Evidence map›Paper›PMID 30106981›Full record

ArticlePloS one2018

FGF21 increases water intake, urine output and blood pressure in rats.

Tod Turner, Xian Chen, Matthew Zahner, Alan Opsahl, George DeMarco, Magalie Boucher, Bryan Goodwin, Mylène Perreault

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed, 1 pooled it
1.9field-weighted citation impact, top 13% 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

22 citing papers in PubMed, 1 synthesis or guideline pooled it, 34 citations in OpenAlex.

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  20. Metal-induced nephrotoxicity to diabetic and non-diabetic Wistar rats.Environmental science and pollution research international · 2019
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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.

Tod TurnerInternal Medicine Research Unit, Pfizer Inc, Cambridge, Massachusetts, United States of America.
Xian ChenComparative Medicine, Pfizer Inc, Cambridge, Massachusetts, United States of America.
Matthew ZahnerDrug Safety Research and Development (DSRD), Pfizer Inc, Groton, Connecticut, United States of America.
Alan OpsahlDrug Safety Research and Development (DSRD), Pfizer Inc, Groton, Connecticut, United States of America.
George DeMarcoComparative Medicine, Pfizer Inc, Cambridge, Massachusetts, United States of America.
Magalie BoucherDrug Safety Research and Development (DSRD), Pfizer Inc, Cambridge, Massachusetts, United States of America.
Bryan GoodwinInternal Medicine Research Unit, Pfizer Inc, Cambridge, Massachusetts, United States of America.
Mylène PerreaultInternal Medicine Research Unit, Pfizer Inc, Cambridge, Massachusetts, United States of America.ORCID 0000-0002-3644-6413
Pfizer (United States) · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Fibroblast growth factor 21 (FGF21) is a hormone secreted by the liver in response to metabolic stress. In addition to its well-characterized effects on energy homeostasis, FGF21 has been shown to increase water intake in animals. In this study, we sought to further explore the effects of FGF21 on fluid homeostasis in rats. A single dose of a long-acting FGF21 analog, PF-05231023, significantly increased water consumption, which was accompanied by an elevation in urine output that appeared prior to a significant change in water intake. We observed that FGF21 rapidly and significantly increased heart rate and blood pressure in telemeter-implanted rats, before changes in urine output and water intake were observed. Our data suggest that sympathetic activation may contribute to the pathogenesis by which FGF21 increases blood pressure as the baroreceptor unloading induced reflex tachycardia was significantly elevated in FGF21-treated animals. However, FGF21 was still capable of causing hypertension in animals in which approximately 40% of the sympathetic post-ganglionic neurons were ablated. Our data suggest that FGF21-induced water intake is in fact secondary to diuresis, which we propose to be a compensatory mechanism engaged to alleviate the acute hypertension caused by FGF21.

Indexed as

AnimalsAntibodies, Monoclonal, HumanizedBaroreflexBlood PressureCardiovascular AgentsDelayed-Action PreparationsDiuresisDiureticsDrinkingDrinking WaterElectrolytesFibroblast Growth FactorsGuanethidineHeart RateHypertensionKidneyAntibodies, Monoclonal, HumanizedCardiovascular AgentsDelayed-Action PreparationsDiureticsDrinking WaterElectrolytesfibroblast growth factor 21Fibroblast Growth FactorsGuanethidinePF-05231023

Identifiers

PMID30106981
PMCPMC6091943
OpenAlexW2886713357

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.