Planta Med 2015; 81(12/13): 1175-1181
DOI: 10.1055/s-0035-1545916
Analytical Studies
Original Papers
Georg Thieme Verlag KG Stuttgart · New York

Isolation and Quantification of Oligomeric and Polymeric Procyanidins in the Aerial Parts of St. Johnʼs Wort (Hypericum perforatum)[*]

Nils Hellenbrand
University of Münster, Institute of Pharmaceutical Biology and Phytochemistry, Münster, Germany
,
Matthias Lechtenberg
University of Münster, Institute of Pharmaceutical Biology and Phytochemistry, Münster, Germany
,
Frank Petereit
University of Münster, Institute of Pharmaceutical Biology and Phytochemistry, Münster, Germany
,
Jandirk Sendker
University of Münster, Institute of Pharmaceutical Biology and Phytochemistry, Münster, Germany
,
Andreas Hensel
University of Münster, Institute of Pharmaceutical Biology and Phytochemistry, Münster, Germany
› Author Affiliations
Further Information

Publication History

received 12 November 2014
revised 05 March 2015

accepted 08 March 2015

Publication Date:
23 April 2015 (online)

Abstract

Proanthocyanidins (condensed tannins) constitute a class of oligomeric and polymeric polyphenols with flavan-3-ols as monomeric building blocks. Despite the high impact of proanthocyanidins, these polyphenols are mostly quantified by colorimetric methods or by chromatographic determination of the flavan-3-ols as cleavage products or low molecular oligomers as lead compounds. For St. Johnʼs wort (Hyperici herba) from Hypericum perforatum, a protocol for preparative isolation of oligomeric and polymeric proanthocyanidins from an acetone-water extract by chromatography on Sephadex®LH20 in combination with preparative high-performance liquid chromatography on the diol stationary phase was developed, yielding procyanidin reference clusters with a defined degree of polymerization from 3 to 10. Identity and purity of these clusters was proven by high-performance liquid chromatography (RP18 and diol phase) and mass spectrometry. For identification and quantification of proanthocyanidin clusters from St. Johnʼs wort, an ICH-Q2 (International harmonized guideline for analytical validation) validated high-performance liquid chromatography method with fluorimetric detection was developed using an acetone-water extract of the herbal material, purified by solid-phase extraction for the removal of naphthodianthrones. The method enabled the quantification of procyanidin clusters with a degree of polymerization from 2 to 10. Analysis of nine batches of Hyperici herba from different sources indicated a high variability of proanthocyanidin content in the range from 8 to 37 mg/g. In all of the batches investigated, the trimer cluster DP3 was the dominant proanthocyanidin (about 40 %), followed by DP 4 (about 15 %) and DP5 (about 12 %). Monitoring of procyanidin distribution during seasonal growth of fresh plants of H. perforatum indicated the highest proanthocyanidin content in young plants (about 50 mg/g) and a time-dependent decrease during the growing season to about 16 mg/g. The highest proanthocyanidin content was found in young leaves and flowers, while the fruits were proanthocyanidin-free; older parts of the stem and the herb had a lower proanthocyanidin content. From these data, it can be concluded that proanthocyanidins serve as part of the plant defense system in the reproductive organs.

* Dedicated to the 75th birthday of Prof. Dr. A. Nahrstedt.


Supporting Information

 
  • References

  • 1 De Bruyne T, Pieters L, Deelstra H, Vlietink A. Condensed vegetable tannins: Biodiversity in structure and biological activities. Biochem Syst Ecol 1999; 27: 445-459
  • 2 He F, Pan QH, Shi Y, Duan CQ. Biosynthesis and genetic regulation of proanthocyanidins in plants. Molecules 2008; 13: 2674-2703
  • 3 Arranz S, Valderas-Martinez P, Chiva-Blanch G, Casas R, Urpi-Sarda M, Lamuela-Raventos RM, Estruch R. Cardioprotective effects of cocoa: clinical evidence from randomized clinical intervention trials in humans. Mol Nutr Food Res 2013; 57: 936-947
  • 4 Holt RR, Heiss C, Kelm M, Keen CL. The potential of flavanol and procyanidin intake to influence age-related vascular disease. J Nutr Gerontol Geriatr 2012; 31: 290-323
  • 5 de Pascual-Teresa S, Moreno DG, García-Viguera G. Flavanols and anthocyanins in cardiovascular health: a review of current evidence. Int J Mol Sci 2010; 11: 1679-1703
  • 6 Gescher K, Hensel A, Hafezi W, Derksen A, Kühn J. Oligomeric proanthocyanidins from Rumex acetosa L. inhibit the attachment of herpes simplex virus type-1. Antivir Res 2011; 89: 9-18
  • 7 Dauer A, Hensel A, Lhoste E, Knasmüller S, Mersch-Sundermann V. Genotoxic and antigenotoxic effects of catechin and tannins from the bark of Hamamelis virginiana L. in metabolically competent, human hepatoma cells (Hep G2) using single cell gel electrophoresis. Phytochem 2003; 63: 199-207
  • 8 Deters A, Dauer A, Schnetz E, Fartasch M, Hensel A. High-molecular products (proanthocyanidins and polysaccharides) from Hamamelis bark: influence on human keratinocyte proliferation and differentiation. Phytochem 2001; 58: 949-958
  • 9 ESCOP (European Scientific Cooperative on Phytotherapy). Monographs: Hyperici Herba (St. Johnʼs wort). 2nd. edition. Stuttgart, New York: Thieme; 2003: 257-281
  • 10 Ploss O, Petereit F, Nahrstedt A. Procyanidins from the herb of Hypericum perforatum . Pharmazie 2001; 6: 509-511
  • 11 Butterweck V, Petereit F, Winterhoff H, Nahrstedt A. Solubilized hypericin and pseudohypericin from Hypericum perforatum exert antidepressant activity in the forced swimming test. Planta Med 1998; 64: 291-294
  • 12 Butterweck V, Liefländer-Wulf U, Winterhoff H, Nahrstedt A. Plasma levels of hypericin in presence of procyanidin B2 and hyperoside: a pharmacokinetic study in rats. Planta Med 2003; 69: 189-192
  • 13 Brantner A, Kartnig T, Quehenberger F. Vergleichende phytochemische Untersuchungen an Hypericum perforatum L. und Hypericum maculatum Crantz. Sci Pharm 1994; 62: 261-276
  • 14 Koupai-Abyazani MR, McCallum J, Bohm BA. Identification of the constituent flavanoid units in sainfoin proanthocyanidins by reversed-phase high-performance liquid chromatography. J Chromatogr 1992; 594: 117-123
  • 15 Hümmer W, Schreier P. Analysis of proanthocyanidins. Mol Nutr Food Res 2008; 52: 1381-1398
  • 16 Sultana T, Stecher G, Mayer R, Trojer L, Qureshi MN, Abel G, Popp M, Bonn GK. Quality assessment and quantitative analysis of flavonoids from tea samples of different origins by HPLC-DAD-ESI-MS. J Agric Food Chem 2008; 56: 3444-3453
  • 17 Svedström U, Vuorela H, Kostianen R, Huovinen K, Laakso I, Hiltunen R. High-performance liquid chromatographic determination of oligomeric procyanidins from dimers up to the hexamer in hawthorn. J Chromatogr A 2002; 968: 53-60
  • 18 Papagiannopoulos M, Wollseifen HR, Mellenthin A, Haber B, Galensa R. Identification and quantification of polyphenols in carob fruits (Ceratonia sliqua L.) and derived products by HPLC-UV-ESI/MS. J Agric Food Chem 2004; 52: 3784-3791
  • 19 Rigaud J, Escribano-Bailón MT, Prieur C, Souquet JM, Cheynier V. Normal-phase high-performance liquid chromatographic separation of procyanidins from cocoa beans and grape seeds. J Chromatogr 1993; 654: 255-260
  • 20 Karonen M, Ossipov V, Sinkkonen J, Loponen J, Haukioja E, Pihlaja K. Quantitative analysis of polymeric proanthocyanidins in birch leaves with normal-phase HPLC. Phytochem Anal 2006; 17: 149-156
  • 21 Kelm MA, Johnson JC, Robbins RJ, Hammerstone JF, Schmitz HH. High-performance liquid chromatography separation and purification of cacao (Theobroma cacao L.) procyanidins according to degree of polymerization using a diol stationary phase. J Agric Food Chem 2006; 54: 1571-1576
  • 22 Zumdick S, Petereit F, Luftmann H, Hensel A. Preparative isolation of oligomeric procyanidins of oligomeric procyanidins from hawthorn (Crataegus spp.). Pharmazie 2009; 64: 286-288
  • 23 Hellenbrand N, Petereit F, Lechtenberg M, Sendker JD, Hensel A. Isolation and quantification of oligomeric and polymeric procyanidins in leaves and flowers of Hawthorn (Crataegus spp.). Submitted.
  • 24 Bicker J, Petereit F, Hensel A. Proanthocyanidins and a phloroglucinol derivative of Rumex acetosa L. Fitoterapia 2009; 80: 483-495
  • 25 Hurst WJ, Stanley B, Glinski JA, Davey M, Payne ML, Stuart DA. Characterization of primary standards for use in the HPLC analysis of the procyanidin content of cocoa and chocolate containing products. Molecules 2009; 14: 4136-4146
  • 26 Rohr G. Analytical investigations on and isolation of procyanidines from Crataegus leaves and flowers [dissertation No. 13020]. Zürich: ETH Zürich; 1999: 156-165
  • 27 Gu L, Kelm M, Hammerstone JF, Beecher G, Cunningham D, Vannozzi S, Prior RL. Fractionation of polymeric procyanidins from lowbush blueberry and quantification of procyanidins in selected foods with an optimized normal-phase HPLC-MS fluorescent detection method. J Agric Food Chem 2002; 50: 4852-4860
  • 28 Awika JM, Dykes I, Gu L, Rooney L, Prior RL. Processing of sorghum (Sorghum bicolor) and sorghum products alters procyanidin oligomer and polymer distribution and content. J Agric Food Chem 2003; 51: 5516-5521
  • 29 ICH. International Conference on Harmonization of Technical Requirements for Registration of Pharmaceuticals for Human Use; ICH Harmonized Tripartite Guideline; Validation of Analytical Procedures: Text and Methodology Q2(R1); Finalised Guidelines: October 1994/November 1996. Geneva: ICH; 1996