Unbound MEDLINE

Swelling-Activated Cl(-) Current in Isolated Rabbit Articular Chondrocytes: Inhibition by Arachidonic Acid. Journal of pharmacological sciences [J Pharmacol Sci] Journal article

 
TitleSwelling-Activated Cl(-) Current in Isolated Rabbit Articular Chondrocytes: Inhibition by Arachidonic Acid.
Author(s)Isoya E, Toyoda F, Imai S, Okumura N, Kumagai K, Omatsu-Kanbe M, Kubo M, Matsuura H, Matsusue Y 
InstitutionDepartment of Orthopaedic Surgery, Shiga University of Medical Science, Japan.
SourceJ Pharmacol Sci 2009 Feb 10.
AbstractArticular chondrocytes play an important role in maintaining the structure and function of the cartilage in synovial joints, which is closely influenced by mechanical or osmotic stress. In the present study, isolated rabbit articular chondrocytes were examined during hyposmotic stress using the whole-cell patch-clamp method. When exposed to hyposmotic external solutions (about 5% or 32% decrease in osmolarity), isolated rabbit articular chondrocytes exhibited hyposmotic cell swelling, accompanied by the activation of the swelling-activated Cl(-) current (I(Cl,swell)). I(Cl,swell) was practically time-independent at potentials negative to +50 mV but exhibited rapid inactivation at more positive potentials. I(Cl,swell) was potently inhibited by the Cl(-) channel blockers 5-nitro-2-(3-phenylpropylamino)benzoic acid, glibenclamide, and tamoxifen, but was little affected by pimozide. I(Cl,swell) was also found to be acutely inhibited by arachidonic acid in a concentration-dependent manner with an IC(50) of 0.81 muM. The maximal effect (approximately 100% block) was obtained with 10 muM arachidonic acid. The arachidonic acid metabolites prostaglandin E(2), leukotriene B(4), and leukotriene D(4) had no appreciable effect on I(Cl,swell), suggesting that the inhibitory effect of arachidonic acid did not require its metabolism. The present study thus reveals the presence of I(Cl,swell) in rabbit articular chondrocytes and I(Cl,swell) exhibits high sensitivity to direct inhibition by arachidonic acid.
LanguageENG
Pub Type(s)JOURNAL ARTICLE
PubMed ID19212094
  
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