Sex differences in the impact of parental obesity on offspring cardiac SIRT3 expression, mitochondrial efficiency, and diastolic function early in life

Parental obesity contributes to diastolic dysfunction in young offspring (1–3 days after weaning) in a sex-dependent manner, as well as reduced cardiac SIRT3 expression and altered mitochondrial bioenergetics, resting Ca 2+ levels, and reduced phospholamban protein levels. Previous studies suggest t...

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Published inAmerican journal of physiology. Heart and circulatory physiology Vol. 321; no. 3; pp. H485 - H495
Main Authors do Carmo, Jussara M., Omoto, Ana C. M., Dai, Xuemei, Moak, Sydney P., Mega, Gabriela S., Li, Xuan, Wang, Zhen, Mouton, Alan J., Hall, John E., da Silva, Alexandre A.
Format Journal Article
LanguageEnglish
Published Bethesda American Physiological Society 01.09.2021
SeriesIntegrative Cardiovascular Physiology and Pathophysiology
Subjects
Online AccessGet full text
ISSN0363-6135
1522-1539
1522-1539
DOI10.1152/ajpheart.00176.2021

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Abstract Parental obesity contributes to diastolic dysfunction in young offspring (1–3 days after weaning) in a sex-dependent manner, as well as reduced cardiac SIRT3 expression and altered mitochondrial bioenergetics, resting Ca 2+ levels, and reduced phospholamban protein levels. Previous studies suggest that parental obesity may adversely impact long-term metabolic health of the offspring. We tested the hypothesis that parental (paternal + maternal) obesity impairs cardiac function in the offspring early in life. Within 1–3 days after weaning, offspring from obese rats fed a high-fat diet (HFD-Offs) and age-matched offspring from lean rats (ND-Offs) were submitted to echocardiography and cardiac catheterization for assessment of pressure-volume relationships. Then, hearts were digested and isolated cardiomyocytes were used to determine contractile function, calcium transients, proteins related to calcium signaling, and mitochondrial bioenergetics. Female and male HFD-Offs were heavier (72 ± 2 and 61 ± 4 g vs. 57 ± 2 and 49 ± 1 g), hyperglycemic (112 ± 8 and 115 ± 12 mg/dL vs. 92 ± 10 and 96 ± 8 mg/dL) with higher plasma insulin and leptin concentrations compared with female and male ND-Offs. When compared with male controls, male HFD-Offs exhibited similar systolic function but impaired diastolic function as indicated by increased IVRT (22 ± 1 vs. 17 ± 1 ms), E/E′ ratio (29 ± 2 vs. 23 ± 1), and tau (5.7 ± 0.2 vs. 4.8 ± 0.2). The impaired diastolic function was associated with reduced resting free Ca 2+ levels and phospholamban protein expression, increased activated matrix metalloproteinase 2, and reduced SIRT3 protein expression, mitochondrial ATP reserve, and ATP-linked respiration. These results indicate that male and female Offs from obese parents have multiple metabolic abnormalities early in life (1–3 days after weaning) and that male, but not female, Offs have impaired diastolic function as well as reductions in cardiac SIRT3, resting free Ca 2+ levels, and mitochondrial biogenesis. NEW & NOTEWORTHY Parental obesity contributes to diastolic dysfunction in young offspring (1–3 days after weaning) in a sex-dependent manner, as well as reduced cardiac SIRT3 expression and altered mitochondrial bioenergetics, resting Ca 2+ levels, and reduced phospholamban protein levels.
AbstractList Previous studies suggest that parental obesity may adversely impact long-term metabolic health of the offspring. We tested the hypothesis that parental (paternal + maternal) obesity impairs cardiac function in the offspring early in life. Within 1–3 days after weaning, offspring from obese rats fed a high-fat diet (HFD-Offs) and age-matched offspring from lean rats (ND-Offs) were submitted to echocardiography and cardiac catheterization for assessment of pressure-volume relationships. Then, hearts were digested and isolated cardiomyocytes were used to determine contractile function, calcium transients, proteins related to calcium signaling, and mitochondrial bioenergetics. Female and male HFD-Offs were heavier (72 ± 2 and 61 ± 4 g vs. 57 ± 2 and 49 ± 1 g), hyperglycemic (112 ± 8 and 115 ± 12 mg/dL vs. 92 ± 10 and 96 ± 8 mg/dL) with higher plasma insulin and leptin concentrations compared with female and male ND-Offs. When compared with male controls, male HFD-Offs exhibited similar systolic function but impaired diastolic function as indicated by increased IVRT (22 ± 1 vs. 17 ± 1 ms), E/E′ ratio (29 ± 2 vs. 23 ± 1), and tau (5.7 ± 0.2 vs. 4.8 ± 0.2). The impaired diastolic function was associated with reduced resting free Ca2+ levels and phospholamban protein expression, increased activated matrix metalloproteinase 2, and reduced SIRT3 protein expression, mitochondrial ATP reserve, and ATP-linked respiration. These results indicate that male and female Offs from obese parents have multiple metabolic abnormalities early in life (1–3 days after weaning) and that male, but not female, Offs have impaired diastolic function as well as reductions in cardiac SIRT3, resting free Ca2+ levels, and mitochondrial biogenesis.
Parental obesity contributes to diastolic dysfunction in young offspring (1–3 days after weaning) in a sex-dependent manner, as well as reduced cardiac SIRT3 expression and altered mitochondrial bioenergetics, resting Ca 2+ levels, and reduced phospholamban protein levels. Previous studies suggest that parental obesity may adversely impact long-term metabolic health of the offspring. We tested the hypothesis that parental (paternal + maternal) obesity impairs cardiac function in the offspring early in life. Within 1–3 days after weaning, offspring from obese rats fed a high-fat diet (HFD-Offs) and age-matched offspring from lean rats (ND-Offs) were submitted to echocardiography and cardiac catheterization for assessment of pressure-volume relationships. Then, hearts were digested and isolated cardiomyocytes were used to determine contractile function, calcium transients, proteins related to calcium signaling, and mitochondrial bioenergetics. Female and male HFD-Offs were heavier (72 ± 2 and 61 ± 4 g vs. 57 ± 2 and 49 ± 1 g), hyperglycemic (112 ± 8 and 115 ± 12 mg/dL vs. 92 ± 10 and 96 ± 8 mg/dL) with higher plasma insulin and leptin concentrations compared with female and male ND-Offs. When compared with male controls, male HFD-Offs exhibited similar systolic function but impaired diastolic function as indicated by increased IVRT (22 ± 1 vs. 17 ± 1 ms), E/E′ ratio (29 ± 2 vs. 23 ± 1), and tau (5.7 ± 0.2 vs. 4.8 ± 0.2). The impaired diastolic function was associated with reduced resting free Ca 2+ levels and phospholamban protein expression, increased activated matrix metalloproteinase 2, and reduced SIRT3 protein expression, mitochondrial ATP reserve, and ATP-linked respiration. These results indicate that male and female Offs from obese parents have multiple metabolic abnormalities early in life (1–3 days after weaning) and that male, but not female, Offs have impaired diastolic function as well as reductions in cardiac SIRT3, resting free Ca 2+ levels, and mitochondrial biogenesis. NEW & NOTEWORTHY Parental obesity contributes to diastolic dysfunction in young offspring (1–3 days after weaning) in a sex-dependent manner, as well as reduced cardiac SIRT3 expression and altered mitochondrial bioenergetics, resting Ca 2+ levels, and reduced phospholamban protein levels.
Previous studies suggest that parental obesity may adversely impact long-term metabolic health of the offspring. We tested the hypothesis that parental (paternal + maternal) obesity impairs cardiac function in the offspring early in life. Within 1-3 days after weaning, offspring from obese rats fed a high-fat diet (HFD-Offs) and age-matched offspring from lean rats (ND-Offs) were submitted to echocardiography and cardiac catheterization for assessment of pressure-volume relationships. Then, hearts were digested and isolated cardiomyocytes were used to determine contractile function, calcium transients, proteins related to calcium signaling, and mitochondrial bioenergetics. Female and male HFD-Offs were heavier (72 ± 2 and 61 ± 4 g vs. 57 ± 2 and 49 ± 1 g), hyperglycemic (112 ± 8 and 115 ± 12 mg/dL vs. 92 ± 10 and 96 ± 8 mg/dL) with higher plasma insulin and leptin concentrations compared with female and male ND-Offs. When compared with male controls, male HFD-Offs exhibited similar systolic function but impaired diastolic function as indicated by increased IVRT (22 ± 1 vs. 17 ± 1 ms), E/E' ratio (29 ± 2 vs. 23 ± 1), and tau (5.7 ± 0.2 vs. 4.8 ± 0.2). The impaired diastolic function was associated with reduced resting free Ca2+ levels and phospholamban protein expression, increased activated matrix metalloproteinase 2, and reduced SIRT3 protein expression, mitochondrial ATP reserve, and ATP-linked respiration. These results indicate that male and female Offs from obese parents have multiple metabolic abnormalities early in life (1-3 days after weaning) and that male, but not female, Offs have impaired diastolic function as well as reductions in cardiac SIRT3, resting free Ca2+ levels, and mitochondrial biogenesis.NEW & NOTEWORTHY Parental obesity contributes to diastolic dysfunction in young offspring (1-3 days after weaning) in a sex-dependent manner, as well as reduced cardiac SIRT3 expression and altered mitochondrial bioenergetics, resting Ca2+ levels, and reduced phospholamban protein levels.Previous studies suggest that parental obesity may adversely impact long-term metabolic health of the offspring. We tested the hypothesis that parental (paternal + maternal) obesity impairs cardiac function in the offspring early in life. Within 1-3 days after weaning, offspring from obese rats fed a high-fat diet (HFD-Offs) and age-matched offspring from lean rats (ND-Offs) were submitted to echocardiography and cardiac catheterization for assessment of pressure-volume relationships. Then, hearts were digested and isolated cardiomyocytes were used to determine contractile function, calcium transients, proteins related to calcium signaling, and mitochondrial bioenergetics. Female and male HFD-Offs were heavier (72 ± 2 and 61 ± 4 g vs. 57 ± 2 and 49 ± 1 g), hyperglycemic (112 ± 8 and 115 ± 12 mg/dL vs. 92 ± 10 and 96 ± 8 mg/dL) with higher plasma insulin and leptin concentrations compared with female and male ND-Offs. When compared with male controls, male HFD-Offs exhibited similar systolic function but impaired diastolic function as indicated by increased IVRT (22 ± 1 vs. 17 ± 1 ms), E/E' ratio (29 ± 2 vs. 23 ± 1), and tau (5.7 ± 0.2 vs. 4.8 ± 0.2). The impaired diastolic function was associated with reduced resting free Ca2+ levels and phospholamban protein expression, increased activated matrix metalloproteinase 2, and reduced SIRT3 protein expression, mitochondrial ATP reserve, and ATP-linked respiration. These results indicate that male and female Offs from obese parents have multiple metabolic abnormalities early in life (1-3 days after weaning) and that male, but not female, Offs have impaired diastolic function as well as reductions in cardiac SIRT3, resting free Ca2+ levels, and mitochondrial biogenesis.NEW & NOTEWORTHY Parental obesity contributes to diastolic dysfunction in young offspring (1-3 days after weaning) in a sex-dependent manner, as well as reduced cardiac SIRT3 expression and altered mitochondrial bioenergetics, resting Ca2+ levels, and reduced phospholamban protein levels.
Previous studies suggest that parental obesity may adversely impact long-term metabolic health of the offspring. We tested the hypothesis that parental (paternal + maternal) obesity impairs cardiac function in the offspring early in life. Within 1–3 days after weaning, offspring from obese rats fed a high-fat diet (HFD-Offs) and age-matched offspring from lean rats (ND-Offs) were submitted to echocardiography and cardiac catheterization for assessment of pressure-volume relationships. Then, hearts were digested and isolated cardiomyocytes were used to determine contractile function, calcium transients, proteins related to calcium signaling, and mitochondrial bioenergetics. Female and male HFD-Offs were heavier (72 ± 2 and 61 ± 4 g vs. 57 ± 2 and 49 ± 1 g), hyperglycemic (112 ± 8 and 115 ± 12 mg/dL vs. 92 ± 10 and 96 ± 8 mg/dL) with higher plasma insulin and leptin concentrations compared with female and male ND-Offs. When compared with male controls, male HFD-Offs exhibited similar systolic function but impaired diastolic function as indicated by increased IVRT (22 ± 1 vs. 17 ± 1 ms), E/E′ ratio (29 ± 2 vs. 23 ± 1), and tau (5.7 ± 0.2 vs. 4.8 ± 0.2). The impaired diastolic function was associated with reduced resting free Ca 2+ levels and phospholamban protein expression, increased activated matrix metalloproteinase 2, and reduced SIRT3 protein expression, mitochondrial ATP reserve, and ATP-linked respiration. These results indicate that male and female Offs from obese parents have multiple metabolic abnormalities early in life (1–3 days after weaning) and that male, but not female, Offs have impaired diastolic function as well as reductions in cardiac SIRT3, resting free Ca 2+ levels, and mitochondrial biogenesis. NEW & NOTEWORTHY Parental obesity contributes to diastolic dysfunction in young offspring (1–3 days after weaning) in a sex-dependent manner, as well as reduced cardiac SIRT3 expression and altered mitochondrial bioenergetics, resting Ca 2+ levels, and reduced phospholamban protein levels.
Author Omoto, Ana C. M.
Li, Xuan
Dai, Xuemei
Mega, Gabriela S.
da Silva, Alexandre A.
Wang, Zhen
Mouton, Alan J.
Hall, John E.
do Carmo, Jussara M.
Moak, Sydney P.
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Cites_doi 10.1016/j.jacc.2009.05.012
10.1093/cvr/cvaa336
10.1172/JCI120849
10.1002/uog.14841
10.1152/ajpendo.00434.2010
10.1111/j.1474-9726.2012.00844.x
10.1152/physiol.00021.2014
10.4274/Jcrpe.1471
10.1007/978-3-642-21631-2_8
10.1016/j.hfc.2007.10.007
10.1038/nrcardio.2017.154
10.3945/ajcn.2009.28838
10.1161/JAHA.120.018298
10.1016/j.molmet.2015.12.002
10.1161/01.CIR.0000125741.88712.77
10.1007/s10741-013-9405-8
10.1161/01.CIR.103.18.2303
10.1161/CIRCULATIONAHA.113.001805
10.1016/j.maturitas.2011.02.018
10.1111/jcmm.12556
10.1002/oby.20144
10.1210/jc.2014-1561
10.1007/s10741-012-9340-0
10.1161/01.HYP.0000208840.30778.00
10.1056/NEJMoa020245
10.1146/annurev-publhealth-032315-021859
10.1186/s12933-018-0762-4
10.4274/jcrpe.3790
10.1152/physrev.00012.2007
10.1681/ASN.2014040393
10.1016/j.jacbts.2020.11.007
10.1038/ijo.2013.177
10.1210/er.2009-0038
10.1016/s0008-6363(02)00694-6
10.1136/bmj.38470.670903.E0
10.1371/journal.pone.0226142
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  doi: 10.1016/j.jacc.2009.05.012
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  doi: 10.1093/cvr/cvaa336
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  doi: 10.1172/JCI120849
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  doi: 10.1002/uog.14841
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  doi: 10.1152/ajpendo.00434.2010
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  doi: 10.1111/j.1474-9726.2012.00844.x
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  doi: 10.1152/physiol.00021.2014
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  doi: 10.4274/Jcrpe.1471
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  doi: 10.1007/978-3-642-21631-2_8
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  doi: 10.1016/j.hfc.2007.10.007
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  doi: 10.1038/nrcardio.2017.154
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  doi: 10.3945/ajcn.2009.28838
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  doi: 10.1161/JAHA.120.018298
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  doi: 10.1016/j.molmet.2015.12.002
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  doi: 10.1161/01.CIR.0000125741.88712.77
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  doi: 10.1007/s10741-013-9405-8
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  doi: 10.1161/01.CIR.103.18.2303
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  doi: 10.1161/CIRCULATIONAHA.113.001805
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  doi: 10.1016/j.maturitas.2011.02.018
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  doi: 10.1111/jcmm.12556
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  doi: 10.1002/oby.20144
– ident: B6
  doi: 10.1210/jc.2014-1561
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  doi: 10.1007/s10741-012-9340-0
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  doi: 10.1161/01.HYP.0000208840.30778.00
– ident: B35
  doi: 10.1056/NEJMoa020245
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  doi: 10.1146/annurev-publhealth-032315-021859
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  doi: 10.1186/s12933-018-0762-4
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  doi: 10.4274/jcrpe.3790
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  doi: 10.1152/physrev.00012.2007
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  doi: 10.1681/ASN.2014040393
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  doi: 10.1016/j.jacbts.2020.11.007
– ident: B14
  doi: 10.1038/ijo.2013.177
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  doi: 10.1210/er.2009-0038
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  doi: 10.1016/s0008-6363(02)00694-6
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Snippet Parental obesity contributes to diastolic dysfunction in young offspring (1–3 days after weaning) in a sex-dependent manner, as well as reduced cardiac SIRT3...
Previous studies suggest that parental obesity may adversely impact long-term metabolic health of the offspring. We tested the hypothesis that parental...
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StartPage H485
SubjectTerms Abnormalities
Bioenergetics
Calcium
Calcium (mitochondrial)
Calcium ions
Calcium signalling
Cardiomyocytes
Catheterization
Echocardiography
Electron transport
Gender aspects
Gender differences
Heart
High fat diet
Insulin
Leptin
Males
Matrix metalloproteinase
Matrix metalloproteinases
Metabolism
Metalloproteinase
Mitochondria
Muscle contraction
Obesity
Offspring
Phospholamban
Protein expression
Proteins
Sex differences
Weaning
Title Sex differences in the impact of parental obesity on offspring cardiac SIRT3 expression, mitochondrial efficiency, and diastolic function early in life
URI https://www.proquest.com/docview/2577526226
https://www.proquest.com/docview/2555114360
https://pubmed.ncbi.nlm.nih.gov/PMC8461840
Volume 321
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