Search Results - "LUNDY, Paul M"

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  1. 1

    Development of the bisquaternary oxime HI-6 toward clinical use in the treatment of organophosphate nerve agent poisoning by LUNDY, Paul M, RAVEH, Lily, AMITAI, Gabriel

    Published in Toxicological reviews (2006)
    “…The traditional therapeutic treatment of organophosphate cholinesterase inhibitor (nerve agents) poisoning consists of co-treatment with an antimuscarinic…”
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    Journal Article
  2. 2

    Comparative protective effects of HI-6 and MMB-4 against organophosphorous nerve agent poisoning by Lundy, Paul M, Hamilton, Murray G, Sawyer, Thomas W, Mikler, John

    Published in Toxicology (Amsterdam) (29-07-2011)
    “…Abstract The oximes pralidoxime (2-PAM), its dimethanesulphonate salt derivative P2S, and obidoxime (toxogonin) are currently licensed and fielded for the…”
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    Journal Article
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    Medical countermeasures to WMDs: Defence research for civilian and military use by Hamilton, Murray G, Lundy, Paul M

    Published in Toxicology (Amsterdam) (20-04-2007)
    “…Abstract This document will address the contributions of defence research to both military and civilian applications. Compared to civilian research…”
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    Journal Article Conference Proceeding
  5. 5

    The pharmacokinetics and pharmacodynamics of two HI-6 salts in swine and efficacy in the treatment of GF and soman poisoning by Lundy, Paul M., Hill, Ira, Lecavalier, Pierre, Hamilton, Murray G., Vair, Cory, Davidson, Corey, Weatherby, Kendal L., Berger, Bradley J.

    Published in Toxicology (Amsterdam) (30-03-2005)
    “…Anesthetized pigs were injected i.m. with 500 mg HI-6 dichloride (HI-6 2Cl) (1-[[[4-(aminocarbonyl)-pyridinio]methoxy]methyl]-2[(hydroxyimino)methyl]pyridinium…”
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    Journal Article
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    Clinical aspects of percutaneous poisoning by the chemical warfare agent VX: effects of application site and decontamination by Hamilton, Murray G, Hill, Ira, Conley, John, Sawyer, Thomas W, Caneva, Duane C, Lundy, Paul M

    Published in Military medicine (01-11-2004)
    “…O-ethyl S-(2-diisopropylaminoethyl) methylphosphonothioate (VX) is an extremely toxic organophosphate nerve agent that has been weaponized and stockpiled in a…”
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    Journal Article
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    Pharmacological differentiation of the P2X7 receptor and the maitotoxin-activated cationic channel by LUNDY, Paul M, NELSON, Peggy, LEI MI, FREW, Robert, MINAKER, Sean, VAIR, Cory, SAWYER, Thomas W

    Published in European journal of pharmacology (08-03-2004)
    “…The ATP-P2X(7) receptor subtype and a maitotoxin-activated ion channel were studied to determine factors which identify them as separate entities in the…”
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    Journal Article
  8. 8

    Stimulation of Ca2+ influx through ATP receptors on rat brain synaptosomes: identification of functional P2X7 receptor subtypes by Lundy, Paul M, Hamilton, Murray G, Mi, Lei, Gong, Wenrong, Vair, Cory, Sawyer, Thomas W, Frew, Robert

    Published in British journal of pharmacology (01-04-2002)
    “…ATP receptors of the P2X class have previously been identified on autonomic nerve endings and on a limited population of CNS neurons. In the present study P2X…”
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    Journal Article
  9. 9

    Effects of bis(2-chloroethyl)sulfide on ATP receptor-mediated responses of the rat vas deferens: possible relationship to cytotoxicity by Lundy, P M, Sawyer, T W, Hand, B T, Frew, R

    “…Extracellular ATP is a broad-spectrum cytotoxic agent that produces effects via cell surface P2 purinoceptors. The ligand-gated P2X purinoceptor subtype has…”
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    Journal Article
  10. 10

    A comparison of the effects of sarin and succinylcholine on respiratory parameters in anesthetized domestic swine by DUNCAN, E. J, CONLEY, John D, GRYCHOWSKI, Kristen D, CONLEY, Seamus A, LUNDY, Paul M, HAMILTON, Murray G, SAWYER, Thomas W

    Published in Military medicine (01-04-2001)
    “…Differences in the "respiratory paralysis" caused by sarin (GB) and succinylcholine (SDC) were observed in a domestic swine model using a bedside pulmonary…”
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    Journal Article
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    Differential effects of ketamine isomers on neuronal and extraneuronal catecholamine uptake mechanisms by LUNDY, P. M, LOCKWOOD, P. A, THOMPSON, G, FREW, R

    Published in Anesthesiology (Philadelphia) (01-03-1986)
    “…Contractile responses of isolated rabbit aortic strips to epinephrine and norepinephrine were potentiated in a dose-related manner by (+) ketamine but not by…”
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    Journal Article
  12. 12

    Stimulation of Ca 2+ influx through ATP receptors on rat brain synaptosomes: identification of functional P2X 7 receptor subtypes by Lundy, Paul M, Hamilton, Murray G, Mi, Lei, Gong, Wenrong, Vair, Cory, Sawyer, Thomas W, Frew, Robert

    Published in British journal of pharmacology (02-02-2009)
    “…ATP receptors of the P2X class have previously been identified on autonomic nerve endings and on a limited population of CNS neurons. In the present study P2X…”
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    Journal Article
  13. 13

    Stimulation of Ca(2+) influx through ATP receptors on rat brain synaptosomes: identification of functional P2X(7) receptor subtypes by Lundy, Paul M, Hamilton, Murray G, Mi, Lei, Gong, Wenrong, Vair, Cory, Sawyer, Thomas W, Frew, Robert

    Published in British journal of pharmacology (01-04-2002)
    “…1. ATP receptors of the P2X class have previously been identified on autonomic nerve endings and on a limited population of CNS neurons. 2. In the present…”
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    Journal Article
  14. 14

    Ketamine: evidence of tissue specific inhibition of neuronal and extraneuronal catecholamine uptake processes by Lundy, P M, Gverzdys, S, Frew, R

    “…Ketamine (1.1 X 10(-5) to 3.7 X 10(-4) M) potentiated catecholamine responses of rat anococcygeus muscle and rabbit aorta in vitro. In the anococcygeus,…”
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    Journal Article
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    Ketamine potentiates catecholamine responses of vascular smooth muscle by inhibition of extraneuronal uptake by Lundy, P M, Frew, R

    “…Effects of ketamine on responses to sympathomimetic amines were studied using isolated aortic and pulmonary artery strips from the rabbit. Ketamine (1.1 x…”
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    Journal Article
  16. 16

    The ganglionic blocking properties of the cholinesterase reactivator, HS-6 by Lundy, P M

    “…Following intravenous administration of the cholinesterase reactivator HS-6 (30 mg/kg), blood pressure fell (up to 50 mmHg) and maximal blood levels of HS-6…”
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    Journal Article
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    Pharmacological differentiation of the P2X 7 receptor and the maitotoxin-activated cationic channel by Lundy, Paul M., Nelson, Peggy, Mi, Lei, Frew, Robert, Minaker, Sean, Vair, Cory, Sawyer, Thomas W.

    Published in European journal of pharmacology (2004)
    “…The ATP-P2X 7 receptor subtype and a maitotoxin-activated ion channel were studied to determine factors which identify them as separate entities in the control…”
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    Journal Article
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    A role for Q type Ca 2+ channels in neurotransmission in the rat urinary bladder by Frew, Robert, Lundy, Paul M.

    Published in British journal of pharmacology (01-09-1995)
    “…In isolated bladder strips of the rat, a substantial component (46%) of the Ca 2+ ‐dependent contractile response to electrical field stimulation (5 Hz) was…”
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    Journal Article
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    Effect of omega-agatoxin-IVA on autonomic neurotransmission by Lundy, P M, Frew, R

    Published in European journal of pharmacology (11-08-1994)
    “…omega-Agatoxin-IVA, a peptide from the venom of the funnel-web spider Agelenopsis aperta and a P type Ca2+ channel inhibitor, was examined for effects on…”
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    Journal Article