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Am J Physiol Regul Integr Comp Physiol 292: R723-R730, 2007. First published June 29, 2006; doi:10.1152/ajpregu.00112.2006
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Sex Differences in Renal and Cardiovascular Function: Physiology and Pathophysiology

Hyperglycemia and loss of ovarian hormones mediate atheroma formation through endothelial layer disruption and increased permeability

Jeana Benton,1 Andrew Powers,1 Larissa Eiselein,1 Richard Fitch,1 Dennis Wilson,2 Amparo C. Villablanca,1 and John C. Rutledge1

1School of Medicine and 2School of Veterinary Medicine, University of California, Davis, California

Submitted 14 February 2006 ; accepted in final form 22 June 2006

The overall goal of this project was to examine the interactions of hyperglycemia and loss of ovarian hormones on the artery wall in a type I diabetic mouse model. Intact or ovariectomized (OVX) female BALB/C mice were fed a high-cholesterol diet. Half the animals were treated with steptozotocin to induce insulin-deficient diabetes mellitus, generating four treatment groups: control, intact; control, ovariectomized; diabetic, intact; diabetic, ovariectomized (DOVX). We examined arterial structure and function and found that 1) diabetes and ovariectomy additively increased endothelial layer permeability, 2) arterial stiffening was increased in DOVX, 3) DOVX synergistically increased atheroma formation, and 4) ultrastructural evaluation revealed that the basal lamina was often multilayered and formed convoluted aggregates separating endothelium from the internal elastic lamina in diabetic, but not control arteries or arteries from OVX mice. Endothelium overlying these regions formed thin cytoplasmic extensions between these aggregates and was often separated from the basal lamina by electron lucent spaces. Our studies showed that diabetes and loss of ovarian function have additive and synergistic effects to worsen arterial pathophysiology by disrupting the arterial endothelial layer with increased permeability and increased atheroma formation.

diabetes; vascular; atherosclerosis; postmenopause; pathophysiology



Address for reprint requests and other correspondence: J. C. Rutledge, Dept. of Internal Medicine, 5404 GBSF, Univ. of California, Davis, CA 95616 (e-mail: jcrutledge{at}ucdavis.edu)




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Am. J. Physiol. Regul. Integr. Comp. Physiol.Home page
K. Denton and C. Baylis
Physiological and molecular mechanisms governing sexual dimorphism of kidney, cardiac, and vascular function
Am J Physiol Regulatory Integrative Comp Physiol, February 1, 2007; 292(2): R697 - R699.
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