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Volume 8

Journal of Clinical Trials

Pharmacy and Pharmacovigilance 2018

July 16-17, 2018

July 16-17, 2018 Sydney, Australia

Joint Event on

Global Pharmacovigilance and

Advanced Pharmacy

In vitro

immunomodulatory activity of chrysin (5, 7-dihydroxyflavone) isolated from

Indigofera

tinctoria

on macrophage via NF-κB signaling pathway

Ravichandran Ramanibai

*

and Madakkannu Boothapandi

University of Madras, India.

I

n the present investigation, in vitro immunomodulatory effect of natural flavonoid chrysin isolated from Indigofera tinctoria leaves

was evaluated on murine macrophages (RAW 264.7 cells). The chrysin was purified and structure was elucidated by spectroscopic

analysis including UV- visible, FTIR, NMR (13C, 1H) and GC–MS. The immunomodulatory activity of different concentrations of

chrysin (25, 50, 75 and 100 μg/mL) was analyzed on normal and LPS(10 µg/mL) stimulated macrophage with various assays including

cell proliferation, nitric oxide (NO) production, phagocytosis, ROS generation, gene expression and NF-κB nuclear translocation. The

results revealed that, chrysin was significantly increased the proliferation of macrophages as well as phagocytic function of macrophages

in dose dependently. Moreover, the preliminary and essential features of phagocytosis such as superoxide anions production, lysosomal

and pinocytic activity of macrophages was significantly enhanced upon chrysin treatment. On the other hand chrysin significantly

debited the ROS generation, NO production and increased the arginase activity on LPS stimulated macrophage. The expression of

pro-inflammatory cytokine such as TNF-α & IL-6 and pro-inflammatory mediators such as iNOS & COX-2 and the expression also

dose dependently decreased by chrysin in LPS treated macrophages. Moreover, the chrysin treatment was greatly reduced the NF-κB

activation and subsequently decreased the NF-κB nuclear translocation. Collectively, the present findings suggested that a natural

flavonoid chrysin can increased the innate immune response by enhancing macrophages functions through NF-κB signaling pathway

and explored the strong immunomodulatory potential.

rramani8@hotmail.com

J Clin Trials 2018, Volume 8

DOI: 10.4172/2167-0870-C2-026