Biological Safety and Anti-hepatofibrogenic Effects of Brassica rapa (Turnip) Nanoparticle

  • Park, Dae-Hun (College of Pharmacy, Kangwon National University) ;
  • Li, Lan (School of Veterinary Medicine, Kangwon National University) ;
  • Jang, Hyung-Kwan (Department of Veterinary Infectious Diseases and Avian Disease, College of Veterinary Medicine, Chonbuk National University) ;
  • Kim, Young-Jin (Traditional Food Research Group, Korea Food Research Institute) ;
  • Jang, Ja-June (Department of Pathology, College of Medicine, Seoul National University) ;
  • Choi, Yeon-Shik (Department of Laboratory Animals, Korea Bio Polytechnic) ;
  • Park, Seung-Kee (Department of Microbiology, College of Medicine, Hallym University) ;
  • Lee, Min-Jae (School of Veterinary Medicine, Kangwon National University)
  • Published : 2009.12.31

Abstract

Hepatic fibrosis is one of chronic liver diseases which spread in worldwide and it has high risk to turn advanced cirrhosis and hepatocellualr carcinoma. Brassica family has been produced for commercial purpose and in Korea Brassica rapa (Turnip) is cultivated in Ganghwa County, Gyeonggi-do Korea and used for making Kimchi. Recently pharmacological effects of turnip have been known; diabete mellitus modulation, alcohol oxidization, and fibrosis inhibition. In previous study we found antifibrogenic effect of turnip water extract and in this study we made turnip nanoparticle to promote turnip delivery into liver. At the same time we assessed the biological safety of turnip nanoparticle. Thioacetamide (TAA) induced hepatic nodular formation and fibrosis (mean of fibrosis score: 4). However, 1% turnip nanoparticle inhibited TAA-induced hepatic nodular formation and fibrosis (mean of fibrosis score: 2-3). Activities of serum enzymes (aspartic acid transaminase (AST), alanine transaminase (ALT), and total bilirubin (T-Bil)), complete blood count (CBC), and the appearance of organs were not different from control and 1% turnip nanoparticle treatment. Conclusively 1% turnip nanoparticle significantly reduced TAA-induced hepatic fibrosis and was safe in 7-weeks feeding.

Keywords

References

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