Abstract

Chronic, low-level inflammation may be an independent marker of Metabolic Syndrome (MetS). Systemic Enzyme Therapy (SET), the oral administration of proteolytic enzymes, is safe and effective in the management of inflammation. Therefore, the effects of SET, as Wobenzym&reg, on the prevention and treatment of inflammation and other metabolic risk factors were assessed in a rabbit model of diet-induced MetS. Animals were fed a lipid-enriched diet for 8 weeks during which they were administered a vehicle control (control group) or Wobenzym either throughout the study period (prevention group) or beginning at the 5th week, after the development of biomarkers of MetS (treatment group). At the 8th week, both prevention and treatment groups demonstrated improved insulin sensitivity relative to the control group and reduced serum C-reactive protein (CRP) and glycosylated hemoglobin (HbA1c, P < 0.001). At 8 weeks, the prevention group, but not the treatment group, exhibited reduced total cholesterol and oxidative stress, measured as serum malondialdehyde (P < 0.001). Triglycerides and free fatty acids were reduced in both the treatment (P < 0.01) and prevention groups (P < 0.001) relative to the control group at the 8th week. Body weight and blood glucose were not affected. Enzyme therapy may have a positive effect on inflammation, insulin sensitivity, and other metabolic risk factors of MetS.

Highlights

  • Metabolic Syndrome (MetS) is generally characterized by obesity and the presence of two additional metabolic risk factors [1]

  • Lipid Loading Induced Insulin Resistance and Metabolic Alterations Chronic lipid loading over 8 weeks induced a deterioration of systemic insulin sensitivity, determined as a reduction in percent glucose clearance following subcutaneous insulin injection (Figure 1(a), P < 0.001)

  • Lipid loading was associated with increased inflammation (Figure 1(b), P < 0.001), oxidative stress (Figure 1(c), P < 0.001), HbA1c (Figure 1(h), P < 0.001), and increased in lipid levels (total cholesterol, total TG and free fatty acids (FFA) levels (Figure 1(d)-(f), P < 0.001) compared to baseline values

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Summary

Introduction

Metabolic Syndrome (MetS) is generally characterized by obesity and the presence of two additional metabolic risk factors [1]. The risk factors encompassing MetS include abdominal obesity (waist circumference ≥ 40 inches for men and ≥35 inches for women), impaired fasting blood glucose (≥100 mg/dL), elevated triglycerides (≥150 mg/dL), low high-density lipoprotein (HDL < 40 mg/dL for men and

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