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COMPLEX FUNCTION OF THE CENTRAL NERVOUS SYSTEM, SLEEP AND LOCOMOTION

Lactoferrin enhances opioid-mediated analgesia via nitric oxide in the rat spinal cord

¹Department of Veterinary Physiology, Faculty of Agriculture, Tottori University, Tottori 680-0945; and ²Nuclear Receptor Ligand Co. Ltd., Kawasaki, Kanagawa 213-0012, Japan

Submitted 16 December 2002 ; accepted in final form 11 April 2003

Lactoferrin (LF) is a multifunctional protein that is found in milk, neutrophils, and other biological fluids, and its receptors have also been identified in the central nervous system. Recently, we found that bovine milk-derived LF (BLF) produced analgesia via a µ-opioid receptor-mediated response in the spinal cord. However, the precise mechanism of this analgesic effect remains unclear. In this study, spinally applied BLF produced analgesia that was reversed by coadministration with a nitric oxide (NO) synthase inhibitor, N^G-nitro-L-arginine methyl ester, during phases 1 and 2 in the formalin test. Spinal coadministration of a µ-opioid receptor agonist, morphine, with a subeffective dose of BLF produced a much more highly potentiated analgesia than that produced by morphine alone during phases 1 and 2 in the formalin test. This potentiated analgesia by morphine with BLF was reversed by a µ-opioid receptor antagonist, D-Phe-Cys-Tyr-D-Trp-Orn-Thr-NH₂, or by N^G-nitro-L-arginine methyl ester. In the tail-flick test, continuous spinal infusion of morphine via an osmotic minipump over 6 days resulted in development of tolerance by day 4, but no tolerance of BLF was observed throughout the experiment. These results suggest that BLF acts as an enhancer of the spinal opioidergic system via an NO-mediated mechanism.

formalin test; tail-flick test; N^G-nitro-L-arginine methyl ester; D-Phe-Cys-Tyr-D-Trp-Orn-Thr-NH₂; tolerance

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