组胺能
组胺H3受体
反激动剂
内分泌学
组胺
能量稳态
内科学
组胺H1受体
兴奋剂
食欲
受体
组胺受体
化学
生物
敌手
药理学
神经科学
医学
作者
Néstor Fabián Díaz,Héctor Flores‐Herrera,Guadalupe García‐López,Anayansí Molina‐Hernández
出处
期刊:Cns & Neurological Disorders-drug Targets
[Bentham Science]
日期:2019-12-09
卷期号:18 (7): 516-522
被引量:5
标识
DOI:10.2174/1871527318666190703094846
摘要
The brain histaminergic system plays a pivotal role in energy homeostasis, through H1- receptor activation, it increases the hypothalamic release of histamine that decreases food intake and reduces body weight. One way to increase the release of hypothalamic histamine is through the use of antagonist/inverse agonist for the H3-receptor. Histamine H3-receptors are auto-receptors and heteroreceptors located on the presynaptic membranes and cell soma of neurons, where they negatively regulate the synthesis and release of histamine and other neurotransmitters in the central nervous system. Although several compounds acting as H3-receptor antagonist/inverse agonists have been developed, conflicting results have been reported and only one has been tested as anti-obesity in humans. Animal studies revealed the opposite effect in food intake, energy expeditor, and body weight, depending on the drug, spice, and route of administration, among others. The present review will explore the state of art on the effects of H3-receptor ligands on appetite and body-weight, going through the following: a brief overview of the circuit involved in the control of food intake and energy homeostasis, the participation of the histaminergic system in food intake and body weight, and the H3-receptor as a potential therapeutic target for obesity.
科研通智能强力驱动
Strongly Powered by AbleSci AI