The Effects of Different Concentrations of Acetylsalicylic Acid on Proliferation and Viability of Lymphocytes in Cell Culture

Numerous studies conducted on acetylsalicylic acid (ASA, aspirin) confirmed that ASA inhibits proliferation and induces apoptosis in various types of human cells. Therefore, it was of interest to examine possible effects of different concentrations of ASA on viability and proliferation of lymphocyte...

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Main Authors: Tanja Dujić, Adlija Čaušević, Maja Malenica
Format: Article
Language:English
Published: Association of Basic Medical Sciences of Federation of Bosnia and Herzegovina 2008-08-01
Series:Bosnian Journal of Basic Medical Sciences
Subjects:
Online Access:http://www.bjbms.org/ojs/index.php/bjbms/article/view/2919
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spelling doaj-6d8b6813b6bc4e82a8c868266486752e2020-11-24T21:41:36ZengAssociation of Basic Medical Sciences of Federation of Bosnia and HerzegovinaBosnian Journal of Basic Medical Sciences1512-86011840-48122008-08-018310.17305/bjbms.2008.2919546The Effects of Different Concentrations of Acetylsalicylic Acid on Proliferation and Viability of Lymphocytes in Cell CultureTanja Dujić0Adlija Čaušević1Maja Malenica2Department of Clinical Biochemistry, Faculty of Pharmacy, University of SarajevoDepartment of Clinical Biochemistry, Faculty of Pharmacy, University of SarajevoDepartment of Clinical Biochemistry, Faculty of Pharmacy, University of SarajevoNumerous studies conducted on acetylsalicylic acid (ASA, aspirin) confirmed that ASA inhibits proliferation and induces apoptosis in various types of human cells. Therefore, it was of interest to examine possible effects of different concentrations of ASA on viability and proliferation of lymphocytes in the cell culture. After separation from blood, lymphocytes were suspended in RPMI 1640 medium and cultured at 37°C. Solution of ASA was added to cultures after 24h, in final concentrations of 1, 3 and 5 mmol/l. After 48h, proliferative response was evaluated by WST-1 assay. Significant difference in viability between controls and cell cultures treated with ASA in three different concentrations was observed (p < 0,01). Percents of viable cells in cultures after application of 1, 3 and 5 mmol/l ASA were 9,9%, 2,5% and 16,9% (compared to controls), respectively. To determine whether this cytotoxic effect was result of induction of apoptosis, DNA from cell cultures was isolated and subjected to agarose gel electrophoresis. Fragmentation of DNA was not detected, excluding apoptosis as possible cause of cytotoxic effects. Addition of ASA caused change of initial extracellular pH value for each treated culture. After addition of 1 mmol/l ASA, pH of culture was 7,19, after 3 mmol/L, 6,99 and after addition of 5 mmol/l solution, pH was 6,75. Decreased lymphocyte viability could be attributed to either the effects of the added substance or possible further acidification of cell cultures during three days of incubation.http://www.bjbms.org/ojs/index.php/bjbms/article/view/2919acetylsalicylic acid (aspirin)lymphocyte cell culture
collection DOAJ
language English
format Article
sources DOAJ
author Tanja Dujić
Adlija Čaušević
Maja Malenica
spellingShingle Tanja Dujić
Adlija Čaušević
Maja Malenica
The Effects of Different Concentrations of Acetylsalicylic Acid on Proliferation and Viability of Lymphocytes in Cell Culture
Bosnian Journal of Basic Medical Sciences
acetylsalicylic acid (aspirin)
lymphocyte cell culture
author_facet Tanja Dujić
Adlija Čaušević
Maja Malenica
author_sort Tanja Dujić
title The Effects of Different Concentrations of Acetylsalicylic Acid on Proliferation and Viability of Lymphocytes in Cell Culture
title_short The Effects of Different Concentrations of Acetylsalicylic Acid on Proliferation and Viability of Lymphocytes in Cell Culture
title_full The Effects of Different Concentrations of Acetylsalicylic Acid on Proliferation and Viability of Lymphocytes in Cell Culture
title_fullStr The Effects of Different Concentrations of Acetylsalicylic Acid on Proliferation and Viability of Lymphocytes in Cell Culture
title_full_unstemmed The Effects of Different Concentrations of Acetylsalicylic Acid on Proliferation and Viability of Lymphocytes in Cell Culture
title_sort effects of different concentrations of acetylsalicylic acid on proliferation and viability of lymphocytes in cell culture
publisher Association of Basic Medical Sciences of Federation of Bosnia and Herzegovina
series Bosnian Journal of Basic Medical Sciences
issn 1512-8601
1840-4812
publishDate 2008-08-01
description Numerous studies conducted on acetylsalicylic acid (ASA, aspirin) confirmed that ASA inhibits proliferation and induces apoptosis in various types of human cells. Therefore, it was of interest to examine possible effects of different concentrations of ASA on viability and proliferation of lymphocytes in the cell culture. After separation from blood, lymphocytes were suspended in RPMI 1640 medium and cultured at 37°C. Solution of ASA was added to cultures after 24h, in final concentrations of 1, 3 and 5 mmol/l. After 48h, proliferative response was evaluated by WST-1 assay. Significant difference in viability between controls and cell cultures treated with ASA in three different concentrations was observed (p < 0,01). Percents of viable cells in cultures after application of 1, 3 and 5 mmol/l ASA were 9,9%, 2,5% and 16,9% (compared to controls), respectively. To determine whether this cytotoxic effect was result of induction of apoptosis, DNA from cell cultures was isolated and subjected to agarose gel electrophoresis. Fragmentation of DNA was not detected, excluding apoptosis as possible cause of cytotoxic effects. Addition of ASA caused change of initial extracellular pH value for each treated culture. After addition of 1 mmol/l ASA, pH of culture was 7,19, after 3 mmol/L, 6,99 and after addition of 5 mmol/l solution, pH was 6,75. Decreased lymphocyte viability could be attributed to either the effects of the added substance or possible further acidification of cell cultures during three days of incubation.
topic acetylsalicylic acid (aspirin)
lymphocyte cell culture
url http://www.bjbms.org/ojs/index.php/bjbms/article/view/2919
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