Anti-inflammatory and antioxidant properties of Sargassum polycystum ethyl acetate extract from Indonesia

Introduction: Inflammatory diseases, including asthma, osteoarthritis, rheumatoid arthritis, and cancer persist with relatively high incidence, which highlights the need to explore natural alternatives such as the bioactive substances of brown algae (Sargassum polycystum). Certain substances, such a...

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Main Authors: Erlia Anggrainy Sianipar, Shannen Ivanka Gunardi
Format: Article
Language:English
Published: Shahrekord University of Medical Sciences 2023-06-01
Series:Journal of HerbMed Pharmacology
Subjects:
Online Access:http://herbmedpharmacol.com/PDF/jhp-12-407.pdf
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author Erlia Anggrainy Sianipar
Shannen Ivanka Gunardi
author_facet Erlia Anggrainy Sianipar
Shannen Ivanka Gunardi
author_sort Erlia Anggrainy Sianipar
collection DOAJ
description Introduction: Inflammatory diseases, including asthma, osteoarthritis, rheumatoid arthritis, and cancer persist with relatively high incidence, which highlights the need to explore natural alternatives such as the bioactive substances of brown algae (Sargassum polycystum). Certain substances, such as phenolics and flavonoids, have been demonstrated to have an association with antioxidant activity because of their capacity to fend off free radicals, which cause inflammation. The purpose of this study was to look into the inflammatory inhibition and antioxidant activity of an ethyl acetate extract of S. polycystum from Indonesia. Methods: After maceration in ethyl acetate (1:4 w/v) for 24 hours, the total phenolic and flavonoid content of S. polycystum extract was measured using the colorimetric method. The antioxidant activity was tested using 1,1-diphenyl-2-picrylhydrazyl (DPPH), and the models of paw edema induced by carrageenan were used to assess inflammatory inhibition activity. Results: The findings revealed that S. polycystum had a weak antioxidant with a half-maximal inhibitory concentration (IC50) value of 605.24 ± 26.53 g/mL. Furthermore, it had 23.509 ± 0.109 mg gallic acid equivalents/gram (GAE/g) and 15.186 ± 0.046 mg quercetin equivalents/ gram (QE/g) of total phenolic and flavonoid compounds, respectively. At 200, 400, and 800 mg/ kg BW doses, S. polycystum had inflammatory inhibition percentages of 53.80 ± 4.68%, 62.35 ± 4.05%, and 60.90 ± 2.88%, respectively. Conclusion: Sargassum polycystum ethyl acetate extract inhibited inflammation. However, further study is needed to examine the safety, identification, separation of the relevant substances involved, and the precise mechanism of action.
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spelling doaj.art-4593e22aa03f4174ae04549f1c48f1672023-11-25T08:27:27ZengShahrekord University of Medical SciencesJournal of HerbMed Pharmacology2345-50042023-06-0112340741210.34172/jhp.2023.44jhp-44840Anti-inflammatory and antioxidant properties of Sargassum polycystum ethyl acetate extract from IndonesiaErlia Anggrainy Sianipar0Shannen Ivanka Gunardi1Department of Pharmacy, School of Medicine and Health Science, Atma Jaya Catholic University of Indonesia, Pluit Raya 2, Jakarta Utara, DKI Jakarta 14440, IndonesiaDepartment of Pharmacy, School of Medicine and Health Science, Atma Jaya Catholic University of Indonesia, Pluit Raya 2, Jakarta Utara, DKI Jakarta 14440, IndonesiaIntroduction: Inflammatory diseases, including asthma, osteoarthritis, rheumatoid arthritis, and cancer persist with relatively high incidence, which highlights the need to explore natural alternatives such as the bioactive substances of brown algae (Sargassum polycystum). Certain substances, such as phenolics and flavonoids, have been demonstrated to have an association with antioxidant activity because of their capacity to fend off free radicals, which cause inflammation. The purpose of this study was to look into the inflammatory inhibition and antioxidant activity of an ethyl acetate extract of S. polycystum from Indonesia. Methods: After maceration in ethyl acetate (1:4 w/v) for 24 hours, the total phenolic and flavonoid content of S. polycystum extract was measured using the colorimetric method. The antioxidant activity was tested using 1,1-diphenyl-2-picrylhydrazyl (DPPH), and the models of paw edema induced by carrageenan were used to assess inflammatory inhibition activity. Results: The findings revealed that S. polycystum had a weak antioxidant with a half-maximal inhibitory concentration (IC50) value of 605.24 ± 26.53 g/mL. Furthermore, it had 23.509 ± 0.109 mg gallic acid equivalents/gram (GAE/g) and 15.186 ± 0.046 mg quercetin equivalents/ gram (QE/g) of total phenolic and flavonoid compounds, respectively. At 200, 400, and 800 mg/ kg BW doses, S. polycystum had inflammatory inhibition percentages of 53.80 ± 4.68%, 62.35 ± 4.05%, and 60.90 ± 2.88%, respectively. Conclusion: Sargassum polycystum ethyl acetate extract inhibited inflammation. However, further study is needed to examine the safety, identification, separation of the relevant substances involved, and the precise mechanism of action.http://herbmedpharmacol.com/PDF/jhp-12-407.pdfsargassumfree radicalsflavonoidsphenolicsinflammation
spellingShingle Erlia Anggrainy Sianipar
Shannen Ivanka Gunardi
Anti-inflammatory and antioxidant properties of Sargassum polycystum ethyl acetate extract from Indonesia
Journal of HerbMed Pharmacology
sargassum
free radicals
flavonoids
phenolics
inflammation
title Anti-inflammatory and antioxidant properties of Sargassum polycystum ethyl acetate extract from Indonesia
title_full Anti-inflammatory and antioxidant properties of Sargassum polycystum ethyl acetate extract from Indonesia
title_fullStr Anti-inflammatory and antioxidant properties of Sargassum polycystum ethyl acetate extract from Indonesia
title_full_unstemmed Anti-inflammatory and antioxidant properties of Sargassum polycystum ethyl acetate extract from Indonesia
title_short Anti-inflammatory and antioxidant properties of Sargassum polycystum ethyl acetate extract from Indonesia
title_sort anti inflammatory and antioxidant properties of sargassum polycystum ethyl acetate extract from indonesia
topic sargassum
free radicals
flavonoids
phenolics
inflammation
url http://herbmedpharmacol.com/PDF/jhp-12-407.pdf
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