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桑色素预处理可减轻实验动物模型中的精神分裂症样行为。

Morin Pretreatment Attenuates Schizophrenia-Like Behaviors in Experimental Animal Models.

作者信息

Ben-Azu Benneth, Aderibigbe Adegbuyi Oladele, Omogbiya Itivere Adrian, Ajayi Abayomi Mayowa, Iwalewa Ezekiel O

机构信息

Neuropharmacology Unit, Department of Pharmacology and Therapeutics, College of Medicine, University of Ibadan, Ibadan, Oyo State, Nigeria.

Department of Pharmacology and Therapeutics, Faculty of Basic Medical Sciences, Delta State University, Abraka, Nigeria.

出版信息

Drug Res (Stuttg). 2018 Mar;68(3):159-167. doi: 10.1055/s-0043-119127. Epub 2017 Sep 29.

Abstract

OBJECTIVES

Morin is a naturally occurring flavonoid with strong anti-oxidant and anti-inflammatory properties. Studies have shown that flavones modulate neurotransmission through enhancement of gamma amino butyric acid activity in the central nervous system; which led to the hypothesis that they could exert tranquilizing effects in rodents. Hence, this study was designed to evaluate the antipsychotic effect of morin on experimental animal models.

METHODS

The antipsychotic effect of morin (25, 50 and 100 mg/kg) administered intraperitoneally (i.p.) was assessed on novelty-induced locomotion, apomorphine-induced stereotypy, ketamine-induced stereotypy, ketamine-induced hyperlocomotion and ketamine-enhanced immobility in forced swim test (FST). Catalepsy and rota rod tests were also carried out to evaluate the extrapyramidal side effects of morin.

RESULTS

Morin (25, 50 and 100 mg/kg, i.p.) pretreatments significantly (p<0.05) demonstrated anti-schizophrenia-like behavior by inhibiting ketamine-induced hyperlocomotion in mice. Moreover, morin (50 and 100 mg/kg, i.p.) significantly (p<0.05) reduced spontaneous locomotor activity. Also, morin suppressed apomorphine-induced stereotypy and ketamine-induced stereotypy. The increase in immobility in FST due to ketamine administration was reduced by morin in a significant dose-dependent manner. Furthermore, the antipsychotic activity of morin was not associated with extrapyramidal side effects, as evidenced by decreased decent latency and increased motoric coordination and performance in mice.

CONCLUSION

The results of the study revealed that morin demonstrated antipsychotic-like property devoid of extrapyramidal side effects in experimental animal models and may be beneficial in the treatment of schizophrenia-like behaviors; particularly in patients with behavioral hyperactivity and negative symptoms.

摘要

目的

桑色素是一种天然存在的黄酮类化合物,具有强大的抗氧化和抗炎特性。研究表明,黄酮类化合物可通过增强中枢神经系统中γ-氨基丁酸的活性来调节神经传递;由此提出假说,认为它们可能对啮齿动物产生镇静作用。因此,本研究旨在评估桑色素对实验动物模型的抗精神病作用。

方法

通过对新奇诱导的运动、阿扑吗啡诱导的刻板行为、氯胺酮诱导的刻板行为、氯胺酮诱导的运动亢进以及强迫游泳试验(FST)中氯胺酮增强的不动行为,评估腹腔注射(i.p.)桑色素(25、50和100mg/kg)的抗精神病作用。还进行了僵住症和转棒试验,以评估桑色素的锥体外系副作用。

结果

桑色素(25、50和100mg/kg,i.p.)预处理通过抑制小鼠氯胺酮诱导的运动亢进,显著(p<0.05)表现出抗精神分裂症样行为。此外,桑色素(50和100mg/kg,i.p.)显著(p<0.05)降低了自发运动活性。而且,桑色素抑制了阿扑吗啡诱导的刻板行为和氯胺酮诱导的刻板行为。桑色素以显著的剂量依赖性方式减少了因注射氯胺酮导致的FST中不动行为的增加。此外,桑色素的抗精神病活性与锥体外系副作用无关,小鼠的下降潜伏期缩短、运动协调性和表现增加证明了这一点。

结论

研究结果表明,桑色素在实验动物模型中表现出抗精神病样特性且无锥体外系副作用,可能对治疗精神分裂症样行为有益;特别是对行为多动和阴性症状的患者。

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