Evidence map›Paper›PMID 26254330›Full record

ArticleAmerican journal of physiology. Heart and circulatory physiology2015

α-Lipoic acid reduces neurogenic hypertension by blunting oxidative stress-mediated increase in ADAM17.

Thyago M de Queiroz, Huijing Xia, Catalin M Filipeanu, Valdir A Braga, Eric Lazartigues

Open access · greenAbstract read
In one paragraph

Article in American journal of physiology. Heart and circulatory physiology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
1.8field-weighted citation impact, top 15% 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

20 citing papers in PubMed, 35 citations in OpenAlex.

  1. Article
  2. Oxidative Stress, Antioxidants and Hypertension.Antioxidants (Basel, Switzerland) · 2023
    Review
  3. Article
  4. Article
  5. Article
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  17. Article
  18. Clinical Relevance and Role of Neuronal ATCirculation research · 2017
    Article
  19. Review
  20. 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

5 authors at 2 institutions in 2 countries.

Thyago M de QueirozDepartment of Pharmacology and Experimental Therapeutics, Louisiana State University Health Sciences Center, New Orleans, Louisiana; Department of Biotechnology, Federal University of Paraíba, João Pessoa, PB, Brazil.
Huijing XiaDepartment of Pharmacology and Experimental Therapeutics, Louisiana State University Health Sciences Center, New Orleans, Louisiana; Cardiovascular Center of Excellence, Louisiana State University Health Sciences Center, New Orleans, Louisiana; and.
Catalin M FilipeanuDepartment of Pharmacology and Experimental Therapeutics, Louisiana State University Health Sciences Center, New Orleans, Louisiana; Cardiovascular Center of Excellence, Louisiana State University Health Sciences Center, New Orleans, Louisiana; and.
Valdir A BragaDepartment of Biotechnology, Federal University of Paraíba, João Pessoa, PB, Brazil.
Eric LazartiguesDepartment of Pharmacology and Experimental Therapeutics, Louisiana State University Health Sciences Center, New Orleans, Louisiana; Neurosciences Center of Excellence, Louisiana State University Health Sciences Center, New Orleans, Louisiana; Cardiovascular Center of Excellence, Louisiana State University Health Sciences Center, New Orleans, Louisiana; and elazar@lsuhsc.edu.
Louisiana State University Health Sciences Center New Orleans · USUniversidade Federal da Paraíba · BR

Funding

Vascular and Cardiac Function Core - "Mentoring in Cardiovascular BiologyP30GM106392 · NIGMS · LSU HEALTH SCIENCES CENTER · PI KAPUSTA, DANIEL R · 2014 to 2018
$5.5M
Mechanisms of ACE2 Regulation in Neurogenic HypertensionR01HL093178 · NHLBI · LSU HEALTH SCIENCES CENTER · PI LAZARTIGUES, ERIC D · 2008 to 2017
$3.4M
NHLBI NIH HHS R01 HL093178NIGMS NIH HHS P30 GM106392
6 · The paper itself

Abstract

We previously reported that type 2 angiotensin-converting enzyme (ACE2) compensatory activity is impaired by the disintegrin and metalloprotease 17 (ADAM17), and lack of ACE2 is associated with oxidative stress in neurogenic hypertension. To investigate the relationship between ADAM17 and oxidative stress, Neuro2A cells were treated with ANG II (100 nM) 24 h after vehicle or α-lipoic acid (LA, 500 μM). ADAM17 expression was increased by ANG II (120.5 ± 9.1 vs. 100.2 ± 0.8%, P < 0.05) and decreased after LA (69.0 ± 0.3 vs. 120.5 ± 9.1%, P < 0.05). In another set of experiments, LA reduced ADAM17 (92.9 ± 5.3 vs. 100.0 ± 11.2%, P < 0.05) following its overexpression. Moreover, ADAM17 activity was reduced by LA in ADAM17-overexpressing cells [109.5 ± 19.8 vs. 158.0 ± 20.0 fluorescence units (FU)·min(-1)·μg protein(-1), P < 0.05], in which ADAM17 overexpression increased oxidative stress (114.1 ± 2.5 vs. 101.0 ± 1.0%, P < 0.05). Conversely, LA-treated cells attenuated ADAM17 overexpression-induced oxidative stress (76.0 ± 9.1 vs. 114.1 ± 2.5%, P < 0.05). In deoxycorticosterone acetate (DOCA)-salt hypertensive mice, a model in which ADAM17 expression and activity are increased, hypertension was blunted by pretreatment with LA (119.0 ± 2.4 vs. 131.4 ± 2.2 mmHg, P < 0.05). In addition, LA improved dysautonomia and baroreflex sensitivity. Furthermore, LA blunted the increase in NADPH oxidase subunit expression, as well as the increase in ADAM17 and decrease in ACE2 activity in the hypothalamus of DOCA-salt hypertensive mice. Taken together, these data suggest that LA might preserve ACE2 compensatory activity by breaking the feedforward cycle between ADAM17 and oxidative stress, resulting in a reduction of neurogenic hypertension.

Indexed as

Oxidative StressADAM17 ProteinADAM ProteinsAngiotensin-Converting Enzyme 2Angiotensin IIAnimalsAntioxidantsBaroreflexCell Line, TumorHypertensionHypothalamusMaleMiceMice, Inbred C57BLNADPH OxidasesNeuronsAce2 protein, mouseADAM17 ProteinAdam17 protein, mouseADAM ProteinsAngiotensin-Converting Enzyme 2Angiotensin IIAntioxidantsNADPH OxidasesPeptidyl-Dipeptidase AThioctic Acidantioxidantdeoxycorticosterone acetate-salt hypertensionmetalloprotease 17type 2 angiotensin-converting enzyme

Identifiers

PMID26254330
PMCPMC4591409
OpenAlexW1801528881

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.