O'Shea R D, Gundlach A L
University of Melbourne, Department of Medicine, Austin and Repatriation Hospital, Heidelberg, Victoria, Australia.
J Neuroendocrinol. 1993 Dec;5(6):697-704. doi: 10.1111/j.1365-2826.1993.tb00542.x.
Cholecystokinin (CCK) has been suggested to mediate satiety in a number of non-primate species via its peripheral actions as well as a possible central mechanism involving magnocellular and parvocellular oxytocin release. Quantitative in vitro autoradiography employing [125I]-Bolton-Hunter labelled CCK-8S ([125I]-CCK-8S) was used to examine the distribution and density of CCK receptors in sections of brain from normal rats and rats deprived of food, water or both food and water for 4 days. In food-deprived rats, specific [125I]-CCK-8S binding was reduced by 64 +/- 5% in the hypothalamic supraoptic nucleus (SON) and by 44 +/- 13% in the paraventricular nucleus of the hypothalamus (PVN). In contrast, water deprivation increased binding of [125I]-CCK-8S by 128 +/- 15% in the SON and by 196% +/- 24% in the PVN, while combined food and water deprivation produced smaller increases in both nuclei (30 +/- 5% and 98 +/- 26% in SON and PVN respectively). Changes in receptor density in the PVN appeared to be most prominent in the magnocellular (especially oxytocin-rich) subdivisions. None of the treatments employed produced changes in [125I]-CCK-8S binding in the ventromedial hypothalamic nucleus or the reticular thalamic nucleus. Both CCK-A and CCK-B receptor subtypes were visualized in the nucleus of the solitary tract and the area postrema of normal rats, but levels of binding to both of these subtypes were unaffected by the experimental treatments. These selective alterations demonstrate the plasticity of CCK receptors in the SON and PBN, and are probably associated with changes in the level of neurochemical activity of magnocellular oxytocinergic neurones in these areas. These results, together with reports of changes in the level of CCK synthesis in cells of the SON and PVN after hyperosmotic stimuli, suggest that CCK may act in an autocrine fashion on these neurones and that both CCK receptors and peptide levels are altered in the same direction following cellular activation or inhibition.
胆囊收缩素(CCK)已被认为可通过其外周作用以及一种可能涉及大细胞和小细胞催产素释放的中枢机制来介导多种非灵长类动物的饱腹感。采用[125I]-博尔顿-亨特标记的CCK-8S([125I]-CCK-8S)进行定量体外放射自显影,以检测正常大鼠以及禁食、禁水或禁食禁水4天的大鼠脑切片中CCK受体的分布和密度。在禁食大鼠中,下丘脑视上核(SON)的特异性[125I]-CCK-8S结合减少了64±5%,下丘脑室旁核(PVN)减少了44±13%。相反,禁水使SON中[125I]-CCK-8S的结合增加了128±15%,PVN中增加了196%±24%,而禁食禁水则使两个核中的增加幅度较小(SON和PVN分别为30±5%和98±26%)。PVN中受体密度的变化似乎在大细胞(尤其是富含催产素的)亚区最为显著。所采用的任何处理均未引起下丘脑腹内侧核或丘脑网状核中[125I]-CCK-8S结合的变化。在正常大鼠的孤束核和最后区中均可观察到CCK-A和CCK-B受体亚型,但这两种亚型的结合水平均不受实验处理的影响。这些选择性改变证明了SON和PBN中CCK受体的可塑性,并且可能与这些区域中大细胞催产素能神经元的神经化学活性水平变化有关。这些结果,连同高渗刺激后SON和PVN细胞中CCK合成水平变化的报道,表明CCK可能以自分泌方式作用于这些神经元,并且在细胞激活或抑制后,CCK受体和肽水平会朝着相同方向改变。