PMID- 19556004 OWN - NLM STAT- MEDLINE DCOM- 20091014 LR - 20131121 IS - 1532-2785 (Electronic) IS - 0143-4179 (Linking) VI - 43 IP - 4 DP - 2009 Aug TI - Involvement of neuropeptide Y in the acute, chronic and withdrawal responses of morphine in nociception in neuropathic rats: behavioral and neuroanatomical correlates. PG - 303-14 LID - 10.1016/j.npep.2009.05.003 [doi] AB - Although morphine is a potent antinociceptive agent, its chronic use developed tolerance in neuropathic pain (NP). Furthermore, opioid antagonist naloxone attenuated the antinociceptive effect of neuropeptide Y (NPY). The present study investigated the role of NPY and NPY Y1/Y5 receptors in acute and chronic actions of morphine in neuropathic rats using thermal paw withdrawal test and immunocytochemistry. In acute study, intracerebroventricular (icv) administration of morphine, NPY or NPY Y1/Y5 receptors agonist [Leu(31),Pro(34)]-NPY produced antinociception, whereas selective NPY Y1 receptors antagonist BIBP3226 caused hyperalgesia. While NPY or [Leu(31),Pro(34)]-NPY potentiated, BIBP3226 attenuated morphine induced antinociception. Chronic icv infusion of morphine via osmotic minipumps developed tolerance to its antinociceptive effect, and produced hyperalgesia following withdrawal. However, co-administration of NPY or [Leu(31),Pro(34)]-NPY prevented the development of tolerance and withdrawal hyperalgesia. Sciatic nerve ligation resulted in significant increase in the NPY-immunoreactive (NPY-ir) fibers in ventrolateral periaqueductal gray (VLPAG) and locus coeruleus (LC); fibers in the dorsal part of dorsal raphe nucleus (DRD) did not respond. While chronic morphine treatment significantly reduced NPY-ir fibers in VLPAG and DRD, morphine withdrawal triggered significant augmentation in NPY-immunoreactivity in the VLPAG. NPY-immunoreactivity profile of LC remained unchanged in all the morphine treatment conditions. Furthermore, removal of sciatic nerve ligation reversed the effects of NP, increased pain threshold and restored NPY-ir fiber population in VLPAG. NPY, perhaps acting via Y1/Y5 receptors, might profoundly influence the processing of NP information and interact with the endogenous opioid system primarily within the framework of the VLPAG. FAU - Upadhya, Manoj A AU - Upadhya MA AD - Department of Pharmaceutical Sciences, Rashtrasant Tukadoji Maharaj Nagpur University Campus, Nagpur 440 033, India. FAU - Dandekar, Manoj P AU - Dandekar MP FAU - Kokare, Dadasaheb M AU - Kokare DM FAU - Singru, Praful S AU - Singru PS FAU - Subhedar, Nishikant K AU - Subhedar NK LA - eng PT - Journal Article PT - Research Support, Non-U.S. Gov't DEP - 20090624 PL - Netherlands TA - Neuropeptides JT - Neuropeptides JID - 8103156 RN - 0 (Analgesics, Opioid) RN - 0 (BIBP 3226) RN - 0 (Neuropeptide Y) RN - 0 (Receptors, Neuropeptide Y) RN - 76I7G6D29C (Morphine) RN - 94ZLA3W45F (Arginine) SB - IM MH - Analgesics, Opioid/*therapeutic use MH - Animals MH - Arginine/analogs & derivatives/metabolism MH - Behavior, Animal/*physiology MH - Drug Tolerance MH - Hyperalgesia/*drug therapy/physiopathology MH - Male MH - Morphine/*therapeutic use MH - Neuropeptide Y/chemistry/*metabolism MH - Pain Measurement MH - Peripheral Nervous System Diseases/pathology/physiopathology MH - Random Allocation MH - Rats MH - Rats, Sprague-Dawley MH - Receptors, Neuropeptide Y/agonists/antagonists & inhibitors/*metabolism MH - Sciatic Nerve/pathology/physiopathology MH - Substance Withdrawal Syndrome/*physiopathology EDAT- 2009/06/27 09:00 MHDA- 2009/10/15 06:00 CRDT- 2009/06/27 09:00 PHST- 2009/02/04 00:00 [received] PHST- 2009/05/14 00:00 [revised] PHST- 2009/05/20 00:00 [accepted] PHST- 2009/06/27 09:00 [entrez] PHST- 2009/06/27 09:00 [pubmed] PHST- 2009/10/15 06:00 [medline] AID - S0143-4179(09)00049-3 [pii] AID - 10.1016/j.npep.2009.05.003 [doi] PST - ppublish SO - Neuropeptides. 2009 Aug;43(4):303-14. doi: 10.1016/j.npep.2009.05.003. Epub 2009 Jun 24.