Search Results - "Gogas, K R"
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Central infusion of the melanocortin receptor antagonist agouti-related peptide (AgRP(83-132)) prevents cachexia-related symptoms induced by radiation and colon-26 tumors in mice
Published in Peptides (New York, N.Y. : 1980) (01-03-2007)“…Cachexia is a clinical wasting syndrome that occurs in multiple disease states, and is associated with anorexia and a progressive loss of body fat and lean…”
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Central administration of peptide and small molecule MC4 receptor antagonists induce hyperphagia in mice and attenuate cytokine-induced anorexia
Published in Peptides (New York, N.Y. : 1980) (01-11-2005)“…We investigated the effect of melanocortin 4 receptor (MC4) antagonists on food intake in mice. Food intake during the light phase was significantly increased…”
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The effect of novel anti-epileptic drugs in rat experimental models of acute and chronic pain
Published in European journal of pharmacology (01-04-1997)“…The novel anti-epileptic drugs lamotrigine, felbamate and gabapentin were compared in rat experimental models of acute (tail flick) and chronic pain: the…”
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Glutamate-based therapeutic approaches: NR2B receptor antagonists
Published in Current opinion in pharmacology (01-02-2006)“…Over the past decade, there have been major advances in our understanding of the role of glutamate and N-methyl- d-aspartate (NMDA) receptors in several…”
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Inhibition of noxious stimulus-evoked pain behaviors and neuronal fos-like immunoreactivity in the spinal cord of the rat by supraspinal morphine
Published in Pain (Amsterdam) (01-04-1996)“…In previous studies, we reported that supraspinally administered DAMGO, a mu-opioid agonist, produces a dose-related, naloxone-reversible inhibition of…”
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Walking evokes a distinctive pattern of Fos-like immunoreactivity in the caudal brainstem and spinal cord of the rat
Published in Neuroscience (01-01-1994)“…We have evaluated the pattern of c-fos expression induced in the rat spinal cord, caudal brainstem and cerebellum by a behavior that is associated with…”
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Morphine or U-50,488 suppresses Fos protein-like immunoreactivity in the spinal cord and nucleus tractus solitarii evoked by a noxious visceral stimulus in the rat
Published in Journal of comparative neurology (1911) (08-01-1992)“…Immunohistochemical visualization of Fos protein, the nuclear phosphoprotein product of the early-immediate gene c-fos, permits identification of populations…”
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Differential contribution of descending controls to the antinociceptive actions of kappa and mu opioids: an analysis of formalin-evoked C-fos expression
Published in The Journal of pharmacology and experimental therapeutics (01-02-1996)“…In this study, the effect of intracerebroventricular (icv) administration of (5R)-(5 alpha, 7 alpha, 8 beta)-N-methyl-N-[7-(1-pyrrolindinyl)-1-…”
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The antinociceptive action of supraspinal opioids results from an increase in descending inhibitory control: correlation of nociceptive behavior and c-fos expression
Published in Neuroscience (1991)“…In an earlier report, we demonstrated that subcutaneous injection of formalin in the rat hindpaw evokes a characteristic pattern of expression of the fos…”
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Diffuse noxious inhibitory controls reduce the expression of noxious stimulus-evoked Fos-like immunoreactivity in the superficial and deep laminae of the rat spinal cord
Published in Pain (Amsterdam) (01-03-1994)“…Behavioral and electrophysiological studies have shown that a noxious stimulus applied to one part of the body can reduce the response to a subsequent noxious…”
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Distribution of the Tetrodotoxin-Resistant Sodium Channel PN3 in Rat Sensory Neurons in Normal and Neuropathic Conditions
Published in The Journal of neuroscience (15-03-1998)“…The novel sodium channel PN3/alpha-SNS, which was cloned from a rat dorsal root ganglion (DRG) cDNA library, is expressed predominantly in small sensory…”
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A role for histamine and H2-receptors in opioid antinociception
Published in The Journal of pharmacology and experimental therapeutics (01-08-1989)“…To investigate the role of brain H2-receptors in opioid antinociceptive mechanisms, the effects of several antagonists of histamine H2-receptors were…”
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Inhibition of naloxone-resistant antinociception by centrally administered H2-antagonists
Published in The Journal of pharmacology and experimental therapeutics (01-01-1989)“…In order to test directly the hypothesis that brain histamine and H2-receptors mediate the naloxone-resistant footshock-induced antinociception (FSIA) elicited…”
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Effects of zolantidine a brain-penetrating H2-receptor antagonist, on naloxone-sensitive and naloxone-resistant analgesia
Published in Neuropharmacology (01-04-1988)“…The action of zolantidine, a histamine H2-receptor antagonist which penetrates the brain, was characterized on the analgesia elicited by brief continuous…”
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Cross-tolerance and cross-sensitization between morphine analgesia and naloxone-sensitive and cimetidine-sensitive stress-induced analgesia
Published in The Journal of pharmacology and experimental therapeutics (01-01-1988)“…Recent studies have shown that different regimens of footshock elicit either "opiate" (naloxone-sensitive) or "histaminergic" (cimetidine-sensitive but…”
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H2-receptor-mediated stress-induced analgesia is dependent on neither pituitary nor adrenal activation
Published in Pharmacology, biochemistry and behavior (01-07-1988)“…The effects of hypophysectomy and adrenalectomy were studied on the analgesia elicited by a 3 min exposure to 3.5 mA of continuous inescapable footshock, a…”
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Opposing actions of cimetidine on naloxone-sensitive and naloxone-insensitive forms of footshock-induced analgesia
Published in Brain research (09-04-1986)“…The effects of the opiate antagonist naloxone (10 mg/kg) and the histamine H2-antagonist cimetidine (100 mg/kg; both administered i.p.) were studied on the…”
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Actions of the brain-penetrating H2-antagonist zolantidine on histamine dynamics and metabolism in rat brain
Published in Biochemical pharmacology (15-12-1988)“…The effects of zolantidine, the first brain-penetrating H2-receptor antagonist, on the brain levels of histamine (HA) and the HA metabolite…”
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Mechanisms of opioid-mediated antinociception: correlation of Fos expression and behavior
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