Abstract
The protective effects of the 5-lipoxygenase inhibitor ardisiaquinone A, a compound
isolated from Ardisia sieboldii, on hepatic ischemia-reperfusion (I/R) injury was studied in rats. Hepatic I/R injury
was induced by occlusion of the portal vein and the hepatic artery for 60 min, followed
by reperfusion for 24 h. The content of leukotriene B4 (LTB4) in the liver increased during ischemia. Serum alanine aminotransferase (ALT) levels,
a marker of hepatic parenchymal cell injury, and hepatic myeloperoxidase (MPO) activity,
a marker of neutrophil accumulation, significantly increased 6 - 9 h after reperfusion.
Treatment with ardisiaquinone A (0.1 - 2 mg/kg, i. p.) 30 min prior to ischemia dose-dependently prevented the increase in LTB4 content during ischemia (ID50 = 0.645 mg/kg) with a slightly higher potency than that of AA-861 (ID50 = 0.728 mg/kg), a known reference 5-lipoxygenase inhibitor. Ardisiaquinone A also
attenuated the increase in MPO activity and serum ALT levels at 6 h after reperfusion
(ID50 = 1.71 mg/kg and 4.28 mg/kg, respectively). These protective effects were more efficient
than those of AA-861 (ID50 = 1.86 mg/kg and no effect, respectively), LY255283 (ID50 = 18.1 mg/kg and 11.5 mg/kg, respectively), and ONO-4057 (ID50 = 8.38 mg/kg and 9.44 mg/kg, respectively), which are LTB4 receptor antagonists. These results suggest that ardisiaquinone A may protect the
liver against damage due to I/R in rats.
Key words
Ardisiaquinone A -
Ardisia sieboldii
- Myrsinaceae - leukotriene B4
- ischemia-reperfusion - liver - rat
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Nobuaki Matsui
Department of Pharmacology
Faculty of Pharmaceutical Sciences
Tokushima Bunri University
180 Nishihama-bouji
Yamashiro-cho
Tokushima City
Tokushima 770-8514
Japan
Phone: +81-88-622-9611 ext. 5722
Fax: +81-88-655-3051
Email: matsui@ph.bunri-u.ac.jp