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Review
. 2017 Jun;174(11):1244-1262.
doi: 10.1111/bph.13630. Epub 2016 Oct 21.

Proanthocyanidins and hydrolysable tannins: occurrence, dietary intake and pharmacological effects

Affiliations
Review

Proanthocyanidins and hydrolysable tannins: occurrence, dietary intake and pharmacological effects

Antonella Smeriglio et al. Br J Pharmacol. 2017 Jun.

Abstract

Tannins are a heterogeneous group of high MW, water-soluble, polyphenolic compounds, naturally present in cereals, leguminous seeds and, predominantly, in many fruits and vegetables, where they provide protection against a wide range of biotic and abiotic stressors. Tannins exert several pharmacological effects, including antioxidant and free radical scavenging activity as well as antimicrobial, anti-cancer, anti-nutritional and cardio-protective properties. They also seem to exert beneficial effects on metabolic disorders and prevent the onset of several oxidative stress-related diseases. Although the bioavailability and pharmacokinetic data for these phytochemicals are still sparse, gut absorption of these compounds seems to be inversely correlated with the degree of polymerization. Further studies are mandatory to better clarify how these molecules and their metabolites are able to cross the intestinal barrier in order to exert their biological properties. This review summarizes the current literature on tannins, focusing on the main, recently proposed mechanisms of action that underlie their pharmacological and disease-prevention properties, as well as their bioavailability, safety and toxicology.

Linked articles: This article is part of a themed section on Principles of Pharmacological Research of Nutraceuticals. To view the other articles in this section visit http://onlinelibrary.wiley.com/doi/10.1111/bph.v174.11/issuetoc.

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Figures

Figure 1
Figure 1
Basic chemical features of B‐ and A‐type proanthocyanidins and their monomeric units.
Figure 2
Figure 2
Chemical structure of pentagalloyl‐glucose.
Figure 3
Figure 3
Formation of ellagic acid in aqueous solution.
Figure 4
Figure 4
Chemical structure of eugeniin and casuarictin.

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