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A type proanthocyanidins are a specific type of proanthocyanidins, which are a class of flavonoid. Proanthocyanidins fall under a wide range of names in the nutritional and scientific vernacular, including oligomeric proanthocyanidins, flavonoids, polyphenols, condensed tannins, and OPCs. Proanthocyanidins were first popularized by French scientist Jacques Masquelier.^[1]

Distribution in plants

A-type linkage is a less common feature in proanthocyanidins with both 4β→8 (B-type) and 2β→O→7 interflavanoid bonds.^[2]

A-type proanthocyanidin glycosides can be isolated from cocoa liquor.^[3]

Dimers

Procyanidin A1 is an epicatechin-(2β→7,4β→8)-catechin dimer.
Procyanidin A2 is a dimeric (-)epicatechin.

Other A-type proanthocyanidins can be found in cranberries,^[2] cinnamon,^[4] peanut skins^[5]^[6] and Geranium niveum.^[7]

Chemistry

B-type procyanidins (catechin dimers) can be converted to A-type procyanidins by radical oxidation.^[8] Fragmentation patterns for A-type proanthocyanidins include heterocyclic ring fission (HRF), retro-Diels-Alder (RDA) fission, benzofuran-forming fission (BFF) and quinone methide fission (QM).^[9]

Metabolism

The metabolism of type-A proanthocyanidins is significant since a large number of metabolites are detected in urine and feces soon after ingestion of foods rich in polymers, indicating rapid elimination and absence of physiological effect. Polymeric type-A proanthocyanidins are depolymerized into epicatechin units in the small intestine, then cleaved into smaller phenolic acids with no known biological role.^[10]

Research

In vitro, A-type proanthocyanidins isolated from cranberry juice cocktail demonstrated anti-adhesion activity against E. coli binding to urinary tract epithelial cells, whereas B-type proanthocyanidins from grape exhibited minor activity.^[11] In humans, a 2014 review indicated there was insufficient clinical evidence that cranberry type-A proanthocyanidins are effective in lowering the risk of urinary tract infections (UTIs),^[12] while a 2023 review concluded that long-term consumption of cranberry products may reduce the risk of UTIs in certain groups.^[13]

References

^ Fine, AM (2000). "Oligomeric proanthocyanidin complexes: history, structure, and phytopharmaceutical applications" (PDF). Alternative Medicine Review. 5 (2): 144–51. PMID 10767669. Archived from the original (PDF) on 4 November 2009. Retrieved 22 September 2009.
^ ^a ^b Neto, CC (2007). "Cranberry and its phytochemicals: a review of in vitro anticancer studies". The Journal of Nutrition. 137 (1 Suppl): 186S – 193S. doi:10.1093/jn/137.1.186S. PMID 17182824.
^ Hatano, T; Miyatake, H; Natsume, M; Osakabe, N; Takizawa, T; Ito, H; Yoshida, T (2002). "Proanthocyanidin glycosides and related polyphenols from cacao liquor and their antioxidant effects". Phytochemistry. 59 (7): 749–58. doi:10.1016/S0031-9422(02)00051-1. PMID 11909632.
^ María Luisa Mateos-Martín; Elisabet Fuguet; Carmen Quero; Jara Pérez-Jiménez; Josep Lluís Torres (2012). "New identification of proanthocyanidins in cinnamon (Cinnamomum zeylanicum L.) using MALDI-TOF/TOF mass spectrometry". Analytical and Bioanalytical Chemistry. 402 (3): 1327–1336. doi:10.1007/s00216-011-5557-3. hdl:10261/88579. PMID 22101466.
^ de Camargo, A. C.; Regitano-d'Arce, M. A. B.; Gallo, C. R.; Shahidi, F. (2015). "Gamma-irradiation induced changes in microbiological status, phenolic profile and antioxidant activity of peanut skin". Journal of Functional Foods. 12: 129–143. doi:10.1016/j.jff.2014.10.034.
^ Hongxiang Lou; Yamazaku Y.; Sasaku T.; Uchida M.; Tanaka H.; Oka S. (1999). "A-type proanthocyanidins from peanut skins". Phytochemistry. 51 (2): 297–308. doi:10.1016/S0031-9422(98)00736-5.
^ Calzada, F; Cerda-García-Rojas, CM; Meckes, M; Cedillo-Rivera, R; Bye, R; Mata, R (1999). "Geranins a and B, new antiprotozoal A-type proanthocyanidins from Geranium niveum". Journal of Natural Products. 62 (5): 705–9. doi:10.1021/np980467b. PMID 10346950.
^ Kondo, Kazunari; Kurihara, Masaaki; Fukuhara, Kiyoshi; Tanaka, Takashi; Suzuki, Takashi; Miyata, Naoki; Toyoda, Masatake (2000). "Conversion of procyanidin B-type (catechin dimer) to A-type: Evidence for abstraction of C-2 hydrogen in catechin during radical oxidation". Tetrahedron Letters. 41 (4): 485–488. doi:10.1016/S0040-4039(99)02097-3.
^ Li, Hui-Jing; Deinzer, Max L. (2008). "The mass spectral analysis of isolated hops A-type proanthocyanidins by electrospray ionization tandem mass spectrometry". Journal of Mass Spectrometry. 43 (10): 1353–63. doi:10.1002/jms.1411. PMID 18416438.
^ María Luisa Mateos-Martín; Jara Pérez-Jiménez; Elisabet Fuguet; Josep Lluís Torres (2012). "Profile of urinary and fecal proanthocyanidin metabolites from common cinnamon (Cinnamomum zeylanicum L.) in rats". Mol. Nutr. Food Res. 56 (4): 671–675. doi:10.1002/mnfr.201100672. hdl:10261/88578. PMID 22383303.
^ Howell AB, Reed JD, Krueger CG, Winterbottom R, Cunningham DG, Leahy M (2005). "A-type cranberry proanthocyanidins and uropathogenic bacterial anti-adhesion activity". Phytochemistry. 66 (18): 2281–91. doi:10.1016/j.phytochem.2005.05.022. PMID 16055161.
^ "Scientific Opinion on the substantiation of a health claim related to CranMax® and reduction of the risk of urinary tract infection by inhibiting the adhesion of certain bacteria in the urinary tract pursuant to Article 14 of Regulation (EC) No 1924/20061". EFSA Journal. 12 (5): 3657. 2014. doi:10.2903/j.efsa.2014.3657.
^ Williams, Gabrielle; Hahn, Deirdre; Stephens, Jacqueline H.; Craig, Jonathan C.; Hodson, Elisabeth M. (17 April 2023). "Cranberries for preventing urinary tract infections". The Cochrane Database of Systematic Reviews. 4 (4): CD001321. doi:10.1002/14651858.CD001321.pub6. ISSN 1469-493X. PMC 10108827. PMID 37068952.