Hepatic expression of sodium-glucose cotransporter 2 (SGLT2) in patients with chronic liver disease

被引:14
作者
Nakano, Dan [1 ]
Akiba, Jun [2 ]
Tsutsumi, Tsubasa [1 ]
Kawaguchi, Machiko [1 ]
Yoshida, Takafumi [1 ]
Koga, Hironori [1 ,3 ]
Kawaguchi, Takumi [1 ,3 ]
机构
[1] Kurume Univ, Dept Med, Div Gastroenterol, Sch Med, 67 Asahi Machi Kurume, Kurume, Fukuoka 8300011, Japan
[2] Kurume Univ Hosp, Dept Pathol, Kurume, Fukuoka, Japan
[3] Kurume Univ, Res Ctr Innovat Canc Therapy, Liver Canc Div, Kurume, Fukuoka, Japan
基金
日本学术振兴会;
关键词
Glucose transporter; SGLT2; Liver; Human tissue; Graphical model; CANAGLIFLOZIN; INHIBITOR; TRANSPORTERS; METABOLISM;
D O I
10.1007/s00795-022-00334-9
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Sodium-glucose cotransporter 2 (SGLT2) occurs in the proximal renal tubule cells. We investigate the hepatic expression of SGLT2 and its related factors in patients with chronic liver disease. This is a retrospective human study. The liver tissues were biopsied from patients with chronic liver disease (n = 30). The expression levels of SGLT2 were evaluated by immunostaining. Furthermore, the undirected graphical model was used to identify factors associated with hepatic expression levels of SGLT2. The SGLT2 expression was observed in not only the kidney, but also the liver in immunostaining (SGLT2 intensity: kidney 165.8 +/- 15.6, liver 114.4 +/- 49.0 arbitrary units, P < 0.01) and immunoblotting. There was no significant difference in hepatic expression of SGLT2 in the stratified analysis according to age, sex, BMI, and the severity of the liver disease. In the undirected graphical model, SGLT2 directly interacted with various factors such as sex, fatty change, neutrophil-to-lymphocyte ratio, triglyceride, hemoglobin A1c, creatinine, and albumin (partial correlation coefficient 0.4-0.6 for sex and 0.2-0.4 for others). The expression of SGLT2 was observed in the hepatocytes of patients with chronic liver disease. The undirected graphical model demonstrated the complex interaction of hepatic expression levels of SGLT2 with gender, inflammation, renal function, and lipid/glucose/protein metabolisms.
引用
收藏
页码:304 / 315
页数:12
相关论文
共 31 条
  • [1] Dysfunctional mitochondrial bioenergetics and the pathogenesis of hepatic disorders
    Auger, Christopher
    Alhasawi, Azhar
    Contavadoo, Manuraj
    Appanna, Vasu D.
    [J]. FRONTIERS IN CELL AND DEVELOPMENTAL BIOLOGY, 2015, 3
  • [2] Expression of glucose transporters in duodenal mucosa of patients with type 1 diabetes
    Bolla, Andrea Mario
    Butera, Elena
    Pellegrini, Silvia
    Caretto, Amelia
    Bonfanti, Riccardo
    Zuppardo, Raffaella Alessia
    Barera, Graziano
    Cavestro, Giulia Martina
    Sordi, Valeria
    Bosi, Emanuele
    [J]. ACTA DIABETOLOGICA, 2020, 57 (11) : 1367 - 1373
  • [3] Network analysis for count data with excess zeros
    Choi, Hosik
    Gim, Jungsoo
    Won, Sungho
    Kim, You Jin
    Kwon, Sunghoon
    Park, Changyi
    [J]. BMC GENETICS, 2017, 18
  • [4] Effects of the SGLT2 inhibitor dapagliflozin on HDL cholesterol, particle size, and cholesterol efflux capacity in patients with type 2 diabetes: a randomized placebo-controlled trial
    Fadini, Gian Paolo
    Bonora, Benedetta Maria
    Zatti, Giancarlo
    Vitturi, Nicola
    Iori, Elisabetta
    Marescotti, Maria Cristina
    Albiero, Mattia
    Avogaro, Angelo
    [J]. CARDIOVASCULAR DIABETOLOGY, 2017, 16
  • [5] Preclinical metabolism and disposition of luseogliflozin, a novel antihyperglycemic agent
    Hasegawa, Masatoshi
    Chino, Yukihiro
    Horiuchi, Nobuko
    Hachiuma, Kenji
    Ishida, Masahiro
    Fukasawa, Yoshiki
    Nakai, Yasuhiro
    Yamaguchi, Jun-ichi
    [J]. XENOBIOTICA, 2015, 45 (12) : 1105 - 1115
  • [6] The Na+/Glucose Cotransporter Inhibitor Canagliflozin Activates AMPK by Inhibiting Mitochondrial Function and Increasing Cellular AMP Levels
    Hawley, Simon A.
    Ford, Rebecca J.
    Smith, Brennan K.
    Gowans, Graeme J.
    Mancini, Sarah J.
    Pitt, Ryan D.
    Day, Emily A.
    Salt, Ian P.
    Steinberg, Gregory R.
    Hardie, D. Grahame
    [J]. DIABETES, 2016, 65 (09) : 2784 - 2794
  • [7] Threshold-based segmentation of fluorescent and chromogenic images of microglia, astrocytes and oligodendrocytes in FIJI
    Healy, Sinead
    McMahon, Jill
    Owens, Peter
    Dockery, Peter
    FitzGerald, Una
    [J]. JOURNAL OF NEUROSCIENCE METHODS, 2018, 295 : 87 - 103
  • [8] Non-Invasive Analysis of Human Liver Metabolism by Magnetic Resonance Spectroscopy
    Jones, John G.
    [J]. METABOLITES, 2021, 11 (11)
  • [9] Gender differences in adverse event reports associated with antidiabetic drugs
    Joung, Kyung-In
    Jung, Gyu-Won
    Park, Han-Heui
    Lee, Hyesung
    Park, So-Hee
    Shin, Ju-Young
    [J]. SCIENTIFIC REPORTS, 2020, 10 (01)
  • [10] Sodium glucose cotransporter 2 inhibitor canagliflozin attenuates liver cancer cell growth and angiogenic activity by inhibiting glucose uptake
    Kaji, Kosuke
    Nishimura, Norihisa
    Seki, Kenichiro
    Sato, Shinya
    Saikawa, Soichiro
    Nakanishi, Keisuke
    Furukawa, Masanori
    Kawaratani, Hideto
    Kitade, Mitsuteru
    Moriya, Kei
    Namisaki, Tadashi
    Yoshiji, Hitoshi
    [J]. INTERNATIONAL JOURNAL OF CANCER, 2018, 142 (08) : 1712 - 1722