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含羞草的口腔面部镇痛作用。

Orofacial antinociceptive effect of Mimosa tenuiflora (Willd.) Poiret.

机构信息

Laboratory of Bioprospecting of Natural Products and Biotechnology, Ceará State University, Department of Chemistry, CECITEC, Tauá, Ceará, Brazil; Laboratory of Biotechnology and Molecular Biology, Ceará State University, Department of Nutrition, Fortaleza, Ceará, Brazil; Experimental Biology Center, University of Fortaleza, Fortaleza, Ceará, Brazil.

Laboratory of Bioprospecting of Natural Products and Biotechnology, Ceará State University, Department of Chemistry, CECITEC, Tauá, Ceará, Brazil.

出版信息

Biomed Pharmacother. 2018 Jan;97:1575-1585. doi: 10.1016/j.biopha.2017.11.001. Epub 2017 Nov 24.

Abstract

Mimosa tenuiflora (Willd.) Poiret, popularly known in Brazil as "jurema-preta" is widely used against bronchitis, fever, headache and inflammation. Its antioxidant, anti-inflammatory and antinociceptive potential has already been reported. To assess the orofacial antinociceptive effect of M. tenuiflora, ethanolic extracts of M. tenuiflora (leaves, twigs, barks and roots) were submitted to in vitro tests of antioxidant activity. The extract with the highest antioxidant potential was partitioned and subjected to preliminary chemical prospecting, GC-MS, measurement of phenolic content and cytotoxicity tests of the fraction with the highest antioxidant activity. The nontoxic fraction with the highest antioxidant activity (FATEM) was subjected to tests of acute and chronic orofacial nociception and locomotor activity. The possible mechanisms of neuromodulation were also assessed. The EtOAc fraction, obtained from the ethanolic extract of M. tenuiflora barks, was the one with the highest antioxidant potential and nontoxic (FATEM), and Benzyloxyamine was the major constituent (34.27%). FATEM did not alter the locomotor system of mice and reduced significantly the orofacial nociceptive behavior induced by formalin, glutamate, capsaicin, cinnamaldehyde or acidic saline compared to the control group. FATEM also inhibited formalin- or mustard oil-induced temporomandibular nociception. In addition, it also reduced mustard oil-induced orofacial muscle nociception. However, FATEM did not alter hypertonic saline-induced corneal nociception. Neuropathic nociception was reversed by treatment with FATEM. The antinociceptive effect of FATEM was inhibited by naloxone, L-NAME and glibenclamide. FATEM has pharmacological potential for the treatment of acute and neuropathic orofacial pain and this effect is modulated by the opioid system, nitric oxide and ATP-sensitive potassium channels. These results lead us to studies of isolation and characterization of bioactive principles.

摘要

含羞草(Willd.)波雷尔,在巴西俗称“jurema-preta”,被广泛用于治疗支气管炎、发热、头痛和炎症。其抗氧化、抗炎和镇痛潜力已被报道。为了评估含羞草的口腔镇痛作用,含羞草(叶、枝、皮和根)的乙醇提取物进行了体外抗氧化活性测试。抗氧化潜力最高的提取物被分离,并进行了初步的化学展望、GC-MS、酚含量测定和具有最高抗氧化活性的馏分的细胞毒性试验。具有最高抗氧化活性且无毒的馏分(FATEM)进行了急性和慢性口腔痛觉和运动活性测试。还评估了神经调节的可能机制。从含羞草皮的乙醇提取物中获得的 EtOAc 馏分是具有最高抗氧化潜力和无毒(FATEM)的馏分,而苯甲氧基胺是主要成分(34.27%)。FATEM 不改变小鼠的运动系统,与对照组相比,显著减少福尔马林、谷氨酸、辣椒素、肉桂醛或酸性盐水诱导的口腔疼痛行为。FATEM 还抑制福尔马林或芥末油诱导的颞下颌疼痛。此外,它还减轻了芥末油诱导的口腔肌肉疼痛。然而,FATEM 并没有改变高渗盐水诱导的角膜疼痛。用 FATEM 治疗可逆转神经病理性疼痛。FATEM 的镇痛作用被纳洛酮、L-NAME 和格列本脲抑制。FATEM 具有治疗急性和神经病理性口腔疼痛的药理学潜力,这种作用受阿片样物质系统、一氧化氮和 ATP 敏感性钾通道的调节。这些结果促使我们进行了生物活性物质的分离和鉴定研究。

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