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Effects of low-dose candesartan on the rate of re-endothelialisation following vascular wound healing
Prakash Koshy
Departments of Pharmacology and Medicine, Tulane University School of Medicine, New Orleans, LA 70112, USA
Amanda Self
Departments of Pharmacology and Medicine, Tulane University School of Medicine, New Orleans, LA 70112, USA
Philip J Kadowitz
Departments of Pharmacology and Medicine, Tulane University School of Medicine, New Orleans, LA 70112, USA
Vivian A Fonseca
Departments of Pharmacology and Medicine, Tulane University School of Medicine, New Orleans, LA 70112, USA
Dennis B McNamara
Departments of Pharmacology and Medicine, Tulane University School of Medicine, New Orleans, LA 70112, USA, dmcnama@ tulane.edu
The wound healing response of the vascular wall to injury involves re-endothelialisation of the denuded luminal surface and thickening of the intimal area (intimal hyperplasia), as expressed by the intimal-to-medial area ratio (I/M). Candesartan, at doses of 1 mg/kg/day or higher, has been reported to attenuate the intimal hyperplastic response. We tested the hypothesis that candesartan, at doses lower than those associated with attenuation of intimal hyperplasia, may affect re-endothelialisation. New Zealand White rabbits were subjected to balloon catheter injury to the thoracic aorta. Candesartan, at doses of 50, 100, and 500 µg/kg/day, was delivered via an Alzet pump placed in the abdomen one week prior to aortic injury. There was no attenuation of the hyperplastic response of the aortic wall. However, at 50 µg/kg/day the rate of reendothelialisation was significantly increased. These data suggest that candesartan may exhibit pleiotropic effects on vascular wound healing, in addition to the well-known effect of attenuating the development of intimal hyperplasia.
Key Words: vascular wound healing intimal hyperplasia re-endothelialisation angiotensin angiotensin receptor antagonist
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Journal of Renin-Angiotensin-Aldosterone System, Vol. 2, No. 1 suppl,
S81-S83 (2001)
DOI: 10.1177/14703203010020011401

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