Md. Delp et al., EXERCISE TRAINING ALTERS AORTIC VASCULAR REACTIVITY IN HYPOTHYROID RATS, American journal of physiology. Heart and circulatory physiology, 37(4), 1995, pp. 1428-1435
Hypothyroidism induces a number of cardiovascular adaptations in rats,
including decreases in blood flow to high-oxidative skeletal muscle a
nd increases in total peripheral resistance. Conversely, exercise trai
ning results in elevations in blood flow to high-oxidative skeletal mu
scle and decreases in vascular resistance. The purpose of this study w
as to determine whether hypothyroidism induces changes in the vasomoto
r responses of arterial vessels and whether exercise training modifies
these responses. Rats were divided into three groups, sedentary euthy
roid (S-Eut), sedentary hypothyroid (S-Hypo), and exercise-trained hyp
othyroid (ET-Hypo). Responses to vasoactive compounds were examined in
vitro using abdominal aortic rings. Maximal isometric contractile ten
sion (g/mm(2)) evoked by KCl and norepinephrine (NE) were not differen
t among groups. However, sensitivity to KCl [agonist concentration pro
ducing 50% of maximal vasoconstrictor response (EC(50); in mM): S-Eut,
21.1 +/- 1.1; S-Hypo, 35.7 +/- 2.7; ET-Hypo, 43.8 +/- 2.0] and to NE
[EC(50) (in M): S-Eut, 4.0 x 10(-8) +/- 2.3 x 10(-8); S-Hypo, 8.3 x 10
(-8) +/- 3.4 x 10(-8); ET-Hypo, 3.6 x 10(-7) +/- 1.1 x 10(-7)] was dif
ferent among groups, and in the order S-Eut > S-Hypo > ET-Hypo. Maxima
l vasodilator responses induced by acetylcholine (10(-7) M NE preconst
riction) were lower in rings from S-Hypo animals than those from S-Eut
and ET-Hypo rats. Dilatory responses induced by sodium nitroprusside
(SNP) with the same NE preconstriction were not different among groups
. However, with a 10(-4) M NE preconstriction, maximal dilatory respon
ses induced by SNP were lower in vessels from hypothyroid animals. Dil
atory responses to forskolin (10(-4) M NE preconstriction) were not di
fferent among groups. These results indicate that hypothyroidism and e
xercise training alter vasomotor function in rat abdominal aortas thro
ugh adaptations of both endothelial and smooth muscle cells.