Evidence map›Paper›PMID 28369933›Full record

ArticleJournal of cellular physiology2017

Sphingolipids metabolism in the salivary glands of rats with obesity and streptozotocin induced diabetes.

Marta Garbowska, Bartłomiej Łukaszuk, Agnieszka Mikłosz, Igor Wróblewski, Krzysztof Kurek, Lucyna Ostrowska, Adrian Chabowski, Małgorzata Żendzian-Piotrowska, Anna Zalewska

Open access · hybridAbstract readComparative Study
In one paragraph

Article in Journal of cellular physiology, 2017. 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
0.7field-weighted citation impact, top 32% 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, 10 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

9 authors at 1 institution in 1 country.

Marta GarbowskaDepartment of Hygiene, Epidemiology and Ergonomics, Medical University of Bialystok, Bialystok, Poland.
Bartłomiej ŁukaszukDepartment of Physiology, Medical University of Bialystok, Bialystok, Poland.ORCID http://orcid.org/0000-0002-4954-3431
Agnieszka MikłoszDepartment of Physiology, Medical University of Bialystok, Bialystok, Poland.
Igor WróblewskiDepartment of Gastroenterology and Internal Medicine, Medical University of Bialystok, Bialystok, Poland.
Krzysztof KurekDepartment of Gastroenterology and Internal Medicine, Medical University of Bialystok, Bialystok, Poland.
Lucyna OstrowskaDepartment of Conservative Dentistry, Medical University of Bialystok, Bialystok, Poland.
Adrian ChabowskiDepartment of Physiology, Medical University of Bialystok, Bialystok, Poland.
Małgorzata Żendzian-PiotrowskaDepartment of Hygiene, Epidemiology and Ergonomics, Medical University of Bialystok, Bialystok, Poland.
Anna ZalewskaDepartment of Conservative Dentistry, Medical University of Bialystok, Bialystok, Poland.
Medical University of Białystok · PL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Diabetes is considered a major public health problem affecting millions of individuals worldwide. Remarkably, scientific reports regarding salivary glands sphingolipid metabolism in diabetes are virtually non-existent. This is odd given the well-established link between the both in other tissues (e.g., skeletal muscles, liver) and the key role of these glands in oral health preservation. The aim of this paper is to examine sphingolipids metabolism in the salivary glands in (pre)diabetes (evoked by high fat diet feeding or streptozotocin). Wistar rats were allocated into three groups: control, HFD-, or STZ-diabetes. The content of major sphingolipid classes in the parotid (PSG) and submandibular (SMSG) glands was assessed via chromatography. Additionally, Western blot analyses were employed for the evaluation of key sphingolipid signaling pathway enzyme levels. No changes in ceramide content in the PSG were found, whereas an increase in ceramide concentration for SMSG of the STZ group was observed. This was accompanied by an elevation in SPT1 level. Probably also sphingomyelin hydrolysis was increased in the SMSG of the STZ-diabetic rats, since we observed a significant drop in the amount of SM. PSG and SMSG respond differently to (pre)diabetes, with clearer pattern presented by the later gland. An activation of sphingomyelin signaling pathway was observed in the course of STZ-diabetes, that is, metabolic condition with rapid onset/progression. Whereas, chronic HFD lead to an inhibition of sphingomyelin signaling pathway in the salivary glands (manifested in an inhibition of ceramide de novo synthesis and accumulation of S1P).

Indexed as

StreptozocinAnimalsCeramidesDiabetes Mellitus, ExperimentalDiabetes Mellitus, Type 1Diet, High-FatInsulin ResistanceLysophospholipidsMaleObesityParotid GlandPhosphotransferases (Alcohol Group Acceptor)Rats, WistarSignal TransductionSphingolipidsSphingomyelin PhosphodiesteraseCeramidesLysophospholipidsPhosphotransferases (Alcohol Group Acceptor)SphingolipidsSphingomyelin PhosphodiesteraseSphingosinesphingosine 1-phosphateSphingosine KinaseSphingosine N-AcyltransferaseStreptozocinceramideinsulin resistancesalivary glandssphingolipidstype 1 diabetes

Identifiers

PMID28369933
PMCPMC5518447
OpenAlexW2597589157

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.