Singh Shamsher, Kumar Puneet
Department of Pharmacology, I.S.F College of Pharmacy, Ferozepur Road, Ghal Kalan, Moga, 142001, Punjab, India.
Research Scholar, I.K. Gujral Punjab Technical University, Jalandhar, India.
Inflammopharmacology. 2017 Feb;25(1):69-79. doi: 10.1007/s10787-016-0297-9. Epub 2016 Nov 16.
6-hydroxy dopamine (6-OHDA) is a neurotoxin which on intranigral administration produces severe nigrostriatal damage with motor and cognitive deficit in animals. Curcumin (CMN) in combination with bioenhancer piperine (PP) in 6-hydroxydopamine-induced Parkinsonian rats was used to investigate the antioxidant, neuromodulatory and neuroprotective mechanisms.
Hemi-Parkinson's rat model was developed with intranigral infusion of 6-OHDA (8 μg/2 μl, once, unilaterally), treatment with CMN (25 and 50 mg/kg) and combination of PP (2.5 mg/kg) with CMN (25 mg/kg) was given daily for 21 days starting from the 7th day after 6-OHDA infusion. The behavioral (locomotor, grip strength, and narrow beam walk) parameters were studied on weekly basis. On 22nd day, isolated brain preparations were subjected to biochemical (lipid peroxidation, glutathione, and nitrite), neuroinflammatory (IL-1β, IL-6, and TNF- α), and neurochemical (DA, NE, 5- HT, GABA, Glutamate, DOPAC, HVA, and 5-HIAA) analysis.
Oral administration of CMN had significantly prevented behavioral, neuroinflammatory, and neurochemical changes and preserved the antioxidant potential of the nigrostriatum in rats treated with 6-OHDA.
In the present study, PP and CMN had afforded a better neuroprotective effect compared to alone treatment on behavior, biochemical, neuroinflammatory, and neurochemical parameters in rats.
6-羟基多巴胺(6-OHDA)是一种神经毒素,经脑内黑质给药后会在动物体内造成严重的黑质纹状体损伤,并伴有运动和认知缺陷。本研究采用姜黄素(CMN)联合生物增强剂胡椒碱(PP),对6-羟基多巴胺诱导的帕金森病大鼠进行研究,以探讨其抗氧化、神经调节和神经保护机制。
通过脑内注射6-OHDA(8μg/2μl,单侧,一次性)建立半帕金森病大鼠模型,自6-OHDA注射后第7天起,每日给予CMN(25mg/kg和50mg/kg)以及PP(2.5mg/kg)与CMN(25mg/kg)的组合,持续21天。每周研究行为学参数(运动能力、握力和窄梁行走)。在第22天,对分离的脑组织进行生化分析(脂质过氧化、谷胱甘肽和亚硝酸盐)、神经炎症分析(IL-1β、IL-6和TNF-α)以及神经化学分析(多巴胺、去甲肾上腺素、5-羟色胺、γ-氨基丁酸、谷氨酸、3,4-二羟基苯乙酸、高香草酸和5-羟吲哚乙酸)。
口服CMN可显著预防6-OHDA处理大鼠的行为、神经炎症和神经化学变化,并维持黑质纹状体的抗氧化能力。
在本研究中,与单独治疗相比,PP和CMN对大鼠的行为、生化、神经炎症和神经化学参数具有更好的神经保护作用。