Evaluation of anticholinesterase effect of some Epilobium species and quantification of hyperoside by HPLC

被引:7
作者
Karakaya, Songul [1 ]
Suntar, Ipek [2 ]
Aydin, Bilge [3 ]
Dursunoglu, Benan [1 ]
Gozcu, Sefa [3 ]
Senol, Onur [4 ]
Bayrak, Burak [4 ]
Ozbek, Hilal [1 ]
Koca, Mehmet [5 ]
Ceribasi, Songul [6 ]
Yakinci, Omer Faruk [2 ,7 ]
Guvenalp, Zuhal [1 ]
Kadioglu, Yucel [4 ]
机构
[1] Ataturk Univ, Fac Pharm, Dept Pharmacognosy, Erzurum, Turkey
[2] Gazi Univ, Fac Pharm, Dept Pharmacognosy, Ankara, Turkey
[3] Binali Yildirim Univ, Fac Pharm, Dept Pharmacognosy, Erzincan, Turkey
[4] Ataturk Univ, Fac Pharm, Dept Analyt Chem, Erzurum, Turkey
[5] Ataturk Univ, Fac Pharm, Dept Pharmaceut Chem, Erzurum, Turkey
[6] Firat Univ, Fac Vet Med, Dept Pathol, Elazig, Turkey
[7] Minist Hlth, Natl Poison Informat Serv, Ankara, Turkey
关键词
Anatomy; anticholinesterase; Epilobium; hyperoside; Onagraceae;
D O I
10.1080/14786419.2020.1856841
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
This article presents the evaluation of anticholinesterase effects of aerial parts of Epilobium angustifolium, E. stevenii and E. hirsutum and isolated flavonoids from E. angustifolium, and quantification of the flavonoids by HPLC. Besides, the highest acetylcholinesterase inhibition was seen in the EtOAc sub-extracts of E. angustifolium and E. stevenii (36.51 +/- 1.88 and 39.89 +/- 3.09%, respectively), whereas EtOAc sub-extract of E. angustifolium had the best butyrylcholinesterase inhibition (62.09 +/- 1.98%). Hyperoside showed strong inhibition activity on both enzymes. The active EtOAc sub-extract of E. angustifolium was quantitatively analyzed for their content of hyperoside (quercetin-3-O-beta-D-galactoside) by HPLC. The content of hyperoside in EtOAc sub-extract of E. angustifolium was detected as 3.312%. The anatomical structures of the stem, leaf, sepal, petal, anther, and filament of E. angustifolium were investigated. The anatomical properties given in this study provide a description of E. angustifolium.
引用
收藏
页码:1296 / 1299
页数:4
相关论文
共 11 条
  • [1] Antimicrobial activity of Epilobium spp. extracts
    Battinelli, L
    Tita, B
    Evandri, MG
    Mazzanti, G
    [J]. FARMACO, 2001, 56 (5-7): : 345 - 348
  • [2] HPLC-ESI-MS/MS analysis of phenolics and in vitro antioxidant activity of Epilobium angustifolium L.
    Deng, Li-Qing
    Zhou, Si-Yu
    Mao, Jin-Xin
    Liu, Shuang
    Lan, Xiao-Zhong
    Liao, Zhi-Hua
    Chen, Min
    [J]. NATURAL PRODUCT RESEARCH, 2018, 32 (12) : 1432 - 1435
  • [3] A NEW AND RAPID COLORIMETRIC DETERMINATION OF ACETYLCHOLINESTERASE ACTIVITY
    ELLMAN, GL
    COURTNEY, KD
    ANDRES, V
    FEATHERSTONE, RM
    [J]. BIOCHEMICAL PHARMACOLOGY, 1961, 7 (02) : 88 - &
  • [4] Vegetational variation of phenolic compounds in Epilobium angustifolium
    Juergenson, Siiri
    Matto, Vallo
    Raal, Ain
    [J]. NATURAL PRODUCT RESEARCH, 2012, 26 (20) : 1951 - 1953
  • [5] In vivo bioactivity assessment on Epilobium species: A particular focus on Epilobium angustifolium and its components on enzymes connected with the healing process
    Karakaya, Songul
    Suntar, Ipek
    Yakinci, Omer Faruk
    Sytar, Oksana
    Ceribasi, Songul
    Dursunoglu, Benan
    Ozbek, Hilal
    Guvenalp, Zuhal
    [J]. JOURNAL OF ETHNOPHARMACOLOGY, 2020, 262
  • [6] Structure of acetylcholinesterase complexed with E2020 (Aricept®):: implications for the design of new anti-Alzheimer drugs
    Kryger, G
    Silman, I
    Sussman, JL
    [J]. STRUCTURE, 1999, 7 (03) : 297 - 307
  • [7] Crystal structure of human butyrylcholinesterase and of its complexes with substrate and products
    Nicolet, Y
    Lockridge, O
    Masson, P
    Fontecilla-Camps, JC
    Nachon, F
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (42) : 41141 - 41147
  • [8] Olszewska M, 2007, ACTA CHROMATOGR, V19, P253
  • [9] Therapeutic Potential of Polyphenols from Epilobium Angustifolium (Fireweed)
    Schepetkin, Igor A.
    Ramstead, Andrew G.
    Kirpotina, Liliya N.
    Voyich, Jovanka M.
    Jutila, Mark A.
    Quinn, Mark T.
    [J]. PHYTOTHERAPY RESEARCH, 2016, 30 (08) : 1287 - 1297
  • [10] Synthesis, docking and biological evaluation of oxamide and fumaramide analogs as potential AChE and BuChE inhibitors
    Yerdelen, Kadir Ozden
    Tosun, Edip
    [J]. MEDICINAL CHEMISTRY RESEARCH, 2015, 24 (02) : 588 - 602