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...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Journal of ethnopharmacology 2012-09, Vol.143 (2), p.695-700
Hauptverfasser: Carpenter, Caitlyn D., O'Neill, Taryn, Picot, Nadia, Johnson, John A., Robichaud, Gilles A., Webster, Duncan, Gray, Christopher A.
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 700
container_issue 2
container_start_page 695
container_title Journal of ethnopharmacology
container_volume 143
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. [Display omitted]
doi_str_mv 10.1016/j.jep.2012.07.035
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_1125227325</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S0378874112005041</els_id><sourcerecordid>1039037323</sourcerecordid><originalsourceid>FETCH-LOGICAL-c410t-71e6f6c203ecc1658b4a76a1885783e535dc472354b308b6b55379fc351229f63</originalsourceid><addsrcrecordid>eNqFkU1P3DAQhi1UBAvlB_TS5thLgj_ijFc9oVX5EhIHisTNcpxJ69Um2doOEv-eWS3tEU6jkZ559eoZxr4IXgkumvN1tcZtJbmQFYeKK33AFsKALEGD-sQWXIEpDdTimJ2ktOacg6j5ETuW0gAspVmwp4sxh3J48VPrfMYY3KYYXZ4jzW2cutnnVPRxGor8B4uVG10X3FgM2AUfxh20cWMubucxbDHOqfDTMNCSPrPD3m0Snr3NU_Z4-fPX6rq8u7-6WV3clb4WPJcgsOkbL7lC70WjTVs7aJwwRoNRqJXufA1S6bpV3LRNq7WCZe-VFlIu-0adsu_7XGr7d8aU7RCSxw3VwmlOVgippQQl9ccoV0tSpqQiVOxRH6eUIvZ2G8Pg4gtBduferi25tzv3loMl93Tz9S1-bsnP_4t_sgn4tgd6N1n3O4ZkHx8ooabH1GAMEPFjTyAZew4YbfIBR0-2I_psuym8U-AVUeGczw</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1039037323</pqid></control><display><type>article</type><title>Anti-mycobacterial natural products from the Canadian medicinal plant Juniperus communis</title><source>MEDLINE</source><source>Elsevier ScienceDirect Journals</source><creator>Carpenter, Caitlyn D. ; O'Neill, Taryn ; Picot, Nadia ; Johnson, John A. ; Robichaud, Gilles A. ; Webster, Duncan ; Gray, Christopher A.</creator><creatorcontrib>Carpenter, Caitlyn D. ; O'Neill, Taryn ; Picot, Nadia ; Johnson, John A. ; Robichaud, Gilles A. ; Webster, Duncan ; Gray, Christopher A.</creatorcontrib><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><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 &amp; purification</subject><subject>Carboxylic Acids - pharmacology</subject><subject>Communic acid</subject><subject>Deoxypodophyllotoxin</subject><subject>Diterpenes - isolation &amp; 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 &amp; 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 &amp; derivatives</subject><subject>Podophyllotoxin - isolation &amp; purification</subject><subject>Podophyllotoxin - pharmacology</subject><subject>Tetrahydronaphthalenes - isolation &amp; 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 &amp; purification</topic><topic>Carboxylic Acids - pharmacology</topic><topic>Communic acid</topic><topic>Deoxypodophyllotoxin</topic><topic>Diterpenes - isolation &amp; 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 &amp; 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 &amp; derivatives</topic><topic>Podophyllotoxin - isolation &amp; purification</topic><topic>Podophyllotoxin - pharmacology</topic><topic>Tetrahydronaphthalenes - isolation &amp; 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>
fulltext fulltext
identifier ISSN: 0378-8741
ispartof Journal of ethnopharmacology, 2012-09, Vol.143 (2), p.695-700
issn 0378-8741
1872-7573
language eng
recordid cdi_proquest_miscellaneous_1125227325
source MEDLINE; Elsevier ScienceDirect Journals
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
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-07T20%3A13%3A14IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Anti-mycobacterial%20natural%20products%20from%20the%20Canadian%20medicinal%20plant%20Juniperus%20communis&rft.jtitle=Journal%20of%20ethnopharmacology&rft.au=Carpenter,%20Caitlyn%20D.&rft.date=2012-09-28&rft.volume=143&rft.issue=2&rft.spage=695&rft.epage=700&rft.pages=695-700&rft.issn=0378-8741&rft.eissn=1872-7573&rft_id=info:doi/10.1016/j.jep.2012.07.035&rft_dat=%3Cproquest_cross%3E1039037323%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=1039037323&rft_id=info:pmid/22877928&rft_els_id=S0378874112005041&rfr_iscdi=true