Evidence map›Paper›PMID 41036361›Full record

ArticleOpen veterinary journal2025

The equine placental extract ameliorates renal damage in mice with adenine-induced chronic kidney disease by inhibiting indoxyl sulfate production.

Koji Sugimoto, Junichi Nakamura, Dawei Deng, Eiichi Hirano

Abstract read
In one paragraph

Article in Open veterinary journal, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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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

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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

4 authors.

Koji SugimotoResearch Institute, Japan Bio Products Co., Ltd.; 1-1 Kurume Research Center bldg., Fukuoka, Japan.
Junichi NakamuraResearch Institute, Japan Bio Products Co., Ltd.; 1-1 Kurume Research Center bldg., Fukuoka, Japan.
Dawei DengResearch Institute, Japan Bio Products Co., Ltd.; 1-1 Kurume Research Center bldg., Fukuoka, Japan.
Eiichi HiranoResearch Institute, Japan Bio Products Co., Ltd.; 1-1 Kurume Research Center bldg., Fukuoka, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Indoxyl sulfate (IS) is a dietary metabolite of tryptophan that is produced in the liver. It is a uremic toxin that facilitates the progression of chronic kidney disease (CKD). We previously observed that equine placental extract (ePE) inhibited IS synthesis in an Aim: This study was designed to investigate the effects of ePE on adenine-induced renal failure in mice at the histological and molecular levels to understand the mechanism of action of ePE. Methods: We assessed this effect through biochemical and histological Results: ePE significantly suppressed serum, renal, and hepatic IS production in adenine diet-fed mice by inhibiting IS synthesis. Histological and semi-quantitative analyses using the tubulointerstitial injury index revealed that ePE effectively prevented the increase in adenine-induced mesangial-positive cell area. Additionally, ePE administration significantly suppressed adenine-induced renal fibrosis in mice. Moreover, immunohistochemical analysis demonstrated that ePE administration reduced the accumulation of F4/80-positive macrophages in the interstitial inflammatory infiltrates. Conclusion: These results suggest that ePE ameliorates IS-associated renal injury in adenine diet-fed mice by reducing IS production in the interstitium of the kidneys.

Indexed as

IndicanPlacental ExtractsRenal Insufficiency, ChronicAdenineAnimalsFemaleHorsesKidneyMaleMicePregnancyAdenineIndicanPlacental ExtractsEquine placental extractRenal failureTubulointerstitial injuryUremic toxin

Identifiers

PMID41036361
PMCPMC12483479

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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.