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印度楝树标准化提取物对大鼠坐骨神经部分损伤的神经保护作用:来自抗炎、抗氧化和抗凋亡研究的证据。

Neuroprotective effect of Azadirachta indica standardized extract in partial sciatic nerve injury in rats: Evidence from anti-inflammatory, antioxidant and anti-apoptotic studies.

作者信息

Kandhare Amit D, Mukherjee Anwesha A, Bodhankar Subhash L

机构信息

Department of Pharmacology, Poona College of Pharmacy, Bharati Vidyapeeth Deemed University, Erandwane, Paud Road, Pune-411 038, India.

出版信息

EXCLI J. 2017 Apr 18;16:546-565. doi: 10.17179/excli2017-161. eCollection 2017.

DOI:10.17179/excli2017-161
PMID:28694757
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5491907/
Abstract

Chronic neuropathic pain is a common and widely recognized pain syndrome for patients and difficult to manage for physicians. (AI) possesses analgesic, anti-inflammatory, and antioxidant properties. To evaluate the neuroprotective effect of AI standardized extract in an animal model of peripheral neuropathy induced by partial sciatic nerve ligation (PSNL). PSNL was induced in male Wistar rats (180-200 g) with tight ligation of the nerve. Rats received treatment with either vehicle i.e. distilled water (PSNL control), Pyridoxine (100 mg/kg, p.o.) or AI (100, 200 and 400 mg/kg, p.o.) for 28 days. Various behavioral parameters, biochemical, molecular and histological parameters were evaluated. PSNL resulted in a significant decrease ( 0.05) in allodynia, hyperalgesia, motor coordination and motor nerve conduction velocity (MNCV) whereas chronic treatment with AI (200 and 400 mg/kg) significantly attenuated ( 0.05) these behavioral changes. Enhanced activity of oxidative-nitrosative stress, inflammatory mediators (TNF-α, IL-1β, and NF-κB) as well as mRNA expression of Bax, Caspase-3, and iNOs were significantly attenuated ( 0.05) by AI treatment. It also significantly increased ( 0.05) peripheral blood oxygen content and Bcl-2 mRNA expression. The flow cytometric analysis revealed that AI (200 and 400 mg/kg) treatment significantly attenuated neural apoptosis and reactive oxygen species levels. PSNL induced histological aberrations were also decreased by AI treatment. exerts its neuroprotection against PSNL induced neuropathic pain via inhibition of oxidative-nitrosative stress, the release of pro-inflammatory cytokines and apoptosis to improve MNCV (graphical abstract, Figure 1(Fig. 1)).

摘要

慢性神经性疼痛是一种常见且被患者广泛认知的疼痛综合征,对医生而言也难以处理。(姜黄)具有镇痛、抗炎和抗氧化特性。为了评估姜黄标准化提取物在部分坐骨神经结扎(PSNL)诱导的周围神经病变动物模型中的神经保护作用。通过紧密结扎神经在雄性Wistar大鼠(180 - 200克)中诱导PSNL。大鼠接受载体即蒸馏水(PSNL对照组)、吡哆醇(100毫克/千克,口服)或姜黄(100、200和400毫克/千克,口服)治疗28天。评估了各种行为参数、生化、分子和组织学参数。PSNL导致痛觉过敏、痛觉超敏、运动协调性和运动神经传导速度(MNCV)显著降低(P < 0.05),而姜黄(200和400毫克/千克)的慢性治疗显著减轻(P < 0.05)这些行为变化。氧化 - 亚硝化应激、炎症介质(TNF-α、IL-1β和NF-κB)的活性增强以及Bax、Caspase-3和iNOs的mRNA表达通过姜黄治疗显著减轻(P < 0.05)。它还显著增加(P < 0.05)外周血氧含量和Bcl-2 mRNA表达。流式细胞术分析显示,姜黄(200和400毫克/千克)治疗显著减轻神经细胞凋亡和活性氧水平。PSNL诱导的组织学异常也通过姜黄治疗而减少。姜黄通过抑制氧化 - 亚硝化应激、促炎细胞因子的释放和细胞凋亡来改善MNCV,从而对PSNL诱导的神经性疼痛发挥神经保护作用(图形摘要,图1(图1))。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5dc5/5491907/ae80dc183766/EXCLI-16-546-g-006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5dc5/5491907/474fc5f8e64c/EXCLI-16-546-t-001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5dc5/5491907/f2a5b020d85f/EXCLI-16-546-t-002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5dc5/5491907/e31598611f32/EXCLI-16-546-t-003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5dc5/5491907/ed06892f7f91/EXCLI-16-546-g-001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5dc5/5491907/982385261c07/EXCLI-16-546-g-002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5dc5/5491907/4965bc369c5a/EXCLI-16-546-g-003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5dc5/5491907/108149f37ae4/EXCLI-16-546-g-004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5dc5/5491907/002fd52c4bd1/EXCLI-16-546-g-005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5dc5/5491907/ae80dc183766/EXCLI-16-546-g-006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5dc5/5491907/474fc5f8e64c/EXCLI-16-546-t-001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5dc5/5491907/f2a5b020d85f/EXCLI-16-546-t-002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5dc5/5491907/e31598611f32/EXCLI-16-546-t-003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5dc5/5491907/ed06892f7f91/EXCLI-16-546-g-001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5dc5/5491907/982385261c07/EXCLI-16-546-g-002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5dc5/5491907/4965bc369c5a/EXCLI-16-546-g-003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5dc5/5491907/108149f37ae4/EXCLI-16-546-g-004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5dc5/5491907/002fd52c4bd1/EXCLI-16-546-g-005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5dc5/5491907/ae80dc183766/EXCLI-16-546-g-006.jpg

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