Cc. Coulson et al., CENTRAL HEMODYNAMIC-EFFECTS OF RECOMBINANT HUMAN RELAXIN IN THE ISOLATED, PERFUSED RAT-HEART MODEL, Obstetrics and gynecology, 87(4), 1996, pp. 610-612
Objective: To determine the cardiac effects of relaxin in the isolated
, perfused rat heart model, and to see if pregnancy modifies the hormo
ne's actions. Methods: Hearts were excised from 18 female Sprague-Dawl
ey rats (ten pregnant, eight nonpregnant) and attached to a Langendorf
f apparatus. Left ventricular systolic pressure, heart rate, and contr
actility were measured. Hearts were exposed serially to 0.5, 1.0, 2.0,
4.0, 8.0, and 16.0 ng/mL concentrations of recombinant human relaxin.
Results: Hearts from pregnant rats had lower heart rates than those f
rom nonpregnant animals. Relaxin increased heart rate, left ventricula
r systolic pressure, and contractility in a dose-dependent fashion. Pr
egnancy did not modify this response. Conclusion: Recombinant human re
laxin is a potent inotropic and chronotropic agent. The effects couple
d with the physiologic increase of relaxin during human pregnancy indi
cate that relaxin may be involved in the cardiovascular changes of pre
gnancy.