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1Academic Journal
Συγγραφείς: Вадим Зурабович Дзеранов, Евгений Владимирович Зиновьев, Владимир Олегович Сидельников Фон Эссен
Πηγή: Российские биомедицинские исследования, Vol 10, Iss 3 (2025)
Θεματικοί όροι: обожженные, ноцицепция, антиноцицепция, опиоидный наркотический анальгетик (фентанил), анестезиологическое обеспечение, фракция кислорода во вдыхаемой газовой смеси (FiO2), Medicine (General), R5-920
Περιγραφή αρχείου: electronic resource
Relation: https://www.ojs3.gpmu.org/index.php/biomedical-research/article/view/6637; https://doaj.org/toc/2658-6584; https://doaj.org/toc/2658-6576
Σύνδεσμος πρόσβασης: https://doaj.org/article/e3a3af1a631c4c93b4280b593472e8e3
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2Academic Journal
Συγγραφείς: D Shibkova, O Baiguzhina, P Kondrashkin
Πηγή: Human Sport Medicine. 20:34-40
Θεματικοί όροι: 2. Zero hunger, болевой порог, здоровые лица, physical activity, пара- вертебральные точки, paravertebral areas, healthy women, 3. Good health, ноцицепция, tensoalgometry, pressure-pain-threshold, тензоалгометрия, nociception, УДК 612.884
Περιγραφή αρχείου: application/pdf
Σύνδεσμος πρόσβασης: https://hsm.susu.ru/hsm/article/download/1002/351
https://hsm.susu.ru/hsm/ru/article/view/1002
https://cyberleninka.ru/article/n/notsitseptivnyy-porog-u-zdorovyh-zhenschin-v-sostoyanii-pokoya-i-gotovnosti-k-fizicheskoy-nagruzke
https://hsm.susu.ru/hsm/article/download/1002/351
http://dspace.susu.ru/xmlui/handle/0001.74/44924 -
3Academic Journal
Συγγραφείς: Shibkova, D.Z., Kondrashkin, P.V., Shevtsov, A.V.
Θεματικοί όροι: ноцицепция, integrative function, болевой порог, интегративная функция, тензоалгометрия, theoretical analysis, mental state, УДК 159.91, теоретический анализ, психическое состояние, nociception, pain threshold, УДК 612
Περιγραφή αρχείου: application/pdf
Σύνδεσμος πρόσβασης: http://dspace.susu.ru/xmlui/handle/00001.74/56252
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4Academic Journal
Συγγραφείς: O. A. Gromova, I. Yu. Torshin, О. А. Громова, И. Ю. Торшин
Συνεισφορές: Работа выполнена при поддержке гранта Российского научного фонда (№ 20-12-00175-п), Ивановский государственный химико-технологический университет
Πηγή: Neurology, Neuropsychiatry, Psychosomatics; Vol 15, No 3 (2023); 128-138 ; Неврология, нейропсихиатрия, психосоматика; Vol 15, No 3 (2023); 128-138 ; 2310-1342 ; 2074-2711 ; 10.14412/2074-2711-2023-3
Θεματικοί όροι: Комплигам В Комплекс, nociception, analgesia, bioinformatics, Compligam B Complex. Contact, ноцицепция, аналгезия, биоинформатика
Περιγραφή αρχείου: application/pdf
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Неврология, нейропсихиатрия, психосоматика. 2017;9(2):50-7. doi:10.14412/2074-27112017-2-50-57; Taylor JM, Allen AM, Graham A. Targeting mitochondrial 18 kDa translocator protein (TSPO) regulates macrophage cholesterol efflux and lipid phenotype. Clin Sci (Lond). 2014 Nov;127(10):603-13. doi:10.1042/CS20140047; Liu J, Huang J, Zhang Z, et al. Translocator Protein 18 kDa (TSPO) as a Novel Therapeutic Target for Chronic Pain. Neural Plast. 2022 Aug 29;2022:8057854. doi:10.1155/2022/8057854; Bettendorff L, Goessens G, Sluse F, et al. Thiamine deficiency in cultured neuroblastoma cells: effect on mitochondrial function and peripheral benzodiazepine receptors. J Neurochem. 1995 May;64(5):2013-21. doi:10.1046/j.1471-4159.1995.64052013.x; El Hajj Chehadeh S, Dreumont N, Willekens J, et al. Early methyl donor deficiency alters cAMP signaling pathway and neurosteroidogenesis in the cerebellum of female rat pups. Am J Physiol Endocrinol Metab. 2014 Dec 1;307(11):E1009-19. doi:10.1152/ajpendo.00364.2014; Громова ОА, Торшин ИЮ, Кобалава ЖД, Сорокина МА. О фундаментальных и клинических аспектах синергидного действия магния и рибофлавина в терапевтической практике. Терапия. 2018;19(1):119-31.; Gorman KM, Meyer E, Grozeva D, et al. Bi-allelic Loss-of-Function CACNA1B Mutations in Progressive Epilepsy-Dyskinesia. Am J Hum Genet. 2019 May 2;104(5):948-56. doi:10.1016/j.ajhg.2019.03.005; Chen K, Wang T, Li Y, et al. Rhodojaponin VI indirectly targets Cav2.2 channels via N-ethylmaleimide-sensitive fusion protein to alleviate neuropathic pain. Acta Pharm Sin B. 2023 Mar;13(3):1326-36. doi:10.1016/j.apsb.2023.01.021; Huang SK, Lu CW, Lin TY, Wang SJ. Neuroprotective Role of the B Vitamins in the Modulation of the Central Glutamatergic Neurotransmission. CNS Neurol Disord Drug Targets. 2022;21(4):292-301. doi:10.2174/1871527320666210902165739; Громова ОА, Торшин ИЮ. Систематический анализ экспериментальной и клинической фармакологии никотинамида и перспективы лечения атеросклероза. Экспериментальная и клиническая гастроэнтерология. 2022;(10):111-25. doi:10.31146/1682-8658-ecg-206-10-111-125; Kotaka M, Gover S, Vandeputte-Rutten L, et al. Structural studies of glucose-6-phosphate and NADP+ binding to human glucose-6phosphate dehydrogenase. Acta Crystallogr D Biol Crystallogr. 2005 May;61(Pt 5):495-504. doi:10.1107/S0907444905002350; Sun Q, Zhang BY, Zhang PA, et al. Downregulation of glucose-6-phosphate dehydrogenase contributes to diabetic neuropathic pain through upregulation of toll-like receptor 4 in rats. Mol Pain. 2019 JanDec;15:1744806919838659. doi:10.1177/1744806919838659; Громова ОА, Рудаков КВ, Торшин ИЮ. Систематический анализ эффектов холина на нервную систему на основе биохимических маршрутов. Анализ независимой литературы по молекулярной фармакологии и клиническим исследованиям. Трудный пациент. 2009;7(4-5):13-8.; Tsuda M, Tozaki-Saitoh H, Inoue K. Platelet-activating factor and pain. Biol Pharm Bull. 2011;34(8):1159-62. doi:10.1248/bpb.34.1159; Motoyama N, Morita K, Kitayama T, et al. Pain-releasing action of platelet-activating factor (PAF) antagonists in neuropathic pain animal models and the mechanisms of action. Eur J Pain. 2013 Sep;17(8):1156-67. doi:10.1002/j.1532-2149.2013.00289.x; Tager AM, LaCamera P, Shea BS, et al. The lysophosphatidic acid receptor LPA1 links pulmonary fibrosis to lung injury by mediating fibroblast recruitment and vascular leak. Nat Med. 2008 Jan;14(1):45-54. doi:10.1038/nm1685; Carvalho OP, Thornton GK, Hertecant J, et al. A novel NGF mutation clarifies the molecular mechanism and extends the phenotypic spectrum of the HSAN5 neuropathy. J Med Genet. 2011 Feb;48(2):131-5. doi:10.1136/jmg.2010.081455; Einarsdottir E, Carlsson A, Minde J, et al. A mutation in the nerve growth factor beta gene (NGFB) causes loss of pain perception. Hum Mol Genet. 2004 Apr 15;13(8):799-805. doi:10.1093/hmg/ddh096; Berry A, Aloe L, Rossi S, et al. Conjunctivally administered NGF antibody reduces pain sensitivity and anxiety-like behavioral responses in aged female mice. Behav Brain Res. 2010 Jul 11;210(2):284-7. doi:10.1016/j.bbr.2010.02.037. Epub 2010 Feb 25.; Громова ОА, Торшин ИЮ, Лиманова ОА, Никонов АА. Патофизиология вегетативно-сосудистых пароксизмов (приливы) у женщин в период менопаузы и механизм действия бета-аланина. Новая клинико-фармакологическая концепция. Гинекология. 2010;12(2):29-36.; Shi L, Tu BP. Acetyl-CoA and the regulation of metabolism: mechanisms and consequences. Curr Opin Cell Biol. 2015 Apr;33:12531. doi:10.1016/j.ceb.2015.02.003; Violante S, Ijlst L, van Lenthe H, et al. Carnitine palmitoyltransferase 2: New insights on the substrate specificity and implications for acylcarnitine profiling. Biochim Biophys Acta. 2010 Sep;1802(9):728-32. doi:10.1016/j.bbadis.2010.06.002; Arelin M, Zierz S, Ceglarek U, et al. Recurrent Myalgia since Early InfancyMisleading Clinical Course in a Child with Carnitine Palmitoyltransferase-II Deficiency. Neuropediatrics. 2020 Feb;51(1):536. doi:10.1055/s-0039-1694977; Taggart RT, Smail D, Apolito C, Vladutiu GD. Novel mutations associated with carnitine palmitoyltransferase II deficiency. Hum Mutat. 1999;13(3):210-20. doi:10.1002/(SICI)10981004(1999)13:33.0.CO;2-0; Dawkins JL, Hulme DJ, Brahmbhatt SB, et al. Mutations in SPTLC1, encoding serine palmitoyltransferase, long chain base subunit-1, cause hereditary sensory neuropathy type I. Nat Genet. 2001 Mar;27(3):309-12. doi:10.1038/85879; Hanna MC, Turner AJ, Kirkness EF. Human pyridoxal kinase. cDNA cloning, expression, and modulation by ligands of the benzodiazepine receptor. J Biol Chem. 1997 Apr 18;272(16):1075660. doi:10.1074/jbc.272.16.10756; Chelban V, Wilson MP, Warman Chardon J, et al. PDXK mutations cause polyneuropathy responsive to pyridoxal 5'-phosphate supplementation. Ann Neurol. 2019 Aug;86(2):225-40. doi:10.1002/ana.25524; Han G, Gupta SD, Gable K, et al. Identification of small subunits of mammalian serine palmitoyltransferase that confer distinct acyl-CoA substrate specificities. Proc Natl Acad Sci U S A. 2009 May 19;106(20):8186-91. doi:10.1073/pnas.0811269106; Mühle C, Reichel M, Gulbins E, Kornhuber J. Sphingolipids in psychiatric disorders and pain syndromes. Handb Exp Pharmacol. 2013;(216):431-56. doi:10.1007/978-3-7091-1511-4_22; Waldrop GL, Holden HM, St Maurice M. The enzymes of biotin dependent CO2 metabolism: what structures reveal about their reaction mechanisms. Protein Sci. 2012 Nov;21(11):1597-619. doi:10.1002/pro.2156; Zempleni J, Hassan YI, Wijeratne SS. Biotin and biotinidase deficiency. Expert Rev Endocrinol Metab. 2008 Nov 1;3(6):715-24. doi:10.1586/17446651.3.6.715; Abed AR, Abed A, Banafshe HR, et al. Effect of biotin supplementation on neuropathic pain induced by chronic constriction of the sciatic nerve in the rat. Res Pharm Sci. 2021 May 12;16(3):250-9. doi:10.4103/1735-5362.314823; Oguma S, Ando I, Hirose T, et al. Biotin ameliorates muscle cramps of hemodialysis patients: a prospective trial. Tohoku J Exp Med. 2012 Jul;227(3):217-23. doi:10.1620/tjem.227.217; Chu CH, Cheng D. Expression, purification, characterization of human 3methylcrotonyl-CoA carboxylase (MCCC). Protein Expr Purif. 2007 Jun;53(2):421-7. doi:10.1016/j.pep.2007.01.012; Boneh A, Baumgartner M, Hayman M, Peters H. Methylcrotonyl-CoA carboxylase (MCC) deficiency associated with severe muscle pain and physical disability in an adult. J Inherit Metab Dis. 2005;28(6):1139-40. doi:10.1007/s10545-005-0163-1; Лиманова ОА, Громова ОА, Торшин ИЮ и др. Систематический анализ молекулярно-физиологических эффектов миоинозитола: данные молекулярной биологии, экспериментальной и клинической медицины. Эффективная фармакотерапия. Акушерство и гинекология. 2013;28 (3):32-41.; Калачева АГ, Торшин ИЮ, Стельмашук ЕВ и др. Нейропротекторное действие миоинозитола на клеточной модели глутаматного стресса как основа для профилактики нарушений внутриутробного развития головного мозга. Фармакокинетика и фармакодинамика. 2018;(3):9-20. doi:10.24411/2587-7836-2018-10018; Larner J. D-chiro-inositol – its functional role in insulin action and its deficit in insulin resistance. Int J Exp Diabetes Res. 2002;3(1):47-60. doi:10.1080/15604280212528; Rapiejko PJ, Northup JK, Evans T, et al. G-proteins of fat-cells. Role in hormonal regulation of intracellular inositol 1,4,5-trisphosphate. Biochem J. 1986 Nov 15;240(1):35-40. doi:10.1042/bj2400035; Ivison SM, Graham NR, Bernales CQ, et al. Protein kinase D interaction with TLR5 is required for inflammatory signaling in response to bacterial flagellin. J Immunol. 2007 May 1;178(9):5735-43. doi:10.4049/jimmunol.178.9.5735; Zhu H, Yang Y, Zhang H, et al. Interaction between protein kinase D1 and transient receptor potential V1 in primary sensory neurons is involved in heat hypersensitivity. Pain. 2008 Jul 31;137(3):574-88. doi:10.1016/j.pain.2007.10.025; Xu JT, Tu HY, Xin WJ, et al. Activation of phosphatidylinositol 3-kinase and protein kinase B/Akt in dorsal root ganglia and spinal cord contributes to the neuropathic pain induced by spinal nerve ligation in rats. Exp Neurol. 2007 Aug;206(2):269-79. doi:10.1016/j.expneurol.2007.05.029; Jin J, Daniel JL, Kunapuli SP. Molecular basis for ADP-induced platelet activation. II. The P2Y1 receptor mediates ADP-induced intracellular calcium mobilization and shape change in platelets. J Biol Chem. 1998 Jan 23;273(4):2030-4. doi:10.1074/jbc.273.4.2030; Zou Y, Yang R, Li L, et al. Purinergic signaling: a potential therapeutic target for depression and chronic pain. Purinergic Signal. 2023 Mar;19(1):163-72. doi:10.1007/s11302-02109801-x; Jimenez E, Zafra F, Perez-Sen R, et al. P2Y purinergic regulation of the glycine neurotransmitter transporters. J Biol Chem. 2011 Mar 25;286(12):10712-24. doi:10.1074/jbc.M110.167056; Torres R, Croll SD, Vercollone J, et al. Mice genetically deficient in neuromedin U receptor 2, but not neuromedin U receptor 1, have impaired nociceptive responses. Pain. 2007 Aug;130(3):267-78. doi:10.1016/j.pain.2007.01.036; Greenberg JA, Bell SJ, Guan Y, Yu YH. Folic Acid supplementation and pregnancy: more than just neural tube defect prevention. Rev Obstet Gynecol. 2011 Summer;4(2):52-9.; Jiang W, Tan XY, Li JM, et al. DNA Methylation: A Target in Neuropathic Pain. Front Med (Lausanne). 2022 Jul 7;9:879902. doi:10.3389/fmed.2022.879902. eCollection 2022.; Zhang R, Huang M, Cao Z, et al. MeCP2 plays an analgesic role in pain transmission through regulating CREB / miR-132 pathway. Mol Pain. 2015 Apr 12;11:19. doi:10.1186/s12990-015-0015-4; Wolthers KR, Lou X, Toogood HS, et al. Mechanism of coenzyme binding to human methionine synthase reductase revealed through the crystal structure of the FNR-like module and isothermal titration calorimetry. Biochemistry. 2007 Oct 23;46(42):11833-44. doi:10.1021/bi701209p. Epub 2007 Sep 25.; Menon S, Lea RA, Roy B, et al. Genotypes of the MTHFR C677T and MTRR A66G genes act independently to reduce migraine disability in response to vitamin supplementation. Pharmacogenet Genomics. 2012 Oct;22(10):7419. doi:10.1097/FPC.0b013e3283576b6b; Brown GM. The biosynthesis of folic acid. II. Inhibition by sulfonamides. J Biol Chem. 1962 Feb;237:536-40.; Maki T, Takeda K. Benzoic Acid and Derivatives. In: Ullmann’s Encyclopedia of Industrial Chemistry. Wiley-VCH. doi:10.1002/14356007.a03_555. ISBN 3527306730; Takahashi N, Kuwaki T, Kiyonaka S, et al. TRPA1 underlies a sensing mechanism for O2. Nat Chem Biol. 2011 Aug 28;7(10):70111. doi:10.1038/nchembio.640; Kremeyer B, Lopera F, Cox JJ, et al. A gain-of-function mutation in TRPA1 causes familial episodic pain syndrome. Neuron. 2010 Jun 10;66(5):671-80. doi:10.1016/j.neuron.2010.04.030; Bang S, Yang TJ, Yoo S, et al. Inhibition of sensory neuronal TRPs contributes to anti-nociception by butamben. Neurosci Lett. 2012 Jan 11;506(2):297-302. doi:10.1016/j.neulet.2011.11.026; Itoh Y, Hatano N, Hayashi H, et al. An environmental sensor, TRPV4 is a novel regulator of intracellular Ca2+ in human synoviocytes. Am J Physiol Cell Physiol. 2009 Nov;297(5):C1082-90. doi:10.1152/ajpcell.00204.2009; Köttgen M, Buchholz B, Garcia-Gonzalez MA, et al. TRPP2 and TRPV4 form a polymodal sensory channel complex. J Cell Biol. 2008 Aug 11;182(3):437-47. doi:10.1083/jcb.200805124; Boehmerle W, Huehnchen P, Lee SLL, et al. TRPV4 inhibition prevents paclitaxel-induced neurotoxicity in preclinical models. Exp Neurol. 2018 Aug;306:64-75. doi:10.1016/j.expneurol.2018.04.014; Günes HN, Bekircan-Kurt CE, Tan E, Erdem-Özdamar S. The histopathological evaluation of small fiber neuropathy in patients with vitamin B12 deficiency. Acta Neurol Belg. 2018 Sep;118(3):405-10. doi:10.1007/s13760017-0847-y; Wu F, Xu K, Liu L, et al. Vitamin B(12) Enhances Nerve Repair and Improves Functional Recovery After Traumatic Brain Injury by Inhibiting ER Stress-Induced Neuron Injury. Front Pharmacol. 2019 Apr 24;10:406. doi:10.3389/fphar.2019.00406; Xu J, Wang W, Zhong XX, et al. EXPRESS: Methylcobalamin ameliorates neuropathic pain induced by vincristine in rats: Effect on loss of peripheral nerve fibers and imbalance of cytokines in the spinal dorsal horn. Mol Pain. 2016 Jun 15;12:1744806916657089. doi:10.1177/1744806916657089; Громова ОА, Торшин ИЮ, Путилина МВ и др. О механизмах синергидного действия толперизона, мелоксикама и витаминов группы В в терапии периферических болевых синдромов. Медицинский совет. 2020;(8):5464. doi:10.21518/2079-701X-2020-8-54-64; Gharibpoor F, Ghavidel-Parsa B, Sattari N, et al. Effect of vitamin B12 on the symptom severity and psychological profile of fibromyalgia patients; a prospective pre-post study. BMC Rheumatol. 2022 Sep 1;6(1):51. doi:10.1186/s41927-022-00282-y; Karedath J, Batool S, Arshad A, et al. The Impact of Vitamin B12 Supplementation on Clinical Outcomes in Patients With Diabetic Neuropathy: A Meta-Analysis of Randomized Controlled Trials. Cureus. 2022 Nov 22;14(11):e31783. doi:10.7759/cureus.31783; Didangelos T, Karlafti E, Kotzakioulafi E, et al. Vitamin B12 Supplementation in Diabetic Neuropathy: A 1-Year, Randomized, DoubleBlind, Placebo-Controlled Trial. Nutrients. 2021;13(2):395. doi:10.3390/nu13020395; Zhang A, Ackley BD, Yan D. Vitamin B12 Regulates Glial Migration and Synapse Formation through Isoform-Specific Control of PTP-3/LAR PRTP Expression. Cell Rep. 2020 Mar 24;30(12):3981-8.e3. doi:10.1016/j.celrep.2020.02
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5Academic Journal
Συγγραφείς: S. G. Krylova, K. A. Lopatina, E. P. Zueva, E. A. Safonova, T. N. Povet’eva, Yu. V. Nesterova, O. G. Afanas’eva, P. V. Kul’pin, N. I. Suslov, D. A. Kulagina, S. V. Sysolyatin, V. V. Zhdanov
Πηγή: Бюллетень сибирской медицины, Vol 19, Iss 4, Pp 110-118 (2021)
Θεματικοί όροι: гексаазаизовюрцитан, тиовюрцин, анальгетическая активность, соматогенная ноцицепция, trp-ионные каналы, кеторолак, диклофенак, капсаицин, формалиновый тест, противовоспалительная активность, Medicine
Relation: https://bulletin.ssmu.ru/jour/article/view/4158; https://doaj.org/toc/1682-0363; https://doaj.org/toc/1819-3684; https://doaj.org/article/80f5ad2763cf450ca9a0a959b0b2685d
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6Academic Journal
Συγγραφείς: E. A. Beskhmelnitsyna, D. V. Kravchenko, M. V. Pokrovsky, M. V. Korokin, A. A. Peresypkina, E. I. Varavin, D. A. Kostina
Πηγή: Регуляторные исследования и экспертиза лекарственных средств, Vol 7, Iss 3, Pp 186-189 (2018)
Θεματικοί όροι: ионный канал trpa1, боль, ноцицепция, воспаление, высокопроизводительный молекулярный скрининг, молекулы-кандидаты в селективные антагонисты ионного канала trpa1, trpa1 ion channel, pain, nociception, inflammation, high throughput screening, candidate molecules for selective antagonists of trpa1 ion channel, Medicine (General), R5-920
Περιγραφή αρχείου: electronic resource
Relation: https://www.vedomostincesmp.ru/jour/article/view/140; https://doaj.org/toc/3034-3062; https://doaj.org/toc/3034-3453
Σύνδεσμος πρόσβασης: https://doaj.org/article/79de8f60e895454face3ae8ac3204ba4
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7Academic Journal
Συγγραφείς: Kramar, H. I., Stepaniuk, H. I., Voloshchuk, N. I., Alchuk, O. I.
Πηγή: Medical and Clinical Chemistry; No. 4 (2019); 67-73 ; Медицинская и клиническая химия; № 4 (2019); 67-73 ; Медична та клінічна хімія; № 4 (2019); 67-73 ; 2414-9934 ; 2410-681X ; 10.11603/mcch.2410-681X.2019.v.i4
Θεματικοί όροι: 4- [4-oxo (4H) -quinazolin-3-yl] benzoic acid, nociception, mediator mechanisms, bradykinin, 4-[4-оксо-(4Н)-хиназолин-3-ил] бензойной кислоты, ноцицепция, медиаторные механизмы, брадикинин, 4-[4-оксо-(4Н)-хіназолін-3-іл] бензойної кислоти, ноцицепція, медіаторні механізми, брадикінін
Περιγραφή αρχείου: application/pdf
Relation: https://ojs.tdmu.edu.ua/index.php/MCC/article/view/10841/10345; https://ojs.tdmu.edu.ua/index.php/MCC/article/view/10841
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8Academic Journal
Συγγραφείς: E. G. Poltavskaya, D. N. Savochkina, Е. Г. Полтавская, Д. Н. Савочкина
Συνεισφορές: Исследование проведено при поддержке гранта РФФИ №17-36-01113-ОГН «Патофизиологические параметры ноцицепции, обусловленные генетическими особенностями, как предиктор риска формирования зависимости от психоактивных веществ у лиц подростково-юношеского возраста».
Πηγή: Neurology, Neuropsychiatry, Psychosomatics; Vol 12, No 1 (2020); 27-32 ; Неврология, нейропсихиатрия, психосоматика; Vol 12, No 1 (2020); 27-32 ; 2310-1342 ; 2074-2711 ; 10.14412/2074-2711-2020-1
Θεματικοί όροι: ген PRDM12, nociception, PRDM12 gene, ноцицепция
Περιγραφή αρχείου: application/pdf
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An association of prodynorphin polymorphisms and opioid dependence in females in a Chinese population. Addict Biol. 2009 Jul;14(3):366-70. doi:10.1111/j.1369-1600.2009.00151.x. Epub 2009 Mar 5.; Koob GF. Neurocircuitry of alcohol addiction: synthesis from animal models. Handb Clin Neurol. 2014;125:33-54. doi:10.1016/B978-0-444-62619-6.00003-3.; Belin D, Everitt BJ. Cocaine seeking habits depend upon dopamine-dependent serial connectivity linking the ventral with the dorsal striatum. Neuron. 2008 Feb 7;57(3):432-41. doi:10.1016/j.neuron.2007.12.019.; Wise RA. The brain and reward. In: Liebman JM, Cooper SJ, editors. The neuropharmacological basis of reward. Oxford: Clarendon; 1989. P. 377–424.; Everitt BJ, Robbins TW. Neural systems of reinforcement for drug addiction: from actions to habits to compulsion. Nat Neurosci. 2005 Nov;8(11):1481-9.; Sesack SR, Grace AA. Cortico-Basal Ganglia reward network: microcircuitry. Neuropsychopharmacology. 2010 Jan;35(1): 27-47. doi:10.1038/npp.2009.93.; Bailey KP. The brain's rewarding system & addiction. J Psychosoc Nurs Ment Health Serv. 2004 Jun;42(6):14-8.; Лелевич ВВ, Курбат МН, Лелевич СВ. Нейромедиаторные механизмы опиатной наркомании (обзор литературы). Журнал ГрГМУ. 2006;(3):12-5.; Cohen JY, Haesler S, Vong L, et al. Neuron-type-specific signals for reward and punishment in the ventral tegmental area. Nature. 2012 Jan 18;482(7383):85-8. doi:10.1038/nature10754.; Mitsi V, Zachariou V. Modulation of pain, nociception, and analgesia by the brain reward center. Neuroscience. 2016 Dec 3;338:81-92. doi:10.1016/j.neuroscience.2016.05.017. Epub 2016 May 14.; Nevidimova TI, Batukhtina EI, Vetlugina TP, et al. Association of Cytokine Production with Hormone Level and Sensory Responses during the Formation of Psychoactive Drug Addiction in Men. Bull Exp Biol Med. 2015 Oct;159(6):768-71. doi:10.1007/s10517-015-3071-x. Epub 2015 Oct 31.; Chen YC, Auer-Grumbach M, Matsukawa S, et al. Transcriptional regulator PRDM12 is essential for human pain perception. Nat Genet. 2015 Jul;47(7):803-8. doi:10.1038/ng.3308. Epub 2015 May 25.; Hohenauer T, Moore AW. The Prdm family: expanding roles in stem cells and development. Development. 2012 Jul;139(13):2267-82. doi:10.1242/dev.070110.; Cortes D, Holt R, de Knegt VE. Hormonal aspects of the pathogenesis and treatment of cryptorchidism. Eur J Pediatr Surg. 2016 Oct; 26(5):409-417. Epub 2016 Sep 19.; Shirane K, Kurimoto K, Yabuta Y, et al. Global landscape and regulatory principles of DNA methylation reprogramming for germ cell specification by mouse pluripotent stem cells. Dev Cell. 2016 Oct 10;39(1):87-103. doi:10.1016/j.devcel.2016.08.008. Epub 2016 Sep 15.; Kobayashi T, Zhang H, Tang WWC, et al. Principles of early human development and germ cell program from conserved model systems. Nature. 2017 Jun 15;546(7658):416-420. doi:10.1038/nature22812. Epub 2017 Jun 7.; Dickinson ME, Flenniken AM, Ji X, et al. High-throuput discovery of novel developmental phenotypes. Nature. 2016 Sep 22;537(7621): 508-514. doi:10.1038/nature19356. Epub 2016 Sep 14.; Smagulova F, Brick K, Pu Y, et al. The evolutionary turnover of recombination hot spots contributes to speciation in mice. Genes Dev. 2016 Feb 1;30(3):266-80. doi:10.1101/gad.270009.115.; Kinameri E, Inoue T, Aruga J, et al. Prdm proto-oncogene transcription factor family expression and interaction with the Notch-Hes pathway in mouse neurogenesis. PLoS One. 2008; 3(12):e3859. doi:10.1371/journal.pone.0003859. Epub 2008 Dec 3.; Saitou M, Kagiwada S, Kurimoto K. Epigenetic reprogramming in mouse preimplantation development and primordial germ cells. Development. 2012 Jan;139(1):15-31. doi:10.1242/dev.050849.; Yang CM, Shinkai Y. Prdm12 is induced by retinoic acid and exhibits anti-proliferative properties through the cell cycle modulation of P19 embryonic carcinoma cells. 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Способ количественной оценки индивидуальных болевых порогов. Патент на изобретение № 2342063. Зарегистрировано в Государственном реестре изобретений 27.12.2008 г.; Савочкина ДН, Полтавская ЕГ. Оценка психофизиологических характеристик и полиморфизма гена SCN9A при формировании аддиктивного поведения. Сибирский вестник психиатрии и наркологии. 2018;(4):11–5.; Kelley AE, Berridge Kent C. The neuroscience of natural rewards: Relevance to addictive drugs. J Neurosci. 2002 May 1;22(9):3306-11.; Blum K, Gold MS. Reward circuitry dopaminergic activation regulates food and drug craving behavior. Curr Pharm Des. 2011;17(12): 1158-67.; Miller NS, Gold MS. Opiate prescription medication dependence and pain perceptions. J Addict Dis. 2007;26 Suppl 1:65-71. doi:10.1300/J069v26S01_07.; Aniskin DB, Fink E, Prosser J, et al. The effect of pain on stroop performance in; patients with opiate dependence in sustained remission. 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9Academic Journal
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10Academic Journal
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11Academic Journal
Συγγραφείς: E. A. Beskhmelnitsyna, D. V. Kravchenko, M. V. Pokrovsky, M. V. Korokin, A. A. Peresypkina, E. I. Varavin, D. A. Kostina, Е. А. Бесхмельницына, Д. В. Кравченко, М. В. Покровский, М. В. Корокин, А. А. Пересыпкина, Е. И. Варавин, Д. А. Костина
Πηγή: Regulatory Research and Medicine Evaluation; Том 7, № 3 (2017); 186-189 ; Регуляторные исследования и экспертиза лекарственных средств; Том 7, № 3 (2017); 186-189 ; 3034-3453 ; 3034-3062 ; undefined
Θεματικοί όροι: candidate molecules for selective antagonists of TRPA 1 ion channel, боль, ноцицепция, воспаление, высокопроизводительный молекулярный скрининг, молекулы-кандидаты в селективные антагонисты ионного канала TRPA 1, TRPA 1 ion channel, pain, nociception, inflammation, high throughput screening
Περιγραφή αρχείου: application/pdf
Relation: https://www.vedomostincesmp.ru/jour/article/view/140/139; Тактика и неотложная терапия болевого синдрома. Научно-информационный материал. М.: Ассоциация московских ВУЗов; 2010.; Jordt SE, Bautista DM, Chuang HH, McKemy DD, Zygmunt PM, Hogestatt ED, et al. Mustard oils and cannabinoids excite sensory nerve fibres through the TRP channel ANKTM1. Nature 2004; 427(6971): 260-5.; Trevisani M, Siemens J, Materazzi S, Bautista DM, Nassini R, Campi B, et al. 4-Hydroxynonenal, an endogenous aldehyde, causes pain and neurogenic inflammation through activation of the irritant receptor TRPA1. Proc Natl Acad Sci USA 2007; 104(33): 13519-24.; Shelukhina I, Mikhailov N, Abushik P, Nurulin L, Nikolsky EE, Giniatullin R. Cholinergic Nociceptive Mechanisms in Rat Meninges and Trigeminal Ganglia: Potential Implications for Migraine Pain. Front Neurol. 2017; (8): 163.; Bohonyi N, Pohoczky K, Szalontai B, Perkecz A, Kovacs K, Kajtar B, et al. Local upregulation of transient receptor potential ankyrin 1 and transient receptor potential vanilloid 1 ion channels in rectosigmoid deep infiltrating endometriosis. Mol Pain 2017; (13): 1744806917705564.; Asai Y, Holt JR, Geleoc GS. A quantitative analysis of the spatiotemporal pattern of transient receptor potential gene expression in the developing mouse cochlea. J Assoc Res Otolaryngol. 2010; 11(1): 27-37.; Matta JA, Cornett PM, Miyares RL, Abe K, Sahibzada N, Ahern GP. General anesthetics activate a nociceptive ion channel to enhance pain and inflammation. Proc Natl Acad Sci USA 2008; 105(25): 8784-9.; Бесхмельницына ЕА, Покровский МВ, Корокин МВ, Якушев ВИ, Гудырев ОС. Биологическая роль ионного канала TRPA1 при различных патологических состояниях. Научные ведомости Белгородского государственного университета. Серия: Медицина. Фармация 2012; 20(22-3): 30-5.; Nie Y, Huang C, Zhong C, Wortley MA, Luo Y, Luo W, et al. Cigarette smoke extract (CSE) induces transient receptor potential ankyrin 1 (TRPA1) expression via activation of HIF1α in A549 cells. Free Radic Biol Med. 2016; (99): 498-507.; Nakao S, Mabuchi M, Wang S, Koqure Y, Shimizu T, Noguchi K, et al. Synthesis of resveratrol derivatives as new analgesic drugs through desensitization of the TRPA1 receptor. Bioorg Med Chem Lett. 2017; 27(14): 3167-72.; Pryde DC, Marron BE, West CW, Reister S, Amato G, Yoger K, et al. Discovery of a Series of Indazole TRPA1 Antagonists. ACS Med Chem Lett. 2017; 8(6): 666-71.; Kravchenko DV, Beskhmelnitsyna EA, Korokin MV, Avtina TV, Sernov LN, Tishin AN, Kostina DA. Molecular screening of prospective candidates for TRPA1 ion channel selective antagonists. Research Result: Pharmacology and Clinical Pharmacology 2016; 2(1): 63-6.; Skerratt S. Recent Progress in the Discovery and Development of TRPA1 Modulators. Prog Med Chem. 2017; (56): 81-115.; Mukhopadhyay I, Kulkarni A, Aranake S, Karnik P, Shetty M, Thorat S, et al. Transient receptor potential ankyrin 1 receptor activation in vitro and in vivo by pro-tussive agents: GRC 17536 as a promising anti-tussive therapeutic. PLoS One 2014; 9(5): e97005.; https://www.vedomostincesmp.ru/jour/article/view/140; undefined
Διαθεσιμότητα: https://www.vedomostincesmp.ru/jour/article/view/140
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12Academic Journal
Συγγραφείς: Stepaniuk, G.I., Степанюк, Г.И., Kramar, A.I., Крамар, А.И., Voloșciuk, N.I., Волощук, Н.И., Alciuk, A.I., Альчук, А.И.
Πηγή: Sănătate Publică, Economie şi Management în Medicină 78 (4) 143-143
Θεματικοί όροι: 4-[4-оксо-4Н-хиназолин-3-ил] бензойной кислоты, ноцицепция, адренергическая, дофаминергическая и ГАМК -ергическая системы
Περιγραφή αρχείου: application/pdf
Relation: https://ibn.idsi.md/vizualizare_articol/69238; urn:issn:17298687
Διαθεσιμότητα: https://ibn.idsi.md/vizualizare_articol/69238
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13Academic Journal
Συγγραφείς: E. A. Beskhmelnitsyna, D. V. Kravchenko, M. V. Pokrovsky, M. V. Korokin, A. A. Peresypkina, E. I. Varavin, D. A. Kostina
Πηγή: Регуляторные исследования и экспертиза лекарственных средств, Vol 7, Iss 3, Pp 186-189 (2018)
Θεματικοί όροι: ионный канал trpa 1, боль, ноцицепция, воспаление, высокопроизводительный молекулярный скрининг, молекулы-кандидаты в селективные антагонисты ионного канала trpa 1, trpa 1 ion channel, pain, nociception, inflammation, high throughput screening, candidate molecules for selective antagonists of trpa 1 ion channel, Medicine (General), R5-920
Relation: https://www.vedomostincesmp.ru/jour/article/view/140; https://doaj.org/toc/3034-3062; https://doaj.org/toc/3034-3453; https://doaj.org/article/79de8f60e895454face3ae8ac3204ba4
Διαθεσιμότητα: https://doaj.org/article/79de8f60e895454face3ae8ac3204ba4
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14Academic Journal
Συγγραφείς: O. P. Bobrova, N. A. Shnayder, M. M. Petrova, K. S. Zyryanov, D. A. Sychev, О. П. Боброва, Н. А. Шнайдер, М. М. Петрова, С. К. Зырянов, Д. А. Сычев
Πηγή: Siberian journal of oncology; Том 16, № 5 (2017); 87-94 ; Сибирский онкологический журнал; Том 16, № 5 (2017); 87-94 ; 2312-3168 ; 1814-4861 ; 10.21294/1814-4861-2017-16-5
Θεματικοί όροι: цитокиновые рецепторы, oncology, single nucleotide polymorphisms (SNPs), analgesic therapy, review, TNF-α, IL-1, IL-6, IL-10, pharmacogenetics, nociception, cytokine receptors, онкология, однонуклеотидный полиморфизм (ОНП), анальгетическая терапия, обзор, ФНО-α, фармакогенетика, ноцицепция
Περιγραφή αρχείου: application/pdf
Relation: https://www.siboncoj.ru/jour/article/view/617/479; Микаэлян М.Ф., Аджиенко В.Л. Концепции и проблемы лечения хронического болевого синдрома на современном этапе. Лекарствен- ный вестник. 2016; 2 (62): 28–30.; Яхно Н.Н., Кукушкина М.Л. Боль (практическое руководство для врачей). М.: Изд-во РАМН, 2011; 512.; Балашова Т.В., Андреева Н.А., Мнацаканяни Л.А., Котельнико- ва А.Г., Долгунов А.М. Современные представления о патогенезе боли. Тихоокеанский медицинский журнал. 2012; 3: 13–16.; Wang X.B., Li Y.S., Li J., Han Y., Liu Z.D. Interleukin-8 -251A/T gene polymorphism and lung cancer susceptibility: a meta-analysis. J Cell Mol Med. 2015 Jun; 19 (6): 1218–22. doi:10.1111/jcmm.12466.; Schmidt B.L., Hamamoto D.T., Simone D.A., Wilcox G.L. Mechanisms of cancer pain. J Mol Interv. 2010; 10 (3): 164–78. doi:10.1124/mi.10.3.7.; Yoneda T., Hata K., Nakanishi M., Nagae M., Nagayama T., Wakabayashi H., Nishisho T., Sakurai T., Hiraga T. Involvement of acidic microenvironment in the pathophysiology of cancer-associated bone pain. Bone. 2011; 48 (1): 100–5. doi:10.1016/j.bone.2010.07.009.; Grivennikov S.I., Greten F.R., Karin M. Immunity, inflammation, and cancer. Cell. 2010; 140(6): 88399. doi:10.1016/j.cell.2010.01.025.; Матвеева Л.В., Мосина Л.М. Роль цитокинов семейства интерлейкина-1 в желудочном канцерогенезе. Вестник РАМН. 2012; 11: 59–65.; Branford R., Droney J., Ross J.R. Opioid genetics: the key to personalized pain control? Clin Genet. 2012; 82: 301–310. doi:10.1111/j.1399- 0004.2012.01923.x.; Neeb L., Hellen P., Boehnke C., Hoffmann J., Schuh-Hofer S., Dirnagl U., Reuter U. IL-1beta stimulates COX-2 dependent PGE synthesis and CGRP release in rat trigeminal ganglia cells. PLoS One. 2011; 6 (3): e17360. doi:10.1371/journal.pone.0017360.; Hirata H., Tetsumoto S., Kijima T., Kida H., Kumagai T., Takahashi R., Otani Y., Inoue K., Kuhara H., Shimada K., Nagatomo I., Takeda Y., Goya S., Yoshizaki K., Kawase I., Tachibana I., Kishimoto T., Kumanogoh A. Favorable responses to tocilizumab in two patients with cancer – related cachexia. J Pain Symptom Manage. 2013; 46 (2): e9–e13. doi:10.1016/j.jpainsymman.2013.01.009.; Wang X.M., Lehky T.J., Brell J.M., Dorsey S.G. Discovering cytokines as targets for chemotherapy-induced painful peripheral neuropathy. Cytokine. 2012; 59 (1): 3–9. doi:10.1016/j.cyto.2012.03.027.; Guo G., Gao F. CXCR3: latest evidence for the in volvemen to chemokine signaling in bone cancer pain. Exp Neurol. 2015; 265: 1769. doi:10.1016/j.expneurol.2015.02.003.; Vendrell D., Macedo I., Alho M., Dionísio R., Costa L. Treatment of cancer pain by targeting cytokines. Mediators Inflamm. 2015; 2015: 984570. doi:10.1155/2015/984570.; Jaggi A.S., Singh N. Mechanisms in cancer-chemotherapeutic drugs-induced peripheral neuropathy. Toxicology. 2012; 291 (1–3): 1–9. doi:10.1016/j.tox.2011.10.019.; Saijo Y., Tanaka M., Miki M., Usui K., Suzuki T., Maemondo M., Hong X., Tazawa R., Kikuchi T., Matsushima K., Nukiwa T. Proinflammatory cytokine IL-1 beta promotes tumor growth of Lewis lung carcinoma by induction of angiogenic factors: in vivo analysis of tumor-stromal interaction. J Immunol. 2002; 169: 469–475.; Kiguchi N., Kobayashi Y., Kishioka S. Chemokine and cytokines in neuroinflammation leading to neuropathic pain. Curr Opin Pharmacol. 2012; 12 (1): 55–61. doi:10.1016/j.coph.2011.10.007.; Guan X.H., Fu Q.C., Shi D., Bu H.L., Song Z.P., Xiong B.R., Shu B., Xiang H.B., Xu B., Manyande A., Cao F., Tian Y.K. Activation of spinal chemokine receptor CXCR3 mediates bonecancer pain throughanAkt ERKcross talk pathway in rats. Exp Neurol. 2015 Jan; 263: 39–49. doi:10.1016/j.expneurol.2014.09.019.; Doong S.H., Dhruva A., Dunn L.B., West C., Paul S.M., Cooper B.A., Elboim C., Abrams G., Merriman J.D., Langford D.J., Leutwyler H., Baggott C., Kober K., Aouizerat B.E., Miaskowski C. Associations between cytokine genes and a symptom cluster of pain, fatigue, sleep disturbance, and depression in patients prior to breast cancer surgery. Biol Res Nurs. 2015; 17 (3): 23747. doi:10.1177/1099800414550394.; Reyes-Gibby C.C., Shete S., Yennurajalingam S., Frazier M., Bruera E., Kurzrock R., Crane C.H., Abbruzzese J., Evans D., Spitz M.R. Genetic and nongenetic covariates of pain severity in patients with adenocarcinoma of the pancreas: assessing the influence of cytokine genes. J Pain Symptom Manage. 2009; 38 (6): 894–902.doi:10.1016/j. jpainsymman.2009.04.019.; Luo M., Yang Y., Luo D., Liu L., Zhang Y., Xiao F., Yang J., Zhang C., FuS., Luo Z. Tumor necrosis factor-alpha promoter polymorphism 308 G/A is not significantly associated with esophageal cancer risk: a meta-analysis. Oncotarget. 2016; 7 (48): 79901–13. doi:10.18632/oncotarget.13093.; Bandil K., Singhal P., Sharma U., Hussain S., Basu S., Parashari A., Singh V., Sehgal A., Shivam A., Ahuja P., Bharadwaj M., Banerjee B.D., Mehrotra R. Impacts of TNF-LTA SNPs/Haplotypes and Lifestyle Factors on Oral Carcinoma in an Indian Population. Mol Diagn Ther. 2016; 20 (5): 469–80. doi:10.1007/s40291-016-0215-2.; Zhao H., Zhang H.W., Zhang T., Gu X.M. Tumor necrosis factor alpha gene -308G>A polymorphism association with the risk of esophageal cancer in a Han Chinese population. Genet Mol Res. 2016 Oct 7; 15 (4). doi:10.4238/gmr.150458661.; Reyes-Gibby C.C., Spitz M.R., Yennurajalingam S., Swartz M., Gu J., Wu X., Bruera E., Shete S. Role of inflammation gene polymorphisms on pain severity in lung cancer patients. Cancer Epidemiol Biomarkers Prev. 2009; 18 (10): 2636–2642. doi:10.1158/1055-9965.EPI-09-0426.; Sun Q., Guo X., Wang Q., Zhao F. The association of TNF-308 (G/A) gene polymorphisms and hepatocellular carcinoma risk: a metaanalysis. Chin J Cancer Res. 2016; 28 (5): 536–542. doi:10.21147/j. issn.1000-9604.2016.05.09.; Rausch S.M., Gonzalez B.D., Clark M.M., Patten C., Felten S., Liu H., Li Y., Sloan J., Yang P. SNPs in PTGS2 and LTA predict pain and quality of life in long term lung cancer survivors. Lung Cancer. 2012; 77 (1): 217–23. doi:10.1016/j.lungcan.2012.02.017.; Wang Z., Liu Y., Yang L., Yin S., Zang R., Yang G. The polymorphism interleukin-8 -251A/T is associated with a significantly increased risk of cancers from a meta-analysis. Tumour Biol. 2014; 35 (7): 7115–23. doi:10.1007/s13277-014-1881-5.; Baune B.T., Dannlowski U., Domschke K., Janssen D.G., Jordan M.A., Ohrmann P., Bauer J., Biros E., Arolt V., Kugel H., Baxter A.G., Suslow T. The interleukin 1 beta (IL1B) gene is associated with failure to achieve remission and impaired emotion processing in major depression. Biol Psychiatry. 2010; 67 (6): 543–9. doi:10.1016/j. biopsych.2009.11.004; Reyes-Gibby C.C., Spitz M., Wu X., Merriman K., Etzel C., Bruera E., Kurzrock R., Shete S. Cytokine genes and pain severity in lung cancer: exploring the influence of TNF-alpha-308 G/A IL6-174G/C and IL8-251T/A. Cancer Epidemiol Biomarkers Prev. 2007; 16 (12): 2745–2751. doi:10.1158/1055-9965.epi-07-0651.; Reyes Gibby C.C., Spitz M.R., Yennurajalingam S., Swartz M., Gu J., Wu X., Bruera E., Shete S. Role of inflammation gene polymorphisms on pain severity in lung cancer patients. Cancer Epidemiol Biomarkers Prev. 2009; 18 (10): 2636–42. doi:10.1158/1055-9965.EPI-09-0426.; Müerköster S., Wegehenkel K., Arlt A., Witt M., Sipos B., Kruse M.L., Sebens T., Klöppel G., Kalthoff H., Fölsch U.R., Schäfer H. Tumor stroma interactions induce chemoresistance in pancreatic ductal carcinoma cells involving increased secretion and paracrine effects of nitric oxide and interleukin-1beta. Cancer Res. 2004; 64: 1331–1337.; Gan W.Y., Li H.M., Zhang Y.G., Li C.M., Wang Y. Association between IL18-607C/A and -137G/C polymorphisms and susceptibility to non-small cell lung cancer in a Chinese population. Genet Mol Res. 2016; 15 (4). doi:10.4238/gmr15048822.; Zhao K., Xu J., Tian H. Correlation analysis between an IL-6 genetic polymorphism and non-small cell lung cancer prognosis. Genet Mol Res. 2016; 15 (1): 15017021. doi:10.4238/gmr.15017021.; Quesada B.J.R., Talpaz M., Rios A., Kurzrock R., Gutterman J.U. Clinical toxicity of interferons in cancer patients: a review. J Clin Oncol. 2015; 4 (20): 234–243. doi:10.1200/JCO.1986.4.2.234; Von Ah.D.M., Kang D.H., Carpenter J.S. Predictors of cancerrelated fatigue in women with breast cancer before, during, and after adjuvant therapy. Cancer Nurs. 2008; 31 (2): 134–44. doi:10.1097/01. NCC.0000305704.84164.54.; Xu J., Yin Z., Cao S., Gao W., Liu L., Yin Y., Liu P., Shu Y. Systematic review and meta-analysis on the association between IL-1B polymorphisms and cancer risk. PLoS One. 2013; 8 (5): e63654. doi:10.1371/journal. pone.0063654.; Bastami S., Norling C., Trinks C., Holmlund B., Walz T.M., Ahlner J., Uppugunduri S. Inhibitory effect of opiates on LPS mediated release of TNF and IL-8. Acta Oncol. 2013 Jun; 52 (5): 1022–33. doi:10.3109/0284186X.2012.737932.; Dahl A.A., Nesvold I.L., Reinertsen K.V., Fossa S.D. Arm/shoulder problems and insomnia symptoms in breast cancer survivors: crosssectional, controlled and longitudinal observations. Sleep Med. 2011 Jun; 12 (6): 584–90. doi:10.1016/j.sleep.2011.01.011.; McCann B., Miaskowski C., Koetters T., Baggott C., West C., Levine J.D., Elboim C., Abrams G., Hamolsky D., Dunn L., Rugo H., Dodd M., Paul S.M., Neuhaus J., Cooper B., Schmidt B., Langford D., Cataldo J., Aouizerat B.E. Associations between pro- and anti-inflammatory cytokine genes and breast pain in women prior to breast cancer surgery. J Pain. 2012; 13 (5): 425–37. doi:10.1016/j.jpain.2011.02.358.; Barratt D.T., Klepstad P., Dale O., Kaasa S., Somogyi A.A. Innate Immune Signalling Genetics of Pain, Cognitive Dysfunction andSickness Symptoms in Cancer Pain Patients Treated with Transdermal Fentanyl. PLoS One. 2015 Sep 2; 10 (9): e0137179. doi:10.1371/journal. pone.0137179.; Sakamoto K., Takeda S., Kanekiyo S., Nishiyama M., Kitahara M., Ueno T., Yamamoto S., Yoshino S., Hazama S., Okayama N., Nagano H. Association of tumor necrosis factor-α polymorphism with chemotherapyinduced oral mucositis in patients with esophageal cancer. Mol Clin Oncol. 2017 Jan; 6 (1): 125–129. doi:10.3892/mco.2016.1081.; Liu X., Wang Z., Yu J., Lei G., Wang S. Three polymorphisms in interleukin-1beta gene and risk for breast cancer: a meta-analysis. Breast Cancer Res Treat. 2010 Dec; 124 (3): 821–5. doi:10.1007/s10549-010- 0910-3.; Ransohoff R.M. Chemokines and chemokine receptors: standing at the crossroads of immunobiology and neurobiology. Immunity. 2009 Nov 20; 31 (5): 711–21. doi:10.1016/j.immuni.2009.09.010.; Nedoszytko B., Olszewska B., Roszkiewicz J., Glen J., Zabłotna M., Ługowska-Umer H., Nowicki R., Sokołowska-Wojdyło M. The role of polymorphism of interleukin-2, -10, -13 and TNF-α genes in cutaneous T-cell lymphoma pathogenesis. Postepy Dermatol Alergol. 2016 Dec; 33 (6): 429–434. doi:10.5114/ada.2016.63881.; Li Y., Ou C., Shu H., Zhao H., Zhu B. The ERCC1-4533/8092, TNF-α 238/308 polymorphisms and the risk of hepatocellular carcinoma in Guangxi Zhuang populations of China: Case-control study. Medicine (Baltimore). 2016; 95 (44): e5217. doi:10.1097/md.0000000000005217.; Gutiérrez-Hurtado I.A., Puebla-Pérez A.M., Delgado-Saucedo J.I., Figuera L.E., Zúñiga-González G.M., Gomez-Mariscal K., Ronquillo-Carreón C.A., Gallegos-Arreola M.P. Association between TNF-α-308G>A and -238G>A gene polymorphisms and TNF-α serum levels in Mexican colorectal cancer patients. Genet Mol Res. 2016; 15 (2). doi:10.4238/gmr.15028199.; Luo Y., Ye Z., Li K., Chen R., Li S., Pang J. Associations between polymorphisms in the IL-4 and IL-4 receptor genes and urinary carcinomas: a meta-analysis. Int J Clin Exp Med. 2015; 8 (1): 1227–1233.; Burada F., Dumitrescu T., Nicoli R., Ciurea M.E., Angelescu C., Mixich F., Ioana M. IL-1RN +2018T>C polymorphismis correlated with colorectal cancer. Mol Biol Rep. 2013; 40 (4): 2851–7. doi:10.1007/ s11033-012-2300-x.; Sáenz López P., Vázquez Alonso F., Romero J.M., Carretero R., Tallada Buñuel M., Ruiz Cabello F., Cózar Olmo J.M. Polymorphisms in inflammatory response genes in metastatic renal cancer. Actas Urol Esp. 2009; 33 (5): 474–81.; Bapat A.A., Hostetter G., VonHoff D.D., Han H. Perineural invasion and associated pain in pancreatic cancer. Nat Rev Cancer. 2011; 11 (10): 695–707.doi:10.1038/nrc3131.; Reyes-Gibby C.C., Wang J., Spitz M., Wu X., Yennurajalingam S., Shete S. Genetic variations in Interleukin-8 and Interleukin-10 are associated with pain, depressed mood, and fatigue in lung cancer patients. J Pain Symptom Manage. 2013; 46 (2): 161–72. doi:10.1016/j. jpainsymman.2012.07.019.; Ando K., Takahashi F., Motojima S., Nakashima K., Kaneko N., Hoshi K., Takahashi K. Possible role for tocilizumab, an anti-interleukin-6 receptor antibody, in treating cancer cachexia. J Clin Oncol. 2013; 31 (60): e69–e72. doi:10.1200/JCO.2012.44.2020.; https://www.siboncoj.ru/jour/article/view/617
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15Academic Journal
Συγγραφείς: Б.Н. РАИМКУЛОВ, К.Б. РАИМКУЛОВА, Х.Б. РАИМКУЛОВА, Р.А. БАЕШОВ, Н.А. БХАТ
Θεματικοί όροι: боль, механизмы развития боли, ноцицепция, антиноцицепция, перцепция
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16Academic Journal
Συγγραφείς: Бесхмельницына Е.А., Корокин М.В., Автина Т.В., Мартынова О.В., Варавин И.И., Тишин А.Н.
Θεματικοί όροι: ионный канал TRP, TRPA1, боль, кеторолак, ноцицепция, анальгезия
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17Academic Journal
Συγγραφείς: Еремеев, А., Шайхутдинов, И., Шульман, А.
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18Academic Journal
Συγγραφείς: Бесхмельницына, Е. А., Корокин, М. В., Автина, Т. В., Мартынова, О. В., Варавин, И. И.
Θεματικοί όροι: медицина, фармакология, фармакокинетика, лекарственные средства, болевой синдром, лечение, ионный канал TRP, TRPA1, кеторолак, ноцицепция, анальгетики, анальгезия
Διαθεσιμότητα: http://dspace.bsu.edu.ru/handle/123456789/16777
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19Academic Journal
Συγγραφείς: E. V. Igolkina, Е. В. Иголкина
Πηγή: Modern Rheumatology Journal; Том 8, № 3 (2014); 66-72 ; Современная ревматология; Том 8, № 3 (2014); 66-72 ; 2310-158X ; 1996-7012 ; 10.14412/1996-7012-2014-3
Θεματικοί όροι: лечение боли, osteoarthrosis, nociception, neuropathic pain, pain treatment, остеоартроз, ноцицепция, невропатическая боль
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PainDETECT: a new scrining questinnare to identify neuropathic components in patients with back pain. Curr Med Res Opin. 2006;22(10):1911–20. DOI: http://dx.doi.org/10.1185/030079906X132488.; Thakur M, Dickenson AH and Baron R. Osteoarthritis pain: nociceptive or neuropathic? Nat Rev Rheumatol. 2014;10(6):374–80. DOI:10.1038/nrrheum.2014,47. Epub 2014 Apr 1.; Orita S, Ishikawa T, Miyagi M, et al. Pain-related sensory innervation in monoiodoacetate-induced ostheoarhritis in rat knees that gradually develops neuronal injure in addition to inflammatory pain. BMC Musculoskelet Disord. 2011;12:134. DOI:10.1186/1471-2474-12-134.; Ivanavicius SP, Ball AD, Heapy CG, et al. Strucrural pathology in a rodent model of osteoarthritis is assotiated with neuropatic pain: increased expression of ATF-3 and pharmacological characterization. Pain. 2007;128(3):272–82. DOI: http://dx.doi.org/10.1016/j.pain.2006.12.022.; Thakur M, Rahman W, Hobbs C, et al. Characterisation of a peripheral neuropathic component of the rat monoiodoacetate model of ostheoarthrites. PLoS ONE. 2012;7(3):e33730. DOI:10.1371/journal.pone.0033730. Epub 2012 Mar 21.; Kelly S, Dunham JP, Murrey F, et al. Spontaneous firing in C-fibers and increased mechanical sensitivity in A-fibers of knee joint associated mechanoreceptive ptimary afferent neurons during MIA – induced ostheoarthritis in the rat. Ostheoarthritis Cartilage. 2012;20(4):305–13. DOI:10.1016/j.joca.2012.01.002. Epub 2012 Jan 10.; Oteo-Alvaro A, Ruiz-Iban MA, Miguens X, et al. High Prevalence of Neuropathic Pain Features in Patients with Knee Osteoarthritis: A Cross-Sectional Study. Pain Pract. 2014 Apr 21. DOI:10.1111/papr.12220.; Suri S, Gill SE, Camin M, et al. Neurovascular invasion at the osteochondral junction and in osteophites in osteoarthritis. Ann Rheum Dis. 2007;66(11):1423–8. DOI: http://dx.doi.org/10.1136/ard.2006.063354. Epub 2007 Apr 19.; Wolsh DA, McWilliams DF, Turley MJ, et al. Angiogenesis and nerve growth factor at the at the osteochondral junction in rheumatoid rthritis and osteoarthritis.Rheumatology (Oxford). 2010;49(10):1852–61. DOI:10.1093/rheumatology/keq188. Epub 2010 Jun 26.; Eitner A, Pester J, Nietzsche S, et al. The innervation of sinovium of human osteoarthritic joints in comparison with normal rat and sheep synovium. Osteoarthtitis Cartilage. 2013;21(9):1383–91. DOI:10.1016/j.joca.2013.06.018.; Wilde V, Palmer S, Learmonth ID, Dieppe P. Somatosensory abnormalities in knee OA. Rheumatology (Oxford). 2012;51(3):535–43. DOI:10.1093/rheumatology/ ker343. Epub 2011 Nov 24.; Arendt-Nielsen L, Nie H, Laursen MB, et al. Sensitization in patients with painful knee osteoarthritis. Pain. 2010;149(3):573–81. DOI:10.1016/j.pain.2010.04.003. Epub 2010 Apr 24.; Imamura M, Imamura ST, Kaziyama HH, et al. Impact of nervous system hyperalgesia on pain, disabilite, and quality of life in patients with knee osteoarthritis: a controlled analysis. Arthritis Rheum. 2008;59(10):1424–31. DOI:10.1002/art.24120.; Hochman JR, Davis AM, Elkayam J, et al. Neuropathic pain symptoms on the modified painDETECT correlate with signs of central sensitization in knee osteoarthritis. Osteoarthritis Cartilage. 2013;21(9):1236–42. DOI:10.1016/j.joca.2013.06.023.; Gwylim SE, Keltner JR, Warnaby CE, et al. Psycholophysical and functional imaging evidence supporting the presence of central sensitization in a cohort of osteoarthritis patients. Arthritis Rheum. 2009;61(9):1226–34. DOI:10.1002/art.24837. 31. Wilde V, Hewlett S, Learmonth ID, Dieppe P. Persistent pain after joint replacement: prevalence, sensory qualities and postoperative determinants. Pain. 2011;152(3):566–72. DOI:10.1016/j.pain.2010.11.023. Epub 2011 Jan 15.; Ohtori S, Orita S, Yamashita M, et al. Existance of neuropathic pain component in patients with osteoarthritis of the knee. Yonsei Med J. 2012;53(4):801–5. DOI:10.3349/ymj.2012.53.4.801.; Soni A, Batra RN, Gwilym SE, et al. Neuropathic features of joint pain: a community- based study. Arthritis Rheum. 2013;65(7):1942–9. DOI:10.1002/art.37962.; Suokas AK, Walsh DA, McWilliams DF, et al. Quantitative sensory testing in painful osteoarthritis: a systematic review and metaanalysis. Osteoarthritis Cartilage. 2012;20(10):1075–85. DOI:10.1016/j.joca.2012.06.009. Epub 2012 Jul 13.; Hochman JR, Gagliese L, Davis AM, Hawker GA. Neuropathic pain symptoms in a community knee OA cohort. Osteoarthritis Cartilage. 2011;19(6):647–54. DOI:10.1016/j.joca.2011.03.007. Epub 2011 Apr 8.; Hochman GR, French MR, Bermingham SL, Hawker GA. The nerve of osteoarthritis pain. Arthritis Care Res (Hoboken). 2010;62(7):1019–23. DOI:10.1002/acr.20142.; Яхно НН, редактор. Методические рекомендации по диагностике и лечению невропатической боли. Москва: РАМН; 2008. С. 5-7. [Yakhno NN, editor. Metodicheskie rekomendatsii po diagnostike i lecheniyu nevropaticheskoi boli [Methodical recommendations about diagnostics and treatment of nevropatichesky pain]. Moscow: RAMN; 2008. P. 5–7.]; Инструкция по применению лекарственного препарата для медицинского применения Лирика® от 20.07.2011. РУ № ЛС - 0011752 от 20.07.2011, с изм. от 20.08.2012. [Instruktsiya po primeneniyu lekarstvennogo preparata dlya meditsinskogo primeneniya Lirika® ot 20.07.2011 [The instruction on use of medicine for medical application of Lirika® of 20.07.2011]. RU № LS - 0011752 of 20.07.2011, s izm. ot 20.08.2012.]; Roth T, van Seventer R, Murphy TK. The effect of pregabalin on pain-related sleep interference in diabetic peripheral neuropathy or postherpetic neuralgia: a review of nine clinical trials. Curr Med Res Opin. 2010 Oct;26(10):2411Р9. DOI: http://dx.doi.org/ 10.1185/03007995.2010.516142.; Argoff CE, Backonja MM, Belgrade MJ, et al. Consensus guidelines: treatment planning and options. Diabetic peripheral neuropathic pain. Mayo Clin Proc. 2006;81 (4 Suppl):S12Р25. DOI: http://dx.doi.org/10.1016/S0025-6196(11)61475-4.; Moulin DE, Clark AJ, Gilron I, et al. Pharmacological management of chronic neuropathic pain Р consensus statement and guidelines from the Canadian Pain Society. Pain Res Manag. 2007;12(1):13–21. 42. Attal N, Cruccu G, Baron R, et al. EFNS guidelines on the pharmacological treatment on neuropathic pain: 2009 revision. Eur J Neurol. 2010;17(9):1113Рe88. DOI:10.1111/j.1468-1331.2010.02999.x. Epub 2010 Apr 9.; Bohlega S, Alsaadi T, Amir A, et al. Guidelines for the pharmacological treatment of peripheral neuropathic pain: expert panel recommendations for the middle East region. J Int Med Res. 2010;38:295–317. DOI: http://dx.doi.org/10.1177/ 147323001003800201.; Fehrenbacher JC, Tailor CP, Vasko MR. Pregabalin and gabapentin reduce release of substance – and CGRP from rat spinal tissues only after inflammation or activation of protein kinase C. 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20Academic Journal
Συγγραφείς: АГАДЖАНЯН Н.А., БЫКОВ А.Т., МЕДАЛИЕВА Р.Х.
Θεματικοί όροι: КОМПОНЕНТНЫЙ СОСТАВ ТЕЛА, АНТИОКСИДАНТНАЯ ЗАЩИТА, ОКСИДАТИВНЫЙ СТРЕСС, ХОЛОДОВАЯ НОЦИЦЕПЦИЯ
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