Evidence map›Paper›PMID 21846804›Full record

ArticleEndocrinology2011

Inhibition of renin release by arachidonic acid metabolites, 12(s)-HPETE and 12-HETE: role of TRPV1 channels.

Chaoqin Xie, Donna H Wang

Open access · bronzeAbstract read
In one paragraph

Article in Endocrinology, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed, 1 pooled it
1.2field-weighted citation impact, top 20% 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

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

  1. Pooled it
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  10. Emerging targets in lipid-based therapy.Biochemical pharmacology · 2013
    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

2 authors at 1 institution in 1 country.

Chaoqin XieDepartment of Medicine, the Neuroscience Program, Michigan State University, East Lansing, Michigan 48824, USA.
Donna H Wang
Michigan State University · US

Funding

Vanilloid Sensitive Sensory Nerves and Salt SensitivityR01HL073287 · NHLBI · MICHIGAN STATE UNIVERSITY · PI WANG, DONNA H · 2004 to 2011
$2.7M
Molecular Sensing of Sodium Homeostasis: Anandamide RoleR01DK067620 · NIDDK · MICHIGAN STATE UNIVERSITY · PI WANG, DONNA H · 2005 to 2009
$1.4M
RENAL ANGIOTENSIN II RECEPTOR AND SODIUM INTAKER01HL057853 · NHLBI · UNIVERSITY OF TEXAS MEDICAL BR GALVESTON · PI WANG, DONNA H · 1998 to 2007
$1.1M
NHLBI NIH HHS HL-57853NHLBI NIH HHS HL-73287NHLBI NIH HHS R01 HL057853NHLBI NIH HHS R01 HL073287NIDDK NIH HHS DK67620NIDDK NIH HHS R01 DK067620
6 · The paper itself

Abstract

We test the hypothesis that 12-hydroperoxyeicosatetraenoic acid (12(s)-HPETE) and 12-hydroxyeicosatetraenoic acid (12-HETE) perfused into the renal pelvis increase afferent renal nerve activity (ARNA) and suppress renin release in rats fed a low-salt (LS) diet via activation of the transient receptor potential vanilloid type 1 (TRPV1) expressed in renal sensory nerves. 12(s)-HPETE or 12-HETE given into the left renal pelvis dose-dependently increased ARNA, which was abolished by AMG9810, a selective TRPV1 antagonist, or by RP67580, a selective neurokinin 1 receptor antagonist, in normal salt or LS-treated rats. 12(s)-HPETE, 12-HETE, or substance P perfused into the left renal pelvis suppressed plasma angiotensin I (Ang I) levels in LS rats, which was abolished by AMG9810 or attenuated by ipsilateral renal denervation (RD). 12(s)-HPETE or 12-HETE increased release of substance P and calcitonin gene-related peptide from the ipsilateral kidney, which was abolished by AMG9810 but not RP67580, RD, or RP67580 plus RD. Immunofluorescence staining showed that TRPV1-positive nerve fibers located in the renal cortex, medulla, and pelvis, and that the sympathetic nerve marker, neuropeptide Y, but not neurokinin 1 receptors expressed in the juxtaglomerular region colocalized with renin. Thus, our data show that 12(s)-HPETE and 12-HETE enhance ARNA and substance P/calcitonin gene-related peptide release but suppress renin activity in LS rats, and these effects are abolished when TRPV1 is blocked. These results indicate that TRPV1 mediates 12(s)-HPETE and 12-HETE action in the kidney in such a way that dysfunction in TRPV1 may lead to disintegrated regulation of renin and renal function.

Indexed as

Renin Inhibitors12-Hydroxy-5,8,10,14-eicosatetraenoic AcidAngiotensin IAnimalsArachidonic AcidLeukotrienesMaleRatsRats, WistarReceptors, Neurokinin-1ReninTRPV Cation Channels12-HPETE12-Hydroxy-5,8,10,14-eicosatetraenoic AcidAngiotensin IArachidonic AcidLeukotrienesReceptors, Neurokinin-1ReninRenin InhibitorsTrpv1 protein, ratTRPV Cation Channels

Identifiers

PMID21846804
PMCPMC3176648
OpenAlexW2053149254

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

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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.