Cargando…

Repeated dose studies with pure Epigallocatechin-3-gallate demonstrated dose and route dependant hepatotoxicity with associated dyslipidemia

EGCG (Epigallocatechin-3-gallate) is the major active principle catechin found in green tea. Skepticism regarding the safety of consuming EGCG is gaining attention, despite the fact that it is widely being touted for its potential health benefits, including anti-cancer properties. The lack of scient...

Descripción completa

Detalles Bibliográficos
Autores principales: Ramachandran, Balaji, Jayavelu, Subramani, Murhekar, Kanchan, Rajkumar, Thangarajan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5615837/
https://www.ncbi.nlm.nih.gov/pubmed/28959554
http://dx.doi.org/10.1016/j.toxrep.2016.03.001
_version_ 1783266676139098112
author Ramachandran, Balaji
Jayavelu, Subramani
Murhekar, Kanchan
Rajkumar, Thangarajan
author_facet Ramachandran, Balaji
Jayavelu, Subramani
Murhekar, Kanchan
Rajkumar, Thangarajan
author_sort Ramachandran, Balaji
collection PubMed
description EGCG (Epigallocatechin-3-gallate) is the major active principle catechin found in green tea. Skepticism regarding the safety of consuming EGCG is gaining attention, despite the fact that it is widely being touted for its potential health benefits, including anti-cancer properties. The lack of scientific data on safe dose levels of pure EGCG is of concern, while EGCG has been commonly studied as a component of GTE (Green tea extract) and not as a single active constituent. This study has been carried out to estimate the maximum tolerated non-toxic dose of pure EGCG and to identify the treatment related risk factors. In a fourteen day consecutive treatment, two different administration modalities were compared, offering an improved [i.p (intraperitoneal)] and limited [p.o (oral)] bioavailability. A trend of dose and route dependant hepatotoxicity was observed particularly with i.p treatment and EGCG increased serum lipid profile in parallel to hepatotoxicity. Fourteen day tolerable dose of EGCG was established as 21.1 mg/kg for i.p and 67.8 mg/kg for p.o. We also observed that, EGCG induced effects by both treatment routes are reversible, subsequent to an observation period for further fourteen days after cessation of treatment. It was demonstrated that the severity of EGCG induced toxicity appears to be a function of dose, route of administration and period of treatment.
format Online
Article
Text
id pubmed-5615837
institution National Center for Biotechnology Information
language English
publishDate 2016
publisher Elsevier
record_format MEDLINE/PubMed
spelling pubmed-56158372017-09-28 Repeated dose studies with pure Epigallocatechin-3-gallate demonstrated dose and route dependant hepatotoxicity with associated dyslipidemia Ramachandran, Balaji Jayavelu, Subramani Murhekar, Kanchan Rajkumar, Thangarajan Toxicol Rep Article EGCG (Epigallocatechin-3-gallate) is the major active principle catechin found in green tea. Skepticism regarding the safety of consuming EGCG is gaining attention, despite the fact that it is widely being touted for its potential health benefits, including anti-cancer properties. The lack of scientific data on safe dose levels of pure EGCG is of concern, while EGCG has been commonly studied as a component of GTE (Green tea extract) and not as a single active constituent. This study has been carried out to estimate the maximum tolerated non-toxic dose of pure EGCG and to identify the treatment related risk factors. In a fourteen day consecutive treatment, two different administration modalities were compared, offering an improved [i.p (intraperitoneal)] and limited [p.o (oral)] bioavailability. A trend of dose and route dependant hepatotoxicity was observed particularly with i.p treatment and EGCG increased serum lipid profile in parallel to hepatotoxicity. Fourteen day tolerable dose of EGCG was established as 21.1 mg/kg for i.p and 67.8 mg/kg for p.o. We also observed that, EGCG induced effects by both treatment routes are reversible, subsequent to an observation period for further fourteen days after cessation of treatment. It was demonstrated that the severity of EGCG induced toxicity appears to be a function of dose, route of administration and period of treatment. Elsevier 2016-03-05 /pmc/articles/PMC5615837/ /pubmed/28959554 http://dx.doi.org/10.1016/j.toxrep.2016.03.001 Text en © 2016 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Article
Ramachandran, Balaji
Jayavelu, Subramani
Murhekar, Kanchan
Rajkumar, Thangarajan
Repeated dose studies with pure Epigallocatechin-3-gallate demonstrated dose and route dependant hepatotoxicity with associated dyslipidemia
title Repeated dose studies with pure Epigallocatechin-3-gallate demonstrated dose and route dependant hepatotoxicity with associated dyslipidemia
title_full Repeated dose studies with pure Epigallocatechin-3-gallate demonstrated dose and route dependant hepatotoxicity with associated dyslipidemia
title_fullStr Repeated dose studies with pure Epigallocatechin-3-gallate demonstrated dose and route dependant hepatotoxicity with associated dyslipidemia
title_full_unstemmed Repeated dose studies with pure Epigallocatechin-3-gallate demonstrated dose and route dependant hepatotoxicity with associated dyslipidemia
title_short Repeated dose studies with pure Epigallocatechin-3-gallate demonstrated dose and route dependant hepatotoxicity with associated dyslipidemia
title_sort repeated dose studies with pure epigallocatechin-3-gallate demonstrated dose and route dependant hepatotoxicity with associated dyslipidemia
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5615837/
https://www.ncbi.nlm.nih.gov/pubmed/28959554
http://dx.doi.org/10.1016/j.toxrep.2016.03.001
work_keys_str_mv AT ramachandranbalaji repeateddosestudieswithpureepigallocatechin3gallatedemonstrateddoseandroutedependanthepatotoxicitywithassociateddyslipidemia
AT jayavelusubramani repeateddosestudieswithpureepigallocatechin3gallatedemonstrateddoseandroutedependanthepatotoxicitywithassociateddyslipidemia
AT murhekarkanchan repeateddosestudieswithpureepigallocatechin3gallatedemonstrateddoseandroutedependanthepatotoxicitywithassociateddyslipidemia
AT rajkumarthangarajan repeateddosestudieswithpureepigallocatechin3gallatedemonstrateddoseandroutedependanthepatotoxicitywithassociateddyslipidemia