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论四氢小檗碱与GABA受体无关的中枢抑制作用

[On the central inhibition action of tetrahydroberberine without relevance to GABA receptors].

作者信息

Wang X L, Jin G Z, Zhou T C

机构信息

Shanghai Institute of Materia Medica Academy of Sciences.

出版信息

Sheng Li Xue Bao. 1994 Oct;46(5):505-8.

PMID:7846552
Abstract

Using an earthworm (Eisenia foetida) dorsal muscle preparation, it was shown that tetrahydroberberine (THB, 10(-7)-10(-4) mol/L) did not affect both GABA and ACh receptors. DA receptor antagonist haloperidol (HAL) also exerted no effect. Owing to the blocking action of isonicotinyl hydrazine (INH) and thiosemicarbazide (TSC) on biosynthesis of GABA, and of picrotoxin (PT) and bicuculline (Bic) on the GABA-BZ receptor complex mediated transmission, all these agents could induce convulsion in mice. This action could be antagonized by amino- oxyacetic acid (AOAA) and benzodiazepine (BZ), but not by DA receptor antagonists THB and HAL. All the above observations indicate that the GABA inhibition is not involved in the central action of THB.

摘要

利用蚯蚓(赤子爱胜蚓)背肌标本,研究发现四氢小檗碱(THB,10⁻⁷ - 10⁻⁴ mol/L)对GABA和ACh受体均无影响。多巴胺受体拮抗剂氟哌啶醇(HAL)也无作用。由于异烟酰肼(INH)和氨基硫脲(TSC)对GABA生物合成有阻断作用,以及印防己毒素(PT)和荷包牡丹碱(Bic)对GABA - BZ受体复合物介导的传递有阻断作用,所有这些药物均可诱发小鼠惊厥。这种作用可被氨氧乙酸(AOAA)和苯二氮䓬(BZ)拮抗,但不能被多巴胺受体拮抗剂THB和HAL拮抗。上述所有观察结果表明,GABA抑制作用不参与THB的中枢作用。

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