» Articles » PMID: 3857069

Red Wine Contains a Potent Inhibitor of Phenolsulphotransferase

Overview
Specialty Pharmacology
Date 1985 Feb 1
PMID 3857069
Citations 7
Authors
Affiliations
Soon will be listed here.
Abstract

Many ethanolic drinks, especially red wine, contain potent inhibitors of phenolsulphotransferase. At a dilution of 1/75 from the original beverage, extracts from six types of red wine inhibited human platelet phenolsulphotransferase P by a mean of 99% and human platelet phenolsulphotransferase M by 12%. Such extracts had no significant effect on rat liver monoamine oxidase A or human platelet monoamine oxidase B. The inhibitors, which have not yet been identified, can be extracted into ethyl acetate at acid or neutral pH. Thus, they are not monoamines. Flavonoid phenols are plausible candidates. As phenolsulphotransferase M and P are involved in the metabolism of many phenols, including drugs, the inhibition of these enzymes could result in the enhancement of pharmacological potency and have important clinical consequences.

Citing Articles

Polyphenols and metabolism: from present knowledge to future challenges.

Quesada-Vazquez S, Eseberri I, Les F, Perez-Matute P, Herranz-Lopez M, Atgie C J Physiol Biochem. 2024; 80(3):603-625.

PMID: 39377969 PMC: 11502541. DOI: 10.1007/s13105-024-01046-7.


Polyphenols: From Theory to Practice.

Bertelli A, Biagi M, Corsini M, Baini G, Cappellucci G, Miraldi E Foods. 2021; 10(11).

PMID: 34828876 PMC: 8621732. DOI: 10.3390/foods10112595.


Multiple catechols in human plasma after drinking caffeinated or decaffeinated coffee.

Goldstein D, Sullivan P, Corrales A, Isonaka R, Gelsomino J, Cherup J J Chromatogr B Analyt Technol Biomed Life Sci. 2021; 1185:122988.

PMID: 34731744 PMC: 8647204. DOI: 10.1016/j.jchromb.2021.122988.


Pharmacogenetics of SULT1A1.

Daniels J, Kadlubar S Pharmacogenomics. 2014; 15(14):1823-1838.

PMID: 25493573 PMC: 4361945. DOI: 10.2217/pgs.14.134.


Hypothesis: holiday sudden cardiac death: food and alcohol inhibition of SULT1A enzymes as a precipitant.

Eagle K J Appl Toxicol. 2012; 32(10):751-5.

PMID: 22678655 PMC: 3504075. DOI: 10.1002/jat.2764.


References
1.
Bakke O, Midtvedt T . Influence of germ-free status on the excretion of simple phenols of possible significance in tumour promotion. Experientia. 1970; 26(5):519. DOI: 10.1007/BF01898483. View

2.
Foldes A, Meek J . Rat brain phenolsulfotransferase: partial purification and some properties. Biochim Biophys Acta. 1973; 327(2):365-74. DOI: 10.1016/0005-2744(73)90419-1. View

3.
Rein G, Glover V, Sandler M . Sulphate conjugation of biologically active monoamines and their metabolites by human platelet phenolsulphotransferase. Clin Chim Acta. 1981; 111(2-3):247-56. DOI: 10.1016/0009-8981(81)90192-3. View

4.
SINGLETON V . Naturally occurring food toxicants: phenolic substances of plant origin common in foods. Adv Food Res. 1981; 27:149-242. DOI: 10.1016/s0065-2628(08)60299-2. View

5.
Carter S, Glover V, Sandler M, Gillman P, Bridges P . Human platelet phenolsulphotransferase: separate control of the two forms and activity range in depressive illness. Clin Chim Acta. 1981; 117(3):333-44. DOI: 10.1016/0009-8981(81)90121-2. View