Lakshminarayanashastry Viswanatha Gollapalle, Venkatanarasappa Venkataranganna Marikunte, Lingeswara Prasad Nunna Bheema
Research Scholar, JNT University Anantapur, Ananthapuramu 515002, India.
Connexios Life Sciences Pvt Ltd, Basavanagudi, Bangalore 560 004, India.
Iran J Basic Med Sci. 2019 Feb;22(2):187-196. doi: 10.22038/ijbms.2018.30660.7389.
This study was conducted to evaluate the cerebroprotective effect of methanolic leaf extract of (MePG) in Wistar rats.
The MePG was initially assessed for antioxidant activity, and later evaluated on LPS-induced RAW 264.7 cell line assay. Finally, the MePG was evaluated against ischemia-reperfusion (I/R) induced brain injury in Wistar rats.
In DPPH, FRAP and ORAC assays, the MePG has exhibited potent antioxidant activity. Further, the MePG has significantly inhibited the generation of nitrite, ROS and TNF-α in LPS-induced RAW 264.7 cell lines. Besides, global ischemia followed by reperfusion caused significant changes in the neurological and behavioral functions in I/R control animals compared to sham control. Additionally, in the I/R control group there was a substantial decrease in the catalase and superoxide dismutase activities; Likewise, reduced glutathione levels reduced and lipid peroxidation levels enhanced significantly. Also, pro-inflammatory cytokines such as TNF-α, IL-6, and ICAM-I were increased and the levels of IL-10 was decreased significantly. Furthermore, the I/R insult caused increase in brain volume and cerebral infarct formation. Similarly, histopathology of the brain tissue revealed hallmarks like necrosis, leukocyte infiltration, cerebral edema and vascular congestion in I/R control. Notably, MePG (200 and 400 mg/kg) pretreatment for 7 days, has attenuated all the I/R-persuaded pathological changes compared to I/R control. In addition, the LC-MS/MS analysis showed presence of acteoside, apigenin, gallic acid, gossypin, pentagalloyl glucose, quercetin, and rutin as major ingredients in the MePG.
These findings suggest that the MePG possesses significant cerebroprotective activity.
本研究旨在评估[植物名称]甲醇叶提取物(MePG)对Wistar大鼠的脑保护作用。
首先对MePG进行抗氧化活性评估,随后在脂多糖(LPS)诱导的RAW 264.7细胞系试验中进行评价。最后,在Wistar大鼠中评估MePG对缺血再灌注(I/R)诱导的脑损伤的作用。
在二苯基苦味酰基自由基(DPPH)、铁离子还原抗氧化能力(FRAP)和氧自由基吸收能力(ORAC)试验中,MePG表现出强大的抗氧化活性。此外,MePG显著抑制了LPS诱导的RAW 264.7细胞系中亚硝酸盐、活性氧(ROS)和肿瘤坏死因子-α(TNF-α)的生成。此外,与假手术对照组相比,全脑缺血后再灌注导致I/R对照组动物的神经和行为功能发生显著变化。此外,在I/R对照组中,过氧化氢酶和超氧化物歧化酶活性大幅降低;同样,还原型谷胱甘肽水平降低,脂质过氧化水平显著升高。此外,促炎细胞因子如TNF-α、白细胞介素-6(IL-6)和细胞间黏附分子-1(ICAM-1)增加,而IL-10水平显著降低。此外,I/R损伤导致脑体积增加和脑梗死形成。同样,脑组织的组织病理学显示I/R对照组存在坏死、白细胞浸润、脑水肿和血管充血等特征。值得注意的是,与I/R对照组相比,MePG(200和400mg/kg)预处理7天减轻了所有I/R诱导的病理变化。此外,液相色谱-串联质谱(LC-MS/MS)分析表明,MePG中的主要成分有毛蕊花糖苷、芹菜素、没食子酸、棉皮素、五倍子酰葡萄糖、槲皮素和芦丁。
这些发现表明MePG具有显著的脑保护活性。