Potentiation of morphine-induced mechanical antinociception by sigma(1) receptor inhibition: Role of peripheral sigma(1) receptors

作者：Sanchez Fernandez Cristina; Rafael Nieto Francisco; Gonzalez Cano Rafael; Artacho Cordon Antonia; Romero Lucia; Montilla Garcia Angeles; Zamanillo Daniel; Manuel Baeyens Jose; Manuel Entrena Jose; Jose Cobos Enrique

来源：Neuropharmacology, 2013, 70: 348-358.

DOI：10.1016/j.neuropharm.2013.03.002

• Sigma-1 (sigma(1)) receptors
• Morphine
• Pain
• Peripheral antinociception
• Hyperlocomotion
• Gastrointestinal transit

We studied the modulation of morphine-induced mechanical antinociception and side effects by sigma(1) receptor inhibition. Both wild-type (WT) and sigma(1) receptor knockout (sigma(1)-KO) mice showed similar responses to paw pressure (100-600 g). The systemic (subcutaneous) or local (intraplantar) administration of sigma(1) antagonists (BD-1063, BD-1047, NE-100 and Si RA) was devoid of antinociceptive effects in WT mice. However, sigma(1)-KO mice exhibited an enhanced mechanical antinociception in response to systemic morphine (1-16 mg/kg). Similarly, systemic treatment of WT mice with sigma(1) antagonists markedly potentiated morphine-induced antinociception, and its effects were reversed by the selective sigma(1) agonist PRE-084. Although the local administration of morphine (50-200 mu g) was devoid of antinociceptive effects in WT mice, it induced dose-dependent antinociception in sigma(1)-KO mice. This effect was limited to the injected paw. Enhancement of peripheral morphine antinociception was replicated in WT mice locally co-administered with sigma(1) antagonists and the opioid. None of the sigma(1) antagonists tested enhanced morphine-antinociception in sigma(1)-KO mice, confirming a sigma(1)-mediated action. Morphine-induced side-effects (hyperlocomotion and inhibition of gastrointestinal transit) were unaltered in sigma(1)-KO mice. These results cannot be explained by a direct interaction of sigma(1) ligands with mu-opioid receptors or adaptive changes of mu-receptors in sigma(1)-KO mice, given that [H-3]DAMGO binding in forebrain, spinal cord, and hind-paw skin membranes was unaltered in mutant mice, and none of the sigma(1) drugs tested bound to mu-opioid receptors. These results show that sigma(1) receptor inhibition potentiates morphine-induced mechanical analgesia but not its acute side effects, and that this enhanced analgesia can be induced at peripheral level.

• 出版日期2013-7