PAP and NT5E inhibit nociceptive neurotransmission by rapidly hydrolyzing nucleotides to adenosine

• Main Authors: Vihko Pirkko, Guillot Thomas S, Taylor-Blake Bonnie, Sowa Nathaniel A, Walsh Paul L, Street Sarah E, Wightman R Mark, Zylka Mark J
• Format: Article
• Language: English
• Published: SAGE Publishing 2011-10-01
• Series: Molecular Pain
• Subjects: pain; nociception; ectonucleotidase; adenosine; fast-scan cyclic voltammetry; field recordings
• Online Access: http://www.molecularpain.com/content/7/1/80

<p>Abstract</p> <p>Background</p> <p>Prostatic acid phosphatase (PAP) and ecto-5'-nucleotidase (NT5E, CD73) produce extracellular adenosine from the nucleotide AMP in spinal nociceptive (pain-sensing) circuits; however, it is currently unknown if these are the main ectonucleotidases that generate adenosine or how rapidly they generate adenosine.</p> <p>Results</p> <p>We found that AMP hydrolysis, when measured histochemically, was nearly abolished in dorsal root ganglia (DRG) neurons and lamina II of spinal cord from <it>Pap/Nt5e </it>double knockout (dKO) mice. Likewise, the antinociceptive effects of AMP, when combined with nucleoside transport inhibitors (dipyridamole or 5-iodotubericidin), were reduced by 80-100% in dKO mice. In addition, we used fast scan cyclic voltammetry (FSCV) to measure adenosine production at subsecond resolution within lamina II. Adenosine was maximally produced within seconds from AMP in wild-type (WT) mice but production was reduced >50% in dKO mice, indicating PAP and NT5E rapidly generate adenosine in lamina II. Unexpectedly, we also detected spontaneous low frequency adenosine transients in lamina II with FSCV. Adenosine transients were of short duration (<2 s) and were reduced (>60%) in frequency in <it>Pap</it>^<it>-/-</it>, <it>Nt5e</it>^<it>-/-</it> and dKO mice, suggesting these ectonucleotidases rapidly hydrolyze endogenously released nucleotides to adenosine. Field potential recordings in lamina II and behavioral studies indicate that adenosine made by these enzymes acts through the adenosine A₁ receptor to inhibit excitatory neurotransmission and nociception.</p> <p>Conclusions</p> <p>Collectively, our experiments indicate that PAP and NT5E are the main ectonucleotidases that generate adenosine in nociceptive circuits and indicate these enzymes transform pulsatile or sustained nucleotide release into an inhibitory adenosinergic signal.</p>