Evidence map›Paper›PMID 23707905›Full record

ArticleEuropean journal of pharmacology2013

Effects of SGLT2 selective inhibitor ipragliflozin on hyperglycemia, hyperlipidemia, hepatic steatosis, oxidative stress, inflammation, and obesity in type 2 diabetic mice.

Atsuo Tahara, Eiji Kurosaki, Masanori Yokono, Daisuke Yamajuku, Rumi Kihara, Yuka Hayashizaki, Toshiyuki Takasu, Masakazu Imamura, Qun Li, Hiroshi Tomiyama and 4 more

3 registry-linked trialsAbstract read
PubMed Publisher
In one paragraph

Article in European journal of pharmacology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 3 registered trials, which are not on this map. Cited by 157 papers, 8 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
157citing papers in PubMed, 8 pooled it
9.4field-weighted citation impact, top 2% 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.

NCT02964715 phase4unknown statusstarted 2016, after this paper: background citation

The Effect of Empagliflozin on NAFLD in Asian Patients With Type 2 Diabetes

Ran2016Enrolled25Registered outcomes17Posted comparisons0ConditionsNAFLD, Type2 DiabetesArmsempagliflozin
Open the trial in the graph
NCT05459701 phase4completedstarted 2022, after this paper: background citation

The Hepato-protective Effect of Dapagliflozin in Type 2 Diabetes Mellitus Patients (T2DM) With Nonalcoholic Fatty Liver Disease (NAFLD)

Ran2022Enrolled50Registered outcomes3Posted comparisons0ConditionsNonalcoholic Fatty Liver Disease, Type 2 DiabetesArmsDapagliflozin 10mg Tab, Placebo
PMID 26914659PMID 26963613other papers from this trial
Open the trial in the graph
NCT02304081 phase4completednot on this mapstarted 2015, after this paper: background citation

Effect of Saxagliptin in Addition to Dapagliflozin and Metformin on Insulin Resistance, Islet Cell Dysfunction, and Metabolic Control in Subjects With Type 2 Diabetes Mellitus on Previous Metformin Treatment

TypeinterventionalSponsorProf. Dr. Thomas ForstRan2015 to 2016Enrolled64ConditionsType2 Diabetes MellitusArmsSaxagliptin, Placebo for Saxagliptin
3 · Its place in the literature

Who cites it

157 citing papers in PubMed, 8 syntheses or guidelines pooled it, 307 citations in OpenAlex.

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97 more citing papers are in PubMed but not listed here.

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

14 authors at 2 institutions in 2 countries.

Atsuo TaharaDrug Discovery Research, Astellas Pharma Inc., Ibaraki, Japan. atsuo.tahara@jp.astellas.com
Eiji Kurosaki
Masanori Yokono
Daisuke Yamajuku
Rumi Kihara
Yuka Hayashizaki
Toshiyuki Takasu
Masakazu Imamura
Qun Li
Hiroshi Tomiyama
Yoshinori Kobayashi
Atsushi Noda
Masao Sasamata
Masayuki Shibasaki
Astellas Pharma (Japan) · JPAstellas Pharma (Netherlands) · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The sodium-glucose cotransporter 2 (SGLT2) is responsible for most glucose reabsorption in the kidney and has been proposed as a novel therapeutic target for the treatment of type 2 diabetes. In the present study, the therapeutic effects of SGLT2 selective inhibitor ipragliflozin were examined in high-fat diet and streptozotocin-nicotinamide-induced type 2 diabetic mice which exhibit impaired insulin secretion, insulin resistance, hyperlipidemia, hepatic steatosis, and obesity. Single administration of ipragliflozin dose-dependently increased urinary glucose excretion, reduced blood glucose and plasma insulin levels, and improved glucose intolerance. Four-week repeated administration of ipragliflozin improved not only glucose tolerance, hyperglycemia, and hyperinsulinemia but also impaired insulin secretion, hyperlipidemia, hepatic steatosis, and obesity with a concomitant increase in urinary glucose excretion. In addition, ipragliflozin reduced plasma and liver levels of oxidative stress biomarkers (thiobarbituric acid reactive substances and protein carbonyl) and inflammatory markers (interleukin 6, tumor necrosis factor α, monocyte chemotactic protein-1, and c-reactive protein), and improved liver injury as assessed by plasma levels of aminotransferases. These results demonstrate that SGLT2 selective inhibitor ipragliflozin improves not only hyperglycemia but also diabetes/obesity-associated metabolic abnormalities in type 2 diabetic mice and suggest that ipragliflozin may be useful in treating type 2 diabetes with metabolic syndrome.

Indexed as

Sodium-Glucose Transporter 2 InhibitorsAnimalsBlood GlucoseDiabetes Mellitus, Type 2Diet, High-FatFatty LiverGlucose Tolerance TestGlucosidesGlycosuriaHyperglycemiaHyperlipidemiasHypoglycemic AgentsInflammationInsulinInsulin ResistanceInsulin SecretionBlood GlucoseGlucosidesHypoglycemic AgentsInsulinipragliflozinSodium-Glucose Transporter 2 InhibitorsThiophenesDiabetesHyperglycemiaIpragliflozinSGLT2Urinary glucose excretion

Identifiers

PMID23707905
OpenAlexW2095574383

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

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.