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Am J Physiol Heart Circ Physiol 290: H137-H145, 2006. First published August 26, 2005; doi:10.1152/ajpheart.00768.2005
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High-dose oral vitamin C partially replenishes vitamin C levels in patients with Type 2 diabetes and low vitamin C levels but does not improve endothelial dysfunction or insulin resistance

Hui Chen,1 Rajaram J. Karne,1 Gail Hall,1 Umberto Campia,2 Julio A. Panza,2 Richard O. Cannon, III,2 Yaohui Wang,3 Arie Katz,1 Mark Levine,3 and Michael J. Quon

1Diabetes Unit, National Center for Complementary and Alternative Medicine; 2Cardiology Branch, National Heart, Lung, and Blood Institute; 3Molecular and Clinical Nutrition Section, Digestive Diseases Branch, National Institute of Diabetes, Digestive and Kidney Diseases, National Institutes of Health, Bethesda, Maryland

Submitted 19 July 2005 ; accepted in final form 23 August 2005

Endothelial dysfunction is a hallmark of Type 2 diabetes related to hyperglycemia and oxidative stress. Nitric oxide-dependent vasodilator actions of insulin may augment glucose disposal. Thus endothelial dysfunction may worsen insulin resistance. Intra-arterial administration of vitamin C improves endothelial dysfunction in diabetes. In the present study, we investigated effects of high-dose oral vitamin C to alter endothelial dysfunction and insulin resistance in Type 2 diabetes. Plasma vitamin C levels in 109 diabetic subjects were lower than healthy (36 ± 2 µM) levels. Thirty-two diabetic subjects with low plasma vitamin C (<40 µM) were subsequently enrolled in a randomized, double-blind, placebo-controlled study of vitamin C (800 mg/day for 4 wk). Insulin sensitivity (determined by glucose clamp) and forearm blood flow in response to ACh, sodium nitroprusside (SNP), or insulin (determined by plethysmography) were assessed before and after 4 wk of treatment. In the placebo group (n = 17 subjects), plasma vitamin C (22 ± 3 µM), fasting glucose (159 ± 12 mg/dl), insulin (19 ± 7 µU/ml), and SIClamp [2.06 ± 0.29 x 10–4 dl·kg–1·min–1/(µU/ml)] did not change significantly after placebo treatment. In the vitamin C group (n = 15 subjects), basal plasma vitamin C (23 ± 2 µM) increased to 48 ± 6 µM (P < 0.01) after treatment, but this was significantly less than that expected for healthy subjects (>80 µM). No significant changes in fasting glucose (156 ± 11 mg/dl), insulin (14 ± 2 µU/ml), SIClamp [2.71 ± 0.46 x 10–4 dl·kg–1·min–1/(µU/ml)], or forearm blood flow in response to ACh, SNP, or insulin were observed after vitamin C treatment. We conclude that high-dose oral vitamin C therapy, resulting in incomplete replenishment of vitamin C levels, is ineffective at improving endothelial dysfunction and insulin resistance in Type 2 diabetes.

hypertension; hyperglycemia; hypercholesterolemia; insulin sensitivity; sodium nitroprusside



Address for reprint requests and other correspondence: M. J. Quon, Diabetes Unit, NCCAM, NIH, Bldg. 10, Rm. 6C-205, 10 Center Dr. MSC 1632, Bethesda, MD 20892-1632 (e-mail: quonm{at}nih.gov)




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