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KMID : 1149220030110010129
Korean Journal of Oriental Medical Prescription
2003 Volume.11 No. 1 p.129 ~ p.149
Effect of Sachungwhan and its components on acetaminophen induced hepatoxicity in rats
Lee Jae-Eun

Park Sun-Dong
Abstract
Liver is an important target of the toxicity of drugs, xenobiotics and oxidative stress. Acetaminophen pverdose causes acute liver injury in both humans and animals. This study was performed to observe the effect of sachunwhan and its component groups on recovery of hepatoxicity in acetaminophen treated rats. The experimental group was divided into 4 groups: sachungwhan(SC), samultang group(SC-1: Ó×Ïý, ô¹Ïä), chungyul group(SC-2: éÌÓÅõ®, ÓÞüÜ, ö¼í­), and haepyo group(SC-3:˶üÀ, ÛÁù¦). Under the same condition Normal group was fed basal diet and water; Control group was injected acetaminophen and fed basal diet for 2 weeks; Experimental groups were injected acetaminophen and fed each extracts for 2 weeks respectively. The results were obtained as follows: 1. In the study on antioxidative defense system in vivo, SC reduced the amount of lipid peroxide in both serum and liver and showed activity on antioxidative enzymes such as catalase, glutathion. Other groups had effect only on glutathion. 2. In the study on hepatotoxicity(GOT, GPT, -GTP, ALP, LDH, Bilirubin), SC had a significant effect on recovery of hepatoxicity in acetaminophen treated rats. Other groups had no effect except SC-1 having effect on -GTP. As results shown, only Sachungwhan(SC) has significant effects on recovery of hepatoxicity and antioxidative defense system in vivo. These results suggest that Sachungwhan(SC) made antioxidative defense system active and it seemed to be very important to its effect on recovery of hepatoxicity. In the other hand, Component groups had no effect on recoverv of hepatoxicity and antioxidative defense system in vivo. This was thought that component drugs¡¯ cooperative synergy effect would be important to Sachungwhan(SC)¡¯s effects mentioned in this paper.
KEYWORD
Sachungwhan, acetaminophen, hepatoxicity
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