A Novel Chemically Modified Curcumin “Normalizes” Wound-Healing in Rats with Experimentally Induced Type I Diabetes: Initial Studies

Author:

Zhang Yazhou12,McClain Steve A.3,Lee Hsi-Ming1,Elburki Muna S.1,Yu Huiwen1,Gu Ying4,Zhang Yu5,Wolff Mark2,Johnson Francis5,Golub Lorne M.1

Affiliation:

1. Department of Oral Biology and Pathology, School of Dental Medicine, Stony Brook University, Stony Brook, NY 11794, USA

2. Department of Cariology and Comprehensive Care, College of Dentistry, New York University, New York, NY 10010, USA

3. Departments of Dermatology and Emergency Medicine, Stony Brook University, Stony Brook, NY 11794, USA

4. Department of General Dentistry, School of Dental Medicine, Stony Brook University, Stony Brook, NY 11794, USA

5. Department of Pharmacological Sciences, Stony Brook University, Stony Brook, NY 11794, USA

Abstract

Introduction. Impaired wound-healing in diabetics can lead to life-threatening complications, such as limb amputation, associated in part with excessive matrix metalloproteinase- (MMP-) mediated degradation of collagen and other matrix constituents. In the current study, a novel triketonic chemically modified curcumin, CMC2.24, was tested for efficacy in healing of standardized skin wounds in streptozotocin-induced diabetic rats. Initially, CMC2.24 was daily applied topically at 1% or 3% concentrations or administered systemically (oral intubation; 30 mg/kg); controls received vehicle treatment only. Over 7 days, the diabetics exhibited impaired wound closure, assessed by gross and histologic measurements, compared to the nondiabetic controls. All drug treatments significantly improved wound closure with efficacy ratings as follows: 1% 2.24 > systemic 2.24 > 3% 2.24 with no effect on the severe hyperglycemia. In subsequent experiments, 1% CMC2.24 “normalized” wound-healing in the diabetics, whereas 1% curcumin was no more effective than 0.25% CMC2.24, and the latter remained 34% worse than normal. MMP-8 was increased 10-fold in the diabetic wounds and topically applied 1% (but not 0.25%) CMC2.24 significantly reduced this excessive collagenase-2; MMP-13/collagenase-3 did not show significant changes. Additional studies indicated efficacy of 1% CMC2.24 over more prolonged periods of time up to 30 days.

Funder

Research Foundation of Stony Brook University

Publisher

Hindawi Limited

Subject

Endocrinology,Endocrinology, Diabetes and Metabolism

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