Planta Med 2022; 88(02): 152-162
DOI: 10.1055/a-1305-3936
Biological and Pharmacological Activity
Original Papers

Constituents of Passiflora incarnata, but Not of Valeriana officinalis, Interact with the Organic Anion Transporting Polypeptides (OATP)2B1 and OATP1A2

1   Biopharmacy, Department Pharmaceutical Sciences, University of Basel, Basel, Switzerland
,
Pierrine M. Gilgen
1   Biopharmacy, Department Pharmaceutical Sciences, University of Basel, Basel, Switzerland
,
Clara Spirgi
1   Biopharmacy, Department Pharmaceutical Sciences, University of Basel, Basel, Switzerland
,
2   Pharmaceutical Biology, Department Pharmaceutical Sciences, University of Basel, Basel, Switzerland
,
Henriette E. Meyer zu Schwabedissen
1   Biopharmacy, Department Pharmaceutical Sciences, University of Basel, Basel, Switzerland
› Author Affiliations

Abstract

Herbal medication used in the treatment of sleep disorders and anxiety often contain extracts of Valeriana officinalis or Passiflora incarnata. Valerenic acid in V. officinalis and apigenin, orientin, and vitexin in P. incarnata are thought to contribute to their therapeutic effect. It was the aim of this study to test whether these constituents of herbal extracts are interacting with the uptake of estrone 3-sulfate, pregnenolone sulfate, and dehydroepiandrosterone sulfate mediated by the uptake transporters organic anion transporting polypeptide 2B1 (OATP2B1) or organic anion transporting polypeptide 1A2 (OATP1A2). Madin-Darby canine kidney cells overexpressing OATP2B1 or OATP1A2 were used to determine the influence of the constituents on the cellular accumulation of the sulfated steroids. Subsequently, competitive counterflow experiments were applied to test whether identified inhibitors are also substrates of the transporters. Valerenic acid only interacted with OATP2B1, whereas apigenin, orientin, and vitexin interacted with OATP2B1 and OATP1A2. Competitive counterflow revealed that orientin is a substrate of both transporters, while apigenin was transported by OATP1A2 and vitexin by OATP2B1. In a next step, commercially available P. incarnata preparations were assessed for their influence on the transporters, revealing inhibition of transporter-mediated estrone 3-sulfate uptake. HPLC-UV-MS analysis confirmed the presence of orientin and vitexin in these preparations, thereby suggesting that these constituents are involved in the interaction. Our data indicate that constituents of P. incarnata may alter the function of OATP2B1 and OATP1A2, which could affect the uptake of other compounds relying on uptake mediated by the transporters.

Supporting Information



Publication History

Received: 08 July 2020

Accepted after revision: 06 November 2020

Article published online:
28 January 2021

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