Allelic and somatic variations in the endogenous opioid system of humans

Pharmacol Ther. 2001 Sep;91(3):167-77. doi: 10.1016/s0163-7258(01)00154-1.

Abstract

People with a genetic predisposition for substance abuse have defects in genes for the opioid peptides and receptors. A high number of polymorphisms have been detected in the mu-opioid receptor, some of which result in pharmacological alterations. The opioid peptide proopiomelanocortin proved extraordinarily rich in mutations that often lead to severe phenotypical consequences. Prodynorphin displays a polymorphic regulation of transcription. Variants of the mu- and the delta-opioid receptor showed positive associations with opiate and/or alcohol addiction in some studies. However, these associations were weak, indicating a small contribution of the opioid system to these disorders.

Publication types

  • Review

MeSH terms

  • Alleles
  • Enkephalins / genetics
  • Enkephalins / pharmacology
  • Genetic Predisposition to Disease*
  • Humans
  • Polymorphism, Genetic*
  • Protein Precursors / genetics
  • Protein Precursors / pharmacology
  • Receptors, Opioid, delta / genetics*
  • Receptors, Opioid, delta / physiology
  • Receptors, Opioid, kappa / genetics*
  • Receptors, Opioid, kappa / physiology
  • Receptors, Opioid, mu / genetics*
  • Receptors, Opioid, mu / physiology
  • Substance-Related Disorders / genetics*
  • beta-Endorphin / genetics
  • beta-Endorphin / pharmacology

Substances

  • Enkephalins
  • Protein Precursors
  • Receptors, Opioid, delta
  • Receptors, Opioid, kappa
  • Receptors, Opioid, mu
  • proenkephalin
  • beta-Endorphin
  • preproenkephalin