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DOI 10.52547/rbmb.11.1.125

Медицинская библиотека · Reports of biochemistry & molecular biology · 2022

Anti-neuroinflammatory of Chloroform Extract of Panax ginseng Root Culture on Lipopolysaccharide-stimulated BV2 Microglia Cells.

Cheah Chee Hoe, Ling Anna Pick Kiong, Wong Ying Pei, Koh Rhun Yian, Hussein Sobri

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Аннотация

BACKGROUND

It is believed that activation of microglia in the central nervous system upon detection of stimulus like lipopolysaccharides provokes neuroinflammation via the production of pro-inflammatory mediators and cytokines. The cytoprotective and anti-inflammatory properties of various folk medicine has been gaining attention as a strategy to combat various disease. This study aimed to assess the anti-neuroinflammatory properties of chloroform extract of in vitro Panax ginseng root culture based on nitric oxide and cytokines production.

METHODS

The study was initiated with the determination of maximum non-toxic dose (MNTD) of P. ginseng root culture chloroform extract using the MTT assay. The lipopolysaccharides-stimulated BV2 microglia cells were treated with MNTD and ½MNTD of the extract and its anti-neuroinflammatory properties were assessed by measuring the production of nitric oxide (NO) via Griess assay, as well as TNF-α, IL-6 and IL-10 using Quantikine ELISA.

RESULTS

It was found that the MNTD and ½MNTD of the extract did not play a significant role in the production of pro-inflammatory cytokines such as NO, TNF-α and IL-6. However, the MNTD and ½MNTD of chloroform extract significantly increased the anti-inflammatory IL-10 compared to the untreated cells.

CONCLUSION

With this, the chloroform extract of P. ginseng root culture potentially exerts anti-neuroinflammatory properties.

Для цитирования: Cheah Chee Hoe, Ling Anna Pick Kiong, Wong Ying Pei, Koh Rhun Yian, Hussein Sobri. Anti-neuroinflammatory of Chloroform Extract of Panax ginseng Root Culture on Lipopolysaccharide-stimulated BV2 Microglia Cells.. Reports of biochemistry & molecular biology. 2022. DOI: 10.52547/rbmb.11.1.125.
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