Evidence map›Paper›PMID 29629958›Full record

ArticleAnesthesiology2018

Guanylyl Cyclase A in Both Renal Proximal Tubular and Vascular Endothelial Cells Protects the Kidney against Acute Injury in Rodent Experimental Endotoxemia Models.

Hiroaki Kitamura, Daisuke Nakano, Yoshiharu Sawanobori, Takehiko Asaga, Hideki Yokoi, Motoko Yanagita, Masashi Mukoyama, Takeshi Tokudome, Kenji Kangawa, Gotaro Shirakami and 1 more

Abstract read
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In one paragraph

Article in Anesthesiology, 2018. 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
1.3field-weighted citation impact, top 23% 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, 8 citations in OpenAlex.

  1. Article
  2. Review
  3. Septic acute kidney injury: a review of basic research.Clinical and experimental nephrology · 2020
    Review
  4. Observational
  5. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

11 authors at 3 institutions in 1 country.

Hiroaki KitamuraFrom the Department of Anesthesiology (H.K., Y.S., T.A., G.S.) Department of Pharmacology (D.N., A.N.), Kagawa University, Kagawa Department of Nephrology, Graduate School of Medicine, Kyoto University, Kyoto (J.N., H.Y., M.Y.) Department of Nephrology, Kumamoto University Graduate School of Medical Sciences, Kumamoto (M.M.) Department of Biochemistry, National Cerebral and Cardiovascular Center Research Institute, Osaka (T.T., K.K.), Japan.
Daisuke Nakano
Yoshiharu Sawanobori
Takehiko Asaga
Hideki Yokoi
Motoko Yanagita
Masashi Mukoyama
Takeshi Tokudome
Kenji Kangawa
Gotaro Shirakami
Akira Nishiyama
Kyoto University · JPKagawa University · JPKumamoto University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

what we already know about this topicWHAT THIS ARTICLE TELLS US THAT IS NEW:

background: Natriuretic peptides are used, based on empirical observations, in intensive care units as antioliguric treatments. We hypothesized that natriuretic peptides prevent lipopolysaccharide-induced oliguria by activating guanylyl cyclase A, a receptor for natriuretic peptides, in proximal tubules and endothelial cells.

methodsNormal Sprague-Dawley rats and mice lacking guanylyl cyclase A in either endothelial cells or proximal tubular cells were challenged with lipopolysaccharide and assessed for oliguria and intratubular flow rate by intravital imaging with multiphoton microscopy.

resultsRecombinant atrial natriuretic peptide efficiently improved urine volume without changing blood pressure after lipopolysaccharide challenge in rats (urine volume at 4 h, lipopolysaccharide: 0.6 ± 0.3 ml · kg · h; lipopolysaccharide + fluid resuscitation: 4.6 ± 2.0 ml · kg · h; lipopolysaccharide + fluid resuscitation + atrial natriuretic peptide: 9.0 ± 4.8 ml · kg · h; mean ± SD; n = 5 per group). Lipopolysaccharide decreased glomerular filtration rate and slowed intraproximal tubular flow rate, as measured by in vivo imaging. Fluid resuscitation restored glomerular filtration rate but not tubular flow rate. Adding atrial natriuretic peptide to fluid resuscitation improved both glomerular filtration rate and tubular flow rate. Mice lacking guanylyl cyclase A in either proximal tubules or endothelium demonstrated less improvement of tubular flow rate when treated with atrial natriuretic peptide, compared with control mice. Deletion of endothelial, but not proximal tubular, guanylyl cyclase A augmented the reduction of glomerular filtration rate by lipopolysaccharide.

conclusionsBoth endogenous and exogenous natriuretic peptides prevent lipopolysaccharide-induced oliguria by activating guanylyl cyclase A in proximal tubules and endothelial cells.

Indexed as

Acute Kidney InjuryAnimalsAtrial Natriuretic FactorDisease Models, AnimalEndothelial CellsEndotoxemiaEnzyme ActivationHumansInfusions, IntravenousKidney Tubules, ProximalLipopolysaccharidesMiceMice, KnockoutRatsRats, Sprague-DawleyReceptors, Atrial Natriuretic FactorAtrial Natriuretic Factoratrial natriuretic factor receptor ALipopolysaccharidesReceptors, Atrial Natriuretic Factor

Identifiers

PMID29629958
OpenAlexW2796372605

What OpenQuestion holds

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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.