Key result
Rolipram (1-100 microM) had no significant effect on peak isometric twitch in guinea-pig ventricular tissue, but dose-dependently prolonged time to half relaxation (by 25.3% at 30 microM, P<0.001).
Why the study?
Does rolipram alter contractile and electrophysiological properties in guinea-pig ventricular myocytes?
Does rolipram alter contractile and electrophysiological properties in guinea-pig ventricular myocytes?
Rolipram alters relaxation time and action potential duration in guinea-pig ventricular myocytes without affecting the second inward current.
Answers are grounded in this paper and cite their sources.
Warrants caution extrapolating guinea-pig data to patients; leaves open PDE4 effects on human cardiac relaxation.
Isometric force, action potentials and in voltage-clamp Isi (second inward current) and its current voltage relation were recorded in papillary muscles from guinea-pigs and from guinea-pig isolated ventricular myocytes (35-37 degrees C, 0.5-1 Hz). Rolipram (1-100 microM) had no significant effect on peak isometric twitch. The rate of rise of force and time to peak tension (TPT) was likewise unaffected. Time to half relaxation (THR) was increased in a dose-dependent manner and at 30 microM THR was prolonged by 25.3 +/- 6% (n = 10, P < 0.001). The effect of 30 microM rolipram on isometric force was frequency dependent. At 0.25 Hz peak force was increased by 6.3 +/- 3.1% (n = 7, P < 0.05). At 2 Hz rolipram exhibited a negative inotropic effect of 9.8 +/- 3.3% (n = 5, P < 0.02). Action potential duration at 90% repolarization was prolonged by 13 +/- 6 ms (n = 7, P < 0.05), and there was usually no effect on resting potential or action potential amplitude. Sometimes, however, a depressed plateau was recorded. Rolipram was without effect on Isi and its current-voltage relations. Time to full mechanical restitution after a test interval was not changed but the shape of the restitution curve was altered. The restitution process was much slower in the presence of rolipram. Hence, peak force was lower at test intervals shorter than 800 ms. Likewise, the shape of the curve relating postextrasystolic potentiation to test interval was altered by rolipram.(ABSTRACT TRUNCATED AT 250 WORDS)
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Mörner et al. (1994) studied this question. Rolipram was evaluated on Isometric force, action potentials, and voltage-clamp Isi. Rolipram (1-100 microM) had no significant effect on peak isometric twitch in guinea-pig ventricular tissue, but dose-dependently prolonged time to half relaxation (by 25.3% at 30 microM, P<0.001).
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