Evidence map›Paper›PMID 28429785›Full record

ArticleScientific reports2017

Natriuretic peptide receptor guanylyl cyclase-A pathway counteracts glomerular injury evoked by aldosterone through p38 mitogen-activated protein kinase inhibition.

Yukiko Kato, Kiyoshi Mori, Masato Kasahara, Keisuke Osaki, Akira Ishii, Keita P Mori, Naohiro Toda, Shoko Ohno, Takashige Kuwabara, Takeshi Tokudome and 7 more

Abstract read
In one paragraph

Article in Scientific reports, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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

16 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Article
  3. Article
  4. Article
  5. Blood Pressure Management Strategies and Podocyte Health.American journal of hypertension · 2025
    Review
  6. Article
  7. Article
  8. Current and Emerging Classes of Pharmacological Agents for the Management of Hypertension.American journal of cardiovascular drugs : drugs, devices, and other interventions · 2022
    Review
  9. Osteocrin, a bone-derived humoral factor, exerts a renoprotective role in ischemia-reperfusion injury in mice.Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association · 2022
    Article
  10. Article
  11. Novel therapeutics for the treatment of hypertension and its associated complications: peptide- and nonpeptide-based strategies.Hypertension research : official journal of the Japanese Society of Hypertension · 2021
    Review
  12. Review
  13. Article
  14. Review
  15. Article
  16. Review
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

17 authors.

Yukiko KatoDepartment of Nephrology, Graduate School of Medicine, Kyoto University, Kyoto, Japan.
Kiyoshi MoriSchool of Pharmaceutical Sciences, University of Shizuoka, Shizuoka, Japan.
Masato KasaharaInstitute for Clinical and Translational Science, Nara Medical University Hospital, Kashihara, Japan.
Keisuke OsakiDepartment of Nephrology, Graduate School of Medicine, Kyoto University, Kyoto, Japan.
Akira IshiiDepartment of Nephrology, Graduate School of Medicine, Kyoto University, Kyoto, Japan.
Keita P MoriDepartment of Nephrology, Graduate School of Medicine, Kyoto University, Kyoto, Japan.
Naohiro TodaDepartment of Nephrology, Graduate School of Medicine, Kyoto University, Kyoto, Japan.
Shoko OhnoDepartment of Nephrology, Graduate School of Medicine, Kyoto University, Kyoto, Japan.
Takashige KuwabaraDepartment of Nephrology, Graduate School of Medicine, Kyoto University, Kyoto, Japan.
Takeshi TokudomeDepartment of Biochemistry, National Cerebral and Cardiovascular Research Institute, Osaka, Japan.
Ichiro KishimotoDepartment of Endocrinology and Diabetes, Toyooka Public Hospital, Toyooka, Japan.
Moin A SaleemChildren's Renal Unit, Bristol Royal Hospital for Children, University of Bristol, Bristol, UK.
Taiji MatsusakaDepartment of Molecular Life Sciences, Tokai University School of Medicine, Isehara, Japan.
Kazuwa NakaoMedical Innovation Center, Graduate School of Medicine, Kyoto University, Kyoto, Japan.
Masashi MukoyamaDepartment of Nephrology, Graduate School of Medicine, Kyoto University, Kyoto, Japan.
Motoko YanagitaDepartment of Nephrology, Graduate School of Medicine, Kyoto University, Kyoto, Japan.
Hideki YokoiDepartment of Nephrology, Graduate School of Medicine, Kyoto University, Kyoto, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Guanylyl cyclase-A (GC-A) signaling, a natriuretic peptide receptor, exerts renoprotective effects by stimulating natriuresis and reducing blood pressure. Previously we demonstrated massive albuminuria with hypertension in uninephrectomized, aldosterone-infused, and high salt-fed (ALDO) systemic GC-A KO mice with enhanced phosphorylation of p38 mitogen-activated protein kinase (MAPK) in podocytes. In the present study, we examined the interaction between p38 MAPK and GC-A signaling. The administration of FR167653, p38 MAPK inhibitor, reduced systolic blood pressure (SBP), urinary albumin excretion, segmental sclerosis, podocyte injury, and apoptosis. To further investigate the local action of natriuretic peptide and p38 MAPK in podocytes, we generated podocyte-specific (pod) GC-A conditional KO (cKO) mice. ALDO pod GC-A cKO mice demonstrated increased urinary albumin excretion with marked mesangial expansion, podocyte injury and apoptosis, but without blood pressure elevation. FR167653 also suppressed urinary albumin excretion without reducing SBP. Finally, we revealed that atrial natriuretic peptide increased phosphorylation of MAPK phosphatase-1 (MKP-1) concomitant with inhibited phosphorylation of p38 MAPK in response to MAPK kinase 3 activation, thereby resulting in decreased mRNA expression of the apoptosis-related gene, Bax, and Bax/Bcl2 ratio in cultured podocytes. These results indicate that natriuretic peptide exerts a renoprotective effect via inhibiting phosphorylation of p38 MAPK in podocytes.

Indexed as

AlbuminuriaAldosteronePodocytesReceptors, Atrial Natriuretic FactorAnimalsApoptosisMiceMice, KnockoutNatriuretic Peptidesp38 Mitogen-Activated Protein KinasesPyrazolesPyridinesAldosteroneatrial natriuretic factor receptor AFR 167653Natriuretic Peptidesp38 Mitogen-Activated Protein KinasesPyrazolesPyridinesReceptors, Atrial Natriuretic Factor

Identifiers

PMID28429785
PMCPMC5399490

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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.