Chemistry:Inulin

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Short description: Natural plant polysaccharides
Inulin
Inulin strukturformel.svg
Identifiers
ChEMBL
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Properties
C6nH10n+2O5n+1
Molar mass Polymer; depends on n
Pharmacology
1=ATC code }} V04CH01 (WHO)
Hazards
NFPA 704 (fire diamond)
Flammability code 1: Must be pre-heated before ignition can occur. Flash point over 93 °C (200 °F). E.g. canola oilHealth code 1: Exposure would cause irritation but only minor residual injury. E.g. turpentineReactivity code 0: Normally stable, even under fire exposure conditions, and is not reactive with water. E.g. liquid nitrogenSpecial hazards (white): no codeNFPA 704 four-colored diamond
1
1
0
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Inulins are a group of naturally occurring polysaccharides produced by many types of plants,[1] industrially most often extracted from chicory.[2] The inulins belong to a class of dietary fibers known as fructans. Inulin is used by some plants as a means of storing energy and is typically found in roots or rhizomes. Most plants that synthesize and store inulin do not store other forms of carbohydrate such as starch. In the United States in 2018, the Food and Drug Administration approved inulin as a dietary fiber ingredient used to improve the nutritional value of manufactured food products.[3] Using inulin to measure kidney function is the "gold standard" for comparison with other means of estimating glomerular filtration rate.[4]

Origin and history

Inulin is a natural storage carbohydrate present in more than 36,000 species of plants, including agave, wheat, onion, bananas, garlic, asparagus, Jerusalem artichoke, and chicory. For these plants, inulin is used as an energy reserve and for regulating cold resistance.[5][6] Because it is soluble in water, it is osmotically active. Certain plants can change the osmotic potential of their cells by changing the degree of polymerization of inulin molecules by hydrolysis. By changing osmotic potential without changing the total amount of carbohydrate, plants can withstand cold and drought during winter periods.[7]

Inulin was discovered in 1804 by German scientist Valentin Rose. He found "a peculiar substance" from Inula helenium roots by boiling-water extraction.[7][8] In the 1920s, J. Irvine used chemical methods such as methylation to study the molecular structure of inulin, and he designed the isolation method for this new anhydrofructose.[8][9] During studies of renal tubules in the 1930s, researchers searched for a substance that could serve as a biomarker that is not reabsorbed or secreted after introduction into tubules.[10][11] A. N. Richards introduced inulin because of its high molecular weight and its resistance to enzymes.[10] Inulin is used to determine glomerular filtration rate of the kidneys.[12]

Chemical structure and properties

Inulin is a heterogeneous collection of fructose polymers. It consists of chain-terminating glucosyl moieties and a repetitive fructosyl moiety,[13] which are linked by β(2,1) bonds. The degree of polymerization (DP) of standard inulin ranges from 2 to 60. After removing the fractions with DP lower than 10 during manufacturing process, the remaining product is high-performance inulin.[5][6] Some articles considered the fractions with DP lower than 10 as short-chained fructo-oligosaccharides, and only called the longer-chained molecules inulin.[7]

Because of the β(2,1) linkages, inulin is not digested by enzymes in the human alimentary system, contributing to its functional properties: reduced calorie value, dietary fiber, and prebiotic effects. Without color and odor, it has little impact on sensory characteristics of food products. Oligofructose has 35% of the sweetness of sucrose, and its sweetening profile is similar to sugar. Standard inulin is slightly sweet, while high-performance inulin is not. Its solubility is higher than the classical fibers. When thoroughly mixed with liquid, inulin forms a gel and a white creamy structure, which is similar to fat. Its three-dimensional gel network, consisting of insoluble submicron crystalline inulin particles, immobilizes a large amount of water, assuring its physical stability.[14] It can also improve the stability of foams and emulsions.[6]

Uses

Harvesting and extraction

Chicory root is the main source of extraction for commercial production of inulin. The extraction process for inulin is similar to obtaining sugar from sugar beets.[5] After harvest, the chicory roots are sliced and washed, then soaked in a solvent (hot water or ethanol);[15] the inulin is then isolated, purified, and spray dried. Inulin may also be synthesized from sucrose.[5]

Processed foods

Inulin received no-objection status as generally recognized as safe (GRAS) from the US Food and Drug Administration (FDA),[16] including long-chain inulin as GRAS.[17] In the early 21st century, the use of inulin in processed foods was due in part to its adaptable characteristics for manufacturing.[18] It is approved by the FDA as an ingredient to enhance the dietary fiber value of manufactured foods.[3] Its flavor ranges from bland to subtly sweet (about 10% of the sweetness of sugar/sucrose). It can be used to replace sugar, fat, and flour. This is advantageous because inulin contains 25–35% of the food energy of carbohydrates (starch, sugar).[19][20] In addition to being a versatile ingredient, inulin provides nutritional advantages by increasing calcium absorption[21] and possibly magnesium absorption,[22] while promoting the growth of intestinal bacteria.[18] Chicory inulin is reported to increase absorption of calcium in young women with lower calcium absorption[23] and in young men.[1] In terms of nutrition, it is considered a form of soluble fiber and is sometimes categorized as a prebiotic.[18] Conversely, it is also considered a FODMAP, a class of carbohydrates which are rapidly fermented in the colon producing gas.[18] Although FODMAPs can cause certain digestive discomfort in some people, they produce potentially favorable alterations in the intestinal flora that contribute to maintaining health of the colon.[24][25][26]

Due to the body's limited ability to process fructans, inulin has minimal increasing impact on blood sugar, and may potentially have use in managing blood sugar-related illnesses, such as metabolic syndrome.[27]

Medical

Inulin and its analog sinistrin are used to help measure kidney function by determining the glomerular filtration rate (GFR), which is the volume of fluid filtered from the renal (kidney) glomerular capillaries into the Bowman's capsule per unit time.[28]

While inulin is the gold standard for measuring the GFR, it is rarely used in practice due to the expense and difficulty in conducting the test; it requires intravenous (IV) access for the infusion of inulin as well as up to twelve blood samples taken from the patient over the course of four hours.[29] To determine the glomerular filtration rate in humans, a large initial dose of inulin is injected, which is followed by a constant infusion of inulin at a rate which compensates for its loss in the urine, thus maintaining a reasonably constant level in the plasma.[30]:228 In the United States, creatinine clearance is more widely used to estimate GFR.[31]

A 2017 systematic review of low-to-moderate quality clinical trial research showed that dietary supplementation with inulin-type fructans reduced blood levels of low-density cholesterol, a biomarker of cardiovascular disease.[27]

Diet and side effects

The side effects of inulin dietary fiber diet, which may occur, usually in sensitive persons, are:[32]

  • Intestinal discomfort, including flatulence, bloating, stomach noises, belching, and cramping
  • Diarrhea
  • Inflammation – inulin can cause an allergy-related type of inflammation in the gut and lungs[33]
  • Anaphylactic allergic reaction (rare) – inulin is used for GFR testing, and in some isolated cases has resulted in an allergic reaction, possibly linked to a food allergy response.[34]

Industrial use

Nonhydrolyzed inulin can also be directly converted to ethanol in a simultaneous saccharification and fermentation process, which may have potential for converting crops high in inulin into ethanol for fuel.[35]

Biochemistry

Inulins are polymers composed mainly of fructose units (fructans), and typically have a terminal glucose. The fructose units in inulins are joined by a β(2→1) glycosidic bond. The molecule is almost exclusively linear, with only a few percent branching.[36]:58 In general, plant inulins contain between 2 and 70 fructose units[36]:58 or sometimes as high as 200,[37]:17 but molecules with less than 10 units are called fructo-oligosaccharides, the simplest being 1-kestose, which has two fructose units and one glucose unit. Bacterial inulin is more highly branched (more than 15% branching) and contains on the order of tens or hundreds of subunits.[37]:17

Inulins are named in the following manner, where n is the number of fructose residues and py is the abbreviation for pyranosyl:

  • Inulins with a terminal glucose are known as alpha-D-glucopyranosyl-[beta-D-fructofuranosyl](n-1)-D-fructofuranosides, abbreviated as GpyFn.
  • Inulins without glucose are beta-D-fructopyranosyl-[D-fructofuranosyl](n-1)-D-fructofuranosides, abbreviated as FpyFn.

Hydrolysis of inulins may yield fructo-oligosaccharides, which are oligomers with a degree of polymerization (DP) of 10 or less.

Calculation of glomerular filtration rate

Inulin is uniquely treated by nephrons in that it is completely filtered at the glomerulus but neither secreted nor reabsorbed by the tubules. This property of inulin allows the clearance of inulin to be used clinically as a highly accurate measure of glomerular filtration rate (GFR) — the rate of plasma from the afferent arteriole that is filtered into Bowman's capsule measured in ml/min.[citation needed]

It is informative to contrast the properties of inulin with those of para-aminohippuric acid (PAH). PAH is partially filtered from plasma at the glomerulus and not reabsorbed by the tubules, in a manner identical to inulin. PAH is different from inulin in that the fraction of PAH that bypasses the glomerulus and enters the nephron's tubular cells (via the peritubular capillaries) is completely secreted. Renal clearance of PAH is thus useful in calculation of renal plasma flow (RPF), which empirically is (1-hematocrit) times renal blood flow. Of note, the clearance of PAH is reflective only of RPF to portions of the kidney that deal with urine formation, and, thus, underestimates the actual RPF by about 10%.[38]

The measurement of GFR by inulin or sinistrin is still considered the gold standard. However, it has now been largely replaced by other, simpler measures that are approximations of GFR. These measures, which involve clearance of such substrates as EDTA, iohexol, cystatin C, 125I-iothalamate (sodium radioiothalamate), the chromium radioisotope 51Cr (chelated with EDTA), and creatinine, have had their utility confirmed in large cohorts of patients with chronic kidney disease.[citation needed]

For both inulin and creatinine, the calculations involve concentrations in the urine and in the serum. However, unlike creatinine, inulin is not naturally present in the body. This is an advantage of inulin (because the amount infused will be known) and a disadvantage (because an infusion is necessary).[citation needed]

Metabolism in vivo

Inulin is indigestible by the human enzymes ptyalin and amylase, which are adapted to digest starch. As a result, it passes through much of the digestive system intact. Only in the colon do bacteria metabolise inulin, with the release of significant quantities of carbon dioxide, hydrogen, and/or methane. Inulin-containing foods can be rather gassy, in particular for those unaccustomed to inulin, and these foods should be consumed in moderation at first.[citation needed]

Inulin is a soluble fiber, one of three types of dietary fiber including soluble, insoluble, and resistant starch. Soluble fiber dissolves in water to form a gelatinous material. Some soluble fibers may help lower blood cholesterol and glucose levels.[39]

Because normal digestion does not break inulin down into monosaccharides, it does not elevate blood sugar levels and may, therefore, be helpful in the management of diabetes. Inulin also stimulates the growth of bacteria in the gut.[5] Inulin passes through the stomach and duodenum undigested and is highly available to the gut bacterial flora. This makes it similar to resistant starches and other fermentable carbohydrates.[citation needed]

Some traditional diets contain over 20 g per day of inulin or fructo-oligosaccharides. The diet of the prehistoric hunter-forager in the Chihuahuan Desert has been estimated to include 135 g per day of inulin-type fructans.[40] Many foods naturally high in inulin or fructo-oligosaccharides, such as chicory, garlic, and leek, have been seen as "stimulants of good health" for centuries.[41]

As of 2013, no regulatory authority had permitted health claims in the marketing of prebiotics as a class. Inulin's health effects had been studied in small clinical trials, which showed that it causes gastrointestinal adverse effects such as bloating and flatulence, does not affect triglyceride levels or development of fatty liver, may help prevent travelers' diarrhea, and may help increase calcium absorption in adolescents.[18]

Natural sources

Plants that contain high concentrations of inulin include:

References

  1. ↑ 1.0 1.1 Roberfroid, M. B. (2003). "Introducing inulin-type fructans". Br. J. Nutr. 93: 13–26. doi:10.1079/bjn20041350. PMID 15877886. 
  2. ↑ Roberfroid M. B. (2007). "Inulin-type fructans: functional food ingredients". Journal of Nutrition 137 (11 suppl): 2493S–2502S. doi:10.1093/jn/137.11.2493S. PMID 17951492. http://jn.nutrition.org/content/137/11/2493S.long. 
  3. ↑ 3.0 3.1 "The Declaration of Certain Isolated or Synthetic Non-Digestible Carbohydrates as Dietary Fiber on Nutrition and Supplement Facts Labels: Guidance for Industry". US Food and Drug Administration. 14 June 2018. https://www.fda.gov/downloads/Food/GuidanceRegulation/GuidanceDocumentsRegulatoryInformation/UCM610144.pdf. 
  4. ↑ Hsu, C. Y.; Bansal, N. (August 2011). "Measured GFR as 'gold standard'—all that glitters is not gold?". Clinical Journal of the American Society of Nephrology 6 (8): 1813–1814. doi:10.2215/cjn.06040611. PMID 21784836. 
  5. ↑ 5.0 5.1 5.2 5.3 5.4 Niness, K. R. (July 1999). "Inulin and oligofructose: what are they?". The Journal of Nutrition 129 (7 Suppl): 1402S–6S. doi:10.1093/jn/129.7.1402S. PMID 10395607. 
  6. ↑ 6.0 6.1 6.2 Kalyani Nair, K.; Kharb, Suman; Thompkinson, D. K. (18 March 2010). "Inulin Dietary Fiber with Functional and Health Attributes—A Review". Food Reviews International 26 (2): 189–203. doi:10.1080/87559121003590664. 
  7. ↑ 7.0 7.1 7.2 Boeckner, L. S.; Schnepf, M. I.; Tungland, B. C. (2001). Inulin: a review of nutritional and health implications. Advances in Food and Nutrition Research. 43. pp. 1–63. doi:10.1016/s1043-4526(01)43002-6. ISBN 978-0-12-016443-1. https://archive.org/details/advancesinfoodnu0000unse/page/1. 
  8. ↑ 8.0 8.1 Irvine, James Colquhoun; Soutar, Charles William (1920). "CLXV. The constitution of polysaccharides. Part II. The conversion of cellulose into glucose". Journal of the Chemical Society, Transactions 117: 1489–1500. doi:10.1039/CT9201701489. https://zenodo.org/record/1593106. 
  9. ↑ Irvine, James Colquhoun; Stevenson, John Whiteford (July 1929). "The molecular structure of inulin. Isolation of a new anhydrofructose". Journal of the American Chemical Society 51 (7): 2197–2203. doi:10.1021/ja01382a035. 
  10. ↑ 10.0 10.1 Richards, A. N.; Westfall, B. B.; Bott, P. A. (1 October 1934). "Renal Excretion of Inulin, Creatinine and Xylose in Normal Dogs". Experimental Biology and Medicine 32 (1): 73–75. doi:10.3181/00379727-32-7564P. 
  11. ↑ Shannon, J. A.; Smith, H. W. (July 1935). "The excretion of inulin, xylose and urea by normal and phlorinzinized man". The Journal of Clinical Investigation 14 (4): 393–401. doi:10.1172/JCI100690. PMID 16694313. 
  12. ↑ Coulthard, M. G.; Ruddock, V. (February 1983). "Validation of inulin as a marker for glomerular filtration in preterm babies". Kidney International 23 (2): 407–409. doi:10.1038/ki.1983.34. PMID 6842964. 
  13. ↑ Barclay, Thomas, et al. Inulin – a versatile polysaccharide with multiple pharmaceutical and food chemical uses. Diss. International Pharmaceutical Excipients Council, 2010.
  14. ↑ Franck, A. (9 March 2007). "Technological functionality of inulin and oligofructose". British Journal of Nutrition 87 (S2): S287–S291. doi:10.1079/BJN/2002550. PMID 12088531. 
  15. ↑ "What is Inulin? The Ultimate FAQ Guide to Inulin". May 15, 2019. https://blog.supplementplace.co.uk/nutrition/what-is-inulin/. 
  16. ↑ Rulis, Alan M. (5 May 2003). "Agency Response Letter GRAS Notice No. GRN 000118". US Food and Drug Administration. https://www.fda.gov/Food/IngredientsPackagingLabeling/GRAS/NoticeInventory/ucm153932.htm. 
  17. ↑ Keefe, Dennis M. (9 December 2015). "Agency Response Letter GRAS Notice No. GRN 000576". US Food and Drug Administration. https://www.fda.gov/Food/IngredientsPackagingLabeling/GRAS/NoticeInventory/ucm489503.htm. 
  18. ↑ 18.0 18.1 18.2 18.3 18.4 Slavin, Joanne (2013-04-22). "Fiber and Prebiotics: Mechanisms and Health Benefits". Nutrients 5 (4): 1417–1435. doi:10.3390/nu5041417. ISSN 2072-6643. PMID 23609775. 
  19. ↑ Roberfroid, M. B. (1999). "Caloric value of inulin and oligofructose". J. Nutr. 129 (7 Suppl): 1436S–7S. doi:10.1093/jn/129.7.1436S. PMID 10395615. 
  20. ↑ "Caloric Value of Inulin and Oligofructose"[yes|permanent dead link|dead link}}].
  21. ↑ Abrams S.; Griffin I.; Hawthorne K.; Liang L.; Gunn S.; Darlington G.; Ellis K. (2005). "A combination of prebiotic short- and long-chain inulin-type fructans enhances calcium absorption and bone mineralization in young adolescents". Am. J. Clin. Nutr. 82 (2): 471–476. doi:10.1093/ajcn.82.2.471. PMID 16087995. 
  22. ↑ Coudray C.; Demigné C.; Rayssiguier Y. (2003). "Effects of dietary fibers on magnesium absorption in animals and humans". J. Nutr. 133 (1): 1–4. doi:10.1093/jn/133.1.1. PMID 12514257. 
  23. ↑ Griffin, I. J.; P. M. Hicks; R. P. Heaney; S. A. Abrams (2003). "Enriched chicory inulin increases calcium absorption mainly in girls with lower calcium absorption". Nutr. Res. 23 (7): 901–909. doi:10.1016/s0271-5317(03)00085-x. 
  24. ↑ Makharia A.; Catassi C.; Makharia G. K. (2015). "The Overlap between Irritable Bowel Syndrome and Non-Celiac Gluten Sensitivity: A Clinical Dilemma". Nutrients 7 (12): 10417–26. doi:10.3390/nu7125541. PMID 26690475. 
  25. ↑ Greer J. B.; O'Keefe S. J. (2011). "Microbial induction of immunity, inflammation, and cancer". Front Physiol 1: 168. doi:10.3389/fphys.2010.00168. PMID 21423403. 
  26. ↑ Andoh A.; Tsujikawa T.; Fujiyama Y. (2003). "Role of dietary fiber and short-chain fatty acids in the colon". Curr. Pharm. Des. 9 (4): 347–58. doi:10.2174/1381612033391973. PMID 12570825. 
  27. ↑ 27.0 27.1 Liu, F.; Prabhakar, M.; Ju, J.; Long, H.; Zhou, H. W. (2017). "Effect of inulin-type fructans on blood lipid profile and glucose level: A systematic review and meta-analysis of randomized controlled trials". European Journal of Clinical Nutrition 71 (1): 9–20. doi:10.1038/ejcn.2016.156. PMID 27623982. 
  28. ↑ Nosek, Thomas M.. "Section 7, Chapter 4, Glomerular Filtration Rate". Essentials of Human Physiology. http://humanphysiology.tuars.com/program/section7/7ch04/7ch04p11.htm. 
  29. ↑ Langlois, Valerie (2008-01-01), Geary, Denis F.; Schaefer, Franz, eds., "CHAPTER 2 - Laboratory Evaluation at Different Ages" (in en), Comprehensive Pediatric Nephrology (Philadelphia: Mosby): pp. 39–54, doi:10.1016/b978-0-323-04883-5.50008-8, ISBN 978-0-323-04883-5, https://www.sciencedirect.com/science/article/pii/B9780323048835500088, retrieved 2022-02-11 
  30. ↑ Wright, Samson (1972). Samson Wright's applied physiology. Cyril Arthur Keele, Neil Eric (12th ed.). London: English Language Book Society, and Oxford University Press. ISBN 0-19-263321-X. OCLC 396722036. 
  31. ↑ Joffe, Marshall; Hsu, Chi-yuan; Feldman, Harold I.; Weir, Matthew; Landis, J.R.; Hamm, L. Lee (2010). "Variability of Creatinine Measurements in Clinical Laboratories: Results from the CRIC Study" (in en). American Journal of Nephrology 31 (5): 426–434. doi:10.1159/000296250. ISSN 1421-9670. PMID 20389058. PMC 2883847. https://www.karger.com/Article/FullText/296250. 
  32. ↑ Coussement, Paul A. A. (1999). "Inulin and oligofructose: safe intakes and legal status". The Journal of Nutrition 129 (7): 1412S–1417S. doi:10.1093/jn/129.7.1412S. PMID 10395609. 
  33. ↑ Arifuzzaman, Mohammad (2022). "Inulin fibre promotes microbiota-derived bile acids and type 2 inflammation". Nature 611 (7936): 578–584. doi:10.1038/s41586-022-05380-y. PMID 36323778. Bibcode: 2022Natur.611..578A. 
  34. ↑ Bacchetta, Justine (2008). "'Renal hypersensitivity' to inulin and IgA nephropathy". Pediatric Nephrology 23 (10): 1883–1885. doi:10.1007/s00467-008-0819-9. PMID 18535847. 
  35. ↑ Kazuyoshi Ohta; Shigeyuki Hamada; Toyohiko Nakamura (1992). "Production of High Concentrations of Ethanol from Inulin by Simultaneous Saccharification and Fermentation Using Aspergillus niger and Saccharomyces cerevisiae". Applied and Environmental Microbiology 59 (3): 729–733. doi:10.1128/AEM.59.3.729-733.1993. PMID 8481000. 
  36. ↑ 36.0 36.1 Kays, Stanley J.; Nottingham, Stephen F. (2007-08-13) (in en). Biology and Chemistry of Jerusalem Artichoke: Helianthus tuberosus L.. CRC Press. ISBN 978-1-4200-4496-6. https://books.google.com/books?id=XwZJN1HSajcC&pg=PA58. 
  37. ↑ 37.0 37.1 Rauter, Amélia P.; Vogel, Pierre; Queneau, Yves (2010-09-20) (in en). Carbohydrates in Sustainable Development I. Springer Science & Business Media. ISBN 978-3-642-14836-1. https://books.google.com/books?id=u4RWrMh8JR0C&pg=PA17. 
  38. ↑ Costanzo, Linda. Physiology, 4th Edition. Philadelphia: Lippincott Williams and Wilkins, 2007. Pages 156–160.
  39. ↑ McRorie, Johnson W.; McKeown, Nicola M. (1 February 2017). "Understanding the Physics of Functional Fibers in the Gastrointestinal Tract: An Evidence-Based Approach to Resolving Enduring Misconceptions about Insoluble and Soluble Fiber". Journal of the Academy of Nutrition and Dietetics 117 (2): 251–264. doi:10.1016/j.jand.2016.09.021. PMID 27863994. 
  40. ↑ Leach, J. D.; Sobolik, K. D. (2010). "High dietary intake of prebiotic inulin-type fructans in the prehistoric Chihuahuan Desert". Br. J. Nutr. 103 (11): 1558–61. doi:10.1017/S0007114510000966. PMID 20416127. 
  41. ↑ Coussement P. (1999). "Inulin and oligofructose: safe intakes and legal status". J. Nutr. 129 (7 Suppl): 1412S–1417S. doi:10.1093/jn/129.7.1412S. PMID 10395609. http://jn.nutrition.org/cgi/content/full/129/7/1412S#SEC1. 



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