Das Sudeshna, Mishra K P, Ganju Lilly, Singh S B
Defence institute of Physiology and Allied Sciences (DIPAS, DRDO), Delhi 110054, India.
Defence institute of Physiology and Allied Sciences (DIPAS, DRDO), Delhi 110054, India.
J Neuroimmunol. 2017 Dec 15;313:161-175. doi: 10.1016/j.jneuroim.2017.11.003. Epub 2017 Nov 8.
Over activation of glial cell derived innate immune factors induces neuro-inflammation that results in neurodegenerative disease, like working memory impairment. In this study, we have investigated the role of andrographolide, a major constituent of Andrographis paniculata plant, in reduction of reactive glial cell derived working memory impairment. Real time PCR, Western bloting, flow cytometric and immunofluorescence studies demonstrated that andrographolide inhibited lipopolysaccharide (LPS)-induced overexpression of HMGB1, TLR4, NFκB, COX-2, iNOS, and release of inflammatory mediators in primary mix glial culture, adult mice prefrontal cortex and hippocampus region. Active microglial and reactive astrocytic makers were also downregulated after andrographolide treatment. Andrographolide suppressed overexpression of microglial MIP-1α, P2X7 receptor and its downstream signaling mediators including-inflammasome NLRP3, caspase1 and mature IL-1β. Furthermore, in vivo maze studies suggested that andrographolide treatment reversed LPS-induced behavioural and working memory disturbances including regulation of expression of protein markers like PKC, p-CREB, amyloid beta, APP, p-tau, synapsin and PSD-95. Andrographolide, by lowering expression of pro apoptotic genes and enhancing the expression of anti-apoptotic gene showed its anti-apoptotic nature that in turn reduces neurodegeneration. Morphology studies using Nissl and FJB staining also showed the neuroprotective effect of andrographolide in the prefrontal cortex region. The above studies indicated that andrographolide prevented neuroinflammation-associated neurodegeneration and improved synaptic plasticity markers in cortical as well as hippocampal region which suggests that andrographolide could be a novel pharmacological countermeasure for the treatment of neuroinflammation and neurological disorders related to memory impairment.
神经胶质细胞衍生的先天免疫因子过度激活会诱发神经炎症,进而导致神经退行性疾病,如工作记忆障碍。在本研究中,我们探究了穿心莲内酯(穿心莲属植物的主要成分)在减轻反应性神经胶质细胞引起的工作记忆障碍中的作用。实时聚合酶链反应、蛋白质免疫印迹、流式细胞术和免疫荧光研究表明,穿心莲内酯可抑制脂多糖(LPS)诱导的高迁移率族蛋白B1(HMGB1)、Toll样受体4(TLR4)、核因子κB(NFκB)、环氧化酶-2(COX-2)、诱导型一氧化氮合酶(iNOS)的过表达,并抑制原代混合神经胶质细胞培养物、成年小鼠前额叶皮质和海马区中炎症介质的释放。穿心莲内酯处理后,活化的小胶质细胞和反应性星形胶质细胞标志物也下调。穿心莲内酯抑制小胶质细胞巨噬细胞炎性蛋白-1α(MIP-1α)、嘌呤能P2X7受体及其下游信号介质(包括炎性小体NLRP3、半胱天冬酶-1和成熟白细胞介素-1β)的过表达。此外,体内迷宫研究表明,穿心莲内酯处理可逆转LPS诱导的行为和工作记忆障碍,包括调节蛋白标志物如蛋白激酶C(PKC)、磷酸化环磷腺苷反应元件结合蛋白(p-CREB)β淀粉样蛋白、淀粉样前体蛋白(APP)、磷酸化tau蛋白、突触素和突触后密度蛋白95(PSD-95)的表达。穿心莲内酯通过降低促凋亡基因的表达并增强抗凋亡基因的表达,显示出其抗凋亡特性,进而减少神经退行性变。使用尼氏染色和焦油紫染色的形态学研究也显示了穿心莲内酯在前额叶皮质区域的神经保护作用。上述研究表明,穿心莲内酯可预防神经炎症相关的神经退行性变,并改善皮质和海马区的突触可塑性标志物,这表明穿心莲内酯可能是治疗神经炎症和与记忆障碍相关的神经疾病的一种新型药理学对策。