Evidence map›Paper›PMID 31491420›Full record

ArticleBrain research2019

Reduced intrinsic excitability of CA1 pyramidal neurons in human immunodeficiency virus (HIV) transgenic rats.

Irina V Sokolova, Attila Szucs, Pietro Paolo Sanna

Abstract read
In one paragraph

Article in Brain research, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Review
  2. Article
  3. Review
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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.

Irina V SokolovaThe Scripps Research Institute, Department of Immunology and Microbiology, 10550 North Torrey Pines Road, La Jolla, CA 92037-1000, United States.
Attila SzucsThe Scripps Research Institute, Department of Immunology and Microbiology, 10550 North Torrey Pines Road, La Jolla, CA 92037-1000, United States; University of California, San Diego, BioCircuits Institute, 9500 Gilman Drive, La Jolla, CA 92039-0328, United States; MTA-ELTE-NAP B Neuronal Cell Biology Research Group, Eötvös Lóránd University, Budapest, Hungary.
Pietro Paolo SannaThe Scripps Research Institute, Department of Immunology and Microbiology, 10550 North Torrey Pines Road, La Jolla, CA 92037-1000, United States. Electronic address: psanna@scripps.edu.

Funding

UC San Diego Clinical and Translational Research InstituteUL1TR001442 · NCATS · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI FIRESTEIN, GARY S, HOGARTH, MICHAEL · 2015 to 2024
$88.3M
VirologyP30AI036214 · NIAID · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI David Mitchell Smith · 1994 to 2026
$78.4M
Systems biology of HIV, methamphetamine and antiretrovirals interactionsR01DA041750 · NIDA · SCRIPPS RESEARCH INSTITUTE, THE · PI KARAN, CHARLES, RISSMAN, ROBERT · 2016 to 2020
$4.4M
Identification of small molecules for neurological complications of HIV and substance abuse comorbidityR01DA046204 · NIDA · SCRIPPS RESEARCH INSTITUTE, THE · PI SANNA, PIETRO P, SPICER, TIMOTHY PATRICK · 2018 to 2022
$4.2M
Systems biology of RNA Modifications in HIV/AIDS and Substance Use DisordersR01DA046170 · NIDA · SCRIPPS RESEARCH INSTITUTE, THE · PI SANNA, PIETRO P · 2018 to 2022
$3.8M
Neural substrates of opiate-HIV interactions.R01DA043268 · NIDA · SCRIPPS RESEARCH INSTITUTE, THE · PI SANNA, PIETRO P · 2016 to 2020
$2.9M
NCATS NIH HHS UL1 TR001442NIAID NIH HHS P30 AI036214NIDA NIH HHS R01 DA041750NIDA NIH HHS R01 DA043268NIDA NIH HHS R01 DA046170NIDA NIH HHS R01 DA046204
6 · The paper itself

Abstract

The hippocampus is involved in key neuronal circuits that underlie cognition, memory, and anxiety, and it is increasingly recognized as a vulnerable structure that contributes to the pathogenesis of HIV-associated neurocognitive disorder (HAND). However, the mechanisms responsible for hippocampal dysfunction in neuroHIV remain unknown. The present study used HIV transgenic (Tg) rats and patch-clamp electrophysiological techniques to study the effects of the chronic low-level expression of HIV proteins on hippocampal CA1 pyramidal neurons. The dorsal and ventral areas of the hippocampus are involved in different neurocircuits and thus were evaluated separately. We found a significant decrease in the intrinsic excitability of CA1 neurons in the dorsal hippocampus in HIV Tg rats by comparing neuronal spiking induced by current step injections and by dynamic clamp to simulate neuronal spiking activity. The decrease in excitability in the dorsal hippocampus was accompanied by a higher rate of excitatory postsynaptic currents (EPSCs), whereas CA1 pyramidal neurons in the ventral hippocampus in HIV Tg rats had higher EPSC amplitudes. We also observed a reduction of hyperpolarization-activated nonspecific cationic current (I

Indexed as

AIDS Dementia ComplexAnimalsCA1 Region, HippocampalExcitatory Postsynaptic PotentialsFemaleHippocampusHIVHIV InfectionsMemoryNeuronsPatch-Clamp TechniquesPyramidal CellsRatsRats, TransgenicRats, WistarDementiaNeurocognitive disordersneuroHIVNeuronal excitabilitySynaptodendriticTransgenic

Identifiers

PMID31491420
PMCPMC6939992

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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 OpenQuestion graph.