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阿戈美拉汀对强迫障碍模型鼠的作用:与meta-氯苯哌嗪、印防己毒素和地西泮的相互作用。

Effects of agomelatine in a murine model of obsessive-compulsive disorder: interaction with meta-chlorophenylpiperazine, bicuculline, and diazepam.

机构信息

Sinhgad College of Pharmacy, Pharmacology Division, Vadgaon (Bk), Off Sinhgad Road, Pune 411 041, Maharashtra, India.

出版信息

Kaohsiung J Med Sci. 2013 Jul;29(7):362-7. doi: 10.1016/j.kjms.2012.11.003. Epub 2013 Apr 4.

Abstract

The anticompulsive potential of agomelatine, a potent MT1/2 receptor agonist, and its combined effect with m-chlorophenylpiperazine hydrochloride (mCPP), bicuculline, and diazepam, were investigated in male C57BLJ/6 mice using marble-burying behavior (MBB) test. Acute administration of agomelatine (30-40 mg/kg, intraperitoneal (i.p.)) significantly inhibited the MBB in mice without influencing their locomotor activity. Further, chronic (28 days) administration of lower doses of agomelatine (10 and 20 mg/kg, i.p.) dose-dependently reduced the MBB without influencing their locomotor activity. Interaction studies revealed that pretreatment with mCPP (0.5 mg/kg, i.p.), a serotonin 5HT2C agonist, partially attenuated the anticompulsive effect of agomelatine (30 mg/kg). Further, a GABAA receptor agonist (diazepam, 1.25 mg/kg, i.p.) and antagonist (bicuculline, 1 mg/kg, i.p.) had no influence on the effects of agomelatine on MBB and locomotor activity. The doses of modulators were selected on the basis of dose-response studies. The results indicate that agomelatine has a potent anticompulsive effect that can be attributed to 5HT2C antagonism and MT1/2 agonism, and is certainly not mediated via its effects on the GABAergic system. Thus, the study adds to the growing literature on the psychopharmacological effects of agomelatine, and warrants further exploration in multiple paradigms.

摘要

本文采用埋珠实验(MBB),研究了强效 MT1/2 受体激动剂阿戈美拉汀的抗强迫作用,及其与 m-氯苯哌嗪盐酸盐(mCPP)、印防己毒素、地西泮联合使用的效果。在雄性 C57BLJ/6 小鼠中进行实验,结果表明,阿戈美拉汀(30-40mg/kg,腹腔注射)急性给药可显著抑制小鼠的 MBB,而不影响其运动活性。此外,较低剂量的阿戈美拉汀(10 和 20mg/kg,腹腔注射)连续(28 天)给药可剂量依赖性地减少 MBB,而不影响其运动活性。相互作用研究表明,预先给予 5HT2C 激动剂 mCPP(0.5mg/kg,腹腔注射)可部分减弱阿戈美拉汀(30mg/kg)的抗强迫作用。此外,GABAA 受体激动剂(地西泮,1.25mg/kg,腹腔注射)和拮抗剂(印防己毒素,1mg/kg,腹腔注射)对阿戈美拉汀对 MBB 和运动活性的影响没有影响。调节剂的剂量是根据剂量反应研究选择的。结果表明,阿戈美拉汀具有很强的抗强迫作用,这可归因于 5HT2C 拮抗作用和 MT1/2 激动作用,而肯定不是通过其对 GABA 能系统的作用介导的。因此,该研究增加了关于阿戈美拉汀精神药理学作用的文献,并在多种范式中进一步探索。

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