Anti-malarial activity of a polyherbal product (Nefang) during early and established Plasmodium infection in rodent models
Identifieur interne : 000911 ( Pmc/Checkpoint ); précédent : 000910; suivant : 000912Anti-malarial activity of a polyherbal product (Nefang) during early and established Plasmodium infection in rodent models
Auteurs : Protus Arrey Tarkang [Cameroun, Kenya] ; Faith A. Okalebo [Kenya] ; Lawrence S. Ayong [Cameroun] ; Gabriel A. Agbor [Cameroun] ; Anastasia N. Guantai [Kenya]Source :
- Malaria Journal [ 1475-2875 ] ; 2014.
Abstract
The emerging resistance of
Systemic acute oral toxicity of Nefang aqueous and ethanol extracts was assessed in mice up to a dose of 5,000 mgkg−1 body weight. BALB/c mice and Wistar rats were inoculated with
Acute oral toxicity of the extract did not cause any observed adverse effects. Percent suppressions of parasitaemia at 600 mgkg−1 bwt were as follows (
These results indicate that Nefang has excellent
The online version of this article (doi:10.1186/1475-2875-13-456) contains supplementary material, which is available to authorized users.
Url:
DOI: 10.1186/1475-2875-13-456
PubMed: 25421605
PubMed Central: 4251988
Affiliations:
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infection in rodent models</title>
<author><name sortKey="Arrey Tarkang, Protus" sort="Arrey Tarkang, Protus" uniqKey="Arrey Tarkang P" first="Protus" last="Arrey Tarkang">Protus Arrey Tarkang</name>
<affiliation wicri:level="1"><nlm:aff id="Aff6">Centre for Research on Medicinal Plants and Traditional Medicine, Institute of Medical Research and Medicinal Plants Studies (IMPM), P. O. Box 6163, Yaoundé, Cameroon</nlm:aff>
<country xml:lang="fr">Cameroun</country>
<wicri:regionArea>Centre for Research on Medicinal Plants and Traditional Medicine, Institute of Medical Research and Medicinal Plants Studies (IMPM), P. O. Box 6163, Yaoundé</wicri:regionArea>
<wicri:noRegion>Yaoundé</wicri:noRegion>
</affiliation>
<affiliation wicri:level="1"><nlm:aff id="Aff7">Department of Pharmacology and Pharmacognosy, University of Nairobi, P. O. Box 19676–00202, Nairobi, Kenya</nlm:aff>
<country xml:lang="fr">Kenya</country>
<wicri:regionArea>Department of Pharmacology and Pharmacognosy, University of Nairobi, P. O. Box 19676–00202, Nairobi</wicri:regionArea>
<wicri:noRegion>Nairobi</wicri:noRegion>
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<author><name sortKey="Okalebo, Faith A" sort="Okalebo, Faith A" uniqKey="Okalebo F" first="Faith A" last="Okalebo">Faith A. Okalebo</name>
<affiliation wicri:level="1"><nlm:aff id="Aff7">Department of Pharmacology and Pharmacognosy, University of Nairobi, P. O. Box 19676–00202, Nairobi, Kenya</nlm:aff>
<country xml:lang="fr">Kenya</country>
<wicri:regionArea>Department of Pharmacology and Pharmacognosy, University of Nairobi, P. O. Box 19676–00202, Nairobi</wicri:regionArea>
<wicri:noRegion>Nairobi</wicri:noRegion>
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</author>
<author><name sortKey="Ayong, Lawrence S" sort="Ayong, Lawrence S" uniqKey="Ayong L" first="Lawrence S" last="Ayong">Lawrence S. Ayong</name>
<affiliation><nlm:aff id="Aff8">Early Drug Discovery Programme, Institut Pasteur Korea, Sampyeong-dong 696, Bundang-gu, Seongnam-si, Gyeonggi-do South Korea</nlm:aff>
<wicri:noCountry code="subfield">Gyeonggi-do South Korea</wicri:noCountry>
</affiliation>
<affiliation wicri:level="1"><nlm:aff id="Aff9">Public Health and Epidemiology Unit, Centre Pasteur du Cameroun, P. O. Box 1274, Yaoundé, Cameroon</nlm:aff>
<country xml:lang="fr">Cameroun</country>
<wicri:regionArea>Public Health and Epidemiology Unit, Centre Pasteur du Cameroun, P. O. Box 1274, Yaoundé</wicri:regionArea>
<wicri:noRegion>Yaoundé</wicri:noRegion>
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<author><name sortKey="Agbor, Gabriel A" sort="Agbor, Gabriel A" uniqKey="Agbor G" first="Gabriel A" last="Agbor">Gabriel A. Agbor</name>
<affiliation wicri:level="1"><nlm:aff id="Aff6">Centre for Research on Medicinal Plants and Traditional Medicine, Institute of Medical Research and Medicinal Plants Studies (IMPM), P. O. Box 6163, Yaoundé, Cameroon</nlm:aff>
<country xml:lang="fr">Cameroun</country>
<wicri:regionArea>Centre for Research on Medicinal Plants and Traditional Medicine, Institute of Medical Research and Medicinal Plants Studies (IMPM), P. O. Box 6163, Yaoundé</wicri:regionArea>
<wicri:noRegion>Yaoundé</wicri:noRegion>
</affiliation>
</author>
<author><name sortKey="Guantai, Anastasia N" sort="Guantai, Anastasia N" uniqKey="Guantai A" first="Anastasia N" last="Guantai">Anastasia N. Guantai</name>
<affiliation wicri:level="1"><nlm:aff id="Aff7">Department of Pharmacology and Pharmacognosy, University of Nairobi, P. O. Box 19676–00202, Nairobi, Kenya</nlm:aff>
<country xml:lang="fr">Kenya</country>
<wicri:regionArea>Department of Pharmacology and Pharmacognosy, University of Nairobi, P. O. Box 19676–00202, Nairobi</wicri:regionArea>
<wicri:noRegion>Nairobi</wicri:noRegion>
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<idno type="doi">10.1186/1475-2875-13-456</idno>
<date when="2014">2014</date>
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<sourceDesc><biblStruct><analytic><title xml:lang="en" level="a" type="main">Anti-malarial activity of a polyherbal product (Nefang) during early and established <italic>Plasmodium</italic>
infection in rodent models</title>
<author><name sortKey="Arrey Tarkang, Protus" sort="Arrey Tarkang, Protus" uniqKey="Arrey Tarkang P" first="Protus" last="Arrey Tarkang">Protus Arrey Tarkang</name>
<affiliation wicri:level="1"><nlm:aff id="Aff6">Centre for Research on Medicinal Plants and Traditional Medicine, Institute of Medical Research and Medicinal Plants Studies (IMPM), P. O. Box 6163, Yaoundé, Cameroon</nlm:aff>
<country xml:lang="fr">Cameroun</country>
<wicri:regionArea>Centre for Research on Medicinal Plants and Traditional Medicine, Institute of Medical Research and Medicinal Plants Studies (IMPM), P. O. Box 6163, Yaoundé</wicri:regionArea>
<wicri:noRegion>Yaoundé</wicri:noRegion>
</affiliation>
<affiliation wicri:level="1"><nlm:aff id="Aff7">Department of Pharmacology and Pharmacognosy, University of Nairobi, P. O. Box 19676–00202, Nairobi, Kenya</nlm:aff>
<country xml:lang="fr">Kenya</country>
<wicri:regionArea>Department of Pharmacology and Pharmacognosy, University of Nairobi, P. O. Box 19676–00202, Nairobi</wicri:regionArea>
<wicri:noRegion>Nairobi</wicri:noRegion>
</affiliation>
</author>
<author><name sortKey="Okalebo, Faith A" sort="Okalebo, Faith A" uniqKey="Okalebo F" first="Faith A" last="Okalebo">Faith A. Okalebo</name>
<affiliation wicri:level="1"><nlm:aff id="Aff7">Department of Pharmacology and Pharmacognosy, University of Nairobi, P. O. Box 19676–00202, Nairobi, Kenya</nlm:aff>
<country xml:lang="fr">Kenya</country>
<wicri:regionArea>Department of Pharmacology and Pharmacognosy, University of Nairobi, P. O. Box 19676–00202, Nairobi</wicri:regionArea>
<wicri:noRegion>Nairobi</wicri:noRegion>
</affiliation>
</author>
<author><name sortKey="Ayong, Lawrence S" sort="Ayong, Lawrence S" uniqKey="Ayong L" first="Lawrence S" last="Ayong">Lawrence S. Ayong</name>
<affiliation><nlm:aff id="Aff8">Early Drug Discovery Programme, Institut Pasteur Korea, Sampyeong-dong 696, Bundang-gu, Seongnam-si, Gyeonggi-do South Korea</nlm:aff>
<wicri:noCountry code="subfield">Gyeonggi-do South Korea</wicri:noCountry>
</affiliation>
<affiliation wicri:level="1"><nlm:aff id="Aff9">Public Health and Epidemiology Unit, Centre Pasteur du Cameroun, P. O. Box 1274, Yaoundé, Cameroon</nlm:aff>
<country xml:lang="fr">Cameroun</country>
<wicri:regionArea>Public Health and Epidemiology Unit, Centre Pasteur du Cameroun, P. O. Box 1274, Yaoundé</wicri:regionArea>
<wicri:noRegion>Yaoundé</wicri:noRegion>
</affiliation>
</author>
<author><name sortKey="Agbor, Gabriel A" sort="Agbor, Gabriel A" uniqKey="Agbor G" first="Gabriel A" last="Agbor">Gabriel A. Agbor</name>
<affiliation wicri:level="1"><nlm:aff id="Aff6">Centre for Research on Medicinal Plants and Traditional Medicine, Institute of Medical Research and Medicinal Plants Studies (IMPM), P. O. Box 6163, Yaoundé, Cameroon</nlm:aff>
<country xml:lang="fr">Cameroun</country>
<wicri:regionArea>Centre for Research on Medicinal Plants and Traditional Medicine, Institute of Medical Research and Medicinal Plants Studies (IMPM), P. O. Box 6163, Yaoundé</wicri:regionArea>
<wicri:noRegion>Yaoundé</wicri:noRegion>
</affiliation>
</author>
<author><name sortKey="Guantai, Anastasia N" sort="Guantai, Anastasia N" uniqKey="Guantai A" first="Anastasia N" last="Guantai">Anastasia N. Guantai</name>
<affiliation wicri:level="1"><nlm:aff id="Aff7">Department of Pharmacology and Pharmacognosy, University of Nairobi, P. O. Box 19676–00202, Nairobi, Kenya</nlm:aff>
<country xml:lang="fr">Kenya</country>
<wicri:regionArea>Department of Pharmacology and Pharmacognosy, University of Nairobi, P. O. Box 19676–00202, Nairobi</wicri:regionArea>
<wicri:noRegion>Nairobi</wicri:noRegion>
</affiliation>
</author>
</analytic>
<series><title level="j">Malaria Journal</title>
<idno type="eISSN">1475-2875</idno>
<imprint><date when="2014">2014</date>
</imprint>
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<front><div type="abstract" xml:lang="en"><sec><title>Background</title>
<p>The emerging resistance of <italic>Plasmodium</italic>
species to currently available anti-malarials remains a public health concern, hence the need for new effective, safe and affordable drugs. Natural products remain a reliable source of drugs. <italic>Nefang</italic>
is a polyherbal anti-malarial of the Cameroonian folklore medicine with demonstrated <italic>in vitro</italic>
antiplasmodial and antioxidant activities. It is composed of <italic>Mangifera indica</italic>
(bark and leaf), <italic>Psidium guajava, Carica papaya, Cymbopogon citratus, Citrus sinensis, Ocimum gratissimum</italic>
(leaves). This study aimed at investigating the suppressive, prophylactic and curative activities of Nefang in <italic>Plasmodium</italic>
infected rodent models.</p>
</sec>
<sec><title>Methods</title>
<p>Systemic acute oral toxicity of Nefang aqueous and ethanol extracts was assessed in mice up to a dose of 5,000 mgkg<sup>−1</sup>
body weight. BALB/c mice and Wistar rats were inoculated with <italic>Plasmodium chabaudi chabaudi</italic>
and <italic>Plasmodium berghei,</italic>
respectively, and treated with Nefang, the <italic>Mangifera indica</italic>
bark/<italic>Psidium guajava</italic>
combination and a <italic>Psidium guajava</italic>
leaf aqueous extracts (75, 150, 300 and 600 mgkg<sup>−1</sup>
bwt). Their schizonticidal activity was then evaluated using the Peter’s 4-day suppressive test). The prophylactic and curative (Rane’s Test) activity of Nefang was also evaluated by determining the parasitaemia, survival time, body weight and temperature in pre-treated rodents.</p>
</sec>
<sec><title>Results</title>
<p>Acute oral toxicity of the extract did not cause any observed adverse effects. Percent suppressions of parasitaemia at 600 mgkg<sup>−1</sup>
bwt were as follows (<italic>P. berghei</italic>
/<italic>P. chabaudi</italic>
): Nefang – 82.9/86.3, <italic>Mangifera indica</italic>
bark/<italic>Psidium guajava</italic>
leaf combination extract – 79.5/81.2 and <italic>Psidium guajava</italic>
leaf – 58.9/67.4. Nefang exhibited a prophylactic activity of 79.5% and its chemotherapeutic effects ranged from 61.2 – 86.1% with maximum effect observed at the highest experimental dose.</p>
</sec>
<sec><title>Conclusion</title>
<p>These results indicate that Nefang has excellent <italic>in vivo</italic>
anti-malarial activities against <italic>P. berghei</italic>
and <italic>P. chabaudi</italic>
, upholding earlier <italic>in vitro</italic>
antiplasmodial activities against multi-drug resistant <italic>P. falciparum</italic>
parasites as well as its traditional use. Hence, Nefang represents a promising source of new anti-malarial agents.</p>
</sec>
<sec><title>Electronic supplementary material</title>
<p>The online version of this article (doi:10.1186/1475-2875-13-456) contains supplementary material, which is available to authorized users.</p>
</sec>
</div>
</front>
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</author>
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</listBibl>
</div1>
</back>
</TEI>
<pmc article-type="research-article"><pmc-dir>properties open_access</pmc-dir>
<front><journal-meta><journal-id journal-id-type="nlm-ta">Malar J</journal-id>
<journal-id journal-id-type="iso-abbrev">Malar. J</journal-id>
<journal-title-group><journal-title>Malaria Journal</journal-title>
</journal-title-group>
<issn pub-type="epub">1475-2875</issn>
<publisher><publisher-name>BioMed Central</publisher-name>
<publisher-loc>London</publisher-loc>
</publisher>
</journal-meta>
<article-meta><article-id pub-id-type="pmid">25421605</article-id>
<article-id pub-id-type="pmc">4251988</article-id>
<article-id pub-id-type="publisher-id">3607</article-id>
<article-id pub-id-type="doi">10.1186/1475-2875-13-456</article-id>
<article-categories><subj-group subj-group-type="heading"><subject>Research</subject>
</subj-group>
</article-categories>
<title-group><article-title>Anti-malarial activity of a polyherbal product (Nefang) during early and established <italic>Plasmodium</italic>
infection in rodent models</article-title>
</title-group>
<contrib-group><contrib contrib-type="author" corresp="yes"><name><surname>Arrey Tarkang</surname>
<given-names>Protus</given-names>
</name>
<address><email>ptarkang@yahoo.co.uk</email>
</address>
<xref ref-type="aff" rid="Aff6"></xref>
<xref ref-type="aff" rid="Aff7"></xref>
</contrib>
<contrib contrib-type="author"><name><surname>Okalebo</surname>
<given-names>Faith A</given-names>
</name>
<address><email>okalebof@yahoo.com</email>
</address>
<xref ref-type="aff" rid="Aff7"></xref>
</contrib>
<contrib contrib-type="author"><name><surname>Ayong</surname>
<given-names>Lawrence S</given-names>
</name>
<address><email>layong05@yahoo.co.uk</email>
</address>
<xref ref-type="aff" rid="Aff8"></xref>
<xref ref-type="aff" rid="Aff9"></xref>
</contrib>
<contrib contrib-type="author"><name><surname>Agbor</surname>
<given-names>Gabriel A</given-names>
</name>
<address><email>agogae@yahoo.fr</email>
</address>
<xref ref-type="aff" rid="Aff6"></xref>
</contrib>
<contrib contrib-type="author"><name><surname>Guantai</surname>
<given-names>Anastasia N</given-names>
</name>
<address><email>anguantai@yahoo.com</email>
</address>
<xref ref-type="aff" rid="Aff7"></xref>
</contrib>
<aff id="Aff6"><label></label>
Centre for Research on Medicinal Plants and Traditional Medicine, Institute of Medical Research and Medicinal Plants Studies (IMPM), P. O. Box 6163, Yaoundé, Cameroon</aff>
<aff id="Aff7"><label></label>
Department of Pharmacology and Pharmacognosy, University of Nairobi, P. O. Box 19676–00202, Nairobi, Kenya</aff>
<aff id="Aff8"><label></label>
Early Drug Discovery Programme, Institut Pasteur Korea, Sampyeong-dong 696, Bundang-gu, Seongnam-si, Gyeonggi-do South Korea</aff>
<aff id="Aff9"><label></label>
Public Health and Epidemiology Unit, Centre Pasteur du Cameroun, P. O. Box 1274, Yaoundé, Cameroon</aff>
</contrib-group>
<pub-date pub-type="epub"><day>25</day>
<month>11</month>
<year>2014</year>
</pub-date>
<pub-date pub-type="pmc-release"><day>25</day>
<month>11</month>
<year>2014</year>
</pub-date>
<pub-date pub-type="collection"><year>2014</year>
</pub-date>
<volume>13</volume>
<elocation-id>456</elocation-id>
<history><date date-type="received"><day>6</day>
<month>8</month>
<year>2014</year>
</date>
<date date-type="accepted"><day>15</day>
<month>11</month>
<year>2014</year>
</date>
</history>
<permissions><copyright-statement>© Arrey Tarkang et al.; licensee BioMed Central Ltd. 2014</copyright-statement>
<license license-type="open-access"><license-p>This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (<ext-link ext-link-type="uri" xlink:href="http://creativecommons.org/licenses/by/4.0">http://creativecommons.org/licenses/by/4.0</ext-link>
), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (<ext-link ext-link-type="uri" xlink:href="http://creativecommons.org/publicdomain/zero/1.0/">http://creativecommons.org/publicdomain/zero/1.0/</ext-link>
) applies to the data made available in this article, unless otherwise stated.</license-p>
</license>
</permissions>
<abstract id="Abs1"><sec><title>Background</title>
<p>The emerging resistance of <italic>Plasmodium</italic>
species to currently available anti-malarials remains a public health concern, hence the need for new effective, safe and affordable drugs. Natural products remain a reliable source of drugs. <italic>Nefang</italic>
is a polyherbal anti-malarial of the Cameroonian folklore medicine with demonstrated <italic>in vitro</italic>
antiplasmodial and antioxidant activities. It is composed of <italic>Mangifera indica</italic>
(bark and leaf), <italic>Psidium guajava, Carica papaya, Cymbopogon citratus, Citrus sinensis, Ocimum gratissimum</italic>
(leaves). This study aimed at investigating the suppressive, prophylactic and curative activities of Nefang in <italic>Plasmodium</italic>
infected rodent models.</p>
</sec>
<sec><title>Methods</title>
<p>Systemic acute oral toxicity of Nefang aqueous and ethanol extracts was assessed in mice up to a dose of 5,000 mgkg<sup>−1</sup>
body weight. BALB/c mice and Wistar rats were inoculated with <italic>Plasmodium chabaudi chabaudi</italic>
and <italic>Plasmodium berghei,</italic>
respectively, and treated with Nefang, the <italic>Mangifera indica</italic>
bark/<italic>Psidium guajava</italic>
combination and a <italic>Psidium guajava</italic>
leaf aqueous extracts (75, 150, 300 and 600 mgkg<sup>−1</sup>
bwt). Their schizonticidal activity was then evaluated using the Peter’s 4-day suppressive test). The prophylactic and curative (Rane’s Test) activity of Nefang was also evaluated by determining the parasitaemia, survival time, body weight and temperature in pre-treated rodents.</p>
</sec>
<sec><title>Results</title>
<p>Acute oral toxicity of the extract did not cause any observed adverse effects. Percent suppressions of parasitaemia at 600 mgkg<sup>−1</sup>
bwt were as follows (<italic>P. berghei</italic>
/<italic>P. chabaudi</italic>
): Nefang – 82.9/86.3, <italic>Mangifera indica</italic>
bark/<italic>Psidium guajava</italic>
leaf combination extract – 79.5/81.2 and <italic>Psidium guajava</italic>
leaf – 58.9/67.4. Nefang exhibited a prophylactic activity of 79.5% and its chemotherapeutic effects ranged from 61.2 – 86.1% with maximum effect observed at the highest experimental dose.</p>
</sec>
<sec><title>Conclusion</title>
<p>These results indicate that Nefang has excellent <italic>in vivo</italic>
anti-malarial activities against <italic>P. berghei</italic>
and <italic>P. chabaudi</italic>
, upholding earlier <italic>in vitro</italic>
antiplasmodial activities against multi-drug resistant <italic>P. falciparum</italic>
parasites as well as its traditional use. Hence, Nefang represents a promising source of new anti-malarial agents.</p>
</sec>
<sec><title>Electronic supplementary material</title>
<p>The online version of this article (doi:10.1186/1475-2875-13-456) contains supplementary material, which is available to authorized users.</p>
</sec>
</abstract>
<kwd-group xml:lang="en"><title>Keywords</title>
<kwd>Medicinal Plants</kwd>
<kwd>Nefang</kwd>
<kwd>Acute toxicity</kwd>
<kwd>Malaria</kwd>
<kwd>In vivo antiplasmodial activity</kwd>
<kwd>Suppressive activity</kwd>
<kwd>Prophylactic activity</kwd>
<kwd>Curative activity</kwd>
<kwd>Combination phytotherapy</kwd>
</kwd-group>
<custom-meta-group><custom-meta><meta-name>issue-copyright-statement</meta-name>
<meta-value>© The Author(s) 2014</meta-value>
</custom-meta>
</custom-meta-group>
</article-meta>
</front>
</pmc>
<affiliations><list><country><li>Cameroun</li>
<li>Kenya</li>
</country>
</list>
<tree><country name="Cameroun"><noRegion><name sortKey="Arrey Tarkang, Protus" sort="Arrey Tarkang, Protus" uniqKey="Arrey Tarkang P" first="Protus" last="Arrey Tarkang">Protus Arrey Tarkang</name>
</noRegion>
<name sortKey="Agbor, Gabriel A" sort="Agbor, Gabriel A" uniqKey="Agbor G" first="Gabriel A" last="Agbor">Gabriel A. Agbor</name>
<name sortKey="Ayong, Lawrence S" sort="Ayong, Lawrence S" uniqKey="Ayong L" first="Lawrence S" last="Ayong">Lawrence S. Ayong</name>
</country>
<country name="Kenya"><noRegion><name sortKey="Arrey Tarkang, Protus" sort="Arrey Tarkang, Protus" uniqKey="Arrey Tarkang P" first="Protus" last="Arrey Tarkang">Protus Arrey Tarkang</name>
</noRegion>
<name sortKey="Guantai, Anastasia N" sort="Guantai, Anastasia N" uniqKey="Guantai A" first="Anastasia N" last="Guantai">Anastasia N. Guantai</name>
<name sortKey="Okalebo, Faith A" sort="Okalebo, Faith A" uniqKey="Okalebo F" first="Faith A" last="Okalebo">Faith A. Okalebo</name>
</country>
</tree>
</affiliations>
</record>
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