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佐米曲普坦——一种5-HT1B/D激动剂、酒精与小鼠攻击行为

Zolmitriptan--a 5-HT1B/D agonist, alcohol, and aggression in mice.

作者信息

de Almeida R M, Nikulina E M, Faccidomo S, Fish E W, Miczek K A

机构信息

Department of Psychology, Tufts University, Medford, MA 02155, USA

出版信息

Psychopharmacology (Berl). 2001 Sep;157(2):131-41. doi: 10.1007/s002130100778.

Abstract

RATIONALE

Zolmitriptan is an anti-migraine agent with action at 5-HT1B/D receptors. It penetrates into the central nervous system and, like other 5-HT1B/D agonists, its pharmacotherapeutic profile may include significant anti-aggressive effects.

OBJECTIVES

To examine whether zolmitriptan has potential anti-aggressive effects by studying two kinds of aggressive behavior in mice--species-typical and aggression under the influence of alcohol. A second objective was to study whether pre- or post-synaptic receptors mediate these anti-aggressive effects.

METHODS

Initially, the anti-aggressive effects of zolmitriptan were studied in male CFW mice during 5-min resident-intruder confrontations. To confirm the 5-HT1B receptor as a critical site of action for the anti-aggressive effects, the zolmitriptan dose-effect determinations were repeated after pretreatment with GR 127935 (10 mg/kg, i.p.). In further experiments, mice were treated concurrently with alcohol (1.0 g/kg, p.o.) and zolmitriptan (1-30 mg/kg, i.p.) in order to compare the effects of this agonist on species-typical and alcohol-heightened aggression. Finally, mice were infused with the neurotoxin 5,7-DHT (10 microg) into the raphé area to eliminate somatodendritic and presynaptic autoreceptors. The anti-aggressive effects of zolmitriptan (17 mg/kg, i.p.) or CP-94,253 (10 mg/kg, i.p.) were assessed 10 days after the lesion, and levels of 5-HT and 5-HIAA were measured in the hippocampus and prefrontal cortex.

RESULTS

Zolmitriptan exerted behaviorally specific anti-aggressive effects. The reduction in aggression was antagonized by GR 127935, indicated by a rightward shift in the dose-effect curves of zolmitriptan, showing the specificity for the 5-HT1B receptors. Zolmitriptan also decreased alcohol-heightened aggression with equal efficacy. The anti-aggressive effects of CP-94,253 and zolmitriptan remained unaltered by 5,7-DHT lesions that depleted cortical and hippocampal 5-HT by 60-80%.

CONCLUSIONS

Zolmitriptan proved to be an effective and behaviorally specific anti-aggressive agent in situations that engender moderate and alcohol-heightened levels of aggression. These effects are potentially due to activation of post-synaptic 5-HT1BD receptors.

摘要

原理

佐米曲坦是一种作用于5-HT1B/D受体的抗偏头痛药物。它可穿透进入中枢神经系统,与其他5-HT1B/D激动剂一样,其药物治疗特性可能包括显著的抗攻击作用。

目的

通过研究小鼠的两种攻击行为——物种典型攻击行为和酒精影响下的攻击行为,来检验佐米曲坦是否具有潜在的抗攻击作用。第二个目的是研究突触前或突触后受体是否介导这些抗攻击作用。

方法

最初,在5分钟的定居者-入侵者对抗实验中,研究了佐米曲坦对雄性CFW小鼠的抗攻击作用。为了确认5-HT1B受体是抗攻击作用的关键作用位点,在用GR 127935(10毫克/千克,腹腔注射)预处理后,重复进行佐米曲坦的剂量-效应测定。在进一步的实验中,小鼠同时接受酒精(1.0克/千克,口服)和佐米曲坦(1 - 30毫克/千克,腹腔注射)治疗,以比较该激动剂对物种典型攻击行为和酒精增强的攻击行为的影响。最后,将神经毒素5,7 - DHT(10微克)注入小鼠中缝区域,以消除躯体树突状和突触前自身受体。在损伤后10天评估佐米曲坦(17毫克/千克,腹腔注射)或CP - 94,253(10毫克/千克,腹腔注射)的抗攻击作用,并测量海马体和前额叶皮质中5 - HT和5 - HIAA的水平。

结果

佐米曲坦发挥了行为特异性的抗攻击作用。GR 127935拮抗了攻击行为的减少,这表现为佐米曲坦剂量-效应曲线向右移动,表明对5-HT1B受体具有特异性。佐米曲坦还以相同的效力降低了酒精增强的攻击行为。CP - 94,253和佐米曲坦的抗攻击作用在5,7 - DHT损伤后未改变,该损伤使皮质和海马体中的5 - HT减少了60 - 80%。

结论

在引发中度和酒精增强的攻击水平的情况下,佐米曲坦被证明是一种有效且行为特异性的抗攻击药物。这些作用可能是由于突触后5-HT1BD受体的激活。

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