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Известия Национальной академии наук Беларуси. Серия биологических наук

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ЦИРКАДНЫЕ РИТМЫ И МЕТАБОЛИЗМ ЛИПИДОВ В ЖИВОТНЫХ КЛЕТКАХ. ЧАСТЬ II. ВЛИЯНИЕ ЦИРКАДНЫХ РИТМОВ НА ОБЩИЙ ПОКРОВ И ЖИРОВУЮ ТКАНЬ. ДЕСИНХРОНОЗ И ЛИПИДНЫЙ ОБМЕН

Об авторах

И. С. Соболевская
Витебский государственный медицинский университет
Беларусь
канд. биол. наук, доцент


О. Д. Мяделец
Витебский государственный медицинский университет
Беларусь
д-р мед. наук, профессор, заведующий кафедрой


Е. С. Пашинская
Витебский государственный медицинский университет
Беларусь
канд. биол. наук, доцент


Список литературы

1. Lamia, K. Physiological significance of a peripheral tissue circadian clock / K. Lamia, K. Storch, C. Weitz // Proc. Natl. Acad. Sci. USA. – 2008. – Vol. 105. – P. 15172–15177.

2. Analysis of circadian and ultradian rhythms of skin surface properties of face and forearm of healthy women / I. Le Fur [еt al.] // J. Invest. Dermatol. – 2001. – Vol. 117, N 3. – P. 718–724.

3. Time-dependent variations of the skin barrier function in humans: transepidermal water loss, stratum corneum hydration, skin surface pH, and skin temperature / G. Yosipovitch [еt al.] // J. Investig. Dermatol. – 1998. – Vol. 110. – P. 20–23.

4. Luber, A. Therapeutic implications of the circadian clock on skin function / A. Luber, S. Ensanyat, J. Zeichner // J. Drugs Dermatol. – 2014. – Vol. 13. – P. 130–134.

5. Van Someren, E. Mechanisms and functions of coupling between sleep and temperature rhythms / E. Van Someren // Prog. Brain Res. – 2006. – Vol. 153. – P. 309–324.

6. Circadian variations in the number of actively secreting sebaceous follicles and androgen circadian rhythms / M. Verschoore [еt al.] // Chronobiol. Int. – 1993. – Vol. 10. – P. 349–359.

7. Matsui, M. Biological rhythms in the skin / M. Matsui // Int. J. Mol. Sci. – 2016. – Vol. 17, N 6. – P. 801.

8. Circadian activity of topical 0.05 % betamethasone dipropionate in human skin in vivo / L. Pershing [еt al.] // J. In-vestig. Dermatol. – 1994. – Vol. 102. – P. 734–739.

9. Geyfman, M. How the skin can tell time / M. Geyfman, B. Andersen // J. Invest. Dermatol. – 2009. − Vol. 129, N 5. – P. 1063–1066.

10. Desotelle, J. The circadian control of skin and cutaneous photodamage / J. Desotelle, M. Wilking, N. Ahmad // Photochem. Photobiol. – 2012. – Vol. 88, N 5. – P. 1037–1047.

11. Circadian expression of clock genes in human oral mucosa and skin: association with specific cell-cycle phases // G. Bjarnason [еt al.] // Am. J. Pathol. – 2001. – Vol. 158, N 5. – P. 1793–1801.

12. Skin, reactive oxygen species, and circadian clocks / M. Ndiaye [еt al.] // Antioxid. Redox. Signal. – 2014. – Vol. 20. – P. 2982–2996.

13. Melatonin, immune function and cancer / V. Srinivasan [еt al.] // Recent. Pat. Endocr. Metab. Immune. Drug Discov. – 2011. – Vol. 5. – P. 109–123.

14. Abbaszadeh, A. Melatonin role in ameliorating radiation-induced skin damage: from theory to practice (a review of literature) / A. Abbaszadeh, G. Haddadi, Z. Haddadi // J. Biomed. Phys. Eng. – 2017. – Vol. 7, N 2. – P. 127–134.

15. Effect of melatonin on lipid barrier in rats’ skin / N. Kostiuk [еt al.] // Am. J. Biochem. – 2012. – Vol. 2, N 5. – P. 67–73.

16. Effects of short-term melatonin administration on lipoprotein metabolism in normolipidemic postmenopausal women / A. Wakatsuki [еt al.] // Maturitas. – 2001. – Vol. 38, N 2. – P. 171–177.

17. Circadian clocks in rat skin and dermal fibroblasts: differential effects of aging, temperature and melatonin / C. Sandu [еt al.] // Cell. Mol. Life Sci. – 2015. – Vol. 72. – P. 2237–2248.

18. Human epidermal stem cell function is regulated by circadian oscillations / P. Janich [еt al.] // Cell Stem Cell. – 2013. – Vol. 13. – P. 745–753.

19. Kriippel-like factor 9 is a circadian transcription factor in human epidermis that controls proliferation of keratinocytes / R. Sporl [еt al.] // Proc. Natl. Acad. Sci. USA. – 2012. – Vol. 109 (27). – P. 10903–10908.

20. Adipose tissue as an endocrine organ: from theory to practice / M. H. Fonseca-Alaniz [et al.] // J. Pediat. – 2007. – Vol. 83, N 5. – P. s192−s203.

21. Adipose tissue sensitivity to radiation exposure / S. Poglio [et al.] // Am. J. Path. – 2009. − Vol. 174, N 1. – P. 44−53.

22. Терешина, Е. В. Возрастная дисфункция жировой ткани / Е. В. Терешина // Геронтология и гериатрия. – 2005. – N 5. – С. 98−101.

23. Lipid homeostasis, lipotoxicity and the metabolic syndrome / R. Unger [et al.] // Biochim. Biophys. Acta. – 2010. – Vol. 1801. – P. 209–214.

24. Circadian regulation of lipid mobilization in white adipose tissues / A. Shostak [еt al.] // Diabetes. – 2013. – Vol. 62. – P. 2195–2203.

25. The human circadian metabolome / R. Dallmann [еt al.] // Proc. Natl. Acad. Sci. USA. – 2012. – Vol. 109. – P. 2625–2629.

26. Obesity in mice with adipocytespecific deletion of clock component / Paschos G. [еt al.] // Arntl. Nat. Med. – 2012. – Vol. 18. – P. 1768–1777.

27. Green, C. The meter of metabolism / C. Green, J. Takahashi, J. Bass // Cell. – 2008. – Vol. 134. – P. 728–742.

28. Obesity and metabolic syndrome in circadian Clock mutant mice / F. Turek [еt al.] // Science. – 2005. – Vol. 308 (5724). – P. 1043–1045.

29. PER2 controls lipid metabolism by direct regulation of PPARg / B. Grimaldi [еt al.] // Cell Metab. – 2010. – Vol. 12, N 5. – P. 509–520.

30. Nuclear receptor expression links the circadian clock to metabolism / X. Yang [еt al.] // Cell. – 2006. – Vol. 126. – P. 801–810.

31. The clock gene, brain and muscle Arnt-like 1, regulates adipogenesis via Wnt signaling pathway / B. Guo [еt al.] // FASEB J. – 2012. – Vol. 26. – P. 3453–3463.

32. The nuclear receptor REV-ERBα is required for the daily balance of carbohydrate and lipid metabolism / J. Delezie [еt al.] // FASEB J. – 2012. – Vol. 26. – P. 3321–3335.

33. Gimble, J. Fat circadian biology / J. Gimble, Z. Floyd // J. Appl. Physiol. – 2009. – Vol. 107. – P. 1629–1637.

34. Regulation of circadian behaviour and metabolism by REV-ERB-α and REV-ERB-β / H. Cho [еt al.] // Nature. – 2012. – Vol. 485. – P. 123–127.

35. Regulation of adipogenesis by natural and synthetic REV-ERB ligands / N. Kumar [еt al.] // Endocrinology. – 2010. – Vol. 151. – P. 3015–3025.

36. Solt, L. A. Regulation of circadian behaviour and metabolism by synthetic REV-ERB agonists / L. A. Solt, Y. Wang, S. Banerjee // Nature. – 2002. – Vol. 485 (7396). – Р. 62–68.

37. Надольник, Л. И. Стресс и щитовидная железа / Л. И. Надольник // Биомед. химия. – 2010. – Т. 56. – Bып. 4. – С. 443–456.

38. Хныченко, Л. К. Стресс и его роль в развитии патологических процессов / Л. К. Хныченко, Н. С. Сапронов // Обзоры по клин. фармакологии и лекарств. терапии. – 2003. – Т. 2, N 3. – С. 2–15.

39. The metabolic consequences of sleep deprivation / K. Knutson [еt al.] // Sleep Med. Rev. – 2007. – Vol. 11. – P. 163–178.

40. Knutson, K. Associations between sleep loss and increased risk of obesity and diabetes / K. Knutson, E. Van Cauter // Ann. NY Acad. Sci. – 2008. – Vol. 1129. – P. 287–304.

41. The clockwork of metabolism / K. Ramsey [еt al.] // Ann. Rev. Nutr. – 2007. – Vol. 27. – P. 219–240.

42. Carcinogenicity of shift-work, painting, and fire-fighting / K. Straif [еt al.] // Lancet Oncol. – 2007. – Vol. 8. – P. 1065–1066.

43. Inadequate sleep as a risk factor for obesity: analyses of the NHANES / J. Gangwisch [еt al.] // I. Sleep. – 2005. – Vol. 28. – P. 1289–1296.

44. Spiegel, K. Impact of sleep debt on metabolic and endocrine function / K. Spiegel, R. Leproult, E. Van Cauter // Lancet. – 1999. – Vol. 354. – P. 1435–1439.

45. Deletion of the mammalian circadian clock gene BMAL1/Mop3 alters baseline sleep architecture and the response to sleep deprivation / A. Laposky [еt al.] // Sleep. – 2005. – Vol. 28. – P. 395–409.

46. Short sleep duration is associated with reduced leptin, elevated ghrelin, and increased body mass index / S. Taheri [еt al.] // PLoS Med. – 2013. – Vol. 62. – P. E62.

47. Colles, S. Night eating syndrome and nocturnal snacking: association with obesity, binge eating and psychological distress / S. Colles, J. Dixon, P. O’Brien // Int. J. Obes. (Lond.). – 2007. – Vol. 31. – P. 1722–1730.

48. Shoelson, S. Obesity, inflammation, and insulin resistance / S. Shoelson, L. Herrero, A. Naaz // Gastroenterology. – 2007. – Vol. 132. – P. 2169–2180.

49. Clock Genes and Metabolic Disease / B. Marcheva [et al.] // J. Appl. Physiol. – 2009. – Vol. 107, N 5. – P. 1638–1646.

50. BMAL1 and CLOCK, two essential components of the circadian clock, are involved in glucose homeostasis / R. Rudic [et al.] // PLoS Biol. – 2004. – Vol. 2. – P. e377.

51. Circadian control of the NAD+ salvage pathway by CLOCK-SIRT1 / Y. Nakahata [et al.] // Science. – 2009. – Vol. 324. – P. 654–657.

52. Visfatin regulates insulin secretion in beta cells as a systemic NAD biosynthetic enzyme / J. Revollo [et al.] // Cell Metab. – 2007. – Vol. 6. – P. 363–375.

53. Galman, C. Bile acid synthesis in humans has a rapid diurnal variation that is asynchronous with cholesterol synthesis / C. Galman, B. Angelin, M. Rudling // Gastroenterology. – 2005. – Vol. 129. – P. 1445–1453.

54. Regulation of bile acid synthesis by the nuclear receptor Rev-erbalpha / H. Duez [et al.] // Gastroenterology. – 2008. – Vol. 135. – P. 689–698.

55. REV-ERBalpha participates in circadian SREBP signaling and bile acid homeostasis / G. Le Martelot [et al.] // PLoS Biol. – 2009. – Vol. 7. – P. e1000181.

56. Circadian rhythms and metabolic syndrome: from experimental genetics to human disease / E. Maury [et al.] // J. Appl. Physiol. – 2009. − Vol. 107, N 5. – P. 1638–1646.

57. Immunologic principles and immunotherapeutic approaches in ovarian cancer / K. Knutson [et al.] // Hematol. Oncol. Clin. North. Am. – 2003. – Vol. 17. – P. 1051–1073.

58. Durgan, D. The Cardiomyocyte Circadian Clock: Emerging Roles in Health and Disease / D. Durgan, M. Young // Circ. Res. – 2010. – Vol. 106, N 4. – P. 647–658.

59. The transcriptional repressor DEC2 regulates sleep length in mammals / Y. He [et al.] // Science. – 2009. – Vol. 325. – P. 866–870.

60. Intrinsic diurnal variations in cardiac metabolism and contractile function / M. Young [et al.] // Circ. Res. – 2001. – Vol. 89. – P. 1199–1208.

61. Diurnal variations in the responsiveness of cardiac and skeletal muscle to fatty acids / Stavinoha M. [et al.] // Am. J. Physiol. – 2004. – Vol. 287. – P. E878–E887.

62. Imeri, L. How (and why) the immune system makes us sleep / L. Imeri, M. Opp // Nat. Rev. Neurosci. – 2009. – Vol. 10. – P. 199–210.

63. Krueger, J. The role of cytokines in sleep regulation / J. Krueger // Curr. Pharm. Des. – 2008. – Vol. 14. – P. 3408–3416.

64. Hotamisligil, G. Nutrient sensing and inflammation in metabolic diseases / G. Hotamisligil, E. Erbay // Nat. Rev. Immunol. − 2008. – Vol. 8. – P. 923−934.

65. Examination of the melatonin hypothesis in women exposed at night to EMF or bright light / C. Graham [et al.] // Environ. Health. Perspect. – 2001. – Vol. 109. – P. 501–507.

66. Wojtovicz, M. Melatonin and its role in human reproduction / M. Wojtovicz, G. Jakiel // Ginekol. Pol. – 2002. – Vol. 73, N 12. – P. 1217–1231.

67. Giammanco, S. Effects of environmental lighting and tryptophan devoid diet on the rat vaginal cycle / S. Giammanco, M. Ernandes, M. La Guardia // Arch. Physiol. Biochem. – 1997. – Vol. 105, N 5. – P. 445–449.

68. The role of polymorphisms in circadian pathway genes in breast tumorigenesis / H. Dai [et al.] // Breast. Cancer Res. Treatment. – 2011. – Vol. 127. – P. 531–540.

69. Testing the circadian gene hypothesis in prostate cancer: a population-based case-control study / Y. Zhu [et al.] // Cancer Res. – 2009. – Vol. 69. – P. 9315–9322.

70. Genome-wide profile of pleural mesothelioma versus parietal and visceral pleura: the emerging gene portrait of the mesothelioma phenotype / O. Røe [et al.] // PLoS One. – 2009. – Vol. 4. – P. e6554.

71. Circadian disruption accelerates liver carcinogenesis in mice / E. Filipski [et al.] // Mutat. Res. – 2009. – Vol. 680. – P. 95–105.

72. Адаскевич, В. П. Акне вульгарные и розовые / В. П. Адаскевич. – Н. Новгород : НГМА, 2003. – 195 c.

73. Козин, В. М. Псориаз (вопросы патогенеза, клиники, терапии) / В. М. Козин. – Витебск : ВГМУ, 2007. – 227 с.

74. Мяделец, О. Д. Морфофункциональная дерматология / О. Д. Мяделец, В. П. Адаскевич. – М. : Медлит, 2006. – 752 с.

75. Количественный анализ холестерола мембран кератиноцитов эпидермиса при псориазе / Т. М. Повалий [и др.] // Вестн. дерматологии и венерологии. – 1997. – № 1. – С. 4–6.

76. Эрнандес, Е. И. Липидный барьер кожи и косметические средства / Е. И. Эрнандес, А. А. Марголина, А. О. Петрухина. – 3-е изд. – М. : КЛАВЕЛЬ, 2005. – 400 с.

77. Boehncke, W.-H. Managing comorbid disease in patients with psoriasis / W.-H. Boehncke [et al.] // BMJ. – 2010. – Vol. 340. – P. 200–203.

78. Christofers, E. Comorbidities in psoriasis / E. Christofers // J. Eur. Acad. Dermatol. Venereol. – 2006. – Vol. 20, iss. s2. – P. 52–55.

79. Zouboulis, C. Isotretinoin revisited: pluripotent effects on human sebaceous gland cells / C. Zouboulis // J. Investig. Dermatol. – 2006. – Vol. 126. – P. 2154–2156.

80. Морфологические особенности распределения свободного холестерола в эпидермисе при псориазе / О. С. Зыкова [и др.] // Вестн. Витеб. гос. мед. ун-та. – 2012. – Т. 11, № 1. – С. 42–47.

81. Соболевская, И. С. Некоторые морфометрические показатели липиднакапливающих и липидсинтезирующих структур кожи человека / И. С. Соболевская // Вестн. Витеб. гос. мед. ун-та. – 2012. − Т. 11, № 2. – С. 41–51.


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