Effect of trolox C on cardiac contracture induced by hydrogen peroxide

Detalhes bibliográficos
Autor(a) principal: Belló-Klein, Adriane
Data de Publicação: 1997
Outros Autores: Oliveira, Álvaro Reischak de, Miranda, Madalena Freitas Silva de, Irigoyen, Maria Claudia Costa, Bittencourt Junior, Paulo Ivo Homem de, Llesuy, Susana Francisca, Bello, Antonio Andrea
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UFRGS
Texto Completo: http://hdl.handle.net/10183/225994
Resumo: Hydrogen 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.
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spelling Belló-Klein, AdrianeOliveira, Álvaro Reischak deMiranda, Madalena Freitas Silva deIrigoyen, Maria Claudia CostaBittencourt Junior, Paulo Ivo Homem deLlesuy, Susana FranciscaBello, Antonio Andrea2021-08-20T04:12:53Z19970100-879Xhttp://hdl.handle.net/10183/225994001090452Hydrogen 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.application/pdfengBrazilian journal of medical and biological research = Revista brasileira de pesquisas médicas e biológicas. Ribeirão Preto. Vol. 30, no. 11 (Nov. 1997), p. 1337-1342Peróxido de hidrogênioEstresse oxidativoRadicais livresTrolox CStone heartFree radicalsHydrogen peroxideEffect of trolox C on cardiac contracture induced by hydrogen peroxideinfo:eu-repo/semantics/articleinfo:eu-repo/semantics/otherinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/openAccessreponame:Repositório Institucional da UFRGSinstname:Universidade Federal do Rio Grande do Sul (UFRGS)instacron:UFRGSTEXT001090452.pdf.txt001090452.pdf.txtExtracted Texttext/plain21395http://www.lume.ufrgs.br/bitstream/10183/225994/2/001090452.pdf.txtadef3f894d0bb86dd2249824908ad4fcMD52ORIGINAL001090452.pdfTexto completo (inglês)application/pdf185204http://www.lume.ufrgs.br/bitstream/10183/225994/1/001090452.pdf8a63ff699d90d1b9eb87b83b151e1c5cMD5110183/2259942021-09-18 04:52:57.625091oai:www.lume.ufrgs.br:10183/225994Repositório InstitucionalPUBhttps://lume.ufrgs.br/oai/requestlume@ufrgs.bropendoar:2021-09-18T07:52:57Repositório Institucional da UFRGS - Universidade Federal do Rio Grande do Sul (UFRGS)false
dc.title.pt_BR.fl_str_mv Effect of trolox C on cardiac contracture induced by hydrogen peroxide
title Effect of trolox C on cardiac contracture induced by hydrogen peroxide
spellingShingle Effect of trolox C on cardiac contracture induced by hydrogen peroxide
Belló-Klein, Adriane
Peróxido de hidrogênio
Estresse oxidativo
Radicais livres
Trolox C
Stone heart
Free radicals
Hydrogen peroxide
title_short Effect of trolox C on cardiac contracture induced by hydrogen peroxide
title_full Effect of trolox C on cardiac contracture induced by hydrogen peroxide
title_fullStr Effect of trolox C on cardiac contracture induced by hydrogen peroxide
title_full_unstemmed Effect of trolox C on cardiac contracture induced by hydrogen peroxide
title_sort Effect of trolox C on cardiac contracture induced by hydrogen peroxide
author Belló-Klein, Adriane
author_facet Belló-Klein, Adriane
Oliveira, Álvaro Reischak de
Miranda, Madalena Freitas Silva de
Irigoyen, Maria Claudia Costa
Bittencourt Junior, Paulo Ivo Homem de
Llesuy, Susana Francisca
Bello, Antonio Andrea
author_role author
author2 Oliveira, Álvaro Reischak de
Miranda, Madalena Freitas Silva de
Irigoyen, Maria Claudia Costa
Bittencourt Junior, Paulo Ivo Homem de
Llesuy, Susana Francisca
Bello, Antonio Andrea
author2_role author
author
author
author
author
author
dc.contributor.author.fl_str_mv Belló-Klein, Adriane
Oliveira, Álvaro Reischak de
Miranda, Madalena Freitas Silva de
Irigoyen, Maria Claudia Costa
Bittencourt Junior, Paulo Ivo Homem de
Llesuy, Susana Francisca
Bello, Antonio Andrea
dc.subject.por.fl_str_mv Peróxido de hidrogênio
Estresse oxidativo
Radicais livres
topic Peróxido de hidrogênio
Estresse oxidativo
Radicais livres
Trolox C
Stone heart
Free radicals
Hydrogen peroxide
dc.subject.eng.fl_str_mv Trolox C
Stone heart
Free radicals
Hydrogen peroxide
description Hydrogen 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.
publishDate 1997
dc.date.issued.fl_str_mv 1997
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dc.language.iso.fl_str_mv eng
language eng
dc.relation.ispartof.pt_BR.fl_str_mv Brazilian journal of medical and biological research = Revista brasileira de pesquisas médicas e biológicas. Ribeirão Preto. Vol. 30, no. 11 (Nov. 1997), p. 1337-1342
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