Literature DB >> 30537758

Nonalcoholic-Fatty-Liver-Disease and Nonalcoholic Steatohepatitis: Successful Development of Pharmacological Treatment Will Depend on Translational Research.

Aline Gottlieb1, Wesal Mosthael1, Jan-Peter Sowa1, Ali Canbay2.   

Abstract

BACKGROUND: Nonalcoholic-fatty-liver-disease/nonalcoholic steatohepatitis (NAFLD/NASH) is expected to become the leading liver disease worldwide. Typical liver-related complications are fibrosis, cirrhosis, and the development of hepatocellular cancer (HCC) with the need for liver transplantation. Up to now there is no approved pharmacotherapy. Indeed, this might be due to the complexity of this disease. While the cheapest therapeutic approach is still a lifestyle change leading to weight loss, the proportion of people achieving sufficient weight reduction without additional support is low. Newly developed drugs are expensive and lack a breakthrough in therapeutic success. One reason might be that drugs developed often derive from murine models. Unfortunately, there is little overlap between genes in human and mice that are responsible for the development of NAFLD/NASH. This review aims at summarizing latest developments as well as stress again that more translational research is necessary.
SUMMARY: Therapy of NAFLD/NASH is easy and very complex at the same time, as the current main target is weight reduction. Since this is in fact not easily achieved and maintained by many affected individuals, pharmacotherapy to halt the progression of NAFLD/NASH is urgently warranted. More translational studies are needed to understand the metabolic mechanisms and interactions between the liver, gut, oxidative stress and the processes leading to NAFLD progression and HCC development, even in the absence of cirrhosis.
© 2018 S. Karger AG, Basel.

Entities:  

Keywords:  Clinical trials; Fibrosis; Hepatitis; Nonalcoholic steatohepatitis; Steatosis

Year:  2018        PMID: 30537758     DOI: 10.1159/000493259

Source DB:  PubMed          Journal:  Digestion        ISSN: 0012-2823            Impact factor:   3.216


  5 in total

1.  Targeted Delivery of Notch Inhibitor Attenuates Obesity-Induced Glucose Intolerance and Liver Fibrosis.

Authors:  Lauren R Richter; Qianfen Wan; Di Wen; Yuqi Zhang; Junjie Yu; Jin Ku Kang; Changyu Zhu; Elizabeth L McKinnon; Zhen Gu; Li Qiang; Utpal B Pajvani
Journal:  ACS Nano       Date:  2020-05-22       Impact factor: 15.881

Review 2.  Oxidative Stress in Non-alcoholic Fatty Liver Disease. An Updated Mini Review.

Authors:  Anna Pia Delli Bovi; Francesca Marciano; Claudia Mandato; Maria Anna Siano; Marcella Savoia; Pietro Vajro
Journal:  Front Med (Lausanne)       Date:  2021-02-26

3.  Attenuating effects of allantoin on oxidative stress in a mouse model of nonalcoholic steatohepatitis: role of SIRT1/Nrf2 pathway.

Authors:  Zeinab Hamidi-Zad; Azam Moslehi; Maryam Rastegarpanah
Journal:  Res Pharm Sci       Date:  2021-10-15

4.  Hmgcs2-mediated ketogenesis modulates high-fat diet-induced hepatosteatosis.

Authors:  Shaza Asif; Ri Youn Kim; Thet Fatica; Jordan Sim; Xiaoling Zhao; Yena Oh; Alix Denoncourt; Angela C Cheung; Michael Downey; Erin E Mulvihill; Kyoung-Han Kim
Journal:  Mol Metab       Date:  2022-04-12       Impact factor: 8.568

5.  Transcriptome-Wide Analysis of Human Liver Reveals Age-Related Differences in the Expression of Select Functional Gene Clusters and Evidence for a PPP1R10-Governed 'Aging Cascade'.

Authors:  Thomas Schreiter; Robert K Gieseler; Ramiro Vílchez-Vargas; Ruy Jauregui; Jan-Peter Sowa; Susanne Klein-Scory; Ruth Broering; Roland S Croner; Jürgen W Treckmann; Alexander Link; Ali Canbay
Journal:  Pharmaceutics       Date:  2021-11-25       Impact factor: 6.321

  5 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.