Modulation of visceral hyperalgesia by morphine and cholecystokinin from the rat rostroventral medial medulla
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[1] A. Dickenson,et al. Spinal opioid systems in inflammation , 1995, Inflammation Research.
[2] P. Mason,et al. Raphe magnus neurons respond to noxious colorectal distension. , 2003, Journal of neurophysiology.
[3] G. Gebhart,et al. Chronic pain and medullary descending facilitation , 2002, Trends in Neurosciences.
[4] R. Dubner,et al. Plasticity in excitatory amino acid receptor-mediated descending pain modulation after inflammation. , 2002, The Journal of pharmacology and experimental therapeutics.
[5] R. Dubner,et al. Changes in gene expression and neuronal phenotype in brain stem pain modulatory circuitry after inflammation. , 2002, Journal of neurophysiology.
[6] Xiao-jun Xu,et al. Increased level of cholecystokinin in cerebrospinal fluid is associated with chronic pain-like behavior in spinally injured rats , 2001, Peptides.
[7] K. Sluka,et al. Blockade of opioid receptors in rostral ventral medulla prevents antihyperalgesia produced by transcutaneous electrical nerve stimulation (TENS). , 2001, The Journal of pharmacology and experimental therapeutics.
[8] M. Heinricher,et al. Circuitry underlying antiopioid actions of cholecystokinin within the rostral ventromedial medulla. , 2001, Journal of neurophysiology.
[9] P. Mason,et al. Contributions of the medullary raphe and ventromedial reticular region to pain modulation and other homeostatic functions. , 2001, Annual review of neuroscience.
[10] F. Porreca,et al. Supraspinal cholecystokinin may drive tonic descending facilitation mechanisms to maintain neuropathic pain in the rat , 2000, Pain.
[11] P. Mantyh,et al. Murine models of inflammatory, neuropathic and cancer pain each generates a unique set of neurochemical changes in the spinal cord and sensory neurons , 2000, Neuroscience.
[12] G. Gebhart,et al. Effects of spinal cholecystokinin receptor antagonists on morphine antinociception in a model of visceral pain in the rat. , 2000, The Journal of pharmacology and experimental therapeutics.
[13] R. Hurley,et al. The Analgesic Effects of Supraspinal μ and δ Opioid Receptor Agonists Are Potentiated during Persistent Inflammation , 2000, The Journal of Neuroscience.
[14] R. Hurley,et al. The analgesic effects of supraspinal mu and delta opioid receptor agonists are potentiated during persistent inflammation. , 2000, The Journal of neuroscience : the official journal of the Society for Neuroscience.
[15] T. Hökfelt,et al. Cholecystokinin/opioid interactions , 1999, Brain Research.
[16] T. Hökfelt,et al. Effect of morphine on cholecystokinin and μ-opioid receptor-like immunoreactivities in rat spinal dorsal horn neurons after peripheral axotomy and inflammation , 1999, Neuroscience.
[17] M. Urban,et al. Supraspinal contributions to hyperalgesia. , 1999, Proceedings of the National Academy of Sciences of the United States of America.
[18] David J. Smith,et al. Stress reduces morphine's antinociceptive potency: dependence upon spinal cholecystokinin processes , 1999, Brain Research.
[19] A. Basbaum. Opioids in Pain Control , 1999, Nature Medicine.
[20] A. Basbaum. Spinal mechanisms of acute and persistent pain. , 1999, Regional anesthesia and pain medicine.
[21] P. Cabot,et al. Opioids in Pain Control: Peripheral Opioid Analgesia: Mechanisms and Clinical Implications , 1998 .
[22] M. Urban,et al. Role of glutamate receptors and nitric oxide in the rostral ventromedial medulla in visceral hyperalgesia , 1998, Pain.
[23] H. Fields,et al. The contribution of the rostral ventromedial medulla to the antinociceptive effects of systemic morphine in restrained and unrestrained rats , 1998, Neuroscience.
[24] Z. Wiesenfeld‐Hallin,et al. Differential release of cholecystokinin by morphine in rat spinal cord , 1998, Neuroscience Letters.
[25] P. Beart,et al. Histochemistry in rat brain and spinal cord with an antibody directed at the cholecystokininA receptor , 1997, Neuroscience Letters.
[26] T. Gaginella. Handbook of methods in gastrointestinal pharmacology , 1996 .
[27] P. Law,et al. Expression of mu-, delta-, and kappa-opioid receptor-like immunoreactivities in rat dorsal root ganglia after carrageenan-induced inflammation , 1995, The Journal of neuroscience : the official journal of the Society for Neuroscience.
[28] J. Stamford. Descending control of pain. , 1995, British journal of anaesthesia.
[29] Jacqueline N. Crawley,et al. Biological actions of cholecystokinin , 1994, Peptides.
[30] T. Hökfelt,et al. Messenger plasticity in primary sensory neurons following axotomy and its functional implications , 1994, Trends in Neurosciences.
[31] M. Fournié-Zaluski,et al. Cholecystokinin B antagonists strongly potentiate antinociception mediated by endogenous enkephalins. , 1994, The Journal of pharmacology and experimental therapeutics.
[32] Xiao-jun Xu,et al. Cholecystokinin and morphine analgesia: variations on a theme. , 1994, Trends in pharmacological sciences.
[33] J. Han,et al. Increased release of immunoreactive cholecystokinin octapeptide by morphine and potentiation of mu-opioid analgesia by CCKB receptor antagonist L-365,260 in rat spinal cord. , 1993, European journal of pharmacology.
[34] T. Hökfelt,et al. Up-regulation of cholecystokinin in primary sensory neurons is associated with morphine insensitivity in experimental neuropathic pain in the rat , 1993, Neuroscience Letters.
[35] A. Dickenson,et al. Cholecystokinin as a factor in the enhanced potency of spinal morphine following carrageenin inflammation , 1993, British journal of pharmacology.
[36] L. Tseng,et al. Cholecystokinin administered intrathecally selectively antagonizes intracerebroventricular beta-endorphin-induced tail-flick inhibition in the mouse. , 1992, The Journal of pharmacology and experimental therapeutics.
[37] L. Tseng,et al. Intrathecal cholecystokinin octapeptide attenuates the antinociception and release of immunoreactive Met-enkephalin induced by intraventricular β-endorphin in the rat , 1992, Neuropeptides.
[38] R. Dubner,et al. Preproenkephalin mrna in spinal dorsal horn neurons is induced by peripheral inflammation and is co-localized with Fos and Fos-related proteins , 1992, Neuroscience.
[39] A. Randich,et al. Further behavioral evidence that colorectal distension is a ‘noxious’ visceral stimulus in rats , 1991, Neuroscience Letters.
[40] G. Woodruff,et al. Functional role of brain CCK receptors , 1991, Neuropeptides.
[41] M. Hamon,et al. Differential inhibitory/stimulatory modulation of spinal CCK release by μ and δ opioid agonists, and selective blockade of μ-dependent inhibition by κ receptor stimulation , 1991, Neuroscience Letters.
[42] D. Price,et al. Cholecystokinin and its antagonist lorglumide respectively attenuate and facilitate morphine-induced inhibition of C-fiber evoked discharges of dorsal horn nociceptive neurons , 1991, Brain Research.
[43] M. Hamon,et al. Differential inhibitory/stimulatory modulation of spinal CCK release by mu and delta opioid agonists, and selective blockade of mu-dependent inhibition by kappa receptor stimulation. , 1991, Neuroscience Letters.
[44] 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.
[45] N. Baber,et al. The role of CCK, caerulein, and CCK antagonists in nociception , 1989, Pain.
[46] M. Iadarola,et al. Temporal analysis of increases in c-fos, preprodynorphin and preproenkephalin mRNAs in rat spinal cord. , 1989, Brain research. Molecular brain research.
[47] 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.
[48] J. Wallace,et al. Hapten-induced model of chronic inflammation and ulceration in the rat colon. , 1989, Gastroenterology.
[49] R. Dubner,et al. Enhancement of dynorphin gene expression in spinal cord following experimental inflammation: stimulus specificity, behavioral parameters and opioid receptor binding , 1988, Pain.
[50] R. M. Bowker,et al. Distribution of μ-opioid receptors in the nucleus raphe magnus and nucleus gigantocellularis: A quantitative autoradiographic study , 1988, Neuroscience Letters.
[51] T. Ness,et al. Colorectal distension as a noxious visceral stimulus: physiologic and pharmacologic characterization of pseudaffective reflexes in the rat , 1988, Brain Research.
[52] R. M. Bowker,et al. Distribution of mu-opioid receptors in the nucleus raphe magnus and nucleus gigantocellularis: a quantitative autoradiographic study. , 1988, Neuroscience letters.
[53] M. Iadarola,et al. In situ hybridization histochemistry and immunocytochemistry reveal an increase in spinal dynorphin biosynthesis in a rat model of peripheral inflammation and hyperalgesia. , 1988, Proceedings of the National Academy of Sciences of the United States of America.
[54] C. Dourish,et al. Classification and function of CCK receptors , 1987 .
[55] Z. Wiesenfeld‐Hallin,et al. Intrathecal cholecystokinin interacts with morphine but not substance P in modulating the nociceptive flexion reflex in the rat , 1987, Peptides.
[56] J. Lauterborn,et al. Co-localization of enkephalin and cholecystokinin in discrete areas of rat brain , 1987, Brain Research.
[57] T. Jensen,et al. I. Comparison of antinociceptive action of morphine in the periaqueductal gray, medial and paramedial medulla in rat , 1986, Brain Research.
[58] Paul R. McHugh,et al. Two brain cholecystokinin receptors: implications for behavioral actions , 1986, Brain Research.
[59] L. Watkins,et al. Potentiation of morphine analgesia by the cholecystokinin antagonist proglumide , 1985, Brain Research.
[60] L. Watkins,et al. Cholecystokinin antagonists selectively potentiate analgesia induced by endogenous opiates , 1985, Brain Research.
[61] M. Iadarola,et al. Proglumide prevents and curtails acute tolerance to morphine in rats , 1984, Neuropharmacology.
[62] L. Watkins,et al. Potentiation of opiate analgesia and apparent reversal of morphine tolerance by proglumide. , 1984, Science.
[63] P. Mantyh,et al. Evidence for cholecystokinin-like immunoreactive neurons in the rat medulla oblongata which project to the spinal cord , 1984, Brain Research.
[64] L. Watkins,et al. Evidence for the neuropeptide cholecystokinin as an antagonist of opiate analgesia. , 1983, Science.
[65] S. Itoh,et al. Caerulein and cholecystokinin suppress β-endorphin-induced analgesia in the rat , 1982 .
[66] S. Itoh,et al. Caerulein and cholecystokinin suppress beta-endorphin-induced analgesia in the rat. , 1982, European journal of pharmacology.
[67] K. Stengaard-Pedersen,et al. Localization and opiate receptor binding of enkephalin, CCK and ACTH/β-endorphin in the rat central nervous system , 1981, Peptides.
[68] S. Snyder,et al. Distinct cholecystokinin receptors in brain and pancreas. , 1980, Proceedings of the National Academy of Sciences of the United States of America.
[69] I. Goldfine,et al. Cholecystokinin receptors in the brain: characterization and distribution. , 1980, Science.
[70] J. Besson,et al. Role of the nucleus raphe magnus in opiate analgesia as studied by the microinjection technique in the rat , 1979, Brain Research.
[71] G. Dockray,et al. Immunochemical evidence of cholecystokinin-like peptides in brain , 1976, Nature.
[72] J. Mackenzie. Symptoms and Their Interpretation , 1912, The Indian Medical Gazette.