The novel reversible fatty acid amide hydrolase inhibitor ST4070 increases endocannabinoid brain levels and counteracts neuropathic pain in different animal models.
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Chemical probes of endocannabinoid metabolismMarijuana, Spice 'herbal high', and early neural development: implications for rescheduling and legalizationInhibitors of Fatty Acid Amide Hydrolase and Monoacylglycerol Lipase: New Targets for Future AntidepressantsThe endocannabinoid system as a potential therapeutic target for pain modulationFatty acid amide hydrolase inhibitors: a patent review (2009-2014)Latest advances in the discovery of fatty acid amide hydrolase inhibitorsElevating endocannabinoid levels: pharmacological strategies and potential therapeutic applicationsPhysical activity and the endocannabinoid system: an overviewCombined inhibition of FAAH and COX produces enhanced anti-allodynic effects in mouse neuropathic and inflammatory pain models.Regulation of inflammation by cannabinoids, the endocannabinoids 2-arachidonoyl-glycerol and arachidonoyl-ethanolamide, and their metabolites.Novel associations between FAAH genetic variants and postoperative central opioid-related adverse effects.17beta-estradiol counteracts neuropathic pain: a behavioural, immunohistochemical, and proteomic investigation on sex-related differences in mice.Protective Action of Anandamide and Its COX-2 Metabolite against l-Homocysteine-Induced NLRP3 Inflammasome Activation and Injury in Podocytes.Cocaine-induced endocannabinoid release modulates behavioral and neurochemical sensitization in miceCannabinoids in pain management: CB1, CB2 and non-classic receptor ligands.Mechanism-based treatment for chemotherapy-induced peripheral neuropathic pain.The Endogenous Cannabinoid System: A Budding Source of Targets for Treating Inflammatory and Neuropathic Pain.Positive Allosteric Modulation of Cannabinoid Receptor Type 1 Suppresses Pathological Pain Without Producing Tolerance or Dependence.An update on PPAR activation by cannabinoids.Targeting the endogenous cannabinoid system to treat neuropathic pain.A Randomized, Double-Blind, Placebo- and Active Comparator-Controlled Phase I Study of Analgesic/Antihyperalgesic Properties of ASP8477, a Fatty Acid Amide Hydrolase Inhibitor, in Healthy Female Subjects.The MOBILE Study-A Phase IIa Enriched Enrollment Randomized Withdrawal Trial to Assess the Analgesic Efficacy and Safety of ASP8477, a Fatty Acid Amide Hydrolase Inhibitor, in Patients with Peripheral Neuropathic Pain.Targeting the Endocannabinoid System for Prevention or Treatment of Chemotherapy-Induced Neuropathic Pain: Studies in Animal Models
P2860
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P2860
The novel reversible fatty acid amide hydrolase inhibitor ST4070 increases endocannabinoid brain levels and counteracts neuropathic pain in different animal models.
description
2012 nî lūn-bûn
@nan
2012年の論文
@ja
2012年学术文章
@wuu
2012年学术文章
@zh-cn
2012年学术文章
@zh-hans
2012年学术文章
@zh-my
2012年学术文章
@zh-sg
2012年學術文章
@yue
2012年學術文章
@zh
2012年學術文章
@zh-hant
name
The novel reversible fatty aci ...... in in different animal models.
@en
The novel reversible fatty aci ...... in in different animal models.
@nl
type
label
The novel reversible fatty aci ...... in in different animal models.
@en
The novel reversible fatty aci ...... in in different animal models.
@nl
prefLabel
The novel reversible fatty aci ...... in in different animal models.
@en
The novel reversible fatty aci ...... in in different animal models.
@nl
P2093
P50
P921
P356
P1476
The novel reversible fatty aci ...... ain in different animal models
@en
P2093
Antonio Caprioli
Cinzia Rapino
Franco Borsini
Mario Vertechy
Mauro Maccarrone
Monia Di Tommaso
Stefano Di Serio
P304
P356
10.1124/JPET.111.191403
P407
P577
2012-04-18T00:00:00Z