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Digital Plethysmography and Arginine Metabolism in Prehypertension: Effect of Nebivolol Therapy

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Date 2014 Dec 16
PMID 25495953
Citations 2
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Abstract

Prehypertension is an important phenotype for cardiovascular risk and development of established hypertension. To better understand the early circulatory changes in this group, the authors studied 34 patients with prehypertension (blood pressure 120-139/80-89 mm Hg) using digital plethysmography for measurement of blood flow and reactive hyperemic index (RHI). Arterial augmentation index (AI) was also measured. Because prehypertension is associated with endothelial dysfunction and decreased availability of nitric oxide (NO), indices of arginine metabolism (l-arginine, asymmetric dimethylarginine (ADMA), symmetric dimethylarginine, and l-citrulline) were measured. Nebivolol (5 mg/d), a vasodilating β1 -antagonist with β3 -agonist activity, was studied in a double-blind fashion for 8 weeks. Nebivolol increases the bioavailability of NO. Prehypertension was associated with normal RHI and baseline digital blood flow. AI was abnormal and associated with diastolic blood pressure. ADMA concentration was increased at baseline. After 8 weeks of nebivolol therapy, RHI, ADMA, symmetric dimethylarginine, and AI showed no significant change, but digital blood flow and l-citrulline levels were significantly increased. Prehypertension is associated with increased ADMA and evidence of increased arterial stiffness and preserved RHI. Nebivolol therapy is associated with digital vasodilation and increased NO production, as depicted by increased levels of l-citruline and mean digital blood flow.

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References
1.
Garbin U, Fratta Pasini A, Stranieri C, Manfro S, Boccioletti V, Cominacini L . Nebivolol reduces asymmetric dimethylarginine in endothelial cells by increasing dimethylarginine dimethylaminohydrolase 2 (DDAH2) expression and activity. Pharmacol Res. 2007; 56(6):515-21. DOI: 10.1016/j.phrs.2007.09.015. View

2.
Achan V, Broadhead M, Malaki M, Whitley G, Leiper J, MacAllister R . Asymmetric dimethylarginine causes hypertension and cardiac dysfunction in humans and is actively metabolized by dimethylarginine dimethylaminohydrolase. Arterioscler Thromb Vasc Biol. 2003; 23(8):1455-9. DOI: 10.1161/01.ATV.0000081742.92006.59. View

3.
EICHNA L, Bordley J . CAPILLARY BLOOD PRESSURE IN MAN. DIRECT MEASUREMENTS IN THE DIGITS OF NORMAL AND HYPERTENSIVE SUBJECTS DURING VASOCONSTRICTION AND VASODILATATION VARIOUSLY INDUCED. J Clin Invest. 1942; 21(6):711-29. PMC: 435187. DOI: 10.1172/JCI101347. View

4.
Nohria A, Gerhard-Herman M, Creager M, Hurley S, Mitra D, Ganz P . Role of nitric oxide in the regulation of digital pulse volume amplitude in humans. J Appl Physiol (1985). 2006; 101(2):545-8. DOI: 10.1152/japplphysiol.01285.2005. View

5.
Urbina E, Khoury P, McCoy C, Daniels S, Kimball T, Dolan L . Cardiac and vascular consequences of pre-hypertension in youth. J Clin Hypertens (Greenwich). 2011; 13(5):332-42. PMC: 3092159. DOI: 10.1111/j.1751-7176.2011.00471.x. View