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Health benefits of resistant starch

SHALINI K. GHODKE, LAXMI ANANTHANARAYAN*


*Corresponding author
Food Engineering and Technology Department
Institute of Chemical Technology, University of Mumbai
Matunga, Mumbai 400 019, India

ABSTRACT: Resistant starches (RS) have drawn broad interest worldwide for both their potential health benefits and functional
properties. Initial clinical studies demonstrate that resistant starches have properties similar to fiber and show promising physiological
benefits in humans, which may result in prevention of various diseases. The present review highlights a number of these aspects and
describes the metabolic and functional properties of RS such as attenuating blood glucose, maintaining gastrointestinal health, acting as
prebiotic, helping in beneficial lipid metabolism and assisting weight loss.

INTRODUCTION

Natural, wholesome and health promoting food is the current demand


of health conscious consumers. Due to altered life style, diet has
become rich in fat, carbohydrates and animal protein and low in
dietary fiber. Consequently, constipation, obesity, type II diabetes,
cancer, heart diseases and many other diseases are on the rise. A
recent US survey showed functional ingredients such as dietary fiber
to be viewed positively by consumers as ranking high amongst
Starch

functional ingredients (1). The World Health Organization currently


recommends consumption of >25 grams of total dietary fiber/day. In
fact, the WHO has identified dietary fiber as the only dietary
ingredient with "Convincing Evidence" showing a protective effect
against weight gain and obesity (2). Resistant starch (RS) is one of
the best sources of fiber available in diet. This review focuses on
health benefits of RS in the diet.
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HEALTH BENEFITS

TYPES OF RESISTANT STARCH There is ample justification that RS behaves physiologically like fiber.
RS assays as insoluble fiber and has the physiological benefits of
Starch is composed primarily of two polysaccharides - a linear soluble fiber. Numerous studies in rats (8-11) have shown RS to
amylose containing α-1-4 glycosidic bonds and branched amylopectin escape digestion in the small intestine and be slowly fermented in the
in which branching occurs through α-1-6 linkages on the amylose large intestine. Following are some of the metabolic health benefits of
chains. The amount of amylose present in starch varies from 17-38 RS.
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percent and depends on the botanical origin. The way in which these
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polymers pack themselves in their granular and non granular (after


processing) forms makes a starch resistant to enzymatic digestion in BLOOD GLUCOSE AND INSULIN RESPONSE
the intestine (3). RS is resistant to enzymatic digestion by α-amylase
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and has been defined as "the sum of starch and products of starch Insulin is a hormone that enables glucose uptake by muscle and
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degradation not absorbed in the small intestine of healthy individuals". adipose cells, thereby lowering blood glucose level. RS containing
RS is classified as a part of dietary fiber when measured using AACC foods release glucose slowly resulting in lowered insulin response
Approved Methods 32-07 (4) and AOAC Method 991.43 (5). Over the and greater access to and use of stored fat. This helps in
last decade, there has been increased interest in the nutritional management of diabetes and impaired glucose tolerance, and hence
implications of RS because of their low calorie content and in the treatment of obesity and weight management. Literature on the
physiological effects similar to dietary fiber. RS that reaches the large dietary requirements for diabetics is controversial. According to the
intestine acts as a substrate for microbial fermentation, the end- American Diabetes Association (ADA), individuals with diabetes
products being hydrogen, carbon dioxide, methane and short chain should derive a major portion of their calories from starchy foods, and
fatty acids (SCFA) (6). There are four types of RS. RS1 is physically limit sugar and protein intake to USDA-recommended levels. Current
inaccessible starch locked within cell walls, e.g. partially milled grains, comparative diet studies suggest that low fat, high carbohydrate diet
seeds and legume starches, RS2 is native starch granules that are recommended by the ADA may not be as beneficial as a diet low in
resistant, for instance from green banana, raw potato and high carbohydrates and high in unsaturated fats. There are number of
amylose maize (HAM). RS3 is retrograded crystalline non granules, studies on effect of various forms and doses of RS on glucose
e.g. cooked, cooled potato and retrograded HAM starches, RS4 is (glycaemic) and insulin responses, but give contradictory results. Few
chemically modified to inhibit or limit amylase digestion; studies have reported on improvement following the consumption of
repolymerised dextrins with altered glycosidic linkages produced by RS rich food (12-14), while others have showed no effect (15-17).
acid or heat treatment and purified e.g. chain linkage altered dextrins The physicochemical properties of foods can directly affect the
are also included in RS4. Higher amylose levels in the starch are amount of RS present. In the study of Heijnen et al. (18), RS when
associated with slower digestibility or greater resistance to digestion. provided in a pudding resulted in lowered postprandial glucose
High-amylose maize producing RS has been particularly useful in the response and the same RS when incorporated in bread roll did not
preparation of foods (7). affect insulin or glucose response. Behall et al. (19) reported no

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significant effect on glucose responses or insulin sensitivity following DNA adducts reflects exposure to toxic chemicals and their
5 weeks of feeding a high RS diet. Kim et al. (33) showed no bioaccumulation throughout life. In the colonic mucosa increased
improvement on glucose or insulin concentration in streptozocin levels of DNA adducts are thought to increase cancer risk (38). The
induced diabetic rats fed RS rich diet. More research is needed to proliferative activity of epithelial cells is thought to be an intermediate
examine the effect of RS on insulin sensitivity using validated risk marker for colorectal cancer (39). Improved colon function is
methods. The role of food matrix also needs to be investigated. associated with increased production of SCFA, lower pH, lower
production of ammonia and phenol, decreased secondary bile acid
excretion, reduced cytotoxicity of fecal water, reduced transit time and
GLYCAEMIC INDEX AND GLYCAEMIC LOAD altered bacterial activity. A low acid and high concentration of SCFA is
thought to prevent overgrowth of pH sensitive pathogenic bacteria
The ability of particular food to elevate postprandial blood glucose (35). Most RS is readily fermentable and is a good source of SCFA
concentration is glycaemic response or gycaemic index (GI). GI is such as butyric acid (BA) in colon. Butyrate has been observed to
measured as the incremental area under the blood glucose curve induce and influence gene expression through its effect on
after consumption of 50g of available carbohydrate from a test food, transcription (40). BA has also been observed to induce apoptosis
divided by area under the curve after eating a similar amount of and reverse the resistance of colonic cancer cells to programmed cell
available carbohydrate in a control food (generally white bread or death (41). The half life time of BA is very short, and any effect of BA
glucose). Foods with high GI values release glucose rapidly into on colon can be expected when there is a consistent production of BA
blood stream (i.e. elicit a rapid glycaemic response), while food with a over a large segment of the colon.
low GI value release glucose more slowly into the blood stream and Many studies have been done on the impact of consumption of
result in delayed glycaemic and insulinamic response (31). With the substrates which generate high amount of butyrate (wheat bran,
consumption of high amylose (RS) starch, insulin response reduced insulin, fructo oligosaccharide and RS) in the colon. Pierre et al. (42)
by 17 percent (12). studied Min mice and observed that short chain fructo
Glycaemic index refers to the nature of carbohydrate in a food. oligosaccharide reduced the incidence of colon tumors, and
However, when people eat meals (different foods) generally concomitantly developed gut associated lymphoid tissue. Neither
carbohydrate foods are eaten along with protein and fat. Glycaemic starch free bran nor RS3 modified the number of tumors. Hence
load (GL) takes into account both carbohydrate content per serving of further studies using several models are required.
food and its GI value i.e. the quantity and nature of carbohydrate
present. It is possible to lower GI by replacing carbohydrate content
with protein, fat or other lower GI carbohydrate such as RS (32). PREBIOTIC

Starch
Probiotics are strains of living bacteria that survive the passage of the
SHORT CHAIN FATTY ACIDS (SCFA) stomach and are able to adhere to the intestinal wall of the small
intestine and to colonise the large intestine whereas prebiotics are
SCFA are the metabolic products of anaerobic bacterial fermentation "growth substrates specifically directed towards potentially beneficial
of polysaccharides, oligosaccharides, protein, peptide and bacteria already resident in colon". Prebiotics stimulate growth and /or
glycoprotein precursors in the large intestine, including those derived

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activity of bacteria in colon, and improve colon health. Synbiotics refer
from dietary fiber and RS (33). The principal SCFA are butyrate, to a mixture of prebiotic and probiotic where there is a synergistic
propionate and acetate, although other SCFA are also produced in interaction between the two. RS appears to function differently than
lesser amounts (34). SCFA are the preferred respiratory fuel of the well known prebiotics (fructooligosaccharides) (36). It has been found
cells lining the colon (colonocytes). They increase colonic blood flow, that only small proportion of ingested organisms reach the colon, and
lower luminal pH and help prevent the development of abnormal as probiotic consumption decreases these organisms are washed out
colonic cell populations (35). SCFA are mainly found in the proximal of the gastrointestinal tract. These losses are avoided by RS which
colon where fermentation is greatest, and the amount present mirrors gives physical protection by slowing the rate at which the bacteria are

n
supply of carbohydrate in the diet (36). Depending on diet, total SCFA lost once probiotic consumption ceases. RS supplementation in

Jan/Feb 2008
concentrations are usually between 70 and 140 mM in the proximal association with oral hydration therapy reduce fluid loss and halve
colon and 20-70 mM in the distal colon; therefore, SCFA are found in recovery time when fed to people with cholera induced diarrhea (36).
much lower amounts in the distal colon (the site of many colonic
diseases and most human colon cancers). Therefore, dietary n
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interventions that increase the amount of SCFA in the colon are


thought to be beneficial to gut health.
Carbohydrates that are not digested in small intestine will enter the
colon, those that are fermentable will be salvaged as SCFA in the
colon and may stimulate colonic micro flora, such as bifidobacteria.
More important aspect of colonic fermentation is stimulation of colonic
micro flora which may assist in the biotransformation of bioactive food
components including the cleaving of plant phenolics and from their
glycone to produce the more rapidly absorbed aglycone (37).
Increasing SCFA production also lowers colonic pH and increases the
excretion of bile acids. A lowered pH is thought to be protective
against colorectal cancer and inhibits the transformation of primary to
secondary bile acids. Secondary bile acids are cytotoxic to colonic
cells and are thought to be tumor promoters (38). Therefore, RS may
also confer benefits to gut health via the actions of SCFA on pH and a
reduced production of secondary bile acids.

GUT DISORDERS AND COLON CANCER LIPID METABOLISM

DNA adducts are complexes formed from the reaction of toxic RS appears to affect lipid metabolism based on studies in rats where
chemicals or their metabolites with cellular DNA. The presence of reduction in a number of measures of lipid metabolism are observed

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such as total lipids, total cholesterol (33), various lipoprotein fractions resistant starch enhances postprandial insulin sensitivity in healthy
subjects", Diabetologia, 46, pp. 659-665 (2003).
in blood (21, 22). Reported data indicate that replacement of 5.4 13. G.H. Anderson, N.L. Catherine et al., "Inverse association between the
percent of total dietary carbohydrate with RS significantly increased effect of carbohydrates on blood glucose and subsequent short-term
post-prandial lipid oxidation and therefore could decrease long term food intake in young men", American Journal of Clinical Nutrition, 76,
pp. 1023-1030 (2002).
fat accumulation (23, 24). 14. K.M. Behall, J. Hallfrisch, "Plasma glucose and insulin reduction after
consumption of breads varying in amylose content", European Journal
of Clinical Nutrition, 56, pp. 913-920 (2002).
15. P. Nestel, M. Cehun et al., "Effects of long-term consumption and single
SATIETY AND WEIGHT LOSS meals of chickpeas on plasma glucose, insulin, and triacylglycerol
concentrations", American Journal of Clinical Nutrition, 79, pp. 390-395
Respiratory quotient (RQ) is a relative measure of oxygen uptake and (2004)
16. D.J. Jenkins, C.W. Kendal et al., "High-complex carbohydrate or lente
is indicative of the use of fat/carbohydrate as fuel. A high RQ is carbohydrate foods", American Journal of Medicine, 113, pp. 30S-37S
reflective of high carbohydrate oxidation. Achour et al. (25) observed (2002).
17. S. Ranganathan, M. Champ, "Comparative study of the acute effects of
the effect of RS on RQ during a post absorptive period i.e. 27h after resistant starch and dietary fibres on metabolic indexes in men",
an initial RS rich mixed meal and 10 h after second identical RS rich American Journal of Clinical Nutrition, 59, pp.879-883 (1994).
mixed meal. They found significant increase in RQ which might be 18. M.L. Heijnen, J.M. van Amelsvoort et al, "Interaction between physical
structure and amylose: amylopectin ratio of foods on postprandial
due to increased bacterial fermentation in the colon. RS may be of glucose and insulin responses in healthy subjects", European Journal
benefit to healthy individuals who are trying to achieve and maintain a of Clinical Nutrition, 49, pp. 446-457 (1995).
healthy body weight. Ingestion of a diet high in RS can delay 19. K.M. Behall, D.J. Scholfield et al., "Diets containing high amylose vs
amylopectin starch: effects on metabolic variables in human subjects",
postprandial carbohydrate oxidation and increase satiety in healthy American Journal of Clinical Nutrition, 49, pp. 337-344 (1989).
subjects. Delayed hunger after a meal has the potential of helping 20. W.K. Kim, M.K. Chung et al., "Effect of resistant starch from corn or rice
on glucose control, colonic events, and blood lipid concentrations in
subjects to control their total energy intake at the appropriate level to streptozotocin-induced diabetic rats", Journal of Nutritional
maintain or lose weight (26-28). RS has been examined as a satiety Biochemistry, 14, pp. 166-172 (2003).
agent. Roos et al. (29) reported that RS was more satiating than 21. T. Kishida, H. Nogami et al., "Heat moisture treatment of high amylose
cornstarch increases its resistant starch content but not its physiologic
glucose. Skrabanja et al. (30) reported that bread rich in RS imparted effect in rats", Journal of Nutrition, 131, pp. 2716-2721 (2001).
greater satiety than white bread. These studies also showed a 22. H.W. Lopez, M.A. Levrat-Verny et al., "Class 2 resistant starches lower
decrease in glucose levels following consumption of high RS meal. plasma and liver lipids and improve mineral retention in rats", Journal of
Nutrition, 131, pp.1283-1289 (2001).
RS was also known to reduce the activity of lipogenic enzymes such 23. J.A. Higgins, D.R. Higbee et al., "Resistant starch consumption
as fatty acid synthases (the rate limiting enzymes in fat synthesis) promotes lipid oxidation", Nutrition & Metabolism, 1:8, pp.1743-7075-1-
8 (2004).
(10). RS may result in smaller fat pad size and /or mass due to
Starch

24. M. Brown, J. Higgins et al., "Consumption of resistant starch decreases


reduced glucose uptake and lipogenesis by the fat cells (23). postprandial lipogenesis in white adipose tissue of the rat", Nutrition
Journal, 5, p. 25 (2006).
25. L. Achour, B. Flourie et al., "Metabolic effects of digestible and partially
indigestible cornstarch: a study in the absorptive and postabsorptive
CONCLUSIONS periods in healthy humans", American Journal of Clinical Nutrition, 66,
pp. 1151-1159 (1997).
26. J.L. Slavin, "Dietary fiber and body weight", Nutrition, 21, pp. 411-418
RS is an exciting ingredient having proven physiological benefits (2005).
similar to soluble fiber. Day by day RS is gaining importance due its
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27. J. Engels, "Resistant starch: Rx for good health - R&D Applications",


contribution in various health aspects such as modification of blood Prepared Foods, p. 6 (2003).
28. M. Hegsted, "Resistant starch - weight control and gastrointestinal
glucose and GI, lipid metabolism. Interest in RS as a prebiotic is on health", AACC Annual Meeting Charlotte, North Carolina October 14-
the rise. It is likely that RS exerts some or all its effects through the 18, 2001 Charlotte Convention Center (2001).
29. N. de Roos, M.L. Heijnen et al., "Resistant starch has little effect on
action of SCFA. The potential of RS in weight management and appetite, food intake and insulin secretion of healthy young men",
maintenance is challenging in the face of increasing trends of obesity. European Journal of Clinical Nutrition, 49, pp. 532-541 (1995).
However in certain areas of research, which have generated 30. V. Skrabanja, H.G. Liljeberg et al., "Nutritional properties of starch in
buckwheat products: studies in vitro and in vivo", Journal of Agricultural
controversial results further work needs to be done to clearly establish and Food Chemistry, 49, pp. 490-496 (2001).
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the exact mechanism of action of RS. 31. Robertson et al., "Insulin sensitizing effects of dietary resistant starch
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and effect on skeletal muscle and adipose tissue metabolism",


American Journal of Clinical Nutrition, 82, pp. 559-567 (2005).
32. G. Livesey, R. Taylor et al., "Glycaemic response and health-a
REFERENCES AND NOTES systematic review and meta analysis relations between dietary
glycaemic properties and health outcomes", American Journal of
n

1. R. S. Mehta, "Dietary fiber benefits", Cereal Foods World, 50, pp. 66-70 Clinical Nutrition, 87, pp. 258S-268S (2008).
Vol 19 - No. 1

(2005). 33. A. Andoh, T. Tsujikawa et al., "Role of dietary fiber and short-chain fatty
2. World Health Organization, Joint WHO/FAO Expert Consultation "Diet, acids in the colon", Current Pharmaceutical Design, 9, pp. 347-358
Nutrition and the Prevention of Chronic Diseases", WHO Technical (2003).
Report Series 916 (2003). 34. S. MacFarlane, G.T. MacFarlane, "Regulation of short-chain fatty acid
3. R.F. Tester, J. Karkalas et al., "Starch-composition, fine structure and production", Proceedings of the Nutrition Society, 62, pp. 67-72 (2003).
architecture", Journal of Cereal Science, 39, pp.151-165 (2004). 35. D.L. Topping, P.M. Clifton, "Short-chain fatty acids and human colonic
4. AACC Method 32-07: Determination of Soluble, Insoluble and Total function: roles of resistant starch and non starch polysaccharides",
Dietary Fiber in Foods and Food Products. Approved Methods of the Physiological Reviews, 81, pp. 1031-1064 (2001).
American Association of Cereal Chemists, 9th Ed. The Association, St. 36. D.L. Topping, M. Fukushima et al., "Resistant starch as a prebiotic and
Paul, MN, 1995. symbiotic: state of the art", Proceedings of the Nutrition Society, 62,
5. AOAC Association of Official Analytical Chemists Method 991.43, the pp.171-176 (2003).
enzymatic/ chemical method (2000). 37. J.M. Wong, D.J.A. Jenkins, "Carbohydrate digestibility and Metabolic
6. H.N. Englyst, S.M. Kingman et al., "Measurement of resistant starch in effects", Journal of Nutrition, 137, 2539S-2546S (2007).
vitro and in vivo", British Journal of Nutrition, 75, pp.749-755 (1996). 38. G.P. Young, R.K. Le Leu, "Resistant starch and colorectal neoplasia"
7. S.K. Patil, "Resistant starches as low-carb ingredients -current Journal of the Association of Official Analytical Chemists International,
applications and issues", Cereal Foods world, 49, pp. 292-294 (2004). 87, pp. 775-786 (2004).
8. E.A.M. De Deckere, W.J. Kloots et al., "Both raw and retrograded 39. B.A. Van Gorkom, A. Karrenbeld et al., "Calcium or resistant starch
starch decrease serum triacylglycerol concentration and fat accretion in does not affect colonic epithelial cell proliferation throughout the colon
the rat", British Journal of Nutrition, 73, pp. 287-298 (1995). in adenoma patients: a randomized controlled trial", Nutrition and
9. T.G. Gordon, K. Topp et al., "Resistant starch: physical and Cancer, 43, pp. 31-38. (2002).
physiological properties", In M. Yalpani, New technologies for healthy 40. D. Kritchevsky, "Epidemiology of fiber, resistant starch and colorectal
foods and nutraceuticals, USA: ATL Press Inc. pp. 157-178 (1997). cancer", European Journal of Cancer Preview, 4, pp. 345-352 (1995).
10. M.A. Younes, C. Levrat et al., "Resistant starch is more effective than 41. R.S. Chapkin, Y. Fan, et al., "Effect of diet on colonic programmed cell
cholestyramine as a lipid-lowering agent in the rat", Lipids, 30, pp.847- death: molecular mechanism of action", Toxicology Letters, 112-113, pp.
853 (1995). 411-414 (2000).
11. K.L. Rickard, M. Folino et al., "Colonic epithelial biology: comparison of 42. F. Pierre, P. Perrin et al., "Short-Chain Fructo-oligosaccharides reduce
effects of resistant starch to soluble and insoluble dietary fibers", the occurrence of colon tumors and development of gut-associated
Proceedings of the Nutritional Society of Australia, 18, p. 57 (1994). lymphoid tissue in Min Mice", Cancer Research, 57, pp. 225-228
12. M.D. Robertson, J.M. Currie et al., "Prior short-term consumption of (1997).

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