Abstract

Today, more than ever, the search for non-trivial sources of biologically active substances is critical. Plants of the genus Rumex are noteworthy. Plants of this genus stand out for a number of advantages from the dominant plant core of meadow phytocenoses of the temperate climatic zone: a short growing season, an intensive increase in biomass, and undemanding growth conditions. In addition, this plant genus is known as a super-producer of secondary phenolic compounds. The wide distribution and intensive synthesis of biologically active substances make plants from the genus Rumex a promising object for study. Seven species of the genus Rumex (R. acetosa, R. acetosella, R. confertus, R. crispus, R. maritimus, R. obtusifolius, and R. sanguineus) were analyzed. Plants were collected under relatively uniform growing conditions. For subsequent extraction and analysis of phenolic compounds, as well as antioxidant activity, plants leaves were used. R. acetosella, R. crispus, R. maritimus, R. obtusifolius, and R. sanguineus were characterized by a high total content of phenolic compounds (111–131 mg g–1). The maximum content of flavonoids was found in the leaves of R. maritimus and R. acetosella. At the same time, according to high-performance liquid chromatography with diode-array detection (HPLC-DAD) analysis, derivatives of flavones (apigenin and luteolin) predominated in the leaves of R. acetosella, while in other species, mainly derivatives of flavonols (quercetin and kaempferol) were identified. Plants of R. acetosa, in comparison with other studied species, were characterized by a lower content of the studied groups of phenolic compounds, with the exception of hydroxycinnamic acids, the content of which in this species was comparable to the content of flavonoids. The maximum content of catechins was found in R. sanguineus; proanthocyanidins—in R. sanguineus, R. obtusifolius, and R. crispus; and tannins—in R. obtusifolius. Extracts from R. crispus were characterized by high antioxidant activity, measured by 2,2-diphenyl-1-picrylhydrazyl (DPPH), 2,2′-azino-bis(3-ethylbenzothiazoline-6-sulfonic acid (ABTS), and ferric reducing antioxidant power (FRAP) assays. In addition, the assessment of the phenolic profile of the plant made it possible to group the plants within the framework of cluster analysis. The distribution pattern in the clusters corresponded to the generally accepted taxonomy, with a characteristic division into subgenera (Acetosa, Acetosella, and Rumex). Thus, the phenolic profile can be considered as an additional instrumental approach when drawing up a systematic hierarchy.

Highlights

  • In Europe, the consumption of wild edible plants has been an integral part of human nutrition and traditional medicine since ancient times [1,2]

  • Plant leaves of the following species were used as the objects of study: R. acetosa L., R. acetosella L., R. confertus Willd., R. crispus L., R. maritimus L., R. obtusifolius L., and R. sanguineus L

  • The leaves of R. confertus showed an even lower total phenolic content (TPC), whereas R. acetosa was characterized by the lowest value

Read more

Summary

Introduction

In Europe, the consumption of wild edible plants has been an integral part of human nutrition and traditional medicine since ancient times [1,2]. Edible wild plants are known to be a good source of primary nutritional compounds (proteins, fats, sugars, vitamins, and minerals) [3]. Edible wild plants contain various biologically active components that demonstrated health benefits effects (flavonoids, phenolic acids, anthocyanins, tannins, terpenoids, steroidal saponins, glucosinolates, and so on) [2]. This shows their potential as nutritional supplements, feed additives, and medicinal agents [2,4]. Wild plants provide a colossal genetic resource that can be used in breeding programs to increase the resistance of cultivated plants and to improve their nutritional and pharmacological value [5]

Objectives
Methods
Results
Discussion
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call