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Protective Effect of Vitamin B5 (Dexpanthenol) on Nephropathy in Streptozotocin Diabetic Rats
Objective: This study aimed to evaluate the effects of vitamin B5 [dexpanthenol, DEX] treatment on the kidney in a streptozotocin (STZ) diabetes animal model. Materials and Methods: Twenty-four Wistar rats were randomised in one of the four groups: Group 1 served as control, and group 2 was administ...
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Published in: | Meandros medical and dental journal 2021-04, Vol.22 (1), p.53-56 |
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creator | Ceri, Nazli Gulriz Gulle, Kanat Arasli, Mehmet Akpolat, Meryem Demirci, Buket |
description | Objective: This study aimed to evaluate the effects of vitamin B5 [dexpanthenol,
DEX] treatment on the kidney in a streptozotocin (STZ) diabetes animal model.
Materials and Methods: Twenty-four Wistar rats were randomised in one of the
four groups: Group 1 served as control, and group 2 was administered high-dose
DEX (300 mg/kg/day) as a safety group. Diabetes was induced by intraperitoneal
injection of a single dose of STZ (50 mg/kg) in groups 3 and 4. In group 4, DEX was
administered as well. All groups were followed up for 6 weeks. Histopathological
analyses were performed on renal tissue using periodic acid-Schiff and Hematoxylin-
Eosin stains.
Results: Microscopic evaluation of the kidney revealed that the rats demonstrated
kidney damage 6 weeks after STZ administration. However, high-dose and longterm
DEX administration alone did not damage renal tissue; moreover, kidney
damage was prevented if DEX was administered in the early phase of diabetes.
Conclusion: DEX could be a safe and cost-effective vitamin for the prevention of
diabetes complications. |
doi_str_mv | 10.4274/meandros.galenos.2021.65002 |
format | article |
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DEX] treatment on the kidney in a streptozotocin (STZ) diabetes animal model.
Materials and Methods: Twenty-four Wistar rats were randomised in one of the
four groups: Group 1 served as control, and group 2 was administered high-dose
DEX (300 mg/kg/day) as a safety group. Diabetes was induced by intraperitoneal
injection of a single dose of STZ (50 mg/kg) in groups 3 and 4. In group 4, DEX was
administered as well. All groups were followed up for 6 weeks. Histopathological
analyses were performed on renal tissue using periodic acid-Schiff and Hematoxylin-
Eosin stains.
Results: Microscopic evaluation of the kidney revealed that the rats demonstrated
kidney damage 6 weeks after STZ administration. However, high-dose and longterm
DEX administration alone did not damage renal tissue; moreover, kidney
damage was prevented if DEX was administered in the early phase of diabetes.
Conclusion: DEX could be a safe and cost-effective vitamin for the prevention of
diabetes complications.</description><identifier>ISSN: 2149-9063</identifier><identifier>EISSN: 2149-9063</identifier><identifier>DOI: 10.4274/meandros.galenos.2021.65002</identifier><language>eng</language><publisher>Aydın: Adnan Menderes Üniversitesi</publisher><subject>Acids ; Animal models ; Animals ; Antioxidants ; Apoptosis ; Conflicts of interest ; Diabetes ; Diabetes mellitus ; Ethics ; Ischemia ; Kidney diseases ; Kidneys ; Membranes ; Metabolism ; Nephropathy ; Streptozocin ; Tıp</subject><ispartof>Meandros medical and dental journal, 2021-04, Vol.22 (1), p.53-56</ispartof><rights>2021. This work is published under https://creativecommons.org/licenses/by-nc-nd/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c309t-522da5259483f34e2d5d6b6e9ed1ddfd960a12b9aff09a72e18a2907722beb4a3</citedby><orcidid>0000-0002-6337-8962 ; 0000-0002-5931-419X ; 0000-0002-3442-5061 ; 0000-0001-5486-1824 ; 0000-0002-3419-1728</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/2833154603/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2833154603?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>314,780,784,25753,27924,27925,37012,44590,75126</link.rule.ids></links><search><contributor>Turan,Yasemin</contributor><creatorcontrib>Ceri, Nazli Gulriz</creatorcontrib><creatorcontrib>Gulle, Kanat</creatorcontrib><creatorcontrib>Arasli, Mehmet</creatorcontrib><creatorcontrib>Akpolat, Meryem</creatorcontrib><creatorcontrib>Demirci, Buket</creatorcontrib><title>Protective Effect of Vitamin B5 (Dexpanthenol) on Nephropathy in Streptozotocin Diabetic Rats</title><title>Meandros medical and dental journal</title><description>Objective: This study aimed to evaluate the effects of vitamin B5 [dexpanthenol,
DEX] treatment on the kidney in a streptozotocin (STZ) diabetes animal model.
Materials and Methods: Twenty-four Wistar rats were randomised in one of the
four groups: Group 1 served as control, and group 2 was administered high-dose
DEX (300 mg/kg/day) as a safety group. Diabetes was induced by intraperitoneal
injection of a single dose of STZ (50 mg/kg) in groups 3 and 4. In group 4, DEX was
administered as well. All groups were followed up for 6 weeks. Histopathological
analyses were performed on renal tissue using periodic acid-Schiff and Hematoxylin-
Eosin stains.
Results: Microscopic evaluation of the kidney revealed that the rats demonstrated
kidney damage 6 weeks after STZ administration. However, high-dose and longterm
DEX administration alone did not damage renal tissue; moreover, kidney
damage was prevented if DEX was administered in the early phase of diabetes.
Conclusion: DEX could be a safe and cost-effective vitamin for the prevention of
diabetes complications.</description><subject>Acids</subject><subject>Animal models</subject><subject>Animals</subject><subject>Antioxidants</subject><subject>Apoptosis</subject><subject>Conflicts of interest</subject><subject>Diabetes</subject><subject>Diabetes mellitus</subject><subject>Ethics</subject><subject>Ischemia</subject><subject>Kidney diseases</subject><subject>Kidneys</subject><subject>Membranes</subject><subject>Metabolism</subject><subject>Nephropathy</subject><subject>Streptozocin</subject><subject>Tıp</subject><issn>2149-9063</issn><issn>2149-9063</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><recordid>eNpNkF1LwzAUhosoOHT_IbCbedGZjzZd8GpuUwdDxa87CWlz4jq6pqaZOH-9mZvo1fseeDgvPFHUI3iQ0Cw5X4GqtbPt4E1VUIekmJIBTzGmB1GHkkTEAnN2-K8fR922XWKMScZTwXgner131kPhyw9AU2NCQ9agl9KrVVmjyxT1J_DZqNovwkR1hmyNbqFZONsov9igwDx6B423X9bbIpyTUuXgywI9KN-eRkdGVS1093kSPV9Nn8Y38fzuejYezeOCYeHjlFKtUpqKZMgMS4DqVPOcgwBNtDZacKwIzYUyBguVUSBDRQXOMkpzyBPFTqLe7m_j7PsaWi-Xdu3qMCnpkDGSJhyzQPV3VKlBVbauyhr-wNlkOppLQnmWJQG92KFFENw6MLJx5Uq5jSRYbu3LX_tyb19u7csf--wbvmR9jA</recordid><startdate>20210401</startdate><enddate>20210401</enddate><creator>Ceri, Nazli Gulriz</creator><creator>Gulle, Kanat</creator><creator>Arasli, Mehmet</creator><creator>Akpolat, Meryem</creator><creator>Demirci, Buket</creator><general>Adnan Menderes Üniversitesi</general><general>Galenos Publishing House</general><scope>AAYXX</scope><scope>CITATION</scope><scope>IEBAR</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M7P</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><orcidid>https://orcid.org/0000-0002-6337-8962</orcidid><orcidid>https://orcid.org/0000-0002-5931-419X</orcidid><orcidid>https://orcid.org/0000-0002-3442-5061</orcidid><orcidid>https://orcid.org/0000-0001-5486-1824</orcidid><orcidid>https://orcid.org/0000-0002-3419-1728</orcidid></search><sort><creationdate>20210401</creationdate><title>Protective Effect of Vitamin B5 (Dexpanthenol) on Nephropathy in Streptozotocin Diabetic Rats</title><author>Ceri, Nazli Gulriz ; Gulle, Kanat ; Arasli, Mehmet ; Akpolat, Meryem ; Demirci, Buket</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c309t-522da5259483f34e2d5d6b6e9ed1ddfd960a12b9aff09a72e18a2907722beb4a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Acids</topic><topic>Animal models</topic><topic>Animals</topic><topic>Antioxidants</topic><topic>Apoptosis</topic><topic>Conflicts of interest</topic><topic>Diabetes</topic><topic>Diabetes mellitus</topic><topic>Ethics</topic><topic>Ischemia</topic><topic>Kidney diseases</topic><topic>Kidneys</topic><topic>Membranes</topic><topic>Metabolism</topic><topic>Nephropathy</topic><topic>Streptozocin</topic><topic>Tıp</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ceri, Nazli Gulriz</creatorcontrib><creatorcontrib>Gulle, Kanat</creatorcontrib><creatorcontrib>Arasli, Mehmet</creatorcontrib><creatorcontrib>Akpolat, Meryem</creatorcontrib><creatorcontrib>Demirci, Buket</creatorcontrib><collection>CrossRef</collection><collection>Idealonline online kütüphane - Journals</collection><collection>ProQuest Central (Corporate)</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>ProQuest Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Biological Science Database</collection><collection>Publicly Available Content Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><jtitle>Meandros medical and dental journal</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ceri, Nazli Gulriz</au><au>Gulle, Kanat</au><au>Arasli, Mehmet</au><au>Akpolat, Meryem</au><au>Demirci, Buket</au><au>Turan,Yasemin</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Protective Effect of Vitamin B5 (Dexpanthenol) on Nephropathy in Streptozotocin Diabetic Rats</atitle><jtitle>Meandros medical and dental journal</jtitle><date>2021-04-01</date><risdate>2021</risdate><volume>22</volume><issue>1</issue><spage>53</spage><epage>56</epage><pages>53-56</pages><issn>2149-9063</issn><eissn>2149-9063</eissn><abstract>Objective: This study aimed to evaluate the effects of vitamin B5 [dexpanthenol,
DEX] treatment on the kidney in a streptozotocin (STZ) diabetes animal model.
Materials and Methods: Twenty-four Wistar rats were randomised in one of the
four groups: Group 1 served as control, and group 2 was administered high-dose
DEX (300 mg/kg/day) as a safety group. Diabetes was induced by intraperitoneal
injection of a single dose of STZ (50 mg/kg) in groups 3 and 4. In group 4, DEX was
administered as well. All groups were followed up for 6 weeks. Histopathological
analyses were performed on renal tissue using periodic acid-Schiff and Hematoxylin-
Eosin stains.
Results: Microscopic evaluation of the kidney revealed that the rats demonstrated
kidney damage 6 weeks after STZ administration. However, high-dose and longterm
DEX administration alone did not damage renal tissue; moreover, kidney
damage was prevented if DEX was administered in the early phase of diabetes.
Conclusion: DEX could be a safe and cost-effective vitamin for the prevention of
diabetes complications.</abstract><cop>Aydın</cop><pub>Adnan Menderes Üniversitesi</pub><doi>10.4274/meandros.galenos.2021.65002</doi><tpages>4</tpages><orcidid>https://orcid.org/0000-0002-6337-8962</orcidid><orcidid>https://orcid.org/0000-0002-5931-419X</orcidid><orcidid>https://orcid.org/0000-0002-3442-5061</orcidid><orcidid>https://orcid.org/0000-0001-5486-1824</orcidid><orcidid>https://orcid.org/0000-0002-3419-1728</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Acids Animal models Animals Antioxidants Apoptosis Conflicts of interest Diabetes Diabetes mellitus Ethics Ischemia Kidney diseases Kidneys Membranes Metabolism Nephropathy Streptozocin Tıp |
title | Protective Effect of Vitamin B5 (Dexpanthenol) on Nephropathy in Streptozotocin Diabetic Rats |
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