Evidence map›Paper›PMID 8349789›Full record

ArticleThe Journal of clinical investigation1993

Altered renal kallikrein and renin gene expression in nephrotic rats and modulation by converting enzyme inhibition.

F N Hutchison, S K Webster, A A Jaffa

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of clinical investigation, 1993. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact, top 92% 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

1 citing paper in PubMed, 9 citations in OpenAlex.

  1. 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

3 authors at 2 institutions in 1 country.

F N HutchisonDepartment of Internal Medicine, Medical University of South Carolina, Charleston 29425.
S K Webster
A A Jaffa
Medical University of South Carolina · USRalph H. Johnson VA Medical Center · US

Funding

HORMONAL MODULATION OF PROTEINURIA IN DIABETES MELLITUSR01DK043186 · NIDDK · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI HUTCHISON, FLORENCE N. · 1990 to 1994
–
NIDDK NIH HHS DK43186
6 · The paper itself

Abstract

Urinary kallikrein excretion (UKE) is decreased in rats with passive Heymann nephritis (PHN), but increases after converting enzyme inhibition (CEI). Although CEI potentiates bradykinin activity, neither the effect of CEI on kallikrein secretion nor the abnormal renal kallikrein metabolism in PHN has been examined previously. To determine the mechanism by which CEI increases UKE, normal rats and PHN received enalapril, 40 mg/kg per d orally for 4 d. UKE was 85% lower in PHN than in normals and increased in both groups after CEI, although UKE in PHN remained significantly less than in normals. Kallikrein mRNA was significantly lower in PHN compared to normals but not in PHN treated with CEI and did not change in normal rats. Renin mRNA was significantly lower in PHN, and was stimulated by CEI only in normals. Renal kallikrein and renin content were not different and were not altered by CEI. Both kallikrein and renin genes appear to be transcriptionally suppressed in rats with PHN and the depressed kallikrein mRNA levels can be reversed by CEI. The modest increase in UKE despite normalization of kallikrein mRNA after CEI suggests that there is also a posttranscriptional defect in synthesis and/or secretion of kallikrein.

Indexed as

Gene Expression Regulation, EnzymologicAnimalsBase SequenceBlotting, NorthernEnalaprilGlomerulonephritis, MembranousKallikreinsKidneyKineticsMaleMolecular Sequence DataOligonucleotide ProbesRatsRats, Sprague-DawleyReference ValuesReninEnalaprilKallikreinsOligonucleotide ProbesReninRNA, Messenger

Identifiers

PMID8349789
PMCPMC294948
OpenAlexW2013950317

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.