Effect of isobutyl methacrylate and methacrylic acid eluted from chairside denture hard reliners on enzymatic cellular antioxidants: An in vitro study in human primary buccal mucosal fibroblasts

Aim: This study was conducted with the objective to evaluate the cytotoxicity of monomers isobutyl methacrylate (IBMA) and methacrylic acid (MA) in human buccal mucosal fibroblast primary cell culture and to study their effect on cellular enzymatic antioxidants-glutathione peroxidase (GPx), superoxi...

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Main Authors: Sivanesan Karthikeyan Jagdish, Anbazhagan Ganeshkumar, Rajaraman Shakila, Shyam Singh, Balasubramanian Jesudas, Sivanesan Karthikeyan
Format: Article
Language:English
Published: Wolters Kluwer Medknow Publications 2017-01-01
Series:The Journal of Indian Prosthodontic Society
Subjects:
Online Access:http://www.j-ips.org/article.asp?issn=0972-4052;year=2017;volume=17;issue=2;spage=189;epage=195;aulast=Jagdish
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spelling doaj-c03e051fd5c14542be4f5fc1faf6f6cd2020-11-24T22:32:52ZengWolters Kluwer Medknow PublicationsThe Journal of Indian Prosthodontic Society0972-40521998-40572017-01-0117218919510.4103/jips.jips_282_16Effect of isobutyl methacrylate and methacrylic acid eluted from chairside denture hard reliners on enzymatic cellular antioxidants: An in vitro study in human primary buccal mucosal fibroblastsSivanesan Karthikeyan JagdishAnbazhagan GaneshkumarRajaraman ShakilaShyam SinghBalasubramanian JesudasSivanesan KarthikeyanAim: This study was conducted with the objective to evaluate the cytotoxicity of monomers isobutyl methacrylate (IBMA) and methacrylic acid (MA) in human buccal mucosal fibroblast primary cell culture and to study their effect on cellular enzymatic antioxidants-glutathione peroxidase (GPx), superoxide dismutase (SOD), and catalase (CAT). Materials and Methods: The tissue for fibroblast cell culture was harvested from oral buccal mucosa of a healthy donor. Fibroblast cells were plated at a density of 1 × 104 cells per well in 96-well tissue culture plates. Cells were exposed to various concentrations of IBMA and MA. The cell viability and various enzyme activities were evaluated 24 h after exposure to the above treatments. All tests were done in triplicate. Cell viability was assessed by trypan blue dye exclusion assay and all enzyme activities were done using assay kits from Cayman Chemicals, Ann Arbor, USA. Results: At all concentrations tested a statistically significant decrease in viability was observed in IBMA- and MA-treated cells. Around 42% cells were viable at the highest test concentration of IBMA (80 μmol/L) and only 20% cells were viable at the highest dose (144 μmol/L) of MA exposure (P < 0.05). Dose-dependent decrease in the GPx and SOD activities was observed in cells treated with IBMA and MA (P < 0.05). CAT activity was not detectable in the controls. However, a fall in CAT activity was detected in cells exposed to IBMA and MA at all concentrations tested (P < 0.05). Conclusion: IBMA and MA leaching out from the chairside denture hard reliners are cytotoxic on human buccal fibroblast primary cell cultures. This could be due to the oxidative stress caused by the generation of reactive oxygen species which is evidenced by the fall in activities of antioxidant enzymes (GPx, SOD, and CAT) and cytotoxicity.http://www.j-ips.org/article.asp?issn=0972-4052;year=2017;volume=17;issue=2;spage=189;epage=195;aulast=JagdishChairside relinerscytotoxicityenzymatic antioxidantsfree radicaloxidative stress
collection DOAJ
language English
format Article
sources DOAJ
author Sivanesan Karthikeyan Jagdish
Anbazhagan Ganeshkumar
Rajaraman Shakila
Shyam Singh
Balasubramanian Jesudas
Sivanesan Karthikeyan
spellingShingle Sivanesan Karthikeyan Jagdish
Anbazhagan Ganeshkumar
Rajaraman Shakila
Shyam Singh
Balasubramanian Jesudas
Sivanesan Karthikeyan
Effect of isobutyl methacrylate and methacrylic acid eluted from chairside denture hard reliners on enzymatic cellular antioxidants: An in vitro study in human primary buccal mucosal fibroblasts
The Journal of Indian Prosthodontic Society
Chairside reliners
cytotoxicity
enzymatic antioxidants
free radical
oxidative stress
author_facet Sivanesan Karthikeyan Jagdish
Anbazhagan Ganeshkumar
Rajaraman Shakila
Shyam Singh
Balasubramanian Jesudas
Sivanesan Karthikeyan
author_sort Sivanesan Karthikeyan Jagdish
title Effect of isobutyl methacrylate and methacrylic acid eluted from chairside denture hard reliners on enzymatic cellular antioxidants: An in vitro study in human primary buccal mucosal fibroblasts
title_short Effect of isobutyl methacrylate and methacrylic acid eluted from chairside denture hard reliners on enzymatic cellular antioxidants: An in vitro study in human primary buccal mucosal fibroblasts
title_full Effect of isobutyl methacrylate and methacrylic acid eluted from chairside denture hard reliners on enzymatic cellular antioxidants: An in vitro study in human primary buccal mucosal fibroblasts
title_fullStr Effect of isobutyl methacrylate and methacrylic acid eluted from chairside denture hard reliners on enzymatic cellular antioxidants: An in vitro study in human primary buccal mucosal fibroblasts
title_full_unstemmed Effect of isobutyl methacrylate and methacrylic acid eluted from chairside denture hard reliners on enzymatic cellular antioxidants: An in vitro study in human primary buccal mucosal fibroblasts
title_sort effect of isobutyl methacrylate and methacrylic acid eluted from chairside denture hard reliners on enzymatic cellular antioxidants: an in vitro study in human primary buccal mucosal fibroblasts
publisher Wolters Kluwer Medknow Publications
series The Journal of Indian Prosthodontic Society
issn 0972-4052
1998-4057
publishDate 2017-01-01
description Aim: This study was conducted with the objective to evaluate the cytotoxicity of monomers isobutyl methacrylate (IBMA) and methacrylic acid (MA) in human buccal mucosal fibroblast primary cell culture and to study their effect on cellular enzymatic antioxidants-glutathione peroxidase (GPx), superoxide dismutase (SOD), and catalase (CAT). Materials and Methods: The tissue for fibroblast cell culture was harvested from oral buccal mucosa of a healthy donor. Fibroblast cells were plated at a density of 1 × 104 cells per well in 96-well tissue culture plates. Cells were exposed to various concentrations of IBMA and MA. The cell viability and various enzyme activities were evaluated 24 h after exposure to the above treatments. All tests were done in triplicate. Cell viability was assessed by trypan blue dye exclusion assay and all enzyme activities were done using assay kits from Cayman Chemicals, Ann Arbor, USA. Results: At all concentrations tested a statistically significant decrease in viability was observed in IBMA- and MA-treated cells. Around 42% cells were viable at the highest test concentration of IBMA (80 μmol/L) and only 20% cells were viable at the highest dose (144 μmol/L) of MA exposure (P < 0.05). Dose-dependent decrease in the GPx and SOD activities was observed in cells treated with IBMA and MA (P < 0.05). CAT activity was not detectable in the controls. However, a fall in CAT activity was detected in cells exposed to IBMA and MA at all concentrations tested (P < 0.05). Conclusion: IBMA and MA leaching out from the chairside denture hard reliners are cytotoxic on human buccal fibroblast primary cell cultures. This could be due to the oxidative stress caused by the generation of reactive oxygen species which is evidenced by the fall in activities of antioxidant enzymes (GPx, SOD, and CAT) and cytotoxicity.
topic Chairside reliners
cytotoxicity
enzymatic antioxidants
free radical
oxidative stress
url http://www.j-ips.org/article.asp?issn=0972-4052;year=2017;volume=17;issue=2;spage=189;epage=195;aulast=Jagdish
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