Search Results - "Chudapongse, N"

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  1. 1

    Changes in the brain κ-opioid receptor levels of rats in withdrawal from physical dependence upon butorphanol by Fan, L.-W, Tien, L.-T, Tanaka, S, Ma, T, Chudapongse, N, Sinchaisuk, S, Rockhold, R.W, Ho, I.K

    Published in Neuroscience (01-01-2003)
    “…Changes in κ-opioid receptor levels have been implicated in the development of physical dependence upon and withdrawal from the mixed agonist–antagonist…”
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    Journal Article
  2. 2

    Proteomic analysis of phosphotyrosyl proteins in morphine-dependent rat brains by Kim, Seong-Youl, Chudapongse, Nuannoi, Lee, Sang-Min, Levin, Michael C., Oh, Jae-Taek, Park, Hae-Joon, Ho, Ing K.

    Published in Brain research. Molecular brain research. (05-01-2005)
    “…Morphine has been used as a potent analgesic, having a high propensity to induce tolerance and physical dependence following their repeated administration…”
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  3. 3

    Nonopioid receptor-mediated effects of U-50,488H on [Ca super(2+)] sub(i) and extracellular dopamine in PC12 cells by Chudapongse, N, Kim, S-Y, Sasaki, K, Kramer, R E, Ho, I K

    Published in Journal of neuroscience research (01-01-2003)
    “…The present studies were carried out to determine the effects of a Kappa -opioid receptor agonist on cytosolic Ca super(2+) concentration, [Ca super(2+)]…”
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  4. 4

    Proteomic analysis of phosphotyrosyl proteins in the rat brain: Effect of butorphanol dependence by Kim, Seong-Youl, Chudapongse, Nuannoi, Lee, Sang-Min, Levin, Michael C., Oh, Jae-Taek, Park, Hae-Joon, Ho, Ing K.

    Published in Journal of neuroscience research (15-09-2004)
    “…Butorphanol (17‐cyclobutylmethyl‐3,14‐dihydroxymorphinan) tartrate (Stadol) is a mixed agonist‐antagonist opioid analgesic agent that is about five to seven…”
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  5. 5

    Nonspecific Effects of the Selective κ-Opioid Receptor Agonist U-50,488H on Dopamine Uptake and Release in PC12 Cells by Chudapongse, Nuannoi, Kim, Seong-Youl, Kramer, Robert E., Ho, Ing K.

    Published in Journal of Pharmacological Sciences (01-11-2003)
    “…κ-Opioid receptor agonists decrease the levels of extracellular dopamine in vivo and in vitro. However, the mechanism(s) underlying these actions are unclear…”
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    Journal Article