Betaine protects against sodium arsenite-induced diabetes and hepatotoxicity in mice

被引:10
|
作者
Esfahani, Parian Pourmoafi [1 ,2 ]
Mahdavinia, Masoud [1 ,2 ]
Khorsandi, Layasadat [3 ]
Rezaei, Mohsen [4 ]
Nikravesh, Hojatolla [1 ,2 ]
Khodayar, Mohammad Javad [1 ,2 ]
机构
[1] Ahvaz Jundishapur Univ Med Sci, Toxicol Res Ctr, Med Basic Sci Res Inst, Ahvaz, Iran
[2] Ahvaz Jundishapur Univ Med Sci, Fac Pharm, Dept Toxicol, Ahvaz, Iran
[3] Ahvaz Jundishapur Univ Med Sci, Cellular & Mol Res Ctr, Med Basic Sci Res Inst, Ahvaz, Iran
[4] Tarbiat Modares Univ, Fac Med Sci, Dept Toxicol, Tehran, Iran
关键词
Arsenic; Hepatotoxicity; Diabetes; Betaine; Mice; OXIDATIVE STRESS; GLYCINE BETAINE; EXPOSURE; SUPPRESSION; PREVALENCE; GENES;
D O I
10.1007/s11356-022-22941-w
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Epidemiological evidence has associated chronic exposure to inorganic arsenic with an increased occurrence of glucose intolerance and diabetes mellitus. Furthermore, inorganic arsenic induces oxidative stress in organs such as the liver. Betaine, as a methyl donor, plays a pivotal role in homocysteine metabolism. Betaine has antioxidant and anti-inflammatory properties. Therefore, the aim of this study was to evaluate the effects of betaine against sodium arsenite-induced diabetes and hepatotoxicity in mice. Forty-eight male mice were divided into 6 groups of 8. Group 1, received distilled water every day for 4 weeks by gavage. Group 2 received 500 mg/kg betaine every day for 4 weeks by gavage. Group 3 was given 10 mg/kg NaAsO2 every day for 4 weeks by gavage. Groups 4, 5, and 6 were co-treated with 125, 250, and 500 mg/kg betaine half an hour before NaAsO2 (10 mg/kg), respectively, daily for up to 4 weeks by gavage. After 28 days of the study, the mice were fasted overnight and on day 29, fasting blood glucose was measured and glucose tolerance test was performed. On day 30, the mice were anesthetized and a blood sample was taken from the heart. Serum factors (alanine aminotransferase, aspartate transaminase, and alkaline phosphatase activities), oxidative stress factors (malondialdehyde and glutathione levels, and the activity of superoxide dismutase, glutathione peroxidase, and catalase enzymes) and hepatic inflammatory factors (nitric oxide and tumor necrosis factor alpha) were measured. Histopathological studies were also performed on the liver and pancreas. In this study, it was shown that arsenic causes glucose intolerance, and oxidative/inflammatory hepatic damage. Co-administration of betaine prevents hepatotoxicity and glucose intolerance induced by arsenic in mice. Co-treatment of betaine with arsenic improved glucose intolerance and protected the liver against arsenic induced-oxidative damage and inflammation. Betaine at the dose of 500 mg/kg showed better results than the other doses. Accordingly, betaine can be suggested as a therapeutic agent against diabetogenic and hepatotoxic effects of arsenic.
引用
收藏
页码:10880 / 10889
页数:10
相关论文
共 50 条
  • [41] Protective effect of betaine against lead-induced testicular toxicity in male mice
    Elsheikh, Nahla Abdalla Hassan
    Omer, Nagmeldin A.
    Yi-Ru, Wang
    Mei-Qian, Kuang
    Ilyas, Ali
    Abdurahim, Yassin
    Wang, Gen-Lin
    ANDROLOGIA, 2020, 52 (07)
  • [42] NBR1-mediated autophagic degradation of caspase 8 protects vascular endothelial cells against arsenite-induced apoptotic cell death
    Hu, Siyao
    Wang, Fu
    Mao, Lejiao
    Jiang, Xuejun
    Luo, Yilin
    Qin, Xia
    Zou, Zhen
    Chen, Chengzhi
    Yu, Chao
    Zhang, Jun
    BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2024, 715
  • [43] Ellagic acid mitigates sodium arsenite-induced renal and hepatic toxicity in male Wistar rats
    Mehrzadi, Saeed
    Fatemi, Iman
    Malayeri, Ali Reza
    Khodadadi, Ali
    Mohammadi, Fatemeh
    Mansouri, Esrafil
    Rashno, Mohammad
    Goudarzi, Mehdi
    PHARMACOLOGICAL REPORTS, 2018, 70 (04) : 712 - 719
  • [44] Intraperitoneal kisspeptin-10 administration ameliorates sodium arsenite-induced reproductive toxicity in adult male mice
    Fatima, Iffat
    Qureshi, Irfan Zia
    ANDROLOGIA, 2022, 54 (03)
  • [45] Role of vitamin D3 in mitigating sodium arsenite-induced neurotoxicity in male rats
    Abdou, Heba Mohamed
    Saad, Alaa Mohamed
    Abd Elkader, Heba-Tallah Abd Elrahim
    Essawy, Amina E.
    TOXICOLOGY RESEARCH, 2024, 13 (06)
  • [46] Ameliorative role of rolipram, PDE-4 inhibitor, against sodium arsenite-induced vascular dementia in rats
    Virk, Divjot
    Kumar, Amit
    Jaggi, Amteshwar Singh
    Singh, Nirmal
    ENVIRONMENTAL SCIENCE AND POLLUTION RESEARCH, 2021, 28 (44) : 63250 - 63262
  • [47] Role of dietary GSH in the amelioration of sodium arsenite-induced ovarian and uterine disorders
    Chattopadhyay, Sandip
    Ghosh, Debidas
    REPRODUCTIVE TOXICOLOGY, 2010, 30 (03) : 481 - 488
  • [48] The Defensive Effect of Benfotiamine in Sodium Arsenite-Induced Experimental Vascular Endothelial Dysfunction
    Verma, Sanjali
    Reddy, Krishna
    Balakumar, Pitchai
    BIOLOGICAL TRACE ELEMENT RESEARCH, 2010, 137 (01) : 96 - 109
  • [49] Role of thymoquinone and ebselen in the prevention of sodium arsenite-induced nephrotoxicity in female rats
    Al-Brakati, A. Y.
    Kassab, R. B.
    Lokman, M. S.
    Elmahallawy, E. K.
    Amin, H. K.
    Moneim, A. E. Abdel
    HUMAN & EXPERIMENTAL TOXICOLOGY, 2019, 38 (04) : 482 - 493
  • [50] Effects of choline on sodium arsenite-induced neural tube defects in chick embryos
    Song, Ge
    Cui, Yi
    Han, Zhong-Ji
    Xia, Hong-Fei
    Ma, Xu
    FOOD AND CHEMICAL TOXICOLOGY, 2012, 50 (12) : 4364 - 4374