Powell K R, Holtzman S G
Department of Pharmacology, Emory University School of Medicine, Atlanta, GA 30322, USA.
Pharmacol Biochem Behav. 1998 Feb;59(2):433-8. doi: 10.1016/s0091-3057(97)00447-4.
The involvement of NMDA-type glutamate receptors in caffeine's locomotor stimulant effects and the development of tolerance to these effects was examined in rats. Caffeine and the noncompetitive NMDA receptor antagonists, MK-801 and phencyclidine (PCP), were examined alone and in combination. Caffeine produced a biphasic dose-effect curve. Both MK-801 and PCP increased locomotor activity at the highest doses tested. MK-801 and PCP shifted the caffeine curve upward, but only with the highest doses that increased locomotor activity when given alone. For the tolerance experiment, osmotic pumps containing either MK-801 or nothing at all and were implanted in rats that were given either caffeinated or drug-free tap water to drink. All rats drinking caffeine showed tolerance to its locomotor stimulant effects, whereas rats drinking drug-free tap water did not. Chronic infusion of MK-801 (0.1 and 0.3 mg/kg/day) failed to block the development of tolerance to caffeine. The 0.3 mg/kg/day infusion of MK-801 appeared to slightly delay the development of tolerance to caffeine, but this effect was probably due to the locomotor stimulant effects of this infused dose of MK-801 alone. These data provide no evidence that NMDA-type glutamate receptors play a crucial role in mediating caffeine's locomotor stimulant effects or tolerance to these effects.
在大鼠中研究了NMDA型谷氨酸受体在咖啡因的运动兴奋作用及其对这些作用的耐受性发展中的参与情况。单独及联合检测了咖啡因以及非竞争性NMDA受体拮抗剂MK-801和苯环己哌啶(PCP)。咖啡因产生了双相剂量效应曲线。在测试的最高剂量下,MK-801和PCP均增加了运动活性。MK-801和PCP使咖啡因曲线向上移动,但仅在单独给药时增加运动活性的最高剂量下才出现这种情况。对于耐受性实验,将含有MK-801或不含任何物质的渗透泵植入给予含咖啡因或无药物自来水饮用的大鼠体内。所有饮用咖啡因的大鼠均对其运动兴奋作用产生耐受性,而饮用无药物自来水的大鼠则没有。长期输注MK-801(0.1和0.3mg/kg/天)未能阻止对咖啡因耐受性的发展。0.3mg/kg/天的MK-801输注似乎略微延迟了对咖啡因耐受性的发展,但这种作用可能仅归因于该输注剂量的MK-801自身的运动兴奋作用。这些数据没有提供证据表明NMDA型谷氨酸受体在介导咖啡因的运动兴奋作用或对这些作用的耐受性方面起关键作用。