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对竞争性N-甲基-D-天冬氨酸拮抗剂耐受,但与巴比妥类无交叉耐受。

Tolerance to competitive NMDA antagonists, but no crosstolerance with barbiturates.

作者信息

Rabbani M, Wright E J, Little H J

机构信息

Pharmacology Department, Medical School, University Walk, Bristol, England.

出版信息

Pharmacol Biochem Behav. 1995 Jan;50(1):9-15. doi: 10.1016/0091-3057(94)00215-5.

Abstract

Tolerance occurred to the sedative actions of the competitive NMDA antagonists, CGP39551 and CGP37849, as measured by a decrease in spontaneous locomotor activity after 1 week or 2 weeks of administration, respectively, in studies using the TO strain of mice. Crosstolerance was seen between these compounds. When CGP37849 was given after 2 weeks treatment with CGP39551, an increase in locomotor activity was seen. Chronic barbiturate treatment, producing tolerance to the actions of pentobarbitone, did not affect the sedative properties of CGP39551 or CGP37849. Chronic treatment with CGP39551 did not alter the ataxic actions of pentobarbitone. Seven days of treatment with HA966 caused complete tolerance to its sedative actions, but no crosstolerance was seen to pentobarbitone, CGP39551, or CGP37849. A small but significant decrease was seen in the convulsion thresholds to NMDA after 15 days of treatment with CGP39551, and a small significant increase in ratings of convulsive behavior after 16 days injections of CGP37849. No significant changes were found in either Bmax or Kd for [3H]-MK-801 binding in cerebrocortical tissue 24 h after the last chronic treatment with either of the NMDA antagonists.

摘要

在使用TO品系小鼠的研究中,分别给药1周或2周后,通过自发运动活动的减少来衡量,对竞争性N-甲基-D-天冬氨酸(NMDA)拮抗剂CGP39551和CGP37849的镇静作用产生了耐受性。这些化合物之间存在交叉耐受性。在用CGP39551治疗2周后给予CGP37849时,观察到运动活动增加。长期巴比妥酸盐治疗产生了对戊巴比妥作用的耐受性,但不影响CGP39551或CGP37849的镇静特性。用CGP39551进行长期治疗不会改变戊巴比妥的共济失调作用。用HA966治疗7天导致对其镇静作用完全耐受,但对戊巴比妥、CGP39551或CGP37849未见交叉耐受性。在用CGP39551治疗15天后,对NMDA的惊厥阈值出现小幅但显著的降低,在用CGP37849注射16天后,惊厥行为评分出现小幅显著增加。在用任何一种NMDA拮抗剂进行最后一次长期治疗24小时后,在脑皮质组织中,[3H]-MK-801结合的最大结合容量(Bmax)或解离常数(Kd)均未发现显著变化。

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