Formation of heterocyclic amines using model systems

Mutat Res. 1991 Mar-Apr;259(3-4):219-33. doi: 10.1016/0165-1218(91)90119-7.

Abstract

Initially, modeling was used to identify the mutagenic heterocyclic amines and their precursors. Major precursors have been shown to be single amino acids or amino acids together with creatine or creatinine. There is also evidence that Maillard reactions are involved since heating sugar and amino acids together with creatine or creatinine has been shown to produce several of the mutagenic heterocyclic amines, especially the aminoimidazoazaarenes (AIA compounds), e.g., IQ, MeIQ, MeIQx, DiMeIQx and PhIP. Due to a low yield in the model systems, the mechanisms behind the formation of the mutagenic heterocyclic amines are still unclear and need further substantiation. The fact that some AIA compounds are also produced in the absence of sugar casts some doubts on an obligatory participation of the Maillard reaction; alternative routes might exist. Further work using isotopically labeled precursors needs to be done and so far such work has only been performed for PhiP. The formation of mutagenic heterocyclic amines is dependent on time, temperature, pH, concentration of the precursors, type of amino acid, and the presence of certain divalent ions. Water may have an impact both as a temperature regulator and as a solvent medium for the reactants.

Publication types

  • Review

MeSH terms

  • Amines / chemical synthesis
  • Amines / chemistry*
  • Amines / toxicity
  • Animals
  • Heterocyclic Compounds / chemical synthesis
  • Heterocyclic Compounds / chemistry*
  • Heterocyclic Compounds / toxicity
  • Hot Temperature
  • Imidazoles / chemistry
  • Maillard Reaction
  • Models, Chemical
  • Mutagens / chemical synthesis
  • Mutagens / chemistry*
  • Quinolines / chemistry
  • Quinoxalines / chemistry

Substances

  • Amines
  • Heterocyclic Compounds
  • Imidazoles
  • Mutagens
  • Quinolines
  • Quinoxalines