POSTNATAL-DEVELOPMENT OF MULTIPLE OPIOID RECEPTORS IN RAT-BRAIN

被引:140
作者
KORNBLUM, HI [1 ]
HURLBUT, DE [1 ]
LESLIE, FM [1 ]
机构
[1] UNIV CALIF IRVINE,DEPT PHARMACOL,IRVINE,CA 92717
来源
DEVELOPMENTAL BRAIN RESEARCH | 1987年 / 37卷 / 1-2期
关键词
Ontogeny; Opiate receptor; Quantitative autoradiography; δ-Receptor; μ-Receptor; ξ-Receptor;
D O I
10.1016/0165-3806(87)90226-4
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Recent studies have demonstrated that opioid receptors may be functional at early stages of ontogeny, and may modulate specific developmental functions. It is presently unknown, however, which particular opioid receptor subtype(s) may be involved. In the preent study, we have used selective radioligand binding conditions in combination with quantitative autoradiography to examine the ontogeny of μ-, ξ- and δ-opioid receptors in the developing rat brain. Membrane binding data indicate that the affinities of μ-, ξ- and δ- sites for radiolabeled drugs are similar in neonatal and adult rats. μ- And ξ-receptors are present in significant densities during early neonatal periods, while δ-receptors appear much later. Autoradiographic data indicate that μ- and ξ-receptors appear early in the development of several brain regions, including the neostriatum, olfactory tubercle and rostral midbrain, and later in other regions such as the thalamus and hypothalamus. Whereas the densities of ξ-binding sites remain relatively constant throughout development, there is a transient appearance and/or redistribution of μ-receptors in several brain areas. δ-Receptors are present in low densities in the basal forebrain at birth. The level of δ-receptor binding increases markedly during the third postnatal week in all brain areas examined. The early appearance of μ- and ξ-receptors during the ontogeny of the brain suggests that these receptors, at least in part, mediate the developmental actions of exogenous and endogenous opioids. © 1987.
引用
收藏
页码:21 / 41
页数:21
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