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Characterization and visualization of rat and guinea pig brain kappa opioid receptors: evidence for kappa 1 and kappa 2 opioid receptors.

机译:大鼠和豚鼠脑中阿片受体的表征和可视化:kappa 1和kappa 2阿片受体的证据。

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摘要

kappa opioid receptors (kappa receptors) have been characterized in homogenates of guinea pig and rat brain under in vitro binding conditions. kappa receptors were labeled by using the tritiated prototypic kappa opioid ethylketocyclazocine under conditions in which mu and delta opioid binding was suppressed. In the case of guinea pig brain membranes, a single population of high-affinity kappa opioid receptor sites (kappa sites; Kd = 0.66 nM, Bmax = 80 fmol/mg of protein) was observed. In contrast, in the case of rat brain, two populations of kappa sites were observed--high-affinity sites at low density (Kd = 1.0 nM, Bmax = 16 fmol/mg of protein) and low-affinity sites at high density (Kd = 13 nM, Bmax = 111 fmol/mg of protein). To test the hypothesis that the high- and low-affinity kappa sites represent two distinct kappa receptor subtypes, a series of opioids were tested for their abilities to compete for binding to the two sites. U-69,593 and Cambridge 20 selectively displaced the high-affinity kappa site in both guinea pig and rat tissue, but were inactive at the rat-brain low-affinity site. Other kappa opioid drugs, including U-50,488, ethylketocyclazocine, bremazocine, cyclazocine, and dynormphin (1-17), competed for binding to both sites, but with different rank orders of potency. Quantitative light microscopy in vitro autoradiography was used to visualize the neuroanatomical pattern of kappa receptors in rat and guinea pig brain. The distribution patterns of the two kappa receptor subtypes of rat brain were clearly different. The pattern of rat high-affinity kappa sites paralleled that of guinea pig in the caudate-putamen, mid-brain, central gray substance of cerebrum, and substantia nigra; interspecies differences were apparent throughout most of the rest of the brain. Collectively, these data provide direct evidence for the presence of two kappa receptor subtypes; the U-69,593-sensitive, high-affinity kappa 1 site predominates in guinea pig brain, and the U-69,593-insensitive, low-affinity kappa 2 site predominates in rat brain.
机译:在体外结合条件下,豚鼠和大鼠脑匀浆中的阿片受体(κ受体)已经被表征。在抑制了μ和δ阿片样物质结合的条件下,通过使用ti化的原型阿片样物质阿片类乙基环环偶氮cine标记kappa受体。在豚鼠脑膜的情况下,观察到单个高亲和性阿片受体部位(kappa部位; Kd = 0.66 nM,Bmax = 80 fmol / mg蛋白)。相比之下,在大鼠大脑中,观察到了两个kappa位种群-低密度时的高亲和力位点(Kd = 1.0 nM,Bmax = 16 fmol / mg蛋白)和高密度时的低亲和力位点( Kd = 13 nM,Bmax = 111 fmol / mg蛋白质)。为了检验高亲和力和低亲和力κ位点代表两种不同的κ受体亚型的假说,测试了一系列阿片类药物竞争结合两个位点的能力。 U-69,593和Cambridge 20在豚鼠和大鼠组织中选择性置换了高亲和力kappa位点,但在大鼠脑低亲和力位点无活性。其他Kappa阿片类药物,包括U-50,488,乙基酮基环偶氮星,溴代咪唑胺,环偶氮星和强啡肽(1-17),竞争与两个位点的结合,但效力不同。定量光学显微镜体外放射自显影用于观察大鼠和豚鼠脑中κ受体的神经解剖学模式。大鼠脑的两种κ受体亚型的分布模式明显不同。大鼠的高亲和性κ位点的模式与豚鼠的尾状-丘脑,中脑,大脑中部灰色物质和黑质相似。种间差异在大脑的其余大部分区域都显而易见。总的来说,这些数据提供了两种κ受体亚型的直接证据。 U-69,593敏感的高亲和力kappa 1位点在豚鼠脑中占主导地位,而U-69,593敏感的低亲和力kappa 2位点在大鼠脑中占主导地位。

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