Медико-биологический
информационный портал
для специалистов
 
Medline.ru

СОДЕРЖАНИЕ ЖУРНАЛА:
Физико-химическая биология

Клиническая медицина

Профилактическая медицина

Медико-биологические науки


АРХИВ:

Фундаментальные исследования

Организация здравохраниения

История медицины и биологии



Последние публикации

Поиск публикаций

Articles

Архив :  2000 г.  2001 г.  2002 г. 
               2003 г.  2004 г.  2005 г. 
               2006 г.  2007 г.  2008 г. 
               2009 г.  2010 г.  2011 г. 
               2012 г.  2013 г.  2014 г. 
               2015 г.  2016 г.  2017 г. 
               2018 г.  2019 г.  2020 г.  2021 г.  2022 г.  2023 г. 

Редакционная информация:
        Опубликовать статью
        Наша статистика


 РЕДАКЦИЯ:
Главный редактор

Заместители главного редактора

Члены редколлегии
Специализированные редколлегии


 УЧРЕДИТЕЛИ:
Институт теоретической и экспериментальной биофизики Российской академии наук.

ООО "ИЦ КОМКОН".




Адрес редакции и реквизиты

199406, Санкт-Петербург, ул.Гаванская, д. 49, корп.2

ISSN 1999-6314

Российская поисковая система
Искать: 


«
Vol. 21, Art. 20 (pp. 227-235)    |    2020       
»

Early changes in extracellular dna and other parameters in the peripheral blood during irradiation of the bladder
1SBI «N.N. Petrov National Medical Research Center of Oncology» of the Ministry of Healthcare of the Russian Federation
2Granov Russian Scientific Center of Radiology and Surgical Technologies of Ministry of Healthcare of the Russian Federation



Brief summary

On the model of radiation cystitis, the changes in the number of blood cells, extracellular DNA (exDNA) and some indicators of total blood metabolism in serum early after the local exposure of the pelvic area of female Wistar rats at a dose of 25 Gy were studied. The irradiation of the region of the bladder of rats was carried out on a linear electron accelerator. 6 h after the exposure, a decrease in the absolute number of leukocytes, lymphocytes, monocytes were observed, and 24 h - a decrease of granulocytes. At 6 and 24 hours after irradiation, a significant increase in serum exDNA content was observed with normalization after 48 h. Irradiation led to a significant decrease in serum triglycerides content after 24 h after exposure, without changing other studied metabolic parameters. According to the correlation analysis, the relative change in the content of exDNA (0 h vs 6 h) correlated with changes in triglycerides (0 h vs 24 h), in the absence of significant correlations with a decrease in the number of blood cells.


Key words

local radiation, radiation cystitis, blood cells, extracellular DNA, triglycerides.





(The article in PDF format. For preview need Adobe Acrobat Reader)



Open article in new window

Reference list

1. Villeirs L., Tailly Th., Ost P. et al. Hyperbaric oxygen therapy for radiation cystitis after pelvic radiotherapy: systematic review of the recent literature // Int. J. Urology. 2020. Vol. 27, N 2. P. 98-107. doi: 10.1111/iju.14130.


2. Oscarsson N., Müller B., Rosen A. et al. Radiation-induced cystitis treared with hyperbaric oxygen therapy (RICH-ART): a randomized, controlled, phase 2-3 trial // Lancet Oncol. 2019. Vol. 20, N 11. P.1602-1614. doi: 10.1016/S1470-2045(19)30494-2.


3. Lee A.Y., Golden D.W., Bazan J.G. et al. Hematologic nadirs during chemoradiation for anal cancer: temporal characterization and dosimetric predictors // Int. J. Radiation Oncol. Biol. Phys. 2017. Vol. 97, N 2. P. 306-312. doi: 10.1016/j.ijrobp.2016.10.010.


4. Mohamed N.E., Ashour S.E. Role of ethanolic extract of Morus alba leaves on some biochemical and haematological alterations in irradiated male rats // Int. J. Radiat. Biol. 2018. Vol. 94, N 4. P.374-384. doi: 10.1080/09553002.2018.1433888.


5. Snyder M.W., Kircher M., Hill A.J. et al. Cell-free DNA comprises an in vivo nucleosome footprint that informs its tissues-of-origin // Cell. 2016. Vol. 164, ? 1-2. P. 57-68. doi: 10.1016/j.cell.2015.11.050.


6. Vladimirov V.G., Belokhvostov A.S., Sherlina S.S. et al. Extracellular DNA level in the blood of irradiated rats // Int. J. Radiat. Biol. 1992. Vol. 62, ? 6. P.667-671. doi: 10.1080/09553009214552611


7. Vasilyeva I.N. Low-molecular-weight DNA in blood plasma as an index of the influence of ionizing radiation // Ann. NY Acad. Sci. 2001. Vol. 945. P.221-228. doi: 10.1111/j.1749-6632.2001.tb03889.x


8. Vasilyeva I., Bespalov V., Baranova A. Radioprotective combination of α-tocopherol and ascorbic acid promotes apoptosis that is evident by release of low-molecular weight DNA fragments into circulation // Int. J. Radiat. Biol. 2015. Vol. 91, N 11. P.872-877. doi: 10.3109/09553002.2015.1087066.


9. Ashry O.M., Hussein E.M., Abd El-Azime A.SH. Restorative role of persimmon leaf (Diospyros kaki) to gamma irradiation induced oxidative stress and tissue injury in rats / Int. J. Radiat. Biol. 2017. Vol. 93, N 3. P. 324-329. doi: 10.1080/09553002.2016.1254831.


10. Liu J., Au Yeng Sh.L., Kwok M.K. et al. The effect of liver enzyme on bone composition: a mendelian randomization study / PLoS ONE. 2020. Vol. 15, N 2. 18 r. doi: 10.1371/journal.pone.0228737.


11. Lenarczyk M., Kronenberg A., Mader M. et al. Age of exposure to radiatiation determined severity of renal and cardiac disease in rats / Radiat. Res. 2019. Vol. 192, N1. P. 63-67. doi: 10.1667/RR15043.


12. Vasilyeva I.N., Bespalov V.G., Von J.D. et al. Cell-free DNA plasma levels differ in age-specific pattern in healthy rats and castrated with testosterone-induced benign prostatic hyperplasia / Int. J. Genomics. 2019. 6 r. doi: 10.1155/2019/8173630.


13. Brengues M., Lapierre A., Bourgier C. et al. T lymphocytes to predict radiation-induced late effects in normal tissues / Expert Rev Mol Diagn. 2017. Vol.17, N 2. P.119-127. doi: 10.1080/14737159.2017.1271715.


14. Holdenrieder S., Stiber P. Clinical use of circulating nucleosomes / Crit. Rev. Clin. Lab. Sci. 2009. Vol. 46, N 1. P.1-24. doi: 10.1080/10408360802485875.


15. Holdenrieder S. Liquid Profiling of Circulating Nucleic Acids as a Novel Tool for the Management of Cancer Patients / Advances in Experimental Medicine and Biology. 2016. Vol. 924. P.53-60. doi: 10.1007/978-3-319-42044-8_11.


16. Ermakov A.V., Konkova M.S., Kostyuk S.V. et al. Oxidized extracellular DNA as a stress signal in human cells / Oxid. Med. Cell. Longev. 2013. doi: 10.1155/2013/649747.


17. Kostyuk S.V., Ermakov A.V., Alekseeva A.Yu. et al. Role of extracellular DNA oxidative modification in radiation induced bystander effects in human endotheliocytes / Mut. Res. 2012. Vol. 729, N 1-2. P. 52-60. doi: 10.16/j.mrfmmm.2011.09.005.


18. Ko S.H., Lee J.K., Lee H.J. et al. 8-Oxo-2'-deoxyguanosine ameliorates features of metabolic syndrome in obese mice / Biochem. Biophys. Res. Commun. 2014. Vol. 443, N 2. P. 610-616. doi: 10.1016/j.bbrc.2013.12.018.


19. Huh J.Y., Son D.J., Lee Y. et al. 8-Hydroxy-2-deoxyguanosine prevents plaque formation and inhibits vascular smooth muscle cell activation through Rac1 inactivation / Free Radic. Biol. Med. 2012. Vol. 53, N 1. P.109-121. doi: 10.1016/j.freeradbiomed.2012.03.023.


20. Teng M.-Sh., Wu S., Hsu L.A. et al. Pleiotropic association of LIPS variants with lipid and urinary 8-hydroxy deoxyguanosine levels in a Taivanese populations / Lipids Health Dis. 2019. Vol. 18, N 1. P.111. doi: 10.1186/s12944-019-1057-9.





Свидетельство о регистрации сетевого электронного научного издания N 077 от 29.11.2006
Журнал основан 16 ноября 2000г.
Выдано Министерством РФ по делам печати, телерадиовещания и средств массовых коммуникаций
(c) Перепечатка материалов сайта Medline.Ru возможна только с письменного разрешения редакции

Размещение рекламы

Rambler's Top100