Sutin E L, Shiromani P J, Kelsoe J R, Storch F I, Gillin J C
Life Sci. 1986 Dec 22;39(25):2419-27. doi: 10.1016/0024-3205(86)90483-2.
The purpose of this study was to determine whether a seven day, once-daily morning administration of scopolamine produces upregulation of muscarinic receptors and augments REMS during withdrawal. After obtaining two, six-hour baseline sleep recordings, beginning at 0900, independent groups of rats were administered either scopolamine or saline every morning for seven days. Six hour sleep recordings were obtained following the first and seventh day of injection and during the two subsequent withdrawal days. After obtaining the last sleep recording the rats were sacrificed and the following brain areas removed: cerebral cortex, hippocampii, caudate nuclei, brainstem, and cerebellum. 3H-QNB was used as the ligand to assess for changes in muscarinic receptor binding. Compared to baseline, scopolamine produced a significant decrease in REMS during the period of drug administration. During the withdrawal days, however, REMS increased during the morning period. Compared to the saline group, the scopolamine treated animals had increased muscarinic receptor binding in the caudate and hippocampus; no significant change in receptor density was observed in the cortex, brainstem or cerebellum.
本研究的目的是确定每日清晨一次、连续七天给予东莨菪碱是否会导致毒蕈碱受体上调,并在戒断期间增强快速眼动睡眠(REMS)。在从09:00开始获得两次六小时的基线睡眠记录后,将独立的大鼠组每天早晨给予东莨菪碱或生理盐水,持续七天。在注射的第一天和第七天以及随后的两个戒断日期间获得六小时的睡眠记录。在获得最后一次睡眠记录后,处死大鼠并取出以下脑区:大脑皮层、海马、尾状核、脑干和小脑。使用3H-QNB作为配体来评估毒蕈碱受体结合的变化。与基线相比,东莨菪碱在给药期间使快速眼动睡眠显著减少。然而,在戒断日期间,早晨时段的快速眼动睡眠增加。与生理盐水组相比,经东莨菪碱处理的动物在尾状核和海马中的毒蕈碱受体结合增加;在皮层、脑干或小脑中未观察到受体密度的显著变化。