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1Academic Journal
Source: Репродуктивное здоровье. Восточная Европа. :109-116
Subject Terms: 0301 basic medicine, pregnancy management, докозагексаеновая кислота, folate complex, gestosis, профилактика невынашивания беременности, профилактика врожденных пороков развития плода, docosahexaenoic acid, гестоз, фолатный комплекс, 3. Good health, 03 medical and health sciences, 0302 clinical medicine, prevention of miscarriage, планирование беременности, prevention of congenital malformations of the fetus, профилактика преждевременных родов, pregnancy planning, prevention of premature birth, fetoplacental insufficiency, ведение беременности, reproductive health, репродуктивное здоровье, фетоплацентарная недостаточность
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2Academic Journal
Source: Педиатрия. Восточная Европа. :259-267
Subject Terms: 0301 basic medicine, 2. Zero hunger, 0303 health sciences, eicosapentaenoic acid, докозагексаеновая кислота, длинноцепочечные полиненасыщенные жирные кислоты, дети, docosahexaenoic acid, эйкозапентаеновая кислота, immunity, 3. Good health, long-chain polyunsaturated fatty acids, иммунитет, 03 medical and health sciences, nutrition, children, arachidonic acid. cognitive functions, когнитивные функции, питание, арахидоновая кислота
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3Academic Journal
Authors: Lyudinina A.Y., Parshukova O.I., Bojko E.R.
Contributors: The study was carried out at the expense of subsidies for the implementation of State Assignment No. GR1021051201877-3-3.1.8 (2022–2026)., Работа выполнена за счет средств субсидии на выполнение Государственного задания № ГР1021051201877-3-3.1.8 (2022–2026).
Source: Marine Medicine; Vol 9, No 2 (2023); 68-76 ; Морская медицина; Vol 9, No 2 (2023); 68-76 ; 2587-7828 ; 2413-5747
Subject Terms: marine medicine, fatty acids, n-3 docosahexaenoic acid, α-linolenic acid, combat stress, OMON fighters, employees of the MES, functional state, морская медицина, жирные кислоты, n-3 докозагексаеновая кислота, α-линоленовая кислота, боевой стресс, бойцы ОМОНа, сотрудники МЧС, функциональное состояние
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4Academic Journal
Authors: B. R. Gvasalia, A. V. Isaeva, M. U. Babaev, Б. Р. Гвасалия, А. В. Исаева, М. У. Бабаев
Source: Andrology and Genital Surgery; Том 24, № 4 (2023); 59-66 ; Андрология и генитальная хирургия; Том 24, № 4 (2023); 59-66 ; 2412-8902 ; 2070-9781
Subject Terms: эйкозапентаеновая кислота, idiopathic infertility, oxidative stress, antioxidant therapy, DNA fragmentation, L-carnitine, omega-3, docosahexaenoic acid, eicosapentaenoic acid, идиопатическое бесплодие, оксидативный стресс, антиоксидантная терапия, фрагментация ДНК, L-карнитин, омега-3, докозагексаеновая кислота
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Postepy Hig Med Dosw (Online) 2005;59:523–34.; Plante M., De Lamirande E., Gagnon C. Reactive oxygen species released by activated neutrophils, but not by deficient spermatozoa, are sufficient to affect normal sperm motility. Fertil Steril 1994;62(2):387–93. DOI:10.1016/s0015-0282(16)56895-2; Henkel R.R. Leukocytes and oxidative stress: dilemma for sperm function and male fertility. Asian J Androl 2011;13(1):43–52. DOI:10.1038/aja.2010.76; Martins da Silva S.J. Male infertility and antioxidants: one small step for man, no giant leap for andrology? Reprod Biomed Online 2019;39(6):879–83. DOI:10.1016/j.rbmo.2019.08.008; Majzoub A., Agarwal A. Systematic review of antioxidant types and doses in male infertility: benefits on semen parameters, advanced sperm function, assisted reproduction and live-birth rate. Arab J Urol 2018;16(1):113–24. DOI:10.1016/j.aju.2017.11.013; Simon L., Zini A., Dyachenko A. et al. A systematic review and meta-analysis to determine the effect of sperm DNA damage on in vitro fertilization and intracytoplasmic sperm injection outcome. Asian J Androl 2017;19(1):80–90. DOI:10.4103/1008-682X.182822; Henkel R., Morris A., Vogiatzi P. et al. Predictive value of seminal oxidation-reduction potential analysis for reproductive outcomes of ICSI. Reprod Biomed Online 2022;45(5):1007–20. DOI:10.1016/j.rbmo.2022.05.010; Hervás I., Pacheco A., Gil Julia M. et al. Sperm deoxyribonucleic acid fragmentation (by terminal deoxynucleotidyl transferase biotin dUTP nick end labeling assay) does not impair reproductive success measured as cumulative live birth rates per donor metaphase II oocyte used. Fertil Steril 2022;118(1):79–89. DOI:10.1016/j.fertnstert.2022.04.002; Наумов Н.П., Щеплев П.А., Полозов В.В. Роль антиоксидантов в профилактике мужского бесплодия. Андрология и генитальная хирургия 2019; 20(1):22–9. DOI:10.17650/2070-9781-2019-20-1-22-29; Корнеев И.А. Мужское бесплодие при оксидативном стрессе: пути решения проблемы. Урология 2022;1:102–8. DOI:10.18565/urology.2022.1.102-108; Yan L., Liu J., Wu S. et al. Seminal superoxide dismutase activity and its relationship with semen quality and SOD gene polymor-phism. J Assist Reprod Genet 2014;31(5):549–54. DOI:10.1007/s10815-014-0215-2; Macanovic B., Vucetic M., Jankovic A. et al. Correlation between sperm parameters and protein expression of antioxidative defense enzymes in seminal plasma: a pilot study. Dis Markers 2015;2015:436236. DOI:10.1155/2015/436236; Gałecka E., Jacewicz R., Mrowicka M. et al. [Antioxidative enzymes – structure, properties, functions (In Polish)]. Pol Merkur Lekarski 2008;25(147):266–8.; Yeung C.H., Cooper T.G., De Geyter M. et al. Studies on the origin of redox enzymes in seminal plasma and their relationship with results of in vitro fertilization. Mol Hum Reprod 1998;4(9):835–9. DOI:10.1093/molehr/4.9.835; Crisol L., Matorras R., Aspichueta F. et al. Glutathione peroxidase activity in seminal plasma and its relationship to classical sperm parameters and in vitro fertilization intracytoplasmic sperm injection outcome. Fertil Steril 2012;97(4):852–7. DOI:10.1016/j.fertnstert.2012.01.097; Гамидов С.И., Шатылко Т.В., Ли К.И., Гасанов Н.Г. Роль антиоксидантных молекул в терапии мужского бесплодия и подготовке мужчины к зачатию ребенка. Медицинский совет 2020;(3):122–9. DOI:10.21518/2079-701X2020-3-122-129; Walczak-Jedrzejowska R., Wolski J.К., Slowikowska-Hilczer J. The role of oxidative stress and antioxidants in male fertilityю. Cent European J Urol 2013;66(1):60–7. DOI:10.5173/ceju.2013.01.art19; Li X., Long X.Y., Xie Y.J. et al. The roles of retinoic acid in the differentiation of spermatogonia and spermatogenic disorders. Clin Chim Acta 2019;497:54–60. DOI:10.1016/j.cca.2019.07.013; Yang Y., Luo J., Yu D. et al. Vitamin A promotes Leydig cell differentiation via alcohol dehydrogenase 1. Front Endocrinol (Lausanne) 2018;9:644. DOI:10.3389/fendo.2018.00644.; Zhou Y., Zhang D., Hu D. et al Retinoic acid: a potential therapeutic agent for cryptorchidism infertility based on investigation of flutamide-induced cryptorchid rats in vivo and in vitro. Reprod Toxicol 2019;87:108–17. DOI:10.1016/j.reprotox.2019.05.063; Comhaire F. The role of food supplementation in the treatment of the infertile couple and for assisted reproduction. Andrologia 2010;42(5):331–40. DOI:10.1111/j.1439-0272.2009.01025.x; Colagar A.Н., Marzony E.T. Ascorbic acid in human seminal plasma: determination and its relationship to sperm quality. J Clin Biochem Nutr 2009;45(2):144–9. DOI:10.3164/jcbn.08-251; Song G.J., Norkus E.P., Lewis V. Relationship between seminal ascorbic acid and sperm DNA integrity in infertile men. Int J Androl 2006;29(6):569–75. DOI:10.1111/j.1365-2605.2006.00700.x; Lanzafame F.M., La Vignera S., Vicari E., Calogero A.E. Oxidative stress and medical antioxidant treatment in male infertility. Reprod Biomed Online 2009;19(5):638–59. DOI:10.1016/j.rbmo.2009.09.014; Hambidge K.M., Krebs N.F. Zinc deficiency: a special challenge. J Nutr 2007;137(4):1101–5. DOI:10.1093/jn/137.4.1101; Omu A.E., Al-Azemi M.K., Al-Maghrebi M. et al. Molecular basis for the effects of zinc deficiency on spermatogenesis: an experimental study in the Sprague-Dawley rat model. Indian J Urol 2015;31(1):57–64. DOI:10.4103/0970-1591.139570; Giahi L., Mohammadmoradi S., Javidan A., Sadeghi M.R. Nutritional modifications in male infertility: a systematic review covering 2 decades. Nutr Rev 2016;74(2):118–30. DOI:10.1093/nutrit/nuv059; Zhao J., Dong X., Hu X. et al. Zinc levels in seminal plasma and their correlation with male infertility: a systematic review and meta-analysis. Sci Rep 2016;6:22386. DOI:10.1038/srep22386; Atig F., Raffa M., Ali H.B. et al. Altered antioxidant status and increased lipid per-oxidation in seminal plasma of tunisian infertile men. Int J Biol Sci 2012;8(1):139–49. DOI:10.7150/ijbs.8.139; Flohé L. Selenium in mammalian spermiogenesis. Biol Chem 2007;388(10):987–95. DOI:10.1515/BC.2007.112; Mossa M.M., Azzawi M.H., Dekhel H.H. et al. Effect of selenium in treatment of male infertility. Exp Tech Urol Nephrol 2018;1(5): ETUN.000521. DOI:10.31031/ETUN.2018.01.000521; Ma L. , Sun Y. Comparison of L-Carnitine vs. Coq10 and Vitamin E for idiopathic male infertility: a randomized controlled trial. Randomized Controlled Trial. Eur Rev Med Pharmacol Sci 2022;26(13):4698–704. DOI:10.26355/eurrev_202207_29194; Gvozdjáková A., Kucharská J., Dubravicky J. et al. Coenzyme Q10, α-tocopherol, and oxidative stress could be important metabolic biomarkers of male infertility. Dis Markers 2015;2015:827941. DOI:10.1155/2015/827941; Safarinejad M.R. The effect of coenzyme Q10 supplementation on partner pregnancy rate in infertile men with idiopathic oligoasthenoteratozoospermia: an open-label prospective study. Int Urol Nephrol 2012;44(3):689–700. 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Effect of folic acid and Zinc supplementation in men on semen quality and live birth among couples undergoing infertility treatment: a randomized clinical trial. JAMA 2020;323(1):35–48. DOI:10.1001/jama.2019.18714; Ozer Kaya S., Kandemir F.M., Gur S. et al. Evaluation of the role of L-arginine on spermatological parameters, seminal plasma nitric oxide levels and arginase enzyme activities in rams. Andrologia 2020;52(1):e13439. DOI:10.1111/and.13439; Comhaire F., Christophe A., Zalata A. et al. The effects of combined conventional treatment, oral antioxidants and essential fatty acids on sperm biology in subfertile men. Prostaglandins Leukot Essent Fatty Acids 2000;63(3):159–65. DOI:10.1054/plef.2000.0174; Martínez-Soto J.C., Domingo J.C., Cordobilla B. et al. Dietary supplementation with docosahexaenoic acid (DHA) improves seminal antioxidant status and decreases sperm DNA fragmentation. Syst Biol Reprod Med 2016;62(6):387–95. 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5Academic Journal
Authors: Feofilaktova, O.V., Zavorokhina, N.V.
Subject Terms: 664.324.6 [УДК 664.346], эмульсионные соусы, mode of production, ультразвуковая гомогенизация, докозагексаеновая кислота, fish fat, ω-3 fatty acids EPA, эйко-запентаеновая кислота, formulation, linseed oil, mustard oil, DHA, emulsion sauces, ω-3 жирные кислоты, ultrasonic homogenization, комплекс растительных масел, camelina oil, рыбий жир, полиненасыщенные жирные кислоты, PUFA
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6Academic Journal
Authors: N. A. Ishutina, I. A. Andrievskaya, N. G. Prikhodko, Н. А. Ишутина, И. А. Андриевская, Н. Г. Приходько
Contributors: Исследование проводилось за счет средств федерального бюджета в рамках государственного задания ФНИ (тема 061, № госрегистрации АААА-А18-118020790064-4).
Source: Acta Biomedica Scientifica; Том 6, № 3 (2021); 43-52 ; 2587-9596 ; 2541-9420
Subject Terms: докозагексаеновая кислота, cytomegalovirus infection, hypoxia-inducible factor 1α, α-tocopherol, docosahexaenoic acid, цитомегаловирусная инфекция, гипоксией индуцируемый фактор 1α, α-токоферол
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Int J Reprod Biomed. 2020; 18 (7): 501–508. doi:10.18502/ijrm.v13i7.7367; Li JM, Zhang HF, Zhang XQ, Huang GL, Huang HZ, Yu WW. Genetic mechanism associated with congenital cytomegalovirus infection and analysis of effects of the infection on pregnancy outcome. Genet Mol Res. 2015; 14 (4): 13247–13257. doi:10.4238/2015.October.26.21; Njue A, Coyne C, Margulis AV, Wang D, Marks MA, Russell K, et al. The Role of Congenital Cytomegalovirus Infection in Adverse Birth Outcomes: A Review of the Potential Mechanisms. Viruses. 2020; 13 (1): 20. doi:10.3390/v13010020; Pass RF, Arav-Boger R. Maternal and fetal cytomegalovirus infection: diagnosis, management, and prevention. F1000Res. 2018; 7: 255. doi:10.12688/f1000research.12517.1; Стрижаков А. Н., Кушлинский Н. Е., Тимохина Е. В., Тарабрина Т. В. Роль ангиогенных факторов роста в прогнозировании плацентарной недостаточности. Вопросы гинекологии, акушерства и перинатологии. 2009; 8 (4): 5–11; Михайлин Е. С., Толибова Г. Х., Траль Т. Г. Морфофункциональные особенности последов у несовершеннолетних женщин. Журнал акушерства и женских болезней. 2016; 65 (5): 41–48. doi.org/10.17816/JOWD65541-48; Большакова М. В., Беженарь В. Ф., Павлова Н. Г., Пастушенков В. Л., Габаева М. М. Современные представления о патогенезе гипоксии плода и роли в нем гипоксия-индуцируемого фактора (HIF). Акушерство и гинекология Санкт-Петербурга. 2019; 1: 19–24.; Macklin PS, McAuliffe J, Pugh CW, Yamamoto A. Hypoxia and HIF pathway in cancer and the placenta. Placenta. 2017; 56: 8–13. doi:10.1016/j.placenta.2017.03.010; Yu N, Wu JL, Xiao J, Fan L, Chen SH, Li W. HIF-1α regulates angiogenesis via Notch1/STAT3/ETBR pathway in trophoblastic cells. Cell Cycle. 2019; 18 (24): 3502–3512. doi:10.1080/15384101.2019.1689481; Pandya AD, Das MK, Sarkar A, Vilasagaram S, Basak S, Duttaroy AK. Tube formation in the first trimester placental trophoblast cells: Differential effects of angiogenic growth factors and fatty acid. Cell. Biol. Int. 2016; 40 (6): 652–661. doi:10.1002/cbin.10601; Kasture V, Sundrani D, Dalvi S, Swamy M, Kale A, Joshi S. Maternal omega-3 fatty acids and vitamin E improve placental angiogenesis in late-onset but not early-onset preeclampsia. Mol. Cell. Biochem. 2019; 461 (1-2): 159–170. doi:10.1007/s11010-019-03599-4; Taneda S, Honda K, Tomidokoro K, Uto K, Nitta K, Oda H. Eicosapentaenoic acid restores diabetic tubular injury through regulating oxidative stress and mitochondrial apoptosis. Am. J. Physiol. Renal. Physiol. 2010; 299 (6): F1451-F1461. doi:10.1152/ajprenal.00637.2009; Rathod RS, Khaire AA, Kale AA, Joshi SR. Maternal omega-3 fatty acid supplementation to a vitamin B12 deficient diet normalizes angiogenic markers in the pup brain at birth. Int. J. Dev Neurosci. 2015; 43 (1): 43–49. doi:10.1016/j.ijdevneu.2015.04.006; Hansen LG, Warwich WI. Flurometric micromethod for serum tocoferol. Am. J. Chen Pathology. 1966; 36 (1): 137–138.; Морозова О. Л., Мальцева Л. Д., Макарова В. Д. VEGF – маркер гипоксии при повреждении почек различного генеза. Патогенез. 2018; 16 (2): 62–69. doi:10.25557/2310–0435.2018.0262–69; Azliana AF, Zainul-Rashid MR, Chandramaya SF, Farouk WI, Nurwardah A, Wong YP, Tan GC. Vascular endothelial growth factor expression in placenta of hypertensive disorder in pregnancy. Indian J Pathol Microbiol. 2017; 60 (4): 515–520. doi:10.4103/IJPM.IJPM_376_16; Макаров О. В., Волкова Е. В., Лысюк Е. Ю., Копылова Ю. В. Фетоплацентарный ангиогенез у беременных с плацентарной недостаточностью. Акушерство, гинекология, репродукция. 2013; 7 (3): 13–19; Zhao H, Narasimhan P, Kalish F, Wong RJ, Stevenson DK. Dysregulation of hypoxia-inducible factor-1α (Hif1α) expression in the Hmox1-deficient placenta. Placenta. 2020; 99: 108–116. doi:10.1016/j.placenta.2020.07.015; Левченкова О. С., Новиков В. Е. Индукторы регуляторного фактора адаптации к гипоксии. Российский медико-биологический вестник им. акад. И. П. Павлова. 2014; 2: 135–145; Мельник А. А. Гипоксией индуцированный фактор для лечения анемии при хронической болезни почек. Почки. 2018; 7 (4): 311–321. doi:10.22141/2307–257.7.4.2018.148522; Беженарь В. Ф., Павлова Н. Г., Большакова М. В., Пастушенков В. Л., Карев В. Е. Экспрессия гипоксия- индуцированого фактора (HIF1α) в плацентах при хронической плацентарной недостаточности в конце беременности. Уральский медицинский журнал. 2020; 5 (188): 141–145. doi:10.25694/URMJ.2020.05.29; Ишутина Н. А., Андриевская И. А., Дорофиенко Н. Н. Малоновый диальдегид и фактор некроза опухолей α в периферической крови беременных с цитомегаловирусной инфекцией. Бюллетень физиологии и патологии дыхания. 2015; 55: 78–81; de Wit RH, Mujić-Delić A, van Senten JR, Fraile-Ramos A, Siderius M, Smit MJ. Human cytomegalovirus encoded chemokine receptor US28 activates the HIF-1α/PKM2 axis in glioblastoma cells. Oncotarget. 2016; 7 (42): 67966–67985. doi:10.18632/oncotarget.11817; He C, Shan N, Xu P, Ge H, Yuan Y, Liu Y, et al. Hypoxiainduced Downregulation of SRC-3 Suppresses Trophoblastic Invasion and Migration Through Inhibition of the AKT/mTOR Pathway: Implications for the Pathogenesis of Preeclampsia. Sci Rep. 2019; 9 (1): 10349. doi:10.1038/s41598-019-46699-3; Ишутина Н. А., Дорофиенко Н. Н. Пероксидация липидов при беременности, осложненной цитомегаловирусной инфекцией. Бюллетень физиологии и патологии дыхания. 2014; 54: 56–59; Kasimanickam RK, Kasimanickam VR, Haldorson GJ, Tibary A. Effect of tocopherol supplementation during last trimester of pregnancy on mRNA abundances of interleukins and angiogenesis in ovine placenta and uterus. Reprod. Biol. Endocrinol. 2012; 10:4. doi:10.1186/1477-7827-10-4; Kasimanickam RK, Kasimanickam VR, Rodriguez JS, Pelzer KD, Sponenberg PD, Thatcher CD. Tocopherol induced angiogenesis in placental vascular network in late pregnant ewes. Reprod. Biol. Endocrinol. 2010; 8: 86. doi.org/10.1186/1477-7827-8-86; Basak S, Das MK, Duttaroy AK. Fatty acid-induced angiogenesis in first trimester placental trophoblast cells: possible roles of cellular fatty acid-binding proteins. Life Sci. 2013; 93 (21): 755–762. doi:10.1016/j. lfs.2013.09.024; Rada CC, Murray G, England SK. The SK3 channel promotes placental vascularization by enhancing secretion of angiogenic factors. American Journal of physiology, endocrinology and metabolism. 2014; 307 (10): E935–943. doi:10.1152/ajpendo.00319.2014; Irwin DC, McCord JM, Nozik-Grayck E, Beckly G, Foreman B, Sullivan T, White M, T Crossno JJr, Bailey D, Flores SC, Majka S, Klemm D, van Patot MC. A potential role for reactive oxygen species and the HIF-1alpha-VEGF pathway in hypoxiainduced pulmonary vascular leak. Free Radic Biol Med. 2009; 47 (1): 55–61. doi:10.1016/j.freeradbiomed.2009.03.027; https://www.actabiomedica.ru/jour/article/view/2844
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7Academic Journal
Authors: Gladyshev, Michail I., Morgun, Vasiliy N., Guseynova, Valeriya E., Sushchik, Nadezhda N., Гладышев, М. И., Моргун, В. Н., Гусейнова, В. Е., Сущик, Н. Н.
Subject Terms: least cisco, Arctic cisco, muksun, broad whitefish, eicosapentaenoic acid, docosahexaenoic acid, FA profiles, cold smoking, ряпушка, арктический омуль, муксун, чир, эйкозапентаеновая кислота, докозагексаеновая кислота, профили жирных кислот, холодное копчение
Relation: Журнал сибирского федерального университета. 2024 17(4). Journal of Siberian Federal University. Biology 2024 17(4); SJIXGQ
Availability: https://elib.sfu-kras.ru/handle/2311/154342
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8Academic Journal
Source: Reproductive Endocrinology; № 47 (2019); 54-62
Репродуктивная эндокринология; № 47 (2019); 54-62
Репродуктивна ендокринологія; № 47 (2019); 54-62Subject Terms: 2. Zero hunger, довголанцюгові поліненасичені жирні кислоти, докозагексаєнова кислота, арахідонова кислота, ейкозапентаєнова кислота, діти раннього віку, 03 medical and health sciences, long-chain polyunsaturated fatty acids, docosahexaenoic acid, arachidonic acid, eicosapentaenoic acid, infants and toddlers, 0302 clinical medicine, длинноцепочечные полиненасыщенные жирные кислоты, докозагексаеновая кислота, арахидоновая кислота, ейкозапентаеновая кислота, дети раннего возраста, 3. Good health
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Access URL: http://reproduct-endo.com/article/view/170090
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9Report
Authors: A A Makhova, Evgeniya V. Shikh
Source: Voprosy pitaniia. 88(2)
Subject Terms: 0301 basic medicine, Adult, Male, 2. Zero hunger, 0303 health sciences, Adolescent, докозагексаеновая кислота, Anti-Inflammatory Agents, eicosapentaenoicacid, Lipid Metabolism, эйкозапентаеновая кислота, полиненасыщенные жирные кислоты семейства ω-3, 3. Good health, ω-3long-chainpolyunsaturated fatty acids, 03 medical and health sciences, Cognition, Sex Factors, Pregnancy, Child, Preschool, Dietary Supplements, Fatty Acids, Omega-3, Humans, Female, Child, docosahexaenoicacid
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10Academic Journal
Authors: I. V. Vinogradov, A. R. Zhivulko, L. M. Vinogradova, S. V. Korolev, И. В. Виноградов, А. Р. Живулько, Л. М. Виноградова, С. В. Королев
Source: Andrology and Genital Surgery; Том 19, № 4 (2018); 21-27 ; Андрология и генитальная хирургия; Том 19, № 4 (2018); 21-27 ; 2412-8902 ; 2070-9781 ; 10.17650/2070-9781-2018-19-4
Subject Terms: фрагментация ДНК сперматозоидов, docosahexaenoic acid, male infertility, sperm DNA fragmentation, докозагексаеновая кислота, мужское бесплодие
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Relation: https://agx.abvpress.ru/jour/article/view/317/288; Greenhall E., Vessey M. The prevalence of subfertility: a review of the current confusion and a report of two new studies. Fertil Steril 1990;54(6):978—83. PMID: 2245856.; Krausz C., Escamilla A.R., Chianese C. Genetics of male infertility: from research to clinic. Reproduction 2015;150(5):159 —74. DOI:10.1530/REP-15-0261. PMID: 26447148.; Esmaeili V., Shahverdi A. H., Moghadasian M.H., Alizadeh A. R. Dietary fatty acids affect semen quality: a review. Andrology 2015;3(3):450—61. DOI:10.1111/andr.12024. PMID: 25951427.; Sanhueza Catalan J., Duran AgUero S., Torres Garcia J. [The fatty acids and relationship with health (In Spanish)]. Nutr Hosp 2015;32(3):1362—75. DOI:10.3305/nh.2015.32.3.9276. PMID: 26319861.; Zerbinati C., Caponecchia L., Rago R. et al. Fatty acids profiling reveals potential candidate markers of semen quality. Andrology 2016;4(6):1094—101. DOI:10.1111/andr.12236. PMID: 27673576.; Rodriguez-Cruz M., Serna D.S. Nutrigenomics of ю-3 fatty acids: Regulators of the master transcription factors. Nutrition 2017;41:90-6. DOI:10.1016/j.nut.2017.04.012. PMID: 28760435.; Andersen J., Ronning P., Herning H. et al. Fatty acid composition of spermatozoa is associated with BMI and with semen quality. Andrology 2016;4(5):857—65. DOI:10.1111/andr.12227. PMID: 27371336.; Hashimoto M., Hossain S., Mamun A. et al. Docosahexaenoic acid: one molecule diverse functions. Crit Rev Biotechnol 2017;37(5):579—97. DOI:10.1080/07388551.2016.1207153. PMID: 27426008.; Rato L., Alves M.G., Cavaco J.E. et al. High-energy diets: a threat for male fertility? Obes Rev 2014;15(12):996—1007. DOI:10.1111/obr.12226. PMID: 25346452.; Mitre R., Cheminade C., Allaume P. et al. Oral intake of shark liver oil modifies lipid composition and improves motility and velocity of boar sperm. Theriogenology 2004;62(8):1557—66. DOI:10.1016/j.theriogenology.2004.02.004. PMID: 15451263.; Castellano C.-A., Audet I. Bailey J. et al. Effect of dietary n-3 fatty acids(fish oils) on boar reproduction and semen quality. J Anim Sci 2010;88(7):2346—55. DOI:10.2527/jas.2009-2779. PMID: 20348371.; Gholami H., Chamani M., Towhidi A., Fazeli M.H. Effect of feeding a docosahexaenoic acid-enriched nutriceutical on the quality of fresh and frozen-thawed semen in Holstein bulls. Theriogenology 2010;74(9):1548—58. DOI:10.1016/j.theriogenology.2010.06.025. PMID: 20708237.; Roqueta-Rivera M., Abbott T.L., Sivaguru M. et al. Deficiency in the omega-3 fatty acid pathway results in failure of acrosome biogenesis in mice. Biol Reprod 2011;85(4):721 —32. DOI:10.1095/biolreprod.110.089524. PMID: 21653892.; Safarinejad M.R. Effect of omega-3 polyunsaturated fatty acid supplementation on semen profile and enzymatic anti-oxidant capacity of seminal plasma in infertile men with idiopathic oligoasthenoteratospermia: a doubleblind, placebo-controlled, randomised study. Andrologia 2011;43(1):38—47. DOI:10.1111/j.1439-0272.2009.01013.x. PMID: 21219381.; Moallem U., Neta N., Zeron Y. et al. Dietary a-linolenic acid from flaxseed oil or eicosapentaenoic and docosahexaenoic acids from fish oil differentially alter fatty acid composition and characteristics of fresh and frozen-thawed bull semen. Theriogenology 2015;83(7):1110—20. DOI:10.1016/j.theriogenology.2014.12.008. PMID: 25617988.; Filipcikova R., Oborna I., Brezinova J. et al. Lycopene improves the distorted ratio between AA/DHA in the seminal plasma of infertile males and increases the likelihood of successful pregnancy. Biomed Pap Med Fac Univ Palacky Olomouc Czech Repub 2015;159(1):77—82. DOI:10.5507/bp.2013.007. PMID: 23446211.; Hosseini B., Nourmohamadi M., Hajipour S. et al. The effect of omega-3 fatty acids, EPA, and/or DHA on male infertility: a systematic review and metaanalysis. J Diet Suppl 2018;16:1 —12. DOI:10.1080/19390211.2018.1431753. PMID: 29451828.; Attaman J.A., Toth T.L., Furtado J. et al. Dietary fat and semen quality among men attending a fertility clinic. Hum Reprod 2012;27(5):1466—74. DOI:10.1093/humrep/des065. PMID: 22416013.; Eslamian G., Amirjannati N., Rashidkhani B. et al. Dietary fatty acid intakes and asthenozoospermia: a case-control study. Fertil Steril 2015;103(1): 190—8. DOI:10.1016/j.fertnstert.2014.10.010. PMID: 25456794.; Calder P. C. Functional roles of fatty acids and their effects on human health. JPEN J Parenter Enteral Nutr 2015;39(1 Suppl): 18S—32S. DOI:10.1177/0148607115595980. PMID: 26177664.; Ollero M., Powers R.D., Alvarez J.G. Variation of docosahexaenoic acid content in subsets of human spermatozoa at different stages of maturation: implications for sperm lipoperoxidative damage. Mol Reprod Dev 2000;55(3):326—34. PMID: 10657052.; Connor W.E., Lin D.S., Wolf D.P., Alexander M. Uneven distribution of desmosterol and docosahexaenoic acid in the heads and tails of monkey sperm. J Lipid Res 1998;39(7):1404—11. PMID: 9684743.; Martinez-Soto J.C., Landeras J., Gadea J. Spermatozoa and seminal plasma fatty acids as predictors of cryopreservation success. Andrology 2013;1(3):365—75. DOI:10.1111/j.2047-2927.2012.00040.x. PMID: 23596043.; Speake B.K., Surai P.F., Rooke J.A. et al. Regulation of avian and mammalian sperm production by dietary fatty acids. In: Male fertility and lipid metabolism. Ed. by S.R. De Vriese, A.B. Christophe. Champaign, IL: AOCS Press, 2003. Pp. 96e117.; Lenzi A., Picardo M., Gandini L., Dondero F. Lipids of the sperm plasma membrane: from polyunsaturated fatty acids considered as markers of sperm function to possible scavenger therapy. Hum Reprod Update 1996;2(3):246—56. PMID: 9079417.; Murphy E.M., Stanton C., Brien C.O. et al. The effect of dietary supplementation of algae rich in docosahexaenoic acid on boar fertility. Theriogenology 2017;90:78—87. DOI:10.1016/j.theriogenology.2016.11.008. PMID: 28166992.; Comhaire F.H., Christophe A.B., Zalata A.A. et al. The effects of combined conventional treatment, oral antioxidants and essential fatty acids on sperm biology in subfertile men. Prostaglandins Leukot Essent Fatty Acids 2000;63(3):159—65. DOI:10.1054/plef.2000.0174. PMID: 10991774.; Martinez-Soto J.C., Domingo J.C., Cordobilla B. et al. Dietary supplementation with docosahexaenoic acid (DHA) improves seminal antioxidant status and decreases sperm DNA fragmentation. Syst Biol Reprod Med 2016;62(6):387—95. DOI:10.1080/19396368.2016.1246623. PMID: 27792396.; Calder P.C. Polyunsaturated fatty acids and inflammation. Biochem Soc Trans 2005;33(Pt 2):423—7. DOI:10.1042/BST0330423. PMID: 15787620.; Kim Y.J., Chung H.Y. Antioxidative and anti-inflammatory actions of docosahexaenoic acid and eicosapentaenoic acid in renal epithelial cells and macrophages. J Med Food 2007;10(2):225—31. DOI:10.1089/jmf.2006.092. PMID: 17651056.; Lukiw J., Bazan G. Docosahexaenoic acid and the aging brain. J Nutr 2.008;138(12.):2510—14. DOI:10.3945/jn.108.096016. PMID: 19022980.; Schumann J. It is all about fluidity: Fatty acids and macrophage phagocytosis. Eur J Pharmacol 2016;785:18-23. DOI:10.1016/j.ejphar.2015.04.057. PMID: 25987422.; Calder P.C. Omega-3 fatty acids and inflammatory processes: from molecules to man. Biochem Soc Trans 2017;45(5):1105—15. DOI:10.1042/BST20160474. PMID: 28900017.; Browning L.M., Walker C.G., Mander A.P. et al. Incorporation of eicosapentaenoic and docosahexaenoic acids into lipid pools when given as supplements providing doses equivalent to typical intakes of oily fish. Am J Clin Nutr 2012;96(4):748—58. DOI:10.3945/ajcn.112.041343. PMID: 22932281.; Chapkin R.S., Akoh C.C., Miller C. C. Influence of dietary n-3 fatty acids on macrophage glycerophospholipid molecular species and peptidoleukotriene synthesis. J Lipid Res 1991;32(7): 1205—13. PMID: 1940643.; Barros K.V., Cassulino A.P., Schalch L. et al. Pharmaconutrition: acute fatty acid modulation of circulating cytokines in elderly patients in the ICU. JPEN J Parenter Enteral Nutr 2014;38(4):467—74. DOI:10.1177/0148607113480183. PMID: 23471207.; Miles E.A., Wallace F.A., Calder P.C. Dietary fish oil reduces intercellular adhesion molecule 1 and scavenger receptor expression on murine macrophages. Atherosclerosis 2000;152(1):43—50. PMID: 10996338.; Daak A.A., Elderdery A.Y., Elbashir L.M. et al. Omega 3(n-3) fatty acids down-regulate nuclear factor-kappa B (NF-kB) gene and blood cell adhesion molecule expression in patients with homozygous sickle cell disease. Blood Cells Mol Dis 2015;55(1) 48—55. DOI:10.1016/j.bcmd.2015.03.014. PMID: 25976467.; Novak T.E., Babcock T.A., Jho D.H. et al. NF-kappa B inhibition by omega —3 fatty acids modulates LPS-stimulated macrophage TNF-alpha transcription. Am J Physiol Lung Cell Mol Physiol 2003;284(1):84—9. DOI:10.1152/ajplung.00077.2002. PMID: 12388359.; Kong W., Yen J.H., Vassiliou E. et al. Docosahexaenoic acid prevents dendritic cell maturation and in vitro and in vivo expression of the IL-12 cytokine family. Lipids Health Dis 2010;9:12. PMC2827414. DOI:10.1186/1476-511X-9—12. PMID: 20122166.; Weylandt K.H. Docosapentaenoic acid derived metabolites and mediators — the new world of lipid mediator medicine in a nutshell. Eur J Pharmacol 2016;785:108—115. DOI:10.1016/j.ejphar.2015.11.002. PMID: 26546723.; Hsiao H.M., Thatcher T.H., Colas R.A. et al. Resolvin D1 reduces emphysema and chronic inflammation. Am J Pathol 2015;185(12):3189—201. DOI:10.1016/j.ajpath.2015.08.008. PMID: 26468975.; Serhan C.N., Chiang N. Resolution phase lipid mediators of inflammation: agonists of resolution. Curr Opin Pharmacol 2013;13(4):632—40. DOI:10.1016/j.coph. 2013.05.012. PMID: 23747022.; Lima-Garcia J.F., Dutra R.C., da Silva K. et al. The precursor of resolvin D series and aspirin-triggered resolvin D1 display anti-hyperalgesic properties in adjuvant-induced arthritis in rats. Br J Pharmacol 2011;164(2):278—93.DOI:10.1111/j.1476-5381.2011.01345.x. PMID: 21418187.; Schwanke R.C., Marcon R., Bento A.F. et al. EPA- and DHA-derived resolvins» actions in inflammatory bowel disease. Eur J Pharmacol 2016;785:156—64. DOI:10.1016/j.ejphar.2015.08.050. PMID: 26325092.; Rogerio A.P., Haworth O., Croze R. et al. Resolvin D1 and aspirin-triggered resolvin D1 promote resolution of allergic airways responses. J Immunol 2012;189(4):1983—91. DOI:10.4049/jimmunol.1101665. PMID: 22802419.; Mas E., Croft K.D., Zahra P. et al. Resolvins D1, D2, and other mediators of self-limited resolution of inflammation in human blood following n-3 fatty acid supplementation. Clin Chem 2012;58(10):1476—84. DOI:10.1373/clinchem.2012.190199. PMID: 22912397.; Lecchi C., Invernizzi G., Agazzi A. et al. In vitro modulation of caprine monocyte immune functions by ю-3 polyunsaturated fatty acids. Vet J 2011;189(3):353—5. DOI:10.1016/j.tvjl.2010.09.001. PMID: 20889357.; Belluzzi A., Brignola C., Campieri. et al. Effect of an enteric-coated fish-oil preparation on relapses in Crohn’s disease. N Engl J 1996;334(24):1557—60. DOI:10.1056/NEJM199606133342401. PMID: 8628335.; Leeb B.F., Sautner J., Andel I., Rintelen B. Intravenous application of omega-3 fatty acids in patients with active rheumatoid arthritis. The ORA-1 trial. An open pilot study. Lipids 2006;41(1):29—34. PMID: 16555468.; Goldberg R.J., Katz J. A meta-analysis of the analgesic effects of omega-3 polyunsaturated fatty acid supplementation for inflammatory joint pain. Pain 2007;129(1—2):210—23. DOI:10.1016/j.pain.2007.01.020. PMID: 17335973.; Xu Q.H., Cai G.L., Lh X.C. et al. [The effects of ю-3 fish oil lipid emulsion on inflammation-immune response and organ function in patients with severe acute pancreatitis (In Chinese)]. Zhonghua Nei Ke Za Zhi 2012;51(12):962—5. PMID: 23327958.; Sheppard J.D. Jr, Singh R., McClellan A.J. Long-term supplementation with n-6 and n-3 PUFAs improves moderate-to-severe keratoconjunctivitis sicca: a randomized double-blind clinical trial. Cornea 2013;32(10):1297—304. DOI:10.1097/ICO.0b013e318299549c. PMID: 23884332.; Naqvi A.Z., Hasturk H., Mu L. et al. Docosahexaenoic acid and periodontitis in adults: a randomized controlled trial. J Dent Res 2014;93(8):767—73.; Bisht S., Faiq M., Tolahunase M., Dada R. Oxidative stress and male infertility. Nat Rev Urol 2017;14(8):470—85. DOI:10.1038/nrurol.2017.69. PMID: 28508879.; https://agx.abvpress.ru/jour/article/view/317
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11Academic Journal
Source: Репродуктивна ендокринологія; № 39 (2018); 65-67
Репродуктивная эндокринология; № 39 (2018); 65-67
Reproductive Endocrinology; № 39 (2018); 65-67Subject Terms: 03 medical and health sciences, 0302 clinical medicine, докозагексаєнова кислота, вагітність, лактація, психомоторний розвиток, зір, Femibion Natalcare II, docosahexaenoic acid, pregnancy, lactation, psychomotor development, vision, 3. Good health, докозагексаеновая кислота, беременность, лактация, психомоторное развитие, зрение
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Access URL: http://reproduct-endo.com/article/view/128320
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12Academic Journal
Authors: A. Yu. Popova, S. I. Gamidov, R. I. Ovchinnikov, I. V. Ushakova, O. N. Golubeva, А. Ю. Попова, С. И. Гамидов, Р. И. Овчинников, И. В. Ушакова, О. Н. Голубева
Source: Andrology and Genital Surgery; Том 16, № 2 (2015); 51-55 ; Андрология и генитальная хирургия; Том 16, № 2 (2015); 51-55 ; 2412-8902 ; 2070-9781 ; 10.17650/2070-9781-2015-2
Subject Terms: олигоастенотератозооспермия, sperm DNA fragmentation, docosahexaenoic acid, spermogram, infertility treatment, fragmentation index, asthenozoospermia, asthenoteratozoospermia, teratozoospermia, oligoasthenozoospermia, oligoasthenoteratozoospermia, фрагментации ДНК спермы, докозагексаеновая кислота, спермограмма, лечение бесплодия, индекс фрагментации, астенозооспермия, астенотератозооспермия, тератозооспермия, олигоастенозооспермия
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Relation: https://agx.abvpress.ru/jour/article/view/146/139; Guzick D.S., Overstreet J.W., FactorLitvak P. et al. Sperm morphology, motility, and concentration in fertile and infertile men. N Engl J Med 2004;345(19):1388–93.; Osman A., Alsomait H., Seshadri S. et al. The effect of sperm DNA fragmentation on live birth rate after IVF or ICSI: a systematic review and meta-analysis. Reprod Biomed Online 2015;30(2):120–7.; Gandini L., Lombardo F., Paoli D. et al. Study of apoptotic DNA fragmentation in human spermatozoa. Hum Reprod 2000;15(4):830–9.; Evenson D.P. Sperm chromatin structure assay (SCSA®). Methods Mol Biol 2013; 927:147–64.; Kumar K., Deka D., Singh A. et al. Predictive value of DNA integrity analysis in idiopathic recurrent pregnancy loss following spontaneous conception. J Assist Reprod Genet 2012;29(9):861–7.; Spano M., Bonde J.P., Hjøllund H.I. The treatment of obstructive azoospermia by intracytoplasmic sperm injection. Fertil Steril 2000;73(1):43–50.; Zini A., Libman J. Sperm DNA damage: importance in the era of assisted reproduction. Curr Open Urol 2006;16(6):428–34.; Zini A., Albert O., Robaire B. Assessing sperm chromatin and DNA damage: clinical importance and development of standards. Andrology 2014;2(3):322–5.; Nogales-Gadea G., Pinós T., Ruiz J.R. Are mitochondrial haplogroups associated with elite athletic status? A study on a Spanish cohort. Mitochondrion 2011;11(6):905–8.; Ahluwalia B., Holman R.T. Fatty acid composition of lipids of bull, boar, rabbit and human semen. J Reprod Fertil 1969;18(3):431–7.; Poulos A., White I.G. The phospholipid composition of human spermatozoa and seminal plasma. J Reprod Fertil 1973;35(2):265–72.; Lenzi A., Picardo M., Gandini L., Dondero F. Lipids of the sperm plasma membrane: from polyunsaturated fatty acids considered as markers of sperm function to possible scavenger therapy. Hum Reprod Update 1996;2(3):246–56.; Alvarez J.G., Storey B.T. Differential incorporation of fatty acids into and peroxidative loss of fatty acids from phospholipids of human spermatozoa. Mol Reprod Dev 1995;42(3):334–46.; Wang A.W., Zhang H., Ikemoto I. et al. Reactive oxygen species generation by seminal cells during cryopreservation. Urology 1997;49(6):921–5.; Alvarez J.G., Storey B.T. Evidence for increased lipid peroxidative damage and loss of superoxide dismutase activity as a mode of sublethal cryodamage to human sperm during cryopreservation. J Androl 1992;13(3): 232–41.; Lasso J.L., Noiles E.E., Alvarez J.G., Storey B.T. Mechanism of superoxide dismutase loss from human sperm cells during cryopreservation. J Androl 1994;15(3): 255–65.; Gadea J., Molla M., Selles E. et al. Reduced glutathione content in human sperm is decreased after cryopreservation: effect of the addition of reduced glutathione to the freezing and thawing extenders. Cryobiology 2011;62(1):40–6.; Agarwal A., Sekhon L.H. The role of antioxidant therapy in the treatment of male infertility. Hum Fertil (Camb) 2010;13(4):217–25.; Safarinejad M.R. Effect of omega-3 polyunsaturated fatty acid supplementation on semen profile and enzymatic anti-oxidant capacity of seminal plasma in infertile men with idiopathic oligoasthenoteratospermia: a double-blind, placebo-controlled, randomised study. Andrologia 2011;43(1):38–47.; Zini A., Al-Hathal N. Antioxidant therapy in male infertility: fact or fiction? Asian J Androl 2011;13(3):374–81.; Larson-Cook K.L., Brannian J.D., Hansen K.A. et al. Relationship between the outcomes of assisted reproductive techniques and sperm DNA fragmentation as measured by the sperm chromatin structure assay. Fertil Steril 2003;80(4):895–902.; https://agx.abvpress.ru/jour/article/view/146
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13Academic Journal
Authors: Макарова, Светлана, Вишнёва, Е.
Subject Terms: ДЛИННОЦЕПОЧЕЧНЫЕ ПОЛИНЕНАСЫЩЕННЫЕ ЖИРНЫЕ КИСЛОТЫ, НЕРВНАЯ СИСТЕМА, ДОКОЗАГЕКСАЕНОВАЯ КИСЛОТА, АРАХИДОНОВАЯ КИСЛОТА, ЭЙКОЗАПЕНТАЕНОВАЯ КИСЛОТА, ω3 ЖИРНЫЕ КИСЛОТЫ, ω-3 FATTY ACIDS
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14Academic Journal
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15Academic Journal
Authors: Грибакин, Сергей, Боковская, О.
Subject Terms: СОН, РЕБЕНОК, ХРОНОНУТРИЕНТЫ, ТРИПТОФАН, СЕРОТОНИН, ДОКОЗАГЕКСАЕНОВАЯ КИСЛОТА
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16Academic Journal
Authors: Тыртышная, Анна
Subject Terms: ДОКОЗАГЕКСАЕНОВАЯ КИСЛОТА, ПОЛИНЕНАСЫЩЕННЫЕ ЖИРНЫЕ КИСЛОТЫ, НЕЙРОВОСПАЛЕНИЕ
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17Academic Journal
Subject Terms: ДЕТИ, ГРУДНОЕ МОЛОКО, ДЕТСКИЕ МОЛОЧНЫЕ СМЕСИ, ДЛИННОЦЕПОЧЕЧНЫЕ ПОЛИНЕНАСЫЩЕННЫЕ ЖИРНЫЕ КИСЛОТЫ, ДОКОЗАГЕКСАЕНОВАЯ КИСЛОТА, АРАХИДОНОВАЯ КИСЛОТА
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18Academic Journal
Subject Terms: ЭЙКОЗАПЕНТАЕНОВАЯ КИСЛОТА, ДОКОЗАГЕКСАЕНОВАЯ КИСЛОТА, СОСТАВ ПРЕПАРАТОВ ОМЕГА-3 ЖИРНЫХ КИСЛОТ
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19Academic Journal
Source: Вопросы современной педиатрии.
Subject Terms: 0404 agricultural biotechnology, 04 agricultural and veterinary sciences, ДЛИННОЦЕПОЧЕЧНЫЕ ПОЛИНЕНАСЫЩЕННЫЕ ЖИРНЫЕ КИСЛОТЫ, НЕРВНАЯ СИСТЕМА, ДОКОЗАГЕКСАЕНОВАЯ КИСЛОТА, АРАХИДОНОВАЯ КИСЛОТА, ЭЙКОЗАПЕНТАЕНОВАЯ КИСЛОТА, ω3 ЖИРНЫЕ КИСЛОТЫ, ω-3 FATTY ACIDS, 0405 other agricultural sciences, 3. Good health
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20Academic Journal
Source: Андрология и генитальная хирургия.
Subject Terms: 3. Good health, МУЖСКОЕ БЕСПЛОДИЕ,MALE INFERTILITY,ФРАГМЕНТАЦИИ ДНК СПЕРМЫ,SPERM DNA FRAGMENTATION,ДОКОЗАГЕКСАЕНОВАЯ КИСЛОТА,DOCOSAHEXAENOIC ACID,СПЕРМОГРАММА,ЛЕЧЕНИЕ БЕСПЛОДИЯ,INFERTILITY TREATMENT,ИНДЕКС ФРАГМЕНТАЦИИ,FRAGMENTATION INDEX,АСТЕНОЗООСПЕРМИЯ,ASTHENOZOOSPERMIA,АСТЕНОТЕРАТОЗООСПЕРМИЯ,ASTHENOTERATOZOOSPERMIA,ТЕРАТОЗООСПЕРМИЯ,TERATOZOOSPERMIA,ОЛИГОАСТЕНОЗООСПЕРМИЯ,OLIGOASTHENOZOOSPERMIA,ОЛИГОАСТЕНОТЕРАТОЗООСПЕРМИЯ,OLIGOASTHENOTERATOZOOSPERMIA,SPERMOGRAM
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