Ranolazine attenuates behavioral signs of neuropathic pain

Harry J. Gould; Colleen Garrett; Renee R. Donahue; Dennis Paul; Ivan Diamond; Bradley K. Taylor

doi:10.1097/FBP.0b013e3283323c90

Ranolazine attenuates behavioral signs of neuropathic pain

Harry J. Gould, Colleen Garrett, Renee R. Donahue, Dennis Paul, Ivan Diamond, Bradley K. Taylor

Research output: Contribution to journal › Article › peer-review

31 Scopus citations

Abstract

Ranolazine modulates the cardiac voltage-gated sodium channel (NaV 1.5) and is approved by the FDA in the treatment of ischemic heart disease. Ranolazine also targets neuronal (NaV 1.7, 1.8) isoforms that are implicated in neuropathic pain. Therefore, we determined the analgesic efficacy of ranolazine in a preclinical animal model of neuropathic pain. Both intraperitoneal and oral administration of ranolazine dose-dependently inhibited the mechanical and cold allodynia associated with spared nerve injury, without producing ataxia or other behavioral side effects. These data warrant clinical investigation of the potential use of ranolazine in the treatment of neuropathic pain.

Original language	English (US)
Pages (from-to)	755-758
Number of pages	4
Journal	Behavioural Pharmacology
Volume	20
Issue number	8
DOIs	https://doi.org/10.1097/FBP.0b013e3283323c90
State	Published - Dec 2009
Externally published	Yes

Keywords

Allodynia
Hyperalgesia
Na 1.7
NaV 1.8
Rat
Spared nerve injury

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This output contributes to the following UN Sustainable Development Goals (SDGs)

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10.1097/FBP.0b013e3283323c90

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title = "Ranolazine attenuates behavioral signs of neuropathic pain",

abstract = "Ranolazine modulates the cardiac voltage-gated sodium channel (NaV 1.5) and is approved by the FDA in the treatment of ischemic heart disease. Ranolazine also targets neuronal (NaV 1.7, 1.8) isoforms that are implicated in neuropathic pain. Therefore, we determined the analgesic efficacy of ranolazine in a preclinical animal model of neuropathic pain. Both intraperitoneal and oral administration of ranolazine dose-dependently inhibited the mechanical and cold allodynia associated with spared nerve injury, without producing ataxia or other behavioral side effects. These data warrant clinical investigation of the potential use of ranolazine in the treatment of neuropathic pain.",

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T1 - Ranolazine attenuates behavioral signs of neuropathic pain

AU - Gould, Harry J.

AU - Garrett, Colleen

AU - Donahue, Renee R.

AU - Paul, Dennis

AU - Diamond, Ivan

AU - Taylor, Bradley K.

PY - 2009/12

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AB - Ranolazine modulates the cardiac voltage-gated sodium channel (NaV 1.5) and is approved by the FDA in the treatment of ischemic heart disease. Ranolazine also targets neuronal (NaV 1.7, 1.8) isoforms that are implicated in neuropathic pain. Therefore, we determined the analgesic efficacy of ranolazine in a preclinical animal model of neuropathic pain. Both intraperitoneal and oral administration of ranolazine dose-dependently inhibited the mechanical and cold allodynia associated with spared nerve injury, without producing ataxia or other behavioral side effects. These data warrant clinical investigation of the potential use of ranolazine in the treatment of neuropathic pain.

KW - Allodynia

KW - Hyperalgesia

KW - Na 1.7

KW - NaV 1.8

KW - Rat

KW - Spared nerve injury

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Ranolazine attenuates behavioral signs of neuropathic pain

Abstract

Keywords

UN SDGs

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