Tocotrienol preserves ovarian function in cyclophosphamide therapy
Introduction: Cyclophosphamide (CPA) chemotherapy leads to ovarian failure and infertility. Tocotrienol (T3) is an antioxidant and anti-inflammatory agent. The role of T3 in ovarian protection throughout chemotherapy remains unclear. Aim: To investigate the role of T3 in the preservation of female f...
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Veröffentlicht in: | Human & experimental toxicology 2015-10, Vol.34 (10), p.946-952 |
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description | Introduction:
Cyclophosphamide (CPA) chemotherapy leads to ovarian failure and infertility. Tocotrienol (T3) is an antioxidant and anti-inflammatory agent. The role of T3 in ovarian protection throughout chemotherapy remains unclear.
Aim:
To investigate the role of T3 in the preservation of female fertility in CPA treatment.
Method:
Sixty female mice were divided into five treatment groups, namely, normal saline, corn oil only, T3 only, CPA and CPA + T3. The treatment was given for 30 days, followed by administration of gonadotrophin to induce ovulation. After killing, both ovaries were collected and examined histologically.
Results:
There was significant reduction in ovarian size in the CPA group compared with the normal group (CPA versus normal, mean area ± SD; 0.118 ± 0.018 vs. 0.423 ± 0.024 cm2; p ≤ 0.005), whilst concurrent administration of T3 with CPA leads to conservation of ovarian size (CPA + T3 vs. CPA, mean area ± SD; 0.285 ± 0.032 vs. 0.118 ± 0.018 cm2; p ≤ 0.005). Ovaries in CPA group showed abnormal folliculogenesis with accompanied reduced ovulation rate, follicular oedema, increased vascularity and inflammatory cell infiltration. These changes were reversed by concurrent T3 administration.
Conclusion:
Co-administration of T3 with CPA confers protection of ovarian morphology and function in vivo. These findings contribute to the further elucidation of CPA effect on ovary and suggest the potential of T3 use in preserving fertility in chemotherapy. |
doi_str_mv | 10.1177/0960327114564793 |
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Cyclophosphamide (CPA) chemotherapy leads to ovarian failure and infertility. Tocotrienol (T3) is an antioxidant and anti-inflammatory agent. The role of T3 in ovarian protection throughout chemotherapy remains unclear.
Aim:
To investigate the role of T3 in the preservation of female fertility in CPA treatment.
Method:
Sixty female mice were divided into five treatment groups, namely, normal saline, corn oil only, T3 only, CPA and CPA + T3. The treatment was given for 30 days, followed by administration of gonadotrophin to induce ovulation. After killing, both ovaries were collected and examined histologically.
Results:
There was significant reduction in ovarian size in the CPA group compared with the normal group (CPA versus normal, mean area ± SD; 0.118 ± 0.018 vs. 0.423 ± 0.024 cm2; p ≤ 0.005), whilst concurrent administration of T3 with CPA leads to conservation of ovarian size (CPA + T3 vs. CPA, mean area ± SD; 0.285 ± 0.032 vs. 0.118 ± 0.018 cm2; p ≤ 0.005). Ovaries in CPA group showed abnormal folliculogenesis with accompanied reduced ovulation rate, follicular oedema, increased vascularity and inflammatory cell infiltration. These changes were reversed by concurrent T3 administration.
Conclusion:
Co-administration of T3 with CPA confers protection of ovarian morphology and function in vivo. These findings contribute to the further elucidation of CPA effect on ovary and suggest the potential of T3 use in preserving fertility in chemotherapy.</description><identifier>ISSN: 0960-3271</identifier><identifier>EISSN: 1477-0903</identifier><identifier>DOI: 10.1177/0960327114564793</identifier><identifier>PMID: 25585998</identifier><language>eng</language><publisher>London, England: SAGE Publications</publisher><subject>Animals ; Antineoplastic Agents, Alkylating - toxicity ; Antioxidants ; Antioxidants - pharmacology ; Chemotherapy ; Cyclophosphamide - toxicity ; Female ; Fertility ; Mice ; Ovary - drug effects ; Ovary - pathology ; Reproductive system ; Tocotrienols - pharmacology ; Toxicity ; Womens health</subject><ispartof>Human & experimental toxicology, 2015-10, Vol.34 (10), p.946-952</ispartof><rights>The Author(s) 2015</rights><rights>The Author(s) 2015.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c365t-b1db399ce904b4d4ae8ea49821ad24adf0c6fa56b73c3aa6f2245a7c4f00c1603</citedby><cites>FETCH-LOGICAL-c365t-b1db399ce904b4d4ae8ea49821ad24adf0c6fa56b73c3aa6f2245a7c4f00c1603</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://journals.sagepub.com/doi/pdf/10.1177/0960327114564793$$EPDF$$P50$$Gsage$$H</linktopdf><linktohtml>$$Uhttps://journals.sagepub.com/doi/10.1177/0960327114564793$$EHTML$$P50$$Gsage$$H</linktohtml><link.rule.ids>315,782,786,21975,27862,27933,27934,44954,45342</link.rule.ids><linktorsrc>$$Uhttps://journals.sagepub.com/doi/full/10.1177/0960327114564793?utm_source=summon&utm_medium=discovery-provider$$EView_record_in_SAGE_Publications$$FView_record_in_$$GSAGE_Publications</linktorsrc><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/25585998$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Saleh, HS</creatorcontrib><creatorcontrib>Omar, E</creatorcontrib><creatorcontrib>Froemming, GRA</creatorcontrib><creatorcontrib>Said, RM</creatorcontrib><title>Tocotrienol preserves ovarian function in cyclophosphamide therapy</title><title>Human & experimental toxicology</title><addtitle>Hum Exp Toxicol</addtitle><description>Introduction:
Cyclophosphamide (CPA) chemotherapy leads to ovarian failure and infertility. Tocotrienol (T3) is an antioxidant and anti-inflammatory agent. The role of T3 in ovarian protection throughout chemotherapy remains unclear.
Aim:
To investigate the role of T3 in the preservation of female fertility in CPA treatment.
Method:
Sixty female mice were divided into five treatment groups, namely, normal saline, corn oil only, T3 only, CPA and CPA + T3. The treatment was given for 30 days, followed by administration of gonadotrophin to induce ovulation. After killing, both ovaries were collected and examined histologically.
Results:
There was significant reduction in ovarian size in the CPA group compared with the normal group (CPA versus normal, mean area ± SD; 0.118 ± 0.018 vs. 0.423 ± 0.024 cm2; p ≤ 0.005), whilst concurrent administration of T3 with CPA leads to conservation of ovarian size (CPA + T3 vs. CPA, mean area ± SD; 0.285 ± 0.032 vs. 0.118 ± 0.018 cm2; p ≤ 0.005). Ovaries in CPA group showed abnormal folliculogenesis with accompanied reduced ovulation rate, follicular oedema, increased vascularity and inflammatory cell infiltration. These changes were reversed by concurrent T3 administration.
Conclusion:
Co-administration of T3 with CPA confers protection of ovarian morphology and function in vivo. These findings contribute to the further elucidation of CPA effect on ovary and suggest the potential of T3 use in preserving fertility in chemotherapy.</description><subject>Animals</subject><subject>Antineoplastic Agents, Alkylating - toxicity</subject><subject>Antioxidants</subject><subject>Antioxidants - pharmacology</subject><subject>Chemotherapy</subject><subject>Cyclophosphamide - toxicity</subject><subject>Female</subject><subject>Fertility</subject><subject>Mice</subject><subject>Ovary - drug effects</subject><subject>Ovary - pathology</subject><subject>Reproductive system</subject><subject>Tocotrienols - pharmacology</subject><subject>Toxicity</subject><subject>Womens health</subject><issn>0960-3271</issn><issn>1477-0903</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><recordid>eNp1kM1Lw0AUxBdRbK3ePUnAc_Ttd_aopX5AwUs9h5fNxqa02bibFPrfm9IqInh6h_nNDG8IuaZwR6nW92AUcKYpFVIJbfgJGVOhdQoG-CkZ7-V0r4_IRYwrAFBG0nMyYlJm0phsTB4X3vou1K7x66QNLrqwdTHxWww1NknVN7arfZPUTWJ3du3bpY_tEjd16ZJu6QK2u0tyVuE6uqvjnZD3p9li-pLO355fpw_z1HIlu7SgZcGNsc6AKEQp0GUOhckYxZIJLCuwqkKpCs0tR1QVY0KitqICsHT4c0JuD7lt8J-9i12-8n1ohsqcapoxDixTAwUHygYfY3BV3oZ6g2GXU8j3o-V_RxssN8fgvti48sfwvdIApAcg4of71fpf4BeJGXS7</recordid><startdate>201510</startdate><enddate>201510</enddate><creator>Saleh, HS</creator><creator>Omar, E</creator><creator>Froemming, GRA</creator><creator>Said, RM</creator><general>SAGE Publications</general><general>Sage Publications Ltd</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7RV</scope><scope>7ST</scope><scope>7TK</scope><scope>7U7</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>BENPR</scope><scope>C1K</scope><scope>CCPQU</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>KB0</scope><scope>M0S</scope><scope>M1P</scope><scope>NAPCQ</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>SOI</scope></search><sort><creationdate>201510</creationdate><title>Tocotrienol preserves ovarian function in cyclophosphamide therapy</title><author>Saleh, HS ; Omar, E ; Froemming, GRA ; Said, RM</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c365t-b1db399ce904b4d4ae8ea49821ad24adf0c6fa56b73c3aa6f2245a7c4f00c1603</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Animals</topic><topic>Antineoplastic Agents, Alkylating - toxicity</topic><topic>Antioxidants</topic><topic>Antioxidants - pharmacology</topic><topic>Chemotherapy</topic><topic>Cyclophosphamide - toxicity</topic><topic>Female</topic><topic>Fertility</topic><topic>Mice</topic><topic>Ovary - drug effects</topic><topic>Ovary - pathology</topic><topic>Reproductive system</topic><topic>Tocotrienols - pharmacology</topic><topic>Toxicity</topic><topic>Womens health</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Saleh, HS</creatorcontrib><creatorcontrib>Omar, E</creatorcontrib><creatorcontrib>Froemming, GRA</creatorcontrib><creatorcontrib>Said, RM</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Nursing & Allied Health Database</collection><collection>Environment Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Toxicology Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</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 Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ProQuest One Community College</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Nursing & Allied Health Premium</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><collection>Environment Abstracts</collection><jtitle>Human & experimental toxicology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext_linktorsrc</fulltext></delivery><addata><au>Saleh, HS</au><au>Omar, E</au><au>Froemming, GRA</au><au>Said, RM</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Tocotrienol preserves ovarian function in cyclophosphamide therapy</atitle><jtitle>Human & experimental toxicology</jtitle><addtitle>Hum Exp Toxicol</addtitle><date>2015-10</date><risdate>2015</risdate><volume>34</volume><issue>10</issue><spage>946</spage><epage>952</epage><pages>946-952</pages><issn>0960-3271</issn><eissn>1477-0903</eissn><abstract>Introduction:
Cyclophosphamide (CPA) chemotherapy leads to ovarian failure and infertility. Tocotrienol (T3) is an antioxidant and anti-inflammatory agent. The role of T3 in ovarian protection throughout chemotherapy remains unclear.
Aim:
To investigate the role of T3 in the preservation of female fertility in CPA treatment.
Method:
Sixty female mice were divided into five treatment groups, namely, normal saline, corn oil only, T3 only, CPA and CPA + T3. The treatment was given for 30 days, followed by administration of gonadotrophin to induce ovulation. After killing, both ovaries were collected and examined histologically.
Results:
There was significant reduction in ovarian size in the CPA group compared with the normal group (CPA versus normal, mean area ± SD; 0.118 ± 0.018 vs. 0.423 ± 0.024 cm2; p ≤ 0.005), whilst concurrent administration of T3 with CPA leads to conservation of ovarian size (CPA + T3 vs. CPA, mean area ± SD; 0.285 ± 0.032 vs. 0.118 ± 0.018 cm2; p ≤ 0.005). Ovaries in CPA group showed abnormal folliculogenesis with accompanied reduced ovulation rate, follicular oedema, increased vascularity and inflammatory cell infiltration. These changes were reversed by concurrent T3 administration.
Conclusion:
Co-administration of T3 with CPA confers protection of ovarian morphology and function in vivo. These findings contribute to the further elucidation of CPA effect on ovary and suggest the potential of T3 use in preserving fertility in chemotherapy.</abstract><cop>London, England</cop><pub>SAGE Publications</pub><pmid>25585998</pmid><doi>10.1177/0960327114564793</doi><tpages>7</tpages></addata></record> |
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source | Sage Journals GOLD Open Access 2024 |
subjects | Animals Antineoplastic Agents, Alkylating - toxicity Antioxidants Antioxidants - pharmacology Chemotherapy Cyclophosphamide - toxicity Female Fertility Mice Ovary - drug effects Ovary - pathology Reproductive system Tocotrienols - pharmacology Toxicity Womens health |
title | Tocotrienol preserves ovarian function in cyclophosphamide therapy |
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