FP7Individual fellowship2012–2014

FoodPro ForHealth · Investigating the role of food structure and processing in lipid digestion for production of healthier food

FP7 — People (Marie Curie Actions)

Duration
2012-10-01 → 2014-09-30
EU contribution
€200,372
Participants
1
Scheme
MC-IEF

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Results in brief

Investigating the role of food structure and processing in lipid digestion for production of healthier food

FoodPro ForHealth aimed to investigate the role of food structure on the physico-chemical breakdown of emulsified fats during in vitro digestion, in order to develop novel approaches for prolonging satiety and reducing dietary fat intake. A multidisciplinary approach combining fundamental physical and biological sciences was required to better understand the mechanisms underlying fat digestion and the impact of emulsion structure on lipase activity. This proposal involved studies that provided important information about the interaction of food ingredients with digestive enzymes, surfactants and lipids in the gut. Through improved understanding of this effect, we have developed food systems with potential to slow the digestion and sustain the release of fats for uptake in the gut. Bile salts are bio-surfactants secreted by the liver which help breakdown the fats during digestion. FoodPro ForHealth focused on ways of limiting the access of bile salts to the fat, as a potential mechanism of slowing fat digestion, either by designing interfaces that resist displacement by bile salts, or by binding bile salts in the small intestine. Understanding how the bile salts interact with emulsifiers and stabilizers commonly found in processed foods during the digestion process, will help to rationally develop healthier foods, not only capable of promoting satiety but also of reducing blood lipid and cholesterol levels. This will help to address obesity and associated conditions, one of the major challenges currently faced by the EU. At the host institution (Institute of Food Research - IFR), Cristina Fernandez-Fraguas has used, in particular, a range of colloidal and interfacial methodologies to identify the mechanisms by which food ingredients can influence fat digestion through either bulk or interfacial effects. She has also carried out experiments simulating the digestion process, under realistic, physiological conditions, following established IFR protocols. The results demonstrate feasible approaches for modifying both the continuous phase and the interface of emulsions by using specific types of food biopolymers. This will allow the design of food structures able to control bile salt behaviour / transport and hence have a marked impact upon fat digestion and metabolic health. APPROACH The project initially looked at the design of the interfaces between the fat and the water that hinder adsorption of bile salts as a potential mechanism to reduce adsorption of fat digesting enzymes, and thus to limit the rate of lipolysis. Model emulsified foods covering a range of responses to digestive conditions were selected; these included systems representative of protein-based ingredients such as (B-lactoglobulin - B-lg, a-lactalbumin - a-la, whey protein isolate - WPI), polysaccharide–protein complexes (sugar beet pectin - SBP) and gels (Hydroxypropyl methylcellulose - HPMC). A relevant mixture of two common bile salts (BS), sodium taurocholate (NaTC) and sodium glycodeoxycholate (NaGDC), was used. These studies were then extended to investigate the implication of the BS binding properties of dietary fibre in the control of fat digestion. Firstly, colloidal methodologies were used in order to characterize the different ingredients and to investigate emulsion stability. A range of interfacial techniques, including particle electrophoresis analysis, tensiometry, interfacial dilatational rheology, interfacial biosensors and atomic force microscopy, were used to determine changes in interfacial behaviour of the adsorbed layers in presence of BS. The impact of the particularly interesting systems on the extent of lipid digestion was investigated by means of a laboratory-based digestion model simulated conditions encountered in the gut. CONCLUSIONS FoodPro ForHealth has enabled the use of physico-chemical approaches to investigate the interaction of diverse food structures with digestive enzymes, surfactants and fats in a simulated gut environment representing both the stomach and small intestine. FoodPro ForHealth has shown, firstly, that heat treatment is a successful strategy to enhance the resistance of whey protein interfacial layers to displacement by Tween 20 and bile salts. Secondly, digestion of emulsified fats stabilised with a naturally occurring protein-polysaccharide complex (SBP) and a non-ionic polymer (HPMC) was similar despite their different competitive adsorption behaviour at low BS concentrations. This reflected that BS are very effective at adsorbing and disrupting interfaces, and they appear to be the critical step for the progression of fat digestion in the small intestine. Thirdly, the binding of BS to celluloses in solution can affect displacement by BS in two ways, by changing interfacial properties of the cellulose-BS complexes, and by reducing free BS available to displace cellulose and/or complexes. Dr. Fernandez demonstrated that the potential of cellulose ethers to influence satiety is more related to their ability to bind BS in solution than their ability to disrupt adsorption of BS at the interface. This important finding, together with the challenge of designing interfaces to restrict adsorption of bile salts, led us to focus our attention on how a specific dietary fibre with proven cholesterol reducing properties, would impact fat digestion. From here, FoodPro ForHealth provided new insights into how the binding of either soluble (B-Glucans) and insoluble fibres from oats to bile salts in the bulk, impact the interfacial properties of the emulsions related to access for digestion. In addition, the different adsorption behaviour observed between different bile salts structures supports the necessity of filling the gaps in our understanding of the roles of various essential components in fat digestion. FoodPro ForHealth has given us a better, fundamental understanding of how interfacial and bulk properties, solution conditions, and interactions with bile salts determines the digestibility of food structures, and in particular the availability of fat for uptake. This is generating renewed scientific interest due to the growing social and economic consequences of the obesity crisis in the developed world. The design of healthier foods to control obesity is a top priority in the EU: it is estimated that treating obesity and related diseases (such as type 2 diabetes and cardio-vascular disorders) takes up to 5% of the EU’s total healthcare budget. FoodPro ForHealth has made a significant contribution to bridge the knowledge gaps between the physical sciences and nutrition, to improve our understanding of how the structure of food can influence digestion of carbohydrates, proteins and fats, and how this in turn can influence dietary intake, satiety, and metabolic health. This knowledge can be exploited in tailoring novel food systems able to control bile salt behaviour / transport as a potential route to modulate lipid absorption. Applying physical and materials science principles to understand fundamental processes, such as bile salt adsorption/interaction, and to modulate digestion and interfacial/bulk properties of complex food structures is a novel, emerging area of industry-relevant research, and may be associated with further, emerging health benefits such as fat metabolism and gut health. An extended final report is included as an attachment

Data: CORDIS, © European Union

Project objective

FoodPro ForHealth will develop rational strategies to formulate and process foods to control lipid digestion, and combines the Fellow’s food science skills with expertise and techniques at the Institute of Food Research (IFR) in the colloids, interfacial, model gut and health areas.Obesity is a major health problem in Europe/developed countries and a risk factor for chronic diseases (diabetes and cardiovascular disease, CVD) leading to anti-obesity campaigns promoting healthy eating and a healthy lifestyle. Lipids are the most energy dense of macronutrients and excess consumption has been linked to obesity. Most people find it difficult to change their diets to eat healthily. Changes in food manufacturing are needed to develop healthier products and ingredients. Lipids are water insoluble and their breakdown in the digestive tract occurs at the fat/water interface so the composition at the fat interface can affect lipid digestion in vitro. If lipid digestion is controlled, energy release during digestion is prolonged and hyperlipidaemia, a CVD risk factor, reduced. Slowly-digested lipids can also increase satiety, control energy intake and help manage weight loss. State-of-the-art physicochemical techniques will be used to study how common food structures in emulsified foods influence the breakdown/digestion of lipids in vitro. The interaction of these structures with digestive enzymes, surfactants and lipids will be studied in the gastric and duodenal environment. Better understanding the factors affecting the nature/extent of lipid breakdown in model systems and real food models will allow science-based strategies to modify food products or develop new products to optimise fat digestion. The project will assist the Fellow to develop new research projects on her return to Spain and to transfer knowledge to industry. Complementary skills (e.g communication, resource management, IP and awareness of the needs of industry and society) will be transferred to the Fellow

Original text from CORDIS.

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Data: CORDIS, © European Union