Stress-induced tolerance to delta receptor agonist DPDPE and selectivity of the irreversible δ-ligand, DALCE

[1]  W. Bowen,et al.  [D-Ala2,Leu5,Cys6]enkephalin: Short-term agonist effects and long-term antagonism at delta opioid receptors , 1989, Peptides.

[2]  J. Holaday,et al.  beta-FNA binds irreversibly to the opiate receptor complex: in vivo and in vitro evidence. , 1988, The Journal of pharmacology and experimental therapeutics.

[3]  H. Mosberg,et al.  Direct dependence studies in rats with agents selective for different types of opioid receptor. , 1988, The Journal of pharmacology and experimental therapeutics.

[4]  M. Fanselow,et al.  Analgesia produced by centrally administered DAGO, DPDPE and U50488H in the formalin test. , 1988, European journal of pharmacology.

[5]  E. J. Simon,et al.  Effects of stress and beta-funal trexamine pretreatment on morphine analgesia and opioid binding in rats. , 1987, Life sciences.

[6]  W. Bowen,et al.  Affinity labeling of delta-opiate receptors using [D-Ala2,Leu5,Cys6]enkephalin. Covalent attachment via thiol-disulfide exchange. , 1987, The Journal of biological chemistry.

[7]  B. Roques,et al.  Use of μ and δ opioid peptides of various selectivity gives further evidence of specific involvement of μ opioid receptors in supraspinal analgesia (tail-flick test) , 1987 .

[8]  S. Holtzman,et al.  Stress-induced changes in the analgesic and thermic effects of opioid peptides in the rat , 1986, Brain Research.

[9]  S. Holtzman,et al.  Stress-induced changes in the analgesic and thermic effects of morphine administered centrally , 1985, Brain Research.

[10]  S. Holtzman,et al.  Restraint stress enhances morphine-induced analgesia in the rat without changing apparent affinity of receptor. , 1985, Life sciences.

[11]  P. Portoghese,et al.  Affinity labels for opioid receptors. , 1985, Annual review of pharmacology and toxicology.

[12]  S. Holtzman,et al.  Characterization of stress-induced potentiation of opioid effects in the rat. , 1984, The Journal of pharmacology and experimental therapeutics.

[13]  Alexander Levitzki,et al.  Receptors: A Quantitative Approach , 1984 .

[14]  V. Hruby,et al.  Cerebral delta opioid receptors mediate analgesia but not the intestinal motility effects of intracerebroventricularly administered opioids. , 1984, The Journal of pharmacology and experimental therapeutics.

[15]  A. Goldstein,et al.  Site-directed alkylation of multiple opioid receptors. I. Binding selectivity. , 1984, Molecular pharmacology.

[16]  W. Dewey,et al.  A comparison of antinociception induced by foot shock and morphine. , 1983, The Journal of pharmacology and experimental therapeutics.

[17]  R. Lahti,et al.  U-50,488: a selective and structurally novel non-Mu (kappa) opioid agonist. , 1983, The Journal of pharmacology and experimental therapeutics.

[18]  P. Portoghese,et al.  Different receptor sites mediate opioid agonism and antagonism. , 1983, Journal of medicinal chemistry.

[19]  G. Paxinos,et al.  The Rat Brain in Stereotaxic Coordinates , 1983 .

[20]  K. Miczek,et al.  Opioid-like analgesia in defeated mice. , 1982, Science.

[21]  J. Holaday,et al.  Repeated electroconvulsive shock (ECS) and morphine tolerance: demonstration of cross-sensitivity in the rat. , 1981, Life sciences.

[22]  B. Morgan,et al.  Analogues of β-LPH61–64 posessing selective agonist activity at μ-opiate receptors , 1981 .

[23]  G. A. Bentley,et al.  The possibility that a component of morphine-induced analgesia is contributed indirectly via the release of endogenous opioids , 1980, PAIN.

[24]  K. M. Taylor,et al.  1-Methylisoguanosine: an orally active marine natural product with skeletal muscle and cardiovascular effects. , 1980, Life sciences.

[25]  E. J. Simon,et al.  Selective protection of stereospecific enkephalin and opiate binding against inactivation by N-ethylmaleimide: evidence for two classes of opiate receptors. , 1980, Proceedings of the National Academy of Sciences of the United States of America.

[26]  H. Kosterlitz,et al.  Specific protection of the binding sites of D-Ala2-D-Leu5- enkephalin (δ-receptors) and dihydromorphine (μ-receptors) , 1979, Proceedings of the Royal Society of London. Series B. Biological Sciences.

[27]  R. Bodnar,et al.  Opiate and non-opiate mechanisms of stress-induced analgesia: Cross-tolerance between stressors , 1979, Pharmacology Biochemistry and Behavior.

[28]  B. Chan,et al.  Footshock induced analgesia in mice: its reversal by naloxone and cross tolerance with morphine. , 1977, Life sciences.