Evidence map›Paper›PMID 36826683›Full record

ArticleMolecular biology reports2023

PRE-084 ameliorated kidney injury by reducing endoplasmic reticulum stress in the rat model of adenine-induced chronic kidney disease.

Mohanapriya Kumaran, Madhu Cholenahalli Lingaraju, Vivek Srivastava, Karikalan Mathesh, Kesavan Manickam, Subhashree Parida, Thakur Uttam Singh, Dinesh Kumar

Abstract read
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In one paragraph

Article in Molecular biology reports, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.5field-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

5 citing papers in PubMed, 7 citations in OpenAlex.

  1. Sigma-1 Receptor Activation by Fluvoxamine Ameliorates ER Stress, Synaptic Dysfunction and Behavioral Deficits in a Ketamine Model of Schizophrenia.Journal of neuroimmune pharmacology : the official journal of the Society on NeuroImmune Pharmacology · 2025
    Article
  2. Article
  3. Sigma-1 Receptor as a Novel Therapeutic Target in Diabetic Kidney Disease.International journal of molecular sciences · 2024
    Article
  4. Article
  5. 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

8 authors at 1 institution in 1 country.

Mohanapriya KumaranDivision of Pharmacology & Toxicology, ICAR-Indian Veterinary Research Institute, 243 122, Izatnagar, India.
Madhu Cholenahalli LingarajuDivision of Pharmacology & Toxicology, ICAR-Indian Veterinary Research Institute, 243 122, Izatnagar, India. maddyvet@gmail.com.ORCID http://orcid.org/0000-0002-3266-3701
Vivek SrivastavaDivision of Pharmacology & Toxicology, ICAR-Indian Veterinary Research Institute, 243 122, Izatnagar, India.
Karikalan MatheshCentre for Wildlife Conservation, Management and Disease Surveillance, ICAR-Indian Veterinary Research Institute, 243 122, Izatnagar, India.
Kesavan ManickamDivision of Pharmacology & Toxicology, ICAR-Indian Veterinary Research Institute, 243 122, Izatnagar, India.
Subhashree ParidaDivision of Pharmacology & Toxicology, ICAR-Indian Veterinary Research Institute, 243 122, Izatnagar, India.
Thakur Uttam SinghDivision of Pharmacology & Toxicology, ICAR-Indian Veterinary Research Institute, 243 122, Izatnagar, India.
Dinesh KumarDivision of Pharmacology & Toxicology, ICAR-Indian Veterinary Research Institute, 243 122, Izatnagar, India.
Indian Veterinary Research Institute · IN

Funding

Science and Engineering Research Board, India ECR/2016/001918
6 · The paper itself

Abstract

backgroundEndoplasmic reticulum (ER) stress plays an important role in the development of chronic kidney disease (CKD). Sigma-1 receptors (σ1Rs) are novel chaperone proteins that regulate ER stress. However, effect of σ1R activation on renal ER stress is yet unexplored. So, in the present study we investigated the effects of PRE-084, a σ1R agonist on renal injury and ER stress in the rat model of CKD.

methodsCKD group rats were fed adenine for 28 days and CKD treatment group rats were additionally administered PRE-084 intraperitoneally at 1, 3 and 10 mg/kg body weight dose from Day 22-28. ER stress markers were evaluated using molecular biology techniques such as immunohistochemistry and Western blot.

resultsMarked kidney injury was observed in CKD rats as revealed by biochemical and histological findings. Expression of ER stress proteins such as phosphorylated protein kinase R-like ER kinase (p-PERK), cleaved activating transcription factor-6 (ATF-6f), phosphorylated inositol requiring enzyme1α (p-IRE1α) and caspase-12 were higher in CKD rats. Nevertheless, CKD rats treated with PRE-084 particularly at 10 mg/kg dose showed considerably lesser kidney injury along with higher expression of σ1R and marked reduction of all the ER stress proteins studied.

conclusionResults reveal that PRE-084 likely ameliorated the adenine-induced kidney injury by lowering ER stress through increased σ1R expression.

Indexed as

Protein Serine-Threonine KinasesRenal Insufficiency, ChronicAnimalsApoptosisEndoplasmic Reticulum StressEndoribonucleasesHeat-Shock ProteinsKidneyMorpholinesRats2-(4-morpholino)ethyl-1-phenylcyclohexane-1-carboxylateEndoribonucleasesHeat-Shock ProteinsMorpholinesProtein Serine-Threonine KinasesAdenine-induced nephropathyChronic kidney diseaseEndoplasmic reticulum stressRatsSigma-1 receptor

Identifiers

PMID36826683
OpenAlexW4321749615

What Socratic holds

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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 Socratic graph.