Laboratorio de Fisiología Experimental (EPhyL), Instituto Antofagasta (IA), Universidad de Antofagasta, Casilla 170, Antofagasta 1271155, Chile.
Laboratorio de Bioquímica Aplicada, Instituto de EtnoFarmacología, Facultad de Ciencias de la Salud, Universidad Arturo Prat, Iquique 1110939, Chile.
Molecules. 2020 Jan 24;25(3):520. doi: 10.3390/molecules25030520.
The infusion of the desertic plant I.M. Johnst showed vascular smooth muscle relaxation in rat aorta and the presence of several phenolic compounds, which were detected by high resolution UHPLC-Orbitrap-HESI-MS. In addition, five flavonoids were rapidly isolated from a methanolic extract using high-performance counter-current chromatography (HPCCC). The extract showed endothelium-independent relaxation effect in rat aorta. Sixty-one compounds were detected in the infusion, mainly glycosylated flavonoids, flavanones and several oxylipins, suggesting that a synergistic effect between the compounds in the extracts could be responsible for the relaxation activity. Vascular activity experiments were done in isolated organ bath. In rat aorta, a nitric oxide inhibitor did not prevent the relaxation effects of the extract; however, a selective guanylyl cyclase inhibitor partially blunted this effect. The compound ,3'-dihydroxy-4'7-dimethoxyflavone presented higher relaxation effect than 100 μg/mL of extract. The extract and the isolated metabolites from can show relaxation effects on rat aorta by a mechanism that is independent of the endothelium.
荒漠植物 I.M. Johnst 的提取物对大鼠主动脉表现出血管平滑肌松弛作用,其中存在几种酚类化合物,这些化合物通过高分辨 UHPLC-Orbitrap-HESI-MS 检测到。此外,从甲醇提取物中使用高效逆流色谱(HPCCC)快速分离出五种黄酮类化合物。提取物对大鼠主动脉表现出非内皮依赖性松弛作用。在提取物中检测到 61 种化合物,主要为糖基化黄酮类、黄烷酮和几种氧化脂类,表明提取物中化合物之间的协同作用可能是导致这种松弛活性的原因。血管活性实验在离体器官浴中进行。在大鼠主动脉中,一氧化氮抑制剂不能阻止提取物的松弛作用;然而,选择性鸟苷酸环化酶抑制剂部分减弱了这种作用。化合物 3'-二羟基-4'7-二甲氧基黄酮的松弛作用大于 100 μg/mL 的提取物。提取物和从 中分离的代谢物可以通过一种独立于内皮的机制对大鼠主动脉表现出松弛作用。