Opioid-related changes in nociceptive threshold and in tissue levels of enkephalins after target disruption of the gene for neutral endopeptidase (EC 3.4.24.11) in mice

• Published in: Neuroscience letters 1997-09, Vol.234 (1), p.27-30
• Main Authors: Saria, A, Hauser, K.F, Traurig, H.H, Turbek, C.S, Hersh, L, Gerard, C
• Format: Article
• Language: English
• Subjects: Analgesics, Opioid - pharmacology; Animals; Biological and medical sciences; Enkephalin levels; Enkephalin, Leucine - metabolism; Enkephalin, Methionine - metabolism; Enkephalinase; Fundamental and applied biological sciences. Psychology; Hot plate test; Knockout mice; Mice; Mice, Knockout; Morphine - pharmacology; Neprilysin - genetics; Neutral endopeptidase; Pain Threshold; Phenotype; Somesthesis and somesthetic pathways (proprioception, exteroception, nociception); interoception; electrolocation. Sensory receptors; Temperature; Thermonociceptive threshold; Vertebrates: nervous system and sense organs
• ISSN: 0304-3940; 1872-7972
• DOI: 10.1016/S0304-3940(97)00660-5

Neutral endopeptidase EC 3.4.24.11 (NEP) is localized in peptidergic neurons and various colocalized peptides or other humoral mediators may serve as substrates. Target disruption of the NEP gene was reported to enhance the lethal response to endotoxin shock in mice. We examined thermonociceptive thresholds and enkephalin (ENK) tissue levels in transgenic NEP (−/−) and control wild type NEP (+/+) mice. Hot plate (52°C) latency was 13.1±1.4 s in NEP (+/+) mice ( n=16) while latency increased significantly ( P=0.031) to 17.7±1.6 s in NEP (−/−) mice. Naloxone (10 mg/kg) had no effect on hot plate latency in NEP (+/+) mice (12.5 s, n=8), but significantly decreased the latency in NEP (−/−) mice compared to untreated NEP (−/−) deficient mice (10.5 s, n=8). Morphine (3 or 10 mg/kg) analgesic response was similar in knockout mice and wild type mice. Methionine-ENK (MET-ENK) and leucine-ENK (LEU-ENK) levels were determined in extracts from cortex, brain stem, hypothalamus, striatum, spinal cord, trigeminal ganglion and heart in treated and untreated mice. ENK-levels varied in a regionally-dependent manner and were significantly decreased in hypothalamus and spinal cord. We conclude that deletion of the NEP gene results in an opioid-related increase in thermonociceptive threshold. Regional differences in opioid metabolism indicate that NEP evokes tissue-specific patterns of ENK-regulation. NEP selectively controls opioid biosynthesis in hypothalamus and spinal cord presumably by feedback regulation.