Bucharles C, Vaudry H, Leroux P
European Institute for Peptide Research (IFRMP n 23), INSERM U413, UA CNRS, University of Rouen, Mont-Saint-Aignan, France.
J Chem Neuroanat. 1999 May;16(3):223-9. doi: 10.1016/s0891-0618(99)00003-4.
Adult rat cerebellar nuclei contain a single population of [125I][Leu8,D-Trp22,Tyr25]somatostatin-28 binding sites characterized as sst1 receptors. In the present study, we have investigated the evolution of somatostatin receptors in rat cerebellar nuclei during development by means of quantitative autoradiography on tissue sections. The binding of [125I][Leu8,D-Trp22,Tyr25]somatostatin-28, observed in the primordium of the medial cerebellar nuclei at embryonic day 17, reached a maximum at postnatal day 7 or 10 in the different nuclei. Thereafter, the density of binding sites gradually decreased to the adult level. Competition studies were performed using the somatostatin analogues CH-288 and MK-678 as specific sst1 and sst2 ligands, respectively. Partial inhibition of the radioligand binding by CH-288 and MK-678 revealed the presence of a predominant population of sst1 from embryonic day 19-28 day postnatal and a minor population of sst2 receptors. The use of [125I]MK-678 as a radioligand confirmed the presence of a transient population of sst2 receptors, suggesting that somatostatin could act on rat cerebellar nuclei via sst1 and/or sst2 receptors during development.
成年大鼠小脑核含有单一群体的[125I][亮氨酸8、D-色氨酸22、酪氨酸25]生长抑素-28结合位点,其被表征为sst1受体。在本研究中,我们通过对组织切片进行定量放射自显影,研究了大鼠小脑核中生长抑素受体在发育过程中的演变。在胚胎第17天内侧小脑核原基中观察到的[125I][亮氨酸8、D-色氨酸22、酪氨酸25]生长抑素-28的结合,在出生后第7天或第10天在不同核中达到最大值。此后,结合位点密度逐渐下降至成年水平。分别使用生长抑素类似物CH-288和MK-678作为特异性sst1和sst2配体进行竞争研究。CH-288和MK-678对放射性配体结合的部分抑制揭示,从胚胎第19天至出生后第28天存在主要的sst1群体和少量的sst2受体群体。使用[125I]MK-678作为放射性配体证实了sst2受体短暂群体的存在,这表明生长抑素在发育过程中可能通过sst1和/或sst2受体作用于大鼠小脑核。