Mitochondrial dysfunction in the general continuum of non-communicable diseases from the position of systemic medicine. Part I. Literature review and results of theoretical research

February 10, 2022
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Resume

The conceptual issues of the involvement of the mechanisms of mitochondrial dysfunction in the general continuum of non-communicable diseases are considered in the article.

Aim: to improve the knowledge of the etiopathogenesis of non-communicable diseases by conceptualizing the issues of systemic involvement of the mechanisms of mitochondrial dysfunction in their general continuum.

The object of the study: to identify, summarize the issues of systemic involvement of the mechanisms of mitochondrial dysfunction in non-communicable diseases, followed by a conceptual restoration in the cardiovascular and general continuum of non-communicable diseases.

Research methods: general scientific, theoretical, logical methods and normative rules.

Results. Part I presents generalized issues of the role of mitochondrial dysfunction in the pathogenesis of non-communicable diseases, identification of mechanisms and ways of primary prevention. Mitochondrial dysfunction is conceptualized as a universal pathogenetic mechanism.

Conclusions. Mitochondrial dysfunction determines the etiopathogenetic basis for the transition of the human body from a state of functional health to pathology with the gradual onset and progression of non-communicable diseases. Emphasis in the introduction of a healthy lifestyle among all segments of the population in order to prevent non-communicable diseases should be placed on: 1) preventing excess intake of food substrates (overeating); 2) avoidance of frequent, constant eating; 3) adequate nutriceptive provision of the diet; 4) prevention of hypodynamia; 5) the need to use ecological, natural food products with sufficient fiber content, normal shelf life; 6) absence of bad habits; 7) expediency of life in an ecologically clean environment.

References

  • 1. Dzau V.J., Braunwald E. (1991) Resolved and unresolved issues in the prevention and treatment of coronary artery disease: a workshop consensus statement. Am. Heart. J., 121: 1244–1263. DOI: 10.1016/0002-8703(91)90694-d.
  • 2. Мінцер О.П., Потяженко М.М., Невойт Г.В. (2021) Магнітоелектрохімічна теорія обміну речовин. Том1. Концептуалізація. Монографія за заг. ред. О.П. Мінцера, М.М. Потяженка. Інтерсервіс. Київ — Полтава, 352 с.
  • 3. Luis A.V., Marimán A., Ramos B. et al. (2022) Standpoints in mitochondrial dysfunction: Underlying mechanisms in search of therapeutic strategies. Mitochondrion., 63: 9–22. DOI: 10.1016/j.mito.2021.12.006.
  • 4. Шендеров Б.А. (2018) Роль митохондрий в профилактической и оздоровительной медицине. Вестник восстановительной медицины, 1: 21–31.
  • 5. Mach N., Fuster-Botella D. (2017) Endurance exercise and gut microbiota: A review. J Sport Health Science, 6: 179–97. DOI: 10.1016/j. shs.2016.05.001.
  • 6. Popkov V.A., Plotnikov E.Y., Lyamzaev K.G. et al. (2015) Mitodiversity. Biochemistry (Moscow), 80(5): 532–541.
  • 7. Popkov V.A., Plotnikov E.Yu., Zorova L.D. et al. (2017) Quantification od Mitochondrial Morphology in situ. Cell and Tissue Biology, 11(1): 51–58.
  • 8. Nibali L., Henderson B. (Eds.) (2016) The Human Microbiota and Chronic Disease: Dysbiosis as a Cause of Human Pathology, 1th Edition. By John Wiley & Sons, 544 p.
  • 9. Rong Y., Urban L., Monica N., Jian Z. (2020) Regulation of Mammalian Mitochondrial Dynamics: Opportunities and Challenges. Front. Endocrinol., 11. DOI:10.3389/fendo.2020.00374.
  • 10. Saint-Georges-Chaumet Y., Edeas M. (2016) Microbiota-mitochondria inter-talk: consequence for microbiota-host interaction. Pathogens Dis., 74: ftv096. DOI: 10.1093/femspd/ftv096.
  • 11. Mottawea W., Chiang C.-K., Méhlbauer M. et al. (2016) Altered intestinal microbiota-host mitochondria crosstalk in new onset Crohn’s disease. Nat. Commun., 7: 13419. DOI: 10.1038/ncomms13419.
  • 12. Frye G.J., Rose S., Slattery J., MacFabe D.F. (2015) Gastrointestinal dysfunction in autism spectrum disorder: the role of the mitochondria and the enteric microbiome. Microb. Ecol. Health Dis., 26: 27458. DOI: dx.doi.org/10.3402/mehd.v.26.27458.
  • 13. Zorov D.B., Plotnikov E.Y., Silachev D.N. et al. (2014) Putting an Equal Sign between Mitochondria and Bacteria. Biochemistry, Moscow, 79(10): 1017–1031.
  • 14. Torralba D., Baixauli F., Sénchez-Madrid F. (2016) Mitochondria know no boundaries: mechanisms and functions of intercellular mitochondrial transfer. Frontiers in Cell and Development Biology, 4: 107. DOI:10.3389/fcell.2016.00107.
  • 15. Shenderov B.A., Midtvedt T. (2014) Epigenomic programing: a future way to health? Microb. Ecol. Health Dis., 25: 24145. DOI: 10.3402/mehd.v25.24145.
  • 16. Kozjak-Pavlovic V., Ross K., Rudel T. (2008) Import of bacterial pathogenicity factors into mitochondria. Curr. Opin. Microbiol., 11(1): 9–14. DOI: 10.1016/j.mib.2007.12.004.
  • 17. Lobet E., Letesson J.J., Arnould T. (2015) Mitochondria: a target for bacteria. Biochem. Pharmacol., 94(3): 173–85. DOI: 10.1016/j.bcp.2015.02.007.
  • 18. Selma M.V., Beltran D., Luna M.C. et al. (2017) Isolation of human Intestinal Bacteria Capable of producing the bioactive metabolite isourolithin A from Ellagic Acid. Front Microbiol., 8. DOI: 10.3389/fmicb.2017.01521.
  • 19. Franco-Obregon A., Gilbert J.A. (2017) The Microbiome-Mitochondrion connection: Common Ancestries, Common Mechanisms, Common Goals. mSystems, 2(3): e00018–e00017. doi org/10.1128/mSystems.00018-17.
  • 20. Wang Y., Wu Y., Wang Y. et al. (2017) Antioxidant Properties of Probiotic Bacteria. Nutrients, 9: 521. DOI:10.3390/nu9050521.
  • 21. Brown D.A., Perry J.B., Allen M.E. et al. (2017) Mitochondrial function as a therapeutic target in heart failure: Expert consensus document. Nat. Rev. Cardiol., 14(4): 238–250. DOI: 10.1038/nrcardio.2016.203.
  • 22. Castegna A., Iacobazzi V., Infantino V. (2015) The mitochondrial side of epigenetics. Physiol. Genomics, 47: 299–307. DOI: 10.1152/physiolgenomics.00096.2014.
  • 23. Chandel N.S. (2015) Evolution of mitochondria as signaling organelles. Cell Metab., 22: 204–206. DOI: 10.1152/physiolgenomics.00096.2014.
  • 24. Khan N.A., Govindaraj P., Meena A.K., Thangaraj K. (2015) Mitochondrial disorders: challenges in diagnosis & treatment. Indian J. Med. Res., 141(1): 13–26. DOI: 10.4103/0971-5916.154489.
  • 25. Neis E.P.J.G., Dejong C.H.C., Rensen S.S. (2015) The Role of Microbial Amino Acid Metabolism in Host Metabolism. Nutrients, 7(4): 2930–2946. DOI:10.3390/nu7042930.
  • 26. Kesner E.E., Saada-Reich A., Lorberboum-Galski H. (2016) Characteristics of mitochondrial transformation into human cells. Sci. Rep., 6. DOI:10.1038/srep26057.
  • 27. Pernas L., Scorrano L. (2016) Mito-morphosis: mitochondrial fusion, fission, and cristae remodeling as key mediators of cellular function. Ann Rev Physiol., 78(1): 505–531. DOI: 10.1146/annurev-physiol-021115-105011.
  • 28. Picard M., Wallace D.C., Burelle Y. (2016) The rise of mitochondria in medicine. Mitochondrion, 30: 105–116. DOI: 10.1016/j.mito.2016.07.003.
  • 29. Johnsona J., Mercado-Ayona E., Mercado-Ayonb Y. et al. (2021) Mitochondrial dysfunction in the development and progression of neurodegenerative diseases. Arch. Biochem. Biophysics., 702: 108698. doi.org/10.1016/j.abb.2020.108698.
  • 30. Nunes C., Laranjinha J. (2021) Nitric oxide and dopamine metabolism converge via mitochondrial dysfunction in the mechanisms of neurodegeneration in Parkinson’s disease. Archives of Biochemistry and Biophysics, 15(704): 108877. DOI: https:10.1016/j.abb.2021.108877.
  • 31. Yanga Y., Liua Y., Zhua J. et al. (2022) Neuroinflammation-mediated mitochondrial dysregulation involved in postoperative cognitive dysfunction. Free Radical. Biology and Medicine, 178: 134–146. DOI: 10.1016/j.freeradbiomed.2021.12.004.
  • 32. Espin J.C., Gonzalez-Sarrias A., Tomas-Barberan F.A. (2017) The gut microbiota: A key factor in the therapeutic effects of (poly) phenols. Biochem. Pharmacol., 139: 82–93. DOI: 10.1016/j.bcp.2017.04.033.
  • 33. Jin H., Kanthasamy A., Ghosh A. et al. (2014) Mitochondria-targeted antioxidants for treatment of Parkinson’s disease: preclinical and clinical outcomes. Biochim. Biophys. Acta, 1842: 1282–1294. DOI: 10.1016/j.bbadis.2013.09.007.
  • 34. Ramachandran A., Moellering D.R., Ceaser E. et al. (2002) Inhibition of mitochondrial protein synthesis results in increased endothelial cell susceptibility to nitric oxide-induced apoptosis. Proc. Natl. Acad. Sci. USA, 99: 6643–6648. DOI: 10.1073/pnas.102019899.
  • 35. Latorre-Pellicer A., Moreno-Loshuertos R., Lechuga-Vieco A.V. et al. (2016) Mitochondrial and nuclear DNA matching shapes metabolism and healthy ageing. Nature. 535(7613): 561–565. DOI: 10.1038/nature18618.
  • 36. Angelova P.R., Abramov A.Y. (2018) Role of mitochondrial ros in the brain: from physiology to neurodegeneration. FEBS Letters, 592: 692–702. DOI: http://www.ncbi.nlm.nih.gov/pubmed/29292494.
  • 37. Elfawy H.A., Das B. (2019) Crosstalk between mitochondrial dysfunction, oxidative stress, and age related neurodegenerative disease: etiologies and therapeutic strategies. Life Sci., 218: 165–184. DOI: http://www.ncbi.nlm.nih.gov/pubmed/30578866.
  • 38. Walter H., Moos D.V. Faller I.P. et al. (2021) Pathogenic mitochondrial dysfunction and metabolic abnormalities. Biochemical Pharmacology, 193: 114809. DOI: 10.1016/j.bcp.2021.114809.
  • 39. Marchi S., Patergnani S., Missiroli S. et al. (2018) Mitochondrial and endoplasmic reticulum calcium homeostasis and cell death. Cell Calcium., 72: 62–72. DOI: ncbi.nlm.nih.gov/pubmed/28515000.
  • 40. Merlini E., Coleman M.P., Loreto A. (2022) Mitochondrial dysfunction as a trigger of programmed axon death. Elsevier, 45: 53–63. DOI: 10.1016/j.tins.2021.10.014.
  • 41. Maguire D., Neytchev O., Talwar D. et al. (2018) Telomere Homeostasis: Interplay with Magnesium. Int. J. Mol. Sci., 19(1): 157. DOI: 10.3390/ijms19010157.
  • 42. Wallace D.C., Chalkia D. (2013) Mitochondrial DNA genetics and the hetertoplasmy conundrum in evolution and disease. Cold Spring Harb Perspect. Biol., 5: a021220. DOI: 10.1101/cshperspect.a021220.
  • 43. Shenderov B.A. (2016) The microbiota as an epigenetic control mechanism. In book: The Human Microbiota and Chronic Disease: 179–197. DOI:10.1002/9781118982907.ch11.
  • 44. Larson-Casey J.L., He C., Carter A.B. (2020) Mitochondrial quality control in pulmonary fibrosis. Redox Biology, 33, article 101426. DOI: 10.1016/j.redox.2020.101426.
  • 45. Picard M., McManus M.J., Gray J.D. et al. (2015) Mitochondria functions modulate neuroendocrine, metabolic, inflammatory, and transcriptional responses to acute psychological stress. PNAS, 16: 6614–6623. DOI: 10.1073/pnas.15157333112.
  • 46. Senft D., Ronai Z.A. (2016) Regulators of mitochondrial dynamics in cancer. Curr. Opin. Cell Biol., 39: 43–52. DOI: 10.1016/j.ceb.2016.02.001.
  • 47. Walker M.A., Volpi S., Sims K.B. et al. (2014) Powering the immune system: mitochondria in immune function and deficiency. J. Immunol. Res., 2014:164309. DOI: 10.1155/2014/164309.
  • 48. Rongvaux A. (2018) Innate immunity and tolerance toward mitochondria. Mitochondrion, 41: 14–20. DOI: 10.1016/j.mito.2017.10.007.
  • 49. Birsoy K., Wang T., Chen W.W. et al. (2015) An essential role of the mitochondrial electron transport chain in cell proliferation is to enable aspartate synthesis. Cell, 162: 540–551. DOI: 10.1016/j.cell.2015.07.016.
  • 50. Zong W.-X., Rabinowitz J.D., White E. (2016) Mitochondria and cancer. Molecular Cell, 61. DOI: 10.1016/j.molcel.2016.02.011.
  • 51. Song S.B., Jang S.-Y., Kang H.T. et al. (2017) Modulation of mitochondrial membrane potential an ROS generation by nicotinamide in a Manner Independent of SIRT1 and Mitophagy. Mol. Cells, 40(7): 503–514. DOI: 10.14348/molcells.2017.0081.
  • 52. Sinha P., Islam M.N., Bhattacharya S., Bhattacharya J. (2016) Intercellular mitochondrial transfer: bioenergetic crosstalk between cells. Cur. Opin. Gen. Devel., 38: 97–101. DOI: 10.1016/j.gde.2016.05.002.
  • 53. Yue L., Yao H. (2016) Mitochondrial dysfunction in inflammatory responses and cellular senescence: pathogenesis and pharmacological targets for chronic lung diseases. Br. J. Pharmacol., 15(173): 2305–2318. DOI: 10.1111/bph.13518.
  • 54. Akbari M., Kirkwood T.B.L., Bohr V.A. (2019) Mitochondria in the signaling pathways that control longevity and health span. Ageing Res. Rev., 54: 100940. DOI: 10.1016/j.arr.2019.100940.
  • 55. Vringer E., Tait S.W.G. (2019) Mitochondria and inflammation: cell death heats up. Frontiers in Cell and Development. Biology, 7: 100. DOI: http://www.ncbi.nlm.nih.gov/pubmed/31316979.
  • 56. Zorov D.B., Isaev N.K., Plotnikov E.Y. et al. (2013) Perspectives of Mitochondrial Medicine. Biochemistry, Moscow, 78(9): 979–990.
  • 57. Zorov D.B., Juhaszova M., Sollott S.J. (2014) Mitochondrial reactive oxygen species (ROS) and ROS-induced ROS release. Physiol. Rev., 94(3): 909–950.
  • 58. Karaa A., Goldstein A. (2015) The spectrum of clinical presentation, diagnosis, and management of mitochondrial forms of diabetes. Pediatr. Diab.,16(1): 1–9. DOI: 10.1111/pedi.12223.
  • 59. Позднякова А.А., Володина М.А., Рштуни С.Д. и др. (2015) Митохондриальная дисфункция как одна из возможных причин нарушения фолликуло- и стероидогенеза при преждевременной недостаточности яичников. Акуш. Гинекол. Репрод., 4: 55–65.
  • 60. Иванова И.И., Гнусаев С.Ф., Сухоруков В.С. и др. (2019) Проявления митохондриальной дисфункции у детей с дисплазией соединительной ткани и хроническим гастродуоденитом. Рос. вестн. перинатол. педиатр., 64(5): 84–90. DOI: 10.21508/1027-4065-2019-64-5-84-90.
  • 61. Zhou W., Qu J., Xie S. et al. (2021) Mitochondrial Dysfunction in Chronic Respiratory Diseases: Implications for the Pathogenesis and Potential Therapeutics. Oxidative Medicine and Cellular Longevity, 2021: Article ID 5188306. DOI: 10.1155/2021/5188306.
  • 62. Knight-Lozano C.A., Young C.G., Burow D.L. et al. (2002) Cigarette smoke exposure and hypercholeste rolemia increase mitochondrial damage in cardiovas cular tissues. Circulation, 105: 849–854. DOI: 10.1161/hc0702.103977.
  • 63. Cудаков Н.П., Никифоров С.Б., Константинов Ю.М. и др. (2007) Митохондриальная дисфункция в механизмах атерогенеза. Бюл. ВСНЦ СО РАМН, 2(54): 119–123.
  • 64. Hayakawa K., Esposito E., Wang X. et al. (2016) Transfer of mitochondria from astrocytes to neurons after stroke. Nature, 535(7613): 551–555. DOI: 10.1038/nature18928.
  • 65. Егорова Л.А., Ежов М.В., Шиганова Г.М., Постнов А.Ю. (2013) Возможная роль мутаций митохондриального генома при ишемической болезни сердца. Клиницист, 2: 6–13.
  • 66. Wu C., Zhang Z., Zhang W., Liu X. (2022) Mitochondrial dysfunction and mitochondrial therapies in heart failure . Pharmacol. Res., 175: 106038. DOI: 10.3389/FCVM.2021.822969.
  • 67. Bisaccia G., Ricci F., Gallina S. et al. (2021) Mitochondrial dysfunction and heart disease: Critical appraisal of an overlooked association. Int. J. Mol. Sci., 22(2): 614. DOI: 10.3390/ijms22020614.
  • 68. Bordi M., Nazio F., Campello S. (2017) The Close Interconnection between Mitochondrial Dynamics and Mitophagy in cancer. Front Oncol., 7: 1–9. DOI:10.3389/fonc.2017.00081.
  • 69. Birsoy K., Possemato R., Lorbeer F.K. et al. (2014) Metabolic determinants of cancer cell sensitivity to glucose limitation and biguanides. Nature, 508: 108–112. DOI: 10.1038/nature13110.
  • 70. Stewart J.B., Alaei-Mahabadi B., Sabarinathan R. et al. (2015) Simultaneous DNA and RNA mapping of somatic mitochondrial mutations across diverse human cancers. PLoS Genet., 11: e1005333. DOI: 10.1371/journal.pgen.1005333.
  • 71. Оковитый С.В. (2015) Митохондриальная дисфункция при метаболическом синдроме. Эффективная фармакотерапия, 16: 46–48.
  • 72. Wu H., Esteve E., Tremaroli V. et al. (2017) Metformin alters the gut microbiome of individuals with treatment-naéve type 2 diabetes, contributing to the therapeutic effects of the drug. Nat. Med., 23(7): 850–58. DOI: 10.1038/nm.4345.
  • 73. Hughes S.D., Kanabus M., Anderson G. et al. (2014) The ketogenic diet component decaboic acid increases mitochondrial citrate synthase and complex I activity in neuronal cells. J. Neurochem., 129: 426–433. DOI: 10.1111/jnc.12646.
  • 74. Николаева Е.А. (2017) Митохондриальные болезни у детей: клинические проявления, возможности диагностики и лечения. Учебное пособие. Москва, 88 с.
  • 75. Гречаніна Ю.Б., Гречаніна О.Я., Школьнікова Д.В. (2020) Мітохондріальні хвороби: генетична епідеміологія, діагностика та лікування (health-ua.com/article/61887-mtohondraln-hvorobi-genetichna-epdemologya-dagnostika-talkuvannya).
  • 76. Брин И.Л., Неудахин Е.В., Дунайкин М.Л. (2015) Карнитин в педиатрии: исследования и клиническая практика. Медпрактика, Москва, 112 с.
  • 77. Ивянский С.А., Балыкова Л.А., Щекина Н.В. и др. (2016) Нарушения соединительной ткани у детей и подростков, занимающихся спортом. Consilium Medicum. Педиатрия, 4: 94–101.
  • 78. Frohlich J., Chaldakov G.N., Vinciguerra M. (2021) Cardio- and neurometabolic adipobiology: Consequences and implications for therapy. Int. J. Mol. Sci., 8(22): 4137. DOI: 10.3390/ijms22084137.
  • 79. Barteková M., Adameová A., Görbe A. et al. (2021) Natural and synthetic antioxidants targeting cardiac oxidative stress and redox signaling in cardiometabolic diseases. Free Radic. Biol. Med.,169: 446–477. DOI: 10.1016/j.freeradbiomed.2021.03.045.
  • 80. Tilokani L., Nagashima S., Paupe V., Prudent J. (2018) Mitochondrial dynamics: overview of molecular mechanisms. Essays Biochem., 62(3): 341–360. DOI: 10.1042/EBC20170104.
  • 81. Khan M.S., Butler J. (2019) Targeting mitochondrial function in heart failure: Makes sense but will it work? JACC Basic Transl. Sci., 4(2): 158–160. DOI: 10.1016/j.jacbts.2019.03.003.
  • 82. Taddeo E.P., Laker R.C., Breen D.S. et al. (2014) Opening of the mitochondrial permeability transition pore links mitochondrial dysfunction to insulin resistance in skeletal muscle. Mol. Metabol., 3: 124–134.
  • 83. Korzeniewski B. (2015) Effects of OXPHOS complex deficiencies and ESA dysfunction in working intact skeletal muscle: implications for mitochondrial myopathies. Biochimica et Biophysica Acta (BBA). Bioenergetics, 1847: 1310–1319. DOI: 10.1016/j.bbabio.2015.07.007.
  • 84. Clark A., Mach N. (2015) Mitochondria, Microbiota, and Endurance Exercise compounds. Gastroenterol. Res. Pract., e398585. DOI: 10.1155/2015/ 398585.
  • 85. Chen Y.-M., Wei L., Chiu Y.-Sh. et al. (2016) Lactobacillus plantarum TWK10 Supplementation Improves Exercise Performance and Increases Muscle Mass in Mice. Nutrients, 8: 205. DOI:10.3390/nu8040205.
  • 86. Huertas J.R., Casuso R.A., Agustín P.H., Cogliati S. (2019) Stay Fit, Stay Young: Mitochondria in Movement: The Role of Exercise in the New Mitochondrial Paradigm. Oxid Med Cell Longev., eCollection 2019 Jun: 7058350. DOI: 10.1155/2019/7058350.
  • 87. Gremmingera V.L., Harrelsona E.N., Crawforda T.K. et al. (2021) Skeletal muscle specific mitochondrial dysfunction and altered energy metabolism in a murine model (oim/oim) of severe osteogenesis imperfecta. Mol. Genet. Metabol., 4(132): 244–253. DOI: 10.1016/j.ymgme.2021.02.004.
  • 88. Muir R., Diot A., Poulton J. (2016) Mitochondrial content is central to nuclear gene expression: Profound implications for human health. BioEssays, 38(2): 150–156. DOI: 10.1002/bies.201500105.
  • 89. Борисова О. Митохондриальная медицина. Часть 2. Научный обзор. openlongevity.org/mitochondria_medicine_2.
  • 90. Nishimura K., Shiina R., Kashiwagi K., Igarashi K. (2006) Decrease in Polyamines with Aging and Their Ingestion from Food and Drink. J. Biochem., 139: 81–90. DOI:10.1093/jb/mvj003.
  • 91. Щербакова Е. (2020) Питание биохакера. Как питаться, чтобы быть эффективным и замедлить старение, Litres, 286 с.
  • 92. Boelsterli U.A., Redinbo M.R., Saitta K.S. (2013) Multiple NSAID -induced hits injure the small intestine: underlying mechanisms and novel strategies. Toxicol. Sci., 131(2): 654–667. DOI: 10.1093/toxsci/kfs310.
  • 93. Bauer A.Z., Kriebel D. (2013) Prenatal and perinatal analgesic exposure and autism: an ecological link. Environ Health, 12: 41. DOI: 10.1186/1476-069X-12-41.
  • 94. Kalghatgi S., Spina C.S., Costello J.C. et al. (2013) Bactericidal antibiotics induce mitochondrial dysfunction and oxidative damage in Mammalian cells. Sci. Transl. Med., 5: 192ra85. DOI: 10.1126/scitranslmed.3006055.
  • 95. Moullan N., Mouchiroud L., Wang X. et al. (2015) Tetracyclines Disturb Mitochondrial Funcrion across Eukaryotic Models: A Call for Caution in Biomedical Research. Cell Reports, 10: 1681–1691. DOI: 10.1016/j.celrep.2015.02.034
  • 96. Bhonchal S., Nain C.K., Prasad K.K. et al. (2008) Functional and morphological alterations in small intestine mucosa of chronic alcoholics. J. Gastroenterol. Hepatol., 23(2): 278–285. DOI: 10.1111/j.1440-1746.2008.05415.x.
  • 97. Самойлов В.О. (2013) Медицинская биофизика. СпецЛит, Санкт-Петербург, 591 с.