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非竞争性N-甲基-D-天冬氨酸(NMDA)受体拮抗剂给药14天后NMDA和多巴胺D2受体而非毒蕈碱受体的适应性变化

Adaptations of NMDA and dopamine D2, but not of muscarinic receptors following 14 days administration of uncompetitive NMDA receptor antagonists.

作者信息

Hesselink M B, De Boer A G, Breimer D D, Danysz W

机构信息

Department of Pharmacological Research, Merz + Co., Frankfurt/Main, Federal Republic of Germany.

出版信息

J Neural Transm (Vienna). 1999;106(5-6):409-21. doi: 10.1007/s007020050168.

Abstract

Behavioral changes have previously been reported following administrations of uncompetitive NMDA receptor antagonists memantine, amantadine and MK-801 for 14 days, at the doses that produce plasma levels comparable to those seen in patients (20, 100 and 0.31 mg/kg/day respectively). Using the same doses, the effect on receptor binding (autoradiography) was studied in rats. [3H]MK-801 binding was increased in the dentate gyrus and CA3 region of the hippocampus (35.2 and 24.3% respectively) following 3 days S.C. infusion of memantine by ALZET minipumps. One daily injection of memantine for 14 days, increased [3H]MK-801 binding in the frontal cortex by 40.3%. The same treatment with amantadine did increase [3H]raclopride binding to dopamine D2 receptors by 13.5%. None of these treatments changed the expression of muscarinic receptors. It is concluded that subchronic blockade of the NMDA receptor by uncompetitive antagonists at moderate (therapeutically-relevant) doses induced only minor changes in NMDA and dopamine D2 receptor expression.

摘要

先前有报道称,在以产生与患者体内水平相当的血浆浓度的剂量(分别为20、100和0.31mg/kg/天)给予非竞争性NMDA受体拮抗剂美金刚、金刚烷胺和MK-801 14天后,会出现行为变化。使用相同剂量,研究了对大鼠受体结合(放射自显影)的影响。通过ALZET微型泵皮下输注美金刚3天后,海马齿状回和CA3区的[3H]MK-801结合增加(分别为35.2%和24.3%)。每天注射一次美金刚,持续14天,额叶皮质的[3H]MK-801结合增加40.3%。用金刚烷胺进行相同处理确实使[3H]雷氯必利与多巴胺D2受体的结合增加了13.5%。这些处理均未改变毒蕈碱受体的表达。结论是,在中等(治疗相关)剂量下,非竞争性拮抗剂对NMDA受体的亚慢性阻断仅引起NMDA和多巴胺D2受体表达的微小变化。

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