Toxicological studies of aqueous extract of Acacia nilotica root
is a widely used plant in traditional medical practice in Northern Nigeria and many African countries. The aim of this study was to determine the toxicological effects of a single dose (acute) and of repeated doses (sub-acute) administration of aqueous extract of root in rodents, following our earli...
Gespeichert in:
Veröffentlicht in: | Interdisciplinary toxicology 2015-03, Vol.8 (1), p.48-54 |
---|---|
Hauptverfasser: | , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 54 |
---|---|
container_issue | 1 |
container_start_page | 48 |
container_title | Interdisciplinary toxicology |
container_volume | 8 |
creator | Alli, Lukman Adewale Adesokan, Abdulfatai Ayoade Salawu, Oluwakanyinsola Adeola Akanji, Musbau Adewunmi |
description | is a widely used plant in traditional medical practice in Northern Nigeria and many African countries. The aim of this study was to determine the toxicological effects of a single dose (acute) and of repeated doses (sub-acute) administration of aqueous extract of
root in rodents, following our earlier study on antiplasmodial activity. In the acute toxicity test, three groups of Swiss albino mice were orally administered aqueous extract of
(50, 300 and 2000 mg/kg body weight) and signs of toxicity were observed daily for 14 days. In the sub-acute toxicity study, four groups of 12 rats (6 male and 6 female) were used. Group 1 received 10 ml/kg b.w distilled water (control), while groups 2, 3 and 4 received 125, 250 and 500 mg/kg b.w of the extract, respectively, for 28 consecutive days by oral gavage. Signs of toxicity/mortality, food and water intake and body weight changes were observed. Biochemical parameters were analysed in both plasma and liver homogenate. In the acute and sub-acute toxicity studies, the extract did not cause mortality. A significant reduction in the activity of lactate dehydrogenase was observed at 250 and 500 mg/kg b.w, while alanine aminotransferase, aspartate aminotransferase and alkaline phosphatase activities were significantly higher than control values at 500 mg/kg b.w. The aqueous extract of
was found to be safe in single dose administration in mice but repeated administration of doses higher than 250 mg/kg b.w of the extract for 28 days in rats may cause hepatotoxicity. |
doi_str_mv | 10.1515/intox-2015-0005 |
format | Article |
fullrecord | <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_4961926</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>1809048558</sourcerecordid><originalsourceid>FETCH-LOGICAL-c3888-aecdd3c99fe861b82838386470f9eceef8d15140b333bd983fe407f55e620a443</originalsourceid><addsrcrecordid>eNptkUtLxDAUhYMozqCzdicFN26qSfNogiCK-ALBja5DJr0dI51mTFod_72pM4qKZJFL8uXkHA5CewQfEU74sWs7v8wLTHiOMeYbaEwoLXPFhdpcz0JyOkKTGJ8TgSnhkoltNCpKJgUVeIzOHvzSWd_4mbOmyWLXVw5i5uvMvPTg-5jBsgvGdsPRuTXWmax1je8SngXvu120VZsmwmS976DHq8uHi5v87v769uL8LrdUSpkbsFVFrVI1SEGmspA0LcFKXCuwALWsUiaGp5TSaaUkrYHhsuYcRIENY3QHna50F_10DpWFNtlq9CK4uQnv2hunf9-07knP_KtmShBViCRwuBYIPkWLnZ67aKFpTDvk1ERihZnkXCb04A_67PvQpniJEiQZFUWZqOMVZYOPMUD9bYZgPRSkPwvSQ0F6KCi92P-Z4Zv_qiMBJyvgzTQdhApmoX9Pw4___5eWhEn6AauCoME</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1861151627</pqid></control><display><type>article</type><title>Toxicological studies of aqueous extract of Acacia nilotica root</title><source>De Gruyter Open Access Journals</source><source>Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals</source><source>PubMed Central</source><source>PubMed Central Open Access</source><creator>Alli, Lukman Adewale ; Adesokan, Abdulfatai Ayoade ; Salawu, Oluwakanyinsola Adeola ; Akanji, Musbau Adewunmi</creator><creatorcontrib>Alli, Lukman Adewale ; Adesokan, Abdulfatai Ayoade ; Salawu, Oluwakanyinsola Adeola ; Akanji, Musbau Adewunmi</creatorcontrib><description>is a widely used plant in traditional medical practice in Northern Nigeria and many African countries. The aim of this study was to determine the toxicological effects of a single dose (acute) and of repeated doses (sub-acute) administration of aqueous extract of
root in rodents, following our earlier study on antiplasmodial activity. In the acute toxicity test, three groups of Swiss albino mice were orally administered aqueous extract of
(50, 300 and 2000 mg/kg body weight) and signs of toxicity were observed daily for 14 days. In the sub-acute toxicity study, four groups of 12 rats (6 male and 6 female) were used. Group 1 received 10 ml/kg b.w distilled water (control), while groups 2, 3 and 4 received 125, 250 and 500 mg/kg b.w of the extract, respectively, for 28 consecutive days by oral gavage. Signs of toxicity/mortality, food and water intake and body weight changes were observed. Biochemical parameters were analysed in both plasma and liver homogenate. In the acute and sub-acute toxicity studies, the extract did not cause mortality. A significant reduction in the activity of lactate dehydrogenase was observed at 250 and 500 mg/kg b.w, while alanine aminotransferase, aspartate aminotransferase and alkaline phosphatase activities were significantly higher than control values at 500 mg/kg b.w. The aqueous extract of
was found to be safe in single dose administration in mice but repeated administration of doses higher than 250 mg/kg b.w of the extract for 28 days in rats may cause hepatotoxicity.</description><identifier>ISSN: 1337-6853</identifier><identifier>ISSN: 1337-9569</identifier><identifier>EISSN: 1337-9569</identifier><identifier>DOI: 10.1515/intox-2015-0005</identifier><identifier>PMID: 27486360</identifier><language>eng</language><publisher>Slovakia: De Gruyter Open</publisher><subject>acute toxicity ; Aqueous solutions ; Extraction processes ; Original ; sub-acute toxicity ; Toxicology</subject><ispartof>Interdisciplinary toxicology, 2015-03, Vol.8 (1), p.48-54</ispartof><rights>Copyright De Gruyter Open Sp. z o.o. 2015</rights><rights>Copyright © 2015 SETOX & Institute of Experimental Pharmacology and Toxicology, SASc. 2015</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3888-aecdd3c99fe861b82838386470f9eceef8d15140b333bd983fe407f55e620a443</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4961926/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4961926/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,881,27901,27902,53766,53768,66901,68685</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/27486360$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Alli, Lukman Adewale</creatorcontrib><creatorcontrib>Adesokan, Abdulfatai Ayoade</creatorcontrib><creatorcontrib>Salawu, Oluwakanyinsola Adeola</creatorcontrib><creatorcontrib>Akanji, Musbau Adewunmi</creatorcontrib><title>Toxicological studies of aqueous extract of Acacia nilotica root</title><title>Interdisciplinary toxicology</title><addtitle>Interdiscip Toxicol</addtitle><description>is a widely used plant in traditional medical practice in Northern Nigeria and many African countries. The aim of this study was to determine the toxicological effects of a single dose (acute) and of repeated doses (sub-acute) administration of aqueous extract of
root in rodents, following our earlier study on antiplasmodial activity. In the acute toxicity test, three groups of Swiss albino mice were orally administered aqueous extract of
(50, 300 and 2000 mg/kg body weight) and signs of toxicity were observed daily for 14 days. In the sub-acute toxicity study, four groups of 12 rats (6 male and 6 female) were used. Group 1 received 10 ml/kg b.w distilled water (control), while groups 2, 3 and 4 received 125, 250 and 500 mg/kg b.w of the extract, respectively, for 28 consecutive days by oral gavage. Signs of toxicity/mortality, food and water intake and body weight changes were observed. Biochemical parameters were analysed in both plasma and liver homogenate. In the acute and sub-acute toxicity studies, the extract did not cause mortality. A significant reduction in the activity of lactate dehydrogenase was observed at 250 and 500 mg/kg b.w, while alanine aminotransferase, aspartate aminotransferase and alkaline phosphatase activities were significantly higher than control values at 500 mg/kg b.w. The aqueous extract of
was found to be safe in single dose administration in mice but repeated administration of doses higher than 250 mg/kg b.w of the extract for 28 days in rats may cause hepatotoxicity.</description><subject>acute toxicity</subject><subject>Aqueous solutions</subject><subject>Extraction processes</subject><subject>Original</subject><subject>sub-acute toxicity</subject><subject>Toxicology</subject><issn>1337-6853</issn><issn>1337-9569</issn><issn>1337-9569</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>BENPR</sourceid><recordid>eNptkUtLxDAUhYMozqCzdicFN26qSfNogiCK-ALBja5DJr0dI51mTFod_72pM4qKZJFL8uXkHA5CewQfEU74sWs7v8wLTHiOMeYbaEwoLXPFhdpcz0JyOkKTGJ8TgSnhkoltNCpKJgUVeIzOHvzSWd_4mbOmyWLXVw5i5uvMvPTg-5jBsgvGdsPRuTXWmax1je8SngXvu120VZsmwmS976DHq8uHi5v87v769uL8LrdUSpkbsFVFrVI1SEGmspA0LcFKXCuwALWsUiaGp5TSaaUkrYHhsuYcRIENY3QHna50F_10DpWFNtlq9CK4uQnv2hunf9-07knP_KtmShBViCRwuBYIPkWLnZ67aKFpTDvk1ERihZnkXCb04A_67PvQpniJEiQZFUWZqOMVZYOPMUD9bYZgPRSkPwvSQ0F6KCi92P-Z4Zv_qiMBJyvgzTQdhApmoX9Pw4___5eWhEn6AauCoME</recordid><startdate>20150301</startdate><enddate>20150301</enddate><creator>Alli, Lukman Adewale</creator><creator>Adesokan, Abdulfatai Ayoade</creator><creator>Salawu, Oluwakanyinsola Adeola</creator><creator>Akanji, Musbau Adewunmi</creator><general>De Gruyter Open</general><general>De Gruyter Poland</general><general>Slovak Toxicology Society SETOX</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7RV</scope><scope>7U7</scope><scope>7X7</scope><scope>7XB</scope><scope>8AO</scope><scope>8C1</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AEUYN</scope><scope>AFKRA</scope><scope>ATCPS</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>BYOGL</scope><scope>C1K</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>KB0</scope><scope>LK8</scope><scope>M0S</scope><scope>M7P</scope><scope>NAPCQ</scope><scope>PATMY</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>PYCSY</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20150301</creationdate><title>Toxicological studies of aqueous extract of Acacia nilotica root</title><author>Alli, Lukman Adewale ; Adesokan, Abdulfatai Ayoade ; Salawu, Oluwakanyinsola Adeola ; Akanji, Musbau Adewunmi</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3888-aecdd3c99fe861b82838386470f9eceef8d15140b333bd983fe407f55e620a443</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>acute toxicity</topic><topic>Aqueous solutions</topic><topic>Extraction processes</topic><topic>Original</topic><topic>sub-acute toxicity</topic><topic>Toxicology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Alli, Lukman Adewale</creatorcontrib><creatorcontrib>Adesokan, Abdulfatai Ayoade</creatorcontrib><creatorcontrib>Salawu, Oluwakanyinsola Adeola</creatorcontrib><creatorcontrib>Akanji, Musbau Adewunmi</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Nursing & Allied Health Database</collection><collection>Toxicology Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>ProQuest Pharma Collection</collection><collection>Public Health Database</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 Edition)</collection><collection>ProQuest One Sustainability</collection><collection>ProQuest Central UK/Ireland</collection><collection>Agricultural & Environmental Science Collection</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>East Europe, Central Europe Database</collection><collection>Environmental Sciences and Pollution Management</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>Nursing & Allied Health Database (Alumni Edition)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Biological Science Database</collection><collection>Nursing & Allied Health Premium</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>Environmental Science Collection</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Interdisciplinary toxicology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Alli, Lukman Adewale</au><au>Adesokan, Abdulfatai Ayoade</au><au>Salawu, Oluwakanyinsola Adeola</au><au>Akanji, Musbau Adewunmi</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Toxicological studies of aqueous extract of Acacia nilotica root</atitle><jtitle>Interdisciplinary toxicology</jtitle><addtitle>Interdiscip Toxicol</addtitle><date>2015-03-01</date><risdate>2015</risdate><volume>8</volume><issue>1</issue><spage>48</spage><epage>54</epage><pages>48-54</pages><issn>1337-6853</issn><issn>1337-9569</issn><eissn>1337-9569</eissn><abstract>is a widely used plant in traditional medical practice in Northern Nigeria and many African countries. The aim of this study was to determine the toxicological effects of a single dose (acute) and of repeated doses (sub-acute) administration of aqueous extract of
root in rodents, following our earlier study on antiplasmodial activity. In the acute toxicity test, three groups of Swiss albino mice were orally administered aqueous extract of
(50, 300 and 2000 mg/kg body weight) and signs of toxicity were observed daily for 14 days. In the sub-acute toxicity study, four groups of 12 rats (6 male and 6 female) were used. Group 1 received 10 ml/kg b.w distilled water (control), while groups 2, 3 and 4 received 125, 250 and 500 mg/kg b.w of the extract, respectively, for 28 consecutive days by oral gavage. Signs of toxicity/mortality, food and water intake and body weight changes were observed. Biochemical parameters were analysed in both plasma and liver homogenate. In the acute and sub-acute toxicity studies, the extract did not cause mortality. A significant reduction in the activity of lactate dehydrogenase was observed at 250 and 500 mg/kg b.w, while alanine aminotransferase, aspartate aminotransferase and alkaline phosphatase activities were significantly higher than control values at 500 mg/kg b.w. The aqueous extract of
was found to be safe in single dose administration in mice but repeated administration of doses higher than 250 mg/kg b.w of the extract for 28 days in rats may cause hepatotoxicity.</abstract><cop>Slovakia</cop><pub>De Gruyter Open</pub><pmid>27486360</pmid><doi>10.1515/intox-2015-0005</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1337-6853 |
ispartof | Interdisciplinary toxicology, 2015-03, Vol.8 (1), p.48-54 |
issn | 1337-6853 1337-9569 1337-9569 |
language | eng |
recordid | cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_4961926 |
source | De Gruyter Open Access Journals; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; PubMed Central; PubMed Central Open Access |
subjects | acute toxicity Aqueous solutions Extraction processes Original sub-acute toxicity Toxicology |
title | Toxicological studies of aqueous extract of Acacia nilotica root |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-03T05%3A34%3A32IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Toxicological%20studies%20of%20aqueous%20extract%20of%20Acacia%20nilotica%20root&rft.jtitle=Interdisciplinary%20toxicology&rft.au=Alli,%20Lukman%20Adewale&rft.date=2015-03-01&rft.volume=8&rft.issue=1&rft.spage=48&rft.epage=54&rft.pages=48-54&rft.issn=1337-6853&rft.eissn=1337-9569&rft_id=info:doi/10.1515/intox-2015-0005&rft_dat=%3Cproquest_pubme%3E1809048558%3C/proquest_pubme%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=1861151627&rft_id=info:pmid/27486360&rfr_iscdi=true |