The preservative effect of Thai propolis extract on the viability of human periodontal ligament cells

© 2016 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd Background/Aim: Tooth avulsion causes an injury to the periodontal ligament (PDL). The success of tooth replantation depends on the quantity and quality of PDL cells. The aim of this study was to examine the preservative an...

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Main Authors: Prueksakorn A., Puasiri S., Ruangsri S., Makeudom A., Sastraruji T., Krisanaprakornkit S., Chailertvanitkul P.
Format: Journal
Published: 2017
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http://cmuir.cmu.ac.th/jspui/handle/6653943832/41248
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spelling th-cmuir.6653943832-412482017-09-28T04:20:13Z The preservative effect of Thai propolis extract on the viability of human periodontal ligament cells Prueksakorn A. Puasiri S. Ruangsri S. Makeudom A. Sastraruji T. Krisanaprakornkit S. Chailertvanitkul P. © 2016 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd Background/Aim: Tooth avulsion causes an injury to the periodontal ligament (PDL). The success of tooth replantation depends on the quantity and quality of PDL cells. The aim of this study was to examine the preservative and proliferative effects of Thai propolis extract, previously shown to exert anti-inflammatory and antioxidant activities, on human PDL cells. Materials and methods: Ninety-six premolars were left to air dry for 30 min and stored in Hank's balanced salt solution (HBSS), milk, or various concentrations of propolis extract from 0.25 to 10 mg ml −1 for 3 h. PDL cells were isolated by collagenase and trypsin digestion, and their viability was determined by a trypan blue dye exclusion assay. PDL tissues were also scraped off the root surface and cultured to determine cell growth and morphology. The alamarBlue ® and BrdU assays were performed to determine the cytotoxic and proliferative effects of the extract on cultured PDL cells, respectively. Results: A non-toxic dose of 2.5 mg ml −1 of propolis extract yielded the greatest percentage of cell viability (78.84 ± 3.34%), which was significantly higher than those of the other concentrations (P < 0.001). Nevertheless, this percentage was not significantly different from that of HBSS (80.14 ± 2.44%; P = 1.00), but was significantly higher than that of milk (71.27 ± 2.79%; P < 0.001). The cells grown from PDL explants looked like fibroblasts. However, 2.5 mg ml −1 of the extract did not induce PDL cell proliferation. Conclusion: Thai propolis extract at 2.5 mg ml −1 appears to be the most effective dose for preserving the viability of PDL cells, and this was comparable to HBSS. 2017-09-28T04:20:13Z 2017-09-28T04:20:13Z 2016-12-01 Journal 16004469 2-s2.0-84979025625 10.1111/edt.12292 https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84979025625&origin=inward http://cmuir.cmu.ac.th/jspui/handle/6653943832/41248
institution Chiang Mai University
building Chiang Mai University Library
country Thailand
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description © 2016 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd Background/Aim: Tooth avulsion causes an injury to the periodontal ligament (PDL). The success of tooth replantation depends on the quantity and quality of PDL cells. The aim of this study was to examine the preservative and proliferative effects of Thai propolis extract, previously shown to exert anti-inflammatory and antioxidant activities, on human PDL cells. Materials and methods: Ninety-six premolars were left to air dry for 30 min and stored in Hank's balanced salt solution (HBSS), milk, or various concentrations of propolis extract from 0.25 to 10 mg ml −1 for 3 h. PDL cells were isolated by collagenase and trypsin digestion, and their viability was determined by a trypan blue dye exclusion assay. PDL tissues were also scraped off the root surface and cultured to determine cell growth and morphology. The alamarBlue ® and BrdU assays were performed to determine the cytotoxic and proliferative effects of the extract on cultured PDL cells, respectively. Results: A non-toxic dose of 2.5 mg ml −1 of propolis extract yielded the greatest percentage of cell viability (78.84 ± 3.34%), which was significantly higher than those of the other concentrations (P < 0.001). Nevertheless, this percentage was not significantly different from that of HBSS (80.14 ± 2.44%; P = 1.00), but was significantly higher than that of milk (71.27 ± 2.79%; P < 0.001). The cells grown from PDL explants looked like fibroblasts. However, 2.5 mg ml −1 of the extract did not induce PDL cell proliferation. Conclusion: Thai propolis extract at 2.5 mg ml −1 appears to be the most effective dose for preserving the viability of PDL cells, and this was comparable to HBSS.
format Journal
author Prueksakorn A.
Puasiri S.
Ruangsri S.
Makeudom A.
Sastraruji T.
Krisanaprakornkit S.
Chailertvanitkul P.
spellingShingle Prueksakorn A.
Puasiri S.
Ruangsri S.
Makeudom A.
Sastraruji T.
Krisanaprakornkit S.
Chailertvanitkul P.
The preservative effect of Thai propolis extract on the viability of human periodontal ligament cells
author_facet Prueksakorn A.
Puasiri S.
Ruangsri S.
Makeudom A.
Sastraruji T.
Krisanaprakornkit S.
Chailertvanitkul P.
author_sort Prueksakorn A.
title The preservative effect of Thai propolis extract on the viability of human periodontal ligament cells
title_short The preservative effect of Thai propolis extract on the viability of human periodontal ligament cells
title_full The preservative effect of Thai propolis extract on the viability of human periodontal ligament cells
title_fullStr The preservative effect of Thai propolis extract on the viability of human periodontal ligament cells
title_full_unstemmed The preservative effect of Thai propolis extract on the viability of human periodontal ligament cells
title_sort preservative effect of thai propolis extract on the viability of human periodontal ligament cells
publishDate 2017
url https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84979025625&origin=inward
http://cmuir.cmu.ac.th/jspui/handle/6653943832/41248
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