Pharmacological characterization of grooming induced by a selective NK-1 tachykinin receptor agonist

Abstract

Bilateral intranigral administration of the selective NK-1 tachykinin receptor agonist [AcArg 6, Sar 9, Met(O 2) 11]SP 6–11 (0–11 nmol total bilateral dose) selectively induced grooming in rats. This response was blocked by concurrent intranigral administration of the NK-1 tachykinin receptor antagonist RP 67580 (2 nmol), but not by NK-2 (L-659, 877) or NK-3 ([Trp 7, β-Ala 8]NKA 4–10) antagonists. Pretreatment with systemic opioid (naloxone 1.5 mg/kg) and D 1 dopamine (SCH 23390 100 μg/kg) receptor antagonists also attenuated tachykinin-induced grooming, which was unaffected by D 2 dopamine (sulpiride 30 mg/kg) or 5-HT 2A+C (ritanserin 2 mg/kg) antagonists. Grooming induced by intranigral [AcArg 6, Sar 9, Met(O 2) 11]SP 6–11 was also attenuated by bilateral 6-hydroxydopamine lesions of te substantia nigra. These findings indicate that grooming induced by intranigral tachykinins reflects activation of NK-1 receptors and is dependent upon endogenous dopamine and consequent selective stimulation of D 1 dopamine receptors.