McIntosh C H, Dahl M A, Kwok Y N, Mutt V, Spruston N, Brown J C
MRC Regulatory Peptide Group, Department of Physiology, University of British Columbia, Vancouver, Canada.
Can J Physiol Pharmacol. 1988 Nov;66(11):1407-14. doi: 10.1139/y88-229.
A number of different forms of cholecystokinin (CCK) exist in the brain and intestine. Gel permeation and ion exchange chromatography and high performance liquid chromatography have been used to isolate a peptide from partially purified porcine intestinal extracts with N-terminal homology to porcine brain CCK-58. This peptide contracted both the guinea pig ileum longitudinal muscle and gallbladder muscle and these responses were inhibited by dibutyryl cyclic GMP or proglumide. The potency was approximately 1/100 of that of CCK-8. The reason for this low potency is unclear, but it is possible that a critical part of the biologically active region is modified or that it is a truncated form of CCK-58. A further peptide was isolated with a sequence homologous to cytochrome oxidase polypeptide VII and chymodenin.
脑和肠道中存在多种不同形式的胆囊收缩素(CCK)。凝胶渗透色谱法、离子交换色谱法和高效液相色谱法已被用于从部分纯化的猪肠道提取物中分离出一种与猪脑CCK - 58具有N端同源性的肽。该肽能使豚鼠回肠纵肌和胆囊肌收缩,且这些反应可被二丁酰环磷鸟苷或丙谷胺抑制。其效力约为CCK - 8的1/100。效力低的原因尚不清楚,但有可能是生物活性区域的关键部分被修饰了,或者它是CCK - 58的截短形式。还分离出了另一种与细胞色素氧化酶多肽VII和促凝乳酶原具有同源序列的肽。