Schisandrin B: A Double-Edged Sword in Nonalcoholic Fatty Liver Disease

Nonalcoholic fatty liver disease (NAFLD) is a spectrum of liver lesions ranging from hepatic steatosis, nonalcoholic steatohepatitis, hepatic cirrhosis, and hepatocellular carcinoma. The high global prevalence of NAFLD has underlined the important public health implications of this disease. The path...

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Main Authors: Pou Kuan Leong, Kam Ming Ko
Format: Article
Language:English
Published: Hindawi Limited 2016-01-01
Series:Oxidative Medicine and Cellular Longevity
Online Access:http://dx.doi.org/10.1155/2016/6171658
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spelling doaj-1b802dd7394148b98eea093002fc5ab62020-11-24T23:23:09ZengHindawi LimitedOxidative Medicine and Cellular Longevity1942-09001942-09942016-01-01201610.1155/2016/61716586171658Schisandrin B: A Double-Edged Sword in Nonalcoholic Fatty Liver DiseasePou Kuan Leong0Kam Ming Ko1Division of Life Science, The Hong Kong University of Science and Technology, Clear Water Bay, Hong KongDivision of Life Science, The Hong Kong University of Science and Technology, Clear Water Bay, Hong KongNonalcoholic fatty liver disease (NAFLD) is a spectrum of liver lesions ranging from hepatic steatosis, nonalcoholic steatohepatitis, hepatic cirrhosis, and hepatocellular carcinoma. The high global prevalence of NAFLD has underlined the important public health implications of this disease. The pathogenesis of NAFLD involves the abnormal accumulation of free fatty acids, oxidative stress, endoplasmic reticulum (ER) stress, and a proinflammatory state in the liver. Schisandrin B (Sch B), an active dibenzooctadiene lignan isolated from the fruit of Schisandra chinensis (a traditional Chinese herb), was found to possess antihyperlipidemic, antioxidant, anti-ER stress, and anti-inflammatory activities in cultured hepatocytes in vitro and in rodent livers in vivo. Whereas a long-term, low dose regimen of Sch B induces an antihyperlipidemic response in obese mice fed a high fat diet, a single bolus high dose of Sch B increases serum/hepatic lipid levels in mice. This differential action of Sch B is likely related to a dose/time-dependent biphasic response on lipid metabolism in mice. The hepatoprotection afforded by Sch B against oxidative stress, ER stress, and inflammation has been widely reported. The ensemble of results suggests that Sch B may offer potential as a therapeutic agent for NAFLD. The optimal dose and duration of Sch B treatment need to be established in order to ensure maximal efficacy and safety when used in humans.http://dx.doi.org/10.1155/2016/6171658
collection DOAJ
language English
format Article
sources DOAJ
author Pou Kuan Leong
Kam Ming Ko
spellingShingle Pou Kuan Leong
Kam Ming Ko
Schisandrin B: A Double-Edged Sword in Nonalcoholic Fatty Liver Disease
Oxidative Medicine and Cellular Longevity
author_facet Pou Kuan Leong
Kam Ming Ko
author_sort Pou Kuan Leong
title Schisandrin B: A Double-Edged Sword in Nonalcoholic Fatty Liver Disease
title_short Schisandrin B: A Double-Edged Sword in Nonalcoholic Fatty Liver Disease
title_full Schisandrin B: A Double-Edged Sword in Nonalcoholic Fatty Liver Disease
title_fullStr Schisandrin B: A Double-Edged Sword in Nonalcoholic Fatty Liver Disease
title_full_unstemmed Schisandrin B: A Double-Edged Sword in Nonalcoholic Fatty Liver Disease
title_sort schisandrin b: a double-edged sword in nonalcoholic fatty liver disease
publisher Hindawi Limited
series Oxidative Medicine and Cellular Longevity
issn 1942-0900
1942-0994
publishDate 2016-01-01
description Nonalcoholic fatty liver disease (NAFLD) is a spectrum of liver lesions ranging from hepatic steatosis, nonalcoholic steatohepatitis, hepatic cirrhosis, and hepatocellular carcinoma. The high global prevalence of NAFLD has underlined the important public health implications of this disease. The pathogenesis of NAFLD involves the abnormal accumulation of free fatty acids, oxidative stress, endoplasmic reticulum (ER) stress, and a proinflammatory state in the liver. Schisandrin B (Sch B), an active dibenzooctadiene lignan isolated from the fruit of Schisandra chinensis (a traditional Chinese herb), was found to possess antihyperlipidemic, antioxidant, anti-ER stress, and anti-inflammatory activities in cultured hepatocytes in vitro and in rodent livers in vivo. Whereas a long-term, low dose regimen of Sch B induces an antihyperlipidemic response in obese mice fed a high fat diet, a single bolus high dose of Sch B increases serum/hepatic lipid levels in mice. This differential action of Sch B is likely related to a dose/time-dependent biphasic response on lipid metabolism in mice. The hepatoprotection afforded by Sch B against oxidative stress, ER stress, and inflammation has been widely reported. The ensemble of results suggests that Sch B may offer potential as a therapeutic agent for NAFLD. The optimal dose and duration of Sch B treatment need to be established in order to ensure maximal efficacy and safety when used in humans.
url http://dx.doi.org/10.1155/2016/6171658
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