Cover image of the article: EFFECTS OF BLACK TEA EXTRACT AND ITS THEARUBIGINS ON WHOLE GUT TRANSIT TIME IN MICE: INVOLVEMENT OF 5-HT3 RECEPTORS

Image Credit:Jundishapur J Nat Pharm Prod

EFFECTS OF BLACK TEA EXTRACT AND ITS THEARUBIGINS ON WHOLE GUT TRANSIT TIME IN MICE: INVOLVEMENT OF 5-HT3 RECEPTORS

Authors

D Mehri1, H.R Monsef-Esfahani1, S Gharibzadeh1, K Jafari2,*, M Faghihi1
1Department of Pharmacognosy, Faculty of Pharmacy, Tehran University of Medical Sciences, Iran
2Department of Zoology, Iranian Research Institute for Plant protection, Kianoosh.jafari@Gmail.com, Iran
*Corresponding Author: Department of Zoology, Iranian Research Institute for Plant protection, Kianoosh.jafari@Gmail.com, Iran. Email: Kianoosh.jafari@Gmail.com

Jundishapur Journal of Natural Pharmaceutical Products:Vol. 3, issue 1; 39-44
Published online:Nov 30, 2008
Article type:Research Article
Received:Dec 22, 1970
Accepted:Feb 22, 1970
How to Cite:Mehri D, Monsef-Esfahani H, Gharibzadeh S, Jafari K, Faghihi M. EFFECTS OF BLACK TEA EXTRACT AND ITS THEARUBIGINS ON WHOLE GUT TRANSIT TIME IN MICE: INVOLVEMENT OF 5-HT3 RECEPTORS. Jundishapur J Nat Pharm Prod. 2008;3(1):. doi:

Abstract

Tea is the most popular beverage in the world. In the recent decades therapeutic effects of various type of tea drinking has been revealed in many studies. The purpose of this study was to evaluate the effects of the black tea extract (BTE) and its major polyphenolic pigments thearubigins (TRs) on whole gut transit time in mice by use of carmine marker. BTE of Iranian tea was prepared and its polyphenolic pigment TRs extracted by Liquid- liquid partition method. BTE (1.5%, 3%, 4.5%, 6%, and 10%) and extracted TRs (30 mg/kg, 40mg/kg, 50mg/kg, 60 mg/kg, 70mg/kg, and 100mg/kg) were gavaged to the fasted mice to measuring the whole gut transit time. Results showed BTE (3%, 4.5%, 6 %,) and TRs (40mg/kg, 50mg/kg, 60 mg/kg, 70mg/kg) significantly decreased the whole gut transit time dose dependant manner. For determination of serotonergic system involvement as a major neurotransmitter system in transit time alteration caused by BTE and TRs, ondansetron (3mg/kg, i.p) was used.Acquired data showed that 5-HT3 antagonist blocked accelerating effects of BTE and TRs. Based on the results BTE and TRs could be regarded as gut accelerator movement dose dependant manner. Moreover, it was concluded that these effects at least partially involved with serotonergic system via   5-HT3 receptors.

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© 2008, Author(s). This open-access article is available under the Creative Commons Attribution 4.0 (CC BY 4.0) International License (https://creativecommons.org/licenses/by/4.0/), which allows for unrestricted use, distribution, and reproduction in any medium, provided that the original work is properly cited.

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