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迷迭香酸抗抑郁样作用涉及单胺能系统。

Evidence of the involvement of the monoaminergic systems in the antidepressant-like effect of Aloysia gratissima.

机构信息

Departamento de Ciências Naturais, Centro de Ciências Exatas e Naturais, Universidade Regional de Blumenau, Campus I, 89012-900 SC, Brazil.

出版信息

J Ethnopharmacol. 2013 Jul 30;148(3):914-20. doi: 10.1016/j.jep.2013.05.042. Epub 2013 Jun 4.

Abstract

ETHNOPHARMACOLOGICAL RELEVANCE

Aloysia gratissima (Verbenaceae) is an aromatic plant distributed in South America and, employed in folk medicine for the treatment of nervous systems illness, including depression. The neuroprotective and antidepressant-like activities of the aqueous extract of Aloysia gratissima (AE) administered orally has already been demonstrated.In this study the involvement of monoaminergic systems in the antidepressant-like effect of the AE was investigated.

MATERIALS AND METHODS

The implication of the monoaminergic systems in the antidepressant-like activity of Aloysia gratissima was evaluated using different pharmacological antagonists that were administered previously to the acute oral administration of AE (10 mg/kg). The antidepressant-like effect was assessed in the TST and locomotor activity was evaluated in the open-field test in mice.

RESULTS

The anti-immobility effect elicited by AE in the TST was prevented by the pre-treatment of mice with the antagonists, NAN-190 (5-HT(1A) receptor), ketanserin (5-HT(2A/2C) receptor), prazosin (α1-adrenoceptor), yohimbine (α2-adrenoceptor), SCH23390 (dopamine D1 receptor), or sulpiride (dopamine D2 receptor).

CONCLUSIONS

These results indicate that the antidepressant-like effect of AE in the TST is dependent on its interaction with the serotonergic (5-HT(1A) and 5-HT(2A/2C)), noradrenergic (α1 and α2-adrenoceptors) and dopaminergic (D1 and D2 receptors) systems, suggesting that this specie might act as a new potential resource for developing antidepressants to treat depressive disorders.

摘要

民族药理学相关性

甜罗勒(唇形科)是一种芳香植物,分布于南美洲,用于民间医学治疗神经系统疾病,包括抑郁症。已证明口服甜罗勒水提物(AE)具有神经保护和抗抑郁样活性。

在这项研究中,研究了单胺能系统在 AE 抗抑郁样作用中的参与。

材料和方法

使用不同的药理学拮抗剂预先给予 AE(10mg/kg)急性口服给药,评估单胺能系统在甜罗勒抗抑郁样活性中的作用。在 TST 中评估抗不动性作用,在开放场试验中评估运动活性。

结果

AE 在 TST 中引起的抗不动性作用被拮抗剂预处理的小鼠所阻止,这些拮抗剂包括 NAN-190(5-HT1A 受体)、酮色林(5-HT2A/2C 受体)、哌唑嗪(α1-肾上腺素受体)、育亨宾(α2-肾上腺素受体)、SCH23390(多巴胺 D1 受体)或舒必利(多巴胺 D2 受体)。

结论

这些结果表明,AE 在 TST 中的抗抑郁样作用取决于其与 5-羟色胺能(5-HT1A 和 5-HT2A/2C)、去甲肾上腺素能(α1 和 α2-肾上腺素受体)和多巴胺能(D1 和 D2 受体)系统的相互作用,表明该物种可能作为开发抗抑郁药治疗抑郁症的新潜在资源。

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