Evidence map›Paper›PMID 27110378›Full record

ArticleBMJ open gastroenterology2016

Fortification of alcoholic beverages (12% v/v) with tea (Camellia sinensis) reduces harmful effects of alcohol ingestion and metabolism in mouse model.

S O Ochanda, K Rashid, J K Wanyoko, M Ngotho, A K Faraj, C A Onyango, F N Wachira, D N Maranga

Open access · goldAbstract read
In one paragraph

Article in BMJ open gastroenterology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
0.5field-weighted citation impact, top 33% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed, 6 citations in OpenAlex.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors at 7 institutions in 4 countries.

S O OchandaTea and Health Unit, Tea Processing and value addition Programme, Kenya Agricultural and Livestock Research Organization, Tea Research Institute (KALRO-TRI), Kericho, Kenya; Department of Dairy and Food Science and Technology, Egerton University, Egerton, Kenya.
K RashidUniversity of Cologne , Cologne , Germany.
J K WanyokoTea and Health Unit, Tea Processing and value addition Programme , Kenya Agricultural and Livestock Research Organization, Tea Research Institute (KALRO-TRI) , Kericho , Kenya.
M NgothoMount Kenya University , Thika , Kenya.
A K FarajDepartment of Dairy and Food Science and Technology , Egerton University , Egerton , Kenya.
C A OnyangoTaita Taveta University College , Voi , Kenya.
F N WachiraAssociation for Strengthening Agricultural Research in Eastern and Central Africa (ASARECA) , Entebbe , Uganda.
D N MarangaDepartment of Animal Sciences , National Museums of Kenya, Institute of Primate Research (NMK-IPR) , Nairobi , Kenya.
Kenya Agricultural and Livestock Research Organization · KEAssociation for Strengthening Agricultural Research in Eastern and Central Africa · UGEgerton University · KEGandhara University · PKInstitute of Primate Research · KEMount Kenya University · KEUniversity of Cologne · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAn animal model was used to study the health benefits inherent in tea fortified alcoholic beverages fed to laboratory mice.

objectivesAn investigation of the effects of tea fortified alcoholic beverages 12% alcohol (v/v) on antioxidant capacity and liver dysfunction indicators in white Swiss mice including packed cell volume (PCV), albumin, total protein, alkaline phosphatase (ALP) and glutathione (GSH) was carried out.

methodsPlain, black, green and purple tea fortified alcohols were developed with varying tea concentrations of 1, 2 and 4 g/250 mL in 12% v/v. Control alcoholic beverages without teas were also developed. A permit (number IRC/13/12) was obtained for the animal research from the National Museums of Kenya, Institute of Primate Research prior to the start of the study. Alcoholic beverages were orally administered every 2 days for 4 weeks at 1 mL per mouse, and thereafter animals were euthanised and liver and blood samples harvested for analyses. Assays on body weight (bwt), packed cell volume (PCV) albumin, total protein, ALP and GSH were performed. Results were statistically analysed using GraphPad statistical package and significant differences of means of various treatments determined.

resultsConsumption of tea fortified alcohols significantly decreased (p=0.0001) bwt at 0.32-9.58% and PCV at 5.56-22.75% for all teas. Total protein in serum and liver of mice fed on different tea fortified alcohols ranged between 6.26 and 9.24 g/dL and 2.14 and 4.02 g/dL, respectively. Albumin, ALP and GSH range was 0.92-2.88 µg/L, 314.98-473.80 µg/L and 17.88-28.62 µM, respectively. Fortification of alcoholic beverages lowered liver ALP, replenished antioxidants and increased liver albumin, improving the nutritional status of the mice.

conclusionsThe findings demonstrate tea's hepatoprotective mechanisms against alcohol-induced injury through promotion of endogenous antioxidants. The beneficial effects of tea in the fortified alcoholic beverages could be used to develop safer alcoholic beverages.

Indexed as

ALCOHOLANTIOXIDANTSNUTRITIONAL STATUSOXIDATIVE STRESS

Identifiers

PMID27110378
PMCPMC4838668
OpenAlexW2308326496

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.