Torda T, Saavedra J M
Section on Pharmacology, National Institute of Mental Health, Bethesda, Md.
Neuroendocrinology. 1990 Oct;52(4):361-7. doi: 10.1159/000125608.
[125I]-neuropeptide Y receptors were characterized in the rat pituitary gland using quantitative autoradiography. Scatchard analysis of saturation isotherms showed high affinity (Kd 8.5 x 10(-11) M) and single class of binding sites (Bmax 0.22 pmol/mg of protein) in the posterior lobe of the pituitary gland, with no specific binding in the intermediate or anterior lobe. Increasing concentrations of guanine nucleotide analogues and peptide YY inhibited neuropeptide Y binding. In addition, neuropeptide Y binding was pertussis-toxin-sensitive. These results add additional information about a possible neuronal (through neuropeptide Y) and hormonal (through peptide YY) regulation of posterior pituitary function, which is most probably GTP-dependent.
利用定量放射自显影技术对大鼠垂体中的[125I] - 神经肽Y受体进行了表征。对饱和等温线的Scatchard分析表明,垂体后叶存在高亲和力(解离常数Kd为8.5×10⁻¹¹ M)和单一类别的结合位点(最大结合容量Bmax为0.22 pmol/mg蛋白质),而中间叶和前叶无特异性结合。鸟嘌呤核苷酸类似物和肽YY浓度的增加会抑制神经肽Y的结合。此外,神经肽Y的结合对百日咳毒素敏感。这些结果为垂体后叶功能可能的神经元(通过神经肽Y)和激素(通过肽YY)调节提供了更多信息,这种调节很可能依赖于鸟苷三磷酸(GTP)。