Mansour A, Fox C A, Meng F, Akil H, Watson S J
Mental Health Research Institute, University of Michigan, Ann Arbor.
Mol Cell Neurosci. 1994 Apr;5(2):124-44. doi: 10.1006/mcne.1994.1015.
Three opioid receptor types have been identified in the CNS and periphery that are referred to as mu, delta, and kappa. The present study examines the mRNA distribution of the kappa 1 receptor in the rat brain and compares it to the distribution of kappa receptor-binding sites and prodynorphin mRNA using a combination of in situ hybridization and receptor autoradiographic techniques. kappa 1 receptor mRNA was localized with a cRNA probe generated with a BamHI-HindIII cDNA fragment of the rat kappa 1 receptor and corresponds to the last 45 bp of the protein coding region and 728 nucleotides of the 3' untranslated region. Prodynorphin mRNA was localized with a cRNA probe corresponding to a 733-bp BamHI-HincII fragment of prodynorphin. kappa receptor-binding sites were labeled in one of two ways: [3H]U69,593 or [3H]bremazocine in the presence of a 300-fold excess of DAMGO and DPDPE. A high degree of correspondence between the kappa 1 receptor mRNA and kappa receptor binding was observed in several brain regions, including the endopiriform nucleus, claustrum, nucleus accumbens, olfactory tubercle, bed nucleus of the stria terminalis, medial preoptic area, paraventricular, supraoptic, suprachiasmatic, dorsomedial and ventromedial hypothalamic nuclei, basolateral, medial and cortical amygdaloid nuclei, midline thalamic nuclei, periaqueductal grey, parabrachial nucleus, locus coeruleus, and the nucleus of the solitary tract. Differences in the localization of kappa 1 receptor mRNA and binding and the relationship between the distribution of kappa 1 receptor and prodynorphin mRNAs are discussed.
在中枢神经系统和外周已鉴定出三种阿片受体类型,分别称为μ、δ和κ。本研究检测了大鼠脑中κ1受体的mRNA分布,并使用原位杂交和受体放射自显影技术相结合的方法,将其与κ受体结合位点和前强啡肽原mRNA的分布进行比较。κ1受体mRNA用大鼠κ1受体的BamHI-HindIII cDNA片段产生的cRNA探针进行定位,该探针对应于蛋白质编码区的最后45个碱基对和3'非翻译区的728个核苷酸。前强啡肽原mRNA用对应于前强啡肽原733bp BamHI-HincII片段的cRNA探针进行定位。κ受体结合位点用两种方法之一进行标记:在存在300倍过量的DAMGO和DPDPE的情况下,使用[3H]U69,593或[3H]布马佐辛。在几个脑区观察到κ1受体mRNA与κ受体结合之间有高度的对应关系,包括内梨状核、屏状核、伏隔核、嗅结节、终纹床核、内侧视前区、室旁核、视上核、视交叉上核、背内侧和腹内侧下丘脑核、基底外侧、内侧和皮质杏仁核、中线丘脑核、导水管周围灰质、臂旁核、蓝斑和孤束核。讨论了κ1受体mRNA定位与结合的差异以及κ1受体与前强啡肽原mRNA分布之间的关系。