1Department of Quality Assurance, KVPSS Institute of Pharmaceutical Education, Boradi Tal-Shirpur, Dist-Dhule (M.S.) India 425–405
2Department of Pharmacognosy, Annasaheb Ramesh Ajmera College of Pharmacy Nagao Dhule, Dist: Dhule 424002, Maharashtra, India
3Department of Clinical Pharmacy. R. C. Patel Institute of Pharmaceutical Education and Research, Shirpur, Dist.: Dhule (M.S.) India 425–405
*Corresponding Author E-mail: amolraje957@gmail.com
Online published on 10 August, 2020.
Chronic hepatitis C is a slowly progressive liver disease that may evolve into cirrhosis with its potential complications of liver failure or hepatocellular carcinoma. Current therapy with α interferon is directed at viral clearance, but sustained response is only achieved in 20–40% of patients without cirrhosis, and less than 20% in patients with cirrhosis who have the greatest need for therapy. Treatment for those who do not respond to antiviral therapy is highly desirable. In Japan glycyrrhizin has been used for more than 20 years as treatment for chronic hepatitis. In randomized controlled trials, glycyrrhizin induced a significant reduction of serum aminotransferases and an improvement in liver histology compared to placebo. Recently, these short-term effects have been amplified by a well conducted retrospective study suggesting that long-term usage of glycyrrhizin prevents development of hepatocellular carcinoma in chronic hepatitis C. The mechanism by which glycyrrhizin improves liver biochemistry and histology are undefined. Metabolism, pharmacokinetics, side-effects, and antiviral and hepatoprotective effects of glycyrrhizin are discussed.
Glycyrrhizin, hepatocellular carcinoma, Metabolism, pharmacokinetics