Anti-mycobacterial natural products from the Canadian medicinal plant Juniperus communis
Common juniper, Juniperus communis, is amongst the plants most frequently used by the indigenous peoples of North America for medicinal purposes. The First Nations of the Canadian Maritimes use infusions of juniper primarily as a tonic and for the treatment of tuberculosis. Previous investigations o...
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Veröffentlicht in: | Journal of ethnopharmacology 2012-09, Vol.143 (2), p.695-700 |
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creator | Carpenter, Caitlyn D. O'Neill, Taryn Picot, Nadia Johnson, John A. Robichaud, Gilles A. Webster, Duncan Gray, Christopher A. |
description | Common juniper, Juniperus communis, is amongst the plants most frequently used by the indigenous peoples of North America for medicinal purposes. The First Nations of the Canadian Maritimes use infusions of juniper primarily as a tonic and for the treatment of tuberculosis. Previous investigations of extracts derived from the aerial parts of J. communis have shown it to possess anti-mycobacterial activity. The aim of the study is to isolate and identify anti-mycobacterial constituents from the aerial parts of J. communis.
Methanolic extracts of J. communis needles and branches were subjected to bioassay guided fractionation using the microplate resazurin assay (MRA) to assess inhibitory activity against Mycobacterium tuberculosis strain H37Ra. The anti-mycobacterial constituents were identified by NMR, MS and polarimetry.
The diterpenes isocupressic acid and communic acid and the aryltetralin lignan deoxypodophyllotoxin were isolated from the J. communis extract. Isocupressic acid and communic acid (isolated as an inseparable 3:2 mixture of cis and trans isomers) displayed MICs of 78μM and 31μM and IC50s of 46μM and 15μM against M. tuberculosis H37Ra respectively. Deoxypodophyllotoxin was less active, with a MIC of 1004μM and an IC50 of 287μM.
Isocupressic acid, communic acid and deoxypodophyllotoxin were identified as the principal constituents responsible for the anti-mycobacterial activity of the aerial parts of J. communis. Although further research will be required to evaluate the relative activities of the two communic acid isomers, this work validates an ethnopharmacological use of this plant by Canadian First Nations and Native American communities.
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doi_str_mv | 10.1016/j.jep.2012.07.035 |
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Methanolic extracts of J. communis needles and branches were subjected to bioassay guided fractionation using the microplate resazurin assay (MRA) to assess inhibitory activity against Mycobacterium tuberculosis strain H37Ra. The anti-mycobacterial constituents were identified by NMR, MS and polarimetry.
The diterpenes isocupressic acid and communic acid and the aryltetralin lignan deoxypodophyllotoxin were isolated from the J. communis extract. Isocupressic acid and communic acid (isolated as an inseparable 3:2 mixture of cis and trans isomers) displayed MICs of 78μM and 31μM and IC50s of 46μM and 15μM against M. tuberculosis H37Ra respectively. Deoxypodophyllotoxin was less active, with a MIC of 1004μM and an IC50 of 287μM.
Isocupressic acid, communic acid and deoxypodophyllotoxin were identified as the principal constituents responsible for the anti-mycobacterial activity of the aerial parts of J. communis. Although further research will be required to evaluate the relative activities of the two communic acid isomers, this work validates an ethnopharmacological use of this plant by Canadian First Nations and Native American communities.
[Display omitted]</description><identifier>ISSN: 0378-8741</identifier><identifier>EISSN: 1872-7573</identifier><identifier>DOI: 10.1016/j.jep.2012.07.035</identifier><identifier>PMID: 22877928</identifier><language>eng</language><publisher>Ireland: Elsevier Ireland Ltd</publisher><subject><![CDATA[aerial parts ; Anti-Bacterial Agents - chemistry ; Anti-Bacterial Agents - pharmacology ; Anti-mycobacterial ; bioassays ; Biological Products - chemistry ; Biological Products - pharmacology ; branches ; Canada ; Carboxylic Acids - isolation & purification ; Carboxylic Acids - pharmacology ; Communic acid ; Deoxypodophyllotoxin ; Diterpenes - isolation & purification ; Diterpenes - pharmacology ; First Nations ; fractionation ; HEK293 Cells ; Humans ; inhibitory concentration 50 ; Isocupressic acid ; isomers ; Juniperus ; Juniperus communis ; medicinal plants ; Medicine, Traditional ; Microbial Sensitivity Tests ; Mycobacterium tuberculosis ; Mycobacterium tuberculosis - drug effects ; Mycobacterium tuberculosis - growth & development ; nuclear magnetic resonance spectroscopy ; Plant Components, Aerial ; Plant Extracts - chemistry ; Plant Extracts - pharmacology ; Plants, Medicinal ; Podophyllotoxin - analogs & derivatives ; Podophyllotoxin - isolation & purification ; Podophyllotoxin - pharmacology ; Tetrahydronaphthalenes - isolation & purification ; Tetrahydronaphthalenes - pharmacology ; tuberculosis]]></subject><ispartof>Journal of ethnopharmacology, 2012-09, Vol.143 (2), p.695-700</ispartof><rights>2012 Elsevier Ireland Ltd</rights><rights>Copyright © 2012 Elsevier Ireland Ltd. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c410t-71e6f6c203ecc1658b4a76a1885783e535dc472354b308b6b55379fc351229f63</citedby><cites>FETCH-LOGICAL-c410t-71e6f6c203ecc1658b4a76a1885783e535dc472354b308b6b55379fc351229f63</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0378874112005041$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/22877928$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Carpenter, Caitlyn D.</creatorcontrib><creatorcontrib>O'Neill, Taryn</creatorcontrib><creatorcontrib>Picot, Nadia</creatorcontrib><creatorcontrib>Johnson, John A.</creatorcontrib><creatorcontrib>Robichaud, Gilles A.</creatorcontrib><creatorcontrib>Webster, Duncan</creatorcontrib><creatorcontrib>Gray, Christopher A.</creatorcontrib><title>Anti-mycobacterial natural products from the Canadian medicinal plant Juniperus communis</title><title>Journal of ethnopharmacology</title><addtitle>J Ethnopharmacol</addtitle><description>Common juniper, Juniperus communis, is amongst the plants most frequently used by the indigenous peoples of North America for medicinal purposes. The First Nations of the Canadian Maritimes use infusions of juniper primarily as a tonic and for the treatment of tuberculosis. Previous investigations of extracts derived from the aerial parts of J. communis have shown it to possess anti-mycobacterial activity. The aim of the study is to isolate and identify anti-mycobacterial constituents from the aerial parts of J. communis.
Methanolic extracts of J. communis needles and branches were subjected to bioassay guided fractionation using the microplate resazurin assay (MRA) to assess inhibitory activity against Mycobacterium tuberculosis strain H37Ra. The anti-mycobacterial constituents were identified by NMR, MS and polarimetry.
The diterpenes isocupressic acid and communic acid and the aryltetralin lignan deoxypodophyllotoxin were isolated from the J. communis extract. Isocupressic acid and communic acid (isolated as an inseparable 3:2 mixture of cis and trans isomers) displayed MICs of 78μM and 31μM and IC50s of 46μM and 15μM against M. tuberculosis H37Ra respectively. Deoxypodophyllotoxin was less active, with a MIC of 1004μM and an IC50 of 287μM.
Isocupressic acid, communic acid and deoxypodophyllotoxin were identified as the principal constituents responsible for the anti-mycobacterial activity of the aerial parts of J. communis. Although further research will be required to evaluate the relative activities of the two communic acid isomers, this work validates an ethnopharmacological use of this plant by Canadian First Nations and Native American communities.
[Display omitted]</description><subject>aerial parts</subject><subject>Anti-Bacterial Agents - chemistry</subject><subject>Anti-Bacterial Agents - pharmacology</subject><subject>Anti-mycobacterial</subject><subject>bioassays</subject><subject>Biological Products - chemistry</subject><subject>Biological Products - pharmacology</subject><subject>branches</subject><subject>Canada</subject><subject>Carboxylic Acids - isolation & purification</subject><subject>Carboxylic Acids - pharmacology</subject><subject>Communic acid</subject><subject>Deoxypodophyllotoxin</subject><subject>Diterpenes - isolation & purification</subject><subject>Diterpenes - pharmacology</subject><subject>First Nations</subject><subject>fractionation</subject><subject>HEK293 Cells</subject><subject>Humans</subject><subject>inhibitory concentration 50</subject><subject>Isocupressic acid</subject><subject>isomers</subject><subject>Juniperus</subject><subject>Juniperus communis</subject><subject>medicinal plants</subject><subject>Medicine, Traditional</subject><subject>Microbial Sensitivity Tests</subject><subject>Mycobacterium tuberculosis</subject><subject>Mycobacterium tuberculosis - drug effects</subject><subject>Mycobacterium tuberculosis - growth & development</subject><subject>nuclear magnetic resonance spectroscopy</subject><subject>Plant Components, Aerial</subject><subject>Plant Extracts - chemistry</subject><subject>Plant Extracts - pharmacology</subject><subject>Plants, Medicinal</subject><subject>Podophyllotoxin - analogs & derivatives</subject><subject>Podophyllotoxin - isolation & purification</subject><subject>Podophyllotoxin - pharmacology</subject><subject>Tetrahydronaphthalenes - isolation & purification</subject><subject>Tetrahydronaphthalenes - pharmacology</subject><subject>tuberculosis</subject><issn>0378-8741</issn><issn>1872-7573</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkU1P3DAQhi1UBAvlB_TS5thLgj_ijFc9oVX5EhIHisTNcpxJ69Um2doOEv-eWS3tEU6jkZ559eoZxr4IXgkumvN1tcZtJbmQFYeKK33AFsKALEGD-sQWXIEpDdTimJ2ktOacg6j5ETuW0gAspVmwp4sxh3J48VPrfMYY3KYYXZ4jzW2cutnnVPRxGor8B4uVG10X3FgM2AUfxh20cWMubucxbDHOqfDTMNCSPrPD3m0Snr3NU_Z4-fPX6rq8u7-6WV3clb4WPJcgsOkbL7lC70WjTVs7aJwwRoNRqJXufA1S6bpV3LRNq7WCZe-VFlIu-0adsu_7XGr7d8aU7RCSxw3VwmlOVgippQQl9ccoV0tSpqQiVOxRH6eUIvZ2G8Pg4gtBduferi25tzv3loMl93Tz9S1-bsnP_4t_sgn4tgd6N1n3O4ZkHx8ooabH1GAMEPFjTyAZew4YbfIBR0-2I_psuym8U-AVUeGczw</recordid><startdate>20120928</startdate><enddate>20120928</enddate><creator>Carpenter, Caitlyn D.</creator><creator>O'Neill, Taryn</creator><creator>Picot, Nadia</creator><creator>Johnson, John A.</creator><creator>Robichaud, Gilles A.</creator><creator>Webster, Duncan</creator><creator>Gray, Christopher A.</creator><general>Elsevier Ireland Ltd</general><scope>FBQ</scope><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>7X8</scope><scope>7QL</scope><scope>C1K</scope></search><sort><creationdate>20120928</creationdate><title>Anti-mycobacterial natural products from the Canadian medicinal plant Juniperus communis</title><author>Carpenter, Caitlyn D. ; O'Neill, Taryn ; Picot, Nadia ; Johnson, John A. ; Robichaud, Gilles A. ; Webster, Duncan ; Gray, Christopher A.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c410t-71e6f6c203ecc1658b4a76a1885783e535dc472354b308b6b55379fc351229f63</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2012</creationdate><topic>aerial parts</topic><topic>Anti-Bacterial Agents - chemistry</topic><topic>Anti-Bacterial Agents - pharmacology</topic><topic>Anti-mycobacterial</topic><topic>bioassays</topic><topic>Biological Products - chemistry</topic><topic>Biological Products - pharmacology</topic><topic>branches</topic><topic>Canada</topic><topic>Carboxylic Acids - isolation & purification</topic><topic>Carboxylic Acids - pharmacology</topic><topic>Communic acid</topic><topic>Deoxypodophyllotoxin</topic><topic>Diterpenes - isolation & purification</topic><topic>Diterpenes - pharmacology</topic><topic>First Nations</topic><topic>fractionation</topic><topic>HEK293 Cells</topic><topic>Humans</topic><topic>inhibitory concentration 50</topic><topic>Isocupressic acid</topic><topic>isomers</topic><topic>Juniperus</topic><topic>Juniperus communis</topic><topic>medicinal plants</topic><topic>Medicine, Traditional</topic><topic>Microbial Sensitivity Tests</topic><topic>Mycobacterium tuberculosis</topic><topic>Mycobacterium tuberculosis - drug effects</topic><topic>Mycobacterium tuberculosis - growth & development</topic><topic>nuclear magnetic resonance spectroscopy</topic><topic>Plant Components, Aerial</topic><topic>Plant Extracts - chemistry</topic><topic>Plant Extracts - pharmacology</topic><topic>Plants, Medicinal</topic><topic>Podophyllotoxin - analogs & derivatives</topic><topic>Podophyllotoxin - isolation & purification</topic><topic>Podophyllotoxin - pharmacology</topic><topic>Tetrahydronaphthalenes - isolation & purification</topic><topic>Tetrahydronaphthalenes - pharmacology</topic><topic>tuberculosis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Carpenter, Caitlyn D.</creatorcontrib><creatorcontrib>O'Neill, Taryn</creatorcontrib><creatorcontrib>Picot, Nadia</creatorcontrib><creatorcontrib>Johnson, John A.</creatorcontrib><creatorcontrib>Robichaud, Gilles A.</creatorcontrib><creatorcontrib>Webster, Duncan</creatorcontrib><creatorcontrib>Gray, Christopher A.</creatorcontrib><collection>AGRIS</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Environmental Sciences and Pollution Management</collection><jtitle>Journal of ethnopharmacology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Carpenter, Caitlyn D.</au><au>O'Neill, Taryn</au><au>Picot, Nadia</au><au>Johnson, John A.</au><au>Robichaud, Gilles A.</au><au>Webster, Duncan</au><au>Gray, Christopher A.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Anti-mycobacterial natural products from the Canadian medicinal plant Juniperus communis</atitle><jtitle>Journal of ethnopharmacology</jtitle><addtitle>J Ethnopharmacol</addtitle><date>2012-09-28</date><risdate>2012</risdate><volume>143</volume><issue>2</issue><spage>695</spage><epage>700</epage><pages>695-700</pages><issn>0378-8741</issn><eissn>1872-7573</eissn><abstract>Common juniper, Juniperus communis, is amongst the plants most frequently used by the indigenous peoples of North America for medicinal purposes. The First Nations of the Canadian Maritimes use infusions of juniper primarily as a tonic and for the treatment of tuberculosis. Previous investigations of extracts derived from the aerial parts of J. communis have shown it to possess anti-mycobacterial activity. The aim of the study is to isolate and identify anti-mycobacterial constituents from the aerial parts of J. communis.
Methanolic extracts of J. communis needles and branches were subjected to bioassay guided fractionation using the microplate resazurin assay (MRA) to assess inhibitory activity against Mycobacterium tuberculosis strain H37Ra. The anti-mycobacterial constituents were identified by NMR, MS and polarimetry.
The diterpenes isocupressic acid and communic acid and the aryltetralin lignan deoxypodophyllotoxin were isolated from the J. communis extract. Isocupressic acid and communic acid (isolated as an inseparable 3:2 mixture of cis and trans isomers) displayed MICs of 78μM and 31μM and IC50s of 46μM and 15μM against M. tuberculosis H37Ra respectively. Deoxypodophyllotoxin was less active, with a MIC of 1004μM and an IC50 of 287μM.
Isocupressic acid, communic acid and deoxypodophyllotoxin were identified as the principal constituents responsible for the anti-mycobacterial activity of the aerial parts of J. communis. Although further research will be required to evaluate the relative activities of the two communic acid isomers, this work validates an ethnopharmacological use of this plant by Canadian First Nations and Native American communities.
[Display omitted]</abstract><cop>Ireland</cop><pub>Elsevier Ireland Ltd</pub><pmid>22877928</pmid><doi>10.1016/j.jep.2012.07.035</doi><tpages>6</tpages></addata></record> |
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subjects | aerial parts Anti-Bacterial Agents - chemistry Anti-Bacterial Agents - pharmacology Anti-mycobacterial bioassays Biological Products - chemistry Biological Products - pharmacology branches Canada Carboxylic Acids - isolation & purification Carboxylic Acids - pharmacology Communic acid Deoxypodophyllotoxin Diterpenes - isolation & purification Diterpenes - pharmacology First Nations fractionation HEK293 Cells Humans inhibitory concentration 50 Isocupressic acid isomers Juniperus Juniperus communis medicinal plants Medicine, Traditional Microbial Sensitivity Tests Mycobacterium tuberculosis Mycobacterium tuberculosis - drug effects Mycobacterium tuberculosis - growth & development nuclear magnetic resonance spectroscopy Plant Components, Aerial Plant Extracts - chemistry Plant Extracts - pharmacology Plants, Medicinal Podophyllotoxin - analogs & derivatives Podophyllotoxin - isolation & purification Podophyllotoxin - pharmacology Tetrahydronaphthalenes - isolation & purification Tetrahydronaphthalenes - pharmacology tuberculosis |
title | Anti-mycobacterial natural products from the Canadian medicinal plant Juniperus communis |
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