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Anti-oxidative and anti-inflammatory activity of Achatina fulica mucus in streptozocin-nicotinamide-induced diabetic kidney disease: an animal model study
Introduction: Diabetic kidney disease (DKD) progression resulted in increased intrarenal oxidative stress and increased inflammatory resulting in further renal fibrosis. Achatina fulica mucus was regarded to exerts anti-oxidative and anti-inflammatory effect. Objectives: This study aims to observe t...
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Published in: | Journal of nephropathology 2024-08, Vol.13 (4), p.e21465-e21465 |
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creator | Putranto, Wachid Fitriawan, Gigih Dewi, Ratih Tri Kusuma Suseno, Aryo Nurudhin, Arief Werdiningsih, Yulyani Perdhana, Santy Ayu Puspita Prabowo, Nurhasan Agung Pratama, Yeremia Suryo |
description | Introduction: Diabetic kidney disease (DKD) progression resulted in increased intrarenal oxidative stress and increased inflammatory resulting in further renal fibrosis. Achatina fulica mucus was regarded to exerts anti-oxidative and anti-inflammatory effect. Objectives: This study aims to observe the effect of administration of A. fulica mucus on oxidative stress and inflammation biomarkers in DKD-induced rats. Methods and Materials: In this study, we used 32 males white Wistar rats divided into four groups; a control, and other three different groups induced with 45 mg/kg streptozocin (STZ) and 110 mg/kg nicotinamide (NA) intra-peritoneally. Achatina fulica mucus was administered orally in the last groups; 3.5 mL/d (S1), and 7 mL/d (S2). Post-test measurement of inflammatory and oxidative biomarker was used to determine the outcome. Results: The study resulted in reduction of malondialdehyde (MDA), transforming growth factor-β (TGF-β), tumor necrosis factor-α (TNF-α), high sensitivity C-reactive protein (hs-CRP), vascular endothelial growth factor (VEGF), and interleukin-1β (IL-1β) in A. fulica mucus administration in our STZ-NA induced rats, with higher dose of the mucus further reduce the inflammatory and oxidative stress biomarkers. Conclusion: Current study showed the potential of A. fulica mucus usage in future management of inflammation and oxidative stress in diabetes and DKD. |
doi_str_mv | 10.34172/jnp.2023.21465 |
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Achatina fulica mucus was regarded to exerts anti-oxidative and anti-inflammatory effect. Objectives: This study aims to observe the effect of administration of A. fulica mucus on oxidative stress and inflammation biomarkers in DKD-induced rats. Methods and Materials: In this study, we used 32 males white Wistar rats divided into four groups; a control, and other three different groups induced with 45 mg/kg streptozocin (STZ) and 110 mg/kg nicotinamide (NA) intra-peritoneally. Achatina fulica mucus was administered orally in the last groups; 3.5 mL/d (S1), and 7 mL/d (S2). Post-test measurement of inflammatory and oxidative biomarker was used to determine the outcome. Results: The study resulted in reduction of malondialdehyde (MDA), transforming growth factor-β (TGF-β), tumor necrosis factor-α (TNF-α), high sensitivity C-reactive protein (hs-CRP), vascular endothelial growth factor (VEGF), and interleukin-1β (IL-1β) in A. fulica mucus administration in our STZ-NA induced rats, with higher dose of the mucus further reduce the inflammatory and oxidative stress biomarkers. Conclusion: Current study showed the potential of A. fulica mucus usage in future management of inflammation and oxidative stress in diabetes and DKD.</description><identifier>ISSN: 2251-8363</identifier><identifier>EISSN: 2251-8819</identifier><identifier>DOI: 10.34172/jnp.2023.21465</identifier><language>eng</language><publisher>Society of Diabetic Nephropathy Prevention</publisher><subject>diabetes ; diabetic nephropathy ; inflammation ; oxidative stress</subject><ispartof>Journal of nephropathology, 2024-08, Vol.13 (4), p.e21465-e21465</ispartof><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c1475-6651646b5b45a1c48cf51ac409d56c75a620cb0554142c5512fa9a86196cb353</cites><orcidid>0000-0003-2016-5649 ; 0000-0003-0093-0729 ; 0000-0003-2408-8783 ; 0000-0003-4662-0638 ; 0000-0001-9962-5104 ; 0000-0003-3145-4948 ; 0000-0002-4116-5851 ; 0000-0001-5231-2346 ; 0000-0002-9575-9217</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,864,2102,27924,27925</link.rule.ids></links><search><creatorcontrib>Putranto, Wachid</creatorcontrib><creatorcontrib>Fitriawan, Gigih</creatorcontrib><creatorcontrib>Dewi, Ratih Tri Kusuma</creatorcontrib><creatorcontrib>Suseno, Aryo</creatorcontrib><creatorcontrib>Nurudhin, Arief</creatorcontrib><creatorcontrib>Werdiningsih, Yulyani</creatorcontrib><creatorcontrib>Perdhana, Santy Ayu Puspita</creatorcontrib><creatorcontrib>Prabowo, Nurhasan Agung</creatorcontrib><creatorcontrib>Pratama, Yeremia Suryo</creatorcontrib><title>Anti-oxidative and anti-inflammatory activity of Achatina fulica mucus in streptozocin-nicotinamide-induced diabetic kidney disease: an animal model study</title><title>Journal of nephropathology</title><description>Introduction: Diabetic kidney disease (DKD) progression resulted in increased intrarenal oxidative stress and increased inflammatory resulting in further renal fibrosis. Achatina fulica mucus was regarded to exerts anti-oxidative and anti-inflammatory effect. Objectives: This study aims to observe the effect of administration of A. fulica mucus on oxidative stress and inflammation biomarkers in DKD-induced rats. Methods and Materials: In this study, we used 32 males white Wistar rats divided into four groups; a control, and other three different groups induced with 45 mg/kg streptozocin (STZ) and 110 mg/kg nicotinamide (NA) intra-peritoneally. Achatina fulica mucus was administered orally in the last groups; 3.5 mL/d (S1), and 7 mL/d (S2). Post-test measurement of inflammatory and oxidative biomarker was used to determine the outcome. Results: The study resulted in reduction of malondialdehyde (MDA), transforming growth factor-β (TGF-β), tumor necrosis factor-α (TNF-α), high sensitivity C-reactive protein (hs-CRP), vascular endothelial growth factor (VEGF), and interleukin-1β (IL-1β) in A. fulica mucus administration in our STZ-NA induced rats, with higher dose of the mucus further reduce the inflammatory and oxidative stress biomarkers. Conclusion: Current study showed the potential of A. fulica mucus usage in future management of inflammation and oxidative stress in diabetes and DKD.</description><subject>diabetes</subject><subject>diabetic nephropathy</subject><subject>inflammation</subject><subject>oxidative stress</subject><issn>2251-8363</issn><issn>2251-8819</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><sourceid>DOA</sourceid><recordid>eNo9kdtKxDAQhosoKOq1t3mBrkmapK13i3hYELzxPkwniWZtk6VpxfooPq1xPYQJc-Sbgb8oLhhdVYLV_HIbditOebXiTCh5UJxwLlnZNKw9_IsrVR0X5yltaX6tYErWJ8XnOky-jO_ewOTfLIFg8s8lH1wPwwBTHBcCmJt-Wkh0ZI0veTQAcXPvEcgw45yIDyRNo91N8SOiD2XwGL-nBm9sZpkZrSHGQ2cnj-TVm2CXnCcLyV7ljdn8AD0ZorF9Rs1mOSuOHPTJnv_60-Lp9ubp-r58eLzbXK8fSmSilqVSkimhOtkJCQxFg04yQEFbIxXWEhSn2FEpBRMcpWTcQQuNYq3CrpLVabH5wZoIW70b8xnjoiN4vS_E8VnDmI_urXYVsIzsBFdCONOAqqkRTVsrqlgNTWZd_rBwjCmN1v3zGNV7oXQWSn8LpfdCVV9CvojG</recordid><startdate>20240810</startdate><enddate>20240810</enddate><creator>Putranto, Wachid</creator><creator>Fitriawan, Gigih</creator><creator>Dewi, Ratih Tri Kusuma</creator><creator>Suseno, Aryo</creator><creator>Nurudhin, Arief</creator><creator>Werdiningsih, Yulyani</creator><creator>Perdhana, Santy Ayu Puspita</creator><creator>Prabowo, Nurhasan Agung</creator><creator>Pratama, Yeremia Suryo</creator><general>Society of Diabetic Nephropathy Prevention</general><scope>AAYXX</scope><scope>CITATION</scope><scope>DOA</scope><orcidid>https://orcid.org/0000-0003-2016-5649</orcidid><orcidid>https://orcid.org/0000-0003-0093-0729</orcidid><orcidid>https://orcid.org/0000-0003-2408-8783</orcidid><orcidid>https://orcid.org/0000-0003-4662-0638</orcidid><orcidid>https://orcid.org/0000-0001-9962-5104</orcidid><orcidid>https://orcid.org/0000-0003-3145-4948</orcidid><orcidid>https://orcid.org/0000-0002-4116-5851</orcidid><orcidid>https://orcid.org/0000-0001-5231-2346</orcidid><orcidid>https://orcid.org/0000-0002-9575-9217</orcidid></search><sort><creationdate>20240810</creationdate><title>Anti-oxidative and anti-inflammatory activity of Achatina fulica mucus in streptozocin-nicotinamide-induced diabetic kidney disease: an animal model study</title><author>Putranto, Wachid ; Fitriawan, Gigih ; Dewi, Ratih Tri Kusuma ; Suseno, Aryo ; Nurudhin, Arief ; Werdiningsih, Yulyani ; Perdhana, Santy Ayu Puspita ; Prabowo, Nurhasan Agung ; Pratama, Yeremia Suryo</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c1475-6651646b5b45a1c48cf51ac409d56c75a620cb0554142c5512fa9a86196cb353</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>diabetes</topic><topic>diabetic nephropathy</topic><topic>inflammation</topic><topic>oxidative stress</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Putranto, Wachid</creatorcontrib><creatorcontrib>Fitriawan, Gigih</creatorcontrib><creatorcontrib>Dewi, Ratih Tri Kusuma</creatorcontrib><creatorcontrib>Suseno, Aryo</creatorcontrib><creatorcontrib>Nurudhin, Arief</creatorcontrib><creatorcontrib>Werdiningsih, Yulyani</creatorcontrib><creatorcontrib>Perdhana, Santy Ayu Puspita</creatorcontrib><creatorcontrib>Prabowo, Nurhasan Agung</creatorcontrib><creatorcontrib>Pratama, Yeremia Suryo</creatorcontrib><collection>CrossRef</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>Journal of nephropathology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Putranto, Wachid</au><au>Fitriawan, Gigih</au><au>Dewi, Ratih Tri Kusuma</au><au>Suseno, Aryo</au><au>Nurudhin, Arief</au><au>Werdiningsih, Yulyani</au><au>Perdhana, Santy Ayu Puspita</au><au>Prabowo, Nurhasan Agung</au><au>Pratama, Yeremia Suryo</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Anti-oxidative and anti-inflammatory activity of Achatina fulica mucus in streptozocin-nicotinamide-induced diabetic kidney disease: an animal model study</atitle><jtitle>Journal of nephropathology</jtitle><date>2024-08-10</date><risdate>2024</risdate><volume>13</volume><issue>4</issue><spage>e21465</spage><epage>e21465</epage><pages>e21465-e21465</pages><issn>2251-8363</issn><eissn>2251-8819</eissn><abstract>Introduction: Diabetic kidney disease (DKD) progression resulted in increased intrarenal oxidative stress and increased inflammatory resulting in further renal fibrosis. Achatina fulica mucus was regarded to exerts anti-oxidative and anti-inflammatory effect. Objectives: This study aims to observe the effect of administration of A. fulica mucus on oxidative stress and inflammation biomarkers in DKD-induced rats. Methods and Materials: In this study, we used 32 males white Wistar rats divided into four groups; a control, and other three different groups induced with 45 mg/kg streptozocin (STZ) and 110 mg/kg nicotinamide (NA) intra-peritoneally. Achatina fulica mucus was administered orally in the last groups; 3.5 mL/d (S1), and 7 mL/d (S2). Post-test measurement of inflammatory and oxidative biomarker was used to determine the outcome. Results: The study resulted in reduction of malondialdehyde (MDA), transforming growth factor-β (TGF-β), tumor necrosis factor-α (TNF-α), high sensitivity C-reactive protein (hs-CRP), vascular endothelial growth factor (VEGF), and interleukin-1β (IL-1β) in A. fulica mucus administration in our STZ-NA induced rats, with higher dose of the mucus further reduce the inflammatory and oxidative stress biomarkers. 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subjects | diabetes diabetic nephropathy inflammation oxidative stress |
title | Anti-oxidative and anti-inflammatory activity of Achatina fulica mucus in streptozocin-nicotinamide-induced diabetic kidney disease: an animal model study |
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