Enjalbert A, Rasolonjanahary R, Moyse E, Kordon C, Epelbaum J
Endocrinology. 1983 Aug;113(2):822-4. doi: 10.1210/endo-113-2-822.
Specific [125I]-Iodo-NTyr somatostatin binding sites are present in adenohypophyseal and cerebral cortical membranes. Guanine nucleotides reduce the maximal binding capacity of adenohypophyseal binding sites without significantly affecting their apparent affinity. In pituitary as well as in cortex, GTP is the most potent nucleotide followed by GDP and guanylyl imidodiphosphate (GMP-PNP). The effect appears specific of guanine nucleotides since ATP, ADP and AMP are inactive on [125I]-Iodo-NTyr somatostatin binding. These results, showing the nucleotide sensitivity of [125I]-Iodo-NTyr somatostatin binding in pituitary and cerebral cortex, are compatible with a coupling of somatostatin receptors with adenylate cyclase.
特异性的[125I] - 碘 - N - 酪氨酸生长抑素结合位点存在于腺垂体和大脑皮质膜中。鸟嘌呤核苷酸降低腺垂体结合位点的最大结合能力,但对其表观亲和力无显著影响。在垂体以及皮质中,GTP是最有效的核苷酸,其次是GDP和鸟苷酰亚胺二磷酸(GMP - PNP)。由于ATP、ADP和AMP对[125I] - 碘 - N - 酪氨酸生长抑素结合无活性,所以该效应似乎是鸟嘌呤核苷酸特有的。这些结果表明[125I] - 碘 - N - 酪氨酸生长抑素结合在垂体和大脑皮质中对核苷酸敏感,这与生长抑素受体与腺苷酸环化酶的偶联是一致的。