Shaw Janice L, Gackenheimer Susan L, Gehlert Donald R
Neuroscience Research, Lilly Research Laboratories, Eli Lilly and Company, Mail Code 0510, Indianapolis, IN 46285, USA.
J Chem Neuroanat. 2003 Nov;26(3):179-93. doi: 10.1016/j.jchemneu.2003.07.003.
Neuropeptide Y, one of the most abundant brain peptides, has been found to modulate several important biological functions via a family of G-protein coupled receptors. To investigate the localization of functional NPY receptor subtypes in the rat brain, we performed agonist-induced [35S]GTPgammaS autoradiography. The Y1/Y4/Y5 agonist Leu(31), Pro(34)-NPY increased [35S]GTPgammaS binding in several brain areas with a regional distribution consistent with that produced when labeling adjacent sections with [125I]-Leu(31), Pro(34)-PYY. The Y1 selective antagonist BIBP3226 antagonized the Leu(31), Pro(34)-NPY stimulated increase in [35S]GTPgammaS binding in all areas examined. The Y2 agonist C2-NPY stimulated [35S]GTPgamma binding in numerous brain areas with a regional distribution similar to the binding observed with [125I]-PYY 3-36. No increase in [35S]GTPgammaS binding above basal was observed in any brain area evaluated using Y4 and Y5 selective agonists. This study demonstrates abundant Y1 and Y2 receptor activation in the rat brain, while evidence for functional Y4 and Y5 receptors was not observed.
神经肽Y是大脑中含量最为丰富的肽类之一,已发现它可通过一类G蛋白偶联受体调节多种重要的生物学功能。为研究功能性神经肽Y受体亚型在大鼠脑中的定位,我们进行了激动剂诱导的[35S]GTPγS放射自显影。Y1/Y4/Y5激动剂Leu(31), Pro(34)-NPY在几个脑区增加了[35S]GTPγS结合,其区域分布与用[125I]-Leu(31), Pro(34)-PYY标记相邻切片时产生的分布一致。Y1选择性拮抗剂BIBP3226在所有检测区域均拮抗了Leu(31), Pro(34)-NPY刺激的[35S]GTPγS结合增加。Y2激动剂C2-NPY在众多脑区刺激了[35S]GTPγ结合,其区域分布类似于用[125I]-PYY 3-36观察到的结合。使用Y4和Y5选择性激动剂评估时,在任何脑区均未观察到[35S]GTPγS结合高于基础水平的增加。本研究表明大鼠脑中存在丰富的Y1和Y2受体激活,而未观察到功能性Y4和Y5受体的证据。