Evidence map›Paper›PMID 39857655›Full record

ArticleBiomedicines2024

Angiotensin IV Receptors in the Rat Prefrontal Cortex: Neuronal Expression and NMDA Inhibition.

Zsolt Tamás Papp, Polett Ribiczey, Erzsébet Kató, Zsuzsanna E Tóth, Zoltán V Varga, Zoltán Giricz, Adrienn Hanuska, Mahmoud Al-Khrasani, Ákos Zsembery, Tibor Zelles and 2 more

Abstract read
In one paragraph

Article in Biomedicines, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
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

2 citing papers in PubMed.

  1. Review
  2. GPCR Sense Communication Among Interaction Nematodes with Other Organisms.International journal of molecular sciences · 2025
    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

12 authors.

Zsolt Tamás PappDepartment of Oral Biology, Semmelweis University, H-1089 Budapest, Hungary.
Polett RibiczeyDepartment of Oral Biology, Semmelweis University, H-1089 Budapest, Hungary.
Erzsébet KatóDepartment of Pharmacology and Pharmacotherapy, Semmelweis University, H-1089 Budapest, Hungary.ORCID 0000-0001-5786-0405
Zsuzsanna E TóthLaboratory of Neuroendocrinology and In Situ Hybridization, Department of Anatomy, Histology and Embryology, Semmelweis University, H-1094 Budapest, Hungary.ORCID 0000-0002-0628-1320
Zoltán V VargaDepartment of Pharmacology and Pharmacotherapy, Semmelweis University, H-1089 Budapest, Hungary.
Zoltán GiriczDepartment of Pharmacology and Pharmacotherapy, Semmelweis University, H-1089 Budapest, Hungary.ORCID 0000-0003-2036-8665
Adrienn HanuskaDepartment of Oral Biology, Semmelweis University, H-1089 Budapest, Hungary.
Mahmoud Al-KhrasaniDepartment of Pharmacology and Pharmacotherapy, Semmelweis University, H-1089 Budapest, Hungary.ORCID 0000-0001-8488-3266
Ákos ZsemberyDepartment of Oral Biology, Semmelweis University, H-1089 Budapest, Hungary.
Tibor ZellesDepartment of Oral Biology, Semmelweis University, H-1089 Budapest, Hungary.ORCID 0000-0002-0357-0469
Laszlo G HarsingDepartment of Pharmacology and Pharmacotherapy, Semmelweis University, H-1089 Budapest, Hungary.
László KölesDepartment of Oral Biology, Semmelweis University, H-1089 Budapest, Hungary.

Funding

National Research, Development, and Innovation Fund (Hungary) TKP2021-EGA-23National Research, Development, and Innovation Fund (Hungary) TKP2021-EGA-25National Research, Development, and Innovation Office of Hungary NKFI K 146086National Research, Development, and Innovation Office of Hungary OTKA-K128875
6 · The paper itself

Abstract

backgroundN-methyl-D-aspartate type glutamate receptors (NMDARs) are fundamental to neuronal physiology and pathophysiology. The prefrontal cortex (PFC), a key region for cognitive function, is heavily implicated in neuropsychiatric disorders, positioning the modulation of its glutamatergic neurotransmission as a promising therapeutic target. Our recently published findings indicate that AT

methodsImmunohistochemistry and whole-cell patch-clamp techniques were used to map the cell-type-specific localization of AT4R, identical to insulin-regulated aminopeptidase (IRAP), and to investigate the modulatory effects of Ang IV on NMDAR function in layer V pyramidal cells of the rat PFC.

resultsAT4R/IRAP expression was detected in pyramidal cells and GABAergic interneurons, but not in microglia or astrocytes, in layer V of the PFC in 9-12-day-old and 6-month-old rats. NMDA (30 μM) induced stable inward cation currents, significantly inhibited by Ang IV (1 nM-1 µM) in a subset of pyramidal neurons. This inhibition was reproduced by the IRAP inhibitor LVVYP-H7 (10-100 nM). Synaptic isolation of pyramidal neurons did not affect the Ang IV-mediated inhibition of NMDA currents.

conclusionsAng IV/IRAP-mediated inhibition of NMDA currents in layer V pyramidal neurons of the PFC may represent a way of regulating cognitive functions and thus a potential pharmacological target for cognitive impairments and related neuropsychiatric disorders.

Indexed as

AT4 angiotensin receptorinsulin-regulated aminopeptidaseneuromodulationN-methyl-D-aspartate receptorprefrontal cortexrenin–angiotensin system

Identifiers

PMID39857655
PMCPMC11760436

What Socratic holds

Textmetadata
LicenceCC BY
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 Socratic graph.