Institute of Chemistry - Federal University of Alfenas - Unifal-MG, Alfenas, MG, Brazil.
Department of Pathology and Parasitology, Federal University of Alfenas - Unifal-MG, Alfenas, MG, Brazil.
Phytochem Anal. 2021 Sep;32(5):859-883. doi: 10.1002/pca.3031. Epub 2021 Feb 16.
Plants have been considered a promising source for discovering new compounds with pharmacological activities. The Fabaceae family comprises a large variety of species that produce substances with diverse therapeutic potential, including anti-inflammatory activity. The limitations of current anti-inflammatories generate the need to research new anti-inflammatory structures with higher efficacy as well as develop methods for screening multiple samples, reliably and ethically, to assess such therapeutic properties.
Validate and apply a quantification method for prostaglandin E (PGE ) production from an ex vivo assay in human blood in order to screen anti-inflammatory activity present in many Fabaceae species extracts.
Human blood was incubated with extracts from 47 Fabaceae species. After lipopolysaccharide (LPS)-induced inflammation, PGE was quantified in the plasma by liquid chromatography with tandem mass spectrometry (LC-MS/MS). The extracts that presented PGE production inhibition were further assessed through in vivo assay and then chemically characterised through an analysis of ultra-performance liquid chromatography electrospray ionisation quadrupole time-of-flight tandem mass spectrometry (UPLC-ESI-QTOF-MS ) data.
The new ex vivo anti-inflammatory assay showed that five out of the 47 Fabaceae species inhibited PGE production. Results from an in vivo assay and the metabolic profile of the active extracts supported the anti-inflammatory potential of four species.
The quantification method for PGE demonstrated fast, sensitive, precise, and accurate results. The new ex vivo anti-inflammatory assay comprised a great, reliable, and ethical approach for the screening of a large number of samples before an in vivo bioassay. Additionally, the four active extracts in both ex vivo and in vivo assays may be useful for the development of more efficient anti-inflammatory drugs.
植物被认为是发现具有药理活性的新化合物的有前途的来源。豆科植物种类繁多,其产生的物质具有多种治疗潜力,包括抗炎活性。目前抗炎药的局限性使得有必要研究具有更高疗效的新型抗炎结构,并开发可靠和符合伦理道德的筛选多种样品的方法,以评估此类治疗特性。
验证并应用一种从人血液的离体测定中定量测定前列腺素 E(PGE)产生的方法,以筛选许多豆科植物提取物中的抗炎活性。
用人血液孵育 47 种豆科植物的提取物。在脂多糖(LPS)诱导炎症后,通过液相色谱-串联质谱(LC-MS/MS)在血浆中定量测定 PGE。通过体内测定进一步评估产生 PGE 抑制作用的提取物,然后通过超高效液相色谱-电喷雾离子化四极杆飞行时间串联质谱(UPLC-ESI-QTOF-MS)数据分析对其进行化学表征。
新的离体抗炎测定法表明,47 种豆科植物中有 5 种抑制了 PGE 的产生。体内测定结果和活性提取物的代谢谱支持四种植物的抗炎潜力。
PGE 的定量方法显示出快速、灵敏、精确和准确的结果。新的离体抗炎测定法是在进行体内生物测定之前筛选大量样品的一种可靠且符合伦理道德的方法。此外,在离体和体内测定中都具有活性的四种提取物可能有助于开发更有效的抗炎药物。