Imeri L, Bianchi S, Angeli P, Mancia M
Istituto di Fisiologia Umana II, Università degli Studi, Milan, Italy.
Am J Physiol. 1995 Aug;269(2 Pt 2):R294-9. doi: 10.1152/ajpregu.1995.269.2.R294.
The medial preoptic area (MPA), a cholinoceptive brain area devoid of cholinergic cells, plays an important role in the regulation of different physiological functions, particularly sleep control and thermoregulation. To investigate the effects of the stimulation of cholinergic receptors in this area on sleep and cortical temperature (Tcort), carbachol (a mixed cholinergic agonist) was directly microinjected into the MPA of freely moving rats. Carbachol (0.25 and 0.5 microgram, corresponding to 1.37 and 2.74 nmol) microinjection induced an increase in wakefulness and an inhibition of both slow wave and desynchronized sleep phases. The temperature of the cerebral cortex was reduced in comparison with control conditions (saline microinjection). Sterile needle insertion and saline microinjections induced a significant increase in Tcort, but no changes in the sleep-wake cycle compared with the handling of the animal. The results suggest that 1) carbachol microinjection into the MPA can activate an arousal-generating system and affect thermoregulatory mechanisms, and 2) sleep and temperature responses may be dissociated.
内侧视前区(MPA)是一个不含胆碱能细胞的胆碱能感受性脑区,在调节不同生理功能,特别是睡眠控制和体温调节方面发挥着重要作用。为了研究刺激该区域的胆碱能受体对睡眠和皮层温度(Tcort)的影响,将卡巴胆碱(一种混合胆碱能激动剂)直接微量注射到自由活动大鼠的MPA中。注射卡巴胆碱(0.25和0.5微克,分别相当于1.37和2.74纳摩尔)可导致觉醒增加,并抑制慢波睡眠和去同步化睡眠阶段。与对照条件(注射生理盐水)相比,大脑皮层温度降低。无菌针头插入和注射生理盐水可导致Tcort显著升高,但与动物处理相比,睡眠-觉醒周期无变化。结果表明:1)向MPA注射卡巴胆碱可激活一个产生觉醒的系统并影响体温调节机制;2)睡眠和温度反应可能是分离的。