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Association of systemic diseases of connective tissue (SDCT) and gerontological processes. / Shishkin, V. ; Kudriavtseva, G. V. ; Malenkov, Y. ; Shishkin, V. V. .

в: Annals of the Rheumatic Diseases, Том 79, № S1, THU0238, 06.2020, стр. 346.

Результаты исследований: Научные публикации в периодических изданияхстатьяРецензирование

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@article{64e12fb8d75d48caad72a2ad96bdd09e,
title = "Association of systemic diseases of connective tissue (SDCT) and gerontological processes",
abstract = "Background: The approach from the point of view of the evolutionary perspective of finding targets for therapeutic effects among the components of the cellular destruction system is critical both in the treatment of rheumatological diseases and in gerontology.Objectives: To identify the relationships between the pathways of cell death in synovial fluid (SF) of people of different age groups with SDCT.Methods: SF was analyzed in patients of two age groups. Group N 1 of patients: 10 SLE (43±2.3 years), 13 RA (45±1.6 years), 7 SSD (35±1.8 years) and 8 donors (42±2.7 years, postmortem). Group N 2 (age) of patients: 9 SLE (69±1.8 years), 10 RA (65±1.6 years), 5 SSD (65±0.7 years) and 9 donors (66±2.3 years, postmortem). SF treated with 0.1% Triton-x-100, resuspended in 0.1% citrate buffer (pH = 7.4) and centrifuged at 25000 g for 30 minutes. The supernatant has been used in the experiment. The activity of adenosine monophosphate-activated protein kinase (AMPK) was evaluated by Western blotting. The level of p53 protein was analyzed by the enzyme immunoassay method using ELISA kit (eBioscience, (USA). The content of 8-hydroxy-2-deoxyguanosine (8-OH-dG) was evaluated using the EIA Kit (USA). Quantitative determination of cytochrome C (Cyt c) was carried using the ELISA kit. Active forms of oxygen free radicals (АFRF) were registered by EPR.Results: An interaction was established between the pathways of cell death in SDCT (mostly distinctive in SLE), age-related changes and clinical manifestations of the autoimmune process were established. The severity of cell death types depends on the nosological form of SDCT (tab.1).",
author = "V. Shishkin and Kudriavtseva, {G. V.} and Y. Malenkov and Shishkin, {V. V.}",
note = "The EULAR Journal Annals of the Rheumatic Diseases June, 2020 https://ard.bmj.com/content/79/Suppl_1 Vol. 79 suppl 1 ISSN 0003-4967 (print); eISSN 1468-2060 (online) p. 346 Impact Factor 16.102 https://ard.bmj.com/ Impact Factor 16.102, rank 2/32 Rheumatology (2019) CiteScore 25.9, rank 1/56 Rheumatology (2019) https://ard.bmj.com/pages/about/ ; Annual European Congress of Rheumatology (EULAR 2019), EULAR 2019 ; Conference date: 12-06-2019 Through 15-06-2019",
year = "2020",
month = jun,
language = "English",
volume = "79",
pages = "346",
journal = "Annals of the Rheumatic Diseases",
issn = "0003-4967",
publisher = "BMJ Publishing Group",
number = "S1",

}

RIS

TY - JOUR

T1 - Association of systemic diseases of connective tissue (SDCT) and gerontological processes

AU - Shishkin, V.

AU - Kudriavtseva, G. V.

AU - Malenkov, Y.

AU - Shishkin, V. V.

N1 - The EULAR Journal Annals of the Rheumatic Diseases June, 2020 https://ard.bmj.com/content/79/Suppl_1 Vol. 79 suppl 1 ISSN 0003-4967 (print); eISSN 1468-2060 (online) p. 346 Impact Factor 16.102 https://ard.bmj.com/ Impact Factor 16.102, rank 2/32 Rheumatology (2019) CiteScore 25.9, rank 1/56 Rheumatology (2019) https://ard.bmj.com/pages/about/

PY - 2020/6

Y1 - 2020/6

N2 - Background: The approach from the point of view of the evolutionary perspective of finding targets for therapeutic effects among the components of the cellular destruction system is critical both in the treatment of rheumatological diseases and in gerontology.Objectives: To identify the relationships between the pathways of cell death in synovial fluid (SF) of people of different age groups with SDCT.Methods: SF was analyzed in patients of two age groups. Group N 1 of patients: 10 SLE (43±2.3 years), 13 RA (45±1.6 years), 7 SSD (35±1.8 years) and 8 donors (42±2.7 years, postmortem). Group N 2 (age) of patients: 9 SLE (69±1.8 years), 10 RA (65±1.6 years), 5 SSD (65±0.7 years) and 9 donors (66±2.3 years, postmortem). SF treated with 0.1% Triton-x-100, resuspended in 0.1% citrate buffer (pH = 7.4) and centrifuged at 25000 g for 30 minutes. The supernatant has been used in the experiment. The activity of adenosine monophosphate-activated protein kinase (AMPK) was evaluated by Western blotting. The level of p53 protein was analyzed by the enzyme immunoassay method using ELISA kit (eBioscience, (USA). The content of 8-hydroxy-2-deoxyguanosine (8-OH-dG) was evaluated using the EIA Kit (USA). Quantitative determination of cytochrome C (Cyt c) was carried using the ELISA kit. Active forms of oxygen free radicals (АFRF) were registered by EPR.Results: An interaction was established between the pathways of cell death in SDCT (mostly distinctive in SLE), age-related changes and clinical manifestations of the autoimmune process were established. The severity of cell death types depends on the nosological form of SDCT (tab.1).

AB - Background: The approach from the point of view of the evolutionary perspective of finding targets for therapeutic effects among the components of the cellular destruction system is critical both in the treatment of rheumatological diseases and in gerontology.Objectives: To identify the relationships between the pathways of cell death in synovial fluid (SF) of people of different age groups with SDCT.Methods: SF was analyzed in patients of two age groups. Group N 1 of patients: 10 SLE (43±2.3 years), 13 RA (45±1.6 years), 7 SSD (35±1.8 years) and 8 donors (42±2.7 years, postmortem). Group N 2 (age) of patients: 9 SLE (69±1.8 years), 10 RA (65±1.6 years), 5 SSD (65±0.7 years) and 9 donors (66±2.3 years, postmortem). SF treated with 0.1% Triton-x-100, resuspended in 0.1% citrate buffer (pH = 7.4) and centrifuged at 25000 g for 30 minutes. The supernatant has been used in the experiment. The activity of adenosine monophosphate-activated protein kinase (AMPK) was evaluated by Western blotting. The level of p53 protein was analyzed by the enzyme immunoassay method using ELISA kit (eBioscience, (USA). The content of 8-hydroxy-2-deoxyguanosine (8-OH-dG) was evaluated using the EIA Kit (USA). Quantitative determination of cytochrome C (Cyt c) was carried using the ELISA kit. Active forms of oxygen free radicals (АFRF) were registered by EPR.Results: An interaction was established between the pathways of cell death in SDCT (mostly distinctive in SLE), age-related changes and clinical manifestations of the autoimmune process were established. The severity of cell death types depends on the nosological form of SDCT (tab.1).

M3 - Article

VL - 79

SP - 346

JO - Annals of the Rheumatic Diseases

JF - Annals of the Rheumatic Diseases

SN - 0003-4967

IS - S1

M1 - THU0238

T2 - Annual European Congress of Rheumatology (EULAR 2019)

Y2 - 12 June 2019 through 15 June 2019

ER -

ID: 61440619