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dc.contributor.authorBelló-Klein, Adrianept_BR
dc.contributor.authorOliveira, Álvaro Reischak dept_BR
dc.contributor.authorMiranda, Madalena Freitas Silva dept_BR
dc.contributor.authorIrigoyen, Maria Claudia Costapt_BR
dc.contributor.authorBittencourt Junior, Paulo Ivo Homem dept_BR
dc.contributor.authorLlesuy, Susana Franciscapt_BR
dc.contributor.authorBello, Antonio Andreapt_BR
dc.date.accessioned2021-08-20T04:12:53Zpt_BR
dc.date.issued1997pt_BR
dc.identifier.issn0100-879Xpt_BR
dc.identifier.urihttp://hdl.handle.net/10183/225994pt_BR
dc.description.abstractHydrogen peroxide (H2O2) perfused into the aorta of the isolated rat heart induces a positive inotropic effect, with cardiac arrhythmia such as extrasystolic potentiation or cardiac contractures, depending on the dose. The last effect is similar to the “stone heart” observed in reperfusion injury and may be ascribed to lipoperoxidation (LPO) of the membrane lipids, to protein damage, to reduction of the ATP level, to enzymatic alterations and to cardioactive compounds liberated by LPO. These effects may result in calcium overload of the cardiac fibers and contracture (“stone heart”). Hearts from male Wistar rats (300- 350 g) were perfused at 31o C with Tyrode, 0.2 mM trolox C, 256 mM H2O2 or trolox C + H2O2. Cardiac contractures (baseline elevation of the myograms obtained) were observed when hearts were perfused with H2O2 (Tyrode: 5.9 ± 3.2; H2O2: 60.5 ± 13.9% of the initial value); perfusion with H2O2 increased the LPO of rat heart homogenates measured by chemiluminescence (Tyrode: 3,199 ± 259; H2O2: 5,304 ± 133 cps mg protein-1 60 min-1), oxygen uptake (Tyrode: 0.44 ± 0.1; H2O2: 3.2 ± 0.8 nmol min-1 mg protein-1) and malonaldehyde (TBARS) formation (Tyrode: 0.12 ± 0; H2O2: 0.37 ± 0.1 nmol/ml). Previous perfusion with 0.2 mM trolox C reduced the LPO (chemiluminescence: 4,098 ± 531), oxygen uptake (0.51 ± 0) and TBARS (0.13 ± 0) but did not prevent the H2O2-induced contractures (33.3 ± 16%). ATP (Tyrode: 2.84 ± 0; H2O2: 0.57 ± 0) and glycogen levels (Tyrode: 0.46 ± 0; H2O2: 0.26 ± 0) were reduced by H2O2. Trolox did not prevent these effects (ATP: 0.84 ± 0 and glycogen: 0.27 ± 0). Trolox C is known to be more effective than α-tocopherol or γ-tocopherol in reducing LPO though it lacks the phytol portion of vitamin E to be fixed to the cell membranes. Trolox C, unlike vitamin A, did not prevent the glycogen reduction induced by H2O2. Trolox C induced a positive chronotropic effect that resulted in higher energy consumption. The reduction of energy level seemed to be more important than LPO in the mechanism of H2O2-induced contracture.en
dc.format.mimetypeapplication/pdfpt_BR
dc.language.isoengpt_BR
dc.relation.ispartofBrazilian journal of medical and biological research = Revista brasileira de pesquisas médicas e biológicas. Ribeirão Preto. Vol. 30, no. 11 (Nov. 1997), p. 1337-1342pt_BR
dc.rightsOpen Accessen
dc.subjectTrolox Cen
dc.subjectPeróxido de hidrogêniopt_BR
dc.subjectEstresse oxidativopt_BR
dc.subjectStone hearten
dc.subjectFree radicalsen
dc.subjectRadicais livrespt_BR
dc.subjectHydrogen peroxideen
dc.titleEffect of trolox C on cardiac contracture induced by hydrogen peroxidept_BR
dc.typeArtigo de periódicopt_BR
dc.identifier.nrb001090452pt_BR
dc.type.originNacionalpt_BR


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