Nociceptin inhibits the neurogenic vasopressor response in the pithed rat via prejunctional ORL₁ receptors

Abstract.

Nociceptin (or orphanin FQ), the endogenous ligand for the opioid receptor-like 1 (ORL₁) receptor, decreases blood pressure in the conscious and anesthetized rat. This study examined whether prejunctional inhibitory ORL₁ receptors located on the postganglionic sympathetic neurons innervating the resistance vessels are detectable in pithed rats.

In pithed and vagotomized rats electrical stimulation of the preganglionic sympathetic nerve fibers, injection of nicotine (2 µmol/kg) or noradrenaline (1 nmol/kg) increased blood pressure by about 30 mmHg. The electrically induced vasopressor response was decreased dose-dependently by nociceptin (0.001–1 µmol/kg; decrease by about 60% at 1 µmol/kg). Nociceptin 0.1 µmol/kg reduced the nicotine-induced vasopressor response by about 40% but at doses up to 1 µmol/kg failed to affect the increase in blood pressure evoked by noradrenaline. The inhibitory action of nociceptin on the electrically and nicotine-induced increase in blood pressure was attenuated by the ORL₁ receptor antagonists naloxone benzoylhydrazone (5 µmol/kg) and/or [Phe¹Ψ(CH₂-NH)Gly²]-nociceptin(1-13)NH₂ (1 µmol/kg) but was not affected by naloxone 10 µmol/kg.

In conclusion, the present data suggest that the postganglionic sympathetic nerve fibers innervating the resistance vessels of the rat are endowed with prejunctional ORL₁ receptors, activation of which causes inhibition of noradrenaline release.