McBride Shawna M, Flynn Francis W
Graduate Neuroscience Program, Department of Zoology and Physiology, University of Wyoming, 1000 E. University Ave., Laramie, WY 82071, USA.
Am J Physiol Regul Integr Comp Physiol. 2007 Sep;293(3):R1452-8. doi: 10.1152/ajpregu.00048.2007. Epub 2007 Jun 13.
Prior sodium restriction cross-sensitizes rats to the psychomotor effects of amphetamines and vice versa. Repeated central injections of vasopressin (VP) induce a psychomotor sensitization similar to amphetamine sensitization and repeated sodium deficiency. Thus brain VP signaling may be a common mechanism involved in mediating these two motivational systems. In experiment 1, we tested the hypothesis that rats previously sensitized to central VP would show enhanced psychomotor responses to amphetamine. Rats were administered saline, VP (50 ng), or amphetamine (1 mg/kg or 3 mg/kg) on days 1 and 2, and given saline or amphetamine on day 3. Amphetamine produced psychomotor arousal in all groups. However, amphetamine on day 3 elicited a significantly greater psychomotor response in rats that had prior injections of amphetamine or VP than in rats previously treated with saline. In experiment 2, the hypothesis that prior experience with central VP would cross-sensitize rats to drinking hypertonic sodium (NaCl) solutions was tested. Rats were administered VP (50 ng) or saline for 3 days. On the fourth day, nondeprived rats were given access to 0.3 M NaCl and water for 1 h. Control and saline-treated rats only drank 1 ml of 0.3 M NaCl, but rats previously exposed to central VP drank significantly more hypertonic saline (4 ml). These results show that prior experience with central VP cross-sensitizes rats to the psychomotor stimulant effects of amphetamine and the ingestion of concentrated NaCl solutions. This pattern of cross-sensitization links central VP signaling, amphetamine, and sodium deficiency, and therefore it may play a role in the cross-sensitization between sodium appetite and amphetamines.
先前的钠限制会使大鼠对苯丙胺的精神运动效应产生交叉敏感性,反之亦然。反复向中枢注射血管加压素(VP)会诱发类似于苯丙胺敏感性和反复缺钠的精神运动敏化。因此,脑内VP信号传导可能是介导这两种动机系统的共同机制。在实验1中,我们测试了以下假设:先前对中枢VP敏感的大鼠对苯丙胺的精神运动反应会增强。在第1天和第2天给大鼠注射生理盐水、VP(50纳克)或苯丙胺(1毫克/千克或3毫克/千克),并在第3天给它们注射生理盐水或苯丙胺。苯丙胺在所有组中都引起了精神运动兴奋。然而,第3天的苯丙胺在先前注射过苯丙胺或VP的大鼠中引起的精神运动反应明显大于先前用生理盐水处理的大鼠。在实验2中,测试了以下假设:先前接触中枢VP的经历会使大鼠对饮用高渗氯化钠(NaCl)溶液产生交叉敏感性。给大鼠注射VP(50纳克)或生理盐水,持续3天。在第4天,不给食的大鼠可以接触0.3M NaCl和水1小时。对照组和生理盐水处理的大鼠只饮用了1毫升0.3M NaCl,但先前接触过中枢VP的大鼠饮用了明显更多的高渗盐水(4毫升)。这些结果表明,先前接触中枢VP的经历会使大鼠对苯丙胺的精神运动刺激效应和浓缩NaCl溶液的摄取产生交叉敏感性。这种交叉敏感模式将中枢VP信号传导、苯丙胺和缺钠联系起来,因此它可能在钠食欲和苯丙胺之间的交叉敏感中起作用。