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Disruption of nNOS‐PSD95 protein–protein interaction inhibits acute thermal hyperalgesia and chronic mechanical allodynia in rodents

British journal of pharmacology, 2009-09, Vol.158 (2), p.494-506

2009

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Visualization of spinal afferent innervation in the mouse colon by AAV8‐mediated GFP expression

Neurogastroenterology and motility, 2013-02, Vol.25 (2), p.e89-e100

2013

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Agmatine Reverses Pain Induced by Inflammation, Neuropathy, and Spinal Cord Injury

Proceedings of the National Academy of Sciences - PNAS, 2000-09, Vol.97 (19), p.10584-10589

2000

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Ligand requirements for involvement of PKCε in synergistic analgesic interactions between spinal μ and δ opioid receptors

British journal of pharmacology, 2015-01, Vol.172 (2), p.642-653

2015

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Involvement of nitric oxide in spinally mediated hyperalgesia in the mouse

Neuroscience letters, 1992-12, Vol.148 (1), p.1-5

1992

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Transient changes in the synthesis of nitric oxide result in long-term as well as short-term changes in acetic acid-induced writhing in mice

Pain (Amsterdam), 2000-05, Vol.86 (1), p.103-111

2000

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Redox manipulation of NMDA receptors in vivo: alteration of acute pain transmission and dynorphin-induced allodynia

Pain (Amsterdam), 1999-03, Vol.80 (1), p.37-43

1999

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Parenterally administered kainic acid induces a persistent hyperalgesia in the mouse and rat

Pain (Amsterdam), 1999-11, Vol.83 (2), p.347-358

1999

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Chelation of zinc in the extracellular area of the spinal cord, using ethylenediaminetetraacetic acid disodium-calcium salt or dipicolinic acid, inhibits the antinociceptive effect of capsaicin in adult mice

The Journal of pharmacology and experimental therapeutics, 1999-02, Vol.288 (2), p.759

1999

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Substance P N-terminal metabolites and nitric oxide mediate capsaicin-induced antinociception in the adult mouse

The Journal of pharmacology and experimental therapeutics, 1994-12, Vol.271 (3), p.1281

1994

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Sensitization to the behavioral effect of kainic acid in the mouse is mediated by nitric oxide

The Journal of pharmacology and experimental therapeutics, 1995-11, Vol.275 (2), p.544

1995

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Evidence that the NH2-terminus of substance P modulates N-methyl-D-aspartate-induced activity by an action involving σ receptors

European journal of pharmacology, 1996-06, Vol.306 (1-3), p.15-22

1996

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Mutual antagonism between nerve growth factor and substance P N-terminal activity on nociceptive activity in mice

The Journal of pharmacology and experimental therapeutics, 1997-09, Vol.282 (3), p.1345

1997

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Manipulations of zinc in the spinal cord, by intrathecal injection of zinc chloride, disodium-calcium-EDTA, or dipicolinic acid, alter nociceptive activity in mice

The Journal of pharmacology and experimental therapeutics, 1997-09, Vol.282 (3), p.1319

1997

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Ligand requirements for involvement of PKC[epsi] in synergistic analgesic interactions between spinal µ and [delta] opioid receptors

British journal of pharmacology, 2015-01, Vol.172 (2), p.642

2015

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Peripherally mediated opioid combination therapy in mouse and pig

The journal of pain, 2024-11, p.104735, Article 104735

2024

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Pharmacodynamic and pharmacokinetic studies of agmatine after spinal administration in the mouse

The Journal of pharmacology and experimental therapeutics, 2005-09, Vol.314 (3), p.1226-1233

2005

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alpha(2C)-Adrenergic receptors mediate spinal analgesia and adrenergic-opioid synergy

The Journal of pharmacology and experimental therapeutics, 2002-01, Vol.300 (1), p.282

2002

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CP-96,345, which inhibits [3H] substance P binding, selectively inhibits the behavioral response to intrathecally administered N-methyl-D-aspartate, but not substance P, in the mouse

The Journal of pharmacology and experimental therapeutics, 1997-06, Vol.281 (3), p.1231

1997

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Supraspinally administered agmatine prevents the development of supraspinal morphine analgesic tolerance

European journal of pharmacology, 2006-04, Vol.536 (1), p.133-137

2006

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Moxonidine, a selective imidazoline/ α2 adrenergic receptor agonist, synergizes with morphine and deltorphin II to inhibit substance P-induced behavior in mice

Pain (Amsterdam), 2000, Vol.84 (1), p.13-20

2000

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Moxonidine, a selective imidazoline/alpha(2) adrenergic receptor agonist, synergizes with morphine and deltorphin II to inhibit substance P-induced behavior in mice

Pain (Amsterdam), 2000-01, Vol.84 (1), p.13

2000

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Evidence that the NH sub(2)-terminus of substance P modulates N-methyl-D-aspartate-induced activity by an action involving sigma receptors

European journal of pharmacology, 1996-06, Vol.306 (1-3), p.15-22

1996

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The alpha2a adrenergic receptor subtype mediates spinal analgesia evoked by alpha2 agonists and is necessary for spinal adrenergic-opioid synergy

The Journal of neuroscience, 1997-09, Vol.17 (18), p.7157

1997

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The alpha sub(2a) adrenergic receptor subtype mediates spinal analgesia evoked by alpha sub(2) agonists and is necessary for spinal adrenergic-opioid synergy

The Journal of neuroscience, 1997-09, Vol.17 (18), p.7157-7165

1997

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Disruption of nNOS‐PSD95 protein–protein interaction inhibits acute thermal hyperalgesia and chronic mechanical allodynia in rodents

Visualization of spinal afferent innervation in the mouse colon by AAV8‐mediated GFP expression

Agmatine Reverses Pain Induced by Inflammation, Neuropathy, and Spinal Cord Injury

Ligand requirements for involvement of PKCε in synergistic analgesic interactions between spinal μ and δ opioid receptors

Involvement of nitric oxide in spinally mediated hyperalgesia in the mouse

Transient changes in the synthesis of nitric oxide result in long-term as well as short-term changes in acetic acid-induced writhing in mice

Redox manipulation of NMDA receptors in vivo: alteration of acute pain transmission and dynorphin-induced allodynia

Parenterally administered kainic acid induces a persistent hyperalgesia in the mouse and rat

Chelation of zinc in the extracellular area of the spinal cord, using ethylenediaminetetraacetic acid disodium-calcium salt or dipicolinic acid, inhibits the antinociceptive effect of capsaicin in adult mice

Substance P N-terminal metabolites and nitric oxide mediate capsaicin-induced antinociception in the adult mouse

Sensitization to the behavioral effect of kainic acid in the mouse is mediated by nitric oxide

Evidence that the NH2-terminus of substance P modulates N-methyl-D-aspartate-induced activity by an action involving σ receptors

Mutual antagonism between nerve growth factor and substance P N-terminal activity on nociceptive activity in mice

Manipulations of zinc in the spinal cord, by intrathecal injection of zinc chloride, disodium-calcium-EDTA, or dipicolinic acid, alter nociceptive activity in mice

Ligand requirements for involvement of PKC[epsi] in synergistic analgesic interactions between spinal µ and [delta] opioid receptors

Peripherally mediated opioid combination therapy in mouse and pig

Pharmacodynamic and pharmacokinetic studies of agmatine after spinal administration in the mouse

alpha(2C)-Adrenergic receptors mediate spinal analgesia and adrenergic-opioid synergy

CP-96,345, which inhibits [3H] substance P binding, selectively inhibits the behavioral response to intrathecally administered N-methyl-D-aspartate, but not substance P, in the mouse

Supraspinally administered agmatine prevents the development of supraspinal morphine analgesic tolerance

Moxonidine, a selective imidazoline/ α2 adrenergic receptor agonist, synergizes with morphine and deltorphin II to inhibit substance P-induced behavior in mice

Moxonidine, a selective imidazoline/alpha(2) adrenergic receptor agonist, synergizes with morphine and deltorphin II to inhibit substance P-induced behavior in mice

Evidence that the NH sub(2)-terminus of substance P modulates N-methyl-D-aspartate-induced activity by an action involving sigma receptors

The alpha2a adrenergic receptor subtype mediates spinal analgesia evoked by alpha2 agonists and is necessary for spinal adrenergic-opioid synergy

The alpha sub(2a) adrenergic receptor subtype mediates spinal analgesia evoked by alpha sub(2) agonists and is necessary for spinal adrenergic-opioid synergy

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