Mouse models of nonalcoholic fatty liver disease (NAFLD): pathomechanisms and pharmacotherapies

被引:40
作者
Fang, Tingyu [1 ]
Wang, Hua [2 ]
Pan, Xiaoyue [3 ]
Little, Peter J. [4 ]
Xu, Suowen [1 ]
Weng, Jianping [1 ]
机构
[1] Chinese Acad Sci Hefei, Univ Sci & Technol China, Clin Res Hosp,Inst Endocrine & Metab Dis, Div Life Sci & Med,Affiliated Hosp USTC 1,Dept En, Hefei 230001, Peoples R China
[2] Anhui Med Univ, Affiliated Hosp 1, Dept Oncol, Hefei 230022, Anhui, Peoples R China
[3] NYU, Dept Fdn Med, Long Isl Sch Med, Mineola, NY 11501 USA
[4] Univ Queensland, Pharm Australia Ctr Excellence, Sch Pharm, Woolloongabba, Qld 4102, Australia
来源
INTERNATIONAL JOURNAL OF BIOLOGICAL SCIENCES | 2022年 / 18卷 / 15期
基金
中国国家自然科学基金;
关键词
Drug discovery; mouse model; NAFLD; NASH; pharmacotherapy; ENDOPLASMIC-RETICULUM STRESS; ANTIVIRAL SIGNALING PROTEIN; STING-MEDIATED INFLAMMATION; ACID-DEFINED DIET; CHOLINE-DEFICIENT; INDUCED STEATOHEPATITIS; HEPATIC STEATOSIS; RECEPTOR AGONISTS; OBETICHOLIC ACID; GUT MICROBIOTA;
D O I
10.7150/ijbs.65044
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The prevalence of non-alcoholic fatty liver disease (NAFLD) increases year by year, and as a consequence, NAFLD has become one of the most prevalent liver diseases worldwide. Unfortunately, no pharmacotherapies for NAFLD have been approved by the United States Food and Drug Administration despite promising pre-clinical benefits; this situation highlights the urgent need to explore new therapeutic targets for NAFLD and for the discovery of effective therapeutic drugs. The mouse is one of the most commonly used models to study human disease and develop novel pharmacotherapies due to its small size, low-cost and ease in genetic engineering. Different mouse models are used to simulate various stages of NAFLD induced by dietary and/or genetic intervention. In this review, we summarize the newly described patho-mechanisms of NAFLD and review the preclinical mouse models of NAFLD (based on the method of induction) and appraises the use of these models in anti-NAFLD drug discovery. This article will provide a useful resource for researchers to select the appropriate model for research based on the research question being addressed.
引用
收藏
页码:5681 / 5697
页数:17
相关论文
共 189 条
  • [1] Nonalcoholic fatty liver disease: another leap forward
    Abdelmalek, Manal F.
    [J]. NATURE REVIEWS GASTROENTEROLOGY & HEPATOLOGY, 2021, 18 (02) : 85 - 86
  • [2] Longitudinal characterization of diet-induced genetic murine models of non-alcoholic steatohepatitis with metabolic, histological, and transcriptomic hallmarks of human patients
    Abe, Naomichi
    Kato, Sayuka
    Tsuchida, Takuma
    Sugimoto, Kanami
    Saito, Ryuta
    Verschuren, Lars
    Kleemann, Robert
    Oka, Kozo
    [J]. BIOLOGY OPEN, 2019, 8 (05):
  • [3] A Protein-Truncating HSD17B13 Variant and Protection from Chronic Liver Disease
    Abul-Husn, N. S.
    Cheng, X.
    Li, A. H.
    Xin, Y.
    Schurmann, C.
    Stevis, P.
    Liu, Y.
    Kozlitina, J.
    Stender, S.
    Wood, G. C.
    Stepanchick, A. N.
    Still, M. D.
    McCarthy, S.
    O'Dushlaine, C.
    Packer, J. S.
    Balasubramanian, S.
    Gosalia, N.
    Esopi, D.
    Kim, S. Y.
    Mukherjee, S.
    Lopez, A. E.
    Fuller, E. D.
    Penn, J.
    Chu, X.
    Luo, J. Z.
    Mirshahi, U. L.
    Carey, D. J.
    Still, C. D.
    Feldman, M. D.
    Small, A.
    Damrauer, S. M.
    Rader, D. J.
    Zambrowicz, B.
    Olson, W.
    Murphy, A. J.
    Borecki, I. B.
    Shuldiner, A. R.
    Reid, J. G.
    Overton, J. D.
    Yancopoulos, G. D.
    Hobbs, H. H.
    Cohen, J. C.
    Gottesman, O.
    Teslovich, T. M.
    Baras, A.
    Mirshahi, T.
    Gromada, J.
    Dewey, F. E.
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 2018, 378 (12) : 1096 - 1106
  • [4] Hydroxysteroid (17β) dehydrogenase 13 deficiency triggers hepatic steatosis and inflammation in mice
    Adam, Marion
    Heikelae, Hanna
    Sobolewski, Cyril
    Portius, Dorothea
    Maki-Jouppila, Jenni
    Mehmood, Arfa
    Adhikari, Prem
    Esposito, Irene
    Elo, Laura L.
    Zhang, Fu-Ping
    Ruohonen, Suvi T.
    Strauss, Leena
    Foti, Michelangelo
    Poutanen, Matti
    [J]. FASEB JOURNAL, 2018, 32 (06) : 3434 - 3447
  • [5] RIPK3 acts as a lipid metabolism regulator contributing to inflammation and carcinogenesis in non-alcoholic fatty liver disease
    Afonso, Marta B.
    Rodrigues, Pedro M.
    Mateus-Pinheiro, Miguel
    Simao, Andre L.
    Gaspar, Maria M.
    Majdi, Amine
    Arretxe, Enara
    Alonso, Cristina
    Santos-Laso, Alvaro
    Jimenez-Aguero, Raul
    Eizaguirre, Emma
    Bujanda, Luis
    Jesus Pareja, Maria
    Banales, Jesus M.
    Ratziu, Vlad
    Gautheron, Jeremie
    Castro, Rui E.
    Rodrigues, Cecilia M. P.
    [J]. GUT, 2021, 70 (12) : 2359 - 2372
  • [6] Obeticholic acid and INT-767 modulate collagen deposition in a NASH in vitro model
    Anfuso, Beatrice
    Tiribelli, Claudio
    Adorini, Luciano
    Rosso, Natalia
    [J]. SCIENTIFIC REPORTS, 2020, 10 (01)
  • [7] Recent insights on the role of cholesterol in non-alcoholic fatty liver disease
    Arguello, Graciela
    Balboa, Elisa
    Arrese, Marco
    Zanlungo, Silvana
    [J]. BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE, 2015, 1852 (09): : 1765 - 1778
  • [8] Adaptive failure to high-fat diet characterizes steatohepatitis in Alms1 mutant mice
    Arsov, T
    Larter, CZ
    Nolan, CJ
    Petrovsky, N
    Goodnow, CC
    Teoh, NC
    Yeh, MM
    Farrell, GC
    [J]. BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2006, 342 (04) : 1152 - 1159
  • [9] Identification of a Metabolic, Transcriptomic, and Molecular Signature of Patatin-Like Phospholipase Domain Containing 3-Mediated Acceleration of Steatohepatitis
    Banini, Bubu A.
    Kumar, Divya P.
    Cazanave, Sophie
    Seneshaw, Mulugeta
    Mirshahi, Faridoddin
    Santhekadur, Prasanna K.
    Wang, Liangsu
    Guan, Hong Ping
    Oseini, Abdul M.
    Alonso, Cristina
    Bedossa, Pierre
    Koduru, Srinivas V.
    Min, Hae-Ki
    Sanyal, Arun J.
    [J]. HEPATOLOGY, 2021, 73 (04) : 1290 - 1306
  • [10] Silencing hepatic MCJ attenuates non-alcoholic fatty liver disease (NAFLD) by increasing mitochondrial fatty acid oxidation
    Barbier-Torres, Lucia
    Fortner, Karen A.
    Iruzubieta, Paula
    Delgado, Teresa C.
    Giddings, Emily
    Chen, Youdinghuan
    Champagne, Devin
    Fernandez-Ramos, David
    Mestre, Daniela
    Gomez-Santos, Beatriz
    Varela-Rey, Marta
    Gutierrez de Juan, Virginia
    Fernandez-Tussy, Pablo
    Zubiete-Franco, Imanol
    Garcia-Monzon, Carmelo
    Gonzalez-Rodriguez, Agueda
    Oza, Dhaval
    Valenca-Pereira, Felipe
    Fang, Qian
    Crespo, Javier
    Aspichueta, Patricia
    Tremblay, Frederic
    Christensen, Brock C.
    Anguita, Juan
    Luz Martinez-Chantar, Maria
    Rincon, Mercedes
    [J]. NATURE COMMUNICATIONS, 2020, 11 (01)