共 63 条
Endocannabinoid mechanism for orofacial antinociception induced by electroacupuncture in acupoint St36 in rats
被引:8
作者:

Almeida, Renato Teixeira
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Univ Fed Minas Gerais, Dept Pharmacol, Inst Biol Sci, Belo Horizonte, MG, Brazil Univ Fed Minas Gerais, Dept Pharmacol, Inst Biol Sci, Belo Horizonte, MG, Brazil

Lima Romero, Thiago Roberto
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Univ Fed Minas Gerais, Dept Pharmacol, Inst Biol Sci, Belo Horizonte, MG, Brazil Univ Fed Minas Gerais, Dept Pharmacol, Inst Biol Sci, Belo Horizonte, MG, Brazil

Miranda E Castor Romero, Marina Gomes
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机构:
Univ Fed Minas Gerais, Dept Pharmacol, Inst Biol Sci, Belo Horizonte, MG, Brazil Univ Fed Minas Gerais, Dept Pharmacol, Inst Biol Sci, Belo Horizonte, MG, Brazil

de Souza, Giovane Galdino
论文数: 0 引用数: 0
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机构:
Univ Fed Alfenas, Dept Physiotherapy, Alfenas, MG, Brazil Univ Fed Minas Gerais, Dept Pharmacol, Inst Biol Sci, Belo Horizonte, MG, Brazil

Perez, Andrea de Castro
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Univ Fed Minas Gerais, Dept Pharmacol, Inst Biol Sci, Belo Horizonte, MG, Brazil Univ Fed Minas Gerais, Dept Pharmacol, Inst Biol Sci, Belo Horizonte, MG, Brazil

Gama Duarte, Igor Dimitri
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h-index: 0
机构:
Univ Fed Minas Gerais, Dept Pharmacol, Inst Biol Sci, Belo Horizonte, MG, Brazil Univ Fed Minas Gerais, Dept Pharmacol, Inst Biol Sci, Belo Horizonte, MG, Brazil
机构:
[1] Univ Fed Minas Gerais, Dept Pharmacol, Inst Biol Sci, Belo Horizonte, MG, Brazil
[2] Univ Fed Alfenas, Dept Physiotherapy, Alfenas, MG, Brazil
关键词:
Electroacupuncture;
Orofacial nociception;
Endocannabinoid system;
Antinociception;
Acupoint St36;
CANNABINOID RECEPTOR AGONISTS;
NEUROPATHIC PAIN;
PERIPHERAL ANTINOCICEPTION;
ANANDAMIDE AMIDASE;
BRAIN;
CB1;
MODEL;
HYPERALGESIA;
MODULATION;
INHIBITION;
D O I:
10.1016/j.pharep.2016.07.004
中图分类号:
R9 [药学];
学科分类号:
1007 ;
摘要:
Introduction: This study was conducted with the aim of evaluating whether electroacupuncture (EA) at acupoint St36 could produce antinociception through the activation of an endocannabinoid mechanism. Methods: Male Wistar rats were divided into experimental groups. Heat was applied to the faces of rats, and the latency to withdraw the face was measured. Furthermore, the influence of electrical stimulation (100 HzP) of acupoint St36, at a 0.5 mA intensity, was investigated in the facial withdrawal threshold. Results: The EA produced antinociception, which lasted for 180 min. This effect was antagonized by the pre-injection of AM 251, a CB1 cannabinoid receptor antagonist, but not by AM 630, a CB2 cannabinoid receptor antagonist. Additionally, pretreatment with an endocannabinoid metabolizing enzyme inhibitor (MAFP) and an anandamide reuptake inhibitor (VDM11) prolonged and intensified the antinociceptive effect produced by EA. Conclusion: This study demonstrated for the first time that the CB1 cannabinoid receptor participates in the antinociceptive effect induced by EA. (C) 2016 Institute of Pharmacology, Polish Academy of Sciences. Published by Elsevier Sp. z o.o. All rights reserved.
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页码:1095 / 1101
页数:7
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Abbott Labs, Neurol Dis Res, Global Pharmaceut Res & Dev, Abbott Pk, IL 60064 USA Abbott Labs, Expt Imaging Adv Technol, Global Pharmaceut Res & Dev, Abbott Pk, IL 60064 USA

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Yao, B. B.
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Cox, B. F.
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Abbott Labs, Expt Imaging Adv Technol, Global Pharmaceut Res & Dev, Abbott Pk, IL 60064 USA Abbott Labs, Expt Imaging Adv Technol, Global Pharmaceut Res & Dev, Abbott Pk, IL 60064 USA

Fox, G. B.
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Abbott Labs, Expt Imaging Adv Technol, Global Pharmaceut Res & Dev, Abbott Pk, IL 60064 USA Abbott Labs, Expt Imaging Adv Technol, Global Pharmaceut Res & Dev, Abbott Pk, IL 60064 USA