Evidence map›Paper›PMID 29260441›Full record

ArticleJournal of neurovirology2018

Effects of docosahexaenoic acid on locomotor activity in ethanol-treated HIV-1 transgenic rats.

Jianlin He, Wenfei Huang, Shizhong Zheng, Michael Vigorito, Sulie L Chang

Abstract read
In one paragraph

Article in Journal of neurovirology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed, 1 pooled it
0.6field-weighted citation impact, top 28% 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, 1 synthesis or guideline pooled it, 7 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Novel Antiretroviral Structures from Marine Organisms.Molecules (Basel, Switzerland) · 2019
    Review
  5. Binge alcohol and HIV: leaky gut and neurodegeneration through the gut-brain axis.International journal of nutrition, pharmacology, neurological diseases
    Article
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

5 authors at 2 institutions in 2 countries.

Jianlin HeDepartment of Pharmacology, School of Pharmacy, Nanjing University of Chinese Medicine, Nanjing, 210029, People's Republic of China.
Wenfei HuangInstitute of NeuroImmune Pharmacology, Seton Hall University, 400 South Orange Avenue, South Orange, NJ, 07079, USA.
Shizhong ZhengDepartment of Pharmacology, School of Pharmacy, Nanjing University of Chinese Medicine, Nanjing, 210029, People's Republic of China. nytws@163.com.
Michael VigoritoInstitute of NeuroImmune Pharmacology, Seton Hall University, 400 South Orange Avenue, South Orange, NJ, 07079, USA.
Sulie L ChangInstitute of NeuroImmune Pharmacology, Seton Hall University, 400 South Orange Avenue, South Orange, NJ, 07079, USA. sulie.chang@shu.edu.
Seton Hall University · USNanjing University of Chinese Medicine · CN

Funding

Glial-neuronal interactions underlying the molecular feedback between HIV viral pR21DA036175 · NIDA · SETON HALL UNIVERSITY · PI CHANG, SULIE L. · 2013 to 2014
$370k
Involvement of TRP Channels in Ethanol Concentration-Dependent Effects on ImmuneR21AA023172 · NIAAA · SETON HALL UNIVERSITY · PI CHANG, SULIE L. · 2014 to 2015
$353k
NIAAA NIH HHS R21 AA023172NIDA NIH HHS R21 DA036175
6 · The paper itself

Abstract

Binge drinking affects the onset and progression of human immunodeficiency virus (HIV)-associated neurological disorders. The HIV-1 transgenic (HIV-1Tg) rat was created with a gag- and pol-deleted HIV-1 viral genome to mimic HIV-infected patients receiving combination anti-retroviral therapy (cART). Docosahexaenoic acid (DHA) is a marine compound that modulates inflammatory responses. Using HIV-1Tg rats subjected to binge exposure to ethanol (EtOH), this study examined whether DHA could reduce the detrimental neurological effects of EtOH and HIV proteins. Young adult male HIV-1Tg and F344 control rats received 4 mL/kg/day saline as a control (Saline group), 20 mg/kg/day DHA (DHA group), 4.8 g/kg/day 52% w/v EtOH (EtOH group), or 4.8 g/kg/day 52% w/v EtOH and 20 mg/kg/d DHA (DHA + EtOH group) by gavage for 5 weeks (n = 6 per group). EtOH was administrated on days 5, 6, and 7 of each week. Locomotor activity (LMA) was assessed using open field tests before and 45, 90, 135, and 180 min after each treatment. Repeated binge EtOH exposure gradually decreased LMA measured before daily treatments in HIV-1Tg and F344 rats, an effect that was reversed by DHA only in the HIV-1Tg rats. Decreased LMA of rats after treatment and under the influence of EtOH was less pronounced, and the reversal effect of DHA did not reach statistical significance. The plasma endotoxin level was significantly higher in HIV-1Tg rats than in F344 rats. IL-6 and IL-18 expression in the striatum was significantly higher in the HIV-1Tg EtOH group than in the F344 EtOH group. DHA significantly decreased the high levels of IL-6, IL-18, and NF-κB expression observed in the HIV-1Tg EtOH group. DHA appears to ameliorate inflammation and consequently lessen the reductions in LMA produced by the combination of EtOH and HIV-1 viral proteins.

Indexed as

AnimalsBinge DrinkingCorpus StriatumDisease Models, AnimalDocosahexaenoic AcidsEndotoxinsGene ExpressionHIV-1HIV InfectionsInterleukin-18Interleukin-6LocomotionMaleMaze LearningNF-kappa BRatsDocosahexaenoic AcidsEndotoxinsIl6 protein, ratInterleukin-18Interleukin-6NF-kappa BDocosahexaenoic acidEthanolHIVLocomotor activityStriatum

Identifiers

PMID29260441
PMCPMC6402484
OpenAlexW2778024789

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.