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Thymoquinone, a bioactive component of Nigella sativa Linn seeds or traditional spice, attenuates acute hepatic failure and blocks apoptosis via the MAPK signaling pathway in mice
Thymoquinone (TQ), a bioactive natural product obtained from the black cumin seeds of Nigella sativa Linn, is a widely used spice or herb. The present study investigated the hepatoprotective effect of TQ on acute hepatic failure induced by d -galactosamine ( d -GalN) and lipopolysaccharide (LPS) in...
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Published in: | RSC advances 2015-01, Vol.5 (1), p.7285-729 |
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Main Authors: | , , , , , , , , , |
Format: | Article |
Language: | English |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | Thymoquinone (TQ), a bioactive natural product obtained from the black cumin seeds of
Nigella sativa
Linn, is a widely used spice or herb. The present study investigated the hepatoprotective effect of TQ on acute hepatic failure induced by
d
-galactosamine (
d
-GalN) and lipopolysaccharide (LPS) in mice. The mice were intragastrically administrated TQ (5 or 20 mg kg
−1
) for 12 h and 1 h prior to
d
-GalN (700 mg kg
−1
)/LPS (10 μg kg
−1
) injections and then sacrificed 8 h after treatment with
d
-GalN/LPS. TQ pretreatment reduced the mortality induced by
d
-GalN/LPS and reversed liver damage. TQ attenuated
d
-GalN/LPS-induced hepatocyte apoptosis, which was confirmed by suppressing caspase activation, PARP cleavage and the Bax/Bcl-2 ratio. Importantly, TQ attenuated the
d
-GalN/LPS-mediated phosphorylation of JNK, ERK and p38. Furthermore, TQ suppressed the production of proinflammatory cytokines. These findings suggested that TQ could modulate
d
-GalN/LPS-mediated acute hepatic failure by inhibiting caspase activation, consistent with the mitochondrial pathway of apoptosis and the MAPK signaling pathway.
This study is the first report on hepatoprotective effect of thymoquinone induced by
d
-GalN/LPS. Thymoquinone alleviated the progress of
d
-GalN/LPS induced acute hepatic failure via attenuating hepatocytes apoptosis and MAPK signaling pathway. |
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ISSN: | 2046-2069 2046-2069 |
DOI: | 10.1039/c4ra15065a |