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选择性5-羟色胺再摄取抑制剂的抗抑郁样效应涉及胍丁胺对咪唑啉受体的调节。

Antidepressant like effect of selective serotonin reuptake inhibitors involve modulation of imidazoline receptors by agmatine.

作者信息

Taksande Brijesh G, Kotagale Nandkishor R, Tripathi Sunil J, Ugale Rajesh R, Chopde Chandrabhan T

机构信息

Division of Neuroscience, Department of Pharmacology, Shrimati Kishoritai Bhoyar College of Pharmacy, New Kamptee, Nagpur, Maharashtra 441 002, India.

出版信息

Neuropharmacology. 2009 Sep;57(4):415-24. doi: 10.1016/j.neuropharm.2009.06.035. Epub 2009 Jul 7.

Abstract

Recent findings demonstrated the dysregulation of imidazoline receptor binding sites in major depression and their normalization by chronic treatment with antidepressants including selective serotonin reuptake inhibitors (SSRIs). Present study investigated the role of agmatine and imidazoline receptors in antidepressant like effect of SSRIs and imipramine in mouse forced swimming test (FST) paradigm. The antidepressant like effect of fluoxetine or paroxetine was potentiated by imidazoline I(1)/I(2) receptor agonist agmatine (5-10 mg/kg, ip), imidazoline I(1) receptor agonists, moxonidine (0.25-0.5 mg/kg, ip) and clonidine (0.015-0.03 mg/kg, ip), imidazoline I(2) receptor agonist, 2-(2-benzofuranyl)-2-imidazoline (5-10 mg/kg, ip) as well as by the drugs known to increase endogenous agmatine levels in brain viz., L-arginine, an agmatine biosynthetic precursor (40 microg/mouse, icv), ornithine decarboxylase inhibitor, difluoromethyl ornithine (12.5 microg/mouse, icv), diamine oxidase inhibitor, aminoguanidine (6.5 microg/mouse, icv) and agmatinase inhibitor, arcaine (50 microg/mouse, icv). Conversely, prior administration of I(1) receptor antagonist, efaroxan (1 mg/kg, ip), I(2) receptor antagonist, idazoxan (0.25 mg/kg, ip) and arginine decarboxylase inhibitor, d-arginine (100 mg/kg, ip) blocked the antidepressant like effect of paroxetine (10 mg/kg, ip) and fluoxetine (20 mg/kg, ip). On the other hand, antidepressant like effect of imipramine was neither augmented nor attenuated by any of the above drugs. Mice pretreated with SSRIs but not imipramine and exposed to FST showed higher concentration of agmatine in brain as compared to saline control. This effect of SSRIs on agmatine levels was completely blocked by arginine decarboxylase inhibitor d-arginine but not by imidazoline receptor antagonists, efaroxan or idazoxan. These results demonstrate that modulation of imidazoline receptors by agmatine are implicated in the antidepressant like effect of SSRIs and may be projected as a potential therapeutic target for the treatment of depressive disorders.

摘要

最近的研究结果表明,在重度抑郁症中,咪唑啉受体结合位点存在失调,而包括选择性5-羟色胺再摄取抑制剂(SSRI)在内的抗抑郁药长期治疗可使其恢复正常。本研究在小鼠强迫游泳试验(FST)范式中,探究了胍丁胺和咪唑啉受体在SSRI和丙咪嗪抗抑郁样效应中的作用。咪唑啉I(1)/I(2)受体激动剂胍丁胺(5-10毫克/千克,腹腔注射)、咪唑啉I(1)受体激动剂莫索尼定(0.25-0.5毫克/千克,腹腔注射)和可乐定(0.015-0.03毫克/千克,腹腔注射)、咪唑啉I(2)受体激动剂2-(2-苯并呋喃基)-2-咪唑啉(5-10毫克/千克,腹腔注射)以及已知可提高脑内内源性胍丁胺水平的药物,如胍丁胺生物合成前体L-精氨酸(40微克/小鼠,脑室内注射)、鸟氨酸脱羧酶抑制剂二氟甲基鸟氨酸(12.5微克/小鼠,脑室内注射)、二胺氧化酶抑制剂氨基胍(6.5微克/小鼠,脑室内注射)和胍丁胺酶抑制剂阿卡因(50微克/小鼠,脑室内注射),均可增强氟西汀或帕罗西汀的抗抑郁样效应。相反,预先给予I(1)受体拮抗剂依发罗新(1毫克/千克,腹腔注射)、I(2)受体拮抗剂伊达唑新(0.25毫克/千克,腹腔注射)和精氨酸脱羧酶抑制剂D-精氨酸(100毫克/千克,腹腔注射),可阻断帕罗西汀(10毫克/千克,腹腔注射)和氟西汀(20毫克/千克,腹腔注射)的抗抑郁样效应。另一方面,上述任何一种药物均未增强或减弱丙咪嗪的抗抑郁样效应。与生理盐水对照组相比,预先用SSRI而非丙咪嗪处理并接受FST的小鼠,脑内胍丁胺浓度更高。SSRI对胍丁胺水平的这种作用被精氨酸脱羧酶抑制剂D-精氨酸完全阻断,但未被咪唑啉受体拮抗剂依发罗新或伊达唑新阻断。这些结果表明,胍丁胺对咪唑啉受体的调节与SSRI的抗抑郁样效应有关,可能是治疗抑郁症的一个潜在治疗靶点。

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