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小豆蔻油对铝诱导的大鼠神经毒性的神经保护作用。

Neuroprotective Effect of Cardamom Oil Against Aluminum Induced Neurotoxicity in Rats.

作者信息

Auti Sandip T, Kulkarni Yogesh A

机构信息

Shobhaben Pratapbhai Patel School of Pharmacy & Technology Management, SVKM's NMIMS, Mumbai, India.

出版信息

Front Neurol. 2019 Apr 30;10:399. doi: 10.3389/fneur.2019.00399. eCollection 2019.

Abstract

Acetylcholinesterase (AChE) is an enzyme involved in the progression of Alzheimer's disease (AD). Cardamom oil (CO) has been reported to have acetylcholinesterase inhibitory, antioxidant and anti-anxiety effects. Hence, we studied the effect of cardamom oil in aluminum chloride induced neurotoxicity in rats. AD like symptoms were induced in Wistar rats with aluminum chloride (100 mg/kg, .). Cardamom oil was administered concomitantly by oral route at doses of 100 and 200 mg/kg for 42 days. Behavioral parameters like Morris water maze, elevated plus maze, passive avoidance test and locomotor activity were evaluated on day 21 and 42. AChE activity, oxidative stress parameters, histopathological studies and immunohistochemistry studies were carried out in hippocampus and cortex. Cardamom oil treatment showed significant improvement in behavioral parameters, inhibition of AChE activity ( < 0.001) and reduction in oxidative stress in the brain. Histopathological studies of hippocampus and cortex by hematoxylin & eosin (H. & E.) and congo red stain showed inhibition of neuronal damage and amyloid β plaque formation with cardamom oil treatment. Immunohistochemistry showed, CO treatment inhibited amyloid β expression and upregulated brain-derived neurotrophic factor (BDNF). The present study showed that, cardamom oil has neuroprotective effect in aluminum chloride induced neurotoxicity linked with inhibition of AChE activity and reduction in oxidative damage. This effect of cardamom oil may be useful in management of Alzheimer's disease.

摘要

乙酰胆碱酯酶(AChE)是一种与阿尔茨海默病(AD)进展相关的酶。据报道,小豆蔻油(CO)具有乙酰胆碱酯酶抑制、抗氧化和抗焦虑作用。因此,我们研究了小豆蔻油对氯化铝诱导的大鼠神经毒性的影响。用氯化铝(100 mg/kg,.)在Wistar大鼠中诱导出类似AD的症状。以100和200 mg/kg的剂量通过口服途径同时给予小豆蔻油,持续42天。在第21天和第42天评估行为参数,如莫里斯水迷宫、高架十字迷宫、被动回避试验和运动活动。在海马体和皮质中进行乙酰胆碱酯酶活性、氧化应激参数、组织病理学研究和免疫组织化学研究。小豆蔻油治疗在行为参数方面显示出显著改善,抑制了乙酰胆碱酯酶活性(<0.001)并减轻了大脑中的氧化应激。用苏木精和伊红(H. & E.)以及刚果红染色对海马体和皮质进行的组织病理学研究表明,小豆蔻油治疗可抑制神经元损伤和淀粉样β斑块形成。免疫组织化学显示,CO治疗可抑制淀粉样β表达并上调脑源性神经营养因子(BDNF)。本研究表明,小豆蔻油在氯化铝诱导的神经毒性中具有神经保护作用,与抑制乙酰胆碱酯酶活性和减少氧化损伤有关。小豆蔻油的这种作用可能对阿尔茨海默病的治疗有用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/81a9/6502995/45bbe14f6a1f/fneur-10-00399-g0001.jpg

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