PFHxS Exposure and the Risk of Non-Alcoholic Fatty Liver Disease

被引:5
|
作者
Ulhaq, Zulvikar Syambani [1 ,2 ]
Tse, William Ka Fai [1 ]
机构
[1] Kyushu Univ, Fac Agr, Ctr Promot Int Educ & Res, Lab Dev Disorders & Toxicol, Fukuoka 8190395, Japan
[2] Natl Res & Innovat Agcy Republ Indonesia, Res Ctr Preclin & Clin Med, Cibinong 16911, Indonesia
基金
日本学术振兴会;
关键词
transcriptomic; toxicities; PFAS; zebrafish; chronic liver disease; PERFLUOROALKYL SUBSTANCES; PERFLUOROOCTANE SULFONATE; ASSOCIATION;
D O I
10.3390/genes15010093
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Perfluorohexanesulfonic acid (PFHxS) is a highly prevalent environmental pollutant, often considered to be less toxic than other poly- and perfluoroalkyl substances (PFASs). Despite its relatively lower environmental impact compared to other PFASs, several studies have suggested that exposure to PFHxS may be associated with disruptions of liver function in humans. Nevertheless, the precise pathomechanisms underlying PFHxS-induced non-alcoholic fatty liver disease (NAFLD) remain relatively unclear. Therefore, this study applied our previously published transcriptome dataset to explore the effects of PFHxS exposure on the susceptibility to NAFLD and to identify potential mechanisms responsible for PFHxS-induced NAFLD through transcriptomic analysis conducted on zebrafish embryos. Results showed that exposure to PFHxS markedly aggravated hepatic symptoms resembling NAFLD and other metabolic syndromes (MetS) in fish. Transcriptomic analysis unveiled 17 genes consistently observed in both NAFLD and insulin resistance (IR), along with an additional 28 genes identified in both the adipocytokine signaling pathway and IR. These shared genes were also found within the NAFLD dataset, suggesting that hepatic IR may play a prominent role in the development of PFHxS-induced NAFLD. In conclusion, our study suggests that environmental exposure to PFHxS could be a potential risk factor for the development of NAFLD, challenging the earlier notion of PFHxS being safer as previously claimed.
引用
收藏
页数:12
相关论文
共 50 条
  • [21] Non-alcoholic fatty liver disease
    Farrell, Geoffrey C.
    Wardell, Rebecca
    Teoh, Narci
    Chitturi, Shiv
    INTERNAL MEDICINE JOURNAL, 2019, 49 (05) : 681 - 683
  • [22] Non-alcoholic fatty liver disease
    Adams, LA
    Angulo, P
    LIVER DISEASES: ADVANCES IN TREATMENT AND PREVENTION: IN HONOUR OF HANS POPPER'S 100TH BIRTHDAY, 2004, 137 : 250 - 270
  • [23] Non-alcoholic fatty liver disease
    Sattar, Naveed
    Forrest, Ewan
    Preiss, David
    BMJ-BRITISH MEDICAL JOURNAL, 2014, 349
  • [24] Non-alcoholic fatty liver disease
    Li, Wenhao
    Alazawi, William
    CLINICAL MEDICINE, 2020, 20 (05) : 509 - 512
  • [25] Non-alcoholic fatty liver disease
    Brent A. Neuschwander-Tetri
    BMC Medicine, 15
  • [26] Non-Alcoholic Fatty Liver Disease
    Engin, Atilla
    OBESITY AND LIPOTOXICITY, 2017, 960 : 443 - 467
  • [27] Non-alcoholic fatty liver disease
    Alba, LM
    Lindor, K
    ALIMENTARY PHARMACOLOGY & THERAPEUTICS, 2003, 17 (08) : 977 - 986
  • [28] Non-alcoholic Fatty Liver: Nutrition influences the Risk of Disease
    Lorenz, Judith
    ZEITSCHRIFT FUR GASTROENTEROLOGIE, 2018, 56 (10): : 1210 - +
  • [29] Loss of Locomotion Is a Risk of Non-Alcoholic Fatty Liver Disease
    Kanayama, Kengo
    Nakagawa, Ryo
    Kanzaki, Hiroaki
    Maeda, Takahiro
    Kojima, Ryuta
    Kobayashi, Kazuhumi
    Kiyono, Soichiro
    Nakamura, Masato
    Ogasawara, Sadahisa
    Suzuki, Eiichiro
    Nakamoto, Shingo
    Muroyama, Ryosuke
    Yasui, Shin
    Ooka, Yoshihiko
    Chiba, Tetsuhiro
    Maruyama, Hitoshi
    Moriyama, Masaru
    Nakagawa, Takashi
    Kato, Naoya
    HEPATOLOGY, 2018, 68 : 299A - 299A
  • [30] Dietary patterns and risk of non-alcoholic fatty liver disease
    Salehi-sahlabadi, Ammar
    Sadat, Samaneh
    Beigrezaei, Sara
    Pourmasomi, Makan
    Feizi, Awat
    Ghiasvand, Reza
    Hadi, Amir
    Clark, Cain C. T.
    Miraghajani, Maryam
    BMC GASTROENTEROLOGY, 2021, 21 (01)