Peripheral benzodiazepine receptor expression on leukocytes and neutrophil function during anticonvulsant monotherapy

Pharmacology. 1998 Oct;57(4):215-21. doi: 10.1159/000028244.

Abstract

Epileptic patients on long-term therapy with a single anticonvulsant showed enhanced expression of peripheral benzodiazepine receptors (pBZrs) on neutrophils, monocytes and lymphocytes. N-Formyl-methionyl-leucyl-phenylalanine-induced chemotaxis was significantly impaired in neutrophils from patients on carbamazepine (p < 0.01 vs. controls). Neutrophils from patients on phenytoin had enhanced phorbol myristate acetate-stimulated O-2 production (p < 0. 01 vs. controls) and neutrophils from patients on valproic acid had impaired phagocytosis frequency and Staphylococcus aureus lethality index (p < 0.01 vs. controls). Overexpression of pBZrs on leukocytes may reflect the clinical response to anticonvulsants and may play a role in the immunological effects of some of these drugs.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Adult
  • Aged
  • Anticonvulsants / pharmacology
  • Anticonvulsants / therapeutic use*
  • Carbamazepine / pharmacology
  • Carbamazepine / therapeutic use
  • Epilepsy / drug therapy*
  • Epilepsy / immunology
  • Epilepsy / pathology
  • Female
  • Humans
  • Leukocytes / drug effects
  • Leukocytes / metabolism
  • Leukocytes / physiology*
  • Lymphocytes / drug effects
  • Lymphocytes / physiology
  • Male
  • Middle Aged
  • Neutrophils / drug effects
  • Neutrophils / metabolism
  • Neutrophils / physiology*
  • Phenytoin / pharmacology
  • Phenytoin / therapeutic use
  • Receptors, GABA-A / biosynthesis*
  • Receptors, GABA-A / physiology
  • Valproic Acid / pharmacology
  • Valproic Acid / therapeutic use

Substances

  • Anticonvulsants
  • Receptors, GABA-A
  • Carbamazepine
  • Valproic Acid
  • Phenytoin