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]
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 juicecocktail demonstrated anti-adhesion activity against E. coli binding to urinary tractepithelial 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]
^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. PMID11909632.
^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. PMID22101466.
^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. PMID10346950.
^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. PMID18416438.
^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. PMID22383303.