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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.

DOI:10.1016/j.kjms.2012.11.003
PMID:23768699
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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本文引用的文献

1
Endocannabinoid analogues exacerbate marble-burying behavior in mice via TRPV1 receptor.内源性大麻素类似物通过 TRPV1 受体加剧小鼠埋珠行为。
Neuropharmacology. 2012 Apr;62(5-6):2024-33. doi: 10.1016/j.neuropharm.2011.12.030. Epub 2012 Jan 11.
2
Is circadian rhythm disruption important in obsessive-compulsive disorder (OCD)? A case of successful augmentation with agomelatine for the treatment of OCD.昼夜节律紊乱在强迫症(OCD)中重要吗?一例阿戈美拉汀成功增效治疗强迫症的病例。
Clin Neuropharmacol. 2011 Jul-Aug;34(4):139-40. doi: 10.1097/WNF.0b013e318223421f.
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Animal models of obsessive-compulsive disorder: exploring pharmacology and neural substrates.
强迫症动物模型:探索药理学和神经基础。
Neurosci Biobehav Rev. 2012 Jan;36(1):47-63. doi: 10.1016/j.neubiorev.2011.04.006. Epub 2011 Apr 15.
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A systematic, updated review on the antidepressant agomelatine focusing on its melatonergic modulation.系统、更新的抗抑郁药阿戈美拉汀综述,重点关注其对褪黑素能的调节。
Curr Neuropharmacol. 2010 Sep;8(3):287-304. doi: 10.2174/157015910792246227.
5
Switching from serotonin reuptake inhibitors to agomelatine in patients with refractory obsessive-compulsive disorder: a 3 month follow-up case series.从选择性 5-羟色胺再摄取抑制剂转换为阿戈美拉汀治疗难治性强迫症患者:一项 3 个月随访的病例系列研究。
Ann Gen Psychiatry. 2011 Feb 28;10(1):5. doi: 10.1186/1744-859X-10-5.
6
Facilitation of CB1 receptor-mediated neurotransmission decreases marble burying behavior in mice.促进 CB1 受体介导的神经递质传递可减少小鼠的埋珠行为。
Prog Neuropsychopharmacol Biol Psychiatry. 2011 Mar 30;35(2):434-8. doi: 10.1016/j.pnpbp.2010.11.027. Epub 2010 Nov 25.
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Marble burying reflects a repetitive and perseverative behavior more than novelty-induced anxiety.大理石掩埋反映的是一种重复性和持续性的行为,而非新奇诱导的焦虑。
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