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地佐环平对可卡因心脏效应的减弱作用。

Attenuation of the cardiac effects of cocaine by dizocilpine.

作者信息

Hageman G R, Simor T

机构信息

Department of Physiology and Biophysics, University of Alabama, Birmingham 35294.

出版信息

Am J Physiol. 1993 Jun;264(6 Pt 2):H1890-5. doi: 10.1152/ajpheart.1993.264.6.H1890.

Abstract

Cocaine abuse causes autonomic and cardiovascular effects that may be life threatening. Attenuation of cocaine-induced seizures has been produced by the noncompetitive antagonist of the N-methyl-D-aspartate receptor channel complex, dizocilpine. The purpose of the present study was, first, to determine effects of dizocilpine on the incidence of pacing-induced ventricular arrhythmias and, second, to evaluate the effects of dizocilpine on cocaine-induced depression of sympathetic efferent activity to the heart. Adult dogs were anesthetized and instrumented for blood pressure and an electrocardiogram. After vagotomy and thoracotomy, electrodes and strain gauges were sutured onto the right atrium and ventricle. A left thoracic sympathetic efferent nerve was isolated and stimulated for analysis of the innervation pattern. Arrhythmias were induced with programmed electrical stimulation of the heart before and during left cardiac sympathetic efferent nerve stimulation. The control incidence of induced arrhythmias was only 2%, which increased to 21% during left sympathetic stimulation. Cocaine (2 mg/kg iv) significantly increased these to 11 and 42%, respectively. Dizocilpine (0.5 mg/kg iv) reduced the incidence of induced ventricular arrhythmias to 2% with cocaine (P < 0.05) and to 19% with cocaine and left sympathetic stimulation (P < 0.01). One or two sympathetic efferent cardiac nerves were stimulated to evaluate innervation patterns. These nerves were severed and prepared for recording multifiber efferent neurograms. Nerve traffic was analyzed by counting positive spikes for 15 s. Control activities were normalized at 100%. Within 6 min, cocaine (2 mg/kg iv) reduced the sympathetic efferent activity to 83 +/- 4% of control (n = 14 nerves).(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

可卡因滥用会引发可能危及生命的自主神经和心血管效应。N-甲基-D-天冬氨酸受体通道复合物的非竞争性拮抗剂地佐环平可减轻可卡因诱发的癫痫发作。本研究的目的,其一,是确定地佐环平对起搏诱导的室性心律失常发生率的影响;其二,是评估地佐环平对可卡因诱发的心脏交感传出活动抑制的影响。成年犬麻醉后安装监测血压和心电图的仪器。在迷走神经切断术和开胸术后,将电极和应变片缝合到右心房和心室上。分离左侧胸交感传出神经并进行刺激以分析其支配模式。在左心交感传出神经刺激之前和期间,通过心脏程控电刺激诱发心律失常。诱发心律失常的对照发生率仅为2%,在左交感神经刺激期间增至21%。可卡因(静脉注射2mg/kg)分别将其显著提高至11%和42%。地佐环平(静脉注射0.5mg/kg)使可卡因诱发的室性心律失常发生率降至2%(P<0.05),可卡因加左交感神经刺激时降至19%(P<0.01)。刺激一或两条心脏交感传出神经以评估支配模式。切断这些神经并准备记录多纤维传出神经图。通过计数15秒内的正向尖峰来分析神经活动。对照活动标准化为100%。在6分钟内,可卡因(静脉注射2mg/kg)将交感传出活动降至对照的83±4%(n = 14条神经)。(摘要截断于250字)

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