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The Role of Piper sarmentosum Aqueous Extract as a Bone Protective Agent, a Histomorphometric Study
Glucocorticoids are one of the causes of secondary osteoporosis. The aqueous extract of Piper sarmentosum contains flavonoids that possess antioxidant effects. In this study, we determined the effects of aqueous Piper sarmentosum leaf extract on structural, dynamic and static histomorphometric chang...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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MDPI
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7589271/ https://www.ncbi.nlm.nih.gov/pubmed/33086468 http://dx.doi.org/10.3390/ijms21207715 |
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author | Mohamad Asri, Siti Fadziyah Soelaiman, Ima Nirwana Mohd Moklas, Mohamad Aris Mohd Nor, Nurul Huda Mohamad Zainal, Nurul Hayati Mohd Ramli, Elvy Suhana |
author_facet | Mohamad Asri, Siti Fadziyah Soelaiman, Ima Nirwana Mohd Moklas, Mohamad Aris Mohd Nor, Nurul Huda Mohamad Zainal, Nurul Hayati Mohd Ramli, Elvy Suhana |
author_sort | Mohamad Asri, Siti Fadziyah |
collection | PubMed |
description | Glucocorticoids are one of the causes of secondary osteoporosis. The aqueous extract of Piper sarmentosum contains flavonoids that possess antioxidant effects. In this study, we determined the effects of aqueous Piper sarmentosum leaf extract on structural, dynamic and static histomorphometric changes from osteoporotic bones of rats induced with glucocorticoids. Thirty-two Sprague-Dawley rats were divided equally into four groups—Sham control group given vehicles (intramuscular (IM) olive oil and oral normal saline); AC: Adrenalectomised (Adrx) control group given IM dexamethasone (DEX) (120 μg/kg/day) and vehicle (oral normal saline); AP: Adrx group administered IM DEX (120 μg/kg/day) and aqueous Piper sarmentosum leaf extract (125 mg/kg/day) orally; and AG: Adrx group administered IM DEX (120 μg/kg/day) and oral glycyrrhizic acid (GCA) (120 mg/kg/day). Histomorphometric measurements showed that the bone volume, trabecular thickness, trabecular number, osteoid and osteoblast surfaces, double-labelled trabecular surface, mineralizing surface and bone formation rate of rats given aqueous Piper sarmentosum leaf extract were significantly increased (p < 0.05), whereas the trabecular separation and osteoclast surface were significantly reduced (p < 0.05). This study suggests that aqueous Piper sarmentosum leaf extract was able to prevent bone loss in prolonged glucocorticoid therapy. Thus, Piper sarmentosum has the potential to be used as an alternative medicine against osteoporosis and osteoporotic fractures in patients undergoing long-term glucocorticoid therapy. |
format | Online Article Text |
id | pubmed-7589271 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-75892712020-10-29 The Role of Piper sarmentosum Aqueous Extract as a Bone Protective Agent, a Histomorphometric Study Mohamad Asri, Siti Fadziyah Soelaiman, Ima Nirwana Mohd Moklas, Mohamad Aris Mohd Nor, Nurul Huda Mohamad Zainal, Nurul Hayati Mohd Ramli, Elvy Suhana Int J Mol Sci Article Glucocorticoids are one of the causes of secondary osteoporosis. The aqueous extract of Piper sarmentosum contains flavonoids that possess antioxidant effects. In this study, we determined the effects of aqueous Piper sarmentosum leaf extract on structural, dynamic and static histomorphometric changes from osteoporotic bones of rats induced with glucocorticoids. Thirty-two Sprague-Dawley rats were divided equally into four groups—Sham control group given vehicles (intramuscular (IM) olive oil and oral normal saline); AC: Adrenalectomised (Adrx) control group given IM dexamethasone (DEX) (120 μg/kg/day) and vehicle (oral normal saline); AP: Adrx group administered IM DEX (120 μg/kg/day) and aqueous Piper sarmentosum leaf extract (125 mg/kg/day) orally; and AG: Adrx group administered IM DEX (120 μg/kg/day) and oral glycyrrhizic acid (GCA) (120 mg/kg/day). Histomorphometric measurements showed that the bone volume, trabecular thickness, trabecular number, osteoid and osteoblast surfaces, double-labelled trabecular surface, mineralizing surface and bone formation rate of rats given aqueous Piper sarmentosum leaf extract were significantly increased (p < 0.05), whereas the trabecular separation and osteoclast surface were significantly reduced (p < 0.05). This study suggests that aqueous Piper sarmentosum leaf extract was able to prevent bone loss in prolonged glucocorticoid therapy. Thus, Piper sarmentosum has the potential to be used as an alternative medicine against osteoporosis and osteoporotic fractures in patients undergoing long-term glucocorticoid therapy. MDPI 2020-10-19 /pmc/articles/PMC7589271/ /pubmed/33086468 http://dx.doi.org/10.3390/ijms21207715 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Mohamad Asri, Siti Fadziyah Soelaiman, Ima Nirwana Mohd Moklas, Mohamad Aris Mohd Nor, Nurul Huda Mohamad Zainal, Nurul Hayati Mohd Ramli, Elvy Suhana The Role of Piper sarmentosum Aqueous Extract as a Bone Protective Agent, a Histomorphometric Study |
title | The Role of Piper sarmentosum Aqueous Extract as a Bone Protective Agent, a Histomorphometric Study |
title_full | The Role of Piper sarmentosum Aqueous Extract as a Bone Protective Agent, a Histomorphometric Study |
title_fullStr | The Role of Piper sarmentosum Aqueous Extract as a Bone Protective Agent, a Histomorphometric Study |
title_full_unstemmed | The Role of Piper sarmentosum Aqueous Extract as a Bone Protective Agent, a Histomorphometric Study |
title_short | The Role of Piper sarmentosum Aqueous Extract as a Bone Protective Agent, a Histomorphometric Study |
title_sort | role of piper sarmentosum aqueous extract as a bone protective agent, a histomorphometric study |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7589271/ https://www.ncbi.nlm.nih.gov/pubmed/33086468 http://dx.doi.org/10.3390/ijms21207715 |
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