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两种品系大鼠的腹侧被盖区镇痛作用:苯丙胺、纳洛酮和对氯苯丙氨酸的影响。

Ventral tegmental analgesia in two strains of rats: effects of amphetamine, naloxone and parachlorophenylalanine.

作者信息

Moreau J L, Cohen E, Lieblich I

出版信息

Brain Res. 1984 May 21;300(1):1-8. doi: 10.1016/0006-8993(84)91334-9.

Abstract

Pain sensitivity and analgesia induced by the stimulation of the ventral tegmentum (VT) were studied in 72 male rats of two lines, LC2-Hi and LC2-Lo, genetically selected for high and low rates of lateral hypothalamic self-stimulation, respectively. LC2-Lo rats were more sensitive to acute peripheral pain and developed a stronger analgesia than their LC2-Hi counterparts. In order to assess the pharmacological substrate of ventral tegmental stimulation-induced analgesia (VT-SIA), the effects of amphetamine (AMP, 21 animals), naloxone (NX, 24 animals) and parachlorophenylalanine (PCPA, 27 animals) injections were studied. VT-SIA was found to be clearly decreased by PCPA, slightly decreased by AMP and not significantly affected by NX. Ventral tegmental self-stimulation ( VTSS ) was increased by PCPA treatment. The comparison of VTSS and VT-SIA did not reveal any correlation between both phenomena. These data suggest that VT-SIA may be mediated by serotonin while catecholamines may have a modulatory role in this analgesia and that VTSS and VT-SIA seem to be governed by different neuronal systems.

摘要

在分别针对下丘脑外侧自我刺激高频率和低频率进行基因选择培育的两个品系(LC2-Hi和LC2-Lo)的72只雄性大鼠中,研究了腹侧被盖区(VT)刺激所诱导的疼痛敏感性和镇痛作用。与LC2-Hi品系的大鼠相比,LC2-Lo品系的大鼠对急性外周疼痛更为敏感,且产生更强的镇痛作用。为了评估腹侧被盖区刺激诱导的镇痛作用(VT-SIA)的药理学基础,研究了注射苯丙胺(AMP,21只动物)、纳洛酮(NX,24只动物)和对氯苯丙氨酸(PCPA,27只动物)的效果。发现PCPA可明显降低VT-SIA,AMP使其略有降低,而NX对其无显著影响。PCPA处理可增加腹侧被盖区自我刺激(VTSS)。VTSS和VT-SIA的比较未发现这两种现象之间存在任何相关性。这些数据表明,VT-SIA可能由5-羟色胺介导,而儿茶酚胺可能在这种镇痛作用中具有调节作用,并且VTSS和VT-SIA似乎受不同的神经元系统支配。

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