Evidence map›Paper›PMID 30531845›Full record

ArticleHypertension research : official journal of the Japanese Society of Hypertension2019

The exaggerated salt-sensitive response in hypertensive transgenic rats (TGR mRen-2) fostered by a normotensive female.

Pavel Svitok, Zuzana Husková, Lenka Červenková, Soňa Kikerlová, Zdenka Vaňourková, Lenka Sedláková, Šárka Vacková, Hana Šutovska, Michal Zeman, Libor Kopkan

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Article in Hypertension research : official journal of the Japanese Society of Hypertension, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
1.1field-weighted citation impact, top 17% 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

2 citing papers in PubMed, 6 citations in OpenAlex.

  1. Azilsartan causes natriuresis due to its sympatholytic action in kidney disease.Hypertension research : official journal of the Japanese Society of Hypertension · 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

10 authors at 2 institutions in 2 countries.

Pavel SvitokDepartment of Animal Physiology and Ethology, Faculty of Natural Sciences, Comenius University Bratislava, Bratislava, Slovak Republic.
Zuzana HuskováCenter for Experimental Medicine, Institute for Clinical and Experimental Medicine, Prague, Czech Republic.
Lenka ČervenkováCenter for Experimental Medicine, Institute for Clinical and Experimental Medicine, Prague, Czech Republic.
Soňa KikerlováCenter for Experimental Medicine, Institute for Clinical and Experimental Medicine, Prague, Czech Republic.
Zdenka VaňourkováCenter for Experimental Medicine, Institute for Clinical and Experimental Medicine, Prague, Czech Republic.
Lenka SedlákováCenter for Experimental Medicine, Institute for Clinical and Experimental Medicine, Prague, Czech Republic.
Šárka VackováCenter for Experimental Medicine, Institute for Clinical and Experimental Medicine, Prague, Czech Republic.
Hana ŠutovskaDepartment of Animal Physiology and Ethology, Faculty of Natural Sciences, Comenius University Bratislava, Bratislava, Slovak Republic.
Michal ZemanDepartment of Animal Physiology and Ethology, Faculty of Natural Sciences, Comenius University Bratislava, Bratislava, Slovak Republic.
Libor KopkanCenter for Experimental Medicine, Institute for Clinical and Experimental Medicine, Prague, Czech Republic. libor.kopkan@ikem.cz.
Institute of Clinical and Experimental Medicine · CZComenius University Bratislava · SK

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Suboptimal conditions during prenatal and early postnatal development can increase risk of hypertension later in life. We studied consequences of a changed perinatal environment by initiating the cross-fostering of homozygous Ren-2 transgenic rat (TGR) offspring to normotensive, transgene-negative control mothers, and vice versa. We hypothesized that cross-fostering to a normotensive female can attenuate the development of malignant hypertension in TGR offspring (TGRx) and change their salt-sensitive response. Blood pressure (BP) was monitored by the telemetry system under normal salt intake, and BP responses to increased salt intake in the phase of established hypertension. Under normal salt conditions, BP was not markedly different in cross-fostered animals compared with controls. However, BP responses to 2% salt intake led to a stronger BP response in TGRx during the active phase when compared with the control TGR group. The TGRx also exhibited increased albuminuria, lower sodium excretion, and creatinine clearance under higher salt intake compared with control salt intake. Higher salt intake resulted in a significant increase of aldosterone concentrations only in the TGRx group; moreover, TGRx rats exhibited more pronounced renal injury compared with controls. In conclusion, our data indicate that cross-fostering in TGR not only did not attenuate the development of hypertension but, on the contrary, led to the deterioration of BP regulation, particularly due to exaggerated salt sensitivity and sodium retention in TGRx. Results underline the important role of the mother during lactation in postnatal development of the offspring, since these changes reflected different ion content in milk of a particular strain of rats.

Indexed as

Sodium, DietaryAldosteroneAnimalsBlood PressureFemaleHypertensionKidneyMaleRatsRats, TransgenicReninRenin-Angiotensin SystemAldosteroneRen2 protein, ratReninSodium, DietaryCross-fosteringdevelopmental programminghypertensionrenal functionrenin–angiotensin–aldosterone system

Identifiers

PMID30531845
OpenAlexW2904027389

What OpenQuestion holds

Textmetadata
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.