Award details

In vivo and in vitro studies of dietary fatty acids eNOS polymorphisms and insulin resistance in the endothelium

Reference	BB/E021816/1
Principal Investigator / Supervisor	Professor Christine Williams
Co-Investigators / Co-Supervisors	Dr Michael Fry, Dr Kim Jackson, Prof. Anne-Marie Minihane
Institution	University of Reading
Department	Food and Nutritional Sciences
Funding type	Research
Value (£)	350,372
Status	Completed
Type	Research Grant
Start date	01/09/2007
End date	31/08/2010
Duration	36 months

Abstract

Endothelial dysfunction is a characteristic feature of insulin resistance which is thought to arise largely from impaired generation of the vasodilator, nitric oxide (NO), by vascular endothelial cells. Recent cell studies have suggested impaired release of NO in insulin resistance is due to selective resistance to the action of insulin on the Insulin Receptor Substrate-1 (IRS-1) /Phosphoinositide 3-kinase (PI 3K) / Akt pathway, and attenuation of the activation of endothelial nitric oxide synthase (eNOS) and NO production. Furthermore, studies have shown this pathway to be down regulated by the serine phosphorylase IKKB, and that high concentrations of free fatty acids (FFAs) activate IKKB, as well as leading to activation of pro-inflammatory payways via NFKB and MAP kinase. The aims of the proposed programme of work, which builds on recent studies in our group, is to investigate the relevance of these in vitro findings by means of a series of in vivo studies in which we will evalute the effect of elevated circulating concentrations of specific fatty acids on vascular function measured using Laser Doppler Iontophoresis. We will carry out these studies in normal healthy subjects who carry the common variant (Glu/Glu) of the eNOS gene polymorphism Glu298Asp as well as in subjects carrying the rarer isoform (Asp/Asp). We will carry out parallel cell studies to evaluate the effect of a range of fatty acids on the activation of the Insulin Receptor Substrate-1 (IRS-1) /Phosphoinositide 3-kinase (PI 3K) / Akt pathway/ eNOS pathway, using human umbilical vein cells (HUVECs) from subjects carrying the common and rare isoforms of eNOS Glu298Asp and/or HUVECs transfected with the relevant DNA sequences. The studies will provide evidence for likely benefit of modifying dietary fat quality on insulin resistance and endothelial dysfunction, contributing to more effective and scientifically sound approaches to diet and vascular health.

Summary

The hormone insulin is involved in stimulating the uptake and metabolism of dietary carbohydrates (e.g. sugars) and fats by cells such as those in muscle, fat tissue and liver. When insufficient insulin is produced (type 1 diabetes), or when there is lack of effect of insulin on cells (type 2 diabetes and insulin resistance), the metabolism of carbohydrates and fats becomes abnormal. Levels of blood glucose rise, leading to symptoms of diabetes (thirst, tiredness etc) and blood lipids also rise. Lipids are carried in the blood on complex particles called lipoproteins (e.g. LDL and HDL cholesterol). In diabetes these particles are abnormal, with low HDL cholesterol (good cholesterol) and raised concentrations of particles called triglyceride rich lipoproteins. This combination is known to increase the risk of cholesterol penetrating the blood vessel wall, leading to hardening of the arteries and heart disease. For a long time it was thought that the reason people with diabetes have a much higher risk of heart disease was because of these abnormal lipoprotein particles. Whilst this is undoubtedly part of the story, new research is suggesting other mechanisms may also be involved. Although we have known for a long time that cells such as muscle, fat and liver require insulin, it is only recently that insulin has been shown to be required for the normal healthy functioning of the cells that line the blood vessel wall (called endothelial cells). Insulin increases the formation of compounds which keep the blood vessel wall dilated and reduces release of compounds which constrict the blood vessel wall and cause it to become sticky (called inflammatory proteins). This new research is helping to understand how insulin triggers the release of compounds which keep the vessel wall healthy and what happens when people become resistant to the normal actions of insulin. People who are diabetic or insulin resistant are unable to dilate their blood vessels normally when stimulated and release inflammatory proteins which are more likely to lead to cholesterol depositing in the artery wall. The reason there is increasing concern about insulin resistance is that this condition is becoming extremely common because it is linked with overweight and obesity. It is now estimated that as many as 20% of middle aged adults may be insulin resistant and this greatly increases their risk of getting heart disease or having a stroke. Understanding the consequences of insulin resistance in blood vessel cells is therefore very important. Some research has shown that the types of fats in the diet can influence the efficiency with which insulin acts on muscle, fat and liver cells. However very little is known about how the type of dietary fat influences endothelial cells and how the cells behave when exposed to different fats, both in the body and when studied in test tubes. We will use a technique to study the behavior of blood vessels in people when they are exposed to high concentrations of different types of fats and also how it affects their blood vessel response when insulin is given. We will also study cells cultured in the laboratory to see if we can understand the triggers that lead to the cells responding more or less favourably in the presence of different types of fats. One of the compounds which help the blood vessel wall to dilate is a small molecule called nitric oxide. The enzyme which leads to the release of nitric oxide is a protein whose structure varies slightly in some people due to differences in their genes (about 12% the population carry this variation and are known to be more at risk of heart disease). We want to study people with and without this variation and see if they respond differently to different fats. We will also study blood vessel cells (from the umbilical cord) which have been obtained from women with and without the variant to see how this enzyme works.

Committee	Closed Committee - Agri-food (AF)
Research Topics	X – not assigned to a current Research Topic
Research Priority	X – Research Priority information not available
Research Initiative	X - not in an Initiative
Funding Scheme	Industrial Partnership Award (IPA)

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