Regional distribution and age-dependent expression of N-acylphosphatidylethanolamine-hydrolyzing phospholipase D in rat brain

J Neurochem. 2005 Aug;94(3):753-62. doi: 10.1111/j.1471-4159.2005.03234.x. Epub 2005 Jun 30.

Abstract

The endocannabinoid anandamide (N-arachidonoylethanolamine) and other bioactive long-chain N-acylethanolamines are thought to be formed from their corresponding N-acylphosphatidylethanolamines by a specific phospholipase D (NAPE-PLD) in the brain as well as other tissues. However, regional distribution of NAPE-PLD in the brain has not been examined. In the present study, we investigated the expression levels of NAPE-PLD in nine different regions of rat brain by enzyme assay, western blotting and real-time PCR. The NAPE-PLD activity was detected in all the tested brain regions with the highest activity in thalamus. Similar distribution patterns of NAPE-PLD were observed at protein and mRNA levels. We also found a remarkable increase in the expression levels of protein and mRNA of the brain NAPE-PLD with development, which was in good agreement with the increase in the activity. The age-dependent increase was also seen with several brain regions and other NAPE-PLD-enriched organs (heart and testis). p-Chloromercuribenzoic acid and cetyltrimethylammonium chloride, which inhibited recombinant NAPE-PLD dose-dependently, strongly inhibited the enzyme of all the brain regions. These results demonstrated wide distribution of NAPE-PLD in various brain regions and its age-dependent expression, suggesting the central role of this enzyme in the formation of anandamide and other N-acylethanolamines in the brain.

Publication types

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

MeSH terms

  • Age Factors
  • Aging / physiology*
  • Animals
  • Animals, Newborn
  • Blotting, Western / methods
  • Brain / anatomy & histology
  • Brain / enzymology*
  • Brain Chemistry / physiology
  • COS Cells
  • Cetrimonium
  • Cetrimonium Compounds / metabolism
  • Chlorocebus aethiops
  • Gene Expression Regulation, Enzymologic / physiology*
  • Male
  • Phosphatidylethanolamines / genetics
  • Phosphatidylethanolamines / metabolism*
  • Phospholipase D / genetics
  • Phospholipase D / metabolism*
  • Rats
  • Recombinant Proteins / metabolism
  • Reverse Transcriptase Polymerase Chain Reaction / methods
  • Subcellular Fractions / enzymology
  • p-Chloromercuribenzoic Acid / metabolism

Substances

  • Cetrimonium Compounds
  • Phosphatidylethanolamines
  • Recombinant Proteins
  • p-Chloromercuribenzoic Acid
  • Phospholipase D
  • Cetrimonium