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Systematics and health effects of chemically distinct tannins in medicinal plants
Authors:Okuda Takuo
Institution:Okayama University, Tsushima, Okayama 700-8530, Japan. okudatakjp@ybb.ne.jp
Abstract:The research began with an investigation of tannins from traditional medicinal plants and resulted in isolation and structure determination of hundreds of ellagitannins and dehydroellagitannins, as well as their oligomers and oxidized derivatives with various structures specific to each plant species. These polyphenols have been classified according to the stage of oxidative structural transformation and oligomerization, into types I-IV and I+ to IV+, etc. Parallels were found between their oxidative transformations and plant evolution. They were also classified by the linkage units between the monomers, into DOG, GOD, GOG and DOGOD types (D=Diphenoyl, G=Galloyl, O=Oxygen), etc. Besides their fundamental activities, e.g., reduction and anti-peroxidation properties, remarkable biological and pharmacological activities of various potencies have also been found, including, amongst others, inhibition of lipid-peroxidation, mutagenicity of carcinogens and tumor promotion, host-mediated antitumor effects specific to particular tannin structures, antiviral activity and potentiation of antibacterial activity.
Keywords:ACTH  adrenocorticotropic hormone  ADP  adenine 5′-diphosphate  AIBN  2  2′-azobisisobutyronitrile  B[a]p diol epoxide  ±7β 8α-dihydroxy-9α  10α-epoxy-7  8  9  10-tetrahydrobenzo[a]pyrene  DHHDP  dehydrohexahydroxydiphenoyl  DMBA  7  12-dimethylbenz[a]anthracene  DMPO  5  5-dimethyl-1-pyrrolidone-N-oxide  DPPH  1  1-diphenyl-2-picrylhydrazyl  EVB-EA  Epstein-Barr virus early antigen  ECG  (−)-epicatechin gallate  EGCG  (−)-epigallocatechin gallate  ENNG  N-ethyl-N′-nitro-N-nitrosoguanidine  ESR  electron spin resonance  GOT  glutamic oxaloacetic transaminase  GPT  glutamic pyruvic transaminase  HHDP  hexahydroxydiphenoyl  5-HETE  5-hydroxy-6  8  11  14-eicosatetraenoic acid  5-HPETE  5-hydroperoxy-6  8  11  14-eicosatetraenoic acid  MM2  mouse mammary cancer 2  MNNG  N-methyl-N′-nitroso[4  3-b]indole  NADPH  nicotinamide adenine dinucleotide phosphate  NNK  4-(methylnitrosamino)-1-(3-pyridyl)-1-butanone  N-OH-Trp-P-2  3-hydroxyamino-1-methyl-5H-pyrido[4  3-b]indole  RA  relative astringency  RAG  astringency relative to that of geraniin  RMB  relative affinity to methylene blue  RMBG  affinity to methylene blue relative to that of geraniin  TNF-α  tumor necrosis factor-α  TPA  12-O- tetradecanoylphorbol 13-acetate  XOD  xanthine oxidase
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