Israel A, Plunkett L M, Saavedra J M
Cell Mol Neurobiol. 1985 Sep;5(3):211-22. doi: 10.1007/BF00711007.
Autoradiographic techniques coupled with computerized microdensitometry and comparison with 125I standards were used to characterize and quantitate receptors for neuropeptides in rat brain and adrenal and pituitary glands. These techniques are rapidly performed, anatomically precise, and more sensitive than membrane binding techniques. They permit the determination of complete saturation curves and Scatchard analysis in discrete nuclei of the rat brain and in single rat pituitary and adrenal glands. Angiotensin II (AII) receptors were quantitated after incubation of 16-micron tissue sections with the AII agonist 125I-[Sar1]-AII. High-affinity, high-density AII receptors were present in the organon subfornicalis, organon vasculosum laminae terminalis and nuclei triangularis septalis, suprachiasmatis, and paraventricularis of the rat and in rat adrenal capsule-zona glomerulosa area, adrenal medulla, and anterior pituitary. These techniques could be used for precise localization and quantitation of other neuropeptide receptors in single rat brain nuclei, after optimizing the assay conditions and provided that suitable 125I ligands are available.
利用放射自显影技术结合计算机化显微密度测定法,并与125I标准品进行比较,对大鼠脑、肾上腺和垂体中的神经肽受体进行表征和定量。这些技术操作迅速、解剖学定位精确,且比膜结合技术更灵敏。它们能够在大鼠脑的离散核以及单个大鼠垂体和肾上腺中测定完整的饱和曲线并进行Scatchard分析。在用血管紧张素II(AII)激动剂125I-[Sar1]-AII孵育16微米厚的组织切片后,对AII受体进行了定量。大鼠的穹窿下器、终板血管器、三角隔核、视交叉上核和室旁核以及大鼠肾上腺被膜-球状带区域、肾上腺髓质和垂体前叶中存在高亲和力、高密度的AII受体。在优化测定条件并确保有合适的125I配体可用后,这些技术可用于对单个大鼠脑核中的其他神经肽受体进行精确定位和定量。