Beneficial role of naringin against methotrexate-induced injury to rat testes: biochemical and ultrastructural analyses
Methotrexate (MTX) is a commonly used chemotherapeutic drug that has adverse toxic effects on germ cells. Naringin (NG) is a natural flavanone glycoside, with different phytotherapeutic applications, and its possible protective effects against MTX-induced testicular tissue damage were investigated i...
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Veröffentlicht in: | Redox report : communications in free radical research 2022-12, Vol.27 (1), p.158-166 |
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creator | Elsawy, Hany Alzahrani, Abdullah M. Alfwuaires, Manal Abdel-Moneim, Ashraf M. Khalil, Mahmoud |
description | Methotrexate (MTX) is a commonly used chemotherapeutic drug that has adverse toxic effects on germ cells. Naringin (NG) is a natural flavanone glycoside, with different phytotherapeutic applications, and its possible protective effects against MTX-induced testicular tissue damage were investigated in this study.
Low and high doses of NG (40 and 80 mg/kg/day) were given for 10 days by intraperitoneal (i.p.) injection and MTX (20 mg/kg i.p.) was given at the 4th day of the experiment, with or without NG in rats.
The obtained results showed that exposure to MTX increased malondialdehyde (MDA) levels and nitric oxide (NO) production compared with the control. In the meantime, MTX depleted catalse (CAT), superoxide dismutase (SOD), glutathione reductase (GR), glutathione peroxidase (GPx), and reduced glutathione (GSH) in the testicular tissue. Further, serum testosterone levels were significantly decreased in the MTX group. NG significantly counteracted the aforementioned effects of MTX; however, NG80 was more effective in restoring SOD, GR, MDA and NO. Interestingly, NG80 achieved a better improvement in the ultrastructural pattern of the testicular cells in MTX-exposed rats.
These results indicated, for the first time, that NG could be a potential candidate therapy against MTX-reprotoxic impacts. |
doi_str_mv | 10.1080/13510002.2022.2101832 |
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Low and high doses of NG (40 and 80 mg/kg/day) were given for 10 days by intraperitoneal (i.p.) injection and MTX (20 mg/kg i.p.) was given at the 4th day of the experiment, with or without NG in rats.
The obtained results showed that exposure to MTX increased malondialdehyde (MDA) levels and nitric oxide (NO) production compared with the control. In the meantime, MTX depleted catalse (CAT), superoxide dismutase (SOD), glutathione reductase (GR), glutathione peroxidase (GPx), and reduced glutathione (GSH) in the testicular tissue. Further, serum testosterone levels were significantly decreased in the MTX group. NG significantly counteracted the aforementioned effects of MTX; however, NG80 was more effective in restoring SOD, GR, MDA and NO. Interestingly, NG80 achieved a better improvement in the ultrastructural pattern of the testicular cells in MTX-exposed rats.
These results indicated, for the first time, that NG could be a potential candidate therapy against MTX-reprotoxic impacts.</description><identifier>ISSN: 1351-0002</identifier><identifier>EISSN: 1743-2928</identifier><identifier>DOI: 10.1080/13510002.2022.2101832</identifier><identifier>PMID: 35861275</identifier><language>eng</language><publisher>Taylor & Francis</publisher><subject>antioxidants ; Methotrexate ; naringin ; nitric oxide ; oxidative stress ; testicular toxicity ; testosterone ; ultrastructure</subject><ispartof>Redox report : communications in free radical research, 2022-12, Vol.27 (1), p.158-166</ispartof><rights>2022 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group 2022</rights><rights>2022 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group 2022 The Author(s)</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c511t-8b7b938bf35e69051f7db48354fdaea6f5297ef181c5705aae2bcec3d0f50a7f3</citedby><cites>FETCH-LOGICAL-c511t-8b7b938bf35e69051f7db48354fdaea6f5297ef181c5705aae2bcec3d0f50a7f3</cites><orcidid>0000-0001-8250-4023</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC9310850/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC9310850/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,864,885,2102,27502,27924,27925,53791,53793,59143,59144</link.rule.ids></links><search><creatorcontrib>Elsawy, Hany</creatorcontrib><creatorcontrib>Alzahrani, Abdullah M.</creatorcontrib><creatorcontrib>Alfwuaires, Manal</creatorcontrib><creatorcontrib>Abdel-Moneim, Ashraf M.</creatorcontrib><creatorcontrib>Khalil, Mahmoud</creatorcontrib><title>Beneficial role of naringin against methotrexate-induced injury to rat testes: biochemical and ultrastructural analyses</title><title>Redox report : communications in free radical research</title><description>Methotrexate (MTX) is a commonly used chemotherapeutic drug that has adverse toxic effects on germ cells. Naringin (NG) is a natural flavanone glycoside, with different phytotherapeutic applications, and its possible protective effects against MTX-induced testicular tissue damage were investigated in this study.
Low and high doses of NG (40 and 80 mg/kg/day) were given for 10 days by intraperitoneal (i.p.) injection and MTX (20 mg/kg i.p.) was given at the 4th day of the experiment, with or without NG in rats.
The obtained results showed that exposure to MTX increased malondialdehyde (MDA) levels and nitric oxide (NO) production compared with the control. In the meantime, MTX depleted catalse (CAT), superoxide dismutase (SOD), glutathione reductase (GR), glutathione peroxidase (GPx), and reduced glutathione (GSH) in the testicular tissue. Further, serum testosterone levels were significantly decreased in the MTX group. NG significantly counteracted the aforementioned effects of MTX; however, NG80 was more effective in restoring SOD, GR, MDA and NO. Interestingly, NG80 achieved a better improvement in the ultrastructural pattern of the testicular cells in MTX-exposed rats.
These results indicated, for the first time, that NG could be a potential candidate therapy against MTX-reprotoxic impacts.</description><subject>antioxidants</subject><subject>Methotrexate</subject><subject>naringin</subject><subject>nitric oxide</subject><subject>oxidative stress</subject><subject>testicular toxicity</subject><subject>testosterone</subject><subject>ultrastructure</subject><issn>1351-0002</issn><issn>1743-2928</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><sourceid>0YH</sourceid><sourceid>DOA</sourceid><recordid>eNp9kktvFDEMx0cIRMvCR0DKkcuUPCbz4ICAikelSlzgHDkZZzdVJilJpmW_PdnugtQLUuRYjv2z7Pyb5jWjF4yO9C0TklFK-QWnvBpG2Sj4k-acDZ1o-cTHp9WvOe0h6ax5kfNN9UQ_jc-bMyHHnvFBnjf3nzCgdcaBJyl6JNGSAMmFrQsEtuBCLmTBsosl4W8o2LowrwZn4sLNmvakRJKgkIK5nndEu2h2uDhTeRBmsvqSIJe0mrKmhxj4fcb8snlmwWd8dbo3zc8vn39cfmuvv3-9uvx43RrJWGlHPehJjNoKif1EJbPDrLtRyM7OgNBbyacBLRuZkQOVAMi1QSNmaiWFwYpNc3XkzhFu1G1yC6S9iuDUQyCmrYJUnPGoOJ0Yaq5n1vUdjgJ03dAsawfdcWZpZb0_sm5XveBsMNTZ_CPo45fgdmob79Qk6pfJA-DNCZDir7VuTC0uG_QeAsY1K95PtWXH64CbRh5TTYo5J7T_2jCqDgJQfwWgDgJQJwHUug_HOhdsTAvcx-RnVWDvY7IJgnFZif8j_gDtrbkz</recordid><startdate>20221231</startdate><enddate>20221231</enddate><creator>Elsawy, Hany</creator><creator>Alzahrani, Abdullah M.</creator><creator>Alfwuaires, Manal</creator><creator>Abdel-Moneim, Ashraf M.</creator><creator>Khalil, Mahmoud</creator><general>Taylor & Francis</general><general>Taylor & Francis Group</general><scope>0YH</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope><orcidid>https://orcid.org/0000-0001-8250-4023</orcidid></search><sort><creationdate>20221231</creationdate><title>Beneficial role of naringin against methotrexate-induced injury to rat testes: biochemical and ultrastructural analyses</title><author>Elsawy, Hany ; Alzahrani, Abdullah M. ; Alfwuaires, Manal ; Abdel-Moneim, Ashraf M. ; Khalil, Mahmoud</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c511t-8b7b938bf35e69051f7db48354fdaea6f5297ef181c5705aae2bcec3d0f50a7f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>antioxidants</topic><topic>Methotrexate</topic><topic>naringin</topic><topic>nitric oxide</topic><topic>oxidative stress</topic><topic>testicular toxicity</topic><topic>testosterone</topic><topic>ultrastructure</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Elsawy, Hany</creatorcontrib><creatorcontrib>Alzahrani, Abdullah M.</creatorcontrib><creatorcontrib>Alfwuaires, Manal</creatorcontrib><creatorcontrib>Abdel-Moneim, Ashraf M.</creatorcontrib><creatorcontrib>Khalil, Mahmoud</creatorcontrib><collection>Taylor & Francis Open Access</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>Redox report : communications in free radical research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Elsawy, Hany</au><au>Alzahrani, Abdullah M.</au><au>Alfwuaires, Manal</au><au>Abdel-Moneim, Ashraf M.</au><au>Khalil, Mahmoud</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Beneficial role of naringin against methotrexate-induced injury to rat testes: biochemical and ultrastructural analyses</atitle><jtitle>Redox report : communications in free radical research</jtitle><date>2022-12-31</date><risdate>2022</risdate><volume>27</volume><issue>1</issue><spage>158</spage><epage>166</epage><pages>158-166</pages><issn>1351-0002</issn><eissn>1743-2928</eissn><abstract>Methotrexate (MTX) is a commonly used chemotherapeutic drug that has adverse toxic effects on germ cells. Naringin (NG) is a natural flavanone glycoside, with different phytotherapeutic applications, and its possible protective effects against MTX-induced testicular tissue damage were investigated in this study.
Low and high doses of NG (40 and 80 mg/kg/day) were given for 10 days by intraperitoneal (i.p.) injection and MTX (20 mg/kg i.p.) was given at the 4th day of the experiment, with or without NG in rats.
The obtained results showed that exposure to MTX increased malondialdehyde (MDA) levels and nitric oxide (NO) production compared with the control. In the meantime, MTX depleted catalse (CAT), superoxide dismutase (SOD), glutathione reductase (GR), glutathione peroxidase (GPx), and reduced glutathione (GSH) in the testicular tissue. Further, serum testosterone levels were significantly decreased in the MTX group. NG significantly counteracted the aforementioned effects of MTX; however, NG80 was more effective in restoring SOD, GR, MDA and NO. Interestingly, NG80 achieved a better improvement in the ultrastructural pattern of the testicular cells in MTX-exposed rats.
These results indicated, for the first time, that NG could be a potential candidate therapy against MTX-reprotoxic impacts.</abstract><pub>Taylor & Francis</pub><pmid>35861275</pmid><doi>10.1080/13510002.2022.2101832</doi><tpages>9</tpages><orcidid>https://orcid.org/0000-0001-8250-4023</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | antioxidants Methotrexate naringin nitric oxide oxidative stress testicular toxicity testosterone ultrastructure |
title | Beneficial role of naringin against methotrexate-induced injury to rat testes: biochemical and ultrastructural analyses |
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