Role of thalamic ventral posterolateral nucleus histamine H2 and opiate receptors in modulation of formalin-induced muscle pain in rats

• Published in: Pharmacological reports 2017-12, Vol.69 (6), p.1393-1401
• Main Authors: Ghasemi, Hamid, Tamaddonfard, Esmaeal, Soltanalinejad, Farhad
• Format: Article
• Language: English
• Subjects: Drug Safety and Pharmacovigilance; Histamine; Histamine H2 receptor; Muscle pain; Opiate receptor; Original Article; Pharmacotherapy; Pharmacy; Thalamic ventral posterolateral nucleus
• ISSN: 1734-1140; 2299-5684
• DOI: 10.1016/j.pharep.2017.05.001

•Intramuscular injection of formalin produced paw licking and paw flinching.•Ranitidine prevented histamine-, dimaprit- and morphine-antinociception.•Naloxone blocked morphine-, histamine-, and dimaprit-induced antinociception.•Histamine H2 and opiate receptors modulate muscle pain at the PVL level. Histamine and opiate systems contribute to supraspinal processing of pain. In the present study, we investigated the effects of microinjection of histamine and agonists and antagonists of histamine H2 and opiate receptors into the thalamic ventral posterolateral nucleus on muscle pain in rats. The thalamic ventral posterolateral nuclei were bilaterally implanted with two guide cannulas. Muscle pain was induced by intramuscular injection of a diluted formalin solution (2.5%, 50μl) into the belly of gastrocnemius muscle, and pain-related behaviors including paw licking duration and paw flinching number were recorded at five-min blocks for 60min. Formalin produced a biphasic pattern of pain-related behaviors. Ranitidine (a histamine H2 receptor antagonist) alone did not affect pain intensity, whereas it prevented the antinociceptive activities of histamine, dimaprit (a histamine H2 receptor agonist) and morphine (an opiate receptor agonist). Naloxone (an opiate receptor antagonist) alone increased pain, and inhibited histamine-, dimaprit-, and morphine-induced antinociception. Locomotor activity was not changed with these chemicals. Our results showed an interaction between histamine H2 and opiate receptors at the thalamic ventral posterolateral nucleus in modulation of muscle pain.