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Increased Sulfation in Gracilaria fisheri Sulfated Galactans Enhances Antioxidant and Antiurolithiatic Activities and Protects HK-2 Cell Death Induced by Sodium Oxalate

Urolithiasis is a common urological disease characterized by the presence of a stone anywhere along the urinary tract. The major component of such stones is calcium oxalate, and reactive oxygen species act as an essential mediator of calcium oxalate crystallization. Previous studies have demonstrate...

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Autores principales: Sakaew, Waraporn, Phanphak, Jenjiralai, Somintara, Somsuda, Hipkaeo, Wiphawi, Wongprasert, Kanokpan, Kovensky, José, Pariwatthanakun, Choowadee, Rudtanatip, Tawut
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9230550/
https://www.ncbi.nlm.nih.gov/pubmed/35736184
http://dx.doi.org/10.3390/md20060382
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author Sakaew, Waraporn
Phanphak, Jenjiralai
Somintara, Somsuda
Hipkaeo, Wiphawi
Wongprasert, Kanokpan
Kovensky, José
Pariwatthanakun, Choowadee
Rudtanatip, Tawut
author_facet Sakaew, Waraporn
Phanphak, Jenjiralai
Somintara, Somsuda
Hipkaeo, Wiphawi
Wongprasert, Kanokpan
Kovensky, José
Pariwatthanakun, Choowadee
Rudtanatip, Tawut
author_sort Sakaew, Waraporn
collection PubMed
description Urolithiasis is a common urological disease characterized by the presence of a stone anywhere along the urinary tract. The major component of such stones is calcium oxalate, and reactive oxygen species act as an essential mediator of calcium oxalate crystallization. Previous studies have demonstrated the antioxidant and antiurolithiatic activities of sulfated polysaccharides. In this study, native sulfated galactans (N-SGs) with a molecular weight of 217.4 kDa from Gracilaria fisheri were modified to obtain lower molecular weight SG (L-SG) and also subjected to sulfation SG (S-SG). The in vitro antioxidant and antiurolithiatic activities of the modified substances and their ability to protect against sodium oxalate-induced renal tubular (HK-2) cell death were investigated. The results revealed that S-SG showed more pronounced antioxidant activities (DPPH and O(2)(−) scavenging activities) than those of other compounds. S-SG exhibited the highest antiurolithiatic activity in terms of nucleation and aggregation, as well as crystal morphology and size. Moreover, S-SG showed improved cell survival and increased anti-apoptotic BCL-2 protein in HK-2 cells treated with sodium oxalate. Our findings highlight the potential application of S-SG in the functional food and pharmaceutical industries.
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spelling pubmed-92305502022-06-25 Increased Sulfation in Gracilaria fisheri Sulfated Galactans Enhances Antioxidant and Antiurolithiatic Activities and Protects HK-2 Cell Death Induced by Sodium Oxalate Sakaew, Waraporn Phanphak, Jenjiralai Somintara, Somsuda Hipkaeo, Wiphawi Wongprasert, Kanokpan Kovensky, José Pariwatthanakun, Choowadee Rudtanatip, Tawut Mar Drugs Article Urolithiasis is a common urological disease characterized by the presence of a stone anywhere along the urinary tract. The major component of such stones is calcium oxalate, and reactive oxygen species act as an essential mediator of calcium oxalate crystallization. Previous studies have demonstrated the antioxidant and antiurolithiatic activities of sulfated polysaccharides. In this study, native sulfated galactans (N-SGs) with a molecular weight of 217.4 kDa from Gracilaria fisheri were modified to obtain lower molecular weight SG (L-SG) and also subjected to sulfation SG (S-SG). The in vitro antioxidant and antiurolithiatic activities of the modified substances and their ability to protect against sodium oxalate-induced renal tubular (HK-2) cell death were investigated. The results revealed that S-SG showed more pronounced antioxidant activities (DPPH and O(2)(−) scavenging activities) than those of other compounds. S-SG exhibited the highest antiurolithiatic activity in terms of nucleation and aggregation, as well as crystal morphology and size. Moreover, S-SG showed improved cell survival and increased anti-apoptotic BCL-2 protein in HK-2 cells treated with sodium oxalate. Our findings highlight the potential application of S-SG in the functional food and pharmaceutical industries. MDPI 2022-06-07 /pmc/articles/PMC9230550/ /pubmed/35736184 http://dx.doi.org/10.3390/md20060382 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/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 (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Sakaew, Waraporn
Phanphak, Jenjiralai
Somintara, Somsuda
Hipkaeo, Wiphawi
Wongprasert, Kanokpan
Kovensky, José
Pariwatthanakun, Choowadee
Rudtanatip, Tawut
Increased Sulfation in Gracilaria fisheri Sulfated Galactans Enhances Antioxidant and Antiurolithiatic Activities and Protects HK-2 Cell Death Induced by Sodium Oxalate
title Increased Sulfation in Gracilaria fisheri Sulfated Galactans Enhances Antioxidant and Antiurolithiatic Activities and Protects HK-2 Cell Death Induced by Sodium Oxalate
title_full Increased Sulfation in Gracilaria fisheri Sulfated Galactans Enhances Antioxidant and Antiurolithiatic Activities and Protects HK-2 Cell Death Induced by Sodium Oxalate
title_fullStr Increased Sulfation in Gracilaria fisheri Sulfated Galactans Enhances Antioxidant and Antiurolithiatic Activities and Protects HK-2 Cell Death Induced by Sodium Oxalate
title_full_unstemmed Increased Sulfation in Gracilaria fisheri Sulfated Galactans Enhances Antioxidant and Antiurolithiatic Activities and Protects HK-2 Cell Death Induced by Sodium Oxalate
title_short Increased Sulfation in Gracilaria fisheri Sulfated Galactans Enhances Antioxidant and Antiurolithiatic Activities and Protects HK-2 Cell Death Induced by Sodium Oxalate
title_sort increased sulfation in gracilaria fisheri sulfated galactans enhances antioxidant and antiurolithiatic activities and protects hk-2 cell death induced by sodium oxalate
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9230550/
https://www.ncbi.nlm.nih.gov/pubmed/35736184
http://dx.doi.org/10.3390/md20060382
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