Sugaya K, Kubota K
Faculty of Pharmaceutical Sciences, Science University of Tokyo, Japan.
Jpn J Pharmacol. 1988 Sep;48(1):1-6. doi: 10.1254/jjp.48.1.
Effects of diazepam (DZP), a synthetic benzodiazepine drug, and anthramycin (ATM), a benzodiazepine antitumor antibiotic produced by a certain species of streptomyces, on the uptake of 2-deoxy-D-[14C]-glucose (2-DG) in mouse brain neurons with or without cholecystokinin were examined. 2-DG uptake in neurons was evaluated by using an autoradiographic technique. The sulfated octapeptide CCK (CCK8) was injected intracisternally; DZP and ATM, intraperitoneally; and 2-DG, intravenously to mice. Autoradiograms prepared from the slices of the brain were converted to false color images. CCK8 (1 microgram/mouse) markedly stimulated the 2-DG uptake in neurons in the various regions of the brain, but the stimulative effects of CCK8 was almost completely suppressed after an intraperitoneal administration of 1.0 mg/kg of DZP or 0.5 mg/kg of ATM. Since it has been previously shown that these doses of DZP and ATM almost completely reversed the antinociception produced by 1 microgram/mouse of CCK8, the present results on the 2-DG uptake in the mouse brain are considered to further support the antagonism between CCK8 and DZP or ATM in the central nervous system.
研究了合成苯二氮䓬类药物地西泮(DZP)和由某种链霉菌产生的苯二氮䓬类抗肿瘤抗生素氨茴霉素(ATM)对有或无胆囊收缩素的小鼠脑神经元摄取2-脱氧-D-[14C]-葡萄糖(2-DG)的影响。采用放射自显影技术评估神经元对2-DG的摄取。将硫酸化八肽胆囊收缩素(CCK8)脑池内注射给小鼠;地西泮和氨茴霉素腹腔注射;2-DG静脉注射给小鼠。从脑切片制备的放射自显影片被转换为伪彩色图像。CCK8(1微克/小鼠)显著刺激脑不同区域神经元对2-DG的摄取,但在腹腔注射1.0毫克/千克地西泮或0.5毫克/千克氨茴霉素后,CCK8的刺激作用几乎完全被抑制。由于先前已表明这些剂量的地西泮和氨茴霉素几乎完全逆转了1微克/小鼠CCK8产生的镇痛作用,因此目前关于小鼠脑2-DG摄取的结果被认为进一步支持了CCK8与地西泮或氨茴霉素在中枢神经系统中的拮抗作用。