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大鼠帕金森病6-羟基多巴胺模型中纹状体内咖啡酸苯乙酯治疗的神经保护作用

Neuroprotective Effect of Intrastriatal Caffeic Acid Phenethyl Ester Treatment in 6-OH Dopamine Model of Parkinson's Disease in Rats.

作者信息

Soner Burak Cem, Acikgoz Eda, Inan Salim Yalcin, Ayla Sule, Sahin Ayse Saide, Oktem Gulperi

机构信息

Izmir Democracy University, Faculty of Medicine, Department of Pharmacology, 35100 Izmir, Turkey.

Van Yuzuncu Yil University, Faculty of Medicine, Department of Histology and Embryology, 65080 Van, Turkey.

出版信息

Parkinsons Dis. 2021 Aug 30;2021:5553480. doi: 10.1155/2021/5553480. eCollection 2021.

Abstract

Parkinson's disease (PD) is the second most common neurodegenerative disorder, and the main cause of PD is still not known. Until now, no cure for Parkinson's disease is yet in sight. Caffeic acid phenethyl ester (CAPE) is a polyphenolic component of the propolis, which can be derived from honeybee hive propolis. We aimed to determine the effect of intrastriatal CAPE administration as a neuroprotective agent on 6-hydroxydopamine (6-OHDA)-induced PD model. Adult male Wistar rats weighing 280-320 g were used. The PD model was induced with unilateral intrastriatal 6-OHDA injection. Treatment groups received 20 mol/5 L/4 day and 80 mol/5 L/4 day CAPE 24 h after 6-OHDA injection. Eight days after 6-OHDA application, behavioral studies (adhesive tape removal test, open-field test, cylinder test, and apomorphine-induced asymmetric rotational behavior) were performed once more to compare the effects of CAPE on behavior tests. Striatal histological verifications, immunohistochemistry, and stereological quantitation were performed. Our results for the first time showed that, besides improving the motor performance, CAPE treatment also prevents 6-OHDA-induced loss of TH-positive neurons. From our results, CAPE may be a promising clinical agent in the treatment of PD.

摘要

帕金森病(PD)是第二常见的神经退行性疾病,其主要病因仍不明。到目前为止,帕金森病仍无治愈方法。咖啡酸苯乙酯(CAPE)是蜂胶中的一种多酚成分,可从蜂巢蜂胶中提取。我们旨在确定纹状体内注射CAPE作为神经保护剂对6-羟基多巴胺(6-OHDA)诱导的PD模型的影响。使用体重280 - 320克的成年雄性Wistar大鼠。通过单侧纹状体内注射6-OHDA诱导PD模型。治疗组在6-OHDA注射24小时后接受20μmol/5μL/4天和80μmol/5μL/4天的CAPE。在应用6-OHDA八天后,再次进行行为学研究(胶带去除试验、旷场试验、圆筒试验和阿扑吗啡诱导的不对称旋转行为)以比较CAPE对行为测试的影响。进行纹状体组织学验证、免疫组织化学和体视学定量分析。我们的结果首次表明,除了改善运动性能外,CAPE治疗还可防止6-OHDA诱导的TH阳性神经元丢失。从我们的结果来看,CAPE可能是治疗PD的一种有前景的临床药物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4225/8424247/195879ba7a15/PD2021-5553480.001.jpg

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