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毒虫畏与家兔下丘脑胆碱能受体的相互作用。

Interaction of chlorphenvinphos with cholinergic receptors in the rabbit hypothalamus.

作者信息

Gralewicz S, Tomas T, Soćko R

机构信息

Nofer Institute of Occupational Medicine, Laboratory of Neurotoxicity Evaluation, Lódź, Poland.

出版信息

Neurotoxicol Teratol. 1995 May-Jun;17(3):289-95. doi: 10.1016/0892-0362(94)00068-o.

Abstract

The purpose of this study was to find out whether chlorphenvinphos (CVP), an organophosphorous pesticide, interacts with the muscarinic cholinergic receptors in CNS. To attain this goal, the effects of intrahypothalamic injections of oxotremorine (Ox), a muscarinic agonist, and physostigmine (Phys), a carbamate anticholinesterase, were compared with those produced by intrahypothalamic injections of CVP in the rabbit. It was found that the infusion of Ox (20 micrograms) as well as Phys (200 micrograms) into the anterior hypothalamus leads to an increase in the 4-7 Hz theta rhythm in the hippocampus and to the appearance of behavioral symptoms suggestive of a threat response. In the case of Ox, the effects could be prevented by injections of 20 micrograms scopolamine, a muscarinic antagonist. Pretreatment of the hypothalamus with 100 micrograms hemicholinium (HC-3) did not prevent the effects of Phys injected 2 h later. (HC-3 prevents the resynthesis of acetylcholine by blocking choline reuptake. This leads to a gradual depletion of ACh stores and to an inhibition of the cholinergic transmission). It suggests that Phys activates directly postsynaptic muscarinic receptors. Intrahypothalamic injections of CVP in doses of up to 1360 micrograms produced no overt changes in behavior nor in the hippocampal EEG of the rabbit and did not prevent the effect of subsequent injections of Ox. This suggests that CVP is neither an agonist nor antagonist of the muscarinic receptors in the rabbit hypothalamus.

摘要

本研究的目的是探究有机磷农药毒虫畏(CVP)是否与中枢神经系统中的毒蕈碱型胆碱能受体相互作用。为实现这一目标,将毒蕈碱激动剂氧化震颤素(Ox)和氨基甲酸酯类抗胆碱酯酶毒扁豆碱(Phys)下丘脑内注射的效果与家兔下丘脑内注射CVP产生的效果进行了比较。结果发现,向下丘脑前部注入Ox(20微克)以及Phys(200微克)会导致海马体中4-7赫兹的θ节律增加,并出现提示威胁反应的行为症状。对于Ox,注射20微克毒蕈碱拮抗剂东莨菪碱可预防其效果。用100微克半胱氨酸(HC-3)预处理下丘脑并不能预防2小时后注射Phys的效果。(HC-3通过阻断胆碱再摄取来阻止乙酰胆碱的再合成。这会导致乙酰胆碱储备逐渐耗尽,并抑制胆碱能传递)。这表明Phys直接激活突触后毒蕈碱受体。向家兔下丘脑内注射高达1360微克剂量的CVP,并未使其行为或海马脑电图出现明显变化,也未阻止随后注射Ox的效果。这表明CVP既不是家兔下丘脑毒蕈碱受体的激动剂也不是拮抗剂。

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