Antinociceptive effects of the essential oil of Alpinia zerumbet on mice

Alpinia zerumbet (Pers.) Burtt. et Smith is an aromatic plant that is distributed widely in the tropical and sub-tropical regions of the world. In Brazil, where A. zerumbet is called “colonia”, it is used widely in folk medicine for the treatment of various diseases, including hypertension. In the p...

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Veröffentlicht in:Phytomedicine (Stuttgart) 2005-06, Vol.12 (6), p.482-486
Hauptverfasser: de Araújo Pinho, F.V.S., Coelho-de-Souza, A.N., Morais, S.M., Ferreira Santos, C., Leal-Cardoso, J.H.
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container_issue 6
container_start_page 482
container_title Phytomedicine (Stuttgart)
container_volume 12
creator de Araújo Pinho, F.V.S.
Coelho-de-Souza, A.N.
Morais, S.M.
Ferreira Santos, C.
Leal-Cardoso, J.H.
description Alpinia zerumbet (Pers.) Burtt. et Smith is an aromatic plant that is distributed widely in the tropical and sub-tropical regions of the world. In Brazil, where A. zerumbet is called “colonia”, it is used widely in folk medicine for the treatment of various diseases, including hypertension. In the present study, the antinociceptive effects of the orally administered essential oil of A. zerumbet (EOAz) were evaluated in male Swiss mice (20–25 g each). In the acetic acid-induced writhing test, EOAz (30, 100 and 300 mg/kg body wt.; n = 10 , n = 13 and n = 15 , respectively) was effective at all doses. In the hot-plate test, EOAz significantly increased the latency at doses of 100 and 300 mg/kg body wt., but not at 30 mg/kg body wt., at all observation times up to the 180th min ( n = 10 for each dose). In the formalin test, EOAz significantly reduced paw licking time in the second phase of the test at 100 mg/kg body wt. ( n = 10 ), but decreased it in both phases at 300 mg/kg body wt. ( n = 10 ). At 30 mg/kg body wt., the effect of EOAz did not differ from control values in either phase of the formalin test ( n = 10 ). Pretreatment with naloxone (5 mg/kg body wt., i.p.) caused a significant reversal of the analgesic effect of 300 mg/kg body wt. EOAz ( n = 8 ) that was complete for the first phase, but only partial for the second phase of the formalin test. The data show that orally administered OEAz promotes a dose-dependent antinociceptive effect, with a mechanism of action which probably involves the participation of opiate receptors.
doi_str_mv 10.1016/j.phymed.2004.04.006
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Burtt. et Smith is an aromatic plant that is distributed widely in the tropical and sub-tropical regions of the world. In Brazil, where A. zerumbet is called “colonia”, it is used widely in folk medicine for the treatment of various diseases, including hypertension. In the present study, the antinociceptive effects of the orally administered essential oil of A. zerumbet (EOAz) were evaluated in male Swiss mice (20–25 g each). In the acetic acid-induced writhing test, EOAz (30, 100 and 300 mg/kg body wt.; n = 10 , n = 13 and n = 15 , respectively) was effective at all doses. In the hot-plate test, EOAz significantly increased the latency at doses of 100 and 300 mg/kg body wt., but not at 30 mg/kg body wt., at all observation times up to the 180th min ( n = 10 for each dose). In the formalin test, EOAz significantly reduced paw licking time in the second phase of the test at 100 mg/kg body wt. ( n = 10 ), but decreased it in both phases at 300 mg/kg body wt. ( n = 10 ). At 30 mg/kg body wt., the effect of EOAz did not differ from control values in either phase of the formalin test ( n = 10 ). Pretreatment with naloxone (5 mg/kg body wt., i.p.) caused a significant reversal of the analgesic effect of 300 mg/kg body wt. EOAz ( n = 8 ) that was complete for the first phase, but only partial for the second phase of the formalin test. 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Burtt. et Smith is an aromatic plant that is distributed widely in the tropical and sub-tropical regions of the world. In Brazil, where A. zerumbet is called “colonia”, it is used widely in folk medicine for the treatment of various diseases, including hypertension. In the present study, the antinociceptive effects of the orally administered essential oil of A. zerumbet (EOAz) were evaluated in male Swiss mice (20–25 g each). In the acetic acid-induced writhing test, EOAz (30, 100 and 300 mg/kg body wt.; n = 10 , n = 13 and n = 15 , respectively) was effective at all doses. In the hot-plate test, EOAz significantly increased the latency at doses of 100 and 300 mg/kg body wt., but not at 30 mg/kg body wt., at all observation times up to the 180th min ( n = 10 for each dose). In the formalin test, EOAz significantly reduced paw licking time in the second phase of the test at 100 mg/kg body wt. ( n = 10 ), but decreased it in both phases at 300 mg/kg body wt. ( n = 10 ). At 30 mg/kg body wt., the effect of EOAz did not differ from control values in either phase of the formalin test ( n = 10 ). Pretreatment with naloxone (5 mg/kg body wt., i.p.) caused a significant reversal of the analgesic effect of 300 mg/kg body wt. EOAz ( n = 8 ) that was complete for the first phase, but only partial for the second phase of the formalin test. The data show that orally administered OEAz promotes a dose-dependent antinociceptive effect, with a mechanism of action which probably involves the participation of opiate receptors.</description><subject>Acetic Acid</subject><subject>Administration, Oral</subject><subject>Alpinia zerumbet</subject><subject>analgesic effect</subject><subject>Analgesics - administration &amp; dosage</subject><subject>Analgesics - pharmacology</subject><subject>Analgesics - therapeutic use</subject><subject>Analgesics, Opioid - administration &amp; dosage</subject><subject>Analgesics, Opioid - pharmacology</subject><subject>Analgesics, Opioid - therapeutic use</subject><subject>Animals</subject><subject>Antinociceptive effects</subject><subject>Dose-Response Relationship, Drug</subject><subject>Essences and essential oils</subject><subject>Essential oil</subject><subject>essential oils</subject><subject>Formaldehyde</subject><subject>Health aspects</subject><subject>Hot Temperature</subject><subject>In vivo</subject><subject>Male</subject><subject>Medicinal plants</subject><subject>medicinal properties</subject><subject>Mice</subject><subject>oral administration</subject><subject>Pain - chemically induced</subject><subject>Pain - prevention &amp; control</subject><subject>Pain Measurement - drug effects</subject><subject>Phytotherapy</subject><subject>Plant Leaves</subject><subject>Plant Oils - administration &amp; dosage</subject><subject>Plant Oils - pharmacology</subject><subject>Plant Oils - therapeutic use</subject><subject>Zingiberales</subject><issn>0944-7113</issn><issn>1618-095X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2005</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kVFL3TAUx8NQ5p3bNxhbwefWkyZNmxfhIm4OBB9U8C2k6ck1l7YpSRX00y-lMhhc5BwIOfn9DznnT8h3CgUFKs73xfT0OmBXlAC8WBLEJ7KhgjY5yOrxiGxAcp7XlLIT8iXGPQDlsobP5IQKgIaW1YZcb8fZjd44g9PsXjBDa9HMMfM2m5_SNUZMhO4z7_qluO0nNzqdvWF4HlqcMz9mQ1J_JcdW9xG_vZ-n5OHX1f3ldX5z-_vP5fYmN7yRc07bDqXFUjKOQkiNuuM1cqalrjTUDTbYMtN2rMO2ErWWjSlrzWmtmUnB2Sk5W_vudI_KjdbPQZvBRaO2lFWVaFLbROUHqB2OGHTvR7Qulf_jiwN8ig7TcAcFfBWY4GMMaNUU3KDDq6KgFn_UXq3-qMUftSSIJPuxyqbndnn7J3o3JAE_V8Bqr_QuuKge7kqgDCiUrOFlIi5WAtOWXxwGFY3D0WDnQnJOdd59_Ie_GNurVQ</recordid><startdate>20050601</startdate><enddate>20050601</enddate><creator>de Araújo Pinho, F.V.S.</creator><creator>Coelho-de-Souza, A.N.</creator><creator>Morais, S.M.</creator><creator>Ferreira Santos, C.</creator><creator>Leal-Cardoso, J.H.</creator><general>Elsevier GmbH</general><general>Urban &amp; 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Burtt. et Smith is an aromatic plant that is distributed widely in the tropical and sub-tropical regions of the world. In Brazil, where A. zerumbet is called “colonia”, it is used widely in folk medicine for the treatment of various diseases, including hypertension. In the present study, the antinociceptive effects of the orally administered essential oil of A. zerumbet (EOAz) were evaluated in male Swiss mice (20–25 g each). In the acetic acid-induced writhing test, EOAz (30, 100 and 300 mg/kg body wt.; n = 10 , n = 13 and n = 15 , respectively) was effective at all doses. In the hot-plate test, EOAz significantly increased the latency at doses of 100 and 300 mg/kg body wt., but not at 30 mg/kg body wt., at all observation times up to the 180th min ( n = 10 for each dose). In the formalin test, EOAz significantly reduced paw licking time in the second phase of the test at 100 mg/kg body wt. ( n = 10 ), but decreased it in both phases at 300 mg/kg body wt. ( n = 10 ). At 30 mg/kg body wt., the effect of EOAz did not differ from control values in either phase of the formalin test ( n = 10 ). Pretreatment with naloxone (5 mg/kg body wt., i.p.) caused a significant reversal of the analgesic effect of 300 mg/kg body wt. EOAz ( n = 8 ) that was complete for the first phase, but only partial for the second phase of the formalin test. The data show that orally administered OEAz promotes a dose-dependent antinociceptive effect, with a mechanism of action which probably involves the participation of opiate receptors.</abstract><cop>Germany</cop><pub>Elsevier GmbH</pub><pmid>16008125</pmid><doi>10.1016/j.phymed.2004.04.006</doi><tpages>5</tpages></addata></record>
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subjects Acetic Acid
Administration, Oral
Alpinia zerumbet
analgesic effect
Analgesics - administration & dosage
Analgesics - pharmacology
Analgesics - therapeutic use
Analgesics, Opioid - administration & dosage
Analgesics, Opioid - pharmacology
Analgesics, Opioid - therapeutic use
Animals
Antinociceptive effects
Dose-Response Relationship, Drug
Essences and essential oils
Essential oil
essential oils
Formaldehyde
Health aspects
Hot Temperature
In vivo
Male
Medicinal plants
medicinal properties
Mice
oral administration
Pain - chemically induced
Pain - prevention & control
Pain Measurement - drug effects
Phytotherapy
Plant Leaves
Plant Oils - administration & dosage
Plant Oils - pharmacology
Plant Oils - therapeutic use
Zingiberales
title Antinociceptive effects of the essential oil of Alpinia zerumbet on mice
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