Evidence map›Paper›PMID 20970459›Full record

ArticleAntiviral research2010

Metabolic and neurologic consequences of chronic lopinavir/ritonavir administration to C57BL/6 mice.

Paul J Pistell, Sunita Gupta, Alecia G Knight, Michelle Domingue, Romina M Uranga, Donald K Ingram, Indu Kheterpal, Carmen Ruiz, Jeffrey N Keller, Annadora J Bruce-Keller

Open access · greenAbstract read
In one paragraph

Article in Antiviral research, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
2.3field-weighted citation impact, top 11% 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

29 citing papers in PubMed, 42 citations in OpenAlex.

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  8. Neurologic complications of COVID-19.The American journal of emergency medicine · 2020
    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

10 authors at 3 institutions in 2 countries.

Paul J PistellPennington Biomedical Research Center, Louisiana State University System, Baton Rouge, 70808, United States.
Sunita Gupta
Alecia G Knight
Michelle Domingue
Romina M Uranga
Donald K Ingram
Indu Kheterpal
Carmen Ruiz
Jeffrey N Keller
Annadora J Bruce-Keller
Louisiana State University System · USPennington Biomedical Research Center · USUniversidad Nacional del Sur · AR

Funding

Research BaseP30DK072476 · NIDDK · LSU PENNINGTON BIOMEDICAL RESEARCH CTR · PI Peter Todd Katzmarzyk · 2005 to 2026
$26.5M
TROPIC, CHOLINERGIC AND PATHOLOGIC CHANGES IN ALZHEIMER'S DISEASEP01AG005119 · NIA · UNIVERSITY OF KENTUCKY · PI ST CLAIR, DARET K · 1985 to 2012
$15.4M
THE ROLE OF PROTEIN MALNUTRITION ON CIRCADIAN PHYSIOLOGY OF C57BL/6J MOUSE DAMSP20RR021945 · NCRR · LSU PENNINGTON BIOMEDICAL RESEARCH CTR · PI GETTYS, THOMAS W · 2006 to 2011
$9.5M
Tat, NADPH oxidase, and HIV-dementiaR01NS046267 · NINDS · UNIVERSITY OF KENTUCKY · PI BRUCE-KELLER, ANNADORA J · 2004 to 2008
$1.5M
NCRR NIH HHS P20 RR021945NCRR NIH HHS P20-RR021945NIA NIH HHS AG05119NIA NIH HHS P01 AG005119NIDDK NIH HHS P30 DK072476NIDDK NIH HHS P30-DK072476NINDS NIH HHS NS46267NINDS NIH HHS R01 NS046267
6 · The paper itself

Abstract

It is well established that HIV antiretroviral drugs, particularly protease inhibitors, frequently elicit a metabolic syndrome that may include hyperlipidemia, lipodystrophy, and insulin resistance. Metabolic dysfunction in non-HIV-infected subjects has been repeatedly associated with cognitive impairment in epidemiological and experimental studies, but it is not yet understood if antiretroviral therapy-induced metabolic syndrome might contribute to HIV-associated neurologic decline. To determine if protease inhibitor-induced metabolic dysfunction in mice is accompanied by adverse neurologic effects, C57BL/6 mice were given combined lopinavir/ritonavir (50/12.5-200/50 mg/kg) daily for 3 weeks. Data show that lopinavir/ritonavir administration caused significant metabolic derangement, including alterations in body weight and fat mass, as well as dose-dependent patterns of hyperlipidemia, hypoadiponectinemia, hypoleptinemia, and hyperinsulinemia. Evaluation of neurologic function revealed that even the lowest dose of lopinavir/ritonavir caused significant cognitive impairment assessed in multi-unit T-maze, but did not affect motor functions assessed as rotarod performance. Collectively, our results indicate that repeated lopinavir/ritonavir administration produces cognitive as well as metabolic impairments, and suggest that the development of selective aspects of metabolic syndrome in HIV patients could contribute to HIV-associated neurocognitive disorders.

Indexed as

HIV Protease InhibitorsAnimalsCognitionDrug Administration ScheduleDrug CombinationsHIVHIV InfectionsLopinavirMaleMetabolic SyndromeMiceMice, Inbred C57BLMotor ActivityPyrimidinonesRitonavirWeight LossDrug CombinationsHIV Protease InhibitorsLopinavirPyrimidinonesRitonavir

Identifiers

PMID20970459
PMCPMC2991583
OpenAlexW2034532818

What OpenQuestion holds

Textmetadata
LicenceTDM
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.