Pera orange (Citrus sinensis) and Moro orange (Citrus sinensis (L.) Osbeck) juices attenuate left ventricular dysfunction and oxidative stress and improve myocardial energy metabolism in acute doxorubicin-induced cardiotoxicity in rats
•Doxorubicin is a chemotherapeutic agent used in treating cancer; however, it leads to cardiotoxicity.•Consumption of orange juice attenuated cardiac remodeling induced by doxorubicin, improved myocardial energy metabolism, and attenuated oxidative stress.•Moro orange juice was more effective in mod...
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Veröffentlicht in: | Nutrition (Burbank, Los Angeles County, Calif.) Los Angeles County, Calif.), 2021-11, Vol.91-92, p.111350-111350, Article 111350 |
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creator | Ribeiro, Ana Paula Dantas Pereira, Amanda Gomes Todo, Márcia Cristina Fujimori, Anderson Seiji Soares dos Santos, Priscila Portugal Dantas, Danielle Fernandes, Ana Angélica Zanati, Silmeia Garcia Hassimotto, Neuza Mariko Aymoto Zornoff, Leonardo Antônio Mamede Azevedo, Paula Schmidt Minicucci, Marcos Ferreira Paiva, Sergio A.R. Polegato, Bertha Furlan |
description | •Doxorubicin is a chemotherapeutic agent used in treating cancer; however, it leads to cardiotoxicity.•Consumption of orange juice attenuated cardiac remodeling induced by doxorubicin, improved myocardial energy metabolism, and attenuated oxidative stress.•Moro orange juice was more effective in modifying energy metabolism and oxidative stress than Pera orange juice, probably because of its anthocyanin content.
Doxorubicin is a highly effective chemotherapeutic agent for treating several types of cancer; however, it can induce cardiotoxicity. We evaluated the influence of Pera and Moro orange juices on cardiac remodeling induced by acute administration of doxorubicin in rats.
We allocated 120 male Wistar rats into six groups: control (C), Pera orange juice (PO), Moro orange juice (MO), doxorubicin (D), doxorubicin + Pera orange juice (DPO), and doxorubicin + Moro orange juice (DMO). Groups PO and DPO received Pera orange juice, MO and DMO received Moro orange juice, and C and D received water with maltodextrin (100 g/L) for 4 wk. Subsequently, groups D, DPO, and DMO received 20 mg/kg doxorubicin and C, PO, and MO received saline. Echocardiogram and euthanasia were performed 48 h after doxorubicin injection. Juice and animal-serum flavonoid identification and quantification were evaluated by liquid chromatography/electrospray ionization multistage mass spectrometry. Oxidative stress and myocardial metabolism were evaluated by spectrophotometry.
Systolic and diastolic left ventricular dysfunction increased oxidative stress and pathologic changes in myocardial energy metabolism of rats treated with doxorubicin. Intake of both orange juices improved left ventricular function, decreased oxidative stress, and attenuated the myocardial energy metabolism changes. Moro orange juice had a more pronounced effect than Pera orange juice in glutathione peroxidase activity, citrate synthase, and β-hydroxyacyl-CoA dehydrogenase activity.
Pera and Moro orange juices attenuated cardiac remodeling induced by doxorubicin, improved myocardial energy metabolism, and attenuated oxidative stress. However, Moro orange juice was more effective than Pera orange juice in modifying energy metabolism. |
doi_str_mv | 10.1016/j.nut.2021.111350 |
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Doxorubicin is a highly effective chemotherapeutic agent for treating several types of cancer; however, it can induce cardiotoxicity. We evaluated the influence of Pera and Moro orange juices on cardiac remodeling induced by acute administration of doxorubicin in rats.
We allocated 120 male Wistar rats into six groups: control (C), Pera orange juice (PO), Moro orange juice (MO), doxorubicin (D), doxorubicin + Pera orange juice (DPO), and doxorubicin + Moro orange juice (DMO). Groups PO and DPO received Pera orange juice, MO and DMO received Moro orange juice, and C and D received water with maltodextrin (100 g/L) for 4 wk. Subsequently, groups D, DPO, and DMO received 20 mg/kg doxorubicin and C, PO, and MO received saline. Echocardiogram and euthanasia were performed 48 h after doxorubicin injection. Juice and animal-serum flavonoid identification and quantification were evaluated by liquid chromatography/electrospray ionization multistage mass spectrometry. Oxidative stress and myocardial metabolism were evaluated by spectrophotometry.
Systolic and diastolic left ventricular dysfunction increased oxidative stress and pathologic changes in myocardial energy metabolism of rats treated with doxorubicin. Intake of both orange juices improved left ventricular function, decreased oxidative stress, and attenuated the myocardial energy metabolism changes. Moro orange juice had a more pronounced effect than Pera orange juice in glutathione peroxidase activity, citrate synthase, and β-hydroxyacyl-CoA dehydrogenase activity.
Pera and Moro orange juices attenuated cardiac remodeling induced by doxorubicin, improved myocardial energy metabolism, and attenuated oxidative stress. However, Moro orange juice was more effective than Pera orange juice in modifying energy metabolism.</description><identifier>ISSN: 0899-9007</identifier><identifier>EISSN: 1873-1244</identifier><identifier>DOI: 10.1016/j.nut.2021.111350</identifier><identifier>PMID: 34265580</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Animals ; Attenuation ; Cancer therapies ; Cardiotoxicity ; Cardiotoxicity - etiology ; Chromatography ; citrate (si)-synthase ; Citrate synthase ; Citrus fruits ; Citrus sinensis ; Dimensional analysis ; Doxorubicin ; Doxorubicin - toxicity ; drug therapy ; Echocardiography ; electrospray ionization mass spectrometry ; Energy Metabolism ; Euthanasia ; Flavonoids ; Fluorides ; Fruit juices ; Fruits ; Gas flow ; Glutathione ; Glutathione peroxidase ; Heart ; Heart failure ; Ionization ; Juices ; Lipid hydroperoxide ; Liquid chromatography ; Male ; males ; Maltodextrin ; maltodextrins ; Mass spectrometry ; Mass spectroscopy ; Metabolism ; Metabolites ; Mitochondrial respiratory chain ; nutrition ; orange juice ; Oranges ; Oxidative metabolism ; Oxidative Stress ; Peroxidase ; Rats ; Rats, Wistar ; Scientific imaging ; Spectrophotometry ; Ventricle ; Ventricular Dysfunction, Left - chemically induced ; β-Hydroxyacyl-CoA dehydrogenase</subject><ispartof>Nutrition (Burbank, Los Angeles County, Calif.), 2021-11, Vol.91-92, p.111350-111350, Article 111350</ispartof><rights>2021 Elsevier Inc.</rights><rights>Copyright © 2021 Elsevier Inc. All rights reserved.</rights><rights>2021. Elsevier Inc.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c457t-aa965bc2906829364f4ea65884c1eb93dc575d9f3aa711ae0804cba7683719ed3</citedby><cites>FETCH-LOGICAL-c457t-aa965bc2906829364f4ea65884c1eb93dc575d9f3aa711ae0804cba7683719ed3</cites><orcidid>0000-0002-2875-9532 ; 0000-0002-5843-6232 ; 0000-0002-9023-5756 ; 0000-0002-6517-9684 ; 0000-0002-5980-4367</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0899900721002124$$EHTML$$P50$$Gelsevier$$Hfree_for_read</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/34265580$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Ribeiro, Ana Paula Dantas</creatorcontrib><creatorcontrib>Pereira, Amanda Gomes</creatorcontrib><creatorcontrib>Todo, Márcia Cristina</creatorcontrib><creatorcontrib>Fujimori, Anderson Seiji Soares</creatorcontrib><creatorcontrib>dos Santos, Priscila Portugal</creatorcontrib><creatorcontrib>Dantas, Danielle</creatorcontrib><creatorcontrib>Fernandes, Ana Angélica</creatorcontrib><creatorcontrib>Zanati, Silmeia Garcia</creatorcontrib><creatorcontrib>Hassimotto, Neuza Mariko Aymoto</creatorcontrib><creatorcontrib>Zornoff, Leonardo Antônio Mamede</creatorcontrib><creatorcontrib>Azevedo, Paula Schmidt</creatorcontrib><creatorcontrib>Minicucci, Marcos Ferreira</creatorcontrib><creatorcontrib>Paiva, Sergio A.R.</creatorcontrib><creatorcontrib>Polegato, Bertha Furlan</creatorcontrib><title>Pera orange (Citrus sinensis) and Moro orange (Citrus sinensis (L.) Osbeck) juices attenuate left ventricular dysfunction and oxidative stress and improve myocardial energy metabolism in acute doxorubicin-induced cardiotoxicity in rats</title><title>Nutrition (Burbank, Los Angeles County, Calif.)</title><addtitle>Nutrition</addtitle><description>•Doxorubicin is a chemotherapeutic agent used in treating cancer; however, it leads to cardiotoxicity.•Consumption of orange juice attenuated cardiac remodeling induced by doxorubicin, improved myocardial energy metabolism, and attenuated oxidative stress.•Moro orange juice was more effective in modifying energy metabolism and oxidative stress than Pera orange juice, probably because of its anthocyanin content.
Doxorubicin is a highly effective chemotherapeutic agent for treating several types of cancer; however, it can induce cardiotoxicity. We evaluated the influence of Pera and Moro orange juices on cardiac remodeling induced by acute administration of doxorubicin in rats.
We allocated 120 male Wistar rats into six groups: control (C), Pera orange juice (PO), Moro orange juice (MO), doxorubicin (D), doxorubicin + Pera orange juice (DPO), and doxorubicin + Moro orange juice (DMO). Groups PO and DPO received Pera orange juice, MO and DMO received Moro orange juice, and C and D received water with maltodextrin (100 g/L) for 4 wk. Subsequently, groups D, DPO, and DMO received 20 mg/kg doxorubicin and C, PO, and MO received saline. Echocardiogram and euthanasia were performed 48 h after doxorubicin injection. Juice and animal-serum flavonoid identification and quantification were evaluated by liquid chromatography/electrospray ionization multistage mass spectrometry. Oxidative stress and myocardial metabolism were evaluated by spectrophotometry.
Systolic and diastolic left ventricular dysfunction increased oxidative stress and pathologic changes in myocardial energy metabolism of rats treated with doxorubicin. Intake of both orange juices improved left ventricular function, decreased oxidative stress, and attenuated the myocardial energy metabolism changes. Moro orange juice had a more pronounced effect than Pera orange juice in glutathione peroxidase activity, citrate synthase, and β-hydroxyacyl-CoA dehydrogenase activity.
Pera and Moro orange juices attenuated cardiac remodeling induced by doxorubicin, improved myocardial energy metabolism, and attenuated oxidative stress. However, Moro orange juice was more effective than Pera orange juice in modifying energy metabolism.</description><subject>Animals</subject><subject>Attenuation</subject><subject>Cancer therapies</subject><subject>Cardiotoxicity</subject><subject>Cardiotoxicity - etiology</subject><subject>Chromatography</subject><subject>citrate (si)-synthase</subject><subject>Citrate synthase</subject><subject>Citrus fruits</subject><subject>Citrus sinensis</subject><subject>Dimensional analysis</subject><subject>Doxorubicin</subject><subject>Doxorubicin - toxicity</subject><subject>drug therapy</subject><subject>Echocardiography</subject><subject>electrospray ionization mass spectrometry</subject><subject>Energy Metabolism</subject><subject>Euthanasia</subject><subject>Flavonoids</subject><subject>Fluorides</subject><subject>Fruit juices</subject><subject>Fruits</subject><subject>Gas flow</subject><subject>Glutathione</subject><subject>Glutathione peroxidase</subject><subject>Heart</subject><subject>Heart failure</subject><subject>Ionization</subject><subject>Juices</subject><subject>Lipid hydroperoxide</subject><subject>Liquid chromatography</subject><subject>Male</subject><subject>males</subject><subject>Maltodextrin</subject><subject>maltodextrins</subject><subject>Mass spectrometry</subject><subject>Mass spectroscopy</subject><subject>Metabolism</subject><subject>Metabolites</subject><subject>Mitochondrial respiratory chain</subject><subject>nutrition</subject><subject>orange juice</subject><subject>Oranges</subject><subject>Oxidative metabolism</subject><subject>Oxidative Stress</subject><subject>Peroxidase</subject><subject>Rats</subject><subject>Rats, Wistar</subject><subject>Scientific imaging</subject><subject>Spectrophotometry</subject><subject>Ventricle</subject><subject>Ventricular Dysfunction, Left - 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Osbeck) juices attenuate left ventricular dysfunction and oxidative stress and improve myocardial energy metabolism in acute doxorubicin-induced cardiotoxicity in rats</title><author>Ribeiro, Ana Paula Dantas ; Pereira, Amanda Gomes ; Todo, Márcia Cristina ; Fujimori, Anderson Seiji Soares ; dos Santos, Priscila Portugal ; Dantas, Danielle ; Fernandes, Ana Angélica ; Zanati, Silmeia Garcia ; Hassimotto, Neuza Mariko Aymoto ; Zornoff, Leonardo Antônio Mamede ; Azevedo, Paula Schmidt ; Minicucci, Marcos Ferreira ; Paiva, Sergio A.R. ; Polegato, Bertha Furlan</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c457t-aa965bc2906829364f4ea65884c1eb93dc575d9f3aa711ae0804cba7683719ed3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Animals</topic><topic>Attenuation</topic><topic>Cancer therapies</topic><topic>Cardiotoxicity</topic><topic>Cardiotoxicity - etiology</topic><topic>Chromatography</topic><topic>citrate (si)-synthase</topic><topic>Citrate synthase</topic><topic>Citrus fruits</topic><topic>Citrus sinensis</topic><topic>Dimensional analysis</topic><topic>Doxorubicin</topic><topic>Doxorubicin - toxicity</topic><topic>drug therapy</topic><topic>Echocardiography</topic><topic>electrospray ionization mass spectrometry</topic><topic>Energy Metabolism</topic><topic>Euthanasia</topic><topic>Flavonoids</topic><topic>Fluorides</topic><topic>Fruit juices</topic><topic>Fruits</topic><topic>Gas flow</topic><topic>Glutathione</topic><topic>Glutathione peroxidase</topic><topic>Heart</topic><topic>Heart failure</topic><topic>Ionization</topic><topic>Juices</topic><topic>Lipid hydroperoxide</topic><topic>Liquid chromatography</topic><topic>Male</topic><topic>males</topic><topic>Maltodextrin</topic><topic>maltodextrins</topic><topic>Mass spectrometry</topic><topic>Mass spectroscopy</topic><topic>Metabolism</topic><topic>Metabolites</topic><topic>Mitochondrial respiratory chain</topic><topic>nutrition</topic><topic>orange juice</topic><topic>Oranges</topic><topic>Oxidative metabolism</topic><topic>Oxidative Stress</topic><topic>Peroxidase</topic><topic>Rats</topic><topic>Rats, Wistar</topic><topic>Scientific imaging</topic><topic>Spectrophotometry</topic><topic>Ventricle</topic><topic>Ventricular Dysfunction, Left - chemically induced</topic><topic>β-Hydroxyacyl-CoA dehydrogenase</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ribeiro, Ana Paula Dantas</creatorcontrib><creatorcontrib>Pereira, Amanda Gomes</creatorcontrib><creatorcontrib>Todo, Márcia Cristina</creatorcontrib><creatorcontrib>Fujimori, Anderson Seiji Soares</creatorcontrib><creatorcontrib>dos Santos, Priscila Portugal</creatorcontrib><creatorcontrib>Dantas, Danielle</creatorcontrib><creatorcontrib>Fernandes, Ana Angélica</creatorcontrib><creatorcontrib>Zanati, Silmeia Garcia</creatorcontrib><creatorcontrib>Hassimotto, Neuza Mariko Aymoto</creatorcontrib><creatorcontrib>Zornoff, Leonardo Antônio Mamede</creatorcontrib><creatorcontrib>Azevedo, Paula Schmidt</creatorcontrib><creatorcontrib>Minicucci, Marcos Ferreira</creatorcontrib><creatorcontrib>Paiva, Sergio A.R.</creatorcontrib><creatorcontrib>Polegato, Bertha Furlan</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Career & Technical Education Database</collection><collection>Nursing & Allied Health Database</collection><collection>Physical Education Index</collection><collection>Toxicology Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Healthcare Administration Database (Alumni)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Public Health Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Research Library (Alumni Edition)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest One Sustainability</collection><collection>ProQuest Central UK/Ireland</collection><collection>British Nursing Database</collection><collection>British Nursing Index</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>British Nursing Index (BNI) (1985 to Present)</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>Research Library Prep</collection><collection>SciTech Premium Collection</collection><collection>British Nursing Index</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Healthcare Administration Database</collection><collection>Medical Database</collection><collection>Research Library</collection><collection>Biological Science Database</collection><collection>Research Library (Corporate)</collection><collection>Nursing & Allied Health Premium</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central Basic</collection><collection>AGRICOLA</collection><collection>AGRICOLA - Academic</collection><collection>MEDLINE - Academic</collection><jtitle>Nutrition (Burbank, Los Angeles County, Calif.)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ribeiro, Ana Paula Dantas</au><au>Pereira, Amanda Gomes</au><au>Todo, Márcia Cristina</au><au>Fujimori, Anderson Seiji Soares</au><au>dos Santos, Priscila Portugal</au><au>Dantas, Danielle</au><au>Fernandes, Ana Angélica</au><au>Zanati, Silmeia Garcia</au><au>Hassimotto, Neuza Mariko Aymoto</au><au>Zornoff, Leonardo Antônio Mamede</au><au>Azevedo, Paula Schmidt</au><au>Minicucci, Marcos Ferreira</au><au>Paiva, Sergio A.R.</au><au>Polegato, Bertha Furlan</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Pera orange (Citrus sinensis) and Moro orange (Citrus sinensis (L.) Osbeck) juices attenuate left ventricular dysfunction and oxidative stress and improve myocardial energy metabolism in acute doxorubicin-induced cardiotoxicity in rats</atitle><jtitle>Nutrition (Burbank, Los Angeles County, Calif.)</jtitle><addtitle>Nutrition</addtitle><date>2021-11</date><risdate>2021</risdate><volume>91-92</volume><spage>111350</spage><epage>111350</epage><pages>111350-111350</pages><artnum>111350</artnum><issn>0899-9007</issn><eissn>1873-1244</eissn><abstract>•Doxorubicin is a chemotherapeutic agent used in treating cancer; however, it leads to cardiotoxicity.•Consumption of orange juice attenuated cardiac remodeling induced by doxorubicin, improved myocardial energy metabolism, and attenuated oxidative stress.•Moro orange juice was more effective in modifying energy metabolism and oxidative stress than Pera orange juice, probably because of its anthocyanin content.
Doxorubicin is a highly effective chemotherapeutic agent for treating several types of cancer; however, it can induce cardiotoxicity. We evaluated the influence of Pera and Moro orange juices on cardiac remodeling induced by acute administration of doxorubicin in rats.
We allocated 120 male Wistar rats into six groups: control (C), Pera orange juice (PO), Moro orange juice (MO), doxorubicin (D), doxorubicin + Pera orange juice (DPO), and doxorubicin + Moro orange juice (DMO). Groups PO and DPO received Pera orange juice, MO and DMO received Moro orange juice, and C and D received water with maltodextrin (100 g/L) for 4 wk. Subsequently, groups D, DPO, and DMO received 20 mg/kg doxorubicin and C, PO, and MO received saline. Echocardiogram and euthanasia were performed 48 h after doxorubicin injection. Juice and animal-serum flavonoid identification and quantification were evaluated by liquid chromatography/electrospray ionization multistage mass spectrometry. Oxidative stress and myocardial metabolism were evaluated by spectrophotometry.
Systolic and diastolic left ventricular dysfunction increased oxidative stress and pathologic changes in myocardial energy metabolism of rats treated with doxorubicin. Intake of both orange juices improved left ventricular function, decreased oxidative stress, and attenuated the myocardial energy metabolism changes. Moro orange juice had a more pronounced effect than Pera orange juice in glutathione peroxidase activity, citrate synthase, and β-hydroxyacyl-CoA dehydrogenase activity.
Pera and Moro orange juices attenuated cardiac remodeling induced by doxorubicin, improved myocardial energy metabolism, and attenuated oxidative stress. However, Moro orange juice was more effective than Pera orange juice in modifying energy metabolism.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>34265580</pmid><doi>10.1016/j.nut.2021.111350</doi><tpages>1</tpages><orcidid>https://orcid.org/0000-0002-2875-9532</orcidid><orcidid>https://orcid.org/0000-0002-5843-6232</orcidid><orcidid>https://orcid.org/0000-0002-9023-5756</orcidid><orcidid>https://orcid.org/0000-0002-6517-9684</orcidid><orcidid>https://orcid.org/0000-0002-5980-4367</orcidid><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0899-9007 |
ispartof | Nutrition (Burbank, Los Angeles County, Calif.), 2021-11, Vol.91-92, p.111350-111350, Article 111350 |
issn | 0899-9007 1873-1244 |
language | eng |
recordid | cdi_proquest_miscellaneous_2552997225 |
source | MEDLINE; Elsevier ScienceDirect Journals |
subjects | Animals Attenuation Cancer therapies Cardiotoxicity Cardiotoxicity - etiology Chromatography citrate (si)-synthase Citrate synthase Citrus fruits Citrus sinensis Dimensional analysis Doxorubicin Doxorubicin - toxicity drug therapy Echocardiography electrospray ionization mass spectrometry Energy Metabolism Euthanasia Flavonoids Fluorides Fruit juices Fruits Gas flow Glutathione Glutathione peroxidase Heart Heart failure Ionization Juices Lipid hydroperoxide Liquid chromatography Male males Maltodextrin maltodextrins Mass spectrometry Mass spectroscopy Metabolism Metabolites Mitochondrial respiratory chain nutrition orange juice Oranges Oxidative metabolism Oxidative Stress Peroxidase Rats Rats, Wistar Scientific imaging Spectrophotometry Ventricle Ventricular Dysfunction, Left - chemically induced β-Hydroxyacyl-CoA dehydrogenase |
title | Pera orange (Citrus sinensis) and Moro orange (Citrus sinensis (L.) Osbeck) juices attenuate left ventricular dysfunction and oxidative stress and improve myocardial energy metabolism in acute doxorubicin-induced cardiotoxicity in rats |
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