Results 41 to 50 of about 12,113 (164)

The effect of aerobic exercise with ozone and stem cell on anandamide concentration in desert rat with osteoarthritis

open access: yesFiyz̤, 2022
Background: Aerobic exercise, ozone therapy and cell therapy have each been independently proposed as treatments for osteoarthritis. Therefore, the present study aimed to investigate the effect of aerobic exercise with ozone and cell therapy on serum ...
Maryam Rezaei   +3 more
doaj  

Identification of prostamides, fatty acyl ethanolamines, and their biosynthetic precursors in rabbit cornea[S]

open access: yesJournal of Lipid Research, 2015
Arachidonoyl ethanolamine (anandamide) and pros­taglandin ethanolamines (prostamides) are biologically active derivatives of arachidonic acid. Although available through different precursor phospholipids, there is considerable overlap between the ...
Paula Urquhart   +3 more
doaj   +1 more source

Two Vanilloid Ligand Bindings Per Channel Are Required to Transduce Capsaicin-Activating Stimuli

open access: yesFrontiers in Molecular Neuroscience, 2020
The tetrameric capsaicin receptor transient receptor potential vanilloid 1 (TRPV1) in mammals has evolved the capability to integrate pain signal arising from harmful temperature and chemical irritants. The four repetitions of TRPV1 subunits result in an
Ting-Yi Liu   +4 more
doaj   +1 more source

Endocannabinoids and related N-acylethanolamines: biological activities and metabolism

open access: yesInflammation and Regeneration, 2018
The plant Cannabis sativa contains cannabinoids represented by Δ9-tetrahydrocannabinol, which exert psychoactivity and immunomodulation through cannabinoid CB1 and CB2 receptors, respectively, in animal tissues. Arachidonoylethanolamide (also referred to
Kazuhito Tsuboi   +3 more
doaj   +1 more source

Tuning the oviduct to the anandamide tone [PDF]

open access: yesJournal of Clinical Investigation, 2006
Anandamide (N-arachidonoylethanolamide) is a lipid signal molecule that was the first endogenous agonist for cannabinoid receptors to be discovered. Cannabinoid receptor type 1 (CB1) is widely distributed in neurons and nonneuronal cells in brain and peripheral organs including sperm, eggs, and preimplantation embryos. A study by Wang and colleagues in
openaire   +2 more sources

Chemical synthesis, pharmacological characterization, and possible formation in unicellular fungi of 3-hydroxy-anandamide1

open access: yesJournal of Lipid Research, 2009
The fungal pathogen Candida albicans transforms arachidonic acid (AA) into 3-hydroxyarachidonic acid [3(R)-HETE], and we investigated if its nonpathogenic and 3(R)-HETE-producing close relative, Dipodascopsis uninucleata, could similarly transform the ...
L. De Petrocellis   +10 more
doaj   +1 more source

Plasma endocannabinoid alterations in individuals with substance use disorder are dependent on the mirror effect of schizophrenia

open access: yesFrontiers in Psychiatry, 2012
Schizophrenia is a complex psychiatric disorder strongly associated with substance use disorders. Theoretically, schizophrenia and SUD may share endocannabinoid alterations in the brain reward system.
Joelle eDesfossés   +8 more
doaj   +1 more source

Altered Anandamide Degradation in Attention Deficit Hyperactivity Disorder

open access: yesPediatric Neurology Briefs, 2009
Anandamide (AEA) metabolism was investigated in 15 drug-free boys with ADHD (aged 6.5-13 years) and 15 age- and gender-matched healthy controls, in a study at Universita Tor Vergata, Rome, Italy.
J Gordon Millichap
doaj   +1 more source

Pharmacological characterization of a novel, potent, selective, and orally active fatty acid amide hydrolase inhibitor, PKM‐833 [(R)‐N‐(pyridazin‐3‐yl)‐4‐(7‐(trifluoromethyl)chroman‐4‐yl)piperazine‐1‐carboxamide] in rats: Potential for the treatment of inflammatory pain

open access: yesPharmacology Research & Perspectives, 2020
Recently, we identified a novel fatty acid amide hydrolase (FAAH) inhibitor, PKM‐833 [(R)‐N‐(pyridazin‐3‐yl)‐4‐(7‐(trifluoromethyl)chroman‐4‐yl)piperazine‐1‐carboxamide].
Toshiya Endo   +2 more
doaj   +1 more source

The Endocannabinoid System as a Potential Therapeutic Target for Pain Modulation

open access: yesBalkan Medical Journal, 2014
Although cannabis has been used for pain management for millennia, very few approved cannabinoids are indicated for the treatment of pain and other medical symptoms. Cannabinoid therapy re-gained attention only after the discovery of endocannabinoids and
Ahmet Ulugöl
doaj   +1 more source

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