Journal of Traditional Medicines
Online ISSN : 1881-3747
Print ISSN : 1880-1447
ISSN-L : 1880-1447
Regular Article
Shigyakusan extract attenuates enhanced hepatic neutrophil infiltration and oxidative stress with progression of α-naphthylisothiocyanate-induced liver injury in rats
Yoshiji OHTAMutsumi KONGO-NISHIMURATakahiro HAYASHIAkira KITAGAWATatsuya MATSURATakashi HASHIMOTOKazuo YAMADA
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2008 Volume 25 Issue 4 Pages 95-102

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Abstract

In the present study, we examined whether shigyakusan extract, a traditional Kampo medicine, attenuates enhanced hepatic neutrophil infiltration and oxidative stress with the progression of α-naphthylisothiocyanate (ANIT)-induced liver injury in rats. Rats were treated once with ANIT (75 mg/kg body weight, i.p.). Liver injury with cholestasis occurred 24 h after ANIT treatment and progressed at 48 h. A spray-dried material of shigyakusan extract (SGS) (0.15, 0.75 or 1.5 g/kg body weight, p.o.) administered at 24 h after ANIT treatment prevented the progression of ANIT-induced liver injury dose-dependently. At 24 h after ANIT treatment, the treated rats showed increases in hepatic lipid peroxide (LPO) and reduced glutathione (GSH) contents and myeloperoxidase (MPO) activity, an index of tissue neutrophil infiltration, and decreases in hepatic superoxide dismutase (SOD) and glutathione reductase (GSSG-R) activities. At 48 h after ANIT treatment, the treated rats showed enhanced changes in hepatic LPO content and MPO, SOD, and GSSG-R activities except GSH content and decreases in hepatic catalase, Se-glutathione peroxidase, and glucose-6-phosphate dehydrogenase activities. SGS administered at 24 h after ANIT treatment attenuated the ANIT-induced changes in hepatic LPO and GSH content and MPO, catalase, and Se-glutathione peroxidase activities except SOD, GSSG-R, and glucose-6-phosphate dehydrogenase activities at 48 h dose-dependently. These results indicate that orally administered SGS attenuates enhanced hepatic neutrophil infiltration and oxidative stress with liver injury progression and increased hepatic GSH content at the progressed stage of liver injury in rats treated with ANIT, which could contributes to its therapeutic effect on this liver injury.

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© 2008 Medical and Pharmaceutical Society for WAKAN-YAKU
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