Electromagnetic Fields Ameliorate Insulin Resistance and Hepatic Steatosis by Modulating Redox Homeostasis and SREBP-1c Expression in db/db Mice

被引:4
|
作者
Zhai, Mingming [1 ]
Yan, Xi [2 ]
Liu, Jiangzheng [3 ]
Long, Zi [3 ]
Zhao, Siyan [4 ]
Li, Wendan [4 ]
Liu, Ying [4 ]
Hai, Chunxu [3 ]
机构
[1] Air Force Med Univ, Dept Biomed Engn, Xian, Peoples R China
[2] Air Force Med Univ, Affiliated Hosp 2, Dept Dermatol, Xian, Peoples R China
[3] Air Force Med Univ, Sch Publ Hlth,Minist Educ, Key Lab Hazard Assessment & Control Special Opera, Dept Toxicol,Shanxi Prov Key Lab Free Rad Biol &, Xian, Peoples R China
[4] Inst Nucl Biol & Chem Def, 1 Yangfang Zhongxin North St, Beijing 102205, Peoples R China
来源
DIABETES METABOLIC SYNDROME AND OBESITY-TARGETS AND THERAPY | 2021年 / 14卷
关键词
nonalcoholic fatty liver disease; electromagnetic fields; hepatic steatosis; oxidative stress; insulin resistance; OXIDATIVE STRESS; LIPID-ACCUMULATION; ADIPOSE-TISSUE; EXPOSURE; MASS;
D O I
10.2147/DMSO.S294020
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Purpose: The prevalence of nonalcoholic fatty liver disease (NAFLD), which has recently become known as metabolic-associated fatty liver disease (MAFLD), has risen. However, pharmacotherapies for this disease have not been approved. Electromagnetic fields (EMFs) have excellent bioeffects on multiple diseases. However, the effects of EMFs on NAFLD are unknown. This study investigated the bioeffects of EMF exposure on insulin resistance, liver redox homeostasis and hepatic steatosis in db/db mice. Methods: Animals were sacrificed after EMF exposure for 8 weeks. The fasting blood glucose and insulin levels in the serum were tested. The homeostatic model assessment of insulin resistance (HOMA-IR) was calculated by a formula. The levels of MDA, GSSG and GSH, biomarkers of redox, were assessed. The activities of CAT, SOD and GSH-Px were assessed. The body and liver weights were measured. Hepatic lipid accumulation was observed by Oil Red O staining. Hepatic CAT, GR, GSH-Px, SOD1, SOD2 and SREBP-1 expression was determined by Western blotting. Results: EMF exposure ameliorated insulin resistance and oxidative stress in the liver by downregulating the MDA and GSSG levels, increasing the reduced GSH levels, and promoting the GSH-Px levels in db/db mice. In addition, liver weight and triglyceride (TG) levels were reduced by EMF exposure. Simultaneously, EMF exposure improved hepatic steatosis by downregulating the protein expression of SREBP-1c. Conclusion: The present findings suggest that EMF exposure has positive effects in the treatment of NAFLD.
引用
收藏
页码:1035 / 1042
页数:8
相关论文
共 50 条
  • [1] Inhibition of CCR2 Ameliorates Insulin Resistance and Hepatic Steatosis in db/db Mice
    Tamura, Yukinori
    Sugimoto, Masayuki
    Murayama, Toshinori
    Ueda, Yukihiko
    Kanamori, Hiroshi
    Ono, Koh
    Ariyasu, Hiroyuki
    Akamizu, Takashi
    Kita, Toru
    Yokode, Masayuki
    Arai, Hidenori
    ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 2008, 28 (12) : 2195 - 2201
  • [2] Inhibition of C-C chemokine receptor-2 improves insulin resistance and hepatic steatosis in db/db mice
    Tamura, Yukinori
    Sugimoto, Masayuki
    Murayama, Toshinori
    Kita, Toru
    Yokode, Masayuki
    Araikyoto, Hidenori
    DIABETES, 2008, 57 : A169 - A169
  • [3] Honokiol Improves Insulin Resistance, Hepatic Steatosis, and Inflammation in Type 2 Diabetic db/db Mice
    Kim, Young-Je
    Jung, Un Ju
    INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2019, 20 (09)
  • [4] The 11β-hydroxysteroid dehydrogenase type 1 inhibitor protects against the insulin resistance and hepatic steatosis in db/db mice
    Yuan, Xiaohuan
    Li, Hongzhi
    Bai, He
    Zhao, Xiaojin
    Zhang, Chunlei
    Liu, Haifeng
    Zhang, Yufei
    Zhao, Binghai
    Wu, Yan
    Liu, Jieting
    Xiang, Qi
    Feng, Biao
    Chu, Yanhui
    Huang, Yadong
    EUROPEAN JOURNAL OF PHARMACOLOGY, 2016, 788 : 140 - 151
  • [5] C-C chemokine receptor-2 inhibitor ameliorates insulin resistance and hepatic steatosis in db/db mice.
    Tamura, Yukinori
    Arai, Hidenon
    Sugimoto, Masayuki
    Murayama, Toshinori
    Ueda, Yukihiko
    Kanamori, Hiroshi
    Ono, Koh
    Ariyasu, Hiroyuki
    Akamizu, Takashi
    Kita, Toru
    Yokode, Masayuki
    CIRCULATION, 2007, 116 (16) : 170 - 170
  • [6] PHARCOLOGICAL BLOCKADE OF CCR2 INHIBITS THE DEVELOPMENT OF INSULIN RESISTANCE AND HEPATIC STEATOSIS IN DB/DB MICE
    Tamura, Y.
    Sugimoto, M.
    Murayama, T.
    Kita, T.
    Yokode, M.
    Arai, H.
    ATHEROSCLEROSIS SUPPLEMENTS, 2008, 9 (01) : 12 - 13
  • [7] SREBP-1c:: a major mediator of insulin action on hepatic genes expression
    Foufelle, F
    Ferré, P
    Foretz, M
    M S-MEDECINE SCIENCES, 2000, 16 (04): : 559 - 561
  • [8] GRP78 expression inhibits insulin and ER stress-induced SREBP-1c activation and reduces hepatic steatosis in mice
    Kammoun, Helene L.
    Chabanon, Herve
    Hainault, Isabelle
    Luquet, Serge
    Magnan, Christophe
    Koike, Tatsuro
    Ferre, Pascal
    Foufelle, Fabienne
    JOURNAL OF CLINICAL INVESTIGATION, 2009, 119 (05): : 1201 - 1215
  • [9] SREBP-1c mediates the insulin-dependent hepatic glucokinase expression
    Kim, SY
    Kim, HI
    Kim, TH
    Im, SS
    Park, SK
    Lee, IK
    Kim, KS
    Ahn, YH
    JOURNAL OF BIOLOGICAL CHEMISTRY, 2004, 279 (29) : 30823 - 30829
  • [10] Inhibition of sterol regulatory element binding protein (SREBP-1c) by insulin ameliorate insulin signalling and hepatic steatosis in high-fat-fed C57BL/6 mice
    Zhu, Yan Hua
    Chen, Xiang
    Li, Ming
    Yu, Qiu Qiong
    Sun, Wei Ping
    Bi, Yan
    Weng, Jianping
    DIABETES, 2008, 57 : A700 - A700