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首页> 外文期刊>Reviews in the neurosciences >The unappreciated roles of the cholecystokinin receptor CCK(1) in brain functioning
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The unappreciated roles of the cholecystokinin receptor CCK(1) in brain functioning

机译:胆囊蛋白受体CCK(1)在脑功能中的未被覆富的作用

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The CCK(1) receptor is a G-protein-coupled receptor activated by the sulfated forms of cholecystokinin (CCK), a gastrin-like peptide released in the gastrointestinal tract and mammal brain. A substantial body of research supports the hypothesis that CCK(1) r stimulates gallbladder contraction and pancreatic secretion in the gut, as well as satiety in brain. However, this receptor may also fulfill relevant roles in behavior, thanks to its widespread distribution in the brain. The strategic location of CCK(1) r in mesolimbic structures and specific hypothalamic and brainstem nuclei lead to complex interactions with neurotransmitters like dopamine, serotonin, and glutamate, as well as hypothalamic hormones and neuropeptides. The activity of CCK(1) r maintains adequate levels of dopamine and regulates the activity of serotonin neurons of raphe nuclei, which makes CCK(1) r an interesting therapeutic target for the development of adjuvant treatments for schizophrenia, drug addiction, and mood disorders. Unexplored functions of CCK(1) r, like the transmission of interoceptive sensitivity in addition to the regulation of hypothalamic hormones and neurotransmitters affecting emotional states, well-being, and attachment behaviors, may open exciting roads of research. The absence of specific ligands for the CCK(1) receptor has complicated the study of its distribution in brain so that research about its impact on behavior has been published sporadically over the last 30 years. The present review reunites all this body of evidence in a comprehensive way to summarize our knowledge about the actual role of CCK in the neurobiology of mental illness.
机译:CCK(1)受体是由硫化物形式的胆囊蛋白(CCK)活化的G蛋白偶联受体,胃肠道和哺乳动物脑释放的胃泌素样肽。大量研究支持CCK(1)R刺激肠道中的胆囊收缩和胰腺分泌物,以及脑中的饱腹感。然而,由于其在大脑中的广泛分布,这种受体也可能满足行为中的相关角色。 CCK(1)r在培素咪啶结构和特定下丘脑和脑干核中的战略位置导致与多巴胺,血清素和谷氨酸等神经递质的复杂相互作用,以及下丘脑激素和神经肽。 CCK(1)R的活性保持足够的多巴胺水平,并调节Raphe核的血清素神经元的活性,使CCK(1)R成为精神分裂症,吸毒成瘾和情绪障碍的辅助治疗的有趣治疗靶标。 CCK(1)R的未开发功能,例如流动敏感性的传播除了对影响情绪状态的下丘脑激素和神经递质,幸福和附着行为的监管外,可能会打开令人兴奋的研究道路。 CCK(1)受体的特定配体的缺失使其在大脑中分布的研究复杂,因此在过去30年中偶尔出版了关于其对行为的影响的研究。本综述以全面的方式统治所有这一证据的证据,以总结我们关于CCK在精神疾病神经生物学中的实际作用的知识。

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