Evidence map›Paper›PMID 26677947›Full record

ArticleNeuropsychopharmacology : official publication of the American College of Neuropsychopharmacology2016

HIV-1 Transgenic Rat Prefrontal Cortex Hyper-Excitability is Enhanced by Cocaine Self-Administration.

Wesley N Wayman, Lihua Chen, Xiu-Ti Hu, T Celeste Napier

Open access · bronzeAbstract read
In one paragraph

Article in Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed
1.4field-weighted citation impact, top 18% 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

36 citing papers in PubMed, 44 citations in OpenAlex.

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  15. CaTranslational psychiatry · 2021
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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

4 authors at 1 institution in 1 country.

Wesley N WaymanDepartment of Pharmacology, Rush University Medical Center, Chicago, IL, USA.
Lihua ChenDepartment of Pharmacology, Rush University Medical Center, Chicago, IL, USA.
Xiu-Ti HuDepartment of Pharmacology, Rush University Medical Center, Chicago, IL, USA.
T Celeste NapierDepartment of Pharmacology, Rush University Medical Center, Chicago, IL, USA.
Rush University Medical Center · US

Funding

DevelopmentalP30AI082151 · NIAID · RUSH UNIVERSITY MEDICAL CENTER · PI CAFFREY, MICHAEL S. · 2009 to 2014
$4.6M
Interactive effects of Meth, HIV and cART on astrocyte/neuron functionR01DA044552 · NIDA · RUSH UNIVERSITY MEDICAL CENTER · PI HU, XIU-TI · 2017 to 2021
$2.9M
Electrophysiological mechanisms of HIV-mediated neuropathogenesisR01NS084817 · NINDS · RUSH UNIVERSITY MEDICAL CENTER · PI HU, XIU-TI · 2013 to 2017
$2.5M
Cortical pathophysiology in cocaine sef-administering HIV-1 transgenic ratsR21DA033882 · NIDA · RUSH UNIVERSITY MEDICAL CENTER · PI HU, XIU-TI, NAPIER, T. CELESTE · 2012 to 2013
$412k
Pathophysiological effects of cocaine/HIV-1 Tat on the medial prefrontal cortexF31DA033206 · NIDA · RUSH UNIVERSITY MEDICAL CENTER · PI WAYMAN, WESLEY N · 2012 to 2014
$127k
NIAID NIH HHS P30 AI082151NIDA NIH HHS F31 DA033206NIDA NIH HHS R01 DA044552NIDA NIH HHS R21 DA033882NINDS NIH HHS R01 NS084817
6 · The paper itself

Abstract

The medial prefrontal cortex (mPFC) is dysregulated in HIV-1-infected humans and the dysregulation is enhanced by cocaine abuse. Understanding mPFC pathophysiology in this comorbid state has been hampered by the dearth of relevant animal models. To help fill this knowledge gap, electrophysiological assessments were made of mPFC pyramidal neurons (PN) from adult male HIV-1 transgenic (Tg) F344 rats (which express seven of the nine HIV-1 toxic proteins) and non-Tg F344 rats that self-administered cocaine for 14 days (COC-SA), as well as saline-yoked controls (SAL-Yoked) and experimentally naive Tg and non-Tg rats. Forebrain slices were harvested and prepared for whole-cell patch-clamp recording, and in treated rats, this occurred after 14-18 days of forced abstinence. Aged-matched rats were used for immunohistochemical detection of the L-channel protein, Cav1.2-α1c. We determined that: (i) the two genotypes acquired the operant task and maintained similar levels of COC-SA, (ii) forced abstinence from COC-SA enhanced mPFC PN excitability in both genotypes, and neurons from Tg rats exhibited the greatest pathophysiology, (iii) neurons from SAL-Yoked Tg rats were more excitable than those from SAL-Yoked non-Tg rats, and in Tg rats (iv) blockade of L-type Ca(2+) channels reduced the enhanced excitability, and (v) Cav1.2-immunoreactivity was increased. These findings provide the first assessment of the mPFC pathophysiology in a rodent model of HIV-1-mediated neuropathology with and without cocaine self-administration. Outcomes reveal an enhanced cortical excitability during chronic exposure to HIV-1 proteins that is excessively exacerbated with cocaine abuse. Such neuropathophysiology may underlie the cognitive dysregulation reported for comorbid humans.

Indexed as

Action PotentialsAnimalsCocaineConditioning, OperantCortical ExcitabilityHIV-1MalePrefrontal CortexPyramidal CellsRats, Inbred F344Rats, TransgenicSelf AdministrationCocaine

Identifiers

PMID26677947
PMCPMC4908633
OpenAlexW2417501220

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.