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对氧磷对猫血流动力学的中枢效应。

Central effects of paraoxon on haemodynamics in the cat.

作者信息

de Neef J H, Porsius A J

出版信息

Naunyn Schmiedebergs Arch Pharmacol. 1981 Sep;317(2):168-72. doi: 10.1007/BF00500075.

Abstract

Application of paraoxon into the left vertebral artery (8--80 micrograms) or both the left and right vertebral artery (4--8 micrograms) of the anaesthetized cat evoked dose-dependent depressor effects, whereas heart rate was not influenced significantly. Also after systemic administration of paraoxon (150--825 micrograms . kg-1), while peripheral muscarinic receptors were blocked, depressor effects were still observed. Dose-response curves for the depressor response to paraoxon were established. Infusion of low doses of dexetimide via the vertebral artery prevented the hypotensive action of paraoxon. The distribution of this antimuscarinic drug in the brain was investigated. The depressor effect of paraoxon can be attributed to both a decrease in peripheral resistance and cardiac output. Decerebration and midcollicular transection were carried out in order to elucidate the site and mechanism of action. The depressor effect of paraoxon seems to be mediated by a central mechanism of action located within the lower brain stem. It is concluded that stimulation of muscarinic receptors in the pontomedullary region gives rise to the observed changes in haemodynamic parameters. Muscarinic receptors in the hypothalamus seem to be of minor importance for the hypotensive action of paraoxon.

摘要

将对氧磷注入麻醉猫的左椎动脉(8 - 80微克)或左右椎动脉(4 - 8微克)会引起剂量依赖性的降压作用,而心率无明显影响。对氧磷全身给药(150 - 825微克·kg⁻¹)后,尽管外周毒蕈碱受体被阻断,但仍观察到降压作用。建立了对氧磷降压反应的剂量 - 反应曲线。经椎动脉输注低剂量的右美托咪定可防止对氧磷的降压作用。研究了这种抗毒蕈碱药物在脑中的分布。对氧磷的降压作用可归因于外周阻力和心输出量的降低。为阐明作用部位和机制进行了去大脑和中脑横断实验。对氧磷的降压作用似乎由位于脑桥下部的中枢作用机制介导。结论是,脑桥延髓区域毒蕈碱受体的刺激导致观察到的血流动力学参数变化。下丘脑的毒蕈碱受体对对氧磷的降压作用似乎不太重要。

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