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Voluntary wheel running and pacing-induced dysfunction in hypertension
Stephen C Kolwicz1, Scott M MacDonnell, Zebulon V Kendrick
1Department of Kinesiology, Temple University, Philadelphia, Pennsylvania, USA.
Voluntary wheel running did not protect hypertensive rats from heart dysfunction during stress. However, forskolin, a direct adenylyl cyclase activator, improved cardiac function in all groups, highlighting the importance of beta-adrenergic signaling.
Area of Science:
- Cardiovascular Physiology
- Exercise Science
- Pharmacology
Background:
- Spontaneously hypertensive rats (SHR) often exhibit cardiac dysfunction.
- Understanding the effects of exercise and pharmacological interventions on cardiac performance is crucial.
Purpose of the Study:
- To investigate if voluntary wheel running enhances myocardial tolerance to pacing stress in female SHR.
- To determine if direct adenylyl cyclase agonism with forskolin improves cardiac performance during pacing in SHR.
Main Methods:
- Female Wistar Kyoto (WKY) and spontaneously hypertensive rats (SHR) were studied.
- SHR were divided into sedentary (SHR-SED) and voluntary wheel running (SHR-WHL) groups.
- Left ventricular (LV) function was assessed using Langendorff preparations during pacing stress, with and without forskolin infusion.
Main Results:
- Voluntary wheel running in SHR led to cardiac enlargement but did not alter resting hemodynamics.
- Pacing stress similarly impaired cardiac function in all groups.
- Forskolin infusion significantly improved LV function across all experimental groups.
Conclusions:
- Voluntary wheel running does not confer protection against pacing-induced myocardial dysfunction in SHR.
- Direct adenylyl cyclase agonism via forskolin demonstrates a protective effect on cardiac function during stress.
- These findings underscore the critical role of a functional myocardial beta-adrenergic signaling pathway.
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