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Acute and Subacute Toxicity Study of Essential Oil of Cymbopogon Martini in Mice
Background. Local Ethiopians regularly use Cymbopogon martini for cosmetic purposes. The plant’s safety, however, is not supported by any solid facts. This investigation aimed to evaluate the acute and subacute toxicities of C. martini essential oil in mice. Methods. The essential oil was analyzed u...
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Published in: | Journal of toxicology 2022-12, Vol.2022, p.1995578-7 |
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description | Background. Local Ethiopians regularly use Cymbopogon martini for cosmetic purposes. The plant’s safety, however, is not supported by any solid facts. This investigation aimed to evaluate the acute and subacute toxicities of C. martini essential oil in mice. Methods. The essential oil was analyzed using GC-MS. The approach outlined by Chinedu et al., 2013 has been used to calculate the median lethal dose. According to organization for economic cooperation and development (OECD) 407 standard, a 28-day repeated dose oral toxicity study was carried out on female mice. Three groups of ten experimental mice each were distributed at random. Group I received the same saline volume and was considered the control. Groups II and III were treated with doses of C. martini of 500 mg/kg and 1000 mg/kg, respectively, of body weight. Hematological and biochemical markers were assessed. The liver and kidney were taken out after the sacrifice using sodium pentobarbital for pathological analysis. Results. Geraniol (40.89%) was the predominant component in the essential oil composition of C. martini with cyclofenchene (13.91%), myrcene (9.34%), 2, 4, 6, octatriene, 2, 6, dimethyl (8.20%), and ocimene (5.93%) being present in small amounts. The LD50 of C. martini essential oil was discovered to be greater than 5000 mg/kg body weight. During a 4-week follow-up period, mice treated with C. martini, the essential oil, at doses of 500 mg/kg or 1000 mg/kg body weight showed no evidence of toxicity or mortality. Biochemical and hematological parameters were not significantly altered in mice treated with the essential oil of C. martini compared with the control group. Histopathological evaluation of the liver and kidney did not exhibit any adverse results. Conclusions. The essential oil of C. martini from Ethiopia is considered relatively safe and nontoxic. |
doi_str_mv | 10.1155/2022/1995578 |
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Local Ethiopians regularly use Cymbopogon martini for cosmetic purposes. The plant’s safety, however, is not supported by any solid facts. This investigation aimed to evaluate the acute and subacute toxicities of C. martini essential oil in mice. Methods. The essential oil was analyzed using GC-MS. The approach outlined by Chinedu et al., 2013 has been used to calculate the median lethal dose. According to organization for economic cooperation and development (OECD) 407 standard, a 28-day repeated dose oral toxicity study was carried out on female mice. Three groups of ten experimental mice each were distributed at random. Group I received the same saline volume and was considered the control. Groups II and III were treated with doses of C. martini of 500 mg/kg and 1000 mg/kg, respectively, of body weight. Hematological and biochemical markers were assessed. The liver and kidney were taken out after the sacrifice using sodium pentobarbital for pathological analysis. Results. Geraniol (40.89%) was the predominant component in the essential oil composition of C. martini with cyclofenchene (13.91%), myrcene (9.34%), 2, 4, 6, octatriene, 2, 6, dimethyl (8.20%), and ocimene (5.93%) being present in small amounts. The LD50 of C. martini essential oil was discovered to be greater than 5000 mg/kg body weight. During a 4-week follow-up period, mice treated with C. martini, the essential oil, at doses of 500 mg/kg or 1000 mg/kg body weight showed no evidence of toxicity or mortality. Biochemical and hematological parameters were not significantly altered in mice treated with the essential oil of C. martini compared with the control group. Histopathological evaluation of the liver and kidney did not exhibit any adverse results. Conclusions. The essential oil of C. martini from Ethiopia is considered relatively safe and nontoxic.</description><identifier>ISSN: 1687-8191</identifier><identifier>EISSN: 1687-8205</identifier><identifier>DOI: 10.1155/2022/1995578</identifier><identifier>PMID: 36573136</identifier><language>eng</language><publisher>Egypt: Hindawi</publisher><subject>Analysis ; Animals ; Biochemical markers ; Body weight ; Chemical composition ; Creatinine ; Dehydrogenases ; Drug dosages ; Essential oils ; Ethylenediaminetetraacetic acid ; Evaluation ; Hematology ; Hemoglobin ; Herbal medicine ; Kidneys ; Lethal dose ; Liver ; Metabolites ; Mice ; Myrcene ; Ocimene ; Oils & fats ; Pentobarbital ; Phytochemicals ; Subacute toxicity ; Toxicity ; Variance analysis</subject><ispartof>Journal of toxicology, 2022-12, Vol.2022, p.1995578-7</ispartof><rights>Copyright © 2022 Kassahun Dires Ayenew et al.</rights><rights>COPYRIGHT 2022 John Wiley & Sons, Inc.</rights><rights>Copyright © 2022 Kassahun Dires Ayenew et al. This is an open access article distributed under the Creative Commons Attribution License (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. https://creativecommons.org/licenses/by/4.0</rights><rights>Copyright © 2022 Kassahun Dires Ayenew et al. 2022</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c511t-7108e4f3eda8c8b0d91f7fa46c033ef7b034749343bfb09c3ddd631fbed9fb863</citedby><cites>FETCH-LOGICAL-c511t-7108e4f3eda8c8b0d91f7fa46c033ef7b034749343bfb09c3ddd631fbed9fb863</cites><orcidid>0000-0002-3213-0681 ; 0000-0003-0030-9529</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/2758026129/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2758026129?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,25744,27915,27916,37003,37004,44581,53782,53784,74887</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/36573136$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><contributor>Ren, Zongming</contributor><contributor>Zongming Ren</contributor><creatorcontrib>Ayenew, Kassahun Dires</creatorcontrib><creatorcontrib>Sewale, Yihenew</creatorcontrib><creatorcontrib>Amare, Yosef Eshetie</creatorcontrib><creatorcontrib>Ayalew, Amare</creatorcontrib><title>Acute and Subacute Toxicity Study of Essential Oil of Cymbopogon Martini in Mice</title><title>Journal of toxicology</title><addtitle>J Toxicol</addtitle><description>Background. Local Ethiopians regularly use Cymbopogon martini for cosmetic purposes. The plant’s safety, however, is not supported by any solid facts. This investigation aimed to evaluate the acute and subacute toxicities of C. martini essential oil in mice. Methods. The essential oil was analyzed using GC-MS. The approach outlined by Chinedu et al., 2013 has been used to calculate the median lethal dose. According to organization for economic cooperation and development (OECD) 407 standard, a 28-day repeated dose oral toxicity study was carried out on female mice. Three groups of ten experimental mice each were distributed at random. Group I received the same saline volume and was considered the control. Groups II and III were treated with doses of C. martini of 500 mg/kg and 1000 mg/kg, respectively, of body weight. Hematological and biochemical markers were assessed. The liver and kidney were taken out after the sacrifice using sodium pentobarbital for pathological analysis. Results. Geraniol (40.89%) was the predominant component in the essential oil composition of C. martini with cyclofenchene (13.91%), myrcene (9.34%), 2, 4, 6, octatriene, 2, 6, dimethyl (8.20%), and ocimene (5.93%) being present in small amounts. The LD50 of C. martini essential oil was discovered to be greater than 5000 mg/kg body weight. During a 4-week follow-up period, mice treated with C. martini, the essential oil, at doses of 500 mg/kg or 1000 mg/kg body weight showed no evidence of toxicity or mortality. Biochemical and hematological parameters were not significantly altered in mice treated with the essential oil of C. martini compared with the control group. Histopathological evaluation of the liver and kidney did not exhibit any adverse results. Conclusions. The essential oil of C. martini from Ethiopia is considered relatively safe and nontoxic.</description><subject>Analysis</subject><subject>Animals</subject><subject>Biochemical markers</subject><subject>Body weight</subject><subject>Chemical composition</subject><subject>Creatinine</subject><subject>Dehydrogenases</subject><subject>Drug dosages</subject><subject>Essential oils</subject><subject>Ethylenediaminetetraacetic acid</subject><subject>Evaluation</subject><subject>Hematology</subject><subject>Hemoglobin</subject><subject>Herbal medicine</subject><subject>Kidneys</subject><subject>Lethal dose</subject><subject>Liver</subject><subject>Metabolites</subject><subject>Mice</subject><subject>Myrcene</subject><subject>Ocimene</subject><subject>Oils & fats</subject><subject>Pentobarbital</subject><subject>Phytochemicals</subject><subject>Subacute toxicity</subject><subject>Toxicity</subject><subject>Variance analysis</subject><issn>1687-8191</issn><issn>1687-8205</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNp9kstvEzEQh1cIREvhxhmtxAWppPVr_bggRVGBSkVFajlbfqaOdu2w3oXmv8ebpIUghHzwePzNbzyeqarXEJxB2DTnCCB0DoVoGsafVMeQcjbjCDRPH2wo4FH1IucVAJQAwZ5XR5g2DENMj6uvczMOrlbR1jejVtvDbboPJgyb-mYY7aZOvr7I2cUhqLa-Du3kWGw6ndZpmWL9RfVDiKEOxQzGvayeedVm92q_n1TfPl7cLj7Prq4_XS7mVzPTQDjMGATcEY-dVdxwDayAnnlFqAEYO880wIQRgQnWXgNhsLWWYui1s8JrTvFJdbnTtUmt5LoPneo3Mqkgt47UL-X0MNM6aYRBDVOkZKHEaM2Zot5Dog0C3GhTtD7stNaj7pw1pdZetQeihzcx3Mll-iEF44ILUQTe7QX69H10eZBdyMa1rYoujVki1vDSHixAQd_-ha7S2MfyVVsKIAqR-E0tVSkgRJ9KXjOJynnpHESINLxQZ_-gyrKuCyZF50PxHwS83wWYPuXcO_9YIwRymiY5TZPcT1PB3_z5L4_ww_gU4HQH3IVo1c_wf7lfU4_QcA</recordid><startdate>20221217</startdate><enddate>20221217</enddate><creator>Ayenew, Kassahun Dires</creator><creator>Sewale, Yihenew</creator><creator>Amare, Yosef Eshetie</creator><creator>Ayalew, Amare</creator><general>Hindawi</general><general>John Wiley & Sons, Inc</general><general>Hindawi Limited</general><scope>RHU</scope><scope>RHW</scope><scope>RHX</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7ST</scope><scope>7U7</scope><scope>8FE</scope><scope>8FG</scope><scope>ABJCF</scope><scope>ABUWG</scope><scope>AEUYN</scope><scope>AFKRA</scope><scope>ATCPS</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>BGLVJ</scope><scope>BHPHI</scope><scope>C1K</scope><scope>CCPQU</scope><scope>CWDGH</scope><scope>DWQXO</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>L6V</scope><scope>M7S</scope><scope>PATMY</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>PTHSS</scope><scope>PYCSY</scope><scope>SOI</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope><orcidid>https://orcid.org/0000-0002-3213-0681</orcidid><orcidid>https://orcid.org/0000-0003-0030-9529</orcidid></search><sort><creationdate>20221217</creationdate><title>Acute and Subacute Toxicity Study of Essential Oil of Cymbopogon Martini in Mice</title><author>Ayenew, Kassahun Dires ; Sewale, Yihenew ; Amare, Yosef Eshetie ; Ayalew, Amare</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c511t-7108e4f3eda8c8b0d91f7fa46c033ef7b034749343bfb09c3ddd631fbed9fb863</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Analysis</topic><topic>Animals</topic><topic>Biochemical markers</topic><topic>Body weight</topic><topic>Chemical composition</topic><topic>Creatinine</topic><topic>Dehydrogenases</topic><topic>Drug dosages</topic><topic>Essential oils</topic><topic>Ethylenediaminetetraacetic acid</topic><topic>Evaluation</topic><topic>Hematology</topic><topic>Hemoglobin</topic><topic>Herbal medicine</topic><topic>Kidneys</topic><topic>Lethal dose</topic><topic>Liver</topic><topic>Metabolites</topic><topic>Mice</topic><topic>Myrcene</topic><topic>Ocimene</topic><topic>Oils & fats</topic><topic>Pentobarbital</topic><topic>Phytochemicals</topic><topic>Subacute toxicity</topic><topic>Toxicity</topic><topic>Variance analysis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ayenew, Kassahun Dires</creatorcontrib><creatorcontrib>Sewale, Yihenew</creatorcontrib><creatorcontrib>Amare, Yosef Eshetie</creatorcontrib><creatorcontrib>Ayalew, Amare</creatorcontrib><collection>Hindawi Publishing Complete</collection><collection>Hindawi Publishing Subscription Journals</collection><collection>Hindawi Publishing Open Access</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Environment Abstracts</collection><collection>Toxicology Abstracts</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Technology Collection</collection><collection>Materials Science & Engineering Collection</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest One Sustainability</collection><collection>ProQuest Central</collection><collection>Agricultural & Environmental Science Collection</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>Technology Collection</collection><collection>Natural Science Collection</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ProQuest One Community College</collection><collection>Middle East & Africa Database</collection><collection>ProQuest Central Korea</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Engineering Collection</collection><collection>Engineering Database</collection><collection>Environmental 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><collection>Engineering Collection</collection><collection>Environmental Science Collection</collection><collection>Environment Abstracts</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>Directory of Open Access Journals(OpenAccess)</collection><jtitle>Journal of toxicology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ayenew, Kassahun Dires</au><au>Sewale, Yihenew</au><au>Amare, Yosef Eshetie</au><au>Ayalew, Amare</au><au>Ren, Zongming</au><au>Zongming Ren</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Acute and Subacute Toxicity Study of Essential Oil of Cymbopogon Martini in Mice</atitle><jtitle>Journal of toxicology</jtitle><addtitle>J Toxicol</addtitle><date>2022-12-17</date><risdate>2022</risdate><volume>2022</volume><spage>1995578</spage><epage>7</epage><pages>1995578-7</pages><issn>1687-8191</issn><eissn>1687-8205</eissn><abstract>Background. Local Ethiopians regularly use Cymbopogon martini for cosmetic purposes. The plant’s safety, however, is not supported by any solid facts. This investigation aimed to evaluate the acute and subacute toxicities of C. martini essential oil in mice. Methods. The essential oil was analyzed using GC-MS. The approach outlined by Chinedu et al., 2013 has been used to calculate the median lethal dose. According to organization for economic cooperation and development (OECD) 407 standard, a 28-day repeated dose oral toxicity study was carried out on female mice. Three groups of ten experimental mice each were distributed at random. Group I received the same saline volume and was considered the control. Groups II and III were treated with doses of C. martini of 500 mg/kg and 1000 mg/kg, respectively, of body weight. Hematological and biochemical markers were assessed. The liver and kidney were taken out after the sacrifice using sodium pentobarbital for pathological analysis. Results. Geraniol (40.89%) was the predominant component in the essential oil composition of C. martini with cyclofenchene (13.91%), myrcene (9.34%), 2, 4, 6, octatriene, 2, 6, dimethyl (8.20%), and ocimene (5.93%) being present in small amounts. The LD50 of C. martini essential oil was discovered to be greater than 5000 mg/kg body weight. During a 4-week follow-up period, mice treated with C. martini, the essential oil, at doses of 500 mg/kg or 1000 mg/kg body weight showed no evidence of toxicity or mortality. Biochemical and hematological parameters were not significantly altered in mice treated with the essential oil of C. martini compared with the control group. Histopathological evaluation of the liver and kidney did not exhibit any adverse results. Conclusions. The essential oil of C. martini from Ethiopia is considered relatively safe and nontoxic.</abstract><cop>Egypt</cop><pub>Hindawi</pub><pmid>36573136</pmid><doi>10.1155/2022/1995578</doi><tpages>7</tpages><orcidid>https://orcid.org/0000-0002-3213-0681</orcidid><orcidid>https://orcid.org/0000-0003-0030-9529</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Analysis Animals Biochemical markers Body weight Chemical composition Creatinine Dehydrogenases Drug dosages Essential oils Ethylenediaminetetraacetic acid Evaluation Hematology Hemoglobin Herbal medicine Kidneys Lethal dose Liver Metabolites Mice Myrcene Ocimene Oils & fats Pentobarbital Phytochemicals Subacute toxicity Toxicity Variance analysis |
title | Acute and Subacute Toxicity Study of Essential Oil of Cymbopogon Martini in Mice |
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