4.5 Article

6-Gingerdione Reduces Apoptotic Conditions in HepG2 Cells and Inhibits Inflammatory Cytokine Gene Expression in Alcoholic Liver Injured Zebrafish Larvae

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CHEMISTRY & BIODIVERSITY
卷 20, 期 1, 页码 -

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WILEY-V C H VERLAG GMBH
DOI: 10.1002/cbdv.202200959

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antioxidant activity; HepG2 cells; zebrafish model; liver injury; anti-inflammatory activity; gingerdione

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Antioxidant natural products and their analogs, especially phenolic compounds, have diverse biological activities, including anti-inflammatory, antioxidant, and anticancer activities. Ginger, widely used for its beneficial effects, contains phenolic antioxidants, such as 6-gingerol. However, the molecular mechanism of synthetically synthesized 6-gingerdione (compound 1) from 6-gingerol was unknown. In this study, compound 1 and methylated 6-gingerdione (compound 2) were obtained and their antioxidant and anti-inflammatory activities were analyzed. Compound 1 showed stronger antioxidant and anti-inflammatory activities compared to compound 2. Additionally, compound 1 protected liver injury in zebrafish larvae induced by 2% EtOH.
Antioxidant natural products and their analogs especially phenolic compounds, exhibit diverse biological properties, including anti-inflammatory, antioxidant, and anticancer activities. Ginger which is widely used worldwide for various beneficial effects also contains several phenolic antioxidants, and 6-gingerol is one of the natural products studied extensively. However, the molecular mechanism of synthetically synthesized 6-gingerdione (compound 1) from 6-gingerol was not known. In this study, compound 1 and methylated 6-gingerdione (compound 2) were obtained semi synthetically from 6-gingerol. Compound 1 and 2 are subjected to SwissADME prediction. Then the protective effect of compound 1 was analyzed in 2 % EtOH induced HepG2 cells and zebrafish larvae. Hydroxyl and nitric oxide scavenging assays reveal that compound 1 showed more antioxidant activity than compound 2 at 50 mu M. Moreover, compound 1 exhibited good anti-inflammatory activity via lipoxygenase inhibition and proteinase inhibition. Apoptosis and oxidative stress in HepG2 cells were induced by 2 % EtOH and treated with compound 1. Compound 1 significantly inhibited the EtOH induced nitric oxide production, apoptosis, and ROS generation in HepG2 cells. Encouraged by the in-vitro antioxidant and anti-inflammatory activities, compound 1 was then investigated for its protective effect in 2 % EtOH induced ALD zebrafish larva. Compound 1 protected the zebrafish larvae from liver injury by suppressing inflammatory (COX-2, TNF-alpha, and IL-1 beta) and lipogenic genes (C/EBP-alpha, SREBP1, and IL-1 beta) while upregulating the antioxidant gene. Our findings indicate that compound 1 synthesized from 6-gingerol ameliorated liver injury that likely, contributes to its potential antioxidant and anti-inflammatory properties.

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