Evidence map›Paper›PMID 34129205›Full record

ArticleCurrent medical science2021

Losartan Protects Podocytes against High Glucose-induced Injury by Inhibiting B7-1 Expression.

Hui Gao, Wen-Yan Du, Jing Lin, Shi-Liang Han, Yun-Jing Zhang, Xi-Feng Sun

Abstract read
PubMed Publisher
In one paragraph

Article in Current medical science, 2021. 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
0.6field-weighted citation impact, top 34% 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, 5 citations in OpenAlex.

  1. Therapeutic potential ofFrontiers in pharmacology · 2023
    Article
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

6 authors at 2 institutions in 1 country.

Hui GaoDepartment of Urology, Zibo Central Hospital, Zibo, 255036, China.
Wen-Yan DuDepartment of Science and Education, Zibo Central Hospital, Zibo, 255036, China.
Jing LinDepartment of Cardiology, Shaanxi Provincial People's Hospital, Xi'an, 710068, China.
Shi-Liang HanDepartment of Nephrology, Zibo Central Hospital, Zibo, 255036, China.
Yun-Jing ZhangDepartment of Nephrology, Zibo Central Hospital, Zibo, 255036, China.
Xi-Feng SunDepartment of Nephrology, Zibo Central Hospital, Zibo, 255036, China. sxfgh-1976@163.com.
Central Hospital of Zibo · CNShaanxi Provincial People's Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The role of B7-1 in podocyte injury has received increasing attention. The aim of this study was to investigate whether losartan protects podocytes of patients with diabetic kidney disease (DKD) by regulating B7-1 and the underlying mechanisms. Rats with streptozotocin-induced DKD were treated with losartan for 8 weeks. Biochemical changes in blood and urine were analyzed. Kidneys were isolated for electron microscopy, immunofluorescence, real-time quantitative PCR (RT-PCR), and Western blot analysis. Immortalized mouse podocyte cells were cultured in normal or high glucose medium in the presence or absence of losartan for 48 h, and then the cells were collected for immunofluorescence, PCR, Western blotting and monolayer permeability detection. The phosphatidylinositol 3-kinase (PI3K) 110α subunit and angiotensin II type 1 receptor (AT1R) plasmids were transfected into podocytes, respectively, and then Western blotting was performed to assess the expression of B7-1 protein. The results showed that losartan ameliorated podocyte structure and function in the rat model of DKD, and reduced the expression of B7-1 protein. Overexpression of PI3K 110α subunit in podocytes attenuated the inhibitory effect of losartan on B7-1 expression in high glucose-stimulated podocytes. The expression of B7-1 was significantly increased by overexpression of AT1R and significantly reduced by blocking PI3K 110α subunit. We conclude that losartan protects podocytes against high glucose-induced injury by inhibiting AT1R-mediated B7-1 expression. This effect is dependent on the AT1R-PI3K 110α subunit pathway.

Indexed as

Angiotensin IIAnimalsApoptosisB7-1 AntigenClass I Phosphatidylinositol 3-KinasesDiabetic NephropathiesDisease Models, AnimalGlucoseHumansKidneyLosartanMicePodocytesRatsReceptor, Angiotensin, Type 1StreptozocinAngiotensin IIB7-1 AntigenClass I Phosphatidylinositol 3-KinasesGlucoseLosartanp110delta protein, ratReceptor, Angiotensin, Type 1Streptozocinangiotensin IIB7-1diabetic kidney disease (DKD)losartanPI3K 110α subunitpodocytetype 1 receptor (AT1R)

Identifiers

PMID34129205
OpenAlexW3172188295

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.