This study determined to what extent active and passive wall tensions
increase in in vivo intestinal arterioles of 13- to 15-week-old and 25
- to 27-week-old spontaneously hypertensive rats (SHR) to maintain nor
mal or smaller arteriolar diameters during microvascular hypertension.
Acetylcholine and nitroprusside were used to determine whether vascul
ar muscle relaxation to endothelium-derived relaxing factor or cyclic
GMP is impaired. Large arterioles of hypertensive rats have passive te
nsion-circumference relations that are steeper and shifted to the left
compared with those of age-matched controls; passive resistance to di
stension limits vasodilation in hypertensive rats except at their natu
rally elevated arteriolar pressure. Passive tension contributes approx
imately 30% of the total resting tension in arterioles of hypertensive
and normotensive rats because a greater passive tension occurs at the
20% to 25% constricted resting diameter in hypertensive rats. Absolut
e and relative changes in the diameter of SHR arterioles during acetyl
choline and nitroprusside application were equal to or greater than th
ose in Wistar-Kyoto rats. However, reduction in active tension was sup
pressed in older SHR and remained approximately 50% higher than that f
ound in older Wistar-Kyoto rats during drug application. Vasoconstrict
ion and increased passive resistance to distension of the arteriolar w
all diminish the active tension required to maintain normal or smaller
resting diameters against microvascular hypertension. However, the el
evated microvascular pressure in hypertensive rats is required to allo
w near-normal dilation to compensate for their increased passive resis
tance to stretch and decreased ability to relax active tension through
cyclic GMP mechanisms.