Ja. Schraeger et al., NORMAL LEFT-VENTRICULAR DIASTOLIC COMPLIANCE AFTER REGRESSION OF HYPERTROPHY, Journal of cardiovascular pharmacology, 23(3), 1994, pp. 349-357
We wished to determine whether (a) left ventricular (LV) diastolic cha
mber compliance and tissue elastic modulus were decreased with hypertr
ophy and improved after reversal of hypertension and regression of hyp
ertrophy and whether collagen concentration was a major determinant of
LV chamber compliance during hypertrophy or aging. Spontaneously hype
rtensive rats (SHR) and Wistar-Kyoto rats (WKY), aged 8 months at time
of study, were used for the hypertension-regression experiments. The
aging study was based on 14- and 24-month-old Fischer-344 rats. LV cha
mber compliance was measured in isolated perfused hearts arrested in d
iastole. Length-tension curves (tissue elastic modulus) were obtained
from ventricular strips, and hydroxyproline assays were used to estima
te LV collagen content. Captopril and hydrochlorothizide were given fo
r an 8-week period to both normotensive and hypertensive rats. Treatme
nt normalized arterial pressure and caused regression of LV hypertroph
y in SHR. LV diastolic compliance was less (pressure-volume curve stee
per) in SHR than in WKY, but stiffness was similar in the two groups,
as indicated by similar slopes when volume was adjusted for heart mass
. Treatment significantly decreased ventricular stiffness in both SHR
and WKY. Length-tension curves were almost identical in SHR and WKY, b
ut treated SHR demonstrated less tension per given length. These chang
es occurred although collagen did not decrease in parallel to the decr
ease in LV mass. Aging was associated with 66 and 60% increases in col
lagen content and concentration, respectively, but did not alter LV ch
amber compliance significantly. We conclude that normalization of arte
rial pressure and regression of LV hypertrophy in SHR increase chamber
compliance and decrease tissue elastic modulus and that increased col
lagen concentration does not necessarily affect LV chamber compliance
during LV hypertrophy or during aging.