1. Signaling Pathways
  2. GPCR/G Protein
    Neuronal Signaling
  3. Cholecystokinin Receptor

Cholecystokinin Receptor (胆囊收缩素受体)

CCK Receptor

胆囊收缩素受体 (Cholecystokinin Receptor) 是一组 G 蛋白偶联受体,可结合肽类激素胆囊收缩素 (CCK) 和胃泌素。两种功能性膜受体,胆囊收缩素 A 受体 (CCK-AR)(主要位于胰腺腺泡细胞)和 CCK-BR(主要位于胃和神经系统组织)已被确定为 CCK 的内源性受体。两者对硫酸化 CCK 八肽 (CCK-8) 均具有高亲和力,而只有 CCK-BR 对胃泌素具有高亲和力。

CCK 是在小肠中发现的一种肽类激素。CCK 与促胰液素和胃泌素一起构成了经典的肠道激素三联体。除了胆囊收缩外,CCK 还调节胰酶的分泌和生长、肠道运动、饱腹感信号以及抑制胃酸分泌。CCK 也是中枢和肠道神经元中的一种递质。

Cholecystokinin receptors are a group of G-protein coupled receptors which bind the peptide hormones cholecystokinin (CCK) and gastrin. Two types of functional membrane receptors, cholecystokinin A receptor (CCK-AR), located mainly on pancreatic acinar cells, and CCK-BR, mostly in the stomach and nervous system tissues, have been identified as the endogenous receptors of CCK. Both have high affinity for the sulfated CCK octapeptide (CCK-8), whereas only the CCK-BR has high affinity for gastrin.

CCK is a peptide hormone discovered in the small intestine. Together with secretin and gastrin, CCK constitutes the classical gut hormone triad. In addition to gallbladder contraction, CCK also regulates pancreatic enzyme secretion and growth, intestinal motility, satiety signalling and the inhibition of gastric acid secretion. CCK is also a transmitter in central and intestinal neurons.

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