Synthesis of N pi-methylhistamine and N alpha-methylhistamine by purified rabbit lung indolethylamine N-methyltransferase

J Biol Chem. 1985 Oct 5;260(22):12336-40.

Abstract

N tau-Methylhistamine is a major inactive metabolite of histamine and is formed by histamine N-methyltransferase (EC 2.1.1.8). However, a controversy exists concerning the presence of other N-methylated histamines, such as N pi- and N alpha-methylhistamine in mammalian tissues. Indolethylamine N-methyltransferase is present in mammalian tissues with the rabbit lung containing the highest concentration, but the physiologic function of this enzyme remains unclear. Using rabbit lung as a tissue source, we purified indolethylamine N-methyltransferase 260-fold and separated it completely from histamine N-methyltransferase. Histamine was a substrate for purified indolethylamine N-methyltransferase and unlike histamine N-methyltransferase which exclusively formed N tau-methylhistamine, indolethylamine N-methyltransferase catalyzed the in vitro formation of both N pi-methylhistamine and N alpha-methylhistamine. In contrast to histamine N-methyltransferase, indolethylamine N-methyltransferase activity was not inhibited by either high histamine concentrations or by quinacrine. Thus, mammalian tissues contain an enzyme capable of forming N pi-methylhistamine and N alpha-methylhistamine. This supports the concept of the existence of these compounds and suggests they may serve a physiologic function in mammals.

MeSH terms

  • Animals
  • Histamine / metabolism
  • Kinetics
  • Lung / enzymology*
  • Methylation
  • Methylhistamines / biosynthesis*
  • Methyltransferases / isolation & purification
  • Methyltransferases / metabolism*
  • Quinacrine / pharmacology
  • Rabbits

Substances

  • Methylhistamines
  • 3-methylhistamine
  • Histamine
  • Methyltransferases
  • indoleethylamine N-methyltransferase
  • Quinacrine