Features of the gas transport function of blood in hyperpigmentations of the skin
Maria V. Glushkova , Oleg G. Sarkisian , Olga A. Sidorenko , Anastasia S. Stradanchenko
Russian Journal of Skin and Venereal Diseases ›› 2024, Vol. 27 ›› Issue (2) : 169 -177.
Features of the gas transport function of blood in hyperpigmentations of the skin
BACKGROUND: Acquired hyperpigmentation is widespread in the population and significantly affects the quality of life of the patients. It is known that one of the clinical signs of skin hyperpigmentation is localized hyperkeratosis in the lesion associated with a high level of cell proliferation and cell saturation with melanin. Cellular proliferation and hyperkeratosis are associated with increased local metabolism rates.
AIM: Study of erythrocyte gas transport function in women with skin hyperpigmentation compared to the control group.
MATERIALS AND METHODS: To achieve the objective, the concentrations of lactic acid, pyruvic acid and 2,3-diphosphoglycerate levels in venous blood erythrocytes were investigated.
RESULTS: The phenomenon of skin hyperpigmentation is accompanied by a restructuring of blood cell metabolism aimed at preserving oxygen and energy homeostasis of skin structures. The obtained data indicate redistribution of oxygen in cellular structures and tissues, which is accompanied by a significant increase in lactate concentration and formation of local tissue hypoxia.
CONCLUSION: The formation of skin pigmentation is considered as a physiological mechanism in response to inflammation, mainly associated with ultraviolet radiation. The general strategy of the course of the inflammatory process under normal regulation or dysregulation has similar features, but there are also differences. It seems necessary to further study systemic adaptation mechanisms in dysregulation and formation of skin hyperpigmentation.
hyperpigmentation / melisma / lactate / pyruvate
| [1] |
Guide to cosmetology. Ed. by A.A. Kubanov, N.E. Manturova, Y.A. Galliamova. Moscow: Nauchnoe obozrenie; 2020. 728 р. (In Russ). |
| [2] |
Руководство по косметологии / под ред. А.А. Кубанова, Н.Е. Мантуровой, Ю.А. Галлямовой. Москва: Научное обозрение, 2020. 728 с. |
| [3] |
Atlas of cosmetic dermatology. Translation from English N.N. Potekaev, M.R. Avram, S. Tszao, et al. Moscow: Binnom; 2013. 295 р. (In Russ). |
| [4] |
Атлас косметической дерматологии / пер. с англ. под ред. Н.Н. Потекаева, М.Р. Аврам, С. Цзао, и др. Москва: Бинном, 2013. 295 с. |
| [5] |
Kim NH, Lee CH, Lee AY. H19 RNA downregulation stimulated melanogenesis in melisma. Pigment Cell Melanoma Res. 2010;23(1):84–92. doi: 10.1111/j.1755-148X.2009.00659.x |
| [6] |
Kim N.H., Lee C.H., Lee A.Y. H19 RNA downregulation stimulated melanogenesis in melisma // Pigment Cell Melanoma Res. 2010. Vol. 23, N 1. P. 84–92. doi: 10.1111/j.1755-148X.2009.00659.x |
| [7] |
Burylina OM, Karpova AV. Cosmetology: Clinical guide. Moscow: GEOTAR-Media; 2018. 744 р. (In Russ). |
| [8] |
Бурылина О.М., Карпова А.В. Косметология: клиническое руководство. Москва: ГЭОТАР-Медиа, 2018. 744 с. |
| [9] |
Kim EH, Kim YC, Lee ES, Kang HY. The vascular characteristics of melasma. J Dermatol Sci. 2007;46(2):111–116. doi: 10.1016/j.jdermsci.2007.01.009 |
| [10] |
Kim E.H., Kim Y.C., Lee E.S., Kang H.Y. The vascular characteristics of melisma // J Dermatol Sci. 2007. Vol. 46, N 2. P. 111–116. doi: 10.1016/j.jdermsci.2007.01.009 |
| [11] |
Torres-Alvarez B, Mesa-Garza IG, Castanedo-Cazares JP, et al. Histochemical and immunohistochemical study in melasma: Evidence of damage in the basal membrane. Am J Dermatopathol. 2011;33(3):291–295. doi: 10.1097/DAD.0b013e3181ef2d45 |
| [12] |
Torres-Alvarez B., Mesa-Garza I.G., Castanedo-Cazares J.P., et al. Histochemical and immunohistochemical study in melasma: Evidence of damage in the basal membrane // Am J Dermatopathol. 2011. Vol. 33, N 3. P. 291–295. doi: 10.1097/DAD.0b013e3181ef2d45 |
| [13] |
Ryazantseva NV, Novitsky VV. Erythrocyte in dysregulation pathology: “Outside observer” or “Active participant”. In: Barkagan Z.S., Butorina E.V., Goldberg E.D., et al. Dysregulation pathology of the blood system. Moscow: Meditsinskoe informatsionnoe agentstvo; 2009. Р. 231–256. (In Russ). EDN: SLIERL |
| [14] |
Рязанцева Н.В., Новицкий В.В. Эритроцит при дизрегуляционной патологии: «Сторонний наблюдатель» или «Активный участник». Глава в кн.: Баркаган З.С., Буторина Е.В., Гольдберг Е.Д., и др. Дизрегуляционная патология системы крови. Москва: Медицинское информационное агентство, 2009. С. 231–256. EDN: SLIERL |
| [15] |
Dayce BJ, Bressman SP. A rapid nonezyraatic assay for 2.3-DPG in muetiple specimens of blood. Arch Environ Health. 1973;27(2):112–115. doi: 10.1080/00039896.1973.10666331 |
| [16] |
Dayce B.J., Bressman S.P. A rapid nonezyraatic assay for 2.3-DPG in muetiple specimens of blood // Arch Environ Health. 1973. Vol. 27, N 2. P. 112–115. doi: 10.1080/00039896.1973.10666331 |
| [17] |
Luganova IS, Blinov MN. Determination of 2,3-BFG by a nonenzymatic method and ATP in erythrocytes of patients with chronic lymphocytic leukemia. Laboratornoe delo. 1975;(7):652–654. (In Russ). |
| [18] |
Луганова И.С., Блинов М.Н. Определение 2,3-БФГ неэнзиматическим методом и АТФ в эритроцитах больных хроническим лимфолейкозом // Лабораторное дело. 1975. № 7. С. 652–654. |
| [19] |
Klimov AN, Parfenova NS, Golikov YuP. To the 100th anniversary of the creation of the cholesterol model of atherosclerosis. Biomedical Chemistry. 2012;58(1):5–11. EDN: OPUYIN doi: 10.18097/pbmc20125801005 |
| [20] |
Климов А.Н., Парфенова Н.С., Голиков Ю.П. К 100-летию создания холестериновой модели атеросклероза // Биомедицинская химия. 2012. Т. 58, № 1. С. 5–11. EDN: OPUYIN doi: 10.18097/pbmc20125801005 |
| [21] |
Kryzhanovsky GN. Dysregulatory pathology. Pathogenesis. 2002;2(1):34–35. EDN: RMMAHV |
| [22] |
Крыжановский Г.Н. Дизрегуляционная патология // Патогенез. 2002. Т. 2, № 1. С. 34–35. EDN: RMMAHV |
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