Increased cell viability and proliferation in post-hypoxic hippocampal tissue culture treated with<em> Acalypha indica</em> root extract

<p><strong>Background:</strong> This research was done to study the influence of <em>Acalypha indica</em> Linn root extract towards relative cell viability and proliferation as parameters of neurogenesis in post-hypoxic hippocampal tissue culture.</p><p><...

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Main Authors: Sophie Yolanda, Endang W. Bachtiar, Nurhadi Ibrahim
Format: Article
Language:English
Published: Faculty of Medicine Universitas Indonesia 2011-05-01
Series:Medical Journal of Indonesia
Online Access:http://mji.ui.ac.id/journal/index.php/mji/article/view/433
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spelling doaj-1173831a4ccb4348a5d44aa6f132cb4e2020-11-25T01:32:27ZengFaculty of Medicine Universitas Indonesia Medical Journal of Indonesia0853-17732252-80832011-05-0120294910.13181/mji.v20i2.433430Increased cell viability and proliferation in post-hypoxic hippocampal tissue culture treated with<em> Acalypha indica</em> root extractSophie YolandaEndang W. BachtiarNurhadi Ibrahim<p><strong>Background:</strong> This research was done to study the influence of <em>Acalypha indica</em> Linn root extract towards relative cell viability and proliferation as parameters of neurogenesis in post-hypoxic hippocampal tissue culture.</p><p><strong>Methods:</strong> Experimental<em> in vitro</em> study using 24 primary neuronal cell cultures obtained from adult <em>Sprague Dawley</em> rat exposed to hypoxia with 5% O<sub>2</sub>/5% CO<sub>2</sub>/N<sub>2</sub> balance gas for 24 hours. Post-hypoxia, <em>Acalypha indica</em> Linn root extract was added at doses of 10, 15, and 20 mg/mL to 3 treatment groups. No treatment was given to the control group. Each group consists of 6 samples. After 90 hours of incubation, relative cell viability was measured by using <em>3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide</em> (MTT) examination, and cell proliferation was measured by using <em>5-bromo2’-deoxy-uridine</em> (BrdU) for cell proliferation. Data was analyzed using one way ANOVA parametric tests, then further analyzed with post-hoc analysis.</p><p><strong>Results:</strong> The relative cell viability of rat hippocampal tissue culture treated with<em> Acalypha indica</em> Linn root extract with dose of 10, 15, and 20 mg/mL was significantly higher than control (176.95%, 220.62%, and 386.02% vs. 100%). Cell proliferation of rat hippocampal tissue culture treated with <em>Acalypha indica</em> Linn root extract with dose of 10, 15, and 20 mg/mL was significantly higher than control (0.132, 0.117, 0.114 vs 0.096).</p><p><strong>Conclusion:</strong><em> Acalypha indica</em> Linn root extract with doses of 10, 15, and 20 mg/mL can increase relative cell viability and proliferation in post-hypoxic hippocampal tissue culture. <em><strong>(Med J Indones 2011; 20:94-9)</strong></em></p><p><strong>Keywords:</strong><em> Acalypha indica Linn (akar kucing), cell proliferation, hypoxia, neurogenesis, relative cell viability</em></p>http://mji.ui.ac.id/journal/index.php/mji/article/view/433
collection DOAJ
language English
format Article
sources DOAJ
author Sophie Yolanda
Endang W. Bachtiar
Nurhadi Ibrahim
spellingShingle Sophie Yolanda
Endang W. Bachtiar
Nurhadi Ibrahim
Increased cell viability and proliferation in post-hypoxic hippocampal tissue culture treated with<em> Acalypha indica</em> root extract
Medical Journal of Indonesia
author_facet Sophie Yolanda
Endang W. Bachtiar
Nurhadi Ibrahim
author_sort Sophie Yolanda
title Increased cell viability and proliferation in post-hypoxic hippocampal tissue culture treated with<em> Acalypha indica</em> root extract
title_short Increased cell viability and proliferation in post-hypoxic hippocampal tissue culture treated with<em> Acalypha indica</em> root extract
title_full Increased cell viability and proliferation in post-hypoxic hippocampal tissue culture treated with<em> Acalypha indica</em> root extract
title_fullStr Increased cell viability and proliferation in post-hypoxic hippocampal tissue culture treated with<em> Acalypha indica</em> root extract
title_full_unstemmed Increased cell viability and proliferation in post-hypoxic hippocampal tissue culture treated with<em> Acalypha indica</em> root extract
title_sort increased cell viability and proliferation in post-hypoxic hippocampal tissue culture treated with<em> acalypha indica</em> root extract
publisher Faculty of Medicine Universitas Indonesia
series Medical Journal of Indonesia
issn 0853-1773
2252-8083
publishDate 2011-05-01
description <p><strong>Background:</strong> This research was done to study the influence of <em>Acalypha indica</em> Linn root extract towards relative cell viability and proliferation as parameters of neurogenesis in post-hypoxic hippocampal tissue culture.</p><p><strong>Methods:</strong> Experimental<em> in vitro</em> study using 24 primary neuronal cell cultures obtained from adult <em>Sprague Dawley</em> rat exposed to hypoxia with 5% O<sub>2</sub>/5% CO<sub>2</sub>/N<sub>2</sub> balance gas for 24 hours. Post-hypoxia, <em>Acalypha indica</em> Linn root extract was added at doses of 10, 15, and 20 mg/mL to 3 treatment groups. No treatment was given to the control group. Each group consists of 6 samples. After 90 hours of incubation, relative cell viability was measured by using <em>3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide</em> (MTT) examination, and cell proliferation was measured by using <em>5-bromo2’-deoxy-uridine</em> (BrdU) for cell proliferation. Data was analyzed using one way ANOVA parametric tests, then further analyzed with post-hoc analysis.</p><p><strong>Results:</strong> The relative cell viability of rat hippocampal tissue culture treated with<em> Acalypha indica</em> Linn root extract with dose of 10, 15, and 20 mg/mL was significantly higher than control (176.95%, 220.62%, and 386.02% vs. 100%). Cell proliferation of rat hippocampal tissue culture treated with <em>Acalypha indica</em> Linn root extract with dose of 10, 15, and 20 mg/mL was significantly higher than control (0.132, 0.117, 0.114 vs 0.096).</p><p><strong>Conclusion:</strong><em> Acalypha indica</em> Linn root extract with doses of 10, 15, and 20 mg/mL can increase relative cell viability and proliferation in post-hypoxic hippocampal tissue culture. <em><strong>(Med J Indones 2011; 20:94-9)</strong></em></p><p><strong>Keywords:</strong><em> Acalypha indica Linn (akar kucing), cell proliferation, hypoxia, neurogenesis, relative cell viability</em></p>
url http://mji.ui.ac.id/journal/index.php/mji/article/view/433
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