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Long-Term N-Acetylcysteine and l-Arginine Administration Reduces Endothelial Activation and Systolic Blood Pressure in Hypertensive Patients With Type 2 Diabetes

  1. Valentino Martina, MD1,
  2. Andi Masha, MD1,
  3. Valentina Ramella Gigliardi, MD1,
  4. Loredana Brocato, MD1,
  5. Enzo Manzato, MD, PHD3,
  6. Arrigo Berchio, MD1,
  7. Paola Massarenti, MD1,
  8. Fabio Settanni, PHD1,
  9. Lara Della Casa, PHD2,
  10. Stefania Bergamini, PHD2 and
  11. Anna Iannone, MD, PHD2
  1. 1Department of Internal Medicine, University of Torino, Torino, Italy
  2. 2Department of Biomedical Sciences, University of Modena and Reggio Emilia, Modena, Italy
  3. 3Department of Medical and Surgical Sciences, University of Padova, Padova, Italy
  1. Corresponding author: Valentino Martina, MD, Department of Internal Medicine, University of Torino, Corso Dogliotti 14, I-10121 Torino, Italy. E-mail: valentino.martina{at}unito.it

Abstract

OBJECTIVE—Reactive oxygen and nitric oxide (NO) have recently been considered to be involved in the cardiovascular complications of patients with type 2 diabetes, as NO is thought to lose its beneficial physiological effects in the presence of oxygen radicals. For this reason, we tested the effects of l-arginine (ARG) and N-acetylcysteine (NAC) administration in increasing NO bioavailability by reducing free radical formation.

RESEARCH DESIGN AND METHODS—A double-blind study was performed on 24 male patients with type 2 diabetes and hypertension divided into two groups of 12 patients that randomly received either an oral supplementation of placebo or NAC + ARG for 6 months.

RESULTS—The NAC + ARG treatment caused a reduction of both systolic (P < 0.05) and diastolic (P < 0.05) mean arterial blood pressure, total cholesterol (P < 0.01), LDL cholesterol (P < 0.005), oxidized LDL (P < 0.05), high-sensitive C-reactive protein (P < 0.05), intracellular adhesion molecule (P < 0.05), vascular cell adhesion molecule (P < 0.01), nitrotyrosine (P < 0.01), fibrinogen (P < 0.01), and plasminogen activator inhibitor-1 (P < 0.05), and an improvement of the intima-media thickness during endothelial postischemic vasodilation (P < 0.02). HDL cholesterol increased (P < 0.05). No changes in other parameters studied were observed.

CONCLUSIONS—NAC + ARG administration seems to be a potential well-tolerated antiatherogenic therapy because it improves endothelial function in hypertensive patients with type 2 diabetes by improving NO bioavailability via reduction of oxidative stress and increase of NO production. Our study's results give prominence to its potential use in primary and secondary cardiovascular prevention in these patients.

Footnotes

  • Published ahead of print at http://care.diabetesjournals.org on 11 February 2008. DOI: 10.2337/dc07-2251.

    The costs of publication of this article were defrayed in part by the payment of page charges. This article must therefore be hereby marked “advertisement” in accordance with 18 U.S.C Section 1734 solely to indicate this fact.

    • Accepted February 2, 2008.
    • Received December 7, 2007.
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This Article

  1. Diabetes Care May 2008 vol. 31 no. 5 940-944
  1. All Versions of this Article:
    1. dc07-2251v1
    2. 31/5/940 most recent
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