Dirceu de Sousa Melo, Liliane Costa-Pereira, Carina Sousa Santos, Bruno Ferreira Mendes, Isaac Konig, Bruna Chaves Garcia, Ilkilene Queiroz, Lauane Gomes Moreno, Ricardo Cardoso Cassilhas, Elizabethe Adriana Esteves, Etel Vieira Rocha, Flávio Castro Magalhães, Luciano Dos Santos Aggum Capettini, Ricardo Augusto Leoni, Kinulpe Sampaio, Marco Fabrício Dias-Peixoto
{"title":"出生后严格的热量限制可以防止大鼠心血管衰老。","authors":"Dirceu de Sousa Melo, Liliane Costa-Pereira, Carina Sousa Santos, Bruno Ferreira Mendes, Isaac Konig, Bruna Chaves Garcia, Ilkilene Queiroz, Lauane Gomes Moreno, Ricardo Cardoso Cassilhas, Elizabethe Adriana Esteves, Etel Vieira Rocha, Flávio Castro Magalhães, Luciano Dos Santos Aggum Capettini, Ricardo Augusto Leoni, Kinulpe Sampaio, Marco Fabrício Dias-Peixoto","doi":"10.1089/rej.2023.0032","DOIUrl":null,"url":null,"abstract":"<p><p>We previously demonstrated that a 50% caloric restriction (CR) from birth improves several cardiometabolic risk factors in young rats. In this study, we investigated in middle-aged rats the consequences of a 50% CR from birth on cardiometabolic risk factors, heart function/morphology, ventricular arrhythmia, and fibrillation incidence, and cardiac intracellular proteins involved with redox status and cell survival. From birth to the age of 18 months, rats were divided into an <i>Ad Libitum</i> (AL18) group, which had free access to food, and a CR18 group, which had food limited to 50% of that consumed by the AL18. Resting metabolic rate, blood pressure, and heart rate were recorded, and oral glucose and intraperitoneal insulin tolerance tests were performed. Blood was collected for biochemical analyses, and visceral fat and liver were harvested and weighed. Hearts were harvested for cardiac function, histological, redox status, and western blot analyses. The 50% CR from birth potentially reduced several cardiometabolic risk factors in 18-month-old rats. Moreover, compared with AL18, the CR18 group showed a ∼50% increase in cardiac contractility and relaxation, nearly three to five times less incidence of ventricular arrhythmia and fibrillation, ∼18% lower cardiomyocyte diameter, and ∼60% lower cardiac fibrosis. CR18 hearts also improved biomarkers of antioxidant defense and cell survival. Collectively, these results reveal several metabolic and cardiac antiaging effects of a 50% CR from birth in middle-aged rats.</p>","PeriodicalId":20979,"journal":{"name":"Rejuvenation research","volume":" ","pages":"194-205"},"PeriodicalIF":2.2000,"publicationDate":"2023-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Intense Caloric Restriction from Birth Prevents Cardiovascular Aging in Rats.\",\"authors\":\"Dirceu de Sousa Melo, Liliane Costa-Pereira, Carina Sousa Santos, Bruno Ferreira Mendes, Isaac Konig, Bruna Chaves Garcia, Ilkilene Queiroz, Lauane Gomes Moreno, Ricardo Cardoso Cassilhas, Elizabethe Adriana Esteves, Etel Vieira Rocha, Flávio Castro Magalhães, Luciano Dos Santos Aggum Capettini, Ricardo Augusto Leoni, Kinulpe Sampaio, Marco Fabrício Dias-Peixoto\",\"doi\":\"10.1089/rej.2023.0032\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>We previously demonstrated that a 50% caloric restriction (CR) from birth improves several cardiometabolic risk factors in young rats. In this study, we investigated in middle-aged rats the consequences of a 50% CR from birth on cardiometabolic risk factors, heart function/morphology, ventricular arrhythmia, and fibrillation incidence, and cardiac intracellular proteins involved with redox status and cell survival. From birth to the age of 18 months, rats were divided into an <i>Ad Libitum</i> (AL18) group, which had free access to food, and a CR18 group, which had food limited to 50% of that consumed by the AL18. Resting metabolic rate, blood pressure, and heart rate were recorded, and oral glucose and intraperitoneal insulin tolerance tests were performed. Blood was collected for biochemical analyses, and visceral fat and liver were harvested and weighed. Hearts were harvested for cardiac function, histological, redox status, and western blot analyses. The 50% CR from birth potentially reduced several cardiometabolic risk factors in 18-month-old rats. 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Intense Caloric Restriction from Birth Prevents Cardiovascular Aging in Rats.
We previously demonstrated that a 50% caloric restriction (CR) from birth improves several cardiometabolic risk factors in young rats. In this study, we investigated in middle-aged rats the consequences of a 50% CR from birth on cardiometabolic risk factors, heart function/morphology, ventricular arrhythmia, and fibrillation incidence, and cardiac intracellular proteins involved with redox status and cell survival. From birth to the age of 18 months, rats were divided into an Ad Libitum (AL18) group, which had free access to food, and a CR18 group, which had food limited to 50% of that consumed by the AL18. Resting metabolic rate, blood pressure, and heart rate were recorded, and oral glucose and intraperitoneal insulin tolerance tests were performed. Blood was collected for biochemical analyses, and visceral fat and liver were harvested and weighed. Hearts were harvested for cardiac function, histological, redox status, and western blot analyses. The 50% CR from birth potentially reduced several cardiometabolic risk factors in 18-month-old rats. Moreover, compared with AL18, the CR18 group showed a ∼50% increase in cardiac contractility and relaxation, nearly three to five times less incidence of ventricular arrhythmia and fibrillation, ∼18% lower cardiomyocyte diameter, and ∼60% lower cardiac fibrosis. CR18 hearts also improved biomarkers of antioxidant defense and cell survival. Collectively, these results reveal several metabolic and cardiac antiaging effects of a 50% CR from birth in middle-aged rats.
期刊介绍:
Rejuvenation Research publishes cutting-edge, peer-reviewed research on rejuvenation therapies in the laboratory and the clinic. The Journal focuses on key explorations and advances that may ultimately contribute to slowing or reversing the aging process, and covers topics such as cardiovascular aging, DNA damage and repair, cloning, and cell immortalization and senescence.
Rejuvenation Research coverage includes:
Cell immortalization and senescence
Pluripotent stem cells
DNA damage/repair
Gene targeting, gene therapy, and genomics
Growth factors and nutrient supply/sensing
Immunosenescence
Comparative biology of aging
Tissue engineering
Late-life pathologies (cardiovascular, neurodegenerative and others)
Public policy and social context.