Evidence map›Paper›PMID 27412955›Full record

ArticleExperimental biology and medicine (Maywood, N.J.)2017

Formononetin exhibits anti-hyperglycemic activity in alloxan-induced type 1 diabetic mice.

Guizhen Qiu, Wei Tian, Mei Huan, Jinlong Chen, Haitao Fu

Open access · greenAbstract read
In one paragraph

Article in Experimental biology and medicine (Maywood, N.J.), 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
4.7field-weighted citation impact, top 5% 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

20 citing papers in PubMed, 48 citations in OpenAlex.

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  12. Frontiers in pharmacology · 2020
    Review
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  16. International journal of molecular sciences · 2018
    Article
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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

5 authors at 1 institution in 1 country.

Guizhen Qiu1 Department of Health, Linyi People's Hospital of Shandong University, Linyi 276003, Shandong Province, China.
Wei Tian2 Department of Nursing, Linyi Oncosurgical Hospital, Linyi 276002, Shandong Province, China.
Mei Huan2 Department of Nursing, Linyi Oncosurgical Hospital, Linyi 276002, Shandong Province, China.
Jinlong Chen3 Department of Ophthalmology, Chinese Medicine Hospital of Linshu County, Linshu 276700, Shandong Province, China.
Haitao Fu4 Department of Ophthalmology, Linyi People's Hospital of Shandong University, Linyi 276003, Shandong Province, China.
Linyi People's Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The aim of this study was to investigate the anti-hyperglycemic activity and mechanism of formononetin in alloxan-induced type 1 diabetic mice by determining its effect on some diabetes-related indices as described below. Body weight, fasting blood glucose, hepatic glycogen, serum insulin, and serum glucagon were determined by electronic scales, glucometer, and ELISA kits. Fas, Caspase-3, pancreatic and duodenal homeobox-1 , insulin receptor substrate 2, glucokinase and glucose transporter 2, mRNA and proteins levels in pancreas tissue, and glucokinase and glucose-6-phosphatase mRNA, and proteins levels in liver tissue were detected by fluorogenic quantitative-polymerase chain reaction and Western blot assays. The results indicated that formononetin (5, 10, and 20 mg/kg; oral administration) reversed the alloxan-induced increase of some indices (fasting blood glucose level and Fas and Caspase-3 mRNA and proteins levels in pancreas tissue) and reduction of some indices (body weight gain, oral glucose tolerance, insulin activity, hepatic glycogen level, pancreatic and duodenal homeobox-1, insulin receptor substrate 2, glucokinase and glucose transporter 2, mRNA and proteins levels in pancreas tissue, and glucokinase mRNA and protein levels in liver tissue). The glucagon level and glucose-6-phosphatase mRNA and protein levels in liver tissue were not affected by the drugs administration. In conclusion, formononetin exhibited anti-hyperglycemic activity in alloxan-induced type 1 diabetic mice by inhibiting islet B cell apoptosis and promoting islet B cell regeneration, insulin secretion, hepatic glycogen synthesis, and hepatic glycolysis.

Indexed as

AlloxanAnimalsBlood GlucoseBody WeightDiabetes Mellitus, ExperimentalDiabetes Mellitus, Type 1Disease Models, AnimalGlucagonHypoglycemic AgentsInsulinIslets of LangerhansIsoflavonesLiverLiver GlycogenMaleMiceAlloxanBlood GlucoseformononetinGlucagonHypoglycemic AgentsInsulinIsoflavonesLiver Glycogenanti-hyperglycemic activityFormononetinglycolysisinsulin secretionislet B cell apoptosis and regenerationtype 1 diabetes

Identifiers

PMID27412955
PMCPMC5167112
OpenAlexW2462339939

What OpenQuestion holds

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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.