Iveta Bernatova, Ol'ga Pechanova and Frantisek Kristek
Department of Cardiovascular Physiology, Institute of Normal and Pathological
Physiology, Slovak Academy of Sciences,
Sienkiewiczova 1, 813 71 Bratislava, Slovak Republic
Abstract: The aim of the present study was to determine whether
decreased nitric oxide (NO) synthase production or rather NG-nitro-l-arginine
methyl ester (L-NAME)-induced hypertension was responsible for metabolic
and structural remodelling of the rat aorta during four-week L-NAME treatment.
Three groups of male Wistar rats were investigated: control, treated with
20 mg/kg per day L-NAME (L-NAME20), and treated with 40 mg/kg
per day L-NAME (L-NAME40). Systolic blood pressure significantly
increased in L-NAME20 to 146% and in L-NAME40 to 149%
of the control value. NO synthase activity in the aorta significantly decreased
in L-NAME20 and L-NAME40 to 86% and 65% of the control
values, respectively. Proteosynthesis was significantly elevated in both
L-NAME groups, while nuclear DNA concentration was significantly elevated
only in the L-NAME40 group. Cyclic GMP concentration significantly
decreased in L-NAME20 to 73% and in L-NAME40 to 46%
of the control. Cyclic AMP concentration significantly increased in L-NAME20
and L-NAME40 to 128% and 145% of the control value, respectively.
The diameter and wall thickness-to-diameter ratio were significantly elevated
only in the L-NAME40 group. We conclude that remodelling of the
aorta in L-NAME-treated rats was rather associated with NO deficiency than
L-NAME-induced hypertension.
Keywords: Nitric oxide, NG-Nitro-l-arginine methyl
ester, Blood pressure, cAMP, Aorta