Suppr超能文献

豚鼠海马苔藓纤维突触处代谢型谷氨酸受体的药理学

Pharmacology of metabotropic glutamate receptors at the mossy fiber synapses of the guinea pig hippocampus.

作者信息

Manzoni O J, Castillo P E, Nicoll R A

机构信息

Department of Cellular and Molecular Pharmacology, University of California-San Francisco 94143-0450, USA.

出版信息

Neuropharmacology. 1995 Aug;34(8):965-71. doi: 10.1016/0028-3908(95)00060-j.

Abstract

We have tested the ability of several specific agonists of glutamate metabotropic receptors (mGluRs) to depress synaptic transmission at mossy fiber synapses in the CA3 region of the guinea pig hippocampus. 1S,3R-1-amino-cyclopentyl-1,3-dicarboxylate (ACPD) reversibly inhibited monosynaptic mossy fiber field potentials, presumably by a presynaptic mechanism, with an EC50 of 2.0 +/- 0.4 microM (n = 3), suggesting the presence of mGluRs on mossy fiber synaptic terminals of the group 1 or 2 category. L-2-amino-4-phosphono butanoate (L-AP4) also inhibited responses with an EC50 of 1.1 +/- 0.2 microM suggesting that mGluRs of the group 3 (mGluR4, 6, 7 and 8) category of receptors are also present on mossy fiber terminals. Both (2S,1'S,2'S)-2-(2'-carboxycyclopropyl)glycine (L-CCG1) and (S)-4-carboxy-3-hydroxy phenylglycine (4C3HPG) were also efficacious at blocking mossy fiber transmission, with an EC50 of 1.1 +/- 0.1 microM (n = 4) and 4.8 +/- 0.6 microM (n = 3) respectively. The latter finding indicates the involvement of mGluRs belonging to the group 2 (mGluR2, 3) category of receptors. The effects of L-AP4 and L-CCG1 were both antagonized by (+)-alpha-methyl-4-carboxyphenylglycine [(+)MCPG]. MAP4, an antagonist of group 3 mGluRs in other systems, blocked the effect of L-AP4, but not the effect of L-CCG1, while MCCG, an antagonist of group 2 mGluRs in other systems, blocked the effect of L-CCG1, but not the effect of L-AP4. These pharmacological findings provide strong evidence for the coexistence of group 2 and 3 mGluRs on the terminals of mossy fibers in the guinea pig.

摘要

我们测试了几种谷氨酸代谢型受体(mGluRs)特异性激动剂抑制豚鼠海马体CA3区苔藓纤维突触处突触传递的能力。1S,3R-1-氨基环戊基-1,3-二羧酸(ACPD)可逆性抑制单突触苔藓纤维场电位,推测是通过一种突触前机制,其半数有效浓度(EC50)为2.0±0.4微摩尔/升(n = 3),这表明在1类或2类苔藓纤维突触终末存在mGluRs。L-2-氨基-4-膦酰丁酸(L-AP4)也能抑制反应,其EC50为1.1±0.2微摩尔/升,这表明3类(mGluR4、6、7和8)受体的mGluRs也存在于苔藓纤维终末。(2S,1'S,2'S)-2-(2'-羧基环丙基)甘氨酸(L-CCG1)和(S)-4-羧基-3-羟基苯甘氨酸(4C3HPG)在阻断苔藓纤维传递方面也有效,其EC50分别为1.1±0.1微摩尔/升(n = 4)和4.8±0.6微摩尔/升(n = 3)。后一发现表明属于2类(mGluR2、3)受体的mGluRs也参与其中。L-AP4和L-CCG1的作用均被(+)-α-甲基-4-羧基苯甘氨酸[(+)MCPG]拮抗。MAP4是其他系统中3类mGluRs的拮抗剂,它阻断了L-AP4的作用,但不阻断L-CCG1的作用,而MCCG是其他系统中2类mGluRs的拮抗剂,它阻断了L-CCG1的作用,但不阻断L-AP4的作用。这些药理学发现为豚鼠苔藓纤维终末存在2类和3类mGluRs提供了有力证据。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验