G protein-coupled endothelial receptor for atypical cannabinoid ligands modulates a Ca2+-dependent K+ current. - Wikidata - wikimedia - TriplyDB

G protein-coupled endothelial receptor for atypical cannabinoid ligands modulates a Ca2+-dependent K+ current.

G protein-coupled endothelial receptor for atypical cannabinoid ligands modulates a Ca2+-dependent K+ current.

http://www.wikidata.org/entity/Q44571657

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N-Arachidonyl glycine does not activate G protein-coupled receptor 18 signaling via canonical pathways CB2 receptors in the brain: role in central immune function The endocannabinoid system as an emerging target of pharmacotherapy Novel cannabinoid receptors Vascular targets for cannabinoids: animal and human studies Is the cardiovascular system a therapeutic target for cannabidiol?Δ(9) -Tetrahydrocannabinol and N-arachidonyl glycine are full agonists at GPR18 receptors and induce migration in human endometrial HEC-1B cells The endocannabinoid system as a target for the treatment of neurodegenerative disease.Endocannabinoid-like N-arachidonoyl serine is a novel pro-angiogenic mediator Architecture of cannabinoid signaling in mouse retina Psychotropic and nonpsychotropic cannabis derivatives inhibit human 5-HT(3A) receptors through a receptor desensitization-dependent mechanism."Venopathy" at work: recasting neointimal hyperplasia in a new light.Cannabinoids and neuroinflammation.Heterogeneity in the mechanisms of vasorelaxation to anandamide in resistance and conduit rat mesenteric arteries.Vasorelaxant effects of oleamide in rat small mesenteric artery indicate action at a novel cannabinoid receptor.Cannabinoid receptor-mediated translocation of NO-sensitive guanylyl cyclase and production of cyclic GMP in neuronal cells.Cannabinoid receptors and endocannabinoids: evidence for new players.Cannabidiol causes endothelium-dependent vasorelaxation of human mesenteric arteries via CB1 activation Blood pressure regulation by endocannabinoids and their receptors Angiotensin II induces vascular endocannabinoid release, which attenuates its vasoconstrictor effect via CB1 cannabinoid receptors.Cardiovascular pharmacology of cannabinoids.Kaempferol stimulates large conductance Ca2+ -activated K+ (BKCa) channels in human umbilical vein endothelial cells via a cAMP/PKA-dependent pathway The endogenous brain constituent N-arachidonoyl L-serine is an activator of large conductance Ca2+-activated K+ channels (-)-Trans-Δ(9)-Tetrahydrocannabinol-Like Discriminative-Stimulus Effects of Gabapentin in Cannabis Users Endocannabinoid signaling in microglial cells The therapeutic potential of novel cannabinoid receptors Calycosin and Formononetin Induce Endothelium-Dependent Vasodilation by the Activation of Large-Conductance Ca2+-Activated K+ Channels (BKCa).Cannabinoid and cannabinoid-like receptors in microglia, astrocytes, and astrocytomas.N-acyl amino acids and N-acyl neurotransmitter conjugates: neuromodulators and probes for new drug targets.Prospects for Creation of Cardioprotective Drugs Based on Cannabinoid Receptor Agonists.The GPR55 agonist lysophosphatidylinositol acts as an intracellular messenger and bidirectionally modulates Ca2+ -activated large-conductance K+ channels in endothelial cells.Activation of large-conductance, Ca2+-activated K+ channels by cannabinoids.Big conductance calcium-activated potassium channel openers control spasticity without sedation.N-arachidonoyl glycine, an endogenous lipid that acts as a vasorelaxant via nitric oxide and large conductance calcium-activated potassium channels.The GPR55 agonist lysophosphatidylinositol relaxes rat mesenteric resistance artery and induces Ca(2+) release in rat mesenteric artery endothelial cells.Characterization of the vasorelaxant mechanisms of the endocannabinoid anandamide in rat aorta.Vasorelaxant activities of the putative endocannabinoid virodhamine in rat isolated small mesenteric artery.Endothelin-1-induced proliferation of human endothelial cells depends on activation of K+ channels and Ca+ influx.The Effect of Chronic Activation of the Novel Endocannabinoid Receptor GPR18 on Myocardial Function and Blood Pressure in Conscious Rats.Nicotine inhibits large conductance Ca(2+)-activated K(+) channels and the NO/-cGMP signaling pathway in cultured human endothelial cells.

P2860

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P2860

G protein-coupled endothelial receptor for atypical cannabinoid ligands modulates a Ca2+-dependent K+ current.

http://www.wikidata.org/entity/Q44571657

description

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2003年学术文章

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2003年学术文章

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2003年學術文章

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2003年學術文章

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name

G protein-coupled endothelial ...... s a Ca2+-dependent K+ current.

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G protein-coupled endothelial ...... s a Ca2+-dependent K+ current.

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type

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G protein-coupled endothelial ...... s a Ca2+-dependent K+ current.

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prefLabel

G protein-coupled endothelial ...... s a Ca2+-dependent K+ current.

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Journal of Biological Chemistry

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G protein-coupled endothelial ...... s a Ca2+-dependent K+ current.

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P2093

David M Lovinger

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Fong-Ming Mo

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

George Kunos

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László Offertaler

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Raj K Razdan

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

Sándor Bátkai

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P2860

Improved patch-clamp techniques for high-resolution current recording from cells and cell-free membrane patches

Cannabinoid-induced mesenteric vasodilation through an endothelial site distinct from CB1 or CB2 receptors

Structure of a cannabinoid receptor and functional expression of the cloned cDNA

Molecular characterization of a peripheral receptor for cannabinoids

Vanilloid receptors on sensory nerves mediate the vasodilator action of anandamide

CB(1) receptor antagonist SR141716A inhibits Ca(2+)-induced relaxation in CB(1) receptor-deficient mice.

Selective ligands and cellular effectors of a G protein-coupled endothelial cannabinoid receptor.

A cannabinoid with cardiovascular activity but no overt behavioral effects.

EDHF: bringing the concepts together.

Characterization of a charybdotoxin-sensitive intermediate conductance Ca2+-activated K+ channel in porcine coronary endothelium: relevance to EDHF.

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46188-46194

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10.1074/JBC.M307258200

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278

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10585049

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12952947

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G protein-coupled receptor

cannabinoid receptor