巴豆鼠李糖叶精油及包合物(OEFC/β-CD)在抗伤害性动物模型中的作用

Macromol Pub Date : 2021-04-06 DOI:10.3390/MACROMOL1020008
Anita Oliveira Brito Pereira Bezerra Martins, Maria Rayane Correia de Oliveira, I. S. Alcântara, Lindaiane Bezerra Rodrigues, Francisco Rafael Alves Santana Cesário, Maria Sanádia Alexandre da Silva, F. Castro, E. P. Nascimento, T. R. Albuquerque, L. Q. Quintans Júnior, A. Araújo, H. Coutinho, I. A. Menezes, A. Wanderley
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引用次数: 3

摘要

本研究旨在评价鼠李叶精油(OEFC)和β-环糊精包合物(COEFC)的抗伤感受作用,并探讨其抗伤感受反应的疼痛信号通路。采用开野法和旋转棒法观察OEFC和COEFC对大鼠中枢神经系统(CNS)的影响,并通过醋酸致腹部扭曲、福尔马林和热板模型评价其抗伤感受作用。两项试验均使用瑞士(小家鼠)雄性小鼠(20-30 g)。口服OEFC (200mg /kg/v.o)和COEFC (83.5 mg/kg/v.o)对中枢神经系统没有影响。OEFC(25、50、100和200 mg/kg/v.)和COEFC(8.35、41.75和83.5 mg/kg/v.o.)在腹部扭曲、福尔马林和热板试验中显示出抗伤感受作用。OEFC (25 mg/kg/v.o.)和COEFC (8.35 mg/kg/v.o. o.)剂量表明其抗伤害性作用涉及阿片系统、胆碱系统和香草素系统,以及l -精氨酸/NO和α-2肾上腺素能受体途径的激活。OEFC和COEFC的抗感知潜能为疼痛治疗提供了可能的选择。然而,COEFC在较低剂量下比分离的OEFC表现出更显著的效果,这种作用可能是由络合物的性质和优势所证明的。
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Effect of the Croton rhamnifolioides Essential Oil and the Inclusion Complex (OEFC/β-CD) in Antinociceptive Animal Models
This study aims to evaluate the antinociceptive effect of the C. rhamnifolioides leaf essential oil (OEFC) and the β-cyclodextrin inclusion complex (COEFC) and investigate the pain signaling pathways involved in the antinociceptive response. The effects of the OEFC and COEFC on the central nervous system (CNS) were determined by open field and rota-rod assays, and the antinociceptive effect was evaluated via the acetic acid-induced abdominal contortions, formalin, and hot plate models. Swiss (Mus musculus) male mice (20–30 g) were used in both trials. The OEFC (200 mg/kg/v.o-orally) and COEFC (83.5 mg/kg/v.o.) did not present alterations in the CNS. The OEFC (25, 50, 100, and 200 mg/kg/vo.) and COEFC (8.35, 41.75, and 83.5 mg/kg/v.o.) demonstrated antinociceptive effects in the abdominal contortions, formalin, and hot plate tests. The OEFC (25 mg/kg/v.o.) and COEFC (8.35 mg/kg/v.o.) doses showed that the antinociceptive effect involves the activation of the opioid, cholinergic, and vanilloid systems, as well as the L-arginine/NO and α-2 adrenergic receptor pathways. The antinociceptive potential the OEFC and COEFC demonstrate possible alternatives for the therapy of pain. However, the COEFC presented more significant effects at lower doses than the isolated OEFC, where this action may be justified by the properties and advantages of the complexation.
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