E. Cerbai et al., Long-term treatment of spontaneously hypertensive rats with losartan and electrophysiological remodeling of cardiac myocytes, CARDIO RES, 45(2), 2000, pp. 388-396
Citations number
48
Categorie Soggetti
Cardiovascular & Respiratory Systems","Cardiovascular & Hematology Research
Objective: Cardiac hypertrophy due to pressure overload is associated with
several cellular electrophysiological alterations such as prolongation of a
ction potential duration (APD), decrease in transient outward current (I-to
) and occurrence of the pacemaker current I-f. These alterations may play a
role in sudden arrhythmic death, which is a major risk factor in myocardia
l hypertrophy and failure. Since angiotensin LI is a key signal for myocyte
hypertrophy, we tested if an 8-week treatment of old spontaneously hyperte
nsive rats (SHR) with the antagonist of type-1 angiotensin II receptor (AT(
1)), losartan (10 mg/kg/day), was able to influence the cellular electrophy
siologic remodeling associated with cardiac hypertrophy. Methods: Left vent
ricular myocytes were isolated from control (CTR) or losartan-treated (LOS)
18-month old SHR. Patch-clamped LVM were superfused with a normal Tyrode's
solution (to measure action potential) or appropriately modified Tyrode's
solution (to measure I-to and I-f). Results: Heart weight to body weight ra
tio (HW/BW) was significantly smaller in LOS (5.69+/-0.25 mg/g) than in CTR
rats (6.67+/-0.37 mg/g; P<0.05). Membrane capacitance, an index of cell si
ze, was significantly reduced in LOS (342+/-12, n=92) vs. CTR (422+/-14 pF,
n=96, P<0.001). APD was significantly shorter in LOS than in CTR (at -60 m
V: 197+/-23 vs. 277+/-19 ms, n=28, P<0.001); this effect was paralleled by
a larger maximum I-to density in the LOS group (LOS: 15.1+/-1.4 pA/pF, CTR:
10.0+/-0.8 pA/pF) (n=27, P<0.02). I-f, elicited by hyperpolarizing steps (
range: -60 to -130 mV), was consistently recorded in SHR cells; however, it
s maximal specific conductance was significantly lower in LOS than in CTR r
ats (28.6+/-3.6 vs. 54.2+/-8.0 pS/pF, n=55, P<0.001). Voltage of half-maxim
al activation (V-1/2) Of both I-to and I-f was unchanged by the treatment.
Conclusions: AT(1) receptor blockade with losartan prevents the development
of myocyte hypertrophy and associated electrophysiological alterations in
old SHR. (C) 2000 Elsevier Science B.V. All rights reserved.