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体外乙醇戒断性过度兴奋可被一种竞争性N-甲基-D-天冬氨酸(NMDA)受体拮抗剂选择性降低。

Ethanol withdrawal hyperexcitability in vitro is selectively decreased by a competitive NMDA receptor antagonist.

作者信息

Ripley T L, Little H J

机构信息

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

出版信息

Brain Res. 1995 Nov 13;699(1):1-11. doi: 10.1016/0006-8993(95)00445-v.

DOI:10.1016/0006-8993(95)00445-v
PMID:8616595
Abstract

Hippocampal slices were prepared immediately after withdrawal from chronic ethanol in vivo. The decreases in thresholds for production of single and multiple population spikes seen after the ethanol treatment were not evident when CGP39551 was included in the perfusion medium at 20 microM. The decrease in paired pulse potentiation seen during ethanol withdrawal, however, was not prevented by CGP39551. For comparison, the effects of CGP39551, at the same concentration, were examined on the changes in field potentials seen in control slices when the magnesium concentration in the bathing medium was lowered to 250 microM. The decreases in thresholds for multiple population spikes produced by the lowered magnesium were prevented, but not other changes including decreases in single spike thresholds. In addition, this 20 microM concentration of CGP39551 did not prevent epileptiform activity, measured by decreases in thresholds for production of single and multiple population spikes caused by addition of the GABAA antagonist, bicuculline, to control hippocampal slices.

摘要

海马切片在体内从慢性乙醇戒断后立即制备。当在灌注培养基中加入20微摩尔的CGP39551时,乙醇处理后观察到的单一群峰和多群峰产生阈值的降低并不明显。然而,CGP39551并不能阻止乙醇戒断期间配对脉冲增强的降低。为了进行比较,在相同浓度下,研究了CGP39551对对照切片中当浴液中镁浓度降低至250微摩尔时所观察到的场电位变化的影响。降低镁浓度所产生的多群峰阈值的降低被阻止了,但其他变化,包括单峰阈值的降低,并未被阻止。此外,20微摩尔浓度的CGP39551并不能阻止癫痫样活动,癫痫样活动通过向对照海马切片中加入GABAA拮抗剂荷包牡丹碱所导致的单一群峰和多群峰产生阈值的降低来衡量。

相似文献

1
Ethanol withdrawal hyperexcitability in vitro is selectively decreased by a competitive NMDA receptor antagonist.体外乙醇戒断性过度兴奋可被一种竞争性N-甲基-D-天冬氨酸(NMDA)受体拮抗剂选择性降低。
Brain Res. 1995 Nov 13;699(1):1-11. doi: 10.1016/0006-8993(95)00445-v.
2
Effects on ethanol withdrawal hyperexcitability of chronic treatment with a competitive N-methyl-D-aspartate receptor antagonist.竞争性N-甲基-D-天冬氨酸受体拮抗剂长期治疗对乙醇戒断性兴奋过度的影响。
J Pharmacol Exp Ther. 1995 Jan;272(1):112-8.
3
A calcium channel antagonist stereoselectively decreases ethanol withdrawal hyperexcitability but not that due to bicuculline, in hippocampal slices.在海马切片中,一种钙通道拮抗剂能立体选择性地降低乙醇戒断引起的过度兴奋,但对荷包牡丹碱引起的过度兴奋无此作用。
Br J Pharmacol. 1991 Jun;103(2):1313-20. doi: 10.1111/j.1476-5381.1991.tb09786.x.
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Effect of CGP39551 administration on the kindling of ethanol-withdrawal seizures.给予CGP39551对乙醇戒断性癫痫发作点燃的影响。
Psychopharmacology (Berl). 2002 Sep;163(2):157-65. doi: 10.1007/s00213-002-1138-7. Epub 2002 Jul 13.
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Comparison of the effects of drugs on hyperexcitability induced in hippocampal slices by withdrawal from chronic ethanol consumption.比较药物对慢性乙醇摄入戒断所致海马切片超兴奋性的影响。
Br J Pharmacol. 1998 Jan;123(2):215-22. doi: 10.1038/sj.bjp.0701596.
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The competitive NMDA receptor antagonist, CGP 39551, inhibits ethanol withdrawal seizures.竞争性N-甲基-D-天冬氨酸受体拮抗剂CGP 39551可抑制乙醇戒断性癫痫发作。
Eur J Pharmacol. 1991 Jan 3;192(1):197-8. doi: 10.1016/0014-2999(91)90092-5.
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Nitrendipine, given during drinking, decreases the electrophysiological changes in the isolated hippocampal slice, seen during ethanol withdrawal.在饮酒期间给予尼群地平,可减少在乙醇戒断期间分离海马切片中所见的电生理变化。
Br J Pharmacol. 1991 Jul;103(3):1677-84. doi: 10.1111/j.1476-5381.1991.tb09846.x.
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Changes in voltage-operated calcium channels modify ethanol withdrawal hyperexcitability in mouse hippocampal slices.
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Greater contribution of N-methyl-D-aspartic acid receptors in ventral compared to dorsal hippocampal slices in the expression and long-term maintenance of epileptiform activity.与背侧海马切片相比,N-甲基-D-天冬氨酸受体在腹侧海马切片癫痫样活动的表达和长期维持中起更大作用。
Neuroscience. 2005;135(3):765-79. doi: 10.1016/j.neuroscience.2005.06.024. Epub 2005 Sep 9.
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Possible involvement of NMDA receptor-mediated transmission in barbiturate physical dependence.N-甲基-D-天冬氨酸受体介导的传递可能参与巴比妥类药物身体依赖性的形成。
Br J Pharmacol. 1994 Jan;111(1):89-96. doi: 10.1111/j.1476-5381.1994.tb14028.x.

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