Isolation and structural determination of the first 8-epi-type tetrodotoxin analogs from the newt, Cynops ensicauda popei, and comparison of tetrodotoxin analogs profiles of this newt and the puffer fish, Fugu poecilonotus

Mar Drugs. 2012 Mar;10(3):655-667. doi: 10.3390/md10030655. Epub 2012 Mar 22.

Abstract

Identification of new tetrodotoxin (TTX) analogs from TTX-possessing animals might provide insight into its biosynthesis and metabolism. In this study, four new analogs, 8-epi-5,6,11-trideoxyTTX, 4,9-anhydro-8-epi-5,6,11-trideoxyTTX, 1-hydroxy-8-epi-5,6,11-trideoxyTTX, and 1-hydroxy-4,4a-anhydro-8-epi-5,6,11-trideoxyTTX, were isolated from the newt, Cynops ensicauda popei, and their structures were determined using spectroscopic methods. These are the first 8-epi-type analogs of TTX that have been found in a natural source. Furthermore, we examined the composition of the TTX analogs in this newt and in the ovary of the puffer fish, Fugu poecilonotus, using LC/MS. The results indicate that TTX and 11-deoxyTTX were present in both sources. However, 6-epiTTX and 8-epi-type analogs were detected only in the newt, while 5,6,11-trideoxyTTX was a specific and major analog in the puffer fish. Such considerable differences among analog compositions might reflect differences in the biosynthesis or metabolism of TTX between these animals.

Keywords: 8-epi-5,6,11-trideoxytetrodotoxin; LC/MS; newt; puffer fish; tetrodotoxin.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Aquatic Organisms
  • Chromatography, High Pressure Liquid
  • Indicators and Reagents
  • Magnetic Resonance Spectroscopy
  • Mass Spectrometry
  • Salamandridae / metabolism*
  • Species Specificity
  • Spectrometry, Mass, Fast Atom Bombardment
  • Takifugu / metabolism*
  • Tetrodotoxin / analogs & derivatives*
  • Tetrodotoxin / biosynthesis
  • Tetrodotoxin / chemistry*

Substances

  • Indicators and Reagents
  • Tetrodotoxin