Search Results - "Amagasu, S."

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  1. 1

    Discovery of a selective, state-independent inhibitor of NaV1.7 by modification of guanidinium toxins by Pajouhesh, H., Beckley, J. T., Delwig, A., Hajare, H. S., Luu, G., Monteleone, D., Zhou, X., Ligutti, J., Amagasu, S., Moyer, B. D., Yeomans, D. C., Du Bois, J., Mulcahy, J. V.

    Published in Scientific reports (09-09-2020)
    “…The voltage-gated sodium channel isoform Na V 1.7 is highly expressed in dorsal root ganglion neurons and is obligatory for nociceptive signal transmission…”
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    Journal Article
  2. 2

    Glia modulate the response of murine cortical neurons to excitotoxicity: glia exacerbate AMPA neurotoxicity by Dugan, LL, Bruno, VM, Amagasu, SM, Giffard, RG

    Published in The Journal of neuroscience (01-06-1995)
    “…We have developed "pure" neuronal cultures (< 1% astrocytes) from mouse neocortex to study the effect of glial cells on the response of neurons to injury…”
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  3. 3

    Volatile anesthetics depress glutamate transmission via presynaptic actions by MACIVER, M. B, MIKULEC, A. A, AMAGASU, S. M, MONROE, F. A

    Published in Anesthesiology (Philadelphia) (01-10-1996)
    “…Recent evidence for a presynaptic depression of glutamate release produced by volatile anesthetics prompted the current study of isoflurane and halothane…”
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  4. 4

    Evidence for a multivalent interaction of symmetrical, N-linked, lidocaine dimers with voltage-gated Na+ channels by Smith, J A M, Amagasu, S M, Hembrador, J, Axt, S, Chang, R, Church, T, Gee, C, Jacobsen, J R, Jenkins, T, Kaufman, E, Mai, N, Vickery, R G

    Published in Molecular pharmacology (01-03-2006)
    “…The interaction of symmetrical lidocaine dimers with voltage-gated Na+ channels (VGSCs) was examined using a FLIPR membrane potential assay and voltage-clamp…”
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  5. 5

    Characterization of prostanoid receptor‐evoked responses in rat sensory neurones by Smith, Jacqueline A M, Amagasu, Shanti M, Eglen, Richard M, Hunter, John C, Bley, Keith R

    Published in British journal of pharmacology (01-06-1998)
    “…Prostanoid receptor‐mediated sensitization, or excitation, of sensory nerve fibres contributes to the generation of hyperalgesia. To characterize the…”
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  6. 6

    Riluzole anesthesia : Use-dependent block of presynaptic glutamate fibers by MACLVER, M. B, AMAGASU, S. M, MIKULEC, A. A, MONROE, F. A

    Published in Anesthesiology (Philadelphia) (01-09-1996)
    “…Riluzole (RP 54274) is an experimental benzothiazole with anesthetic properties, but little is known about its synaptic or cellular actions. The authors…”
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  7. 7

    Halothane depresses action potential conduction in hippocampal axons by Mikulec, Anthony A, Pittson, Sky, Amagasu, Shanti M, Monroe, Frances A, MacIver, M.Bruce

    Published in Brain research (15-06-1998)
    “…General anesthetics are thought to depress the central nervous system (CNS) by acting at synapses; however, only a few studies have compared effects on axonal…”
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  8. 8

    Discovery of a selective, state-independent inhibitor of Na V 1.7 by modification of guanidinium toxins by Pajouhesh, H, Beckley, J T, Delwig, A, Hajare, H S, Luu, G, Monteleone, D, Zhou, X, Ligutti, J, Amagasu, S, Moyer, B D, Yeomans, D C, Du Bois, J, Mulcahy, J V

    Published in Scientific reports (09-09-2020)
    “…The voltage-gated sodium channel isoform Na 1.7 is highly expressed in dorsal root ganglion neurons and is obligatory for nociceptive signal transmission…”
    Get full text
    Journal Article
  9. 9

    An in vitro investigation of the cardiovascular effects of the 5-HT4 receptor selective agonists, velusetrag and TD-8954 by Beattie, D.T, Higgins, D.L, Ero, M.P, Amagasu, S.M, Vickery, R.G, Kersey, K, Hopkins, A, Smith, J.A.M

    Published in Vascular pharmacology (01-01-2013)
    “…Abstract The 5-HT4 receptor agonists, and gastrointestinal (GI) prokinetic agents, cisapride and tegaserod, lack selectivity for the 5-HT4 receptor. Cisapride…”
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  10. 10

    Comparison of the pharmacological properties of rat Na(V)1.8 with rat Na(V)1.2a and human Na(V)1.5 voltage-gated sodium channel subtypes using a membrane potential sensitive dye and FLIPR by Vickery, R G, Amagasu, S M, Chang, R, Mai, N, Kaufman, E, Martin, J, Hembrador, J, O'Keefe, M D, Gee, C, Marquess, D, Smith, J A M

    Published in Receptors & channels (2004)
    “…A novel, membrane potential sensitive dye and a fluorescence imaging plate reader (FLIPR) have been used to characterize the pharmacological properties of rat…”
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  11. 11

    An in vitro investigation of the cardiovascular effects of the 5-HT(4) receptor selective agonists, velusetrag and TD-8954 by Beattie, D T, Higgins, D L, Ero, M P, Amagasu, S M, Vickery, R G, Kersey, K, Hopkins, A, Smith, J A M

    Published in Vascular pharmacology (01-01-2013)
    “…The 5-HT(4) receptor agonists, and gastrointestinal (GI) prokinetic agents, cisapride and tegaserod, lack selectivity for the 5-HT(4) receptor. Cisapride is a…”
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    Journal Article
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