Hordiienko L. P.

INFLUENCE OF MONOSODIUM GLUTAMATE ON BODY MASS AND DEVELOPMENT OF OBESITY (LITERATURE REVIEW)


About the author:

Hordiienko L. P.

Heading:

LITERATURE REVIEWS

Type of article:

Scentific article

Annotation:

Obesity is one of the most widespread public health problems worldwide. According to WHO more than 1.9 billion adults, 18 years and older, are overweight. Of these over 600 million were obese. Excessive energy intake, physical inactivity and uncontrolled use of food addictives, especially monosodium glutamate, are the main causal factors contributing to the onset of obesity. The aim of the study was to analyze a modern scientific literature on the influence of monosodium glutamate on body weight and the development of obesity in animals and humans. Monosodium glutamate is a flavor enhancer largely used in the food industry with individual consumption steadily increasing worldwide. As a flavor enhancer, monosodium glutamate increases the sapidity of food. Monosodium glutamate produces a flavor that cannot be provided by other foods. It elicits a taste described in Japanese as umami, which is translated to “savory”. Higher amounts of individual monosodium glutamate consumption are associated with risk of being overweight of other major determinants. Studies providing the evidence of monosodium glutamate toxic effects have raised the increasing interest in monosodium glutamate intake as flavor enhancer. Neurotoxic effects in brain, obesity and metabolic defects and „Chinese restaurant syndrome“ are the most discussed in the connection with monosodium glutamate intake. Introduction of monosodium glutamate to newborn rats is one of the experimental models of obesity. The administration of monosodium glutamate to newborn rats causes the destruction of the ventromedial hypothalamic and arcuate nuclei, leading the rats to develop obesity due to the lack of control between absorption and energy expenditure. Monosodium glutamate retains its toxicity when administered orally. The results of the studies indicate that the use of monosodium glutamate in rats at concentrations that are only slightly higher than normal ones causes the development of obesity. Today there is a debate about the participation of monosodium glutamate in the obesity of most people who abuse food in fast food restaurants. Some scientists suggest that this food additive causes metabolic disorders and weight gain, but others argue that the consumption of monosodium glutamate even in large doses does not cause a development of obesity. Thus, the results of experimental studies have shown that neonatal injection of monosodium glutamate causes destruction of arcuate and ventromedial nuclei of the hypothalamus, leads to leptin resistance and development of the neuroendocrine form of obesity. A large number of scientific studies postulate that monosodium glutamate as a dietary supplement may be one of the causes of obesity in animals. However, contradictory results obtained in the animal and human studies require further intensive investigation to assess the effect of monosodium glutamate consumption as a food additive on the development of obesity.

Tags:

food additives, monosodium glutamate, obesity

Bibliography:

  • Vorobev V.V. Vrednoe vozdeystvie pischevyih dobavok na bezopasnost moreproduktov i zdorove naseleniya / V.V. Vorobev // Ryibnoe hozyaystvo. – 2008. – № 5. – S. 8-11.
  • Hordiienko L.P. Mehanizmi rozvitku patologIchnih zmin u slinnih zalozah schuriv za umov eksperimentalnogo ozhirinnya: avtoref. dis. na zdobuttya nauk. stupenya kand. med. nauk: spets. 14.03.04 “Patologichna fiziologiya” / L.P. Hordiienko. – Zaporizhzhya, 2016. – 23 s.
  • Kosyigina A.V. Novoe v patogeneze ozhireniya: adipokinyi – gormonyi zhirovoy tkani / A.V. Kosyigina, O.V. Vasyukova // Problemyi endokrinologii. – 2009. – T. 55, № 1. – S. 44-50.
  • Pasieshvili L.M. Imunniy disbalans yak pidgruntya progresuvannya steatogepatitu u hvorih na arterialnu gipertenzIyu ta ozhirInnya / L.M. Pasieshvili, T.F. HoroshavIna // Ukrayinskiy terapevtichniy zhurnal. – 2014. – № 2. – S. 40-44.
  • Patofiziologichna harakteristika eksperimentalnoyi modeli ozhirinnya u samits schurIv, viklikanoyi neonatalnim vvedennyam glutamatu natriyu / V.V. Konopelnyuk, I.Yu. Pribitko, O.I. Tsiryuk [ta in.] // Science Rise: Biological Science. – 2016. – T. 3, № – S. 14-18.
  • Rutska A.V. Toksichniy vpliv glutamatu natriyu na zhiviy organizm (oglyad literaturi) / A.V. Rutska, N.V. Getsko, I.Ya. Krinitska // Medichna ta klinichna himIya. – 2017. – T. 19, № 1. – S. 119-127.
  • Sarafanova L.A. Pischevyie dobavki: Entsiklopediya. – 2-e izd. / L.A. Sarafanova. – SPb: GIORD, 2004. – 808 s.
  • Svistilnik T.V. Fenomen eksaytotoksichnosti. Mehanizmi viniknennya, znachennya v rozvitku neyronalnogo poshkodzhennya ta mozhlivosti yogo korektsiyi pri patologiyah TsNS / T.V. Svistilnik // Biomedical and biosocial anthropology. – 2012. – № 1. – S. 207-215.
  • Falaleeva T.M. Vpliv trivalogo vvedennya glutamatu natriyu na strukturno-funktsionalniy stan shlunka ta massu tila schuriv / T.M. Falaleeva, V.M. Kuharskiy, T.V. Beregova // FizIiologichniy zhurnal. – 2010. – T. 56, № 4. – S. 102-110.
  • Falaleeva T.M. Zmini masi tila schuriv za umov dovgotrivalogo vvedennya glutamatu natriyu / T.M. Falaleeva // Svit meditsini ta biologiyi. – 2012. – № 2. – S. 170-172.
  • Acquired flavor acceptance and intake facilitated by monosodium glutamate in humans / M.R. Yeomans, N.J. Gould, S. Mobini [et al.] // Physiol Behav. – 2008. – Vol. 93, № 4-5. – P. 958-966.
  • Association of monosodium glutamate intake with overweight in Chinese adults: the INTERMAP Study / K. He, L. Zhao, M.L. Daviglus [et al.] // Obesity. – 2008. – Vol. 16, № 8. – P. 1875-1880.
  • Effect of food restriction on energy expenditure of monosodium glutamate-induced obese rats / J. Luz, V.P. Pasin, D.J. Silva [et al.] // Nutr. Metab. – 2010. – Vol. 56, № 1. – P. 31-35.
  • Effect of treatment with MSG on growth, satiety and epididymal adiposity in neonatal rats / L.C. Lemos, J.A. Pochapski, A. Raczenski [et al.] // Journal of Applied Pharmaceutical Science. – 2013. – Vol. 3, № 1. – P. 21-25.
  • Epidemiological studies of monosodium glutamate and health / H. VuThiThu, A. Wakita, S. Shikanai [et al.] // J Nutr Food Sci. – 2013. – Vol. 10. – P. 1-4.
  • Glutamate-induced obesity leads to decreased sperm reserves and acceleration of transit time in the epididymis of adult male rats / G.S. Fernandes, A.C. Arena, K.E. Campos [et al.] // Reproductive Biology and Endocrinology. – 2012. – Vol. 10, № 105. – P. 1-6.
  • Hermanussen M. Obesity, voracity, and short stature: the impact of glutamate on the regulation of appetite / M. Hermanussen, A.P. Garsia, M. Sunder // Eur J ClinNutr. – 2006. – Vol. 60, № 1. – P. 25-31.
  • Hermanussen M. Overweight, appetite control, and the role of glutamate and excess nutritional protein during child development / M. Hermanussen, J.F. Tresguerres // Hum ontogenet. – 2007. – Vol. 1, № 1. – P. 23-35.
  • Husarova V. Monosodium Glutamate toxic effects and their implications for human intake: A review / V. Husarova, D. Ostatnikova // JMED Research. – 2013. – Vol. 2013. – P. 1-12.
  • Insawang T. Monosodium glutamate (MSG) intake is associated with the prevalence of metabolic syndrome in a rural Thai population / T. Insawang, C. Selmi, U. Cha’on // NutrMetab (Lond). – 2012. – Vol. 1, № 9. – P. 50-52.
  • Interactive effects of neonatal exposure to monosodium glutamate and aspartame on glucose homeostasis / K.S. Collison, N.J. Makhoul, M.Z. Zaidi [et al.] // Nutrition & Metabolism. – 2012. – Vol. 9. – P. 1-14.
  • Monosodium glutamate neonatal intoxication associated with obesity in adult Stage is characterized by chronic inflammation and increased mRNA expression of peroxisome proliferator-activated receptors in mice / R. Roman-Ramos, J.C. Almanza-Perez, R. Garcia-Macedo [et al.] // Basic & Clinical Pharmacology & Toxicology. – 2011. – Vol. 108, № 6. – P. 406-413.
  • Monosodium glutamate raises antral distension and plasma amino acid after a standard meal in humans / B. Boutry, H. Matsumoto, G. Airinei [et al.] // Am J Physiol Gastrointest Liver Physiol. – 2011. – Vol. 300, № 1. – P. 137-145.
  • Monosodium glutamate stimulates secretion of glucagon-like peptide-1 and reduces postprandial glucose after a lipid-containing meal / H. Hosaka, M. Kusano, H. Zai [et al.] // Aliment Pharmacol Ther. – 2012. – Vol. 36. – P. 895-903.
  • Samuels A. Monosodium glutamate is not associated with obesity or a greater prevalence of weight gain over 5 years: findings from the Jiangsu Nutrition Study of Chinese adults – comments by Samuels / A. Samuels // Br. J Nutr. – 2010. – Vol. 9. – P. 11-13.
  • Sensitivity to food additives, vasoactive amines and salicylates: a review of the evidence / I.J. Skypala, M. Williams, L. Reeves [et al.] // Clin Transl Allergy. – 2015. – Vol. 5, № 34. – P. 1-11.
  • Tarasoff L. Monosodium L-glutamate: A double-blind study and review / L. Tarasoff, M.F. Kelly // Food and Chemical Toxicol. – 1993. – Vol. 31. – P. 1019-1035.
  • The endocrine disrupting potential of monosodium glutamate (MSG) on secretion of the glucagon-like peptide-1 (GLP-1) gut hormone and GLP-1 receptor interaction / M. Shannon, B. Green, G. Willars [et al.] // Toxicol Lett. – 2017. – Vol. 265. – P. 97-105.
  • Type 2 diabetes mellitus in obese mouse model induced by monosodium glutamate / M. Nagata, W. Suzuki, S. Iizuka [et al.] // Exp. Anim. – 2006. – Vol. 55, № 2. – P. 109-115.
  • Von Diemen V. Experimental model to induce obesity in rats / V. Von Diemen, E.N. Trindade, M.R. Trindade // Acta Cir Bras. – 2006. – Vol. 21, № 6. – P. 425-429.
  • WHO fact sheet № 311, jan. 2015. – Available from URL: http: // www.who.int/mediacentre/factsheets/fs311/en/.
  • Zhao J. Biomechanical and morphometric intestinal remodelling during experimental diabetes in rats / J. Zhao, J. Yang, H. Gregersen // Diabetologia. – 2003. – Vol. 46, № 12. – P. 1688-1697.

Publication of the article:

«Bulletin of problems biology and medicine» Issue 4 Part 3 (141), 2017 year, 33-37 pages, index UDK 616-056.5:612.393(-035.8)

DOI: