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麻柳树皮提取物对小鼠的镇痛和抗炎作用。

Antinociceptive and anti-inflammatory effects of extract of Celtis iguanaea (Jacq.) Sargent leaves in mice.

机构信息

Federal University of Goiás, Natural Products Research Laboratory, Faculty of Pharmacy, Av. Universitária com 1a Avenida s/n, Setor Universitário, 74605-220 Goiânia, GO, Brazil.

Federal University of Goiás, Laboratory of Pharmacology of Natural and Synthetic Products, Institute of Biological Sciences, Avenida Esperança, s/n, Campus Samambaia, 74690-900 Goiânia, GO, Brazil.

出版信息

An Acad Bras Cienc. 2022 Sep 5;94(suppl 3):e20191339. doi: 10.1590/0001-3765202220191339. eCollection 2022.

Abstract

The antinociceptive and anti-inflammatory activities of crude ethanolic extract of Celtis iguanaea leaves and their active fractions are reported. The oral treatment with crude ethanolic extract (CEE; 100, 300 or 1000 mg/Kg) inhibited the number of writhings in a dose-dependent manner. The intermediate dose also inhibited formalin-induced nociception in both phases. The oral treatment with dichloromethane fraction (DF; 9 mg/Kg) produced antinociceptive effect in both phases of formalin test; however, the treatment with ethyl acetate fraction (EAF; 16 mg/Kg) reduced pain only in the second phase of this test. The oral treatments with CEE (300 mg/Kg) or DF (9 mg/Kg) reduced the nociception induced by capsaicin and pre-treatment with naloxone did not change these effects. The oral administration of CEE (300 mg/Kg), DF (9 mg/Kg) or ethyl EAF (16 mg/Kg) reduced ear edema, leukocytes migration and myeloperoxidase activity. Furthermore, the oral treatment with CEE (300 mg/Kg) or EAF (16 mg/Kg) reduced the level of Tumor Necrosis Factor - Alpha (TNF-α) in the pleurisy test. In conclusion, the DF showed antinociceptive activity that involves the vanilloid system as well as anti-inflammatory effect and the EAF showed anti-inflammatory activity involving the reduction of TNF-α cytokine.

摘要

报道了碧玉木叶的粗乙醇提取物及其活性部位的镇痛和抗炎活性。粗乙醇提取物(CEE;100、300 或 1000mg/Kg)的口服治疗可剂量依赖性地抑制扭体次数。中间剂量也抑制了福尔马林诱导的两阶段疼痛。二氯甲烷部分(DF;9mg/Kg)的口服治疗在福尔马林试验的两个阶段均产生镇痛作用;然而,乙酸乙酯部分(EAF;16mg/Kg)的治疗仅减轻了该试验第二阶段的疼痛。CEE(300mg/Kg)或 DF(9mg/Kg)的口服治疗减轻了辣椒素诱导的疼痛,而纳洛酮预处理并未改变这些作用。CEE(300mg/Kg)、DF(9mg/Kg)或乙基 EAF(16mg/Kg)的口服给药减轻了耳肿胀、白细胞迁移和髓过氧化物酶活性。此外,CEE(300mg/Kg)或 EAF(16mg/Kg)的口服治疗降低了胸膜炎试验中肿瘤坏死因子-α(TNF-α)的水平。总之,DF 表现出涉及香草素系统的镇痛活性以及抗炎作用,而 EAF 表现出涉及 TNF-α 细胞因子减少的抗炎活性。

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