Andrographolide - A promising therapeutic agent, negatively regulates glial cell derived neurodegeneration of prefrontal cortex, hippocampus and working memory impairment

被引:42
作者
Das, Sudeshna [1 ]
Mishra, K. P. [1 ]
Ganju, Lilly [1 ]
Singh, S. B. [1 ]
机构
[1] DRDO, DIPAS, Delhi 110054, India
关键词
Andrographolide; Neuro-inflammation; Glial cells; Innate immune receptors; Prefrontal cortex; Working memory; LPS-INDUCED NEUROINFLAMMATION; KAPPA-B; ALZHEIMERS-DISEASE; INFLAMMATION; LIPOPOLYSACCHARIDE; ACTIVATION; EXPRESSION; PATHWAY; BRAIN; COMPONENTS;
D O I
10.1016/j.jneuroim.2017.11.003
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
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, NF kappa B, 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 down regulated after andrographolide treatment. Andrographolide suppressed overexpression of microglial MIP-1 alpha, P2X7 receptor and its downstream signaling mediators including-inflammasome NLRP3, caspasel and mature IL-1 beta. 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.
引用
收藏
页码:161 / 175
页数:15
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