Cadmium-induced changes in lipid peroxidation, blood hematology, biochemical parameters and semen quality of male rats: protective role of vitamin E and beta-carotene

Food Chem Toxicol. 2004 Oct;42(10):1563-71. doi: 10.1016/j.fct.2004.05.001.

Abstract

Cadmium is a well-known human carcinogen and a potent nephrotoxin. Lipid peroxidation is involved in cadmium-related toxicity. Vitamin E and beta-carotene are effective antioxidants and free radical scavengers. Therefore, the present study was carried out to investigate the potential protective effects of vitamin E and beta-carotene alone or in combination against cadmium (Cd) toxicity. Cadmium chloride (CdCl2, 5 mg/kg BW, 1/15 LD50), vitamin E (100 mg/kg BW), beta-carotene (10 mg/kg BW), and vitamin E with beta-carotene (100 + 10 mg/kg BW, respectively) were orally administered by gavage alone or in combination. The tested doses were given to rats every other day (15 times). Results obtained showed that CdCl2 significantly (P < 0.05) induced free radicals in plasma, liver and brain. The activities of glutathione S-transferase (GST) (plasma and liver), alkaline phosphatase (AlP) (plasma and liver), aspartate aminotransferase (AST), alanine aminotransferase (ALT) (liver) and acetylcholinesterase (AChE) (plasma and brain) were significantly (P < 0.05) decreased due to CdCl2 administration, whereas, the activities of AST and ALT were increased in plasma. Treatment with CdCl2 caused a significant (P < 0.05) increase in glucose, urea, creatinine and bilirubin in plasma. On the other hand, results showed that CdCl2 significantly (P < 0.05) decreased plasma total protein (TP), albumin (A), blood hemoglobin (Hb), total erythrocytic count (TEC) and packed cell volume (PCV), while total leukocyte count (TLC) increased. Treatment with CdCl2 caused a significant (P < 0.05) decrease in sperm concentration, motility (%), weight of testes and epididymis, and increase in dead and abnormal sperm. Results demonstrated the beneficial influences of vitamin E, -carotene alone and/or in combination in reducing the harmful effects of CdCl2.

MeSH terms

  • Alanine Transaminase / blood
  • Alanine Transaminase / metabolism
  • Alkaline Phosphatase / blood
  • Alkaline Phosphatase / metabolism
  • Animals
  • Antioxidants / pharmacology*
  • Aspartate Aminotransferases / blood
  • Aspartate Aminotransferases / metabolism
  • Blood Cell Count
  • Brain / drug effects
  • Brain / enzymology
  • Cadmium / antagonists & inhibitors*
  • Cadmium / pharmacology*
  • Enzymes / blood
  • Free Radicals / metabolism
  • Glutathione Transferase / blood
  • Glutathione Transferase / metabolism
  • Lipid Peroxidation / drug effects*
  • Liver / drug effects
  • Liver / enzymology
  • Liver / metabolism
  • Male
  • Organ Size / drug effects
  • Rats
  • Rats, Sprague-Dawley
  • Semen / drug effects*
  • Sperm Motility / drug effects
  • Testis / drug effects
  • Testis / enzymology
  • Testis / metabolism
  • Thiobarbituric Acid Reactive Substances / metabolism
  • Vitamin E / pharmacology*
  • beta Carotene / pharmacology*

Substances

  • Antioxidants
  • Enzymes
  • Free Radicals
  • Thiobarbituric Acid Reactive Substances
  • Cadmium
  • beta Carotene
  • Vitamin E
  • Glutathione Transferase
  • Aspartate Aminotransferases
  • Alanine Transaminase
  • Alkaline Phosphatase