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http://purl.uniprot.org/citations/31194991http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/31194991http://www.w3.org/2000/01/rdf-schema#comment"

Aims

Caffeine is a methylxanthine with multiple actions in vascular smooth muscle cells (VSMCs), including the increase in the intracellular Ca2+ (iCa2+) concentration by the activation of ryanodine receptors (RyRs). The present study aimed at investigating the participation of Ca2+-influx through different Ca2+-channels on the transient contraction (TC) induced by caffeine in mice mesenteric arteries.

Main methods

Second-order of mesenteric arteries was isolated from male Swiss mice. Vessels without functional endothelium were stimulated with caffeine (10 mM). The caffeine-induced TC was evaluated after the incubation of artery rings for 30 min with the following drugs: nifedipine (10 μM), a Cav1.2 blocker; 2-aminoethoxydiphenyl borate (2-APB; 10 μM) and ruthenium red (RuR; 10 μM), transient receptor potential (TRPs) channels blockers; capsazepine (10 μM) and HC067047 (10 μM), TRPV1 and TRPV4 antagonists, respectively; paxilline (1 μM), a selective BKCa blocker; and SKF-96365 (30 μM), an Orai blocker. Ca2+-fluorescence measurements were also performed on the investigated arteries.

Key findings

The TC induced by caffeine was partially dependent on Ca2+-influx. However, the blockage of Cav1.2 increased the TC while reduced the iCa2+ signal. Similar results were observed after the blockage of TRPs or BKCa. Therefore, caffeine promoted Ca2+-influx via TRPs and Cav1.2, and hyperpolarization through the activation of BKCa, inducing negative feedback of TC.

Significance

Our results indicate an alternative mechanism for the control of VSMCs contraction in resistance arteries. The evidence of the negative feedback of contraction via TRP-Cav1.2-BKCa provides a new perspective for understanding the mechanism involved in the vascular responses triggered by caffeine."xsd:string
http://purl.uniprot.org/citations/31194991http://purl.org/dc/terms/identifier"doi:10.1016/j.lfs.2019.116555"xsd:string
http://purl.uniprot.org/citations/31194991http://purl.uniprot.org/core/author"Lemos V.S."xsd:string
http://purl.uniprot.org/citations/31194991http://purl.uniprot.org/core/author"Cortes S.F."xsd:string
http://purl.uniprot.org/citations/31194991http://purl.uniprot.org/core/author"Lopes M.J."xsd:string
http://purl.uniprot.org/citations/31194991http://purl.uniprot.org/core/author"Garcia D.C.G."xsd:string
http://purl.uniprot.org/citations/31194991http://purl.uniprot.org/core/author"Mbiakop U.C."xsd:string
http://purl.uniprot.org/citations/31194991http://purl.uniprot.org/core/date"2019"xsd:gYear
http://purl.uniprot.org/citations/31194991http://purl.uniprot.org/core/name"Life Sci"xsd:string
http://purl.uniprot.org/citations/31194991http://purl.uniprot.org/core/pages"116555"xsd:string
http://purl.uniprot.org/citations/31194991http://purl.uniprot.org/core/title"Activation of Cav1.2 and BKCa is involved in the downregulation of caffeine-induced contraction in mice mesenteric arteries."xsd:string
http://purl.uniprot.org/citations/31194991http://purl.uniprot.org/core/volume"231"xsd:string
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