ACYLATED FLAVONOIDS OF SPIRAEA GENUS AS α-AMYLASE INHIBITORS

  • Нина (Nina) Игоревна (Igorevna) Кащенко (Kashchenko) Institute of General and Experimental Biology, Siberian Branch, Russian Academy of Science Email: ninkk@mail.ru
  • Надежда (Nadezhda) Константиновна (Konstantinovna) Чирикова (Chirikova) North-Eastern Federal University Email: hofnung@mail.ru
  • Даниил (Daniil) Николаевич (Nikolaevich) Оленников (Olennikov) Institute of General and Experimental Biology, Siberian Branch, Russian Academy of Science http://orcid.org/0000-0001-8194-1061 Email: olennikovdn@mail.ru
Keywords: Spiraea, Rosaceae, Spiraea salicifolia, flavonoids, 6′′-О-caffeoyl-hyperoside, HPLC, α-amylase inhibition

Abstract

Spiraea L. is a genus of deciduous shrubs of Rosaceae family widespread on the territory of Eastern Siberia. As a result of the study of six Spiraea species growing on the Baikal region, it was shown that they characterized by a high content of phenolic compounds and their extracts had an inhibitory effect on α-amylase. The use of correlation analysis made it possible to reveal the leading role of flavonoids as carriers of the biological effect of extracts. The most active was the extract of S. salicifolia leaves with an IC50 value 69,30 μg/mL After fractionation and chromatographic separation of the extractive substances, 18 compounds were isolated from the ethyl acetate fraction of S. salicifolia and fifteen of them for the first time for the species, including trifolin, 6′′-O-caffeoyl-hyperoside, 6′′-O-caffeoyl-isoquercitrin, 6′′-O-caffeoyl-astragalin, 1-O-p-hydroxybenzoyl-6-O-p-coumaroyl-β-d-glucopyranoside, 3,4,5-tri-O-caffeoylquinic acid, isoramnetinin-3-O-β-d-glucopyranoside, tiliroside, isoramnetin-3-O-α-l-rhamnopyranoside, 1-O-cis-cinnamoyl-6-O-(2′-methylene-4′-hydroxybutyroyl)-β-d-glucopyranose, 1-О-(4′′-hydroxy-3′′-methylfurane-2′′-one)-6-О-trans-cinnamoyl-β-d-glucopyranose, 1-О-(4′′-hydroxy-3′′-methylfurane-2′′-one)-6-О-cis-cinnamoyl-β-d-glucopyranose, 6-tuliposide A and tulipalin A. The most active inhibitors of α-amylase were flavonoid caffeoyl glycosides with 6′′-O-caffeoyl-hyperoside as a most effective inhibitor with IC50 value 46.18 μg/mL. Latter compound determined the total anti-α-amylase effect of S. salicifolia. The content of 6′′-O-caffeoyl-hyperoside in leaves of S. salicifolia was 0,60-10,53 mg/g and flavonoids – 12,02-23,17 mg/g. This study demonstrated the fact that the acylated flavonoids of Spiraea are effective inhibitors of α-amylase.

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Author Biographies

Нина (Nina) Игоревна (Igorevna) Кащенко (Kashchenko), Institute of General and Experimental Biology, Siberian Branch, Russian Academy of Science
кандидат фармацевтических наук, научный сотрудник лаборатории медико-биологических исследований
Надежда (Nadezhda) Константиновна (Konstantinovna) Чирикова (Chirikova), North-Eastern Federal University
кандидат фармацевтических наук, доцент кафедры биохимии и биотехнологии
Даниил (Daniil) Николаевич (Nikolaevich) Оленников (Olennikov), Institute of General and Experimental Biology, Siberian Branch, Russian Academy of Science
доктор фармацевтических наук, ведущий научный сотрудник лаборатории медико-биологических исследований

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Published
2017-06-02
How to Cite
1. Кащенко (Kashchenko)Н. (Nina) И. (Igorevna), Чирикова (Chirikova)Н. (Nadezhda) К. (Konstantinovna), Оленников (Olennikov)Д. (Daniil) Н. (Nikolaevich) ACYLATED FLAVONOIDS OF SPIRAEA GENUS AS α-AMYLASE INHIBITORS // chemistry of plant raw material, 2017. № 4. P. 81-90. URL: http://journal.asu.ru/cw/article/view/2144.
Section
Low-molecular weight compounds