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dc.contributor.authorBaker, J. G.en
dc.contributor.authorKemp, P.en
dc.contributor.authorMarch, J.en
dc.contributor.authorFretwell, L.en
dc.contributor.authorHill, S. J.en
dc.contributor.authorGardiner, S. M.en
dc.date.accessioned2013-04-10T08:22:24Z
dc.date.available2013-04-10T08:22:24Z
dc.date.issued2011-08-24
dc.identifier.citationBaker, J., Kemp, P., March, J., Fretwell, L., Hill, S., and Gardiner, S. (2011) Predicting in vivo cardiovascular properties of blockers from cellular and cardiovascular pharmacological responses. The FASEB Journal. 25 (12), pp. 4486-4497en
dc.identifier.urihttp://hdl.handle.net/2086/8333
dc.description.abstractBeta -Adrenoceptor antagonists differ in their degree of partial agonism. In vitro assays have provided information on ligand affinity, selectivity, and intrinsic efficacy. However, the extent to which these properties are manifest in vivo is less clear. Conscious freely moving rats, instrumented for measurement of heart rate ( 1; HR) and hindquarters vascular conductance ( 2; HVC) were used to measure receptor selectivityand ligand efficacy in vivo. CGP 20712A caused a dose-dependent decrease in basal HR (P<0.05, ANOVA) at 5 doses between 6.7 and 670 g/kg (i.v.) and shifted the dose-response curve for isoprenaline to higher agonist concentrations without altering HVC responses. In contrast, at doses of 67 g/kg (i.v.) and above, ICI 118551 substantially reduced the HVC response to isoprenaline without affecting HR responses. ZD 7114, xamoterol, and bucindolol significantly increased basal HR ( HR: 122 12, 129 11, and 59 11 beats/min, respectively; n 6), whereas other -blockers caused significant reductions (all at 2 mg/kg i.v.). The agonist effects of xamoterol and ZD 7114 were equivalent to that of the highest dose of isoprenaline. Bucindolol, however, significantly antagonized the response to the highest doses isoprenaline. An excellent correlation was obtained between in vivo and in vitro measures of 1-adrenoceptor efficacy(R2 0.93; P<0.0001).en
dc.language.isoenen
dc.publisherFASEBen
dc.subjectpartial agonismen
dc.subjectintrinsic sympathomimeticen
dc.subjectheart rateen
dc.subjectvascular conductanceen
dc.titlePredicting in vivo cardiovascular properties of blockers from cellular assays: a quantitative comparison of cellular and cardiovascular pharmacological responsesen
dc.typeArticleen
dc.identifier.doihttp://dx.doi.org/10.1096/fj.11-192435
dc.peerreviewedYesen
dc.ref2014.selected1365591152_1310680262232_3_3
dc.researchinstituteInstitute for Allied Health Sciences Researchen


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