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Cardioprotective Effects of Leucine Supplementation against Doxorubicin-Induced Cardiotoxicit.
Guimarães, Lucas C; Fidale, Thiago M; Pereira, Talita C R; Lopes, Paulo R; Ferreira-Junior, Marcos D; Deconte, Simone R; Ferreira-Neto, Marcos L; Brito, Willams S; Gomes, Rodrigo M; de Souza, Fernanda R; Cavalcante, Keilah V N; Herrera, Gustavo C; de Moura, Francyelle B R; Resende, Elmiro S.
Afiliación
  • Guimarães LC; Laboratory of Experimental Medicine, Department of Health Sciences - PGCS, Faculty of Medicine, Federal University of Uberlândia, Uberlândia, Brazil. lucasimetria@gmail.com.
  • Fidale TM; Biotechnology Institute. Department of Medicine, Federal University of Catalão, Catalão, Goiás, Brazil.
  • Pereira TCR; Institute of Biomedical Sciences, Department of Physiology, Federal University of Uberlândia, Uberlândia, MG, Brazil.
  • Lopes PR; School of Dentistry-FOAr, Department of Physiology and Pathology, Universidade Estadual Paulista "Júlio de Mesquita Filho"-UNESP, Araraquara, SP, Brazil.
  • Ferreira-Junior MD; Laboratory of Endocrine Physiology and Metabolism, ICB, Universidade Federal de Goiás, Goiânia, GO, Brazil.
  • Deconte SR; UFU-ICBIM. Department of Physiology and Biophysics, Federal University of Uberlândia, Uberlândia, Brazil.
  • Ferreira-Neto ML; UFU-ICBIM. Department of Physiology and Biophysics, Federal University of Uberlândia, Uberlândia, Brazil.
  • Brito WS; Federal University of Piauí, Teresina, PI, Brazil.
  • Gomes RM; Laboratory of Endocrine Physiology and Metabolism, ICB, Universidade Federal de Goiás, Goiânia, GO, Brazil.
  • de Souza FR; Laboratory of Experimental Medicine, Department of Medicine, Federal University of Uberlândia, Uberlândia, MG, Brazil.
  • Cavalcante KVN; Laboratory of Endocrine Physiology and Metabolism, ICB, Universidade Federal de Goiás, Goiânia, GO, Brazil.
  • Herrera GC; The Veterinary Hospital, Federal University of Uberlândia, Uberlândia, MG, Brazil.
  • de Moura FBR; Department of Biological Sciences, Federal University of Catalão, Catalão, Goiás, Brazil.
  • Resende ES; Laboratory of Experimental Medicine, Department of Health Sciences - PGCS, Faculty of Medicine, Federal University of Uberlândia, Uberlândia, Brazil.
Cardiovasc Toxicol ; 24(2): 122-132, 2024 Feb.
Article en En | MEDLINE | ID: mdl-38165500
ABSTRACT
Doxorubicin is one of the most important antitumor drugs used in oncology; however, its cardiotoxic effect limits the therapeutic use and raises concerns regarding patient prognosis. Leucine is a branched-chain amino acid used in dietary supplementation and has been studied to attenuate the toxic effects of doxorubicin in animals, which increases oxidative stress. Oxidative stress in different organs can be estimated using several methods, including catalase expression analysis. This study aimed to analyze the effect of leucine on catalase levels in rat hearts after doxorubicin administration. Adult male Wistar rats were separated into two groups Standard diet (SD) and 5% Leucine-Enriched Diet (LED). The animals had free access to diet from D0 to D28. At D14, the groups were subdivided in animals injected with Doxorubicin and animals injected with vehicle, until D28, and the groups were SD, SD + Dox, LED and LED + Dox. At D28, the animals were submitted do Transthoracic Echocardiography and euthanized. Despite Dox groups had impaired body weight gain, raw heart weight was not different between the groups. No substantial alterations were observed in macroscopic evaluation of the heart. Although, Doxorubicin treatment increased total interstitial collagen in the heart, which in addition to Type I collagen, is lower in LED groups. Western blot analysis showed that catalase expression in the heart of LED groups was lower than that in SD groups. In conclusion, leucine supplementation reduced both the precocious Dox-induced cardiac remodeling and catalase levels in the heart.
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Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Doxorrubicina / Cardiotoxicidad Límite: Animals / Humans / Male Idioma: En Revista: Cardiovasc Toxicol Asunto de la revista: ANGIOLOGIA / CARDIOLOGIA / TOXICOLOGIA Año: 2024 Tipo del documento: Article País de afiliación: Brasil

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Doxorrubicina / Cardiotoxicidad Límite: Animals / Humans / Male Idioma: En Revista: Cardiovasc Toxicol Asunto de la revista: ANGIOLOGIA / CARDIOLOGIA / TOXICOLOGIA Año: 2024 Tipo del documento: Article País de afiliación: Brasil