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.

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