Hyq. Zhou et al., REACTIVITY AND SENSITIVITY OF THE MESENTERIC-ARTERY IN ADULT SPONTANEOUSLY HYPERTENSIVE RATS AFTER CHRONIC TREATMENT WITH INDAPAMIDE, Journal of cardiovascular pharmacology, 22, 1993, pp. 190000013-190000017
The effects of chronic treatment with indapamide (3 mg/kg/day) on the
structure and function of the mesenteric artery were studied in two gr
oups of spontaneously hypertensive rats (SHRs) using an experimental m
odel of in situ localized mesenteric artery. Indapamide (n = 12) or pl
acebo (n = 12) were given to 8-week-old rats for 4 weeks. After anesth
esia and laparotomy, a segment of mesenteric artery (external diameter
, 300-400 mum) was exposed for video-microscopic measurements. The dia
meter-pressure relationships were established under active conditions
(phenylephrine, 10(-6) M) and passive conditions (potassium cynanide,
KCN) for transmural pressure ranging from atmospheric pressure to 200
mm Hg. These studied arterial segments were then fixed and their wall
cross-sectional areas (CSA) measured in transverse sections. Active wa
ll stress and tension were defined as the differences in wall stresses
and wall tensions calculated for active and passive conditions. Systo
lic arterial pressure and mesenteric CSA were decreased in treated rat
s (197 +/- 15 mm Hg vs. 211 +/- 12 mm Hg, p < 0.05; 16,230 +/- 1048 mu
m2 vs. 19,033 +/- 1082 mum2, p < 0.05). In both groups, mesenteric dia
meters were smaller under active than under passive conditions without
significant differences in treated vs. untreated group under active c
onditions. The active wall tension was lower in treated (0.4 +/- 0.19
N/m) than in untreated rats (1.19 +/- 0.62 N/m, p < 0.05). However, th
ere were no differences in active wall stress in both groups (103 +/-
47 kPa and 134 +/- 30 kPa). These results suggest that chronic treatme
nt with indapamide induced a reduction of the mesenteric arterial smoo
th-muscle mass associated with a marked decrease in its maximal contra
ctile tone. The latter was related to the smooth-muscle mass reduction
and not to alteration of the vascular muscle contractility.