A. Rodrigues, D. Guimarães, T. Konno, L. Tinoco, T. Barth, F. Aguiar, N. Lopes, I. Leal, J. Raimundo, M. Muzitano
{"title":"Phytochemical Study of Tapirira guianensis Leaves Guided by Vasodilatory and Antioxidant Activities","authors":"A. Rodrigues, D. Guimarães, T. Konno, L. Tinoco, T. Barth, F. Aguiar, N. Lopes, I. Leal, J. Raimundo, M. Muzitano","doi":"10.3390/molecules22020304","DOIUrl":null,"url":null,"abstract":"The aim of this research was to perform a phytochemical study of the methanol leaves extract of T. guianensis (MET) guided by vasodilatory and antioxidant activities. The chemical profile of MET and the ethyl acetate fraction (EA fraction) was determined by HPLC-UV-MS and EA fraction guided fractionation by reverse-phase chromatography. The vasorelaxant effects of MET, fractions, sub-fractions and constituents were assessed on rat aorta pre-contracted with phenylephrine. Antioxidant activity was evaluated by using a DPPH assay. The results show that MET-induced vasodilation was dependent on NO/cGMP; and that the PI3K/Akt pathway seems to be the main route involved in eNOS activation. The EA fraction showed greater vasodilatory and antioxidant potency and was submitted to further fractionation. This allowed the isolation and characterization of quercetin, quercetin 3-O-(6″-O-galloyl)-β-d-galactopyranoside and 1,4,6-tri-O-galloyl-β-d-glucose. Also, galloyl-HHDP-hexoside and myricetin deoxyhexoside were identified by HPLC-UV-MS. These compounds are being described for the first time for T. guianensis. 1,4,6-tri-O-galloyl-β-d-glucose and quercetin 3-O-(6″-O-galloyl)-β-d-galactopyranoside showed no vasodilatory activity. Quercetin and myricetin glycoside seems to contribute to the MET activity, since they have been reported as vasodilatory flavonoids. MET-induced vasodilation could contribute to the hypotensive effect of T. guianensis previously reported.","PeriodicalId":19033,"journal":{"name":"Molecules : A Journal of Synthetic Chemistry and Natural Product Chemistry","volume":"42 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2017-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"8","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Molecules : A Journal of Synthetic Chemistry and Natural Product Chemistry","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.3390/molecules22020304","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 8
Abstract
The aim of this research was to perform a phytochemical study of the methanol leaves extract of T. guianensis (MET) guided by vasodilatory and antioxidant activities. The chemical profile of MET and the ethyl acetate fraction (EA fraction) was determined by HPLC-UV-MS and EA fraction guided fractionation by reverse-phase chromatography. The vasorelaxant effects of MET, fractions, sub-fractions and constituents were assessed on rat aorta pre-contracted with phenylephrine. Antioxidant activity was evaluated by using a DPPH assay. The results show that MET-induced vasodilation was dependent on NO/cGMP; and that the PI3K/Akt pathway seems to be the main route involved in eNOS activation. The EA fraction showed greater vasodilatory and antioxidant potency and was submitted to further fractionation. This allowed the isolation and characterization of quercetin, quercetin 3-O-(6″-O-galloyl)-β-d-galactopyranoside and 1,4,6-tri-O-galloyl-β-d-glucose. Also, galloyl-HHDP-hexoside and myricetin deoxyhexoside were identified by HPLC-UV-MS. These compounds are being described for the first time for T. guianensis. 1,4,6-tri-O-galloyl-β-d-glucose and quercetin 3-O-(6″-O-galloyl)-β-d-galactopyranoside showed no vasodilatory activity. Quercetin and myricetin glycoside seems to contribute to the MET activity, since they have been reported as vasodilatory flavonoids. MET-induced vasodilation could contribute to the hypotensive effect of T. guianensis previously reported.
本研究的目的是在血管扩张和抗氧化活性的指导下,对桂枝甲醇叶提取物(MET)进行植物化学研究。采用HPLC-UV-MS法测定MET和乙酸乙酯组分(EA组分)的化学谱,反相色谱法测定EA组分。研究了MET、组分、亚组分和组份对大鼠肾上腺素预收缩主动脉的血管松弛作用。采用DPPH法测定抗氧化活性。结果表明,met诱导的血管舒张作用依赖于NO/cGMP;PI3K/Akt通路似乎是eNOS激活的主要途径。EA部分显示出更大的血管扩张和抗氧化能力,并提交进一步的分离。这使得槲皮素、槲皮素3-O-(6″- o -没食子酰)-β-d-半乳糖苷和1,4,6-三- o -没食子酰-β-d-葡萄糖得以分离和表征。HPLC-UV-MS鉴定没食子酰- hhdp -己糖苷和杨梅素脱氧己糖苷。这些化合物均为首次在贵州滴虫中被描述。1,4,6-三- o -没食子酰-β-d-葡萄糖和槲皮素3-O-(6″- o -没食子酰)-β-d-半乳糖苷没有血管扩张活性。槲皮素和杨梅苷似乎有助于MET活性,因为它们已被报道为血管扩张类黄酮。此前有报道称,met诱导的血管舒张可能有助于豚鼠的降压作用。