Comprehensive Characterization of Phytochemical Composition, Membrane Permeability, and Antiproliferative Activity of Juglans nigra Polyphenols

Author:

Osztie Rita1ORCID,Czeglédi Tamás1,Ross Sarah2,Stipsicz Bence34,Kalydi Eszter5,Béni Szabolcs6ORCID,Boldizsár Imre17ORCID,Riethmüller Eszter1,Bősze Szilvia E.48,Alberti Ágnes1ORCID

Affiliation:

1. Department of Pharmacognosy, Semmelweis University, Üllői út 26, 1085 Budapest, Hungary

2. Department Pharmaceutical Biology, Institute for Drug Discovery, University of Leipzig, Eilenburger Str. 14, 04317 Leipzig, Germany

3. Institute of Biology, Doctoral School of Biology, ELTE Eötvös Loránd University, Pázmány Péter sétány 1/C, 1117 Budapest, Hungary

4. HUN-REN-ELTE Research Group of Peptide Chemistry, Hungarian Research Network, ELTE Eötvös Loránd University, Pázmány Péter sétány 1/A, 1117 Budapest, Hungary

5. Institute of Organic Chemistry, Semmelweis University, Hőgyes Endre u. 7., 1092 Budapest, Hungary

6. Institute of Chemistry, ELTE Eötvös Loránd University, Pázmány Péter sétány 1/A, 1117 Budapest, Hungary

7. Department of Plant Anatomy, Institute of Biology, ELTE Eötvös Loránd University, Pázmány Péter sétány 1/C, 1117 Budapest, Hungary

8. Department of Genetics, Cell- and Immunobiology, Semmelweis University, Nagyvárad tér 4., 1089 Budapest, Hungary

Abstract

The aim of our study was the detailed polyphenol profiling of Juglans nigra and the characterization of the membrane permeability and antiproliferative properties of its main phenolics. A total of 161 compounds were tentatively identified in J. nigra bark, leaf, and pericarp extracts by ultrahigh-performance liquid chromatography–high-resolution tandem mass spectrometry (UHPLC-HR-MS/MS). Eight compounds including myricetin-3-O-rhamnoside (86), quercetin-3-O-rhamnoside (106), quercetin-3-O-xyloside (74), juglone (141), 1,2,3,4-tetrahydro-7,8-dihydroxy-4-oxonaphthalen-1-yl-6-O-galloyl-glucoside (92), ellagic acid (143), gallic acid (14), and ethyl gallate (58) were isolated from J. nigra pericarp. The in vitro antiproliferative activity of the isolated compounds was investigated against three human cancer cell lines, confirming that juglone (141) inhibits cell proliferation in all of them, and has similar activity as the clinical standards. The permeability of the isolated compounds across biological membranes was evaluated by the parallel artificial membrane permeability assay (PAMPA). Both juglone (141) and ethyl-gallate (58) showed positive results in the blood–brain-barrier-specific PAMPA-BBB study. Juglone (141) also possesses logPe values which indicates that it may be able to cross both the GI and BBB membranes via passive diffusion.

Funder

National Research, Development and Innovation Office: NKFIH

Doctoral School of Biology, Eötvös Loránd University

European Union

Publisher

MDPI AG

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