Literature DB >> 30021122

Future trends in the treatment of non-alcoholic steatohepatitis.

Stefano Fiorucci1, Michele Biagioli2, Eleonora Distrutti3.   

Abstract

With an estimated prevalence of ≈25% in Western and Asian countries, non alcoholic fatty liver disease (NAFLD), caused by chronic excessive caloric intake, is the emerging as the most prevalent liver disorder worldwide. NAFLD exists in two clinical entities, non-alcoholic fatty liver disease (NAFL), a relative benign disease that carry on minimal risk of liver-related morbidity but significant risk of cardiovascular complications, and non-alcoholic steatohepatitis (NASH), a progressive liver disorder with a significant risk for development of liver-related morbidities and mortality. While, liver injury in NASH is contributed by lipid overload in hepatocytes, lipotoxicity, the main determinant of disease progression is an inflammation-driven fibrotic response. Here, we review the landscape of emerging pharmacological interventions in the treatment of NAFL and NASH. A consensus exists that, while treating the liver component of NASH requires development of novel pharmacological approaches, the future therapy of NASH needs to be tailored to the single patient and most likely will be a combination of agents acting on specific pathogenic mechanisms at different disease stage.
Copyright © 2018 Elsevier Ltd. All rights reserved.

Entities:  

Keywords:  Apoptosis; FXR; Fibrosis; GPBAR1; Inflammation; Intestine; Lipids; Liver; Nuclear receptors; PPARs; Steatohepatitis

Mesh:

Year:  2018        PMID: 30021122     DOI: 10.1016/j.phrs.2018.07.014

Source DB:  PubMed          Journal:  Pharmacol Res        ISSN: 1043-6618            Impact factor:   7.658


  16 in total

1.  Ursodeoxycholic acid exerts hepatoprotective effects by regulating amino acid, flavonoid, and fatty acid metabolic pathways.

Authors:  Da Jung Kim; Hyewon Chung; Sang Chun Ji; SeungHwan Lee; Kyung-Sang Yu; In-Jin Jang; Joo-Youn Cho
Journal:  Metabolomics       Date:  2019-02-27       Impact factor: 4.290

2.  Strategies Targeting the Innate Immune Response for the Treatment of Hepatitis C Virus-Associated Liver Fibrosis.

Authors:  Daniel Sepulveda-Crespo; Salvador Resino; Isidoro Martinez
Journal:  Drugs       Date:  2021-01-05       Impact factor: 9.546

3.  ACC inhibitor alone or co-administered with a DGAT2 inhibitor in patients with non-alcoholic fatty liver disease: two parallel, placebo-controlled, randomized phase 2a trials.

Authors:  Roberto A Calle; Neeta B Amin; Santos Carvajal-Gonzalez; Trenton T Ross; Arthur Bergman; Sudeepta Aggarwal; Collin Crowley; Anthony Rinaldi; Jessica Mancuso; Naresh Aggarwal; Veena Somayaji; Malgorzata Inglot; Theresa A Tuthill; Kou Kou; Magalie Boucher; Greg Tesz; Robert Dullea; Kendra K Bence; Albert M Kim; Jeffrey A Pfefferkorn; William P Esler
Journal:  Nat Med       Date:  2021-10-11       Impact factor: 53.440

Review 4.  FXR: structures, biology, and drug development for NASH and fibrosis diseases.

Authors:  Si-Yu Tian; Shu-Ming Chen; Cheng-Xi Pan; Yong Li
Journal:  Acta Pharmacol Sin       Date:  2022-02-25       Impact factor: 7.169

5.  Discovery of a Potent and Orally Active Dual GPBAR1/CysLT1R Modulator for the Treatment of Metabolic Fatty Liver Disease.

Authors:  Stefano Fiorucci; Pasquale Rapacciuolo; Bianca Fiorillo; Rosalinda Roselli; Silvia Marchianò; Cristina Di Giorgio; Martina Bordoni; Rachele Bellini; Chiara Cassiano; Paolo Conflitti; Bruno Catalanotti; Vittorio Limongelli; Valentina Sepe; Michele Biagioli; Angela Zampella
Journal:  Front Pharmacol       Date:  2022-04-25       Impact factor: 5.988

6.  Diagnostic accuracy assessment of molecular prediction model for the risk of NAFLD based on MRI-PDFF diagnosed Chinese Han population.

Authors:  Qing Zhang; Yueli Zhu; Wanjiang Yu; Zhipeng Xu; Zhenzhen Zhao; Shousheng Liu; Yongning Xin; Kuirong Lv
Journal:  BMC Gastroenterol       Date:  2021-02-25       Impact factor: 3.067

7.  Transcriptome Analysis of Dual FXR and GPBAR1 Agonism in Rodent Model of NASH Reveals Modulation of Lipid Droplets Formation.

Authors:  Adriana Carino; Silvia Marchianò; Michele Biagioli; Chiara Fiorucci; Angela Zampella; Maria Chiara Monti; Elva Morretta; Martina Bordoni; Cristina Di Giorgio; Rosalinda Roselli; Patrizia Ricci; Eleonora Distrutti; Stefano Fiorucci
Journal:  Nutrients       Date:  2019-05-21       Impact factor: 5.717

8.  TRIB1 rs17321515 and rs2954029 gene polymorphisms increase the risk of non-alcoholic fatty liver disease in Chinese Han population.

Authors:  Qun Liu; Feng Xue; Jing Meng; Shou-Sheng Liu; Li-Zhen Chen; Hui Gao; Ning Geng; Wen-Wen Jin; Yong-Ning Xin; Shi-Ying Xuan
Journal:  Lipids Health Dis       Date:  2019-03-09       Impact factor: 3.876

9.  The Aryl Hydrocarbon Receptor (AhR) Mediates the Counter-Regulatory Effects of Pelargonidins in Models of Inflammation and Metabolic Dysfunctions.

Authors:  Michele Biagioli; Adriana Carino; Chiara Fiorucci; Giannamaria Annunziato; Silvia Marchianò; Martina Bordoni; Rosalinda Roselli; Cristina Di Giorgio; Federica Castiglione; Patrizia Ricci; Agostino Bruno; Andrea Faccini; Eleonora Distrutti; Monia Baldoni; Gabriele Costantino; Stefano Fiorucci
Journal:  Nutrients       Date:  2019-08-07       Impact factor: 5.717

10.  Role and mechanisms of action of microRNA‑21 as regards the regulation of the WNT/β‑catenin signaling pathway in the pathogenesis of non‑alcoholic fatty liver disease.

Authors:  Xiu-Mei Wang; Xiao-Yi Wang; Yu-Mei Huang; Xia Chen; Mu-Han Lü; Lei Shi; Chang-Ping Li
Journal:  Int J Mol Med       Date:  2019-10-18       Impact factor: 4.101

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