Science for Education Today, 2022, vol. 12, no. 6, pp. 189–211
UDC: 
615.3+37.01

Evaluation of the biological effect of the brown algae Laminaria digitata (based on studies on experimental animals)

Ogudov A. S. 1 (Novosibirsk, Russian Federation), Shepeleva O. A. 2 (Arkhangelsk, Russian Federation), Chuenko N. F. 1 (Novosibirsk, Russian Federation), Shestakov N. A. 1 (Novosibirsk, Russian Federation), Shevkun I. I. 3 (Moscow, Russian Federation), Novikova I. I. 1 (Novosibirsk, Russian Federation)
1 Novosibirsk Research Institute of Hygiene
2 Northern State Medical University
3 Rospotrebnadzor
Abstract: 

Introduction. Currently, the problem of keeping schoolchildren healthy is acute. One of the leading risk factors for the health of schoolchildren is nutrition, in the organization of which much attention has recently been paid to the inclusion of special foods that help prevent diet-related diseases. The White Sea brown alga, Laminaria digitata, has been shown to be a natural source of bioactive compounds. However, the mechanisms of the kinetics of health-promoting effects during long-term dietary intake of Laminaria digitata are poorly studied which makes it difficult to solve practical problems in the use of products and dishes containing Laminaria digitata for health purposes.
The purpose of this research is to study the biological effects of Laminaria digitata in a 28-day experiment in white Wistar rats to address practical issues of justifying food formulation and food processing for school nutrition, and to assess the risk of side effects.
Materials and Methods. The study used dry concentrates of Laminaria digitata. The sample comprised white Wistar rats divided into 4 groups of 10 animals each. The animals were examined on the 14th and 28th days of the experiment using standard methods. The experiment was conducted in accordance with the rules adopted in the European Convention for the Protection of Animals Used for Experimental Scientific Purposes (Strasburg, 1986), after approval by the Ethics Committee of Novosibirsk Research Hygiene Institute. The statistical processing of the research materials was performed using Statistica 10.0.
Results. The analysis of the dynamics of the indicators showed the stages of the interaction process of the organism with bioactive substances contained in the brown alga Laminaria digitata.
Strengthening of stress-protective, antihypercholesterolemic effects and metabolic function of the liver at the stage of primary reactions is replaced by a significant weakening at the stage of physiological adaptation. The bioavailability of a form of iodine accumulated by the brown algae Laminaria digitata has been experimentally confirmed. The assessment of biological significance consisted of classifying the effects manifested using benefit and safety criteria.
Conclusions. Based on the results of the experiment, new knowledge was gained on the criteria for the usefulness and safety of Laminaria digitata algae, which can be used to solve practical problems of proving the quantitative values of the inclusion of Laminaria digitata as an ingredient in recipes and to solve practical problems with Laminaria digitata enriched food production technologies in the development of school meals, the inclusion of which in students' diets minimizes the risk of diet-related diseases.

Keywords: 

Laminaria digitata algae; Toxicology experiment; Wistar rats; Biological effect; Lipid metabolism; Hypoglycaemic effect; Hormones; Special foods for school nutrition.

For citation:
Ogudov A. S., Shepeleva O. A., Chuenko N. F., Shestakov N. A., Shevkun I. I., Novikova I. I. Evaluation of the biological effect of the brown algae Laminaria digitata (based on studies on experimental animals). Science for Education Today, 2022, vol. 12, no. 6, pp. 189–211. DOI: http://dx.doi.org/10.15293/2658-6762.2206.08
References: 
  1. Semenova E. V., Bilimenko A. S., Chebotok V. V. The use of seaweed in medicine and pharmacy. Modern Problems of Science and Education, 2019, no. 5, pp. 118. (In Russian) URL: https://elibrary.ru/item.asp?id=41258216
  2. Balázs A. Role of phytotherapy in the prevention and treatment of obesity. Orvosi Hetilap, 2010, vol. 151 (19), pp. 763–773. DOI: https://doi.org/10.1556/OH.2010.28812  
  3. Bitto A., Wang A. M., Bennett C. F., Kaeberlein M. Biochemical genetic pathways that modulate aging in multiple species. Cold Spring Harbor Perspectives in Medicine, 2015, vol. 5 (11), pp.  a025114. DOI:  https://doi.org/10.1101/cshperspect.a025114
  4. Zhang J., Tiller C., Shen J., Wang C., Girouard G. S., Dennis D., Barrow C. J., Miao M., Ewart  H.  S. Antidiabetic properties of polysaccharide- and polyphenolic-enriched fractions from the brown seaweed Ascophyllum nodosum. Canadian Journal of Physiology and Pharmacology, 2007, vol. 85 (11), pp. 1116–1123. DOI: https://doi.org/10.1139/y07-105 
  5. Walpole S. S., Prieto-Merino D., Edwards P., Cleland J., Stephens G., Roberts I. The weight of nations: An estimation of adult human biomass. BMC Public Health, 2012, vol. 12 (1), pp. 439. DOI: https://doi.org/10.1186/1471-2458-12-439
  6. Tanna B., Mishra A. Nutraceutical potential of seaweed polysaccharides: Structure, bioactivity, safety and toxicity. Comprehensive Reviews in Food Science and Food Safety, 2019, vol. 18, pp.  817–831. DOI: http://doi.org/10.1111/1541-4337.12441
  7. Kim Y. M., Jang M-S. Anti-obesity effects of Laminaria japonica fermentation on 3T3-L1 adipocytes are mediated by the inhibition of C/EBP-α/β and PPAR-γ. Cellular and Molecular Biology, 2018, vol. 64 (4), pp. 71–77. DOI: https://doi.org/10.14715/CMB/2018.64.4.12 
  8. Aitbaev K. A., Murkamilov I. T., Murkamilova Zh. A., Kudaibergenova I. O., Yusupov F. A. Epigenetic mechanisms of cardioprotection: Focus is on activation of sirtuins. Archives of Internal Medicine, 2021, vol. 11 (6), pp. 424–432. (In Russian) DOI: https://doi.org/10.20514/2226-6704-2021-11-6-424-432 URL: https://elibrary.ru/item.asp?id=47247409
  9. Yamanashi Y., Takada T., Yamamoto H., Suzuki H. NPC1L1 Facilitates sphingomyelin absorption and regulates diet-induced production of VLDL/LDL-associated S1P. Nutrients, 2020, vol. 12 (9), pp. 2641. DOI: https://doi.org/10.3390/nu12092641
  10. Oh J. H., Kim J., Lee Y. Anti-inflammatory and anti-diabetic effects of brown seaweeds in high-fat diet-induced obese mice. Nutrition Research and Practice, 2016, vol. 10 (1), pp. 42–48. DOI: https://doi.org/10.4162/nrp.2016.10.1.42
  11. Zhang Q., Fan X. Y., Guo W. L., Cao Y. J., Lin Y. C., Cheng W. J., Chen L. J., Rao P. F., Ni L., Lv X. C. The protective mechanisms of macroalgae Laminaria japonica consumption against lipid metabolism disorders in high-fat diet-induced hyperlipidemic rats. Food & Function, 2020, vol.  11  (4), pp. 3256–3270. DOI: https://doi.org/10.1039/d0fo00065e 
  12. Barde S. R., Sakhare R. S., Kanthale S. B., Chandak P. G., Jamkhande P. G. Marine bioactive agents: A short review on new marine antidiabetic compounds. Asian Pacific Journal of Tropical Disease, 2015, vol. 5 (1), pp. S209–S213. DOI: http://doi.org/10.1016/S2222-1808(15)60891-X
  13. Roslyy I. M., Abramov S. V., Pokrovsky V. I. Enzymemia – an adaptive mechanism or a marker of cytolysis? Bulletin of the Russian Academy of Medical Sciences, 2002, no. 8, pp. 3–10. (In Russian) URL: https://www.elibrary.ru/item.asp?id=18084698  EDN PFTLDB.
  14. Shen W. J., Azhar S., Kraemer F. B. SR-B1: A unique multifunctional receptor for cholesterol influx and efflux. Annual Review of Physiology, 2018, vol. 80, pp. 95–116. DOI: https://doi.org/10.1146/annurev-physiol-021317-121550
  15. Peteiro C. Alginate production from marine macroalgae, with emphasis on kelp farming. In: Rehm B., Moradali M. (eds)  Alginates and Their Biomedical Applications, 2018, pp. 27–66. DOI: https://doi.org/10.1007/978-981-10-6910-9_2
  16. Egorov A. D., Penkov D. N., Tkachuk V. A. Molecular and cellular mechanisms of adipogenesis. Diabetes Mellitus, 2015, vol. 18 (2), pp. 12–19. (In Russian) DOI: https://doi.org/10.14341/БМ2015212-19  URL: https://elibrary.ru/item.asp?id=23701202
  17. Walpole S. C., Merino D. P., Phil E., Cleland J., Stevens G., Roberts I. The weight of nations: An estimation of adult human biomass. BMC Public Health, 2012, vol. 12 (1), pp. 439. DOI: https://doi.org/10.1186/1471-2458-12-439
  18. Asrian L., Giri N. Sexual differences in nutrition physiology. Regulatory, Integrative and Comparative Physiology, 2013, vol. 305 (11), pp. R1215–R1267. DOI: https://doi.org/10.1152/ajpregu.00446.2012  
  19. Bloor I. D., Symondрs M. E. Sexual dimorphism in white and brown adipose tissue with obesity and inflammation. Hormones and Behavior, 2014, vol. 66 (1), pp. 95–103. DOI: https://doi.org/10.1016/j.yhbeh.2014.02.007
  20. Chen X., Clusky R., Chen J., Beaven S. W., Tontonoz P., Arnold A. P., Reue K. The number of X chromosomes causes sex differences in adiposity in mice. PLoS Genetics, 2012, vol. 8 (5), pp.  e1002709. DOI: https://doi.org/10.1371/journal.pgen.1002709
  21. Thomson C. D. Dietary recommendations for iodine around the world. IDD Newsletter, 2002, vol. 18 (3), pp. 38–42. URL: https://scholar.google.com/scholar_lookup?title=Dietary+recommendations+of+iodine+around+the+world&author=Thomson+CD&publication+year=2002&journal=IDD+Newsletter&volume=18&pages=38-42
Date of the publication 31.12.2022