Relaxation Kinetics of Rat Aorta During Pregnancy
Departments of Obstetrics and Gynecology and Physiology and Biophysics, The University of Texas Medical Health, Galveston, Texas, and Research Laboratories of Schering MD Berlin, Germany
Departments of Obstetrics and Gynecology and Physiology and Biophysics, The University of Texas Medical Health, Galveston, Texas, and Research Laboratories of Schering MD Berlin, Germany; Division of Reproductive Sciences, Department of Obstetrics and Gynecology, The University of Texas Medical Branch, 301 University Boulevard, Rt J-62, Galveston, TX 77555-1062 rgarfiel{at}marlin.utmb.edu Objective: To examine the hypothesis that kinetics of vasorelaxation are altered during pregnancy.
Methods: Rings of aorta from rats at different stages of pregnancy (early, late, and term) and from nonpregnant female rats were precontracted with high-K+ and then allowed to relax in normal-K+ physiologic saline solution. The time to reach 50% and 80% relaxation were determined in the absence or presence of a cycloxygenase inhibitor (indomethacin) and a nitric oxide synthase inhibitor (N
Results: The aortic relaxation was progressively faster in later stages of gestation. N Conclusion: Aortic relaxation is faster in the presence of endothelium. The effect of endothelium on relaxation is independent of nitric oxide synthase or cycloxygenase systems. Progression of gestation is associated with acceleration of aortic relaxation, which cannot be totally ascribed to an endothelial factor and may involve a change intrinsic to the vascular smooth muscle. Faster relaxation kinetics of the vasculature during pregnancy may be a mechanism to decrease peripheral vascular resistance.
Key Words: Rat aorta pregnancy endothelium vascular smooth muscle relaxation kinetics
Journal of the Society for Gynecologic Investigation, Vol. 5, No. 2,
81-86 (1998) |
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-nitro-L-arginine methyl ester) or after removal of the endothelium. 