Blockade of the polyamine site of NMDA receptors produces antinociception and enhances the effect of morphine, in mice.
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[1] A. Bertolini. The opioid/anti-opioid balance in shock: a new target for therapy in resuscitation. , 1995, Resuscitation.
[2] H. Suh,et al. Multiplicative interaction between intrathecally and intracerebroventricularly administered morphine for antinociception in the mouse: involvement of supraspinal NMDA but not non-NMDA receptors. , 1995, Life sciences.
[3] A. Larson,et al. Morphine modulates excitatory amino acid-induced activity in the mouse spinal cord: short-term effects on N-methy-D-aspartate (NMDA) and long-term effects on kainic acid , 1994, Brain Research.
[4] M. Kavaliers,et al. Antagonistic effects of the selective, competitive N-methyl-d-aspartate (NMDA) receptor antagonist, NPC 12626, on kappa opiate-induced analgesia in male deer mice , 1994, Brain Research.
[5] S. Genedani,et al. Influence of ifenprodil on the ACTH-induced behavioral syndrome in rats. , 1994, European journal of pharmacology.
[6] Nobuko Minami,et al. The NMDA Receptor antagonists, LY274614 and MK-801, and the nitric oxide synthase inhibitor, NG-nitro-l-arginine, attenuate analgesic tolerance to the mu-opioid morphine but not to kappa opioids , 1994, Pain.
[7] T. Gordh,et al. The NMDA antagonist 3-(2-carboxypiperazin-4-yl)propyl-1-phosphonic acid (CPP) has antinociceptive effect after intrathecal injection in the rat , 1994, Pain.
[8] D. Hurlbut,et al. Blockade of morphine-induced analgesia and tolerance in mice by MK-801 , 1993, Brain Research.
[9] K. Abe,et al. Spermine facilitates the generation of long-term potentiation of evoked potential in the dentate gyrus of anesthetized rats , 1992, Brain Research.
[10] T. Yamamoto,et al. Comparison of the antinociceptive effects of pre- and posttreatment with intrathecal morphine and MK801, an NMDA antagonist, on the formalin test in the rat. , 1992, Anesthesiology.
[11] B. Kest,et al. The specific N-methyl-d-aspartate (NMDA) receptor antagonist MK-801 blocks U-50,488, but not morphine antinociception , 1992, Brain Research.
[12] C. Post,et al. Antinociceptive actions of different classes of excitatory amino acid receptor antagonists in mice. , 1992, European journal of pharmacology.
[13] G. Page,et al. N-methyl-d-aspartic acid (NMDA) receptor antagonist MK-801 blocks non-opioid stress-induced analgesia. I. Comparison of opiate receptor-deficient and opiate receptor-rich strains of mice , 1991, Brain Research.
[14] M. Kavaliers,et al. Sex differences in the inhibitory effects of the NMDA antagonist, MK-801, on morphine and stress-induced analgesia , 1990, Brain Research Bulletin.
[15] H. Schoemaker,et al. Binding of [3H]ifenprodil, a novel NMDA antagonist, to a polyamine-sensitive site in the rat cerebral cortex. , 1990, European journal of pharmacology.
[16] C. Carter,et al. Ifenprodil and SL 82.0715 are antagonists at the polyamine site of the N-methyl-D-aspartate (NMDA) receptor. , 1989, European journal of pharmacology.
[17] J. Han,et al. Effect of calcium ion on analgesia of opioid peptides. , 1989, The International journal of neuroscience.
[18] Y. Jacquet. The NMDA receptor: central role in pain inhibition in rat periaqueductal gray. , 1988, European journal of pharmacology.
[19] A. Vergoni,et al. Cross‐Species Comparison of the ACTH‐induced Behavioral Syndrome , 1988, Annals of the New York Academy of Sciences.
[20] E. Contreras,et al. Calcium channel antagonists increase morphine-induced analgesia and antagonize morphine tolerance. , 1988, European journal of pharmacology.
[21] S. Guarini,et al. Evidence that melanocortins are physiological antagonists of opioids , 1986 .
[22] D. Wied,et al. Central actions of ACTH and related peptides , 1986 .
[23] A. Adeagbo,et al. Pharmacological actions of ifenprodil in the rat isolated anococcygeus muscle , 1985, The Journal of pharmacy and pharmacology.
[24] S. Genedani,et al. Effect of α-difluoromethylornithine (DFMO) on the behavioral syndrome induced by intracerebroventricular injection of ACTH1–24, in rats , 1984, Neuropeptides.
[25] G. Paxinos,et al. The Rat Brain in Stereotaxic Coordinates , 1983 .
[26] J. Jolles,et al. Neuropeptides derived from pro-opiocortin: behavioral, physiological, and neurochemical effects. , 1982, Physiological reviews.
[27] T. O'donohue,et al. The opiomelanotropinergic neuronal and endocrine systems , 1982, Peptides.
[28] S. Amir. Effects of ACTH on pain responsiveness in mice: Interaction with morphine , 1981, Neuropharmacology.
[29] W. Fratta,et al. Reciprocal antagonism between ACTH1–24 and β-endorphin in rats , 1981, Neuroscience Letters.
[30] G. Gessa,et al. Behavioral effects of ACTH and MSH peptides , 1981, Journal of endocrinological investigation.
[31] S. Amir,et al. The pituitary gland mediates acute and chronic pain responsiveness in stressed and non-stressed rats. , 1979, Life sciences.
[32] J. P. Heybach,et al. The effect of pituitary‐adrenal function in the modulation of pain sensitivity in the rat , 1978, The Journal of physiology.
[33] W. Gispen,et al. Interaction between ACTH fragments, brain opiate receptors and morphine-induced analgesia. , 1976, European journal of pharmacology.
[34] W. Gispen,et al. The induction of excessive grooming in the rat by intraventricular application of peptides derived from ACTH: structure-activity studies. , 1975, Life sciences.
[35] G. Gessa,et al. Induction of Sexual Excitement by the Action of Adrenocorticotrophic Hormone in Brain , 1969, Nature.
[36] G. Gessa,et al. BEHAVIORAL EFFECTS INDUCED BY INTRACISTERNALLY INJECTED ACTH AND MSH * , 1963, Annals of the New York Academy of Sciences.
[37] W. Ferrari. Behavioural Changes in Animals after Intracisternal Injection with Adrenocorticotrophic Hormone and Melanocyte-Stimulating Hormone , 1958, Nature.
[38] R. Cadmus,et al. A Method for Evaluating both Non-Narcotic and Narcotic Analgesics , 1957, Proceedings of the Society for Experimental Biology and Medicine. Society for Experimental Biology and Medicine.
[39] N. B. Eddy,et al. Synthetic analgesics. II. Dithienylbutenyl- and dithienylbutylamines. , 1953, The Journal of pharmacology and experimental therapeutics.
[40] G. Woolfe,et al. THE EVALUATION OF THE ANALGESIC ACTION OF PETHIDINE HYDROCHLORIDE (DEMEROL) , 1944 .