Inhibition of protein tyrosine phosphatases unmasks vasoconstriction and potentiates calcium signalling in rat aorta smooth muscle cells in response to an agonist of 5-HT2B receptors BW723C86

dc.cclicenceCC-BY-NC-NDen
dc.contributor.authorMironova, G. Y.en
dc.contributor.authorAvdonin, P. P.en
dc.contributor.authorGoncharov, Nikolay V.en
dc.contributor.authorJenkins, R. O.en
dc.contributor.authorAvdonin, P. V.en
dc.date.acceptance2016-12-12en
dc.date.accessioned2017-01-23T15:04:06Z
dc.date.available2017-01-23T15:04:06Z
dc.date.issued2016-12-13
dc.descriptionThe file attached to this record is the author's final peer reviewed version. The Publisher's final version can be found by following the DOI link.en
dc.description.abstractIn blood vessels, serotonin 5-HT2B receptors mainly mediate relaxation, although their activation by the selective agonist BW723C86 is known to exert contraction of aorta in deoxycorticosterone acetate (DOCA)-salt and N(omega)-nitro-L-arginine (L-NAME) hypertensive rats [Russel et al., 2002; Banes et al., 2003] and in mice with type 2 diabetes [Nelson et al., 2012]. The unmasking effect on vasoconstriction can be caused by a shift in the balance of tyrosine phosphorylation in smooth muscle cells (SMC) due to oxidative stress induced inhibition of protein tyrosine phosphatases (PTP). We have demonstrated that BW723C86 which does not cause contraction of rat aorta and mesenteric artery rings, evoked a vasoconstrictor effect in the presence of PTP inhibitors sodium orthovanadate (Na3VO4) or BVT948. BW723C86 induced a weak rise of [Ca2+]i in the SMC isolated from rat aorta; however, after pre-incubation with Na3VO4 the response to BW723C86 increased more than 5-fold. This effect was diminished by protein tyrosine kinase (PTK) inhibitor genistein, inhibitor of Src-family kinases PP2, inhibitor of NADPH-oxidase VAS2870 and completely suppressed by N-acetylcysteine and 5-HT2B receptor antagonist RS127445. Using fluorescent probe DCFH-DA we have shown that Na3VO4 induces oxidative stress in SMC. In the presence of Na3VO4 BW723C86 considerably increased formation of reactive oxygen species while alone had no appreciable effect on DCFH oxidation. We suggest that oxidative stress causes inhibition of PTP and unmasking of 5-HT2B receptors functional activity.en
dc.funderRussian Science Foundationen
dc.identifier.citationMironova, G.Y. et al. (2017) Inhibition of protein tyrosine phosphatases unmasks vasoconstriction and potentiates calcium signalling in rat aorta smooth muscle cells in response to an agonist of 5-HT2B receptors BW723C86. Biochemical and Biophysical Research Communications, 483 (1), pp. 700-705en
dc.identifier.doihttps://doi.org/10.1016/j.bbrc.2016.12.079
dc.identifier.issn0006-291X
dc.identifier.urihttp://hdl.handle.net/2086/13199
dc.language.isoenen
dc.peerreviewedYesen
dc.projectid14-15-01004en
dc.publisherElsevieren
dc.researchgroupBiomedical and Environmental Healthen
dc.researchinstituteInstitute for Allied Health Sciences Researchen
dc.subject5-HT2B receptorsen
dc.subjectsmooth muscle cellsen
dc.subjectprotein tyrosine phosphatasesen
dc.subjectoxidative stressen
dc.subjectcalciumen
dc.subjecthypertensionen
dc.titleInhibition of protein tyrosine phosphatases unmasks vasoconstriction and potentiates calcium signalling in rat aorta smooth muscle cells in response to an agonist of 5-HT2B receptors BW723C86en
dc.typeArticleen

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