.

出版信息

Res Commun Chem Pathol Pharmacol. 1990 May;68(2):131-42.

PMID:2353129
Abstract

5-Hydroxytryptamine (5-HT) inhibited K(+)-induced [3H]acetylcholine ([3H]ACh) release from rat hippocampal slices dose-dependently. Minaprine [3-(2-morpholino-ethylamino)-4-methyl-6-phenylpyridazine] and 9-amino-1,2,3,4-tetrahydroacridine (THA) attenuated the inhibition of [3H]ACh release by 5-HT. A neurotoxin isolated from the venom of Dendroaspis snake, dendrotoxin (DTX), also attenuated the 5-HT inhibited [3H]ACh release from hippocampal slices dose-dependently at doses of more than 3 x 10(-7) g/ml (about 42 nM). Specific binding of [3H]minaprine to hippocampal membrane was dose-dependently inhibited by THA and DTX. The IC50 of THA and DTX for the [3H]minaprine binding were about 32 and 0.7 mu M, respectively. Scatchard plot analyses showed that the inhibitory effects of THA and DTX were noncompetitive for [3H]minaprine binding. THA and DTX inhibited [3H]ketanserin binding with IC50 of 28.8 and 26.2 mu M, respectively. These results suggest that THA and DTX attenuate the 5-HT-inhibited [3H]ACh release by blocking a voltage-dependent K+ current, and that they interact with the binding site of minaprine in the hippcampus.

摘要

5-羟色胺(5-HT)剂量依赖性地抑制钾离子(K(+))诱导的大鼠海马切片中[3H]乙酰胆碱([3H]ACh)的释放。米那普明[3-(2-吗啉代-乙氨基)-4-甲基-6-苯基哒嗪]和9-氨基-1,2,3,4-四氢吖啶(THA)减弱了5-HT对[3H]ACh释放的抑制作用。从树眼镜蛇毒液中分离出的一种神经毒素——树眼镜蛇毒素(DTX),在剂量高于3×10(-7) g/ml(约42 nM)时,也剂量依赖性地减弱了5-HT对海马切片中[3H]ACh释放的抑制作用。[3H]米那普明与海马膜的特异性结合受到THA和DTX的剂量依赖性抑制。THA和DTX对[3H]米那普明结合的IC50分别约为32和0.7 μM。Scatchard图分析表明,THA和DTX对[3H]米那普明结合的抑制作用是非竞争性的。THA和DTX分别以28.8和26.2 μM的IC50抑制[3H]酮色林结合。这些结果表明,THA和DTX通过阻断电压依赖性钾离子电流减弱了5-HT对[3H]ACh释放的抑制作用,并且它们与海马中米那普明的结合位点相互作用。

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