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给小鼠注射地西泮可预防重复电惊厥休克治疗所引起的单胺介导行为的某些变化。

Diazepam administration to mice prevents some of the changes in monoamine-mediated behaviour produced by repeated electroconvulsive shock treatment.

作者信息

Green A R, Mountford J A

出版信息

Psychopharmacology (Berl). 1985;86(1-2):190-3. doi: 10.1007/BF00431707.

DOI:10.1007/BF00431707
PMID:2991965
Abstract

Administration to mice of electroconvulsive shock (ECS) five times over 10 days results in an enhanced 5-HTP-induced head twitch response, an enhanced apomorphine-induced locomotor response and an attenuated sedation response to the alpha 2-adrenoceptor agonist clonidine. Diazepam (1.25 mg/kg IP) injected 5 min before each ECS abolished the enhanced 5-HT- and dopamine-mediated responses but left the attenuated sedation response unaltered. When diazepam was given 5 min after each convulsion it still had the same effect, although its effects on the ECS-induced changes was blocked by administration of the specific benzodiazepine antagonist Ro 15-1788 (10 mg/kg IP) at the same time as diazepam. It is concluded that diazepam can abolish the ECS-induced changes in 5-HT- and DA-mediated behaviour, but not alpha 2-adrenoceptor-mediated responses, possibly by interfering with post-ictal changes. The implications for administration of benzodiazepines during electroconvulsive therapy (ECT) are discussed.

摘要

在10天内对小鼠进行5次电惊厥休克(ECS)处理,会导致5-羟色胺酸(5-HTP)诱导的头部抽搐反应增强、阿扑吗啡诱导的运动反应增强以及对α2-肾上腺素能受体激动剂可乐定的镇静反应减弱。在每次ECS前5分钟注射地西泮(1.25毫克/千克,腹腔注射)可消除增强的5-羟色胺(5-HT)和多巴胺介导的反应,但对减弱的镇静反应无影响。当在每次惊厥后5分钟给予地西泮时,其仍有相同效果,尽管其对ECS诱导变化的作用在与地西泮同时给予特异性苯二氮䓬拮抗剂Ro 15-1788(10毫克/千克,腹腔注射)时被阻断。得出的结论是,地西泮可能通过干扰发作后变化来消除ECS诱导的5-HT和多巴胺介导行为的变化,但不能消除α2-肾上腺素能受体介导的反应。文中讨论了在电惊厥治疗(ECT)期间给予苯二氮䓬类药物的意义。

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引用本文的文献

1
MK-801 prevents the enhanced behavioural response to apomorphine elicited by repeated electroconvulsive treatment in mice.MK-801可预防小鼠反复电惊厥治疗引起的对阿扑吗啡行为反应增强。
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本文引用的文献

1
A method for assessing the effects of drugs on the central actions of 5-hydroxytryptamine.一种评估药物对5-羟色胺中枢作用影响的方法。
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Effect of single and repeated electroconvulsive shock on serotonergic system in rat brain--II. Behavioural studies.单次及重复电惊厥休克对大鼠脑内5-羟色胺能系统的影响——II. 行为学研究。
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Enhanced 5-hydroxytryptamine and dopamine-mediated behavioural responses following convulsions--II. The effects of anaesthesia and current conditions on the appearance of enhanced responses following electroconvulsive shock.
惊厥后5-羟色胺和多巴胺介导的行为反应增强——II. 麻醉和电流条件对电惊厥休克后增强反应出现的影响
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The effect of some anti-epilepsy drugs on enhancement of the monoamine-mediated behavioural responses following the administration of electroconvulsive shocks to rats.某些抗癫痫药物对大鼠电惊厥休克给药后单胺介导的行为反应增强的影响。
Eur J Pharmacol. 1981 Sep 11;74(2-3):243-7. doi: 10.1016/0014-2999(81)90537-9.
5
Enhancement of responsiveness of the central serotonergic system and serotonin-2 receptor density in rat frontal cortex by electroconvulsive treatment.电休克治疗增强大鼠额叶皮质中央5-羟色胺能系统反应性及5-羟色胺-2受体密度
Eur J Pharmacol. 1981 Nov 19;76(1):81-5. doi: 10.1016/0014-2999(81)90012-1.
6
Repeated electroconvulsive shock attenuates clonidine-induced hypoactivity in rodents.重复电惊厥休克可减轻可乐定诱导的啮齿动物活动减退。
Eur J Pharmacol. 1981 Nov 5;75(4):231-7. doi: 10.1016/0014-2999(81)90549-5.
7
Differential effects of electroconvulsive shock and antidepressant drugs on serotonin-2 receptors in rat brain.电休克和抗抑郁药物对大鼠脑内5-羟色胺-2受体的不同作用。
Eur J Pharmacol. 1981 Feb 19;69(4):515-8. doi: 10.1016/0014-2999(81)90460-x.
8
Further evidence for a relationship between changes in GABA concentration in rat brain and enhanced monoamine-mediated behavioural responses following repeated electroconvulsive shock.大鼠脑内γ-氨基丁酸(GABA)浓度变化与重复电休克后单胺介导的行为反应增强之间关系的进一步证据。
Neuropharmacology. 1982 Oct;21(10):981-4. doi: 10.1016/0028-3908(82)90110-1.
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Benzodiazepines and effectiveness of ect.苯二氮䓬类药物与电休克治疗的有效性
Br J Psychiatry. 1982 Sep;141:314-5. doi: 10.1192/bjp.141.3.314.
10
Antidepressant treatments: effects in rodents on dose-response curves of 5-hydroxytryptamine- and dopamine-mediated behaviours and 5-HT2 receptor number in frontal cortex.抗抑郁药治疗:对啮齿动物5-羟色胺和多巴胺介导行为的剂量反应曲线以及额叶皮质中5-HT2受体数量的影响。
Br J Pharmacol. 1983 Oct;80(2):377-85. doi: 10.1111/j.1476-5381.1983.tb10044.x.