Abstract

Objective: In clinical studies with diabetic patients thiazolidinediones have been shown to restore abnormal vascular function which might be attributed to improved blood sugar control or to restoration of vascular endothelium and smooth muscle responsiveness. The present study was undertaken to investigate whether rosiglitazone modulates vascular responsiveness to different vasoactive agents and exerts renin-angiotensin-system (RAS)-inhibiting properties in healthy subjects in vivo. Methods: 24 healthy male subjects were randomized to receive either rosiglitazone or placebo. Venoconstrictor responses to angiotensin II (Ang II) and phenylephrine, and endothelium-dependent response to histamine and insulin, and endothelium-independent response to glyceroltrinitrate were compared using the dorsal hand vein compliance method. Effects on the RAS were investigated by plasma level determinations of Ang II and angiotensin-(1-7). Treatment effects on the systemic arterial system were investigated by standardized pulse-wave-analysis. Results: Rosiglitazone significantly inhibited venoconstrictor responses to Ang II by 19% (–70% vs. –51% constriction, p = 0.034) and in the presence of rosiglitazone the ED80 for phenylephrine was increased (ED80: 317 ± 86 ng vs. 531 ± 102 ng; p = 0.010). Rosiglitazone treatment was without effect on endothelium-dependent dilation, blood pressure, pulse-wave-velocity and plasma angiotensin peptide levels. Conclusions: The data of the present study in veins of healthy subjects are consistent with data from in vitro and animal studies supporting a direct effect of rosiglitazone on venous tone by modulation of the vascular smooth muscle response via AT1-receptor-downregulation.

Author Details

Authors

• C. Schindler
• C.M. Ferrario
• C. Jatzke
• K. Ahner
• K.B. Brosnihan
• P. Bramlage
• U. Maywald
• R. Oertel
• W. Boecking
• W. Kirch

Departments

• ¹ Institute of Clinical Pharmacology, Medical Faculty, Technical University Dresden, Dresden, Germany, and
• ² Hypertension and Vascular Research Center, Wake Forest University School of Medicine, Winston-Salem, NC, USA

Address

Dr. C. Schindler; Institute of Clinical Pharmacology, Medical Faculty of the Technical University Dresden, Fiedlerstrasse 27, 01307 Dresden, Germany
Email: [email protected]

Citation