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短期氟西汀治疗可增强后肢卸载后压力反射对交感神经系统活动的控制。

Short-term fluoxetine treatment enhances baroreflex control of sympathetic nervous system activity after hindlimb unloading.

作者信息

Moffitt Julia A, Johnson Alan Kim

机构信息

The Cardiovascular Center, University of Iowa, Iowa City, Iowa 52242, USA.

出版信息

Am J Physiol Regul Integr Comp Physiol. 2004 Mar;286(3):R584-90. doi: 10.1152/ajpregu.00223.2002.

Abstract

Data in humans indicate that individuals with orthostatic hypotension that are refractory to other traditional forms of therapy are responsive to selective serotonin reuptake inhibitor (SSRI) treatment. We tested the hypothesis that SSRI administration would help correct the attenuated baroreflex control of sympathetic nervous system activity in the hindlimb-unloaded (HU) rat model of cardiovascular deconditioning. An initial study was conducted to determine the time course of effects of fluoxetine (Flu) administration on baroreflex control of lumbar sympathetic nerve activity (LSNA) in conscious, chronically instrumented rats. Animals received either vehicle (Veh, sterile water) or 10 mg/kg Flu for 1, 4, or 16 days of treatment. Data indicate that while 1-day and 16-day Flu administration did not affect baroreflex function, baroreflex control of LSNA was enhanced after 4-day (short term) Flu administration. HU rats were then treated with Flu for 4 days and compared with HU rats receiving Veh and to casted control rats maintained in the normal posture that received either Veh or short-term Flu treatment. Similar to pilot data, short-term Flu treatment enhanced baroreflex control of LSNA in both HU rats and control rats. These data taken together indicate that baroreflex control of sympathetic nervous system activity is a possible mechanism responsible for the successful treatment of orthostatic intolerance with Flu.

摘要

人体数据表明,对其他传统治疗形式无效的体位性低血压个体对选择性5-羟色胺再摄取抑制剂(SSRI)治疗有反应。我们检验了这样一个假设:在心血管失健的后肢去负荷(HU)大鼠模型中,给予SSRI将有助于纠正交感神经系统活动的压力反射控制减弱的情况。开展了一项初步研究,以确定给予氟西汀(Flu)对清醒、长期植入仪器的大鼠腰交感神经活动(LSNA)的压力反射控制的影响的时间进程。动物接受载体(Veh,无菌水)或10mg/kg氟西汀治疗1、4或16天。数据表明,虽然给予1天和16天的氟西汀不影响压力反射功能,但给予4天(短期)氟西汀后,LSNA的压力反射控制增强。然后对HU大鼠给予氟西汀治疗4天,并与接受载体的HU大鼠以及保持正常姿势、接受载体或短期氟西汀治疗的石膏固定对照大鼠进行比较。与前期数据相似,短期氟西汀治疗增强了HU大鼠和对照大鼠中LSNA的压力反射控制。这些数据共同表明,交感神经系统活动的压力反射控制是氟西汀成功治疗体位性不耐受的一种可能机制。

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