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Inhibitory effect of Salvadora persica extract (Miswak) on collagen degradation in demineralized dentin: In vitro study

BACKGROUND/PURPOSE: Root dentin is vulnerable to acid attack, suggesting a higher risk of demineralization than coronal enamel. This study aimed to evaluate the inhibitory effect of Miswak extract on collagen degradation of demineralized dentin lesion. MATERIALS AND METHODS: Demineralized bovine roo...

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Autores principales: Khunkar, Sahar, Hariri, Ilnaz, Alsayed, Ehab, Linjawi, Amal, Khunkar, Sawsan, Islam, Sofiqul, Bakhsh, Turki A., Nakashima, Syozi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Association for Dental Sciences of the Republic of China 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7770310/
https://www.ncbi.nlm.nih.gov/pubmed/33384799
http://dx.doi.org/10.1016/j.jds.2020.05.025
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author Khunkar, Sahar
Hariri, Ilnaz
Alsayed, Ehab
Linjawi, Amal
Khunkar, Sawsan
Islam, Sofiqul
Bakhsh, Turki A.
Nakashima, Syozi
author_facet Khunkar, Sahar
Hariri, Ilnaz
Alsayed, Ehab
Linjawi, Amal
Khunkar, Sawsan
Islam, Sofiqul
Bakhsh, Turki A.
Nakashima, Syozi
author_sort Khunkar, Sahar
collection PubMed
description BACKGROUND/PURPOSE: Root dentin is vulnerable to acid attack, suggesting a higher risk of demineralization than coronal enamel. This study aimed to evaluate the inhibitory effect of Miswak extract on collagen degradation of demineralized dentin lesion. MATERIALS AND METHODS: Demineralized bovine root dentin specimens were treated for 1 h by 20% Miswak extract and 0.12% Chlorehexidine (CHX) as a positive control group, and then subjected to collagenolytic attack (clostridium histolyticum 0.5 CDU/mL, 16 h). These cyclic treatments were repeated for 3 days. After the cyclic treatment, the images of the specimens were captured with a light microscope and the lesion depth of degraded collagen layer of all specimens was measured. The mean lesion depth was calculated and compared between the groups using descriptive and One-way ANOVA followed by Post hoc Tukey's tests. Significant level was set at p < 0.05. RESULTS: The mean lesion depth of CHX (28.6 ± 3.37 μm) had the least value, followed by Miswak (37.5 ± 4.01 μm) then the control (78.4 ± 18.43 μm) group. There was a significant difference in the mean lesion depth among the three groups (p = 0.000). CONCLUSION: Miswak aqueous extract from S. persica was found to preserve the dentin collagen matrix from collagenase enzyme. This could be due to the organic compounds like flavonoids, saponins, alkaloids, tannins, and others which have been reported in literature. Present finding suggests that Miswak might play a positive effect in dentin caries prevention.
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spelling pubmed-77703102020-12-30 Inhibitory effect of Salvadora persica extract (Miswak) on collagen degradation in demineralized dentin: In vitro study Khunkar, Sahar Hariri, Ilnaz Alsayed, Ehab Linjawi, Amal Khunkar, Sawsan Islam, Sofiqul Bakhsh, Turki A. Nakashima, Syozi J Dent Sci Original Article BACKGROUND/PURPOSE: Root dentin is vulnerable to acid attack, suggesting a higher risk of demineralization than coronal enamel. This study aimed to evaluate the inhibitory effect of Miswak extract on collagen degradation of demineralized dentin lesion. MATERIALS AND METHODS: Demineralized bovine root dentin specimens were treated for 1 h by 20% Miswak extract and 0.12% Chlorehexidine (CHX) as a positive control group, and then subjected to collagenolytic attack (clostridium histolyticum 0.5 CDU/mL, 16 h). These cyclic treatments were repeated for 3 days. After the cyclic treatment, the images of the specimens were captured with a light microscope and the lesion depth of degraded collagen layer of all specimens was measured. The mean lesion depth was calculated and compared between the groups using descriptive and One-way ANOVA followed by Post hoc Tukey's tests. Significant level was set at p < 0.05. RESULTS: The mean lesion depth of CHX (28.6 ± 3.37 μm) had the least value, followed by Miswak (37.5 ± 4.01 μm) then the control (78.4 ± 18.43 μm) group. There was a significant difference in the mean lesion depth among the three groups (p = 0.000). CONCLUSION: Miswak aqueous extract from S. persica was found to preserve the dentin collagen matrix from collagenase enzyme. This could be due to the organic compounds like flavonoids, saponins, alkaloids, tannins, and others which have been reported in literature. Present finding suggests that Miswak might play a positive effect in dentin caries prevention. Association for Dental Sciences of the Republic of China 2021-01 2020-06-11 /pmc/articles/PMC7770310/ /pubmed/33384799 http://dx.doi.org/10.1016/j.jds.2020.05.025 Text en © 2020 Association for Dental Sciences of the Republic of China. Publishing services by Elsevier B.V. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Original Article
Khunkar, Sahar
Hariri, Ilnaz
Alsayed, Ehab
Linjawi, Amal
Khunkar, Sawsan
Islam, Sofiqul
Bakhsh, Turki A.
Nakashima, Syozi
Inhibitory effect of Salvadora persica extract (Miswak) on collagen degradation in demineralized dentin: In vitro study
title Inhibitory effect of Salvadora persica extract (Miswak) on collagen degradation in demineralized dentin: In vitro study
title_full Inhibitory effect of Salvadora persica extract (Miswak) on collagen degradation in demineralized dentin: In vitro study
title_fullStr Inhibitory effect of Salvadora persica extract (Miswak) on collagen degradation in demineralized dentin: In vitro study
title_full_unstemmed Inhibitory effect of Salvadora persica extract (Miswak) on collagen degradation in demineralized dentin: In vitro study
title_short Inhibitory effect of Salvadora persica extract (Miswak) on collagen degradation in demineralized dentin: In vitro study
title_sort inhibitory effect of salvadora persica extract (miswak) on collagen degradation in demineralized dentin: in vitro study
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7770310/
https://www.ncbi.nlm.nih.gov/pubmed/33384799
http://dx.doi.org/10.1016/j.jds.2020.05.025
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