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Pharmacological evidence for the folk use of Nefang: antipyretic, anti-inflammatory and antinociceptive activities of its constituent plants

Identifieur interne : 000506 ( Main/Exploration ); précédent : 000505; suivant : 000507

Pharmacological evidence for the folk use of Nefang: antipyretic, anti-inflammatory and antinociceptive activities of its constituent plants

Auteurs : Protus Arrey Tarkang [Cameroun, Kenya] ; Faith A. Okalebo [Kenya] ; Juma D. Siminyu [Kenya] ; William N. Ngugi [Kenya] ; Amos M. Mwaura [Kenya] ; Jackson Mugweru [Kenya] ; Gabriel A. Agbor [Cameroun] ; Anastasia N. Guantai [Kenya]

Source :

RBID : PMC:4459057

Descripteurs français

English descriptors

Abstract

Background

Nefang is a polyherbal anti-malarial composed of Mangifera indica (MiB and MiL; bark and leaf), Psidium guajava (Pg), Carica papaya (Cp), Cymbopogon citratus (Cc), Citrus sinensis (Cs) and Ocimum gratissimum (Og) (leaves). Previous studies have demonstrated its in vitro and in vivo antiplasmodial activities, antioxidant properties and safety profile. This study aimed at evaluating the antipyretic, anti-inflammatory and antinociceptive activities of the constituent plants of Nefang which are relevant to the symptomatic treatment of malaria fever.

Methods

Antipyretic activities were determined by the D-Amphetamine induced pyrexia and Brewer’s Yeast induced hyperpyrexia methods. Anti-inflammatory activities were investigated using the carrageenan-induced rat paw edema method. Antinociceptive activities were determined by mechanical nociception in the tail pressure and thermal nociception in the radiant heat tail flick and hot plate methods. Data was analysed using the one way ANOVA followed by Neuman-Keuls multiple comparison test.

Results

Best percentage inhibition of induced pyrexia (amphetamine/brewer’s yeast; p < 0.05) was exhibited by Cc (95/97) followed by Og (85/94), MiL (90/89), MiB (88/84) and Cs (82/89). Cc and Og exhibited comparable activities to paracetamol (100/95).

Anti-inflammatory studies revealed paw edema inhibition (%) as follows (p < 0.05): Indomethacin (47), MiL (40), Cp (30), MiB (28) and Og (22), suggesting best activity by MiL.

Antinociceptive studies revealed significant (p < 0.01) pain inhibition (%) as follows: Paracetamol (97), Og (113), MiL (108), Pg (84) and MiB (88). Og and MiL exhibited the best activities.

Conclusion

The results obtained suggest that the constituent plants possess biologically active compounds with antipyretic, anti-inflammatory and antinociceptive activities. These activities are essential in the symptomatic treatment of malaria fever, thereby justifying the folk use of Nefang. This would be useful in its subsequent development for clinical application.


Url:
DOI: 10.1186/s12906-015-0703-7
PubMed: 26055261
PubMed Central: 4459057


Affiliations:


Links toward previous steps (curation, corpus...)


Le document en format XML

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<wicri:regionArea>Department of Veterinary Anatomy and Physiology, Faculty of Veterinary Medicine, University of Nairobi, P. O. Box 30197-00100, Nairobi</wicri:regionArea>
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<name sortKey="Agbor, Gabriel A" sort="Agbor, Gabriel A" uniqKey="Agbor G" first="Gabriel A." last="Agbor">Gabriel A. Agbor</name>
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<name sortKey="Guantai, Anastasia N" sort="Guantai, Anastasia N" uniqKey="Guantai A" first="Anastasia N." last="Guantai">Anastasia N. Guantai</name>
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<name sortKey="Okalebo, Faith A" sort="Okalebo, Faith A" uniqKey="Okalebo F" first="Faith A." last="Okalebo">Faith A. Okalebo</name>
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<name sortKey="Siminyu, Juma D" sort="Siminyu, Juma D" uniqKey="Siminyu J" first="Juma D." last="Siminyu">Juma D. Siminyu</name>
<affiliation wicri:level="1">
<nlm:aff id="Aff2">Department of Pharmacology and Pharmacognosy, School of Pharmacy, University of Nairobi, P. O. Box 19676-00202, Nairobi, Kenya</nlm:aff>
<country xml:lang="fr">Kenya</country>
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<name sortKey="Ngugi, William N" sort="Ngugi, William N" uniqKey="Ngugi W" first="William N." last="Ngugi">William N. Ngugi</name>
<affiliation wicri:level="1">
<nlm:aff id="Aff2">Department of Pharmacology and Pharmacognosy, School of Pharmacy, 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, School of Pharmacy, University of Nairobi, P. O. Box 19676-00202, Nairobi</wicri:regionArea>
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<name sortKey="Mwaura, Amos M" sort="Mwaura, Amos M" uniqKey="Mwaura A" first="Amos M." last="Mwaura">Amos M. Mwaura</name>
<affiliation wicri:level="1">
<nlm:aff id="Aff2">Department of Pharmacology and Pharmacognosy, School of Pharmacy, 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, School of Pharmacy, University of Nairobi, P. O. Box 19676-00202, Nairobi</wicri:regionArea>
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</affiliation>
</author>
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<name sortKey="Mugweru, Jackson" sort="Mugweru, Jackson" uniqKey="Mugweru J" first="Jackson" last="Mugweru">Jackson Mugweru</name>
<affiliation wicri:level="1">
<nlm:aff id="Aff3">Department of Veterinary Anatomy and Physiology, Faculty of Veterinary Medicine, University of Nairobi, P. O. Box 30197-00100, Nairobi, Kenya</nlm:aff>
<country xml:lang="fr">Kenya</country>
<wicri:regionArea>Department of Veterinary Anatomy and Physiology, Faculty of Veterinary Medicine, University of Nairobi, P. O. Box 30197-00100, Nairobi</wicri:regionArea>
<wicri:noRegion>Nairobi</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="Aff1">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="Aff2">Department of Pharmacology and Pharmacognosy, School of Pharmacy, 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, School of Pharmacy, University of Nairobi, P. O. Box 19676-00202, Nairobi</wicri:regionArea>
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<title level="j">BMC Complementary and Alternative Medicine</title>
<idno type="eISSN">1472-6882</idno>
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<date when="2015">2015</date>
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<term>Analgesics (pharmacology)</term>
<term>Analgesics (therapeutic use)</term>
<term>Angiosperms</term>
<term>Animals</term>
<term>Anti-Inflammatory Agents (pharmacology)</term>
<term>Anti-Inflammatory Agents (therapeutic use)</term>
<term>Antimalarials (pharmacology)</term>
<term>Antimalarials (therapeutic use)</term>
<term>Antipyretics (pharmacology)</term>
<term>Antipyretics (therapeutic use)</term>
<term>Cameroon</term>
<term>Carrageenan</term>
<term>Drug Combinations</term>
<term>Edema (drug therapy)</term>
<term>Fever (drug therapy)</term>
<term>Inflammation (drug therapy)</term>
<term>Malaria (complications)</term>
<term>Malaria (drug therapy)</term>
<term>Mice</term>
<term>Pain (drug therapy)</term>
<term>Pain Measurement</term>
<term>Phytotherapy</term>
<term>Plant Bark</term>
<term>Plant Extracts (pharmacology)</term>
<term>Plant Extracts (therapeutic use)</term>
<term>Plant Leaves (drug effects)</term>
<term>Rats, Wistar</term>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="pharmacology" xml:lang="en">
<term>Analgesics</term>
<term>Anti-Inflammatory Agents</term>
<term>Antimalarials</term>
<term>Antipyretics</term>
<term>Plant Extracts</term>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="therapeutic use" xml:lang="en">
<term>Analgesics</term>
<term>Anti-Inflammatory Agents</term>
<term>Antimalarials</term>
<term>Antipyretics</term>
<term>Plant Extracts</term>
</keywords>
<keywords scheme="MESH" type="geographic" xml:lang="en">
<term>Cameroon</term>
<term>Carrageenan</term>
<term>Drug Combinations</term>
</keywords>
<keywords scheme="MESH" qualifier="complications" xml:lang="en">
<term>Malaria</term>
</keywords>
<keywords scheme="MESH" qualifier="drug effects" xml:lang="en">
<term>Plant Leaves</term>
</keywords>
<keywords scheme="MESH" qualifier="drug therapy" xml:lang="en">
<term>Edema</term>
<term>Fever</term>
<term>Inflammation</term>
<term>Malaria</term>
<term>Pain</term>
</keywords>
<keywords scheme="MESH" xml:lang="en">
<term>Angiosperms</term>
<term>Animals</term>
<term>Mice</term>
<term>Pain Measurement</term>
<term>Phytotherapy</term>
<term>Plant Bark</term>
<term>Rats, Wistar</term>
</keywords>
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<term>Cameroun</term>
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<front>
<div type="abstract" xml:lang="en">
<sec>
<title>Background</title>
<p>
<italic>Nefang</italic>
is a polyherbal anti-malarial composed of
<italic>Mangifera indica (</italic>
<bold>
<italic>MiB</italic>
</bold>
and
<bold>
<italic>MiL</italic>
</bold>
; bark and leaf),
<italic>Psidium guajava (</italic>
<bold>
<italic>Pg</italic>
</bold>
<italic>), Carica papaya (</italic>
<bold>
<italic>Cp</italic>
</bold>
<italic>), Cymbopogon citratus (</italic>
<bold>
<italic>Cc</italic>
</bold>
<italic>), Citrus sinensis (</italic>
<bold>
<italic>Cs</italic>
</bold>
<italic>)</italic>
and
<italic>Ocimum gratissimum (</italic>
<bold>
<italic>Og</italic>
</bold>
<italic>)</italic>
(leaves). Previous studies have demonstrated its in vitro and in vivo antiplasmodial activities, antioxidant properties and safety profile. This study aimed at evaluating the antipyretic, anti-inflammatory and antinociceptive activities of the constituent plants of
<italic>Nefang</italic>
which are relevant to the symptomatic treatment of malaria fever.</p>
</sec>
<sec>
<title>Methods</title>
<p>Antipyretic activities were determined by the D-Amphetamine induced pyrexia and Brewer’s Yeast induced hyperpyrexia methods. Anti-inflammatory activities were investigated using the carrageenan-induced rat paw edema method. Antinociceptive activities were determined by mechanical nociception in the tail pressure and thermal nociception in the radiant heat tail flick and hot plate methods. Data was analysed using the one way ANOVA followed by Neuman-Keuls multiple comparison test.</p>
</sec>
<sec>
<title>Results</title>
<p>Best percentage inhibition of induced pyrexia (amphetamine/brewer’s yeast;
<italic>p</italic>
 < 0.05) was exhibited by
<italic>Cc</italic>
(95/97) followed by
<italic>Og</italic>
(85/94),
<italic>MiL</italic>
(90/89),
<italic>MiB</italic>
(88/84) and
<italic>Cs</italic>
(82/89).
<italic>Cc</italic>
and
<italic>Og</italic>
exhibited comparable activities to paracetamol (100/95).</p>
<p>Anti-inflammatory studies revealed paw edema inhibition (%) as follows (
<italic>p</italic>
 < 0.05): Indomethacin (47),
<italic>MiL</italic>
(40),
<italic>Cp</italic>
(30),
<italic>MiB</italic>
(28) and
<italic>Og</italic>
(22), suggesting best activity by
<italic>MiL.</italic>
</p>
<p>Antinociceptive studies revealed significant (
<italic>p</italic>
 < 0.01) pain inhibition (%) as follows: Paracetamol (97),
<italic>Og</italic>
(113),
<italic>MiL</italic>
(108),
<italic>Pg</italic>
(84) and
<italic>MiB</italic>
(88).
<italic>Og</italic>
and
<italic>MiL</italic>
exhibited the best activities.</p>
</sec>
<sec>
<title>Conclusion</title>
<p>The results obtained suggest that the constituent plants possess biologically active compounds with antipyretic, anti-inflammatory and antinociceptive activities. These activities are essential in the symptomatic treatment of malaria fever, thereby justifying the folk use of
<italic>Nefang</italic>
. This would be useful in its subsequent development for clinical application.</p>
</sec>
</div>
</front>
<back>
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