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首页> 外文期刊>Journal of Neurochemistry: Offical Journal of the International Society for Neurochemistry >The dual peptidase inhibitor RB101 induces a long-lasting increase in the extracellular level of Met-enkephalin-like material in the nucleus accumbens of freely moving rats.
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The dual peptidase inhibitor RB101 induces a long-lasting increase in the extracellular level of Met-enkephalin-like material in the nucleus accumbens of freely moving rats.

机译:双重肽酶抑制剂RB101诱导自由运动大鼠伏隔核中Met-脑啡肽样物质的细胞外水平长期持续增加。

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摘要

This study was carried out to analyze the extracellular levels of Met-enkephalin-like material in the nucleus accumbens, a brain structure involved in the effects of opioids on motor activity and reward processes, using microdialysis in awake and freely moving rats, combined with a sensitive radioimmunoassay. The levels of Met-enkephalin-like material were measured after administration of a dual inhibitor of enkephalin-degrading enzymes, RB101, to evaluate its in vivo protecting effects. The basal levels of Met-enkephalin-like immunoreactivity in the nucleus accumbens were approximately 1.2 pg/30 min or 2.2 fmol/30 min (37 pM). Perfusion of KCI (100 mM) produced a 17-fold increase in the level of Met-enkephalin-like material in this structure. During the 8-h perfusion, which started at 9 a.m., a spontaneous increase of the basal level of Met-enkephalin-like material in the nucleus accumbens occurred between 4 and 4:30 p.m., suggesting the existence of variation in opioid peptide secretion, at least in this structure. Intraperitoneal injection of RB101 induced a dose-dependent and long-lasting (210-min) increase in the extracellular levels of Met-enkephalin-like material. A prolonged effect was also observed in the behavioral studies in which the inhibitor increased global motor activity of rats 210 min after injection. These data represent the first direct evidence that dual inhibitors of enkephalin-degrading enzymes increase in vivo the extracellular levels of Met-enkephalin-like material in awake and freely moving rats.
机译:这项研究是通过在清醒和自由移动的大鼠中进行微透析,结合伏隔核,分析伏隔核中Met-脑啡肽样物质的细胞外水平,该脑结构参与了阿片类药物对运动活动和奖励过程的影响。灵敏的放射免疫分析。给予脑啡肽降解酶双重抑制剂RB101后,测定Met-脑啡肽样物质的水平,以评估其体内保护作用。伏伏核中Met-脑啡肽样免疫反应性的基础水平约为1.2 pg / 30分钟或2.2 fmol / 30分钟(37 pM)。在该结构中,灌注KCI(100 mM)使Met-脑啡肽样物质的水平增加了17倍。在从上午9点开始的8小时灌注过程中,伏隔核中Met-脑啡肽样物质的基础水平自发增加,发生在下午4点至4:30点之间,表明存在阿片类肽分泌的变化,至少在这种结构中。腹膜内注射RB101会引起Met-脑啡肽样物质的细胞外水平剂量依赖性和持久性的提高(210分钟)。在行为研究中还观察到了延长的作用,其中抑制剂在注射后210分钟增加了大鼠的整体运动活性。这些数据代表了首个直接证据,即在醒着和自由活动的大鼠体内,脑啡肽降解酶的双重抑制剂会增加体内Met-脑啡肽样物质的细胞外水平。

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