组胺
组胺受体
组胺H3受体
受体
细胞内
组胺H2受体
组胺H1受体
第二信使系统
生物
组胺H4受体
离子通道
细胞生物学
神经科学
化学
药理学
生物化学
兴奋剂
敌手
出处
期刊:PubMed
日期:1990-03-01
卷期号:42 (1): 45-83
被引量:227
摘要
It is clear from the preceding overview of histamine receptor pharmacology that research into the pharmacology of histamine receptors is at an exciting stage of development. The rapid advance of molecular biology should soon see the structural identification and cloning of all three of the major vertebrate histamine receptors. Further work will continue toward enhancing our understanding of the control by histamine of intracellular signaling via H1- and H2-receptors, and the rapid explosion of work on the H3-receptor should begin to unravel the mechanisms underlying its actions, perhaps via effects on ionic channels. The potential role of histamine as an intracellular second messenger raises exciting possibilities, as does the search for a histamine receptor analogous to the ligand-gated ion channel in the invertebrate nervous system.
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