Evidence map›Paper›PMID 35840638›Full record

ArticleScientific reports2022

Thiosulfate sulfurtransferase prevents hyperglycemic damage to the zebrafish pronephros in an experimental model for diabetes.

Zayana M Al-Dahmani, Xiaogang Li, Lucas M Wiggenhauser, Hannes Ott, Paul D Kruithof, Sergey Lunev, Fernando A Batista, Yang Luo, Amalia M Dolga, Nicholas M Morton and 3 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
2.7field-weighted citation impact, top 10% 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

5 citing papers in PubMed, 8 citations in OpenAlex.

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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

13 authors at 4 institutions in 3 countries.

Zayana M Al-DahmaniDepartment of Pharmacy and Drug Design, University of Groningen, Groningen, The Netherlands.
Xiaogang LiDepartment of Vascular Biology and Tumor Angiogenesis, European Center for Angioscience (ECAS), Medical Faculty Mannheim, Heidelberg University, 68167, Mannheim, Germany.
Lucas M WiggenhauserDepartment of Vascular Biology and Tumor Angiogenesis, European Center for Angioscience (ECAS), Medical Faculty Mannheim, Heidelberg University, 68167, Mannheim, Germany.
Hannes OttDepartment of Vascular Biology and Tumor Angiogenesis, European Center for Angioscience (ECAS), Medical Faculty Mannheim, Heidelberg University, 68167, Mannheim, Germany.
Paul D KruithofDepartment of Pharmacy and Drug Design, University of Groningen, Groningen, The Netherlands.
Sergey LunevDepartment of Pharmacy and Drug Design, University of Groningen, Groningen, The Netherlands.
Fernando A BatistaDepartment of Pharmacy and Drug Design, University of Groningen, Groningen, The Netherlands.
Yang LuoDepartment of Pharmacy, Molecular Pharmacology, University of Groningen, Groningen, The Netherlands.
Amalia M DolgaDepartment of Pharmacy, Molecular Pharmacology, University of Groningen, Groningen, The Netherlands.
Nicholas M MortonCentre for Cardiovascular Science, The Queen's Medical Research Institute, University of Edinburgh, Edinburgh, UK.
Matthew R GrovesDepartment of Pharmacy and Drug Design, University of Groningen, Groningen, The Netherlands. m.r.groves@rug.nl.ORCID http://orcid.org/0000-0001-9859-5177
Jens KrollDepartment of Vascular Biology and Tumor Angiogenesis, European Center for Angioscience (ECAS), Medical Faculty Mannheim, Heidelberg University, 68167, Mannheim, Germany.
Harry van GoorDepartment of Pathology and Medical Biology, University Medical Center Groningen, Groningen, The Netherlands. h.van.goor@umcg.nl.
University of Groningen · NLHeidelberg University · DEUniversity Medical Center Groningen · NLThe Queen's Medical Research Institute · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Thiosulfate sulfurtransferase (TST, EC 2.8.1.1), also known as Rhodanese, was initially discovered as a cyanide detoxification enzyme. However, it was recently also found to be a genetic predictor of resistance to obesity-related type 2 diabetes. Diabetes type 2 is characterized by progressive loss of adequate β-cell insulin secretion and onset of insulin resistance with increased insulin demand, which contributes to the development of hyperglycemia. Diabetic complications have been replicated in adult hyperglycemic zebrafish, including retinopathy, nephropathy, impaired wound healing, metabolic memory, and sensory axonal degeneration. Pancreatic and duodenal homeobox 1 (Pdx1) is a key component in pancreas development and mature beta cell function and survival. Pdx1 knockdown or knockout in zebrafish induces hyperglycemia and is accompanied by organ alterations similar to clinical diabetic retinopathy and diabetic nephropathy. Here we show that pdx1-knockdown zebrafish embryos and larvae survived after incubation with thiosulfate and no obvious morphological alterations were observed. Importantly, incubation with hTST and thiosulfate rescued the hyperglycemic phenotype in pdx1-knockdown zebrafish pronephros. Activation of the mitochondrial TST pathway might be a promising option for therapeutic intervention in diabetes and its organ complications.

Indexed as

Diabetes Mellitus, Type 2HyperglycemiaPronephrosAnimalsModels, TheoreticalThiosulfatesThiosulfate SulfurtransferaseZebrafishThiosulfatesThiosulfate Sulfurtransferase

Identifiers

PMID35840638
PMCPMC9287301
OpenAlexW4285492710

What OpenQuestion holds

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LicenceCC BY
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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.