Low Levels of Hydrogen Sulfide in the Blood of Diabetes Patients and Streptozotocin-Treated Rats Causes Vascular Inflammation?

Sushil K. Jain(Louisiana State University Health Sciences Center New Orleans), Rebeca Bull(Louisiana State University Health Sciences Center New Orleans), Justin Rains(Louisiana State University Health Sciences Center New Orleans), Pat F. Bass(Louisiana State University Health Sciences Center New Orleans), Steven N. Levine(Louisiana State University Health Sciences Center New Orleans), Sudha Reddy(Louisiana State University Health Sciences Center New Orleans), Robert McVie(Louisiana State University Health Sciences Center New Orleans), Joseph A. Bocchini(Louisiana State University Health Sciences Center New Orleans)
Antioxidants and Redox Signaling
January 21, 2010
Cited by 314Open Access
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Abstract

Hydrogen sulfide (H(2)S) is emerging as a physiological neuromodulator as well as a smooth muscle relaxant. We submit the first evidence that blood H(2)S levels are significantly lower in fasting blood obtained from type 2 diabetes patients compared with age-matched healthy subjects, and in streptozotocin-treated diabetic rats compared with control Sprague-Dawley rats. We further observed that supplementation with H(2)S or an endogenous precursor of H(2)S (l-cysteine) in culture medium prevents IL-8 and MCP-1 secretion in high-glucose-treated human U937 monocytes. These first observations led to the hypothesis that lower blood H(2)S levels may contribute to the vascular inflammation seen in diabetes.


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