• Am. J. Physiol. Regul. Integr. Comp. Physiol. · Aug 2003

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

    • Ken-ichiro Hayashida, Takashi Takeuchi, Hirohiko Shimizu, Kunio Ando, and Etsumori Harada.
    • Department of Veterinary Physiology, Faculty of Agriculture, Tottori University, Tottori 680-0945, Japan.
    • Am. J. Physiol. Regul. Integr. Comp. Physiol. 2003 Aug 1; 285 (2): R306-12.

    AbstractLactoferrin (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 mu-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, NG-nitro-l-arginine methyl ester, during phases 1 and 2 in the formalin test. Spinal coadministration of a mu-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 mu-opioid receptor antagonist, d-Phe-Cys-Tyr-d-Trp-Orn-Thr-NH2, or by NG-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.

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