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Antioxidant and antimalarial properties of Sophora exigua Craib. root extract in Plasmodium berghei-infected mice

BACKGROUND: Sophora exigua Craib. is commonly used in Thailand to reduce fever and increase postpartum breast milk production in women who have hypogalactia. However, there has been no report on the antioxidant and antimalarial properties of this plant. This study aimed to investigate the antioxidan...

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Autores principales: Kaewdana, Kantarakorn, Chaniad, Prapaporn, Jariyapong, Pitchanee, Phuwajaroanpong, Arisara, Punsawad, Chuchard
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7980637/
https://www.ncbi.nlm.nih.gov/pubmed/33741053
http://dx.doi.org/10.1186/s41182-021-00314-2
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author Kaewdana, Kantarakorn
Chaniad, Prapaporn
Jariyapong, Pitchanee
Phuwajaroanpong, Arisara
Punsawad, Chuchard
author_facet Kaewdana, Kantarakorn
Chaniad, Prapaporn
Jariyapong, Pitchanee
Phuwajaroanpong, Arisara
Punsawad, Chuchard
author_sort Kaewdana, Kantarakorn
collection PubMed
description BACKGROUND: Sophora exigua Craib. is commonly used in Thailand to reduce fever and increase postpartum breast milk production in women who have hypogalactia. However, there has been no report on the antioxidant and antimalarial properties of this plant. This study aimed to investigate the antioxidant and antimalarial activities of S. exigua root extract and to evaluate its acute toxicity in mice to confirm its safety. METHODS: The in vitro antioxidant activities were determined using 2,2-diphenyl-1-picrylhydrazyl (DPPH), superoxide radical, and hydroxyl radical scavenging assays. The in vivo antioxidant activities were determined by detecting the malondialdehyde (MDA) content and superoxide dismutase (SOD) activity in the livers of malaria-infected mice. The in vivo antimalarial activity was determined by Peters’ 4-day suppressive test in mice infected with Plasmodium berghei ANKA and orally administered S. exigua root aqueous and ethanolic extracts at different doses (200, 400, and 600 mg/kg body weight). In addition, the acute oral toxicity of the plant extracts was assessed in mice at a dose of 2000 mg/kg body weight. RESULTS: The ethanolic extract of S. exigua root exhibited inhibition of DPPH radicals, superoxide anions, and hydroxyl radicals, with half maximal inhibitory concentration (IC(50)) values of 24.63 ± 1.78, 129.78 ± 0.65, and 30.58 ± 1.19 μg/ml, respectively. Similarly, research on the in vivo antioxidant activity indicated that the ethanolic extract of S. exigua root exerted a stronger effect than the aqueous extract. The aqueous extract at doses of 200, 400, and 600 mg/kg had stronger antimalarial activity than the ethanolic extract. The aqueous extract at 600 mg/kg exhibited 60.46% suppression of parasitemia. Increased levels of aspartate aminotransferase (AST), alanine aminotransferase (ALT), and alkaline phosphatase (ALP) and blood urea nitrogen (BUN) were detected in the mice treated with 2000 mg/kg ethanolic extract, which was related to the results of histopathological analysis of liver tissue, showing ballooning degeneration of hepatocytes, diffuse hepatic hemorrhage, and infiltration of inflammatory cells. CONCLUSIONS: This study demonstrated that the ethanolic S. exigua root extract possessed antioxidant properties, and the aqueous extract also had antimalarial activity. Therefore, this plant is an alternative source of new antioxidant and antimalarial agents.
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spelling pubmed-79806372021-03-22 Antioxidant and antimalarial properties of Sophora exigua Craib. root extract in Plasmodium berghei-infected mice Kaewdana, Kantarakorn Chaniad, Prapaporn Jariyapong, Pitchanee Phuwajaroanpong, Arisara Punsawad, Chuchard Trop Med Health Research BACKGROUND: Sophora exigua Craib. is commonly used in Thailand to reduce fever and increase postpartum breast milk production in women who have hypogalactia. However, there has been no report on the antioxidant and antimalarial properties of this plant. This study aimed to investigate the antioxidant and antimalarial activities of S. exigua root extract and to evaluate its acute toxicity in mice to confirm its safety. METHODS: The in vitro antioxidant activities were determined using 2,2-diphenyl-1-picrylhydrazyl (DPPH), superoxide radical, and hydroxyl radical scavenging assays. The in vivo antioxidant activities were determined by detecting the malondialdehyde (MDA) content and superoxide dismutase (SOD) activity in the livers of malaria-infected mice. The in vivo antimalarial activity was determined by Peters’ 4-day suppressive test in mice infected with Plasmodium berghei ANKA and orally administered S. exigua root aqueous and ethanolic extracts at different doses (200, 400, and 600 mg/kg body weight). In addition, the acute oral toxicity of the plant extracts was assessed in mice at a dose of 2000 mg/kg body weight. RESULTS: The ethanolic extract of S. exigua root exhibited inhibition of DPPH radicals, superoxide anions, and hydroxyl radicals, with half maximal inhibitory concentration (IC(50)) values of 24.63 ± 1.78, 129.78 ± 0.65, and 30.58 ± 1.19 μg/ml, respectively. Similarly, research on the in vivo antioxidant activity indicated that the ethanolic extract of S. exigua root exerted a stronger effect than the aqueous extract. The aqueous extract at doses of 200, 400, and 600 mg/kg had stronger antimalarial activity than the ethanolic extract. The aqueous extract at 600 mg/kg exhibited 60.46% suppression of parasitemia. Increased levels of aspartate aminotransferase (AST), alanine aminotransferase (ALT), and alkaline phosphatase (ALP) and blood urea nitrogen (BUN) were detected in the mice treated with 2000 mg/kg ethanolic extract, which was related to the results of histopathological analysis of liver tissue, showing ballooning degeneration of hepatocytes, diffuse hepatic hemorrhage, and infiltration of inflammatory cells. CONCLUSIONS: This study demonstrated that the ethanolic S. exigua root extract possessed antioxidant properties, and the aqueous extract also had antimalarial activity. Therefore, this plant is an alternative source of new antioxidant and antimalarial agents. BioMed Central 2021-03-19 /pmc/articles/PMC7980637/ /pubmed/33741053 http://dx.doi.org/10.1186/s41182-021-00314-2 Text en © The Author(s) 2021 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Research
Kaewdana, Kantarakorn
Chaniad, Prapaporn
Jariyapong, Pitchanee
Phuwajaroanpong, Arisara
Punsawad, Chuchard
Antioxidant and antimalarial properties of Sophora exigua Craib. root extract in Plasmodium berghei-infected mice
title Antioxidant and antimalarial properties of Sophora exigua Craib. root extract in Plasmodium berghei-infected mice
title_full Antioxidant and antimalarial properties of Sophora exigua Craib. root extract in Plasmodium berghei-infected mice
title_fullStr Antioxidant and antimalarial properties of Sophora exigua Craib. root extract in Plasmodium berghei-infected mice
title_full_unstemmed Antioxidant and antimalarial properties of Sophora exigua Craib. root extract in Plasmodium berghei-infected mice
title_short Antioxidant and antimalarial properties of Sophora exigua Craib. root extract in Plasmodium berghei-infected mice
title_sort antioxidant and antimalarial properties of sophora exigua craib. root extract in plasmodium berghei-infected mice
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7980637/
https://www.ncbi.nlm.nih.gov/pubmed/33741053
http://dx.doi.org/10.1186/s41182-021-00314-2
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