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Toxicity of mixtures of parathion, toxaphene and/or 2,4-D in mice

D J Kuntz1, N G Rao, I E Berg

  • 1Department of Pharmaceutical Sciences/Toxicology, North Dakota State University College of Pharmacy, Fargo 58105.

Insights

Mixtures of parathion, toxaphene, and 2,4-D reduced weight gain in mice. Parathion inhibited cholinesterase, while toxaphene and 2,4-D showed varied effects on enzyme activity and liver health.

Area of Science:

  • Toxicology
  • Environmental Health
  • Biochemistry

Background:

  • Agricultural chemicals (ACs) like parathion (PA), toxaphene (TOX), and 2,4-dichlorophenoxyacetic acid (2,4-D) are widely used.
  • Understanding the toxicity of individual ACs and their mixtures is crucial for risk assessment.

Purpose of the Study:

  • To investigate the toxicity of PA, TOX, and 2,4-D, individually and in mixtures, in ICR male mice.
  • To assess the effects on body weight, cholinesterase (ChE) activity, liver enzymes, and histopathology.

Main Methods:

  • Male ICR mice were administered PA, TOX, and/or 2,4-D via oral intubation daily for 14 days.
  • Animals were monitored for body weight changes, ChE activity (serum and brain), serum glutamic pyruvic transaminase (SGPT), and liver/body weight ratio.
  • Histopathological examination of brain and liver tissues was performed. Pentobarbital-induced sleep was also assessed.

Main Results:

  • Body weight gain was reduced by individual ACs and their mixtures.
  • Parathion significantly inhibited serum and brain ChE activity.
  • Toxaphene initially inhibited serum ChE but later increased its activity, with minimal brain ChE effects. 2,4-D increased serum ChE but decreased brain ChE.
  • SGPT levels increased in TOX, 2,4-D, and mixture groups. TOX and mixtures increased liver/body weight ratio and reduced pentobarbital-induced sleep time.

Conclusions:

  • The study highlights the differential toxicological effects of PA, TOX, and 2,4-D on mice.
  • Mixtures exhibited complex interactions, affecting body weight, enzyme activities, and physiological responses.
  • No significant pathological changes were observed at the light microscopic level, suggesting sub-acute toxicity profiles.

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