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可乐定和BS 100 - 141对大鼠脑电图睡眠模式的影响。

Effects of clonidine and BS 100-141 on the EEG sleep pattern in rats.

作者信息

Kleinlogel H, Scholtysik G, Sayers A C

出版信息

Eur J Pharmacol. 1975 Aug;33(1):159-63. doi: 10.1016/0014-2999(75)90151-x.

Abstract

The effects of the peripheral and central alpha-adrenoceptor stimulant and antihypertensive agents clonidine and BS 100-141 (N-amidino-2[2,6-dichlorophenyl]acetamide - HCl) on EEG sleep patterns in rats and on blood pressure in pithed rats have been investigated. Whereas both compounds abolished paradoxical sleep (PS), clonidine, in contrast to BS 100-141, markedly increased the sleeping time. Both drugs caused a dose-dependent increase in the blood pressure of pithed rats. The pressor action was abolished by the alpha-adrenoceptor blocking agent phentolamine, but was not influenced by reserpine, indicating a direct stimulation of vascular alpha-adrenoceptors by both drugs. It is suggested that sedation or sleep induction by adrenergic drugs cannot be explained exclusively by an action on central alpha-adrenoceptors. Rather, the findings suggest that such an action may be involved in the modulation of PS.

摘要

研究了外周和中枢α-肾上腺素能受体兴奋剂及降压药可乐定和BS 100 - 141(N-脒基-2[2,6-二氯苯基]乙酰胺盐酸盐)对大鼠脑电图睡眠模式以及对脊髓麻醉大鼠血压的影响。两种化合物均消除了异相睡眠(PS),但与BS 100 - 141不同,可乐定显著增加了睡眠时间。两种药物均使脊髓麻醉大鼠的血压呈剂量依赖性升高。α-肾上腺素能受体阻断剂酚妥拉明可消除升压作用,但利血平对其无影响,表明两种药物均直接刺激血管α-肾上腺素能受体。提示肾上腺素能药物的镇静或诱导睡眠作用不能仅用其对中枢α-肾上腺素能受体的作用来解释。相反,这些发现表明这种作用可能参与了异相睡眠的调节。

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