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氟西汀抑制大鼠5-羟色胺再摄取所产生的高血压和心动过速。

Hypertension and tachycardia produced by inhibition of reuptake of 5-hydroxytryptamine by fluoxetine in the rat.

作者信息

Tsai M L, Lin M T

出版信息

Neuropharmacology. 1986 Jul;25(7):799-802. doi: 10.1016/0028-3908(86)90099-7.

Abstract

In rats anaesthetized with urethane, increasing the activity of 5-hydroxytryptamine receptors or the level of cuntional serotonin in the brain with the inhibitors of the reuptake of serotonin, fluoxetine, produced both hypertension and tachycardia. The hypertension induced by fluoxetine was significantly inhibited by pretreatment of the animals with ketanserin (a serotonin receptor antagonist), by bilateral vagotomy, spinal transection or bilateral adrenalectomy. On the other hand, the tachycardia induced by fluoxetine was significantly inhibited by pretreatment with ketanserin or bilateral vagotomy, but not by spinal transection or adrenalectomy. The data indicate that fluoxetine acts through serotonin receptors in the central nervous system by influencing autonomic outflow to induce both hypertension and tachycardia.

摘要

在用乌拉坦麻醉的大鼠中,使用5-羟色胺再摄取抑制剂氟西汀来增加大脑中5-羟色胺受体的活性或功能性血清素水平,会导致高血压和心动过速。用酮色林(一种血清素受体拮抗剂)对动物进行预处理、双侧迷走神经切断术、脊髓横断术或双侧肾上腺切除术,可显著抑制氟西汀诱发的高血压。另一方面,用酮色林或双侧迷走神经切断术进行预处理可显著抑制氟西汀诱发的心动过速,但脊髓横断术或肾上腺切除术则不能。数据表明,氟西汀通过影响自主神经输出,作用于中枢神经系统中的血清素受体,从而诱发高血压和心动过速。

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