Daugé V, Mauborgne A, Cesselin F, Fournié-Zaluski M C, Roques B P
Départment de Pharmacochimie Moléculaire et Structurale, U. 266 INSERM, URA D1500 CNRS, Faculté de Pharmacie, Université René Descartes, Paris, France.
J Neurochem. 1996 Sep;67(3):1301-8. doi: 10.1046/j.1471-4159.1996.67031301.x.
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.
本研究旨在利用清醒且自由活动大鼠的微透析技术,并结合灵敏的放射免疫分析法,分析伏隔核中脑啡肽样物质的细胞外水平。伏隔核是一种参与阿片类药物对运动活动和奖赏过程影响的脑结构。在给予脑啡肽降解酶双重抑制剂RB101后,测量脑啡肽样物质的水平,以评估其体内保护作用。伏隔核中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)。灌注KCl(100 mM)使该结构中脑啡肽样物质的水平增加了17倍。在上午9点开始的8小时灌注过程中,伏隔核中脑啡肽样物质的基础水平在下午4点至4点30分之间出现自发升高,这表明至少在该结构中存在阿片肽分泌的变化。腹腔注射RB101可诱导脑啡肽样物质的细胞外水平出现剂量依赖性和长期(210分钟)的升高。在行为学研究中也观察到了延长效应,即该抑制剂在注射后210分钟增加了大鼠的整体运动活动。这些数据代表了首个直接证据,表明脑啡肽降解酶双重抑制剂在清醒且自由活动的大鼠体内可提高脑啡肽样物质的细胞外水平。