Effects of alpha-melanocortin enantiomers on acetaminophen-induced hepatotoxicity in CBA mice

Molecules. 2009 Dec 2;14(12):5017-26. doi: 10.3390/molecules14125017.

Abstract

Proteins and peptides in mammals are based exclusively on L-amino acids. Recent investigations show that D-amino acids exhibit physiological effects in vivo, despite of their very small quantities. We have investigated the hepatoprotective effects of the Land D-enantiomers of alpha-melanocortin peptide (alpha-MSH). The results showed that peptide-enantiomerism is related to the protective effects of melanocortin peptides in vivo. L-alpha-MSH exhibited potent hepatoprotective effect in the experimental model of acetaminophen induced hepatotoxicity in male CBA mice, while its D-mirror image was inefficient. Furthermore, the antibody to the L-peptide did not recognize the D-structure. The results indicate that the opposite peptide configuration may be used to modulate its function and metabolism in vivo and in vitro.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acetaminophen / toxicity*
  • Animals
  • Circular Dichroism
  • Liver / drug effects*
  • Melanocortins / chemistry
  • Melanocortins / pharmacology*
  • Mice
  • Mice, Inbred CBA
  • Stereoisomerism

Substances

  • Melanocortins
  • Acetaminophen