Evidence map›Paper›PMID 28660012›Full record

ArticleWorld journal of hepatology2017

Angiotensin II or epinephrine hemodynamic and metabolic responses in the liver of L-NAME induced hypertension and spontaneous hypertensive rats.

Debora Conte Kimura, Marcia Regina Nagaoka, Durval Rosa Borges, Maria Kouyoumdjian

Open access · diamondAbstract read
In one paragraph

Article in World journal of hepatology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
0.4field-weighted citation impact, top 35% 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

0 citing papers in PubMed, 4 citations in OpenAlex.

No citing paper in PubMed yet.

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

4 authors at 1 institution in 1 country.

Debora Conte KimuraDebora Conte Kimura, Maria Kouyoumdjian, Department of Biochemistry, Federal University of São Paulo, Experimental Hepatology Laboratory, São Paulo 04023-900, Brazil.
Marcia Regina NagaokaDebora Conte Kimura, Maria Kouyoumdjian, Department of Biochemistry, Federal University of São Paulo, Experimental Hepatology Laboratory, São Paulo 04023-900, Brazil.
Durval Rosa BorgesDebora Conte Kimura, Maria Kouyoumdjian, Department of Biochemistry, Federal University of São Paulo, Experimental Hepatology Laboratory, São Paulo 04023-900, Brazil.
Maria KouyoumdjianDebora Conte Kimura, Maria Kouyoumdjian, Department of Biochemistry, Federal University of São Paulo, Experimental Hepatology Laboratory, São Paulo 04023-900, Brazil.
Universidade Federal de Santa Maria · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

aimTo study hepatic vasoconstriction and glucose release induced by angiotensin (Ang)II or Epi in rats with pharmacological hypertension and spontaneously hypertensive rat (SHR).

methodsIsolated liver perfusion was performed following portal vein and vena cava cannulation; AngII or epinephrine (Epi) was injected

resultsThe portal hypertensive response (PHR) and the glucose release induced by AngII of L-NAME were similar to normal rats (WIS). On the other hand, the PHR induced by Epi in L-NAME was higher whereas the glucose release was lower compared to WIS. Despite the similar glycogen content, glucose release induced by AngII was lower in SHR compared to Wistar-Kyoto rats although both PHR and glucose release induced by Epi in were similar.

conclusionAngII and Epi responses are altered in different ways in these hypertension models. Our results suggest that inhibition of NO production seems to be involved in the hepatic effects induced by Epi but not by AngII; the diminished glucose release induced by AngII in SHR is not related to glycogen content.

Indexed as

Angiotensin IIEpinephrineGlucoseLiver perfusionL-NAMESpontaneously hypertensive rat

Identifiers

PMID28660012
PMCPMC5474724
OpenAlexW2626632585

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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.