A-type proanthocyanidin

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

Distribution in plants

Schematic chemical structure of an A type proanthocyanidin dimer

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

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] However, in humans, there is no sufficient clinical evidence that cranberry type-A proanthocyanidins are effective in lowering risk of urinary tract infection.[12][13]

References

  1. ↑ Fine, AM (2000). "Oligomeric proanthocyanidin complexes: history, structure, and phytopharmaceutical applications" (PDF). Alternative medicine review. 5 (2): 144–51. PMID 10767669.
  2. 1 2 Neto, CC (2007). "Cranberry and its phytochemicals: a review of in vitro anticancer studies". The Journal of Nutrition. 137 (1 Suppl): 186S–193S. PMID 17182824.
  3. ↑ 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.
  4. ↑ 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. PMID 22101466.
  5. ↑ de Camargo, A. C.; Regitano-d'Arce, M. A. B.; Gallo, C. R.; Shahidi, F., Gamma-irradiation induced changes in microbiological status, phenolic profile and antioxidant activity of peanut skin. Journal of Functional Foods 2015, 12, 129-143
  6. ↑ 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.
  7. ↑ 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.
  8. ↑ 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.
  9. ↑ 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.
  10. ↑ 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. PMID 22383303.
  11. ↑ 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.
  12. ↑ "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" (PDF). EFSA Journal. European Food Safety Authority. 12 (5): 3657. 2014. Retrieved 22 May 2014.
  13. ↑ Jepson, RG; Williams, G; Craig, JC (Oct 17, 2012). Jepson, Ruth G, ed. "Cranberries for preventing urinary tract infections". Cochrane database of systematic reviews (Online). 10: CD001321. doi:10.1002/14651858.CD001321.pub5. PMID 23076891.
This article is issued from Wikipedia - version of the 11/21/2016. The text is available under the Creative Commons Attribution/Share Alike but additional terms may apply for the media files.