Evidence map›Paper›PMID 27599802›Full record

ArticleBMC complementary and alternative medicine2016

A dietary strategy for the management of artemether-lumefantrine-induced cardiovascular and renal toxicity.

Isaac Julius Asiedu-Gyekye, Mahmood Abdulai Seidu, Banga Benoit N'guessan, Samuel Frimpong-Manso, Joseph Edusei Sarkodie, Samuel Adjei, Schevadnazy Kutu, Joseph Osei-Little, Alexander Kwadwo Nyarko, Philip Debrah

Open access · goldAbstract read
In one paragraph

Article in BMC complementary and alternative medicine, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
1.7field-weighted citation impact, top 14% 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

1 citing paper in PubMed, 6 citations in OpenAlex.

  1. Reproductive Toxicity ofJournal of toxicology · 2021
    Article
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

10 authors at 3 institutions in 1 country.

Isaac Julius Asiedu-GyekyeDepartment of Pharmacology and Toxicology, College of Health Sciences, University of Ghana School of Pharmacy, P. O. Box LG 43, Legon, Ghana. asiedugyekye@yahoo.co.uk.
Mahmood Abdulai SeiduDepartment of Medical Laboratory Sciences, College of Health Sciences, School of Biomedical and Allied Health Sciences, Legon, Ghana.
Banga Benoit N'guessanDepartment of Pharmacology and Toxicology, College of Health Sciences, University of Ghana School of Pharmacy, P. O. Box LG 43, Legon, Ghana.
Samuel Frimpong-MansoDepartment of Pharmaceutical Chemistry, College of Health Sciences, University of Ghana School of Pharmacy, Legon, Ghana.
Joseph Edusei SarkodieDepartment of Pharmacognosy and Herbal Medicine, College of Health Sciences, University of Ghana School of Pharmacy, Legon, Accra, Ghana.
Samuel AdjeiDepartment of animal experimentation unit, College of Health Sciences, Noguchi Memorial Institute for Medical Research, Legon, Accra, Ghana.
Schevadnazy KutuDepartment of Pharmacology and Toxicology, College of Health Sciences, University of Ghana School of Pharmacy, P. O. Box LG 43, Legon, Ghana.
Joseph Osei-LittleDepartment of Pharmacology and Toxicology, College of Health Sciences, University of Ghana School of Pharmacy, P. O. Box LG 43, Legon, Ghana.
Alexander Kwadwo NyarkoDepartment of Pharmacology and Toxicology, College of Health Sciences, University of Ghana School of Pharmacy, P. O. Box LG 43, Legon, Ghana.
Philip DebrahDepartment of Pharmaceutics and Microbiology, College of Health Sciences, University of Ghana School of Pharmacy, Legon, Ghana.
University of Ghana · GHNoguchi Memorial Institute for Medical Research · GHUniversity of Health and Allied Sciences · GH

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundUnsweetened natural cocoa has antimalarial properties. Unsweetened natural cocoa powder (UNCP), obtained as a result of the removal of cocoa butter from a cocoa bean protects against malaria episodes. Cocoa powder, which is prepared after removal of the cocoa butter, contains about 1.9 % theobromine and 0.21 % caffeine. Concomitant consumption of cocoa and artemether/lumefantrine (A/L) is a common practice in Ghana, West Africa. This study seeks to determine the elemental composition of UNCP and its protective effect on the heart and kidney against (A/L) administration.

methodsEnergy dispersive x-ray fluorescence spectroscopy was used to detect the quality and quantity of the elemental composition in UNCP. Thereafter, 30 nonmalarious male guinea pigs were divided into five groups of six animals each. One group was administered with 75 mg/kg body weight A/L only and another group distilled water (control group). The rest received 300 mg/kg, 900 mg/kg and 1500 mg/kg body weight UNCP for 14 days orally and A/L for the last 3 days (ie day 11 to day 14). Biochemical and histopathological examinations were carried out after euthanisation of the animals.

resultsA total of thirty-eight (38) micro and macro elements were detected with the ED-XRF. Macro elements like sodium (Na), magnesium (Mg), aluminium (Al), phosphorus (P), chlorine (Cl), potassium (K), calcium (Ca), manganese (Mn) and iron (Fe) and micro elements like chromium (Cr), copper (Cu), zinc (Zn), arsenic (As), and lead (Pb) were identified and evaluated. Biochemical analysis revealed increases in HDL levels (p>0.05) while there were decreases in LDL levels (p>0.05), creatine kinase and AST levels (P<0.05) in animals that received UNCP compared to A/L only administered group. Urea levels reduced significantly by 53 % (p<0.05) in group that received 1500 mg/kg UNCP. Histopathological examinations of the heart and kidney buttressed the protective effects of cocoa administration.

conclusionThe percentage of recommended daily allowance of UNCP for chromium is 3750 % for men and 5250 % for women while % RDA for copper corresponds to 103.6 % in both sexes. UNCP proved to possess cardioprotective and renoprotective potential during artemether-lumefantrine administration.

Indexed as

AnimalsAntimalarialsArtemether, Lumefantrine Drug CombinationArtemisininsCacaoCreatine KinaseDrug CombinationsDrug-Related Side Effects and Adverse ReactionsEthanolaminesFluorenesGuinea PigsKidneyLipidsMalePlant PreparationsAntimalarialsArtemether, Lumefantrine Drug CombinationArtemisininsCreatine KinaseDrug CombinationsEthanolaminesFluorenesLipidsPlant PreparationsArtemether-LumefantrineCocoaEDXRFHistopathologyLipid profileRenal function test

Identifiers

PMID27599802
PMCPMC5012013
OpenAlexW2518021631

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.