Patel Y C, Baquiran G, Srikant C B, Posner B I
Endocrinology. 1986 Nov;119(5):2262-9. doi: 10.1210/endo-119-5-2262.
Quantitative in vivo autoradiography was used to identify and compare the regional distribution of specific binding sites for blood-borne [125I-Tyr11]somatostatin-14 (S-14 section) and [Leu8,D-Trp22-125I-Tyr25]somatostatin-28 (S-28 section) in the rat brain. Rats were given intracardiac injections of 17 pmol S-14 section (with or without unlabeled S-14) or 17 pmol S-28 section (with or without unlabeled S-28). After whole body perfusion and fixation, brains were processed for light microscopic autoradiography of S-14 section- and S-28 section-binding sites. Of the peripheral tissues, the adrenal glands showed the highest uptake of S-14 section and S-28 section (determined by counting) and were subsequently processed for autoradiography for comparison with brain. Specific autoradiographic grains (ARG) associated with both radioligands were identified only in the circumventricular organs (CVOs). The highest ARG density associated with S-14 section was found in the area postrema, followed in decreasing order by the subfornical organ and the organum vasculosum lamina terminalis region. Median eminence (ME) contained virtually no specific S-14 section ARG. As with S-14 section, the highest ARG density of S-28 section-binding sites was also found in the area postrema, which labeled approximately equally with the two radioligands. This was followed by the ME, subfornical organ, and organum vasculosum lamina terminalis. The overall patterns of labeling of the CVOs with S-14 section and S-28 section showed significant differences, especially in the ME. Within the ME, labeled S-28 section was concentrated in a broad band throughout the external zone in a location identical to that of immunoreactive S-14. Analysis of dose-response curves obtained with 0.3-30 nmol unlabeled S-14 or S-28 revealed IC50 values for S-14 3- to 6-fold lower than those for S-28 for all labeled CVOs. With both S-14 section and S-28 section, the labelling density of the adrenal glands was double that of the area postrema. Adrenal binding of the radioligands was confined to the cells of the zona glomerulosa. We conclude: specific high affinity binding sites for S-14 section and S-28 section exist in the CVOs and the adrenal glomerulosa; and the 3- to 6-fold higher affinity of binding of S-14 to CVOs compared to S-28 together with the dissimilar patterns of labelling of the different CVOs by the two radioligands suggest the existence of separate populations of S-14 and S-28 receptors.
采用定量体内放射自显影技术来鉴定和比较大鼠脑中血源性[125I-酪氨酸11]生长抑素-14(S-14片段)和[亮氨酸8,D-色氨酸22-125I-酪氨酸25]生长抑素-28(S-28片段)特异性结合位点的区域分布。给大鼠心内注射17 pmol S-14片段(有或无未标记的S-14)或17 pmol S-28片段(有或无未标记的S-28)。全身灌注固定后,对脑进行处理,以对S-14片段和S-28片段结合位点进行光学显微镜放射自显影。在外周组织中,肾上腺对S-14片段和S-28片段的摄取量最高(通过计数确定),随后对其进行放射自显影处理以与脑进行比较。仅在室周器官(CVO)中鉴定出与两种放射性配体相关的特异性放射自显影颗粒(ARG)。与S-14片段相关的最高ARG密度出现在最后区,其次依次为穹窿下器官和终板血管器区域。正中隆起(ME)几乎没有特异性S-14片段ARG。与S-14片段一样,S-28片段结合位点的最高ARG密度也出现在最后区,该区域与两种放射性配体的标记程度大致相同。其次是ME、穹窿下器官和终板血管器。S-14片段和S-28片段对CVO的整体标记模式显示出显著差异,尤其是在ME中。在ME内,标记的S-28片段集中在整个外部区域的一条宽带中,其位置与免疫反应性S-14相同。对用0.3 - 30 nmol未标记的S-14或S-28获得的剂量反应曲线进行分析,结果显示所有标记的CVO中S-14的半数抑制浓度(IC50)值比S-28低3至6倍。对于S-14片段和S-28片段,肾上腺的标记密度是最后区的两倍。放射性配体与肾上腺的结合局限于球状带细胞。我们得出结论:CVO和肾上腺球状带中存在S-14片段和S-28片段的特异性高亲和力结合位点;与S-28相比,S-14与CVO结合的亲和力高3至6倍,并且两种放射性配体对不同CVO的标记模式不同,这表明存在单独的S-14和S-28受体群体。