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Journal Abstract Search

139 related items for PubMed ID: 8131071

  • 1. The nature of conditioned anti-analgesia: spinal cord opiate and anti-opiate neurochemistry.
    Wiertelak EP, Yang HY, Mooney-Heiberger K, Maier SF, Watkins LR.
    Brain Res; 1994 Jan 21; 634(2):214-26. PubMed ID: 8131071
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  • 2. Reversal of spinal cord non-opiate analgesia by conditioned anti-analgesia in the rat.
    Watkins LR, McGorry M, Schwartz B, Sisk D, Wiertelak EP, Maier SF.
    Pain; 1997 Jul 21; 71(3):237-47. PubMed ID: 9231866
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  • 9. Heroin acts on different opioid receptors than morphine in Swiss Webster and ICR mice to produce antinociception.
    Rady JJ, Roerig SC, Fujimoto JM.
    J Pharmacol Exp Ther; 1991 Feb 21; 256(2):448-57. PubMed ID: 1847196
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  • 10. Dynorphinergic mechanism mediating endomorphin-2-induced antianalgesia in the mouse spinal cord.
    Wu HE, Sun HS, Darpolar M, Leitermann RJ, Kampine JP, Tseng LF.
    J Pharmacol Exp Ther; 2003 Dec 21; 307(3):1135-41. PubMed ID: 14557378
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  • 11. Evidence for delta opioid receptor subtypes in rat spinal cord: studies with intrathecal naltriben, cyclic[D-Pen2, D-Pen5] enkephalin and [D-Ala2, Glu4]deltorphin.
    Stewart PE, Hammond DL.
    J Pharmacol Exp Ther; 1993 Aug 21; 266(2):820-8. PubMed ID: 8394918
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  • 13. Streptozotocin-induced diabetes selectively alters the potency of analgesia produced by mu-opioid agonists, but not by delta- and kappa-opioid agonists.
    Kamei J, Ohhashi Y, Aoki T, Kawasima N, Kasuya Y.
    Brain Res; 1992 Feb 07; 571(2):199-203. PubMed ID: 1319265
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  • 14. Antinociception and delta-1 opioid receptors in the rat spinal cord: studies with intrathecal 7-benzylidenenaltrexone.
    Hammond DL, Stewart PE, Littell L.
    J Pharmacol Exp Ther; 1995 Sep 07; 274(3):1317-24. PubMed ID: 7562504
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  • 15. Role of mu 1-opiate receptors in supraspinal opiate analgesia: a microinjection study.
    Bodnar RJ, Williams CL, Lee SJ, Pasternak GW.
    Brain Res; 1988 Apr 26; 447(1):25-34. PubMed ID: 2838129
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  • 16. The antinociception produced by intrathecal morphine, calcium, A23187, U50,488H, [D-Ala2, N-Me-Phe4, Gly-ol]enkephalin and [D-Pen2, D-Pen5]enkephalin after intrathecal administration of calcitonin gene-related peptide in mice.
    Welch SP, Singha AK, Dewey WL.
    J Pharmacol Exp Ther; 1989 Oct 26; 251(1):1-8. PubMed ID: 2552070
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  • 17. Selective antagonism by naltrindole of the antinociceptive effects of the delta opioid agonist cyclic[D-penicillamine2-D-penicillamine5]enkephalin in the rat.
    Drower EJ, Stapelfeld A, Rafferty MF, de Costa BR, Rice KC, Hammond DL.
    J Pharmacol Exp Ther; 1991 Nov 26; 259(2):725-31. PubMed ID: 1658309
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  • 18. Nonopioidergic mechanism mediating morphine-induced antianalgesia in the mouse spinal cord.
    Wu HE, Thompson J, Sun HS, Leitermann RJ, Fujimoto JM, Tseng LF.
    J Pharmacol Exp Ther; 2004 Jul 26; 310(1):240-6. PubMed ID: 14999057
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  • 19. Cholecystokinin antagonists selectively potentiate analgesia induced by endogenous opiates.
    Watkins LR, Kinscheck IB, Kaufman EF, Miller J, Frenk H, Mayer DJ.
    Brain Res; 1985 Feb 18; 327(1-2):181-90. PubMed ID: 3838691
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  • 20. Mu and delta opioid receptors mediate opposite modulations by morphine of the spinal release of cholecystokinin-like material.
    Benoliel JJ, Collin E, Mauborgne A, Bourgoin S, Legrand JC, Hamon M, Cesselin F.
    Brain Res; 1994 Aug 08; 653(1-2):81-91. PubMed ID: 7982079
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