2015Tropical Journal of Pharmaceutical ResearchOpen access

Suppression of Lipopolysaccharide-Stimulated Neuroinflammatory Mediators by Chenopodiacea Mangrove, Suaedea maritima (L) Dumort, in BV-2 Microglial Cells

Hee‐Ju Kang

Open full text 2 citations

Abstract

Purpose: To investigate the in-vitro antioxidant and anti-neuroinflammatory effects of Suaeda maritime (L) Dumort ethyl acetate (SM-EA) extract in lipopolysaccharide (LPS)-stimulated BV-2 microglial cells.Methods: LPS-stimulated BV- microglia were used to study the expression and production of inflammatory mediators, viz, nitric oxide (NO), inducible NO synthase (iNOS, interleukin (IL)-6) and tumor necrosis alpha (TNF-α). Antioxidant activity was measured using 1, 1-diphenyl-2-picryl-hydrazyl (DPPH) assay. Cell viability was estimated by 3-(4, 5-dimethylthiazol-2-yl)-2, 5- diphenyl-tetrazolium bromide (MTT) assay.Results: SM-EA extract significantly suppressed LPS-induced production of NO (p < 0.001 at 80 and 100 ìg/ml) and expression of iNOS in BV-2 cells. SM-EA also suppressed LPS-induced increase in IL-6 and TNF-α levels (p < 0.001at 100 ìg/ml) in BV- cells. Further, DPPH-generated free radicals were inhibited by SM-EA extract in a concentration-dependent manner (p < 0.01 at 0.1 mg/ml and p < 0.001 at 1 mg/ml) with half maximal inhibitory concentration (IC50) of 0.42 mg/ml.Conclusion: The findings imply that SM-EA extract can be developed as a potential therapeutic agent in regulating microglia-mediated neuroinflammatory responses observed in several neurodegenerative diseases.Keywords: Suaedea maritime, Chenopodiaceae, Anti-oxidant, Anti-inflammatory, Microglial cells, Inducible nitric oxide synthase, Interleukin-6

Open-access reader

About this research paper

What this paper is about

Purpose: To investigate the in-vitro antioxidant and anti-neuroinflammatory effects of Suaeda maritime (L) Dumort ethyl acetate (SM-EA) extract in lipopolysaccharide (LPS)-stimulated BV-2 microglial cells.Methods: LPS-stimulated BV- microglia were used to study the expression and production of inflammatory mediators, viz, nitric oxide (NO), inducible NO synthase (iNOS, interleukin (IL)-6) and tumor necrosis alpha (TNF-α). Antioxidant activity was measured using 1, 1-diphenyl-2-picryl-hydrazyl (DPPH) assay. Cell viability was estimated by 3-(4, 5-dimethylthiazol-2-yl)-2, 5- diphenyl-tetrazolium bromide (MTT) assay.Results: SM-EA extract significantly suppressed LPS-induced production of NO (p < 0.001 at 80 and 100 ìg/ml) and expression of iNOS in BV-2 cells. SM-EA also suppressed LPS-induced increase in IL-6 and TNF-α levels (p < 0.001at 100 ìg/ml) in BV- cells. Further, DPPH-generated free radicals were inhibited by SM-EA extract in a concentration-dependent manner (p < 0.01 at 0.1 mg/ml and p < 0.001 at 1 mg/ml) with half maximal inhibitory concentration (IC50) of 0.42 mg/ml.Conclusion: The findings imply that SM-EA extract can be developed as a potential therapeutic agent in regulating microglia-mediated neuroinflammatory responses observed in several neurodegenerative diseases.Keywords: Suaedea maritime, Chenopodiaceae, Anti-oxidant, Anti-inflammatory, Microglial cells, Inducible nitric oxide synthase, Interleukin-6

Why it matters

OpenAlex reports 2 citations for this work. Citation counts describe recorded attention and do not establish research quality.

Key contribution

A contribution statement is not available in the OpenAlex record.

Method / approach

Method details are not available in the OpenAlex metadata.

Main findings

Findings are not separately available in the OpenAlex metadata.

Limitations

Limitations are not available in the OpenAlex metadata.

Applications

Application details are not available in the OpenAlex metadata.

Available abstract

Purpose: To investigate the in-vitro antioxidant and anti-neuroinflammatory effects of Suaeda maritime (L) Dumort ethyl acetate (SM-EA) extract in lipopolysaccharide (LPS)-stimulated BV-2 microglial cells.Methods: LPS-stimulated BV- microglia were used to study the expression and production of inflammatory mediators, viz, nitric oxide (NO), inducible NO synthase (iNOS, interleukin (IL)-6) and tumor necrosis alpha (TNF-α). Antioxidant activity was measured using 1, 1-diphenyl-2-picryl-hydrazyl (DPPH) assay. Cell viability was estimated by 3-(4, 5-dimethylthiazol-2-yl)-2, 5- diphenyl-tetrazolium bromide (MTT) assay.Results: SM-EA extract significantly suppressed LPS-induced production of NO (p < 0.001 at 80 and 100 ìg/ml) and expression of iNOS in BV-2 cells. SM-EA also suppressed LPS-induced increase in IL-6 and TNF-α levels (p < 0.001at 100 ìg/ml) in BV- cells. Further, DPPH-generated free radicals were inhibited by SM-EA extract in a concentration-dependent manner (p < 0.01 at 0.1 mg/ml and p < 0.001 at 1 mg/ml) with half maximal inhibitory concentration (IC50) of 0.42 mg/ml.Conclusion: The findings imply that SM-EA extract can be developed as a potential therapeutic agent in regulating microglia-mediated neuroinflammatory responses observed in several neurodegenerative diseases.Keywords: Suaedea maritime, Chenopodiaceae, Anti-oxidant, Anti-inflammatory, Microglial cells, Inducible nitric oxide synthase, Interleukin-6

Key concepts: Lipopolysaccharide, Nitric oxide, Nitric oxide synthase, Chemistry, Microglia, IC50, DPPH, Tumor necrosis factor alpha

Related papers

Back to paper searchBrowse research topicsOriginal source
Suppression of Lipopolysaccharide-Stimulated Neuroinflammatory Mediators by Chenopodiacea Mangrove, Suaedea maritima (L) Dumort, in BV-2 Microglial Cells — Research Paper | ScholarLens