Chemical profiling, toxicity assessment, anti-diarrhoeal, anti-inflammatory and antinociceptive activities of Canarium schweinfurthii Engl. (Burseraceae) bark in rats
The bark of Canarium schweinfurthii is used in ethnomedicine for the treatment of diabetes, pain, malaria, fever and diarrhoea. The chemical phytoconstituents, antidiarrheal, anti-inflammatory and antinociceptive effects and safety profile of the aqueous extract of Canarium schweinfurthii bark (AECS...
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creator | Umeh, Nkiruka Edith Onuorah, Remigius Tochukwu Ekweogu, Celestine Nwabu Ijioma, Solomon Nnah Egeduzu, Ozioma Glory Nwaru, Ezeibe Chidi Iweala, Emeka Joshua Ugbogu, Eziuche Amadike |
description | The bark of Canarium schweinfurthii is used in ethnomedicine for the treatment of diabetes, pain, malaria, fever and diarrhoea.
The chemical phytoconstituents, antidiarrheal, anti-inflammatory and antinociceptive effects and safety profile of the aqueous extract of Canarium schweinfurthii bark (AECSB) were investigated.
Gas chromatography-mass spectrometry (GC-MS) was used to analyse the phytochemical composition. In the acute toxicity test, AECSB were administered up to 2 g/kg by oral gavage. For the subacute toxicity test (28 days), rats in group 1 (control) received no AECSB, while rats in groups 2–4 were administered different doses of AECSB. Charcoal meal transit and castor oil-induced diarrhoea models were used to study the antidiarrheal effect, while egg albumin/carrageenan and acetic acid/tail immersion models were used for the anti-inflammatory and antinociceptive studies, respectively. With the exception of the acute toxicity experiment, AECSB was administered orally at doses of 200, 400 and 800 mg/kg.
Bioactive phytoconstituents identified include p-cymene, δ-terpinene, linalool and phytol. No adverse effects or mortality were observed in acute and subacute studies. Treatment with AECSB (28 days) had no significant effect on organ weight, biochemical, hematologic and histopathologic parameters compared to the control groups (p > 0.05). Comparable antidiarrheal and antinociceptive effects were observed in both AECSB- and standard drug-treated groups, while the 400 and 800 mg/kg AECSB-treated groups showed remarkable anti-inflammatory effects compared to the standard drug-treated and control groups (p |
doi_str_mv | 10.1016/j.jep.2024.118460 |
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The chemical phytoconstituents, antidiarrheal, anti-inflammatory and antinociceptive effects and safety profile of the aqueous extract of Canarium schweinfurthii bark (AECSB) were investigated.
Gas chromatography-mass spectrometry (GC-MS) was used to analyse the phytochemical composition. In the acute toxicity test, AECSB were administered up to 2 g/kg by oral gavage. For the subacute toxicity test (28 days), rats in group 1 (control) received no AECSB, while rats in groups 2–4 were administered different doses of AECSB. Charcoal meal transit and castor oil-induced diarrhoea models were used to study the antidiarrheal effect, while egg albumin/carrageenan and acetic acid/tail immersion models were used for the anti-inflammatory and antinociceptive studies, respectively. With the exception of the acute toxicity experiment, AECSB was administered orally at doses of 200, 400 and 800 mg/kg.
Bioactive phytoconstituents identified include p-cymene, δ-terpinene, linalool and phytol. No adverse effects or mortality were observed in acute and subacute studies. Treatment with AECSB (28 days) had no significant effect on organ weight, biochemical, hematologic and histopathologic parameters compared to the control groups (p > 0.05). Comparable antidiarrheal and antinociceptive effects were observed in both AECSB- and standard drug-treated groups, while the 400 and 800 mg/kg AECSB-treated groups showed remarkable anti-inflammatory effects compared to the standard drug-treated and control groups (p < 0.05).
AECSB has antidiarrheal, antinociceptive and anti-inflammatory effects and can be safely used for therapeutic purposes.
[Display omitted]
•Bark of Canarium schweinfurthii is traditionally used to treat diarrhoea, pain and inflammation.•Methanol ECSB contains biologically active compounds with various pharmacological effects.•AECSB caused no adverse effects on haematology and serum biochemistry.•AECSB has analgesic, anti-inflammatory and anti-diarrhoeal effects.</description><identifier>ISSN: 0378-8741</identifier><identifier>ISSN: 1872-7573</identifier><identifier>EISSN: 1872-7573</identifier><identifier>DOI: 10.1016/j.jep.2024.118460</identifier><identifier>PMID: 38878840</identifier><language>eng</language><publisher>Ireland: Elsevier B.V</publisher><subject>acetic acid ; acute toxicity ; Anti-inflammatory ; antidiarrheal effect ; bark ; Bioactive compounds ; Canarium schweinfurthii ; Canarium schweinfurthii bark ; carrageenan ; charcoal ; chemical constituents of plants ; diabetes ; diarrhea ; egg albumen ; fever ; gas chromatography-mass spectrometry ; histopathology ; linalool ; malaria ; mortality ; oral gavage ; p-cymene ; pain ; subacute toxicity ; tail ; therapeutics ; tissue weight ; Toxicity profile ; toxicity testing ; traditional medicine</subject><ispartof>Journal of ethnopharmacology, 2024-10, Vol.333, p.118460, Article 118460</ispartof><rights>2024 Elsevier B.V.</rights><rights>Copyright © 2024. Published by Elsevier B.V.</rights><rights>Copyright © 2024 Elsevier B.V. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c338t-d1a34eb63d84f5dc33a414a71a02f13dc0b78857eedff16f3f56139d21bc0a5c3</cites><orcidid>0000-0003-3145-5473 ; 0000-0002-1393-1416</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0378874124007591$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/38878840$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Umeh, Nkiruka Edith</creatorcontrib><creatorcontrib>Onuorah, Remigius Tochukwu</creatorcontrib><creatorcontrib>Ekweogu, Celestine Nwabu</creatorcontrib><creatorcontrib>Ijioma, Solomon Nnah</creatorcontrib><creatorcontrib>Egeduzu, Ozioma Glory</creatorcontrib><creatorcontrib>Nwaru, Ezeibe Chidi</creatorcontrib><creatorcontrib>Iweala, Emeka Joshua</creatorcontrib><creatorcontrib>Ugbogu, Eziuche Amadike</creatorcontrib><title>Chemical profiling, toxicity assessment, anti-diarrhoeal, anti-inflammatory and antinociceptive activities of Canarium schweinfurthii Engl. (Burseraceae) bark in rats</title><title>Journal of ethnopharmacology</title><addtitle>J Ethnopharmacol</addtitle><description>The bark of Canarium schweinfurthii is used in ethnomedicine for the treatment of diabetes, pain, malaria, fever and diarrhoea.
The chemical phytoconstituents, antidiarrheal, anti-inflammatory and antinociceptive effects and safety profile of the aqueous extract of Canarium schweinfurthii bark (AECSB) were investigated.
Gas chromatography-mass spectrometry (GC-MS) was used to analyse the phytochemical composition. In the acute toxicity test, AECSB were administered up to 2 g/kg by oral gavage. For the subacute toxicity test (28 days), rats in group 1 (control) received no AECSB, while rats in groups 2–4 were administered different doses of AECSB. Charcoal meal transit and castor oil-induced diarrhoea models were used to study the antidiarrheal effect, while egg albumin/carrageenan and acetic acid/tail immersion models were used for the anti-inflammatory and antinociceptive studies, respectively. With the exception of the acute toxicity experiment, AECSB was administered orally at doses of 200, 400 and 800 mg/kg.
Bioactive phytoconstituents identified include p-cymene, δ-terpinene, linalool and phytol. No adverse effects or mortality were observed in acute and subacute studies. Treatment with AECSB (28 days) had no significant effect on organ weight, biochemical, hematologic and histopathologic parameters compared to the control groups (p > 0.05). Comparable antidiarrheal and antinociceptive effects were observed in both AECSB- and standard drug-treated groups, while the 400 and 800 mg/kg AECSB-treated groups showed remarkable anti-inflammatory effects compared to the standard drug-treated and control groups (p < 0.05).
AECSB has antidiarrheal, antinociceptive and anti-inflammatory effects and can be safely used for therapeutic purposes.
[Display omitted]
•Bark of Canarium schweinfurthii is traditionally used to treat diarrhoea, pain and inflammation.•Methanol ECSB contains biologically active compounds with various pharmacological effects.•AECSB caused no adverse effects on haematology and serum biochemistry.•AECSB has analgesic, anti-inflammatory and anti-diarrhoeal effects.</description><subject>acetic acid</subject><subject>acute toxicity</subject><subject>Anti-inflammatory</subject><subject>antidiarrheal effect</subject><subject>bark</subject><subject>Bioactive compounds</subject><subject>Canarium schweinfurthii</subject><subject>Canarium schweinfurthii bark</subject><subject>carrageenan</subject><subject>charcoal</subject><subject>chemical constituents of plants</subject><subject>diabetes</subject><subject>diarrhea</subject><subject>egg albumen</subject><subject>fever</subject><subject>gas chromatography-mass spectrometry</subject><subject>histopathology</subject><subject>linalool</subject><subject>malaria</subject><subject>mortality</subject><subject>oral gavage</subject><subject>p-cymene</subject><subject>pain</subject><subject>subacute toxicity</subject><subject>tail</subject><subject>therapeutics</subject><subject>tissue weight</subject><subject>Toxicity profile</subject><subject>toxicity testing</subject><subject>traditional medicine</subject><issn>0378-8741</issn><issn>1872-7573</issn><issn>1872-7573</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><recordid>eNqFkU1v1DAQhiMEokvhB3BBPhapWew4iV1xglX5kCpxgbM1scfdWRJnsZ1C_xC_Ey-7cITTSKPnfaWZp6qeC74WXPSvdusd7tcNb9q1ELrt-YNqJbRqatUp-bBacal0rVUrzqonKe0450q0_HF1JrVWWrd8Vf3cbHEiCyPbx9nTSOH2kuX5B1nK9wxSwpQmDPmSQchUO4IYtzPCeFpQ8CNME-Q5Fjy439swW7K4z3SHDGwZlAkTmz3bQIBIy8SS3X7HEl5i3hKx63A7rtnF2yUmjGAR8CUbIH5lFFiEnJ5WjzyMCZ-d5nn15d31582H-ubT-4-bNze1lVLn2gmQLQ69dLr1nStLaEULSgBvvJDO8qHc3SlE573ovfRdL-SVa8RgOXRWnlcXx97yjW8LpmwmShbHEQLOSzJSdLLvr_q--z_Ke626g46CiiNq45xSRG_2kSaI90ZwczBpdqaYNAeT5miyZF6c6pdhQvc38UddAV4fASz_uCOMJlnCYNFRRJuNm-kf9b8AoWSyJA</recordid><startdate>20241028</startdate><enddate>20241028</enddate><creator>Umeh, Nkiruka Edith</creator><creator>Onuorah, Remigius Tochukwu</creator><creator>Ekweogu, Celestine Nwabu</creator><creator>Ijioma, Solomon Nnah</creator><creator>Egeduzu, Ozioma Glory</creator><creator>Nwaru, Ezeibe Chidi</creator><creator>Iweala, Emeka Joshua</creator><creator>Ugbogu, Eziuche Amadike</creator><general>Elsevier B.V</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>7S9</scope><scope>L.6</scope><orcidid>https://orcid.org/0000-0003-3145-5473</orcidid><orcidid>https://orcid.org/0000-0002-1393-1416</orcidid></search><sort><creationdate>20241028</creationdate><title>Chemical profiling, toxicity assessment, anti-diarrhoeal, anti-inflammatory and antinociceptive activities of Canarium schweinfurthii Engl. (Burseraceae) bark in rats</title><author>Umeh, Nkiruka Edith ; Onuorah, Remigius Tochukwu ; Ekweogu, Celestine Nwabu ; Ijioma, Solomon Nnah ; Egeduzu, Ozioma Glory ; Nwaru, Ezeibe Chidi ; Iweala, Emeka Joshua ; Ugbogu, Eziuche Amadike</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c338t-d1a34eb63d84f5dc33a414a71a02f13dc0b78857eedff16f3f56139d21bc0a5c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>acetic acid</topic><topic>acute toxicity</topic><topic>Anti-inflammatory</topic><topic>antidiarrheal effect</topic><topic>bark</topic><topic>Bioactive compounds</topic><topic>Canarium schweinfurthii</topic><topic>Canarium schweinfurthii bark</topic><topic>carrageenan</topic><topic>charcoal</topic><topic>chemical constituents of plants</topic><topic>diabetes</topic><topic>diarrhea</topic><topic>egg albumen</topic><topic>fever</topic><topic>gas chromatography-mass spectrometry</topic><topic>histopathology</topic><topic>linalool</topic><topic>malaria</topic><topic>mortality</topic><topic>oral gavage</topic><topic>p-cymene</topic><topic>pain</topic><topic>subacute toxicity</topic><topic>tail</topic><topic>therapeutics</topic><topic>tissue weight</topic><topic>Toxicity profile</topic><topic>toxicity testing</topic><topic>traditional medicine</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Umeh, Nkiruka Edith</creatorcontrib><creatorcontrib>Onuorah, Remigius Tochukwu</creatorcontrib><creatorcontrib>Ekweogu, Celestine Nwabu</creatorcontrib><creatorcontrib>Ijioma, Solomon Nnah</creatorcontrib><creatorcontrib>Egeduzu, Ozioma Glory</creatorcontrib><creatorcontrib>Nwaru, Ezeibe Chidi</creatorcontrib><creatorcontrib>Iweala, Emeka Joshua</creatorcontrib><creatorcontrib>Ugbogu, Eziuche Amadike</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>AGRICOLA</collection><collection>AGRICOLA - Academic</collection><jtitle>Journal of ethnopharmacology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Umeh, Nkiruka Edith</au><au>Onuorah, Remigius Tochukwu</au><au>Ekweogu, Celestine Nwabu</au><au>Ijioma, Solomon Nnah</au><au>Egeduzu, Ozioma Glory</au><au>Nwaru, Ezeibe Chidi</au><au>Iweala, Emeka Joshua</au><au>Ugbogu, Eziuche Amadike</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Chemical profiling, toxicity assessment, anti-diarrhoeal, anti-inflammatory and antinociceptive activities of Canarium schweinfurthii Engl. (Burseraceae) bark in rats</atitle><jtitle>Journal of ethnopharmacology</jtitle><addtitle>J Ethnopharmacol</addtitle><date>2024-10-28</date><risdate>2024</risdate><volume>333</volume><spage>118460</spage><pages>118460-</pages><artnum>118460</artnum><issn>0378-8741</issn><issn>1872-7573</issn><eissn>1872-7573</eissn><abstract>The bark of Canarium schweinfurthii is used in ethnomedicine for the treatment of diabetes, pain, malaria, fever and diarrhoea.
The chemical phytoconstituents, antidiarrheal, anti-inflammatory and antinociceptive effects and safety profile of the aqueous extract of Canarium schweinfurthii bark (AECSB) were investigated.
Gas chromatography-mass spectrometry (GC-MS) was used to analyse the phytochemical composition. In the acute toxicity test, AECSB were administered up to 2 g/kg by oral gavage. For the subacute toxicity test (28 days), rats in group 1 (control) received no AECSB, while rats in groups 2–4 were administered different doses of AECSB. Charcoal meal transit and castor oil-induced diarrhoea models were used to study the antidiarrheal effect, while egg albumin/carrageenan and acetic acid/tail immersion models were used for the anti-inflammatory and antinociceptive studies, respectively. With the exception of the acute toxicity experiment, AECSB was administered orally at doses of 200, 400 and 800 mg/kg.
Bioactive phytoconstituents identified include p-cymene, δ-terpinene, linalool and phytol. No adverse effects or mortality were observed in acute and subacute studies. Treatment with AECSB (28 days) had no significant effect on organ weight, biochemical, hematologic and histopathologic parameters compared to the control groups (p > 0.05). Comparable antidiarrheal and antinociceptive effects were observed in both AECSB- and standard drug-treated groups, while the 400 and 800 mg/kg AECSB-treated groups showed remarkable anti-inflammatory effects compared to the standard drug-treated and control groups (p < 0.05).
AECSB has antidiarrheal, antinociceptive and anti-inflammatory effects and can be safely used for therapeutic purposes.
[Display omitted]
•Bark of Canarium schweinfurthii is traditionally used to treat diarrhoea, pain and inflammation.•Methanol ECSB contains biologically active compounds with various pharmacological effects.•AECSB caused no adverse effects on haematology and serum biochemistry.•AECSB has analgesic, anti-inflammatory and anti-diarrhoeal effects.</abstract><cop>Ireland</cop><pub>Elsevier B.V</pub><pmid>38878840</pmid><doi>10.1016/j.jep.2024.118460</doi><orcidid>https://orcid.org/0000-0003-3145-5473</orcidid><orcidid>https://orcid.org/0000-0002-1393-1416</orcidid></addata></record> |
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source | Elsevier ScienceDirect Journals |
subjects | acetic acid acute toxicity Anti-inflammatory antidiarrheal effect bark Bioactive compounds Canarium schweinfurthii Canarium schweinfurthii bark carrageenan charcoal chemical constituents of plants diabetes diarrhea egg albumen fever gas chromatography-mass spectrometry histopathology linalool malaria mortality oral gavage p-cymene pain subacute toxicity tail therapeutics tissue weight Toxicity profile toxicity testing traditional medicine |
title | Chemical profiling, toxicity assessment, anti-diarrhoeal, anti-inflammatory and antinociceptive activities of Canarium schweinfurthii Engl. (Burseraceae) bark in rats |
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