CYBERMED LIFE - ORGANIC  & NATURAL LIVING

Tea

  • An in vitro study of theaflavins extracted from black tea to neutralize bovine rotavirus and bovine coronavirus infections.

    Abstract Title:

    An in vitro study of theaflavins extracted from black tea to neutralize bovine rotavirus and bovine coronavirus infections.

    Abstract Source:

    Vet Microbiol. 1998 Oct ;63(2-4):147-57. PMID: 9850995

    Abstract Author(s):

    K J Clark, P G Grant, A B Sarr, J R Belakere, C L Swaggerty, T D Phillips, G N Woode

    Article Affiliation:

    K J Clark

    Abstract:

    Crude theaflavin was extracted from black tea and then fractionated by HPLC into five components (initial peaks (IP), TF1, TF2A, TF2B, and TF3). The crude extract and the various fractions of theaflavin were collected and tested, individually and in combination, for antirotaviral activity. The mean effective concentration (EC50) was calculated and compared. Activity varied from the most active being the uncharacterized theaflavin-like initial peaks (IP) with an EC50 of 0.125 microgram/ml to the least active being theaflavin-3 monogallate (TF2A) with an EC50 of 251.39 micrograms/ ml. The combination of TF1 + TF2A + TF2B + TF3 was more active than the sum of the activities of these four fractions individually, indicating synergism among the peaks. Only the crude extract was assayed for activity against coronavirus; the EC50 was 34.7 micrograms/ml.

  • An in vitro study of theaflavins extracted from black tea to neutralize bovine rotavirus and bovine coronavirus infections.

    Abstract Title:

    An in vitro study of theaflavins extracted from black tea to neutralize bovine rotavirus and bovine coronavirus infections.

    Abstract Source:

    Vet Microbiol. 1998 Oct ;63(2-4):147-57. PMID: 9850995

    Abstract Author(s):

    K J Clark, P G Grant, A B Sarr, J R Belakere, C L Swaggerty, T D Phillips, G N Woode

    Article Affiliation:

    K J Clark

    Abstract:

    Crude theaflavin was extracted from black tea and then fractionated by HPLC into five components (initial peaks (IP), TF1, TF2A, TF2B, and TF3). The crude extract and the various fractions of theaflavin were collected and tested, individually and in combination, for antirotaviral activity. The mean effective concentration (EC50) was calculated and compared. Activity varied from the most active being the uncharacterized theaflavin-like initial peaks (IP) with an EC50 of 0.125 microgram/ml to the least active being theaflavin-3 monogallate (TF2A) with an EC50 of 251.39 micrograms/ ml. The combination of TF1 + TF2A + TF2B + TF3 was more active than the sum of the activities of these four fractions individually, indicating synergism among the peaks. Only the crude extract was assayed for activity against coronavirus; the EC50 was 34.7 micrograms/ml.

  • Inhibition of nicotine-DNA adduct formation in mice by six dietary constituents.

    Abstract Title:

    Inhibition of nicotine-DNA adduct formation in mice by six dietary constituents.

    Abstract Source:

    Food Chem Toxicol. 2003 Jul;41(7):1045-50. PMID: 12804663

    Abstract Author(s):

    Y Cheng, H L Li, H F Wang, H F Sun, Y F Liu, S X Peng, K X Liu, Z Y Guo

    Article Affiliation:

    Department of Applied Chemistry, College of Chemistry and Molecular Engineering, Peking University, Beijing 100871, P.R. China.

    Abstract:

    Nicotine [3-(1-methyl-2-pyrrolidinyl)-pyridine] is a major alkaloid in tobacco products and has proven to be a potential genotoxic compound. Many natural dietary products can suppress the DNA adduction, and hence act as inhibitors of cancer. In this study, we investigated the inhibitory effects of curcumin, garlic squeeze, grapeseed extract, tea polyphenols, vitamin C, and vitamin E on nicotine-DNA adduction in vivo using an ultrasensitive method of accelerator mass spectrometry (AMS). The results demonstrated that all the dietary constituents induced marked dose-dependent decrease in nicotine-DNA adducts as compared with the control. The reduction rate reached about 50% for all agents, except garlic squeeze (40%), even at its highest dose level. Amongst the six agents, grapeseed extract exhibited the strongest inhibition to the DNA adduct formation. Therefore, we may arrive at a point that these dietary constituents are beneficial to prevent the harmful adduct formation, and thus to block the potential carcinogenesis induced by nicotine.

  • Inhibition of nitrobenzene-induced DNA and hemoglobin adductions by dietary constituents.

    Abstract Title:

    Inhibition of nitrobenzene-induced DNA and hemoglobin adductions by dietary constituents.

    Abstract Source:

    Appl Radiat Isot. 2003 Mar;58(3):291-8. PMID: 12595006

    Abstract Author(s):

    Hongli Li, Yan Cheng, Haifang Wang, Hongfang Sun, Yuanfang Liu, Kexin Liu, Shixiang Peng

    Article Affiliation:

    Department of Applied Chemistry, College of Chemistry and Molecular Engineering, Peking University, Beijing 100871, People's Republic of China.

    Abstract:

    Nitrobenzene (NB), a widely used industrial chemical, is a likely human carcinogen. Many dietary constituents can suppress the DNA-adduction, acting as the inhibitors of cancer. In this study, we investigated the inhibitory effects of vitamin C (VC), vitamin E (VE), tea polyphenols (TP), garlic squeeze, curcumin, and grapestone extract on NB-DNA and NB-hemoglobin (Hb) adductions in mice using an ultrasensitive method of accelerator mass spectrometry (AMS) with 14C-labelled nitrobenzene. All of these dietary constituents showed their inhibitory effects on DNA or Hb adduction. VC, VE, TP and grapestone extract could efficaciously inhibit the adductions by 33-50%, and all of these six agents could inhibit Hb adduction by 30-64%. We also investigated resveratrol, curcumin, VC and VE as inhibitors of NB-DNA adduction in vitro using liquid scintillation counting technique. These agents in the presence of NADPH and S9 components also pronouncedly blocked DNA adduction in a dose-dependent profile. Our study suggests that these seven constituents may interrupt the process of NB-induced chemical carcinogenesis.

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