Mechanisms of μ-opioid receptor inhibition of NMDA receptor-induced substance P release in the rat spinal cord.

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Peripheral Mu-Opioid receptors Attenuate the Responses of Group III and IV Afferents to Contraction in Rats with Simulated Peripheral Artery Disease.Mu-opioid receptors in nociceptive afferents produce a sustained suppression of hyperalgesia in chronic pain.

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Mechanisms of μ-opioid receptor inhibition of NMDA receptor-induced substance P release in the rat spinal cord.

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http://www.wikidata.org/entity/Q44349884

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Mechanisms of μ-opioid recepto ...... elease in the rat spinal cord.

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Mechanisms of μ-opioid recepto ...... elease in the rat spinal cord.

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Item

label

Mechanisms of μ-opioid recepto ...... elease in the rat spinal cord.

@en

Mechanisms of μ-opioid recepto ...... elease in the rat spinal cord.

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Mechanisms of μ-opioid recepto ...... elease in the rat spinal cord.

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Mechanisms of μ-opioid recepto ...... elease in the rat spinal cord.

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Mechanisms of μ-opioid recepto ...... elease in the rat spinal cord.

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Helena S Ennes

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James A McRoberts

http://www.w3.org/2001/XMLSchema#string

Wenling Chen

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P2860

Acute inflammation induces segmental, bilateral, supraspinally mediated opioid release in the rat spinal cord, as measured by mu-opioid receptor internalization

Differential actions of PKA and PKC in the regulation of glutamate release by group III mGluRs in the entorhinal cortex.

Mechanisms of inward-rectifier K+ channel inhibition by tertiapin-Q.

Inverse, protean, and ligand-selective agonism: matters of receptor conformation.

BDNF released during neuropathic pain potentiates NMDA receptors in primary afferent terminals

Src family kinases mediate the inhibition of substance P release in the rat spinal cord by μ-opioid receptors and GABA(B) receptors, but not α2 adrenergic receptors.

Spinal G-protein-gated potassium channels contribute in a dose-dependent manner to the analgesic effect of mu- and delta- but not kappa-opioids.

Alternative splicing controls G protein-dependent inhibition of N-type calcium channels in nociceptors.

Why the Schild method is better than Schild realised.

Evidence for presynaptic N-methyl-D-aspartate autoreceptors in the spinal cord dorsal horn.

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255-268

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scholarly article

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10.1016/J.NEUROPHARM.2017.10.014

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128

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P50

Juan Carlos Marvizón

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2017-10-14T00:00:00Z

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29042318

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substance P

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5726399

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Mechanisms of μ-opioid receptor inhibition of NMDA receptor-induced substance P release in the rat spinal cord.

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P2860

P2860

Mechanisms of μ-opioid receptor inhibition of NMDA receptor-induced substance P release in the rat spinal cord.

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P1476

P2093

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