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氟西汀和丁螺环酮对大鼠中脑导水管周围灰质背侧5-HT1A和5-HT2A受体激活诱导的类抗惊恐反应的影响。

Effects of fluoxetine and buspirone on the panicolytic-like response induced by the activation of 5-HT1A and 5-HT2A receptors in the rat dorsal periaqueductal gray.

作者信息

de Bortoli Valquíria Camin, Nogueira Regina Lúcia, Zangrossi Hélio

机构信息

Department of Pharmacology, School of Medicine, University of São Paulo, 14049-900, Ribeirão Preto, SP, Brazil.

出版信息

Psychopharmacology (Berl). 2006 Jan;183(4):422-8. doi: 10.1007/s00213-005-0189-y. Epub 2005 Oct 29.

Abstract

RATIONALE

Administration of 5-hydroxytryptamine (5-HT)1A and 5-HT2A receptor agonists into the dorsal periaqueductal gray (DPAG) inhibits escape, a defensive behavior associated with panic attacks. Long-term treatment with the antipanic compound imipramine enhances the DPAG 5-HT1A- and 5-HT2A-receptor-mediated inhibition of escape, implicating these receptors in the mode of action of panicolytic drugs.

OBJECTIVES

In the present study, we investigated whether the inhibitory effect on escape elicited by the intra-DPAG injection of 5-HT1A and 5-HT2A receptor agonists is also enhanced after treatment with fluoxetine, another widely used antipanic drug. The effects of fluoxetine were compared to those of buspirone, an anxiolytic drug without major effect on panic disorder.

METHODS

Male Wistar rats, subchronically (3-6 days) or chronically (21-24 days) treated with fluoxetine (10 mg/kg i.p.) or chronically treated with buspirone (0.3 mg/kg i.p.), were intra-DPAG injected with 5-HT (20 nmol), the 5-HT1A receptor agonist (+/-)-8-hydroxy-2-(di-n-propylamino)tetralin hydrobromide (8-OH-DPAT; 8 nmol) or the preferential 5-HT2A receptor agonist (+/-)-1-(2,5-dimethoxy-4-iodophenyl) piperazine dihydrochloride (DOI; 16 nmol). The intensity of electrical current that applied to the DPAG-evoked escape behavior was measured before and after the microinjection of these agonists.

RESULTS

The electrical current necessary to produce escape was increased after the microinjection of the three 5-HT receptor agonists in all groups of animals tested. However, this panicolytic-like effect was significantly higher in animals receiving long-term treatment with fluoxetine.

CONCLUSIONS

The results suggest that facilitation of the 5-HT1A- and 5-HT2A-receptor-mediated inhibition of DPAG neuronal activity is implicated in the beneficial effect of antidepressants in panic disorder.

摘要

理论依据

向中脑导水管周围灰质背侧(DPAG)注射5-羟色胺(5-HT)1A和5-HT2A受体激动剂可抑制逃避反应,逃避反应是一种与惊恐发作相关的防御行为。抗惊恐化合物丙咪嗪的长期治疗可增强DPAG中5-HT1A和5-HT2A受体介导的对逃避反应的抑制作用,提示这些受体与抗惊恐药物的作用方式有关。

目的

在本研究中,我们调查了另一种广泛使用的抗惊恐药物氟西汀治疗后,DPAG内注射5-HT1A和5-HT2A受体激动剂对逃避反应的抑制作用是否也会增强。将氟西汀的作用与丁螺环酮(一种对惊恐障碍无主要影响的抗焦虑药物)的作用进行比较。

方法

对雄性Wistar大鼠进行亚慢性(3 - 6天)或慢性(21 - 24天)氟西汀(10mg/kg腹腔注射)治疗,或对其进行慢性丁螺环酮(0.3mg/kg腹腔注射)治疗,然后向DPAG内注射5-HT(20nmol)、5-HT1A受体激动剂(±)-8-羟基-2-(二正丙基氨基)四氢萘溴酸盐(8-OH-DPAT;8nmol)或优先的5-HT2A受体激动剂(±)-1-(2,5-二甲氧基-4-碘苯基)哌嗪二盐酸盐(DOI;16nmol)。在微量注射这些激动剂之前和之后,测量施加于DPAG诱发逃避行为的电流强度。

结果

在所有测试的动物组中,微量注射三种5-HT受体激动剂后,产生逃避反应所需的电流增加。然而,在接受氟西汀长期治疗的动物中,这种抗惊恐样效应明显更高。

结论

结果表明,5-HT1A和5-HT2A受体介导的对DPAG神经元活动的抑制作用的促进与抗抑郁药对惊恐障碍的有益作用有关。

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