Planta Med 2019; 85(18): 1500
DOI: 10.1055/s-0039-3399926
Main Congress Poster
Poster Session 1
© Georg Thieme Verlag KG Stuttgart · New York

Phytochemical investigation of the fruits of Paliurus spina-christi Mill.

V Amountzias
School of Pharmacy, National & Kapodistrian University of Athens,, Department of Pharmacognosy & Chemistry of Natural Products, Panepistimiopolis, Zografou, Greece
,
D Abatis
School of Pharmacy, National & Kapodistrian University of Athens,, Department of Pharmacognosy & Chemistry of Natural Products, Panepistimiopolis, Zografou, Greece
,
N Aligiannis
School of Pharmacy, National & Kapodistrian University of Athens,, Department of Pharmacognosy & Chemistry of Natural Products, Panepistimiopolis, Zografou, Greece
› Author Affiliations
Further Information

Publication History

Publication Date:
20 December 2019 (online)

 

Paliurus spina-christi Mill. (Rhamnaceae) is a much-branched, deciduous, thorny shrub with green fruits that become brown during maturation. The shrub is found in dry slopes in Mediterranean, Southwest and Central Asia and North America. Its common name is ‘Christ’s thorn’ because it is said that its spiny branches were used to make the crown of thorns which had been placed on Christ’s head before his crucifixion. P. ramosissimus Lour., P. orientalis Franch. and P. hemsleyanus Rehder are well known species of the Eastern Asia [1]. Traditionally, P. spina-christi is used for its diuretic and anti-hypercholesterolemic properties, as well as a palliative against gastrointestinal pain [2]-[5]. Thus, it was decided to investigate the shrub’s fruits phytochemically.

Powdered mature fruits were exhaustively extracted with cyclohexane, dichloromethane, methanol and water. In order to remove fats and sugars, the dried methanolic extract was subjected to liquid-liquid extraction with c-Hex., EtOAc and water. The EtOAc fraction was initially chromatographed on Si-gel using Vacuum Liquid Chromatography (NP-VLC), followed by prepTLC and NP-HPLC for the final separations and isolation of the pure secondary metabolites. The water phase was treated using adsorption resin technology and the obtained fractions were further chromatographed using Reversed Phase-Solid Phase Extraction (RP-SPE) and RP-HPLC. Structure determination was based on NMR spectroscopy and LC-MS.

So far, there have been isolated and identified 12 secondary metabolites, 1 flavonoid-diglycoside, 2 phenolics, 2 triterpenoids, 1 lignan, 3 phytosterols and 3 cyclopeptide alkaloids (CPAs). One of the CPAs, metabolite 8, has been recognized as a new natural product.

 
  • References

  • 1 Tutin TG, Heyword VH, Burges NA, Moore DM, Valentine DH, Walters SM, Webb DA. Flora Europeaea 1968; 2: 243.
  • 2 Polat R, Satıl F. An ethnobotanical survey of medicinal plants in Edremit Gulf (Balıkesir –Turkey). Journal of Ethnopharmacol 2012; 139: 626- 641.
  • 3 Montse P, Carriό E, MÀ Bonet, Vallès J. Ethnobotany of the Alt Empordà region (Catalonia, Iberian Peninsula). Plants used in human traditional medicine. J Ethnopharmacol 2009; 124: 609-618.
  • 4 Bulut G, Tuzlaci E. An ethnobotanical study of medicinal plants in Turgutlu (Manisa - Turkey). Journal of Ethnopharmacology 2013; 149: 633-647
  • 5 Tetik F, Civelek S, Cakilcioglu U. Traditional uses of some medicinal plants in Malatya (Turkey). J Ethnopharmacol 2013; 146: 331-346.