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A Comprehensive Insight on the Health Benefits and Phytoconstituents of and Recent Approaches for Its Quality Control

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Date 2019 Oct 9
PMID 31590466
Citations 21
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Abstract

Tea, Camellia sinensis, which belongs to the family Theaceae, is a shrub or evergreen tree up to 16 m in height. Green tea is very popular because of its marked health benefits comprising its anticancer, anti-oxidant, and antimicrobial activities, as well as its effectiveness in reducing body weight. Additionally, it was recognized by Chinese people as an effective traditional drink required for the prophylaxis against many health ailments. This is due to the complex chemical composition of green tea, which comprises different classes of chemical compounds, such as polyphenols, alkaloids, proteins, minerals, vitamins, amino acids, and others. The beneficial health effects of green tea ultimately led to its great consumption and increase its liability to be adulterated by either low-quality or non-green tea products with concomitant decrease in activity. Thus, in this review, green tea was selected to highlight its health benefits and phytoconstituents, as well as recent approaches for its quality-control monitoring that guarantee its incorporation in many pharmaceutical industries. More research is needed to find out other more biological activities, active constituents, and other simple and cheap techniques for its quality assurance that ascertain the prevention of its adulteration.

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References
1.
Ali M, Afzal M, GUBLER C, Burka J . A potent thromboxane formation inhibitor in green tea leaves. Prostaglandins Leukot Essent Fatty Acids. 1990; 40(4):281-3. DOI: 10.1016/0952-3278(90)90050-u. View

2.
Satoh K, Sakamoto Y, Ogata A, Nagai F, Mikuriya H, Numazawa M . Inhibition of aromatase activity by green tea extract catechins and their endocrinological effects of oral administration in rats. Food Chem Toxicol. 2002; 40(7):925-33. DOI: 10.1016/s0278-6915(02)00066-2. View

3.
Dyer P, Kotha A, Gollings A, Shorter S, Shepherd T, Pettit M . An in vitro evaluation of epigallocatechin gallate (eGCG) as a biocompatible inhibitor of ricin toxin. Biochim Biophys Acta. 2016; 1860(7):1541-50. DOI: 10.1016/j.bbagen.2016.03.024. View

4.
Wasilewski R, Ubara E, Klonizakis M . Assessing the effects of a short-term green tea intervention in skin microvascular function and oxygen tension in older and younger adults. Microvasc Res. 2016; 107:65-71. DOI: 10.1016/j.mvr.2016.05.001. View

5.
Oyama J, Shiraki A, Nishikido T, Maeda T, Komoda H, Shimizu T . EGCG, a green tea catechin, attenuates the progression of heart failure induced by the heart/muscle-specific deletion of MnSOD in mice. J Cardiol. 2016; 69(2):417-427. DOI: 10.1016/j.jjcc.2016.05.019. View