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1.
Molecules ; 23(4)2018 Apr 16.
Article in English | MEDLINE | ID: mdl-29659496

ABSTRACT

Numerous epidemiological and interventional clinical studies have consistently reported that black tea is good for human health. The polyphenolic compound, theaflavin, and its galloyl esters (theaflavins) are the primary red pigments in black tea that possess several health benefits, including fat-reducing and glucose-lowering capabilities and lifestyle-related disease prevention related to anti-obesity, anticancer, anti-atherosclerotic, anti-inflammatory, antiviral, antibacterial, anti-osteoporotic, and anti-dental caries properties. These compounds are produced by key enzymes, such as polyphenol oxidase and peroxidase, from parent green tea catechins present in fresh green tea leaves during the production of black tea leaves or the fermentation of green tea. However, theaflavins are only present in low concentrations in black tea; thus, their extraction from black tea leaves at sufficient levels for use in medical studies has been difficult. To circumvent this issue, different procedures for the synthesis of theaflavins using chemical oxidizing reagents or enzymes have been studied; however, low yields have limited their utility. Recently, however, several biosynthetic methods have been developed for the mass production of theaflavins. Using these methods, the physiological functions of theaflavins in lifestyle-related diseases in mice and humans have also been studied. In this review, we present the synthesis of theaflavins and their health benefits.


Subject(s)
Biflavonoids/biosynthesis , Camellia sinensis/metabolism , Catechin/biosynthesis , Animals , Biflavonoids/therapeutic use , Catechin/therapeutic use , Catechol Oxidase/metabolism , Fermentation , Food , Humans , Mice , Peroxidase/metabolism , Plant Leaves/metabolism , Tea
2.
Biol Pharm Bull ; 40(6): 860-866, 2017 Jun 01.
Article in English | MEDLINE | ID: mdl-28381812

ABSTRACT

The polyphenolic compound theaflavin, the main red pigment in black tea, possesses many beneficial properties, such as fat-reducing and glucose-lowering capabilities. To produce theaflavin-containing fermentation water on a large scale, we have developed a simple, inexpensive, and selective enzymatic biotransformation method to obtain sufficient levels from fresh green tea leaves. Subsequent administration of theaflavin-containing fermentation water to obese mice on a high-fat diet inhibited body weight gain, decreased casual blood glucose and fasting blood glucose levels, and lowered mesenteric and total fat composition. To note, there were no significant differences observed in food consumption between the experimental and control (water without theaflavin) mice groups. Next, we investigated the effect of this water on blood glucose levels in healthy humans and found that it significantly inhibited blood glucose levels. Thus, we showed that theaflavin-containing fermentation water can be efficiently generated from fresh green tea leaves and demonstrated its significantly potent effects in vivo.


Subject(s)
Biflavonoids/pharmacology , Blood Glucose/drug effects , Camellia sinensis , Catechin/pharmacology , Plant Preparations/pharmacology , Adipose Tissue/drug effects , Adult , Animals , Biflavonoids/pharmacokinetics , Biflavonoids/therapeutic use , Biflavonoids/urine , Biotransformation , Catechin/pharmacokinetics , Catechin/therapeutic use , Catechin/urine , Diet, High-Fat , Female , Fermentation , Humans , Male , Mice, Inbred C57BL , Middle Aged , Obesity/blood , Obesity/drug therapy , Plant Leaves , Plant Preparations/pharmacokinetics , Plant Preparations/therapeutic use , Plant Preparations/urine , Water , Weight Gain/drug effects , Young Adult
3.
Biol Pharm Bull ; 39(8): 1347-52, 2016 Aug 01.
Article in English | MEDLINE | ID: mdl-27237789

ABSTRACT

The polyphenolic compound theaflavin, which is the main red pigment present in black tea, is reported to elicit various physiological effects. Because of the extremely low concentration of theaflavin present in black tea, its extraction from black tea leaves in quantities sufficient for use in medical studies has been difficult. We have developed a simple, inexpensive, selective, domino-type, one-pot enzymatic biotransformation method for the synthesis of theaflavin that is suitable for use in medical studies. Subsequent administration of this synthetic theaflavin to high-fat diet-induced obese mice inhibited both body weight gain and visceral fat accumulation, with no significant difference in the amount of faeces between the experimental and control mice.


Subject(s)
Biflavonoids , Camellia sinensis , Catechin , Obesity/drug therapy , Animals , Biflavonoids/biosynthesis , Biflavonoids/chemistry , Biflavonoids/therapeutic use , Biotransformation , Camellia sinensis/chemistry , Camellia sinensis/cytology , Camellia sinensis/metabolism , Catechin/biosynthesis , Catechin/chemistry , Catechin/therapeutic use , Diet, High-Fat , Intra-Abdominal Fat/drug effects , Male , Mice, Inbred C57BL , Peroxidases/metabolism , Plant Extracts/chemistry , Plant Leaves/chemistry , Plant Leaves/cytology , Plant Leaves/metabolism , Weight Gain/drug effects
4.
Biochem Biophys Res Commun ; 417(1): 287-93, 2012 Jan 06.
Article in English | MEDLINE | ID: mdl-22155236

ABSTRACT

The incidence of non-alcoholic fatty liver disease (NAFLD) has been increasing, and there is a shortage of liver donors, which has led to the acceptance of steatotic livers for transplantation. However, steatotic livers are known to experience more severe acute ischemia-reperfusion (I/R) injury than normal livers upon transplantation. In the present study, we investigated the role of theaflavin, a polyphenol substance extracted from black tea, in attenuating acute I/R injury in a fatty liver model. We induced I/R in normal and steatotic livers treated with or without theaflavin. We also separated primary hepatocytes from the normal and steatotic livers, and applied RAW264.7 cells, a mouse macrophage cell line, that was pretreated with theaflavin. We observed that liver steatosis, oxidative stress, inflammation and hepatocyte apoptosis were increased in the steatotic liver compared to the normal liver, however, these changes were significantly decreased by theaflavin treatment. In addition, theaflavin significantly diminished the ROS production of steatotic hepatocytes and TNF-α production by LPS-stimulated RAW264.7 cells. We concluded that theaflavin has protective effects against I/R injury in fatty livers by anti-oxidant, anti-inflammatory, and anti-apoptotic mechanisms.


Subject(s)
Antioxidants/administration & dosage , Biflavonoids/administration & dosage , Catechin/administration & dosage , Fatty Liver/physiopathology , Liver Transplantation , Reperfusion Injury/drug therapy , Reperfusion Injury/physiopathology , Animals , Apoptosis/drug effects , Cell Line , Cytokines/antagonists & inhibitors , Cytokines/biosynthesis , Fatty Liver/drug therapy , Fatty Liver/pathology , Hepatocytes/drug effects , Male , Mice , Mice, Inbred C57BL , Non-alcoholic Fatty Liver Disease , RNA, Messenger/antagonists & inhibitors , RNA, Messenger/biosynthesis , Reperfusion Injury/pathology , Tissue Donors , Tumor Necrosis Factor-alpha/metabolism
5.
Chem Pharm Bull (Tokyo) ; 54(2): 226-9, 2006 Feb.
Article in English | MEDLINE | ID: mdl-16462069

ABSTRACT

We have synthesized lyoniresinol with the combined utilization of synthetic chemistry and biotechnological methods, specifically using plant cell cultures as an "enzyme source."


Subject(s)
Anisoles/chemical synthesis , Biotechnology , Naphthalenes/chemical synthesis , Biotransformation , Camellia sinensis/enzymology , Cells, Cultured , Indicators and Reagents , Indolequinones/chemistry , Magnetic Resonance Spectroscopy , Peroxidases/chemistry
6.
Phytochemistry ; 49(6): 1627-1629, 1998 Nov 20.
Article in English | MEDLINE | ID: mdl-11711075

ABSTRACT

Immobilized cells of Catharanthus roseus synthesized (R)-4-pyridyl-1-ethanol from the corresponding racemate in 100% yield by stereoinversion of the (S)-alcohol in the racemate to the (R)-alcohol. Furthermore, in the reduction of 4-acetylpyridine, we could synthesize both (R) and (S)-4-pyridyl-1-ethanol during a short or a long incubation.

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