5-羟色胺受体
(重定向自血清素受體)
5-羥色胺受體,也被稱為血清素受體或5-HT受體,是一羣於中樞神經系統中央處和末梢神經系統周邊出現的G蛋白偶聯受體及配體門控離子通道。[1][2]它們同時調節興奮性和抑制性神經傳導物質的傳遞。
分類
血清素受體可分為七個亞科 5-HT1, 5-HT2, 5-HT3, 5-HT4, 5-HT5, 5-HT6, 5-HT7。至少有十四種受體亞型已被發現,包含G蛋白偶聯受體(G protein-coupled receptor)和配體門控離子通道(ligand-gated ion channel)。
- 5-HT1受體是5-HT受體家族中最龐大的一科,包括5-HT1A、5-HT1B、5-HT1D、5-HT1E、5-HT1F五種受體蛋白。沒有5-HT1C受體,因為它被重新分類為5-HT2C受體。
- 5-HT2受體亚家族包括5-HT2A、5-HT2B,和5-HT2C三種受體蛋白。
- 5-HT3受體
- 5-HT4受體
- 5-HT5受體亚家族包括5-HT5A、5-HT5B两種受體蛋白。(其中5B受体在人类中为假基因,无受体表达)
- 5-HT6受體
- 5-HT7受體
總共有十四種受體亞型。
除了5-HT3受体是配体门控离子通道以外,其它的所有血清素受体都是G蛋白偶联受体,激活细胞内的第二信使来产生效应。在2014年,在菜粉蝶基因组中发现了一种新的5-HT受体,被命名为pr5-HT8。它与已知的各类5-HT受体相似度很低,在哺乳动物中没有类似基因。[3]
家族
七個亞科 5-HT1, 5-HT2, 5-HT3, 5-HT4, 5-HT5, 5-HT6, 5-HT7。
家族 | 類型 | 作用機制 | 類別 |
5-HT1 | Gi/Go-蛋白偶聯受体 | 減少cAMP在細胞內的水平 | 抑制性 |
5-HT2 | Gq/G11-蛋白偶聯受体 | 增加細胞內IP3和DAG的水平 | 興奮性 |
5-HT3 | 配體門控Na+,K+离子通道 | 使質膜去極化 | 興奮性 |
5-HT4 | Gs蛋白偶聯受体 | 增加細胞內cAMP的水平 | 興奮性 |
5-HT5 | Gi/Go-蛋白偶聯受体[4] | 減少cAMP在細胞內的水平 | 抑制性 |
5-HT6 | Gs-蛋白偶聯受体 | 增加細胞內cAMP的水平 | 興奮性 |
5-HT7 | Gs-蛋白偶聯受体 | 增加細胞內cAMP的水平 | 興奮性 |
亞型
血清素受體功能概述 | ||||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|
受體 | 首次克隆 | 基因 | 分佈 | 作用 | 激動劑 | 拮抗劑 | 用途 | |||||
血管 | 中樞神經系統 | 胃腸道 | 血小板 | 外周神經系統 | 平滑肌 | |||||||
5-HT1A | 1987 | 是 | 是 | 否 | 否 | 否 | 否 |
選擇性
非選擇性
|
| |||
5-HT1B | 1992 | 是 | 是 | 否 | 否 | 否 | 否 | |||||
5-HT1D | 1991 | 是 | 是 | 否 | 否 | 否 | 否 |
|
||||
5-HT1E | 1992 | 是 | 是 | 否 | 否 | 否 | 否 |
| ||||
5-HT1F | 1993 | 否 | 是 | 否 | 否 | 否 | 否 |
|
| |||
5-HT2A | 1988 | 是 | 是 | 是 | 是 | 是 | 是 |
| ||||
5-HT2B | 1992 | 是 | 是 | 是 | 是 | 是 | 是 |
| ||||
5-HT2C | 1988 | 是 | 是 | 是 | 是 | 是 | 是 | |||||
5-HT3 | 1993 | 否 | 是 | 是 | 否 | 是 | 否 | |||||
5-HT4 | 1995 | 否 | 是 | 是 | 否 | 是 | 否 |
| ||||
5-HT5A | 1994 | 否 | 是 | 否 | 否 | 否 | 否 |
|
|
| ||
5-HT5B | 1993 | 否 | 否 | 否 | 否 | 否 | 否 |
Functions in rodents, |
| |||
5-HT6 | 1993 | 否 | 是 | 否 | 否 | 否 | 否 |
| ||||
5-HT7 | 1993 | 是 | 是 | 是 | 否 | 否 | 否 |
|
注意没有5-HT1C受体。这是因为在克隆这个受体并进一步分类之后,发现它和5-HT2家族共同点更多,于是就改名成了5-HT2C受体。
对各5-HT受体亚型选择性极弱的激动剂有麦角胺(一种antimigraine,激活5-HT1A、5-HT1D、5-HT1B、D2、去甲肾上腺素受体[28])、LSD(一种合成迷幻药物,可以激活5-HT1A、5-HT2A、5-HT2C、5-HT5A、5-HT6)。[28]
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外部链接
- 醫學主題詞表(MeSH):Serotonin+Receptors
- 5-Hydroxytryptamine Receptors. IUPHAR Database of Receptors and Ion Channels. International Union of Basic and Clinical Pharmacology. (原始内容存档于2016-06-01).
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