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Related Experiment Video

Updated: Jul 5, 2026

Behavioral Disturbances: An Innovative Approach to Monitor the Modulatory Effects of a Nutraceutical Diet
07:05

Behavioral Disturbances: An Innovative Approach to Monitor the Modulatory Effects of a Nutraceutical Diet

Published on: January 3, 2017

Potentially adverse interactions between haloperidol and valerian.

C L Dalla Corte1, R Fachinetto, D Colle

  • 1Universidade Federal de Santa Maria, Centro de Ciências Naturais e Exatas, Departamento de Química, Programa de Pós-graduação em Ciências Biológicas: Bioquímica Toxicológica, Camobi, Cep 97105-900, Santa Maria, RS, Brazil.

Food and Chemical Toxicology : an International Journal Published for the British Industrial Biological Research Association
|May 14, 2008
PubMed
Summary

This study investigated haloperidol (HP) and valerian interactions, finding they may cause adverse liver effects. Concomitant use increased oxidative stress and inhibited delta-aminolevulinate dehydratase (delta-ALA-D) in the liver.

Related Experiment Videos

Last Updated: Jul 5, 2026

Behavioral Disturbances: An Innovative Approach to Monitor the Modulatory Effects of a Nutraceutical Diet
07:05

Behavioral Disturbances: An Innovative Approach to Monitor the Modulatory Effects of a Nutraceutical Diet

Published on: January 3, 2017

Area of Science:

  • Pharmacology
  • Toxicology
  • Biochemistry

Background:

  • Haloperidol (HP) is an antipsychotic, and valerian is a herbal supplement.
  • Investigating potential drug-herb interactions is crucial for patient safety.
  • Oxidative stress and liver/kidney function are key indicators of drug toxicity.

Purpose of the Study:

  • To evaluate the impact of haloperidol (HP), valerian, and their combination on liver and kidney functions in rats.
  • To assess the effects on oxidative stress markers and specific enzyme activities.

Main Methods:

  • Rats were treated with HP, valerian, or both.
  • Liver and kidney functions were assessed by measuring oxidative stress parameters, enzyme activities (delta-ALA-D, AST, ALT), and reactive species.
  • Glutathione (GSH) levels, lipid peroxidation, and dichlorofluorescein (DCFH) were quantified.

Main Results:

  • Valerian alone had no significant effect on oxidative stress.
  • HP alone caused GSH depletion in the liver.
  • Combined HP and valerian increased hepatic lipid peroxidation, DCFH production, and inhibited hepatic delta-ALA-D activity.
  • Serum ALT levels were elevated in rats treated with HP and with the HP-valerian combination.

Conclusions:

  • Concomitant administration of haloperidol and valerian may lead to adverse hepatic effects, including oxidative stress.
  • Hepatic delta-aminolevulinate dehydratase (delta-ALA-D) inhibition and elevated ALT suggest potential liver toxicity from the combination.
  • These findings highlight the importance of considering potential adverse interactions between antipsychotics and herbal supplements.