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Review

A Systematic Review of the Potential Effects of Thylakoids in the Management of Obesity and Its Related Issues

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References

  • Hasani-Ranjbar, S.; Nayebi, N.; Larijani, B.; Abdollahi, M. A Systematic Review of the Efficacy and Safety of Herbal Medicines Used in the Treatment of Obesity. World J. Gastroenterol. 2009, 15(25), 3073–3085. DOI: 10.3748/wjg.15.3073.
  • Obesity and Overweight [Internet]. http://www.who.int/news-room/fact-sheets/detail/obesity-and-overweighthttp://www.who.int/news-room/fact-sheets/detail/obesity-and-overweight (accessed Oct 24, 2018).
  • NCD Risk Factor Collaboration (NCD-RisC). Trends in Adult Body-Mass Index in 200 Countries from 1975 to 2014: A Pooled Analysis of 1698 Population-Based Measurement Studies with 19·2 Million Participants. Lancet. 2016, 387(10026), 1377–1396. DOI:10.1016/S0140-6736(16)30054-X.
  • Hales, C. M.; Carroll, M. D.; Fryar, C. D.; Ogden, C. L. Prevalence of Obesity among Adults and Youth: United States, 2015–2016. NCHS Data Brief. 2017, (288), 1–8. https://www.cdc.gov/nchs/data/databriefs/db288.pdf
  • Lozano, R.; Naghavi, M.; Foreman, K.; Lim, S.; Shibuya, K.; Aboyans, V.; Abraham, J.; Adair, T.; Aggarwal, R.; Ahn, S. Y.;, et al. Global and Regional Mortality from 235 Causes of Death for 20 Age Groups in 1990 and 2010: A Systematic Analysis for the Global Burden of Disease Study 2010. Lancet.2012, 380(9859), 2095–2128. DOI:10.1016/S0140-6736(12)61728-0.
  • Lu, Y.; Hajifathalian, K.; Ezzati, M.; Woodward, M.; Rimm, E. B.; Danaei, G. Metabolic Mediators of the Effects of Body-Mass Index, Overweight, and Obesity on Coronary Heart Disease and Stroke: A Pooled Analysis of 97 Prospective Cohorts with 1·8 Million Participants. Lancet. 2014, 383(9921), 970–983. DOI: 10.1016/S0140-6736(13)61836-X.
  • Wilde, P. J.;. Eating for Life: Designing Foods for Appetite Control. J. Diabetes Sci. Technol. 2009, 3(2), 366–370. DOI: 10.1177/193229680900300219.
  • Erlanson-Albertsson, C.; Albertsson, P.-Å. The Use of Green Leaf Membranes to Promote Appetite Control, Suppress Hedonic Hunger and Loose Body Weight. Plant Foods Hum. Nutr. 2015, 70(3), 281–290. DOI: 10.1007/s11130-015-0491-8.
  • Albertsson, P.-Å.; Köhnke, R.; Emek, S. C.; Mei, J.; Rehfeld, J. F.; Åkerlund, H.-E.; Erlanson-Albertsson, C. Chloroplast Membranes Retard Fat Digestion and Induce Satiety: Effect of Biological Membranes on Pancreatic Lipase/Co-Lipase. Biochem. J. 2007, 401(3), 727–733. DOI: 10.1042/BJ20061463.
  • Rebello, C. J.; Chu, J.; Beyl, R.; Edwall, D.; Erlanson-Albertsson, C.; Greenway, F. L. Acute Effects of A Spinach Extract Rich in Thylakoids on Satiety: A Randomized Controlled Crossover Trial. J. Am. Coll. Nutr. 2015, 34(6), 470–477. DOI: 10.1080/07315724.2014.1003999.
  • Stenblom, E.-L.; Egecioglu, E.; Landin-Olsson, M.; Erlanson-Albertsson, C. Consumption of Thylakoid-Rich Spinach Extract Reduces Hunger, Increases Satiety and Reduces Cravings for Palatable Food in Overweight Women. Appetite. 2015, 91, 209–219. DOI: 10.1016/j.appet.2015.04.051.
  • Montelius, C.; Szwiec, K.; Kardas, M.; Lozinska, L.; Erlanson-Albertsson, C.; Pierzynowski, S.; Rehfeld, J. F.; Weström, B. Dietary Thylakoids Suppress Blood Glucose and Modulate Appetite-Regulating Hormones in Pigs Exposed to Oral Glucose Tolerance Test. Clin. Nutr. 2014, 33(6), 1122–1126. DOI: 10.1016/j.clnu.2013.12.009.
  • Stenblom, E. L.; Montelius, C.; Erlandsson, D.; Skarping, L.; Fransson, M.; Egecioglu, E.; Podgórski, K.; Erlanson-Albertsson, C. H. Decreased Urge for Palatable Food after a Two-Month Dietary Intervention with Green-Plant Membranes in Overweight Women. J. Obes. Weight. Loss Ther.2014, 04(04), 1–8. DOI:10.4172/2165-7904.1000238.
  • Stenblom, E.-L.; Egecioglu, E.; Montelius, C.; Ramachandran, D.; Bonn, B.; Weström, B.; Mansouri, A.; Langhans, W.; Erlanson-Albertsson, C. Dietary Thylakoids Reduce Visceral Fat Mass and Increase Expression of Genes Involved in Intestinal Fatty Acid Oxidation in High-Fat Fed Rats. Am. J. Physiol. Integr. Comp. Physiol. 2016, 311(3), R618–R627. DOI: 10.1152/ajpregu.00212.2016.
  • Montelius, C.; Osman, N.; Weström, B.; Ahrné, S.; Molin, G.; Albertsson, P. Å.; Erlanson-Albertsson, C. Feeding Spinach Thylakoids to Rats Modulates the Gut Microbiota, Decreases Food Intake and Affects the Insulin Response. J. Nutr. Sci. 2013, 2, 1–9. DOI: 10.1017/jns.2012.29.
  • Stenblom, E. L.; Weström, B.; Linninge, C.; Bonn, P.; Farrell, M.; Rehfeld, J. F.; Montelius, C. Dietary Green-Plant Thylakoids Decrease Gastric Emptying and Gut Transit, Promote Changes in the Gut Microbial Flora, but Does Not Cause Steatorrhea. Nutr. Metab. 2016, 13(1), 1–9. DOI: 10.1186/s12986-016-0128-4.
  • Masih, D.; Rakhra, G.; Singh, S. N. Effect of Thylakoid Supplementation on Activities of Glucose Metabolizing Enzymes in Rats. Adv. Weight Loss Manag. Med. Dev. 2016, 1(1), 1–5. DOI: 10.4172/awmd.1000101.
  • Montelius, C.; Gustafsson, K.; Weström, B.; Albertsson, P.-Å.; Emek, S. C.; Rayner, M.; Erlanson-Albertsson, C. Chloroplast Thylakoids Reduce Glucose Uptake and Decrease Intestinal Macromolecular Permeability. Br. J. Nutr. 2011, 106(6), 836–844. DOI: 10.1017/S0007114511001267.
  • Otokozawa, R.; Matsuda, H.; Kumazaki, K.; Tanaka, M.; Udagawa, E.; Nishida, T.; Shirai, T. Effects of Dietary Thylakoid Intake Just before Diet on Postprandial Serum Hypertriglyceridemia in Rats. J. Integr. Study Diet. Habits. 2017, 27(4), 237–242. DOI: 10.2740/jisdh.27.4_237.
  • Matsuda, H.; Ooi, S.; Otokozawa, R.; Kumazaki, K.; Udagawa, E.; Asakura, M.; Suzuki, D.; Shirai, T. Intake of Green-Plant Membrane with Dietary Oil Suppresses Postprandial Hypertriglyceridemia in Rats via Promoting Excretion of Bile Acids. Biosci. Biotechnol. Biochem. 2018, 82(1), 114–119. DOI: 10.1080/09168451.2017.1409070.
  • Köhnke, R.; Svensson, L.; Valverde Piedra, J. L.; Pierzynowski, S. G.; Weström, B.; Erlanson-Albertsson, C. Feeding Appetite Suppressing Thylakoids to Pigs Alters Pancreatic Lipase/Colipase Secretion. Livest. Sci. 2010, 134(1–3), 68–71. DOI: 10.1016/J.LIVSCI.2010.06.100.
  • Stenkula, K. G.; Stenblom, E.-L.; Montelius, C.; Egecioglu, E.; Erlanson-Albertsson, C. Thylakoids Reduce Body Fat and Fat Cell Size by Binding to Dietary Fat Making It Less Available for Absorption in High-Fat Fed Mice. Nutr. Metab. 2017, 14, 4. DOI: 10.1186/s12986-016-0160-4.
  • Panda, V.; Shinde, P. Appetite Suppressing Effect of Spinacia Oleracea in Rats: Involvement of the Short Term Satiety Signal Cholecystokinin. Appetite. 2017, 113, 224–230. DOI: 10.1016/j.appet.2017.02.030.
  • Köhnke, R.; Lindqvist, A.; Göransson, N.; Emek, S. C.; Albertsson, P. A.; Rehfeld, J. F.; Hultgårdh-Nilsson, A.; Erlanson‐Albertsson., C. Thylakoids Suppress Appetite by Increasing Cholecystokinin Resulting in Lower Food Intake and Body Weight in High-Fat Fed Mice. Phyther. Res. 2009, 23(12), 1778–1783. DOI: 10.1002/ptr.2855.
  • Montelius, C.; Erlandsson, D.; Vitija, E.; Stenblom, E.-L.; Egecioglu, E.; Erlanson-Albertsson, C. Body Weight Loss, Reduced Urge for Palatable Food and Increased Release of GLP-1 through Daily Supplementation with Green-Plant Membranes for Three Months in Overweight Women. Appetite. 2014, 81, 295–304. DOI: 10.1016/j.appet.2014.06.101.
  • Stenblom, E.-L.; Montelius, C.; Östbring, K.; Håkansson, M.; Nilsson, S.; Rehfeld, J. F.; Erlanson-Albertsson, C. Supplementation by Thylakoids to a High Carbohydrate Meal Decreases Feelings of Hunger, Elevates CCK Levels and Prevents Postprandial Hypoglycaemia in Overweight Women. Appetite. 2013, 68, 118–123. DOI: 10.1016/j.appet.2013.04.022.
  • Köhnke, R.; Lindbo, A.; Larsson, T.; Lindqvist, A.; Rayner, M.; Emek, S. C.; Albertsson, P.-Å.; Rehfeld, J. F.; Landin-Olsson, M.; Erlanson-Albertsson, C. Thylakoids Promote Release of the Satiety Hormone Cholecystokinin while Reducing Insulin in Healthy Humans. Scand. J. Gastroenterol. 2009, 44(6), 712–719. DOI: 10.1080/00365520902803499.
  • Westerterp, K. R.;. Energy Requirements Assessed Using the Doubly-Labelled Water Method. Br. J. Nutr. 1998, 80(3), 217–218. DOI: 10.1017/S0007114598001251.
  • Erlanson-Albertsson, C.;. How Palatable Food Disrupts Appetite Regulation. Basic Clin. Pharmacol. Toxicol. 2005, 97(2), 61–73. DOI: 10.1111/j.1742-7843.2005.pto_179.x.
  • Maljaars, J.; Peters, H. P. F.; Masclee, A. M. Review Article: The Gastrointestinal Tract: Neuroendocrine Regulation of Satiety and Food Intake. Aliment. Pharmacol. Ther. 2007, 26, 241–250. DOI: 10.1111/j.1365-2036.2007.03550.x.
  • Asarian, L.;. Loss of Cholecystokinin and Glucagon-like Peptide-1-Induced Satiation in Mice Lacking Serotonin 2C Receptors. Am. J. Physiol. Integr. Comp. Physiol. 2009, 296(1), R51–R56. DOI: 10.1152/ajpregu.90655.2008.
  • Mehta, A.; Marso, S. P.; Neeland, I. J. Liraglutide for Weight Management: A Critical Review of the Evidence. Obes. Sci. Pract. 2017, 3(1), 3–14. DOI: 10.1002/osp4.84.
  • Drent, M. L.; Larsson, I.; William-Olsson, T.; Quaade, F.; Czubayko, F.; von Bergmann, K.; Strobel, W.; Sjöström, L.; van der Veen, E. A. Orlistat (Ro 18-0647), A Lipase Inhibitor, in the Treatment of Human Obesity: A Multiple Dose Study. Int. J. Obes. Relat. Metab. Disord. 1995, 19(4), 221–226.
  • Tai, N.; Wong, F. S.; Wen, L. The Role of Gut Microbiota in the Development of Type 1, Type 2 Diabetes Mellitus and Obesity. Rev. Endocr. Metab. Disord. 2015, 16(1), 55–65. DOI: 10.1007/s11154-015-9309-0.
  • Turroni, F.; Ribbera, A.; Foroni, E.; van Sinderen, D.; Ventura, M. Human Gut Microbiota and Bifidobacteria: From Composition to Functionality. Antonie Van Leeuwenhoek. 2008, 94(1), 35–50. DOI: 10.1007/s10482-008-9232-4.
  • Wang, J.; Tang, H.; Zhang, C.; Zhao, Y.; Derrien, M.; Rocher, E.; Van-Hylckama Vlieg, J. E.; Strissel, K.; Zhao, L.; Obin, M.;, et al. Modulation of Gut Microbiota during Probiotic-Mediated Attenuation of Metabolic Syndrome in High Fat Diet-Fed Mice. Isme J.2015, 9(1), 1–15. DOI:10.1038/ismej.2014.99.
  • Elvira-Torales, L. I.; Periago, M. J.; González-Barrio, R.; Hidalgo, N.; Navarro-González, I.; Gómez-Gallego, C.; Masuero, D.; Soini, E.; Vrhovsek, U.; García-Alonso, F. J. Spinach Consumption Ameliorates the Gut Microbiota and Dislipaemia in Rats with Diet-Induced Non-Alcoholic Fatty Liver Disease (NAFLD). Food Funct. 2019, 10(4), 2148–2160. DOI: 10.1039/c8fo01630e.
  • Li, Y.; Cui, Y.; Lu, F.; Wang, X.; Liao, X.; Hu, X.; Zhang, Y. Beneficial Effects of a Chlorophyll-Rich Spinach Extract Supplementation on Prevention of Obesity and Modulation of Gut Microbiota in High-Fat Diet-Fed Mice. J. Funct. Foods. 2019, 60. DOI: 10.1016/j.jff.2019.103436.
  • Li, Y.; Cui, Y.; Hu, X.; Liao, X.; Zhang, Y. Chlorophyll Supplementation in Early Life Prevents Diet‐Induced Obesity and Modulates Gut Microbiota in Mice. Mol. Nutr. Food Res. 2019, 63(21), 1801219. DOI: 10.1002/mnfr.201801219.
  • Ley, R. E.; Turnbaugh, P. J.; Klein, S.; Gordon, J. I. Microbial Ecology: Human Gut Microbes Associated with Obesity. Nature. 2006, 444(7122), 1022–1023. DOI: 10.1038/4441022a.
  • Chen, G.; Xie, M.; Dai, Z.; Wan, P.; Ye, H.; Zeng, X.; Sun, Y. Kudingcha and Fuzhuan Brick Tea Prevent Obesity and Modulate Gut Microbiota in High-Fat Diet Fed Mice. Mol. Nutr. Food Res. 2018, 62, 6. DOI: 10.1002/mnfr.201700485.
  • Roberts, J. L.; Moreau, R. Functional Properties of Spinach (Spinacia Oleracea L.) Phytochemicals and Bioactives. Food Funct. 2016, 3337–3353. Royal Society of Chemistry August 1, doi: 10.1039/c6fo00051g.
  • Nejdfors, P.; Wang, Q.; Ekelund, M.; Westrom, B.; Jansson, O.; Lindström, C.; Karlsson, B.; Jeppsson., B. Increased Colonic Permeability in Patients with Ulcerative Colitis: An in Vitro Study. Scand. J. Gastroenterol. 1998, 33(7), 749–753. DOI: 10.1080/00365529850171701.
  • Söderholm, J. D.; Peterson, K. H.; Olaison, G.; Franzén, L. E.; Weström, B.; Magnusson, K.-E.; Sjödahl, R. Epithelial Permeability to Proteins in the Noninflamed Ileum of Crohn’s Disease?. Gastroenterology. 1999, 117(1), 65–72. DOI: 10.1016/S0016-5085(99)70551-2.
  • Emek, S. C.; Åkerlund, H.-E.; Clausén, M.; Ohlsson, L.; Weström, B.; Erlanson-Albertsson, C.; Albertsson, P.-Å. Pigments Protect the Light Harvesting Proteins of Chloroplast Thylakoid Membranes against Digestion by Gastrointestinal Proteases. Food Hydrocoll. 2011, 25(6), 1618–1626. DOI: 10.1016/j.foodhyd.2010.12.004.
  • De Kort, S.; Keszthelyi, D.; Masclee, A. A. M. Leaky Gut and Diabetes Mellitus: What Is the Link? Obes. Rev. 2011, 12(6), 449–458. DOI: 10.1111/j.1467-789X.2010.00845.x.
  • Ducroc, R.; Guilmeau, S.; Akasbi, K.; Devaud, H.; Buyse, M.; Bado, A. Luminal Leptin Induces Rapid Inhibition of Active Intestinal Absorption of Glucose Mediated by Sodium-Glucose Cotransporter 1. Diabetes. 2005, 54(2), 348–354. DOI: 10.2337/DIABETES.54.2.348.
  • Hirsh, A. J.; Cheeseman, C. I. Cholecystokinin Decreases Intestinal Hexose Absorption by a Parallel Reduction in SGLT1 Abundance in the Brush-Border Membrane. J. Biol. Chem. 1998, 273(23), 14545–14549. DOI: 10.1074/jbc.273.23.14545.
  • Kohnke, R.; Lindbo, A.; Larsson, T.; Lindqvist, A.; Rayner, M.; Emek, S. C.; Albertsson, P. K.; Rehfeld, J. F.; Landin-Olsson, M.; Erlanson-Albertsson, C. Thylakoids Promote Release of the Satiety Hormone Cholecystokinin while Reducing Insulin in Healthy Humans. Scand. J. Gastroenterol. 2009, 44(6), 712–719. DOI: 10.1080/00365520902803499.
  • Backhed, F.; Ding, H.; Wang, T.; Hooper, L. V.; Koh, G. Y.; Nagy, A.; Semenkovich, C. F.; Gordon, J. I. The Gut Microbiota as an Environmental Factor that Regulates Fat Storage. Proc. Natl. Acad. Sci. 2004, 101(44), 15718–15723. DOI: 10.1073/pnas.0407076101.
  • Matsuzaki, T.; Yamazaki, R.; Hashimoto, S.; Yokokura, T. Antidiabetic Effects of an Oral Administration of Lactobacillus Casei in a Non-Insulin-Dependent Diabetes Mellitus (NIDDM) Model Using KK-Ay Mice. Endocr. J. 1997, 44(3), 357–365. DOI: 10.1507/endocrj.44.357.
  • Tabuchi, M.; Ozaki, M.; Tamura, A.; Yamada, N.; Ishida, T.; Hosoda, M.; Honsano, A. Antidiabetic Effect of Lactobacillus GG in Streptozotocin-Induced Diabetic Rats. Biosci. Biotechnol. Biochem.2003, 67(6), 1421–1424. DOI:10.1271/bbb.67.1421.
  • Yadav, H.; Jain, S.; Sinha, P. R. Oral Administration of Dahi Containing Probiotic Lactobacillus Acidophilus and Lactobacillus Casei Delayed the Progression of Streptozotocin-Induced Diabetes in Rats. J. Dairy Res. 2008, 75(02), 189–195. DOI: 10.1017/S0022029908003129.
  • Ko, S.-H.; Park, J.-H.; Kim, S.-Y.; Lee, S. W.; Chun, -S.-S.; Park, E. Antioxidant Effects of Spinach (Spinacia Oleracea L.) Supplementation in Hyperlipidemic Rats. Prev. Nutr. Food Sci. 2014, 19(1), 19–26. DOI: 10.3746/pnf.2014.19.1.019.
  • Jolivet, P.; Bergeron, E.; Meunier, J.-C. Evidence for Sulphite Oxidase Activity in Spinach Leaves. Phytochemistry. 1995, 40(3), 667–672. DOI: 10.1016/0031-9422(95)00406-W.
  • St-Pierre, A.; Blondeau, D.; Boivin, M.; Beaupré, V.; Boucher, N.; Desgagné-Penix, I. Study of Antioxidant Properties of Thylakoids and Application in UV Protection and Repair of UV-Induced Damage. J. Cosmet. Dermatol. 2019, 18, 1980–1991. DOI: 10.1111/jocd.12936.
  • Bruno, A.; Rossi, C.; Marcolongo, G.; Di Lena, A.; Venzo, A.; Berrie, C. P.; Corda, D. Selective in Vivo Anti-Inflammatory Action of the Galactolipid Monogalactosyldiacylglycerol. Eur. J. Pharmacol. 2005, 524(1–3), 159–168. DOI: 10.1016/j.ejphar.2005.09.023.
  • Hou, -C.-C.; Chen, Y.-P.; Wu, J.-H.; Huang, -C.-C.; Wang, S.-Y.; Yang, N.-S.; Shyur, L.-F. A Galactolipid Possesses Novel Cancer Chemopreventive Effects by Suppressing Inflammatory Mediators and Mouse B16 Melanoma. Cancer Res. 2007, 67(14), 6907–6915. DOI: 10.1158/0008-5472.CAN-07-0158.
  • Kuriyama, I.; Musumi, K.; Yonezawa, Y.; Takemura, M.; Maeda, N.; Iijima, H.; Hada, T.; Yoshida, H.; Mizushina, Y. Inhibitory Effects of Glycolipids Fraction from Spinach on Mammalian DNA Polymerase Activity and Human Cancer Cell Proliferation. J. Nutr. Biochem. 2005, 16(10), 594–601. DOI: 10.1016/j.jnutbio.2005.02.007.
  • Murakami, C.; Kumagai, T.; Hada, T.; Kanekazu, U.; Nakazawa, S.; Kamisuki, S.; Maeda, N.; Xu, X.; Yoshida, H.; Sugawara, F.;; et al. Effects of Glycolipids from Spinach on Mammalian DNA Polymerases. Biochem. Pharmacol. 2003, 65(2), 259–267.
  • Wang, R.; Furumoto, T.; Motoyama, K.; Okazaki, K.; Kondo, A.; FUKUI., H. Possible Antitumor Promoters in Spinacia Oleracea (Spinach) and Comparison of Their Contents among Cultivars. Biosci. Biotechnol. Biochem. 2002, 66(2), 248–254. DOI: 10.1271/bbb.66.248.
  • Dörmann, P.; Benning, C. Galactolipids Rule in Seed Plants. Trends Plant Sci. 2002, 7(3), 112–118. DOI: 10.1016/S1360-1385(01)02216-6.
  • Hölzl, G.; Dörmann, P. Structure and Function of Glycoglycerolipids in Plants and Bacteria. Prog. Lipid Res. 2007, 46(5), 225–243. DOI: 10.1016/j.plipres.2007.05.001.
  • Ishii, M.; Nakahara, T.; Araho, D.; Murakami, J.; Nishimura, M. Glycolipids from Spinach Suppress LPS-Induced Vascular Inflammation through ENOS and NK-ΚB Signaling. Biomed. Pharmacother. 2017, 91, 111–120. DOI: 10.1016/j.biopha.2017.04.052.
  • Shiota, A.; Hada, T.; Baba, T.; Sato, M.; Yamanaka-Okumura, H.; Yamamoto, H.; Taketani, Y.; Takeda, E. Protective Effects of Glycoglycerolipids Extracted from Spinach on 5-Fluorouracil Induced Intestinal Mucosal Injury. J. Med. Invest. 2010, 57(3–4), 314–320. DOI: 10.2152/jmi.57.314.

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