Evidence map›Paper›PMID 31835675›Full record

ArticleInternational journal of molecular sciences2019

Renal Chemerin Expression is Induced in Models of Hypertensive Nephropathy and Glomerulonephritis and Correlates with Markers of Inflammation and Fibrosis.

Alexander Mocker, Karl F Hilgers, Nada Cordasic, Rainer Wachtveitl, Carlos Menendez-Castro, Joachim Woelfle, Andrea Hartner, Fabian B Fahlbusch

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
2.4field-weighted citation impact, top 11% 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

24 citing papers in PubMed, 32 citations in OpenAlex.

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  17. SPM Receptor Expression and Localization in Irradiated Salivary Glands.The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society · 2021
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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

8 authors at 1 institution in 1 country.

Alexander MockerDepartment of Pediatrics and Adolescent Medicine, University Hospital of Erlangen, 91054 Erlangen, Germany.
Karl F HilgersDepartment of Nephrology and Hypertension, University Hospital of Erlangen, 91054 Erlangen, Germany.
Nada CordasicDepartment of Nephrology and Hypertension, University Hospital of Erlangen, 91054 Erlangen, Germany.
Rainer WachtveitlDepartment of Nephrology and Hypertension, University Hospital of Erlangen, 91054 Erlangen, Germany.
Carlos Menendez-CastroDepartment of Pediatrics and Adolescent Medicine, University Hospital of Erlangen, 91054 Erlangen, Germany.
Joachim WoelfleDepartment of Pediatrics and Adolescent Medicine, University Hospital of Erlangen, 91054 Erlangen, Germany.
Andrea HartnerDepartment of Pediatrics and Adolescent Medicine, University Hospital of Erlangen, 91054 Erlangen, Germany.
Fabian B FahlbuschDepartment of Pediatrics and Adolescent Medicine, University Hospital of Erlangen, 91054 Erlangen, Germany.
Universitätsklinikum Erlangen · DE

Funding

Deutsche Forschungsgemeinschaft / Friedrich-Alexander-University Erlangen-Nürnberg (FAU) within the funding programme Open Access Publishing n/aRobert Pfleger Stiftung n/a
6 · The paper itself

Abstract

Chemerin and its receptor, chemokine-like receptor 1 (CmklR1), are associated with chemotaxis, inflammation, and endothelial function, especially in metabolic syndrome, coronary heart disease, and hypertension. In humans, circulating chemerin levels and renal function show an inverse relation. So far, little is known about the potential role of chemerin in hypertensive nephropathy and renal inflammation. Therefore, we determined systemic and renal chemerin levels in 2-kidney-1-clip (2k1c) hypertensive and Thy1.1 nephritic rats, respectively, to explore the correlation between chemerin and markers of renal inflammation and fibrosis. Immunohistochemistry revealed a model-specific induction of chemerin expression at the corresponding site of renal damage (tubular vs. glomerular). In both models, renal expression of chemerin (RT-PCR, Western blot) was increased and correlated positively with markers of inflammation and fibrosis. In contrast, circulating chemerin levels remained unchanged. Taken together, these findings demonstrate that renal chemerin expression is associated with processes of inflammation and fibrosis-related to renal damage. However, its use as circulating biomarker of renal inflammation seems to be limited in our rat models.

Indexed as

AnimalsBiomarkersChemokinesCollagen Type IVDisease Models, AnimalFibrosisGlomerulonephritisHypertensionHypertension, RenalInflammationKidneyMacrophagesNephritisReceptors, ChemokineRNA, MessengerBiomarkersChemokinesCmklr1 protein, ratCollagen Type IVRarres2 protein, ratReceptors, ChemokineRNA, Messenger2k1c2-kidney-1-clipchemerinCmklR1renal fibrosisrenal inflammationrenal injuryrenovascular hypertensionThy1.1 nephritis

Identifiers

PMID31835675
PMCPMC6941130
OpenAlexW2995834136

What OpenQuestion holds

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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.