Evidence map›Paper›PMID 36313818›Full record

ArticleJournal of diabetes research2022

The Molecular Effects of SGLT2i Empagliflozin on the Autophagy Pathway in Diabetes Mellitus Type 2 and Its Complications.

Ranin Saad, Hagar Tadmor, Offir Ertracht, Nakhoul Nakhoul, Farid Nakhoul, Farber Evgeny, Shaul Atar

Open access · goldAbstract read
In one paragraph

Article in Journal of diabetes research, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed, 1 pooled it
1.3field-weighted citation impact, top 18% 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

9 citing papers in PubMed, 1 synthesis or guideline pooled it, 10 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Article
  4. Review
  5. Article
  6. Acute Hyperglycemia-Induced Injury in Myocardial Infarction.International journal of molecular sciences · 2024
    Review
  7. Review
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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

7 authors at 3 institutions in 1 country.

Ranin SaadDiabetes & Metabolism Lab, Baruch Padeh Poriya Medical Center, Israel.
Hagar TadmorDiabetes & Metabolism Lab, Baruch Padeh Poriya Medical Center, Israel.
Offir ErtrachtCardiovascular Laboratory, Medical Research Institute, Galilee Medical Center, Nahariya, Israel.
Nakhoul NakhoulThe Ophthalmology, Israel.
Farid NakhoulCardiovascular Laboratory, Medical Research Institute, Galilee Medical Center, Nahariya, Israel.ORCID https://orcid.org/0000-0001-8657-1530
Farber EvgenyDiabetes & Metabolism Lab, Baruch Padeh Poriya Medical Center, Israel.
Shaul AtarCardiovascular Laboratory, Medical Research Institute, Galilee Medical Center, Nahariya, Israel.
Poriya Medical Center · ILBar-Ilan University · ILWestern Galilee Hospital · IL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Type 2 diabetes mellitus (T2DM), especially hyperglycemia, is associated with increased glucose cell toxicity and oxidative stress that can lead to irreversible damage in the kidney such as diabetic nephropathy (DN). Autophagy plays a key role in the degradation of damaged intracellular proteins in order to maintain intracellular homeostasis and cell integrity. The disturbance of autophagy is involved in the pathogenesis of diabetic nephropathy. We aim to investigate the molecular effect of sodium-glucose transporter 2 inhibitor (SGLT2i) on the expression of ATG5 and its downstream collaborator LC3-II in diabetic nice model. Results: Histological and Western blot analyses reveal decrease ATG5, LC3-II, and fibronectin levels at renal specimens taken from DM mice. EMPA treatment reduced T2DM mice body weight and blood glucose and increased urine glucose. Further, it upregulated all of the abovementioned proteins. Conclusions: Hyperglycemia reduces LC3-II and ATG5 protein levels which contribute to deficiencies in the autophagy process, with development and progression of DN. SGLT2i significantly reduces progression of DN and onset of end-stage renal disease in T2DM patients, probably through its effect on autophagy.

Indexed as

Diabetes Mellitus, Type 2Diabetic NephropathiesHyperglycemiaSodium-Glucose Transporter 2 InhibitorsAnimalsAutophagyBenzhydryl CompoundsBlood GlucoseFibronectinsGlucosidesMaleMiceMice, Inbred C57BLBenzhydryl CompoundsBlood GlucoseempagliflozinFibronectinsGlucosidesSodium-Glucose Transporter 2 Inhibitors

Identifiers

PMID36313818
PMCPMC9605841
OpenAlexW4306841809

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.