Laboratory of Pharmacology of Pain and Inflammation, Federal University of São João Del Rei, Campus Centro Oeste Dona Lindu, Divinópolis, 35501-296, Brazil; Laboratory of Phytochemistry, Federal University of São João Del Rei, Campus Centro Oeste Dona Lindu, Divinópolis, 35501-296, Brazil.
Laboratory of Pharmacology of Pain and Inflammation, Federal University of São João Del Rei, Campus Centro Oeste Dona Lindu, Divinópolis, 35501-296, Brazil.
J Ethnopharmacol. 2020 Nov 15;262:113125. doi: 10.1016/j.jep.2020.113125. Epub 2020 Jul 29.
Solanum lycocarpum St. Hil. (Solanaceae) is widely distributed in the Brazilian Cerrado and is used in folk medicine for treatment of inflammatory disorders, such as asthma and hepatitis, as weel as antirheumatic.
The aims of this study were to evaluate the antioxidant, anti-inflammatory and antinociceptive activities of the ethanol extract (EE) obtained from the ripe fruits of S. lycocarpum and to identify its chemical constituents.
The extract was obtained by percolation with ethanol. This extract was analyzed by liquid chromatography coupled to a diode array detector and mass spectrometer (LC-DAD-MS) for identify its chemical constituents. The antioxidant activity was determined by the reaction with 1,1-diphenyl-2-picrylhydrazyl radical (DPPH). In vivo anti-inflammatory potential was assessed using carrageenan-induced paw edema model, while qualitative and quantitative histological analyses evaluated of the inflammatory infiltrate at different times and treatments. The antinociceptive effect of the EE was evaluated by acetic acid-induced abdominal writhing test, formalin-induced nociception and hot-plate test.
The main compounds identified in EE were steroidal glycoalkaloids (such as robeneoside B or hydroxysolasonine isomers and solanandaine isomers), the aglycone alkaloids peiminine and solasodine, di- and tri-O-caffeoylquinic acid derivatives, O-coumaroyl caffeoylquinic acid derivatives, N1,N10-bis-(dihydrocaffeoyl)spermidine, di-O-hexoside, and hexonic acid. In addition, the EE showed significant antioxidant activity. Intraperitoneal (i.p.) treatment with EE (300 mg/kg) exhibited anti-inflammatory activity. Qualitative and quantitative histological analyses showed that EE significantly reduced the cell infiltrate in acute inflammation. The EE, in all doses evaluated, significantly reduced the abdominal contortions in mice. Besides, reduced licking time was found in both phases in the formalin test after treatment with EE (100 and 300 mg/kg). In addition, the opioid receptor antagonist naloxone reversed the antinociceptive activity of morphine in the both phases the test, but it did not reverse the antinociceptive activity of the EE. The EE (300 mg/kg) also caused an increase in the latency to response in the hot-plate test.
The ripe fruits of S. lycocarpum exhibit antioxidant, anti-inflammatory, and antinociceptive activities, attributed mainly to the presence of alkaloids, such as solasodine and peiminine, as well as caffeoylquinic acids in their chemical composition. These results contribute to use of S. lycocarpum ripe fruits for the treatment of inflammatory and painful process.
Solanum lycocarpum St. Hil.(茄科)广泛分布于巴西塞拉多,民间医学用于治疗哮喘和肝炎等炎症性疾病,以及抗风湿。
本研究的目的是评估从 S. lycocarpum 成熟果实中获得的乙醇提取物(EE)的抗氧化、抗炎和镇痛活性,并鉴定其化学成分。
通过乙醇渗漉获得提取物。该提取物通过液相色谱-二极管阵列检测-质谱联用仪(LC-DAD-MS)进行分析,以鉴定其化学成分。抗氧化活性通过与 1,1-二苯基-2-苦基肼(DPPH)反应来确定。体内抗炎潜力通过角叉菜胶诱导的爪肿胀模型评估,而定性和定量组织学分析则在不同时间和治疗下评估炎症浸润。EE 的镇痛作用通过醋酸诱导的腹部扭曲试验、福尔马林诱导的疼痛和热板试验进行评估。
EE 中鉴定的主要化合物是甾体糖生物碱(如罗布宁 B 或羟基茄啶异构体和茄啶异构体)、糖苷生物碱佩米宁和茄碱、二-O-和三-O-咖啡酰奎宁酸衍生物、O-咖啡酰奎宁酸衍生物、N1,N10-双(二氢咖啡酰基)亚精胺、二-O-己糖苷和己酮酸。此外,EE 表现出显著的抗氧化活性。腹腔(i.p.)给予 EE(300mg/kg)表现出抗炎活性。定性和定量组织学分析表明,EE 显著减少了急性炎症中的细胞浸润。EE 在所有评估剂量下均显著减少了小鼠的腹部扭曲。此外,在 EE(100 和 300mg/kg)治疗后,在福尔马林试验的两个阶段均发现舔舐时间减少。此外,阿片受体拮抗剂纳洛酮逆转了吗啡在测试的两个阶段的镇痛作用,但它没有逆转 EE 的镇痛作用。EE(300mg/kg)还导致热板试验中反应潜伏期增加。
S. lycocarpum 成熟果实具有抗氧化、抗炎和镇痛活性,这主要归因于其化学成分中存在生物碱,如茄碱和佩米宁,以及咖啡酰奎宁酸。这些结果有助于将 S. lycocarpum 成熟果实用于治疗炎症和疼痛过程。