Actions of intrathecal omega-conotoxins CVID, GVIA, MVIIA, and morphine in acute and neuropathic pain in the rat.

[1]  J. Besson,et al.  Intravenous morphine does not modify dorsal horn touch-evoked allodynia in the mononeuropathic rat: a Fos study , 2001, PAIN®.

[2]  A. Robertson,et al.  Cardiovascular and autonomic effects of ω‐conotoxins MVIIA and CVID in conscious rabbits and isolated tissue assays , 2000 .

[3]  P. Andrews,et al.  Novel ω-Conotoxins from Conus catus Discriminate among Neuronal Calcium Channel Subtypes* , 2000, The Journal of Biological Chemistry.

[4]  R. Luther,et al.  Ziconotide, A New N‐Type Calcium Channel Blocker, Administered Intrathecally for Acute Postoperative Pain , 2000, Regional anesthesia and pain medicine.

[5]  K. Nielsen,et al.  Structure–activity relationships of ω‐conotoxins at N‐type voltage‐sensitive calcium channels , 2000, Journal of molecular recognition : JMR.

[6]  R. Penn,et al.  Adverse effects associated with the intrathecal administration of ziconotide , 2000, Pain.

[7]  Yongxiang Wang,et al.  Interactions of intrathecally administered ziconotide, a selective blocker of neuronal N-type voltage-sensitive calcium channels, with morphine on nociception in rats , 2000, PAIN®.

[8]  G. Sanger,et al.  Rank-order inhibition by ω-conotoxins in human and animal autonomic nerve preparations , 2000 .

[9]  A. Dickenson,et al.  The effectiveness of spinal and systemic morphine on rat dorsal horn neuronal responses in the spinal nerve ligation model of neuropathic pain , 1999, Pain.

[10]  R. Luther,et al.  Use of intrathecal SNX-111, a novel, N-type, voltage-sensitive, calcium channel blocker, in the management of intractable brachial plexus avulsion pain. , 1997, The Clinical journal of pain.

[11]  S. Abram,et al.  Assessment of the Potency and Intrinsic Activity of Systemic versus Intrathecal Opioids in Rats , 1997, Anesthesiology.

[12]  A. Garcı́a,et al.  omega-Conotoxins block neurotransmission in the rat vas deferens by binding to different presynaptic sites on the N-type Ca2+ channel. , 1997, European journal of pharmacology.

[13]  R. Luther,et al.  Selective N-type neuronal voltage-sensitive calcium channel blocker, SNX-111, produces spinal antinociception in rat models of acute, persistent and neuropathic pain. , 1996, The Journal of pharmacology and experimental therapeutics.

[14]  K. Omote,et al.  Spinal Antinociceptive Action of an N‐Type Voltage‐dependent Calcium Channel Blocker and the Synergistic Interaction with Morphine , 1996, Anesthesiology.

[15]  O. Bulbena,et al.  Effects of ω-toxins on noradrenergic neurotransmission in beating guinea pig atria , 1995 .

[16]  A. Malmberg,et al.  Effect of continuous intrathecal infusion of ω-conopeptides, N-type calcium-channel blockers, on behavior and antinociception in the formalin and hot-plate tests in rats , 1995, Pain.

[17]  H. Rhim,et al.  Opioid receptors modulate diverse types of calcium channels in the nucleus tractus solitarius of the rat , 1994, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[18]  T. Yaksh,et al.  Voltage-sensitive calcium channels in spinal nociceptive processing: blockade of N- and P-type channels inhibits formalin-induced nociception , 1994, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[19]  T. Yaksh,et al.  Quantitative assessment of tactile allodynia in the rat paw , 1994, Journal of Neuroscience Methods.

[20]  T. Yaksh,et al.  Role of voltage-dependent calcium channel subtypes in experimental tactile allodynia. , 1994, The Journal of pharmacology and experimental therapeutics.

[21]  J. Leiphart,et al.  Analgesic action of acute and chronic intraspinally administered opiate and alpha 2-adrenergic agonists in chronic neuropathic pain. , 1994, Stereotactic and functional neurosurgery.

[22]  Jin Mo Chung,et al.  An experimental model for peripheral neuropathy produced by segmental spinal nerve ligation in the rat , 1992, PAIN.

[23]  R. Portenoy,et al.  The nature of opioid responsiveness and its implications for neuropathic pain: new hypotheses derived from studies of opioid infusions , 1990, Pain.

[24]  D. Logothetis,et al.  Elementary properties and pharmacological sensitivities of calcium channels in mammalian peripheral neurons , 1989, Neuron.

[25]  W. Dixon,et al.  Efficient analysis of experimental observations. , 1980, Annual review of pharmacology and toxicology.

[26]  T. Yaksh,et al.  Chronic catheterization of the spinal subarachnoid space , 1976, Physiology & Behavior.