Evaluation of the effects of specific opioid receptor agonists in a rodent model of spinal cord injury (original) (raw)

Morphine Undermines Recovery Following Spinal Cord Injury: Evaluation of Opioid Receptors and Cellular Mechanisms

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2017

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Neurobiological Effects of Morphine after Spinal Cord Injury

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Nor-Binaltorphimine Blocks the Adverse Effects of Morphine after Spinal Cord Injury

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Adam F, Dufour E, Le Bars D D (2008) The glycine site-specific NMDA antagonist (+)-HA966 enhances the effect of morphine and reverses morphine tolerance via a spinal mechanism. Neuropharmacology 54 : 588-596.

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Opioid and substance p receptor adaptations in the rat spinal cord following sub-chronic intrathecal treatment with morphine and naloxone

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Antinociceptive and Adverse Effects of µ- and κ-Opioid Receptor Agonists: A Comparison of Morphine and U50488-H

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Sensitivity to μ-opioid receptor-mediated anti-nociception is determined by cross-regulation between μ- and δ-opioid receptors at supraspinal level

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Pre-injury administration of morphine prevents development of neuropathic hyperalgesia through activation of descending monoaminergic mechanisms in the spinal cord in mice

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Analgesia or Addiction?: Implications for Morphine Use after Spinal Cord Injury

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Chronic opioid antagonist treatment selectively regulates trafficking and signaling proteins in mouse spinal cord

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The kappa-opioid receptor is upregulated in the spinal cord and locus ceruleus but downregulated in the dorsal root ganglia of morphine tolerant rats

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Moxonidine, a Selective Imidazoline–α2-Adrenergic Receptor Agonist, Produces Spinal Synergistic Antihyperalgesia with Morphine in Nerve-injured Mice

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Ketamine blocks enhancement of spinal long-term potentiation in chronic opioid treated rats

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Morphine-6-glucuronide-Induced Locomotor Stimulation in Mice: Role of Opioid Receptors

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Spinal Glucocorticoid Receptors Contribute to the Development of Morphine Tolerance in Rats

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Intrathecal Morphine Attenuates Recovery of Function after a Spinal Cord Injury

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A role for heterodimerization of µ and opiate receptors in enhancing morphine analgesia

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Morphine Tolerance in Spinal Cord Is Due to Interaction between micro- and delta -Receptors

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The Effects of Repeated Opioid Administration on Locomotor Activity: I. Opposing Actions of μ and κ Receptors

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MOL-13185 1 Morphine-induced µ-opioid receptor desensitization MOL-13185 2 a. Running title Morphine-induced desensitization

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2020

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Experimental considerations for the assessment of in vivo and in vitro opioid pharmacology

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The loss of antinociceptive efficacy of spinal morphine in rats with nerve ligation injury is prevented by reducing spinal afferent drive

Michael Ossipov

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Opioid Agonists Differentially Regulate μ-Opioid Receptors and Trafficking Proteins in Vivo

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Opioid administration following spinal cord injury: Implications for pain and locomotor recovery

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Intrathecal CART (55-102) enhances the spinal analgesic actions of morphine in mice

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Effect of κ-opioid receptor agonists on morphine analgesia in morphine-naive and morphine-tolerant rats

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Sustained morphine exposure induces a spinal dynorphin-dependent enhancement of excitatory transmitter release from primary afferent fibers

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Mechanisms of opioid-induced pain and antinociceptive tolerance: descending facilitation and spinal dynorphin

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The Role of Spinal Opioid Receptors in Antinociceptive Effects Produced by Intrathecal Administration of Hydromorphone and Buprenorphine in the Rat

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Chronic treatment with the opioid antagonist naltrexone favours the coupling of spinal cord μ-opioid receptors to Gαz protein subunits

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