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Published on: September 17, 2015
Effects of forskolin on inotropic performance and phospholamban phosphorylation in exercise-trained hypertensive
Stephen C Kolwicz1, Hajime Kubo, Scott M MacDonnell
1Department of Kinesiology, Temple Univ., Philadelphia, PA, USA.
Insights
Treadmill training improves beta-adrenergic receptor (beta-AR) responsiveness in hypertensive rats, enhancing left ventricular (LV) function. This improvement is not due to adenylyl cyclase but likely involves other signaling pathways.
Area of Science:
- Cardiovascular Physiology
- Exercise Physiology
- Molecular Cardiology
Background:
- Hypertension-induced left ventricular (LV) hypertrophy is associated with reduced beta-adrenergic receptor (beta-AR) responsiveness.
- Exercise training can improve beta-AR responsiveness in hypertensive states, but the specific role of adenylyl cyclase remains unclear.
Purpose of the Study:
- To investigate whether treadmill running enhances LV responsiveness to forskolin (FOR) or FOR + isoproterenol (ISO) in spontaneously hypertensive rats (SHR).
Main Methods:
- Female SHR and Wistar-Kyoto (WKY) rats were assigned to sedentary or treadmill-trained groups.
- Langendorff, isovolumic LV performance was assessed with incremental FOR and FOR+ISO infusion.
- Key proteins like phospholamban phosphorylation were analyzed.
Main Results:
- Treadmill training (SHR-TRD) improved isoproterenol-stimulated LV function in the presence of forskolin compared to sedentary SHR (SHR-SED).
- Phospholamban phosphorylation at Thr17 was higher in SHR-TRD compared to SHR-SED and WKY rats.
- LV developed pressure correlated with phospholamban phosphorylation.
Conclusions:
- Adenylyl cyclase is not downregulated in early hypertension and is not the primary mediator of enhanced beta-AR responsiveness with training.
- Improved beta-AR inotropic responsiveness in trained SHR hearts occurs at signaling levels beyond adenylyl cyclase.
Abstract:
Beta-adrenergic receptor (beta-AR) responsiveness is downregulated in left ventricular (LV) hypertrophy induced by chronic hypertension. While exercise training in hypertension enhances beta-AR responsiveness, the role of adenylyl cyclase remains unclear. The purpose of the present study was to test whether treadmill running in the spontaneously hypertensive rat (SHR) model improves LV responsiveness to forskolin (FOR) or the combination of FOR + isoproterenol (FOR+ISO). Female SHR (16-wk) were randomly placed into sedentary (SHR-SED; n = 7) or treadmill-trained (SHR-TRD; n = 8) groups. Wistar-Kyoto (WKY; n = 7) animals acted as normotensive controls. Langendorff, isovolumic LV performance was established at baseline and during incremental FOR infusion (1 and 5 micromol/l) and FOR+ISO (5 micromol/l + 1x10(-8) mol/l). Heart rate, systolic blood pressure, and heart-to-body weight ratio were lower in WKY relative to both SHR groups (P < 0.05). LV performance and heart rate significantly increased in all groups to a similar extent with incremental FOR infusion. However, in the presence of 5 micromol/l FOR, ISO increased LV developed pressure, positive change in LV pressure, and negative change in LV pressure to a greater extent in SHR-TRD relative to SHR-SED (P < 0.05). Phospholamban phosphorylation at the Thr17 was greater in SHR-TRD relative to SHR-SED and WKY (P < 0.05). Absolute LV developed pressure was moderately correlated with phospholamban phosphorylation at both the Ser16 (r = 0.64; P < 0.05) and Thr17 (r = 0.52; P < 0.05). Our data suggest that the adenylyl cyclase step in the beta-AR cascade is not downregulated in the early course of hypertension and that the enhanced beta-AR responsiveness with training is likely mediated at levels other than adenylyl cyclase. Our data also suggest that beta-AR inotropic responsiveness in the presence of direct adenylyl cyclase agonism is improved in trained compared with sedentary SHR hearts.
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