Evidence map›Paper›PMID 41872523›Full record

ArticleJournal of molecular histology2026

Development of metabolic syndrome by increasingly fructose-enriched water in Wistar rats.

Youssef S'hih, Ibrahim Hinad, Loubna Mrabet, Hicham Bouasria, Fatiha Grina, Niranjan Koirala, Abdechahid Loukili, Moulay Laarbi Ouahidi

Abstract read
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In one paragraph

Article in Journal of molecular histology, 2026. 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
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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.

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.

Youssef S'hihLaboratory of Biology and Health, Department of Life Sciences, Faculty of Sciences, Ibn Tofail University, Kenitra, Morocco. youssef.shih@uit.ac.ma.ORCID http://orcid.org/0000-0003-4601-3125
Ibrahim HinadLaboratory of Biology and Health, Department of Life Sciences, Faculty of Sciences, Ibn Tofail University, Kenitra, Morocco.ORCID http://orcid.org/0000-0003-3047-594X
Loubna MrabetLaboratory of Multidisciplinary Research in Science, Technology and Society, Higher School of Technology, Sultane Moulay Slimane University, Khenifra, Morocco.ORCID http://orcid.org/0009-0003-6793-0851
Hicham BouasriaLaboratory of Biotechnology, Bio-resources and Bioinformatics, Higher School of Technology, Sultane Moulay Slimane University, Khenifra, Morocco.ORCID http://orcid.org/0009-0006-1815-4544
Fatiha GrinaLaboratory of Biochemistry & Neuroscience, Applied Biochemistry and Toxicology Team, Faculty of Sciences and Technology, Hassan 1st University, Settat, Morocco.ORCID http://orcid.org/0000-0002-2904-5216
Niranjan KoiralaNepal Academy of Science and Technology, Specialized Research Centre, Pokhara, Gandaki, Nepal.ORCID http://orcid.org/0000-0002-7777-1191
Abdechahid LoukiliLaboratory of scientific research and pedagogical innovation, Regional Centre for Education and Training, Khemisset, RABAT-SALE-KENITRA, Morocco.ORCID http://orcid.org/0000-0001-8071-4860
Moulay Laarbi OuahidiLaboratory of Biology and Health, Department of Life Sciences, Faculty of Sciences, Ibn Tofail University, Kenitra, Morocco.ORCID http://orcid.org/0009-0005-8751-8279

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Several studies have shown that excessive fructose consumption increases the risk of developing metabolic syndrome (MS), which can lead to diabetes mellitus. This study aimed to evaluate the metabolic and histological abnormalities accompanying MS induced by progressive high fructose diet (HFr) in Wistar rats. Twelve Wistar rats were used, divided into two groups (n = 6) (NC and HFr). They were fed a HFr with daily administration of increasingly higher doses of fructose solutions (dose 1 = 20% from week 1 to 4, dose 2 = 25% from week 5 to 8 and dose 3 = 30% from week 9 to 12 ), during which body weight and blood glucose were measured, while an oral glucose tolerance test (OGTT) was performed, it's glucose, triglyceride, and total cholesterol concentrations were determined, and pancreatic, liver, and kidney tissues were studied at the end of the experiment. Daily administration of increasingly high doses of fructose caused body weight increase, manifested by a highly significant difference in body weight, a metabolic abnormality, differences in fasting blood glucose (hyperglycaemia), plasma concentration of glucose, glucose intolerance, and by a very significant increase of total cholesterol and triglycerides levels in blood (hyperlipidaemia) between HFr and NC groups of rats. Histopathological study showed a slight swelling of the hepatocytes and a narrowing of the blood sinusoids, as well as an inflammatory infiltration of the portal space in the hepatic section of HFr group, no morphological alterations, necrosis, or steatosis in the pancreatic and renal sections of HFr group of rats. A twelve-week HFr diet can cause some abnormalities in the liver tissue, in carbohydrate and lipid metabolism in Wistar rats without damaging their pancreas and kidneys, which may be explained by the fact that metabolic abnormalities can precede histological lesions.

Indexed as

FructoseMetabolic SyndromeWaterAnimalsBlood GlucoseBody WeightCholesterolGlucose Tolerance TestKidneyLiverMaleRatsRats, WistarTriglyceridesBlood GlucoseCholesterolFructoseTriglyceridesWaterHigh fructose (HFr)HyperglycaemiaHyperlipidaemiaMetabolic syndromes (MS)Wistar rats

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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.