Brown J, Gallagher N D
Biochim Biophys Acta. 1978 Jan 3;538(1):42-9. doi: 10.1016/0304-4165(78)90250-7.
A specific receptor for gastrin I has been demonstrated in the rat stomach fundus. Specific binding of 125I-labelled gastrin I was localised to particles sedimenting between 250--20 000 X g. Saturation of binding sites occurred with a gastrin concentration of 10(-11) M in an assay system containing 0.6--1.7 mg/ml of homogenate protein. Gastrin binding was shown to be reversible, temperature- and pH-dependent, and susceptible to tryptic digestion. Electron microscopic and enzymatic studies showed the binding fraction to contain predominantly mitochondria. Preincubation of the homogenate with 10(-8) M cholecystokinin or secretin inhibited gastrin binding to a greater extent than an equimolar concentration of pentagastrin. Cimetidine, a histamine receptor antagonist, did not affect binding of gastrin to the receptor.
已在大鼠胃底中证实存在胃泌素I的特异性受体。125I标记的胃泌素I的特异性结合定位于在250 - 20000×g之间沉降的颗粒。在含有0.6 - 1.7mg/ml匀浆蛋白的测定系统中,胃泌素浓度为10(-11)M时发生结合位点饱和。胃泌素结合表现为可逆的,依赖温度和pH,并易受胰蛋白酶消化影响。电子显微镜和酶学研究表明,结合部分主要含有线粒体。用10(-8)M胆囊收缩素或促胰液素对匀浆进行预孵育,比等摩尔浓度的五肽胃泌素更能抑制胃泌素结合。组胺受体拮抗剂西咪替丁不影响胃泌素与受体的结合。