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(Hypertension. 2000;36:1065.)
© 2000 American Heart Association, Inc.
Scientific Contributions |
From the Vascular Pathophysiology Unit, School of Medicine, University of Navarra, Pamplona, Spain.
Correspondence to Dr Javier Díez, Unidad de Fisiopatología Vascular, Facultad de Medicina, C/Irunlarrea s/n, 31080 Pamplona, Spain. E-mail jadimar{at}unav.es
AbstractPrevious findings have
shown that hypotensive doses of losartan prevent the excess of
apoptosis present in the hypertrophied left ventricle of
adult spontaneously hypertensive rats (SHR). This study was designed to
determine whether angiotensin II facilitates
apoptosis in cardiomyocytes of adult SHR. Primary
cultures of ventricular cardiomyocytes from
30-week-old normotensive Wistar-Kyoto rats (WKY) and SHR with left
ventricular hypertrophy were exposed to
10-9 mol/L angiotensin II for 24
hours. Apoptotic cells were assessed by terminal
deoxynucleotidyl transferase assay and confirmed by
Annexin V detection. The expression of Bax-
, Bcl-2,
p53, and caspase-3 proteins was assessed by Western blot
assays. The expression of BAX gene was assessed by
Northern blot. Angiotensin II increased
(P<0.01) cardiomyocyte apoptosis,
and this effect was higher (P<0.001) in SHR cells than
in WKY cells. Whereas losartan (10-7
mol/L) blocked the apoptotic effect of the octapeptide in cells
from the two strains of rats, PD123319 (10-7
mol/L) inhibited angiotensin IImediated apoptosis
only in SHR cells. Angiotensin II stimulated
(P<0.01) Bax-
protein, and this effect was higher
(P<0.01) in SHR cells than in WKY cells.
Angiotensin II did not modify Bcl-2, p53, and BAX mRNA in
cells from the two strains of rats. Angiotensin II induced
a similar increase (P<0.05) in the ratio
caspase-3/procaspase-3 (an index of caspase-3 activation) in
cardiomyocytes from the two strains of rats. The
present in vitro results indicate that SHR
cardiomyocytes exhibit enhanced susceptibility to
angiotensin IIinduced apoptosis. Ligand binding
to angiotensin II type 1 and type 2 receptors leading to
changes in posttranscriptional processing of Bax-
and accumulation
of this proapoptotic protein may be involved in the abnormal
response of SHR cardiomyocytes. These data support a role
for angiotensin II in apoptosis observed in the
left ventricle of these rats.
Key Words: angiotensin II apoptosis myocytes rats, spontaneously hypertensive
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