LC-MS Profiling of Kakkonto and Identification of Ephedrine as a Key Component for Its Anti-Glycation Activity

Molecules. 2023 May 29;28(11):4409. doi: 10.3390/molecules28114409.

Abstract

A total of 147 oral Kampo prescriptions, which are used clinically in Japan, were evaluated for their anti-glycation activity. Kakkonto demonstrated significant anti-glycation activity, prompting further analysis of its chemical constituents using LC-MS, which revealed the presence of two alkaloids, fourteen flavonoids, two but-2-enolides, five monoterpenoids, and four triterpenoid glycosides. To identify the components responsible for its anti-glycation activity, the Kakkonto extract was reacted with glyceraldehyde (GA) or methylglyoxal (MGO) and analyzed using LC-MS. In LC-MS analysis of Kakkonto reacted with GA, the peak intensity of ephedrine was attenuated, and three products from ephedrine-scavenging GA were detected. Similarly, LC-MS analysis of Kakkonto reacted with MGO revealed two products from ephedrine reacting with MGO. These results indicated that ephedrine was responsible for the observed anti-glycation activity of Kakkonto. Ephedrae herba extract, which contains ephedrine, also showed strong anti-glycation activity, further supporting ephedrine's contribution to Kakkonto's reactive carbonyl species' scavenging ability and anti-glycation activity.

Keywords: Kakkonto; Kampo; advanced glycation end products; anti-glycation activity; ephedrine.

MeSH terms

  • Chromatography, Liquid
  • Drugs, Chinese Herbal*
  • Ephedrine* / analysis
  • Ephedrine* / pharmacology
  • Glycation End Products, Advanced / analysis
  • Magnesium Oxide
  • Pyruvaldehyde
  • Tandem Mass Spectrometry

Substances

  • kakkon-to
  • Ephedrine
  • Magnesium Oxide
  • Drugs, Chinese Herbal
  • Pyruvaldehyde
  • Glycation End Products, Advanced

Grants and funding

This research received no external funding.