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桉叶油醇的急性及神经性口面部抗伤害感受作用。

Acute and neuropathic orofacial antinociceptive effect of eucalyptol.

作者信息

Melo Júnior José de Maria de Albuquerque de, Damasceno Marina de Barros Mamede Vidal, Santos Sacha Aubrey Alves Rodrigues, Barbosa Talita Matias, Araújo João Ronielly Campêlo, Vieira-Neto Antonio Eufrásio, Wong Deysi Viviana Tenazoa, Lima-Júnior Roberto César Pereira, Campos Adriana Rolim

机构信息

Experimental Biology Center (NUBEX), University of Fortaleza (UNIFOR), Av. Washington Soares 1321, Edson Queiroz, Fortaleza, Ceará, CEP 60811-905, Brazil.

Department of Physiology and Pharmacology, Federal University of Ceará (UFC), Fortaleza, Ceará, Brazil.

出版信息

Inflammopharmacology. 2017 Apr;25(2):247-254. doi: 10.1007/s10787-017-0324-5. Epub 2017 Feb 16.

Abstract

Terpenes have a wide range of pharmacological properties, including antinociceptive action. The anti-inflammatory and antinociceptive effects of eucalyptol are well established. The purpose of this study was to evaluate the antinociceptive effect of eucalyptol on acute and neuropathic orofacial pain in rodent models. Acute orofacial and corneal nociception was induced with formalin, capsaicin, glutamate and hypertonic saline in mice. In another series, animals were pretreated with capsazepine or ruthenium red to evaluate the involvement of TRPV1 receptors in the effect of eucalyptol. In a separate experiment, perinasal tissue levels of IL-1β, TNF-α and IFN-γ were measured. Rats were pretreated with eucalyptol before induction of temporomandibular joint pain with formalin or mustard oil. In another experiment, rats were submitted to infraorbital nerve transection (IONX) to induce chronic pain, followed by induction of mechanical hypersensitivity using Von Frey hairs. Locomotor performance was evaluated with the open-field test, and molecular docking was conducted on the TRPV1 channel. Pretreatment with eucalyptol significantly reduced formalin-induced nociceptive behaviors in all mouse strains, but response was more homogenous in the Swiss strain. Eucalyptol produced antinociceptive effects in all tests. The effect was sensitive to capsazepine but not to ruthenium red. Moreover, eucalyptol significantly reduced IFN-γ levels. Matching the results of the experiment in vivo, the docking study indicated an interaction between eucalyptol and TRPV1. No locomotor activity changes were observed. Our study shows that eucalyptol may be a clinically relevant aid in the treatment of orofacial pain, possibly by acting as a TRPV1 channel antagonist.

摘要

萜类化合物具有广泛的药理特性,包括抗伤害感受作用。桉叶油醇的抗炎和抗伤害感受作用已得到充分证实。本研究的目的是评估桉叶油醇对啮齿动物模型中急性和神经性口面部疼痛的抗伤害感受作用。在小鼠中,用福尔马林、辣椒素、谷氨酸和高渗盐水诱导急性口面部和角膜伤害感受。在另一组实验中,动物用辣椒素受体拮抗剂或钌红预处理,以评估瞬时受体电位香草酸亚型1(TRPV1)受体在桉叶油醇作用中的参与情况。在一项单独的实验中,测量了鼻周组织中白细胞介素-1β(IL-1β)、肿瘤坏死因子-α(TNF-α)和干扰素-γ(IFN-γ)的水平。在用福尔马林或芥子油诱导颞下颌关节疼痛之前,大鼠先用桉叶油醇预处理。在另一项实验中,大鼠接受眶下神经横断术(IONX)以诱导慢性疼痛,随后用von Frey毛发诱导机械性超敏反应。用旷场试验评估运动能力,并对TRPV1通道进行分子对接。桉叶油醇预处理显著降低了所有小鼠品系中福尔马林诱导的伤害感受行为,但瑞士品系的反应更均匀。桉叶油醇在所有试验中均产生抗伤害感受作用。该作用对辣椒素受体拮抗剂敏感,但对钌红不敏感。此外,桉叶油醇显著降低了IFN-γ水平。与体内实验结果一致,对接研究表明桉叶油醇与TRPV1之间存在相互作用。未观察到运动活动变化。我们的研究表明,桉叶油醇可能是治疗口面部疼痛的一种临床相关辅助药物,可能是通过作为TRPV1通道拮抗剂发挥作用。

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