Evidence map›Paper›PMID 31885479›Full record

ArticleSaudi pharmaceutical journal : SPJ : the official publication of the Saudi Pharmaceutical Society2019

Natural substance rutin versus standard drug atorvastatin in a treatment of metabolic syndrome-like condition.

Dominika Micháliková, Barbara Tyukos Kaprinay, Boris Lipták, Karol Švík, Lukáš Slovák, Ružena Sotníková, Vladimír Knezl, Zdenka Gaspárová

Open access · hybridAbstract read
In one paragraph

Article in Saudi pharmaceutical journal : SPJ : the official publication of the Saudi Pharmaceutical Society, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.8field-weighted citation impact, top 25% 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

3 citing papers in PubMed, 9 citations in OpenAlex.

  1. Phytochemical Composition ofAdvances in pharmacological and pharmaceutical sciences · 2025
    Review
  2. Prevention of Metabolic Syndrome by Phytochemicals and Vitamin D.International journal of molecular sciences · 2023
    Review
  3. 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

8 authors at 4 institutions in 1 country.

Dominika MichálikováCentre of Experimental Medicine, Institute of Experimental Pharmacology and Toxicology, Slovak Academy of Sciences, Dúbravská cesta 9, Bratislava, Slovakia.
Barbara Tyukos KaprinayCentre of Experimental Medicine, Institute of Experimental Pharmacology and Toxicology, Slovak Academy of Sciences, Dúbravská cesta 9, Bratislava, Slovakia.
Boris LiptákCentre of Experimental Medicine, Institute of Experimental Pharmacology and Toxicology, Slovak Academy of Sciences, Dúbravská cesta 9, Bratislava, Slovakia.
Karol ŠvíkCentre of Experimental Medicine, Institute of Experimental Pharmacology and Toxicology, Slovak Academy of Sciences, Dúbravská cesta 9, Bratislava, Slovakia.
Lukáš SlovákCentre of Experimental Medicine, Institute of Experimental Pharmacology and Toxicology, Slovak Academy of Sciences, Dúbravská cesta 9, Bratislava, Slovakia.
Ružena SotníkováCentre of Experimental Medicine, Institute of Experimental Pharmacology and Toxicology, Slovak Academy of Sciences, Dúbravská cesta 9, Bratislava, Slovakia.
Vladimír KnezlCentre of Experimental Medicine, Institute of Experimental Pharmacology and Toxicology, Slovak Academy of Sciences, Dúbravská cesta 9, Bratislava, Slovakia.
Zdenka GaspárováCentre of Experimental Medicine, Institute of Experimental Pharmacology and Toxicology, Slovak Academy of Sciences, Dúbravská cesta 9, Bratislava, Slovakia.
Institute of Experimental Pharmacology and Toxicology of the Slovak Academy of Sciences · SKSlovak Academy of Sciences · SKCentre of Experimental Medicine of the Slovak Academy of Sciences · SKComenius University Bratislava · SK

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMetabolic syndrome is a cluster of metabolic risk factors. The clear causes of its development are not known yet and there is no comprehensive treatment of this disease. There is a trend to use natural substances in the treatment of various diseases, but their effects need to be well explored. We decided to test effect of rutin compared to the effect of the standard drug atorvastatin.

methodsAs a model of metabolic syndrome we used males of hypertriacylglycerolemic rats in combination with high-fat-high-fructose diet. Rutin (100 mg/kg) and atorvastatin (50 mg/kg) were administered orally daily for 5 weeks.

resultsWe determined biochemical parameters from blood: HDL-cholesterol, LDL-cholesterol, total cholesterol, triacylglycerols. Relaxation and contraction response of aorta was measured to determine vessel dysfunctions and possible predisposition to cardiovascular disease. The negative influence on cognitive functions could be associated with the development of metabolic cognitive syndrome. Therefore we aimed to monitor spatial memory by Morris water maze test. Both rutin and atorvastatin had a tendency to decrease levels of serum triacylglycerols, but only atorvastatin significantly reduced levels od LDL-cholesterol and increased HDL-cholesterol levels. Both compounds significantly reduced the phenylephrine-induced contractile response of the aorta and improved the relaxation response. Further, treated animals learned better compared to untreated rats in the Morris water maze.

conclusionBased on our results we can assume that atorvastatin and rutin had positive effect on spatial memory and vessel reactivity. Atorvastatin optimized lipid profile of blood serum.

Indexed as

ACh, acetylcholineAD, Alzheimer diseaseANOVA, one-way analysis of varianceAortaAtorvastatincAMP, cyclic adenosine monophosphateDyslipidemiaeNOS, endothelial NO synthaseGlc, glucoseGLUT-4, glucose transporter 4HDL-cholesterol, high density lipoprotein cholesterolHFFD, high-fat-high-fructose dietHMG-CoA, β-hydroxy β-methylglutaryl-CoAHTG-HFFD-A, hypertriacylglycerolemic rat with high-fat-high-fructose diet with atorvastatinHTG-HFFD, hypertriacylglycerolemic rat with high-fat-high-fructose dietHTG-HFFD-R, hypertriacylglycerolemic rat with high-fat-high-fructose diet with rutinHTG, hypertriacylglycerolemicIRS-1, insulin receptor substrate 1LDL-cholesterol, low density lipoprotein cholesterolMetabolic syndromeMetS, metabolic syndromeMWM, Morris water mazeNOS, NO synthaseOOGTT, oral glucose tolerance testPKC, proteinkinase CPXR, pregnane X receptorROS, reactive oxygen speciesRutinSEM, standard error of the meanSpatial memoryTG, triacylglycerols

Identifiers

PMID31885479
PMCPMC6921224
OpenAlexW2979416836

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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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.