Effects of Antioxidative, DPPH Radical Scavenging Activity and Antithrombogenic by the Extract of Sancho ( Zanthoxylum Schinifolium).
- Author:
Mi Jin JANG
1
;
Mi Hee WOO
;
Young Ho KIM
;
Do Youn JUN
;
Soon Jae RHEE
Author Information
1. Department of Food Science and Nutrition, Catholic University of Daegu, Gyeongsan, Korea. sjrhee@cu.ac.kr
- Publication Type:In Vitro ; Original Article
- Keywords:
sancho;
zanthoxylum;
schinifolium;
lipid peroxidation;
DPPH radical scavenging activity;
activated partial thromboplastin time
- MeSH:
1-Butanol;
Animals;
Lipid Peroxidation;
Methylene Chloride;
Microsomes;
Partial Thromboplastin Time;
Rats;
Steam;
Thromboplastin;
Zanthoxylum*
- From:The Korean Journal of Nutrition
2005;38(5):386-394
- CountryRepublic of Korea
- Language:Korean
-
Abstract:
Effects of root, stem and leaf extract of sancho (Zanthoxylum schinifolium) on the inhibition of lipid peroxidation in the hepatic microsome of rat, DPPH radical scavenging activity and activated partial thromboplastin times (APTT) were examined in vitro. The highest inhibition of hepatic microsomal lipid peroxidation was observed by ethyl acetate fraction than that of methylene chloride fraction of the root and stem extracts. The high inhibition of lipid peroxidation was determined in the leaf, the root and the stem in order. The DPPH radical scavenging activity of ethyl acetate fraction was higher than that of n-butanol fraction and it was similar to the root and the steam extract. It was similar to the inhibition of hepatic microsomal lipid peroxidation. The DPPH radical scavenging activity was the highest in 2.500 mg/mL of ethyl acetate fraction and it was 4.4 fold higher than that of h-tocopherol, as an antioxidant standard. The DPPH radical scavenging activity was dependent on the extract concentration in the range of 0.125 - 5.000 mg/mL. The thromboplastin times were higher than that of n-butanol fraction and it was similar to the root and the steam extracts. The leaf extract showed the highest antithrombogenic effect followed by the stem and then the root extract. The activated partial thromboplastin times were dependent on the extract concentration in the range of 0.100 - 2.000 mg/mL. Consequently, the effects of antioxidative, DPPH radical scavenging activity and antithrombogenic of Z. schinifolium was observed due to the inhibition of lipid peroxidation and the DPPH radical scavenging activity by methylene chloride, n-butanol and ethyl acetate fraction of the leaf extract.
