Abstract

Background: The aim of the current study was to determine whether a unique blueberry tea (BT) ameliorates insulin resistance by improving metabolic and vascular actions of insulin in skeletal muscle. Methods: Male Sprague Dawley rats were fed normal (4.8% fat wt/wt, ND) or high (22.6% fat wt/wt, HFD) fat diets for 4 weeks. A second group of HFD rats was provided BT (4.0% wt/vol) in the drinking water during the final 2 weeks. Animals were subjected to an intraperi toneal glucose tolerance test (1g glucose/kg IPGTT) or euglycaemic hyperinsulinaemic clamp (10mU/min/kg x 2hr). Results: HFD rats displayed significantly (p<0.05) higher plasma glucose levels at 15 and 30 mins following the IPGTT compared to ND, and this increase was completely abolished by BT treatment. Glucose infusion rate, muscle glucose uptake, and microvascular perfusion in muscle were significantly (p<0.05) impaired during clamps in HFD and all markedly improved (p<0.05) with BT treatment. Insulin-mediated changes in femoral artery blood flow were unaffected by HFD or BT treatment. Conclusions: We conclude that BT treatment ameliorates glucose intolerance and insulin resistance by restoring both metabolic and microvascular insulin sensitivity in high fat-fed rats. Therefore, BT consumption may have therapeutic implications for insulin resistance and type 2 diabetes.

Highlights

  • Insulin resistance plays a key role in the pathogenesis of type-2 diabetes (T2D)

  • HFD rats displayed significantly (p

  • At the end of the dietary intervention, there were no differences in plasma glucose concentrations between ND, HFD and HFD rats were supplemented with blueberry tea (HFD+BT) rats (Figure 2A and B)

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Summary

Introduction

Insulin resistance plays a key role in the pathogenesis of type-2 diabetes (T2D). While the root causes of insulin resistance are multifactorial, two of the major contributors are increased dietary fat and a sedentary lifestyle [1,2,3,4]. Our research implicates vascular dysfunction in skeletal muscle as one major cause of muscle insulin resistance. Insulin stimulates both total blood flow to skeletal muscle [11,12,13] and increases microvascular perfusion of the myocytes [6,7,8,9,10]. Muscle glucose uptake, and microvascular perfusion in muscle were significantly (p

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