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Journal Abstract Search

256 related items for PubMed ID: 2838332

  • 1. A highly selective ligand for brain delta opiate receptors, a cyclopropyl(E)Phe(4)-enkephalin analog, suppresses mu receptor-mediated thermal analgesia by morphine.
    Shimohigashi Y, Takano Y, Kamiya H, Costa T, Herz A, Stammer CH.
    FEBS Lett; 1988 Jun 20; 233(2):289-93. PubMed ID: 2838332
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  • 5. Role of mu and delta receptors in the supraspinal and spinal analgesic effects of [D-Pen2, D-Pen5]enkephalin in the mouse.
    Porreca F, Heyman JS, Mosberg HI, Omnaas JR, Vaught JL.
    J Pharmacol Exp Ther; 1987 May 20; 241(2):393-400. PubMed ID: 3033214
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  • 6. Morphine-like discriminative stimulus effects of opioid peptides: possible modulatory role of D-Ala2-D-Leu5-enkephalin (DADL) and dynorphin A (1-13).
    Ukai M, Holtzman SG.
    Psychopharmacology (Berl); 1988 May 20; 94(1):32-7. PubMed ID: 2894701
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  • 7. Mu-, delta-, kappa- and epsilon-opioid receptor modulation of the hypothalamic-pituitary-adrenocortical (HPA) axis: subchronic tolerance studies of endogenous opioid peptides.
    Iyengar S, Kim HS, Wood PL.
    Brain Res; 1987 Dec 01; 435(1-2):220-6. PubMed ID: 2892574
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  • 11. Delta but not mu-opioid receptors in the spinal cord are involved in antinociception induced by beta-endorphin given intracerebroventricularly in mice.
    Suh HH, Tseng LF.
    J Pharmacol Exp Ther; 1990 Jun 01; 253(3):981-6. PubMed ID: 2162954
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  • 12. Comparison of two penicillamine-containing enkephalins: mu, not delta, activity produces analgesia.
    Leander JD, Gesellchen PD, Mendelsohn LG.
    Neuropeptides; 1986 Jun 01; 8(2):119-25. PubMed ID: 3020472
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  • 13. Comparison of analgesic potencies of mu, delta and kappa agonists locally applied to various CNS regions relevant to analgesia in rats.
    Satoh M, Kubota A, Iwama T, Wada T, Yasui M, Fujibayashi K, Takagi H.
    Life Sci; 1983 Jun 01; 33 Suppl 1():689-92. PubMed ID: 6141508
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  • 14. Regional interactions of opioid peptides at mu and delta sites in rat brain.
    Hewlett WA, Barchas JD.
    Peptides; 1983 Jun 01; 4(6):853-8. PubMed ID: 6324140
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  • 15. Action at the mu receptor is sufficient to explain the supraspinal analgesic effect of opiates.
    Fang FG, Fields HL, Lee NM.
    J Pharmacol Exp Ther; 1986 Sep 01; 238(3):1039-44. PubMed ID: 3018217
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  • 16. Behavioral effects of opioid peptides selective for mu or delta receptors. I. Morphine-like discriminative stimulus effects.
    Locke KW, Holtzman SG.
    J Pharmacol Exp Ther; 1986 Sep 01; 238(3):990-6. PubMed ID: 3018230
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  • 17. Dermenkephalin (Tyr-D-Met-Phe-His-Leu-Met-Asp-NH2): a potent and fully specific agonist for the delta opioid receptor.
    Amiche M, Sagan S, Mor A, Delfour A, Nicolas P.
    Mol Pharmacol; 1989 Jun 01; 35(6):774-9. PubMed ID: 2543911
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  • 18. Brain passage of BUBU, a highly selective and potent agonist for delta opioid receptors: in vivo binding and mu versus delta receptors occupancy.
    Delay-Goyet P, Ruiz-Gayo M, Baamonde A, Gacel G, Morgat JL, Roques BP.
    Pharmacol Biochem Behav; 1991 Jan 01; 38(1):155-62. PubMed ID: 1850135
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  • 19. Opioid delta-receptor involvement in supraspinal and spinal antinociception in mice.
    Heyman JS, Mulvaney SA, Mosberg HI, Porreca F.
    Brain Res; 1987 Sep 08; 420(1):100-8. PubMed ID: 2823970
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  • 20. 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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