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姜黄烯在抗精神病作用中的抗炎、抗氧化和上调 BDNF 特性:与奥氮平的比较研究。

Involvement of anti-inflammatory, antioxidant, and BDNF up-regulating properties in the antipsychotic-like effect of the essential oil of Alpinia zerumbet in mice: a comparative study with olanzapine.

机构信息

Neuropharmacology Laboratory, Drug Research and Development Center, Department of Physiology and Pharmacology, Faculty of Medicine, Universidade Federal do Ceará, Rua Cel. Nunes de Melo, 1000, 60431-270, Fortaleza, CE, Brazil.

Laboratory of Experimental Oncology, Drug Research and Development Center, Department of Physiology and Pharmacology, Faculty of Medicine, Universidade Federal do Ceará, Fortaleza, Ceará, Brazil.

出版信息

Metab Brain Dis. 2021 Dec;36(8):2283-2297. doi: 10.1007/s11011-021-00821-5. Epub 2021 Sep 7.

Abstract

The current drug therapy for schizophrenia effectively treats acute psychosis and its recurrence; however, this mental disorder's cognitive and negative symptoms are still poorly controlled. Antipsychotics present important side effects, such as weight gain and extrapyramidal effects. The essential oil of Alpinia zerumbet (EOAZ) leaves presents potential antipsychotic properties that need further preclinical investigation. Here, we determined EAOZ effects in preventing and reversing schizophrenia-like symptoms (positive, negative, and cognitive) induced by ketamine (KET) repeated administration in mice and putative neurobiological mechanisms related to this effect. We conducted the behavioral evaluations of prepulse inhibition of the startle reflex (PPI), social interaction, and working memory (Y-maze task), and verified antioxidant (GSH, nitrite levels), anti-inflammatory [interleukin (IL)-6], and neurotrophic [brain-derived neurotrophic factor (BDNF)] effects of this oil in hippocampal tissue. The atypical antipsychotic olanzapine (OLZ) was used as standard drug therapy. EOAZ, similarly to OLZ, prevented and reversed most KET-induced schizophrenia-like behavioral alterations, i.e., sensorimotor gating deficits and social impairment. EOAZ had a modest effect on the prevention of KET-associated working memory deficit. Compared to OLZ, EOAZ showed a more favorable side effects profile, inducing less cataleptic and weight gain changes. EOAZ efficiently protected the hippocampus against KET-induced oxidative imbalance, IL-6 increments, and BDNF impairment. In conclusion, our data add more mechanistic evidence for the anti-schizophrenia effects of EOAZ, based on its antioxidant, anti-inflammatory, and BDNF up-regulating actions. The absence of significant side effects observed in current antipsychotic drug therapy seems to be an essential benefit of the oil.

摘要

目前,用于治疗精神分裂症的药物疗法能有效治疗急性精神病及其复发,但这种精神障碍的认知和阴性症状仍难以控制。抗精神病药物存在重要的副作用,如体重增加和锥体外系反应。Alpinia zerumbet(EAOZ)叶的精油具有潜在的抗精神病特性,需要进一步进行临床前研究。在这里,我们确定了 EAOZ 对预防和逆转氯胺酮(KET)重复给药诱导的类精神分裂症样症状(阳性、阴性和认知)的作用,以及与这种作用相关的潜在神经生物学机制。我们进行了惊吓反射前脉冲抑制(PPI)、社会互动和工作记忆(Y 迷宫任务)的行为评估,并验证了这种油在海马组织中的抗氧化(GSH、亚硝酸盐水平)、抗炎[白细胞介素(IL)-6]和神经营养[脑源性神经营养因子(BDNF)]作用。使用典型抗精神病药奥氮平(OLZ)作为标准药物疗法。与 OLZ 类似,EAOZ 可预防和逆转大多数 KET 诱导的类精神分裂症样行为改变,即感觉运动门控缺陷和社会障碍。EAOZ 对预防 KET 相关的工作记忆缺陷有一定的效果。与 OLZ 相比,EAOZ 表现出更有利的副作用特征,引起的僵住和体重增加变化更少。EAOZ 有效地保护海马免受 KET 诱导的氧化失衡、IL-6 增加和 BDNF 损伤。总之,我们的数据基于其抗氧化、抗炎和 BDNF 上调作用,为 EAOZ 的抗精神分裂症作用提供了更多的机制证据。与目前的抗精神病药物治疗相比,缺乏明显的副作用似乎是该油的一个重要优势。

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