Lead induced disorders in hematopoietic and drug metabolizing enzyme system and their protection by ascorbic acid supplementation

Biomed Environ Sci. 1998 Mar;11(1):7-14.

Abstract

Effect of vitamin C supplementation in restoring lead induced alterations in hematopoietic system and drug metabolizing enzymes were investigated in male rats. Intraperitoneal administration of 20 mg/kg lead produced a significant inhibition of heme synthesis in blood and liver and drug metabolism in liver. Toxic insult by lead also resulted into a marked decline in tissue thiols and vitamin C levels. Oral supplementation of vitamin C (100 mg/kg for 3 days) completely restored blood delta aminolevulinic acid dehydratase, uroporphyrinogen I synthetase and a few drug metabolizing enzymes. Level of vitamin C and sulfhydryl contents too recovered to a great extent. A marked reduction in blood and liver lead concentration occurred on vitamin C supplementation although renal lead contents were marginally reduced in lead exposed animals. The results, thus, indicate a significant protective action of vitamin C against toxic effects of lead on heme synthesis and drug metabolism.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Administration, Oral
  • Aniline Hydroxylase / blood
  • Animals
  • Ascorbic Acid / administration & dosage
  • Ascorbic Acid / metabolism
  • Ascorbic Acid / pharmacology*
  • Hematopoiesis / drug effects
  • Heme / biosynthesis*
  • Hydroxymethylbilane Synthase / blood
  • Kidney / drug effects
  • Kidney / enzymology
  • Lead / blood
  • Lead / toxicity*
  • Lead Poisoning / blood
  • Lead Poisoning / enzymology*
  • Liver / drug effects*
  • Liver / enzymology
  • Male
  • Microsomes, Liver / drug effects
  • Microsomes, Liver / enzymology
  • Mixed Function Oxygenases / metabolism
  • Porphobilinogen Synthase / blood
  • Rats
  • Sulfhydryl Compounds / metabolism

Substances

  • Sulfhydryl Compounds
  • Lead
  • Heme
  • Mixed Function Oxygenases
  • Aniline Hydroxylase
  • Hydroxymethylbilane Synthase
  • Porphobilinogen Synthase
  • Ascorbic Acid