首页> 外文期刊>European Journal of Pharmacology: An International Journal >Effects of systemic injections of Vilazodone, a selective serotonin reuptake inhibitor and serotonin 1(A) receptor agonist, on anxiety induced by predator stress in rats.
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Effects of systemic injections of Vilazodone, a selective serotonin reuptake inhibitor and serotonin 1(A) receptor agonist, on anxiety induced by predator stress in rats.

机译:全身注射Vilazodone,选择性5-羟色胺再摄取抑制剂和5-羟色胺1(A)受体激动剂对捕食者应激所致大鼠焦虑的影响。

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We examined the effect of Vilazodone, a selective serotonin reuptake inhibitor (SSRI) and serotonin 1(A) (5-HT(1A)) receptor agonist [Bartoszyk, G.D., Hegenbart, R., Ziegler, H., 1997. EMD 68843, a serotonin reuptake inhibitor with selective presynaptic 5-HT1A receptor agonistic properties. Eur. J. Pharmacol. 322, 147-153.], on change in affect following predator stress. Vilazodone and vehicle injection (intraperitoneal) occurred either 10 min after predator stress (prophylactic testing), or 90 min prior to behavioral testing for the effects of predator stress (therapeutic testing). Predator stress involved unprotected exposure of rats to a domestic cat. Behavioral effects of stress were evaluated with hole board, plus-maze, and acoustic startle tests 1 week after stress. Predator stress increased anxiety-like behavior in the plus-maze and elevated response to acoustic startle. In prophylactic testing, Vilazodone affected stress potentiation of startle at doses above 5 mg/kg. Vilazodone increased stress elevation of startle at 10 mg/kg. Higher doses of Vilazodone (20 and 40 mg/kg) blocked stress potentiation of startle. In contrast, Vilazodone had no effect on stress potentiation of anxiety in the plus-maze. In therapeutic testing, Vilazodone increased stress elevation of startle at all doses. In contrast, therapeutic Vilazodone had no effect on stress potentiation of anxiety in the plus-maze. Taken together, the data suggest a prophylactic potential for Vilazodone in the treatment of changes in hypervigilance following severe stress.
机译:我们研究了选择性5-羟色胺再摄取抑制剂(SSRI)和5-羟色胺1(A)(5-HT(1A))受体激动剂Vilazodone的作用[Bartoszyk,GD,Hegenbart,R.,Ziegler,H.,1997. EMD 68843 ,一种具有选择性突触前5-HT1A受体激动特性的血清素再摄取抑制剂。欧元。 J.Pharmacol。 322,147-153。],关于捕食者应激后的情感变化。 Vilazodone和媒介物注射(腹膜内注射)发生在掠食者应激后10分钟(预防性测试),或行为测试前90分钟发现掠食者应激的影响(治疗性测试)。捕食者应激涉及大鼠在没有保护的情况下与家猫接触。应激1周后,通过孔板,迷宫和声惊吓测试评估了应激的行为影响。食肉动物的压力增加了迷宫般的焦虑感,并增强了对听觉惊吓的反应。在预防性测试中,Vilazodone以高于5 mg / kg的剂量影响惊吓的应激增强。 Vilazodone以10 mg / kg的剂量增加惊吓的应力升高。更高剂量的维拉唑酮(20和40 mg / kg)阻止了惊吓的应激增强。相反,维拉唑酮对正迷宫中焦虑的应激增强没有作用。在治疗性测试中,Vilazodone在所有剂量下均增加了惊吓的紧张感。相反,治疗性维拉唑酮对正迷宫中焦虑的应激增强没有作用。总体而言,这些数据表明,Vilazodone具有预防严重压力后过度警觉性变化的预防潜力。

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