Role of cholecystokinin in the reduction of endomorphin-2-induced antinociception in diabetic mice.
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[1] J. Kamei,et al. The role of spinal cholecystokinin B receptors in thermal allodynia and hyperalgesia in diabetic mice , 2001, Brain Research.
[2] A. Eschalier,et al. Potentiation of morphine and clomipramine analgesia by cholecystokinin -B antagonist CI-988 in diabetic rats , 2000, Neuroscience Letters.
[3] M. Ohsawa,et al. The antinociceptive effects of endomorphin-1 and endomorphin-2 in diabetic mice. , 2000, European journal of pharmacology.
[4] J. Crawley,et al. International Union of Pharmacology. XXI. Structure, distribution, and functions of cholecystokinin receptors. , 1999, Pharmacological reviews.
[5] M. Ohsawa,et al. Role of intracellular calcium in thermal allodynia and hyperalgesia in diabetic mice , 1999, Brain Research.
[6] M. Ohsawa,et al. Possible involvement of spinal protein kinase C in thermal allodynia and hyperalgesia in diabetic mice. , 1999, European journal of pharmacology.
[7] M. Schwartz,et al. Effect of Intracerebroventricular Insulin Infusion on Diabetic Hyperphagia and Hypothalamic Neuropeptide Gene Expression , 1995, Diabetes.
[8] Xiao-jun Xu,et al. Cholecystokinin and morphine analgesia: variations on a theme. , 1994, Trends in pharmacological sciences.
[9] J. Kamei,et al. Role of spleen or spleen products in the deficiency in morphine-induced analgesia in diabetic mice , 1992, Brain Research.
[10] J. Kamei,et al. Streptozotocin-induced diabetes selectively alters the potency of analgesia produced by μ-opioid agonists, but not by δ- and κ-opioid agonists , 1992, Brain Research.
[11] Xiao-Jing Wang,et al. Cholecystokinin octapeptide antagonized opioid analgesia mediated by μ- and κ- but not δ-receptors in the spinal cord of the rat , 1990, Brain Research.
[12] L. Tseng,et al. Differential effects of sulfated cholecystokinin octapeptide and proglumide injected intrathecally on antinociception induced by beta-endorphin and morphine administered intracerebroventricularly in mice. , 1990, European journal of pharmacology.
[13] S. Iversen,et al. Morphine-induced analgesia in the rat paw pressure test is blocked by CCK and enhanced by the CCK antagonist MK-329 , 1989, Neuropharmacology.
[14] B. Komisaruk,et al. Morphine analgesia potentiated but tolerance not affected by active immunization against cholecystokinin. , 1984, Science.
[15] M. Beinfeld. Cholecystokinin in the central nervous system: A minireview , 1983, Neuropeptides.
[16] L. Watkins,et al. Evidence for the neuropeptide cholecystokinin as an antagonist of opiate analgesia. , 1983, Science.
[17] S. Itoh,et al. Caerulein and cholecystokinin suppress β-endorphin-induced analgesia in the rat , 1982 .
[18] J. Morley,et al. Minireview. The ascent of cholecystokinin (CCK) - from gut to brain. , 1982, Life sciences.