首页> 外文期刊>Neuroscience: An International Journal under the Editorial Direction of IBRO >M2 muscarinic receptors in pontine reticular formation of C57BL/6J mouse contribute to rapid eye movement sleep generation.
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M2 muscarinic receptors in pontine reticular formation of C57BL/6J mouse contribute to rapid eye movement sleep generation.

机译:C57BL / 6J小鼠脑桥网状结构中的M2毒蕈碱受体有助于快速产生眼动睡眠。

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Microinjecting the acetylcholinesterase inhibitor neostigmine into the pontine reticular formation of C57BL/6J (B6) mouse causes a rapid eye movement (REM) sleep-like state. This finding is consistent with similar studies in cat and both sets of data indicate that the REM sleep-like state is caused by increasing levels of endogenous acetylcholine (ACh). Muscarinic cholinergic receptors have been localized to the pontine reticular formation of B6 mouse but no previous studies have examined which of the five muscarinic receptor subtypes participate in cholinergic REM sleep enhancement. This study examined the hypothesis that M2 receptors in pontine reticular formation of B6 mouse contribute to the REM sleep-like state caused by pontine reticular formation administration of neostigmine. B6 mice (n=13) were implanted with electrodes for recording states of sleep and wakefulness and with microinjection cannulae aimed for the pontine reticular formation. States of sleep and wakefulness were recorded for 4 h following pontine reticular formation injection of saline (control) or neostigmine. Experiments designed to gain insight into the muscarinic receptor subtypes mediating REM sleep enhancement involved pontine reticular formation administration of neostigmine after pertussis toxin, neostigmine after methoctramine, and neostigmine after pirenzepine. Pertussis toxin was used to block effects mediated by M2 and M4 receptors. Methoctramine was used to block M2 and M4 receptors, and pirenzepine was used to block M1 and M4 receptors. Pertussis toxin and methoctramine significantly decreased the neostigmine-induced REM sleep-like state. In contrast, pretreatment with pirenzepine did not significantly decrease the REM sleep-like state caused by neostigmine. These results support the interpretation that M2 receptors in the pontine reticular formation of B6 mouse contribute to the generation of REM sleep.
机译:将乙酰胆碱酯酶抑制剂新斯的明微注射到C57BL / 6J(B6)小鼠的脑桥网状结构中会导致快速眼动(REM)睡眠样状态。这一发现与猫的类似研究一致,两组数据均表明,REM睡眠样状态是由内源性乙酰胆碱(ACh)水平升高引起的。毒蕈碱型胆碱能受体已经定位于B6小鼠的桥状网状结构,但之前没有研究检查过5种毒蕈碱受体亚型中的哪一种参与胆碱能性REM睡眠增强。这项研究检验了以下假设:B6小鼠桥状网状结构中的M2受体可导致由新斯的明的桥状网状结构形成引起的REM睡眠状态。 B6小鼠(n = 13)植入电极以记录睡眠和清醒状态,并植入微针套管以形成桥脑网状结构。在脑桥网状注射盐水(对照)或新斯的明后4小时记录睡眠和清醒状态。旨在深入了解介导REM睡眠增强的毒蕈碱受体亚型的实验涉及百日咳毒素后新斯的明,甲氧卡明后的新斯的明和哌仑西平后的新斯的明的桥脑网状结构给药。百日咳毒素被用来阻断M2和M4受体介导的作用。甲硫辛明用于阻断M2和M4受体,吡咯西平用于阻断M1和M4受体。百日咳毒素和methoctramine显着降低了新斯的明诱导的REM睡眠样状态。相反,用哌仑西平预处理并不能显着降低由新斯的明引起的REM睡眠样状态。这些结果支持以下解释:B6小鼠脑桥网状结构中的M2受体有助于REM睡眠的产生。

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