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Published on: May 22, 2018
Age-related changes in cardiac adenosine receptor expression
Tamsin L Jenner1, Albert S Mellick, Glenn J Harrison
1School of Health Sciences, Griffith University Gold Coast Campus, Southport, Qld. 9726, Australia.
Aging reduces key cardiac adenosine receptors, specifically adenosine A(1) and A(2A) receptors, impacting heart function. This study reveals age-related changes at the receptor level, not just functional decline.
Area of Science:
- Cardiovascular Physiology
- Molecular Biology
- Aging Research
Background:
- Adenosine is a cardioprotective agent acting through adenosine receptor (ADOR) subtypes.
- Functional responses to adenosine decrease with age, but the underlying mechanism is unclear.
- This study investigates age-related changes in cardiac ADOR expression.
Purpose of the Study:
- To determine the effect of aging on cardiac adenosine receptor expression in rats.
- To identify which adenosine receptor subtypes are affected by age.
- To clarify whether changes occur at the receptor, second messenger, or translational level.
Main Methods:
- Quantitative analysis of adenosine receptor gene expression in rat hearts.
- Utilized 18S rRNA and adenosine A(2B) receptor gene as internal controls for normalization.
- Compared gene expression levels between young and aged rats.
Main Results:
- 18S rRNA and adenosine A(2B) receptor expression showed no age-related changes.
- Using 18S rRNA as control, a 5.5-fold reduction in adenosine A(1) receptor expression was observed with age.
- Using adenosine A(2B) receptor as control, significant age-related downregulation of adenosine A(1) (5.4-fold) and A(2A) (2.2-fold) receptors was found.
- 18S rRNA's high expression masked age-related changes in adenosine A(2A) receptor expression.
Conclusions:
- Aging leads to a significant reduction in cardiac adenosine A(1) and A(2A) receptor expression in rats.
- The choice of housekeeping gene significantly impacts the interpretation of age-related gene expression changes.
- Age-related decline in cardiac function may be partly due to decreased expression of specific adenosine receptors.
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