Liu C, Gillette M U
Neuroscience Program, University of Illinois at Urbana-Champaign 61801, USA.
J Neurosci. 1996 Jan 15;16(2):744-51. doi: 10.1523/JNEUROSCI.16-02-00744.1996.
In mammals, the suprachiasmatic nucleus (SCN) is responsible for the generation of most circadian rhythms and for their entrainment to environmental cues. Carbachol, an agonist of acetylcholine (ACh), has been shown to shift the phase of circadian rhythms in rodents when injected intracerebroventricularly. However, the site and receptor type mediating this action have been unknown. In the present experiments, we used the hypothalamic brain-slice technique to study the regulation of the SCN circadian rhythm of neuronal firing rate by cholinergic agonists and to identify the receptor subtypes involved. We found that the phase of the oscillation in SCN neuronal activity was reset by a 5 min treatment with a carbachol microdrop (1 microliter, 100 microM), but only when applied during the subjective night, with the largest phase shift (+ 6 hr) elicited during the middle of the subjective night. This effect also was produced by ACh and two muscarinic receptor (mAChR) agonists, muscarine and McN-A-343 (M1-selective), but not by nicotine. Furthermore, the effect of carbachol was blocked by the mAChR antagonist atropine (0.1 microM), not by two nicotinic antagonists, dihydro-beta-erythroidine (10 microM) and d-tubocurarine (10 microM). The M1-selective mAChR antagonist pirenzepine completely blocked the carbachol effect at 1 microM, whereas an M3-selective antagonist, 4,2-(4,4'-diacetoxydiphenylmethyl)pyridine, partially blocked the effect at the same concentration. These results demonstrate that carbachol acts directly on the SCN to reset the phase of its firing rhythm during the subjective night via an M1-like mAChR.
在哺乳动物中,视交叉上核(SCN)负责大多数昼夜节律的产生及其与环境线索的同步。已证明,当脑室内注射时,乙酰胆碱(ACh)的激动剂卡巴胆碱会改变啮齿动物昼夜节律的相位。然而,介导此作用的位点和受体类型尚不清楚。在本实验中,我们使用下丘脑脑片技术研究胆碱能激动剂对SCN神经元放电频率昼夜节律的调节,并确定所涉及的受体亚型。我们发现,用卡巴胆碱微滴(1微升,100微摩尔)处理5分钟可重置SCN神经元活动的振荡相位,但仅在主观夜间应用时才会发生,在主观夜间中期引起最大相位偏移(+6小时)。ACh以及两种毒蕈碱受体(mAChR)激动剂毒蕈碱和McN-A-343(M1选择性)也产生了这种效应,但尼古丁没有。此外,卡巴胆碱的作用被mAChR拮抗剂阿托品(0.1微摩尔)阻断,而不是被两种烟碱拮抗剂二氢-β-刺桐碱(10微摩尔)和d-筒箭毒碱(10微摩尔)阻断。M1选择性mAChR拮抗剂哌仑西平在1微摩尔时完全阻断了卡巴胆碱的作用,而M3选择性拮抗剂4,2-(4,4'-二乙酰氧基二苯基甲基)吡啶在相同浓度下部分阻断了该作用。这些结果表明,卡巴胆碱在主观夜间通过类M1 mAChR直接作用于SCN,以重置其放电节律的相位。