Parental obesity exacerbates cognitive dysfunction and cardiac vulnerability in offspring of an Alzheimer disease model
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Jussara M do Carmo1, John E Hall1, Emily Ladnier1
1Department of Physiology and Biophysics, Mississippi Center for Obesity Research, Cardiorenal and Metabolic Diseases Research Center, University of Mississippi Medical Center, Jackson, Mississippi, United States.
Insights
Parental obesity worsens Alzheimer disease (AD) outcomes in offspring, impairing cognitive and cardiac function. This highlights parental metabolic health as crucial for offspring
Area of Science:
- Neuroscience and Cardiovascular Research
- Metabolic Disease and Aging
Background:
- Alzheimer disease (AD) presents significant neurocognitive and cardiovascular challenges.
- Parental obesity is linked to adverse cardiometabolic outcomes in offspring.
- The impact of parental obesity on AD susceptibility in lean offspring requires investigation.
Purpose of the Study:
- To determine if parental obesity exacerbates cardiac, metabolic, and cognitive dysfunction in lean offspring susceptible to AD.
- To examine sex-specific effects of parental obesity on AD-related pathologies in offspring.
Main Methods:
- Utilized 3xTg-AD mice offspring from control diet-fed (lean) and high-fat diet-fed (obese) parents.
- Assessed cognitive function using Morris Water Maze and New Object Recognition (NOR) tests.
- Evaluated cardiac function via echocardiography and invasive hemodynamic measurements.
- Measured mitochondrial (MT) function in cardiac and brain tissues using high-resolution respirometry.
Main Results:
- Offspring from obese parents (HFD-Offs) showed impaired memory retention compared to offspring from lean parents (ND-Offs).
- Male HFD-Offs exhibited impaired cardiac diastolic relaxation and reduced mitochondrial glucose and fatty acid oxidation in heart and brain.
- Cardiac catheterization revealed significantly reduced contractility and relaxation indices in male HFD-Offs.
Conclusions:
- Parental obesity exacerbates Alzheimer disease-related cognitive decline and cardiac dysfunction in a sex-specific manner.
- Parental metabolic status is a critical determinant of AD-related cardiometabolic vulnerability in offspring.
- Findings underscore the importance of parental metabolic health in mitigating AD risks.
Abstract:
Alzheimer disease (AD) is a growing health problem characterized by neurocognitive and cardiovascular dysfunction. Although parental obesity programs adverse cardiometabolic complications, including obesity, hypertension, and cardiorenal dysfunction in their offspring, whether parental obesity worsens cardiac, metabolic, and cognitive function in lean offspring that are susceptible to AD (3xTg-AD mice) remains unclear. Male and female offspring from control diet-fed or high-fat diet (HFD)-fed parents were examined at 26-28 wk of age. Cognitive function was assessed by Morris water maze and New Object Recognition (NOR) tests, cardiac function by echocardiography and invasive hemodynamic measurements, and mitochondrial (MT) function by high-resolution respirometry in isolated cardiac fibers and brain cortex. AD offspring from obese parents (HFD-Offs) exhibited worse memory retention compared with AD offspring from lean parents [normal diet (ND)-Offs], whereas recognition memory assessed by NOR was not significantly different between groups, although there was greater variability in HFD-Offs. Although systolic function by echocardiography was similar between groups, male HFD-Offs showed impaired diastolic relaxation with prolonged isovolumetric relaxation time, whereas E/e' remained unchanged. Left ventricular catheterization showed reduced indices of contractility and relaxation, including maximal and minimal rates of pressure changes: dP/dtmax (8,038 ± 1,011 vs. 18,704 ± 183 mmHg/s), dP/dtmin (-7,724 ± 471 vs. -13,634 ± 1,139), and prolonged Tau (4.0 ± 0.1 vs. 2.9 ± 0.1) in HFD-Offs compared with ND-Offs. Male HFD-Offs exhibited reduced MT glucose and fatty acid oxidation in the heart and brain. These findings indicate that parental obesity exacerbates AD-related cognitive decline and cardiac dysfunction in a sex-specific manner, suggesting parental metabolic status as an important determinant of AD-related cardiometabolic vulnerability.NEW & NOTEWORTHY Parental obesity is associated with worsened cognitive performance and male-specific impairments in cardiac metabolism and function in AD-susceptible offspring, highlighting developmental programming as a modifier of heart-brain vulnerability.
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