Open Access Open Access  Restricted Access Subscription Access
Open Access Open Access Open Access  Restricted Access Restricted Access Subscription Access

Effect of Cadmium on Glucose, Lipid Profile and Oxidative Stress in Streptozotocin-Induced Diabetic and Non-Diabetic Rats


Affiliations
1 Department of Basic Medical Sciences, Neyshabur University of Medical Sciences, Neyshabur, Iran, Islamic Republic of
2 Department of Immunogenetics, BuAli Research Institute, Mashhad University of Medical Sciences, Mashhad, Iran, Islamic Republic of
3 Medical Plants Research Center, Shahrekord University of Medical Sciences, Shahrekord, Iran, Islamic Republic of
     

   Subscribe/Renew Journal


Cadmium (Cd), highly toxic heavy metal, has been considered as a possible risk factor for diabetes and its complications. However, the underlying mechanisms of Cd-induced diabetes are not clear. The present study was designed to evaluate the effects of Cd on the oxidative system in the diabetic and non-diabetic rats. Rats were divided into the following groups of 8 animals each: control (C), diabetic (D), Cd-exposed (1 mg/kg/bw) and diabetic-exposed to Cd (1 mg/kg/bw) (D + Cd- exposed) groups. Diabetes was induced by streptozotocin (intraperitoneally (i.p.)) at a single dose of 60 mg/kg. Cd (i.p.) was administered 3 days after streptozotocin (STZ) administration to the end of the study. After 4-weeks, blood was drawn to determine the changes of glucose, serum superoxide dismutase (SOD), catalase (CAT), glutathione-S-transfrase (GST) and glutathione peroxidase (GPx) activities as well as the levels of reduced glutathione (GSH), malondialdehyde (MDA) and lipid profile. The results indicated that Cd exposure aggravated increased blood glucose, MDA, triglycerides, total cholesterol, LDL-C as well as decreased GSH levels and the activities of antioxidant enzymes in diabetic rats (p<0.001). These results suggest that Cd exposure deteriorates diabetic effect and its complications in STZ-diabetic model by induction of oxidative stress.

Keywords

Cadmium, Diabetes, Lipid Profile, Oxidative Stress, Rats.
User
Subscription Login to verify subscription
Notifications
Font Size

  • Wild S, Roglic G, Green A, Sicree R, King H. Global prevalence of diabetes: estimates for the year 2000 and projections for 2030. Diabetes Care 2004; 27: 1047–1053.
  • Jarup L. Hazards of heavy metal contamination. Brit. Med. Bull. 2003; 68: 167-182.
  • Treviño S, Waalkes MP, Flores Hernández JA, León-Chavez BA, Aguilar-Alonso P, Brambila E. Chronic cadmium exposure in rats produces pancreatic impairment and insulin resistance in multiple peripheral tissues. Arch. Biochem. Biophys. 2015; 583: 27-35 (2015).
  • Kurata Y, Katsuta O, Doi T. Chronic cadmium treatment induces islet β-cell injury in ovariectomized cynomolgus monkeys. Jpn. J. Vet. Res. 50, 175-83.
  • Demir H, Kanter M, Coskun O, Uz YH, Koc A, Yildiz A. Effect of black cumin (Nigella sativa) on heart rate, some hematological values, and pancreatic β-cell damage in cadmiumtreated rats. Biol. Trace. Elem. Res. 2006; 110: 151-162.
  • Subramanyan G, Bhaskar M, Govindappa S. The role of cadmium in induction of atherosclerosis in rabbits. Indian Heart. J. 1992; 44: 177-180.
  • Onianwa PC, Adetola IG, Iwegbue CMA, Ojo MG, Tella OO. Trace heavy metals composition of some Nigerian beverages and food drinks. Food Chem. J. 1999; 66: 275-279.
  • Edwards JR, Prozialeck WC. Cadmium, diabetes and chronic kidney disease. Appl. Pharmacol. 2009; 238: 289293.
  • Gonzales GF, Gonzales-Castañeda C, Gasco M. A mixture of extracts from Peruvian plants (black maca and yacon) improves sperm count and reduced glycemia in mice with streptozotocin-induced diabetes. Toxicol. Mech. Meth. 2013: 23; 509-518.
  • Samarghandian S, Borji A, Delkhosh MB, Samini F. Safranal treatment improves hyperglycemia, hyperlipidemia and oxidative stress in streptozotocin-induced diabetic rats. J. Pharm. Pharm. Sci. 2013; 16: 352-362.
  • Genet S, Kale RK, Baquer NZ. Alterations in antioxidant enzymes and oxidative damage in experimental diabetic rattissues: effect of vanadate and fenugreek (Trigonella foenum graecum). Mol. Cell. Biochem. 2002; 236: 7-12.
  • Ellman GL. Tissue sulphydryl groups. Arch. Biochem. Biophys. 82, 70-77 (1959).
  • Kakkar P, Das B, Viswanathan PN. A modified spectroscopic assay of superoxide dismutase. Indian J. Biochem. Biophys. 21, 130-132 (1984).
  • Sinha AK. Colorimetric assay of catalase. Anal. Biochem. 1972; 47: 389-394.
  • Rotruck JT, Pope AL, Ganther HE. Selenium: biochemical role as a component of glutathione peroxidase purification assay. Science 1973; 179: 588-590.
  • Habig WH, Pabst ML, Jakpoly WB. Glutathione transferase: a first enzymatic step in mercapturic acid and formation. J. Bio. Chem. 1974; 249: 7130-7139.
  • Bradford MM. A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein dye binding. Anal. Biochem. 1976; 72, 248-254.
  • Samarghandian S, Hadjzadeh MA, Amin Nya F, Davoodi S. (2012). Antihyperglycemic and antihyperlipidemic effects of guar gum on streptozotocin-induced diabetes in male rats. Pharmacogn. Mag. 2012; 8: 65-72.
  • Chen YW, Yang CY, Huang CF, Hung DZ, Leung YM, Liu SH. Heavy metals, islet function and diabetes development. Islets 1. 2009; 169-176.
  • Kaneto H, Kawamori D, Matsuoka TA, Kajimoto Y, Yamasaki Y. Oxidative stress and pancreatic beta-cell dysfunction. Am. J. Ther. 2009; 12: 529-533.
  • Chang KC, Hsu CC, Liu SH, Su3 CC, Yen CC, Lee MJ, Chen KL, Ho TJ, Hung DZ, Wu CC, Lu TH, Su YC, Chen YW, Huang CF. Cadmium induces apoptosis in pancreatic b-Cells through a mitochondria-dependent pathway: The role of oxidative stress-mediated c-Jun N-terminal kinase activation. PLOS ONE 2013; 8: e54374.
  • Milton Prabu S, Muthumani M, Shagirtha K. Quercetin potentially attenuates cadmium induced oxidative stress mediated cardiotoxicity and dyslipidemia in rats. Eur. Rev. Med. Pharmacol. Sci. 2013; 17: 582-595.
  • Wiernsperger NF. Oxidative stress as a therapeutic target in diabetes: revisiting the controversy. Diabet. Metabol. 2003; 29: 579-585.
  • Grune T, Siems WG, Petras T. Identification of metabolic pathways of the lipid peroxidation product 4-hydroxynonenal in in situ perfused rat kidney. J. Lipid. Res. 1997; 38: 1660-1665.

Abstract Views: 673

PDF Views: 3




  • Effect of Cadmium on Glucose, Lipid Profile and Oxidative Stress in Streptozotocin-Induced Diabetic and Non-Diabetic Rats

Abstract Views: 673  |  PDF Views: 3

Authors

Saeed Samarghandian
Department of Basic Medical Sciences, Neyshabur University of Medical Sciences, Neyshabur, Iran, Islamic Republic of
Abasalt Borji
Department of Basic Medical Sciences, Neyshabur University of Medical Sciences, Neyshabur, Iran, Islamic Republic of
Tahereh Farkhondeh
Department of Immunogenetics, BuAli Research Institute, Mashhad University of Medical Sciences, Mashhad, Iran, Islamic Republic of
Asadi-Samani Majid
Medical Plants Research Center, Shahrekord University of Medical Sciences, Shahrekord, Iran, Islamic Republic of

Abstract


Cadmium (Cd), highly toxic heavy metal, has been considered as a possible risk factor for diabetes and its complications. However, the underlying mechanisms of Cd-induced diabetes are not clear. The present study was designed to evaluate the effects of Cd on the oxidative system in the diabetic and non-diabetic rats. Rats were divided into the following groups of 8 animals each: control (C), diabetic (D), Cd-exposed (1 mg/kg/bw) and diabetic-exposed to Cd (1 mg/kg/bw) (D + Cd- exposed) groups. Diabetes was induced by streptozotocin (intraperitoneally (i.p.)) at a single dose of 60 mg/kg. Cd (i.p.) was administered 3 days after streptozotocin (STZ) administration to the end of the study. After 4-weeks, blood was drawn to determine the changes of glucose, serum superoxide dismutase (SOD), catalase (CAT), glutathione-S-transfrase (GST) and glutathione peroxidase (GPx) activities as well as the levels of reduced glutathione (GSH), malondialdehyde (MDA) and lipid profile. The results indicated that Cd exposure aggravated increased blood glucose, MDA, triglycerides, total cholesterol, LDL-C as well as decreased GSH levels and the activities of antioxidant enzymes in diabetic rats (p<0.001). These results suggest that Cd exposure deteriorates diabetic effect and its complications in STZ-diabetic model by induction of oxidative stress.

Keywords


Cadmium, Diabetes, Lipid Profile, Oxidative Stress, Rats.

References





DOI: https://doi.org/10.22506/ti%2F2017%2Fv24%2Fi1%2F149027