Evidence map›Paper›PMID 25585352›Full record

ArticleJournal of insect physiology2015

Perturbations in dopamine synthesis lead to discrete physiological effects and impact oxidative stress response in Drosophila.

Marley E Hanna, Andrea Bednářová, Kuntol Rakshit, Anathbandhu Chaudhuri, Janis M O'Donnell, Natraj Krishnan

Open access · greenAbstract read
In one paragraph

Article in Journal of insect physiology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
2.1field-weighted citation impact, top 14% 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

14 citing papers in PubMed, 44 citations in OpenAlex.

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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

6 authors at 5 institutions in 2 countries.

Marley E HannaDepartment of Biochemistry, Molecular Biology, Entomology and Plant Pathology, Mississippi State University, Mississippi State, MS 39762, USA.
Andrea BednářováDepartment of Biochemistry, Molecular Biology, Entomology and Plant Pathology, Mississippi State University, Mississippi State, MS 39762, USA; Institute of Entomology, Biology Centre, Academy of Sciences and Faculty of Science, University of South Bohemia, Branišovská 31, 370 05 České Budějovice, Czech Republic.
Kuntol RakshitDepartment of Physiology and Biomedical Engineering, Mayo Clinic School of Medicine, Mayo Clinic, 200 First St. SW, Rochester, MN 55905, USA.
Anathbandhu ChaudhuriDepartment of Natural Sciences, Stinson Mathematics and Science Building, 3601 Stillman Blvd, Stillman College, Tuscaloosa, AL 35043, USA.
Janis M O'DonnellDepartment of Biological Sciences, The University of Alabama, Tuscaloosa, AL 35487, USA.
Natraj KrishnanDepartment of Biochemistry, Molecular Biology, Entomology and Plant Pathology, Mississippi State University, Mississippi State, MS 39762, USA. Electronic address: nk260@msstate.edu.
Mississippi State University · USMayo Clinic · USSewanee: The University of the South · USStillman College · USUniversity of Alabama · US

Funding

Inflammatory and hypoxia responses in neurodegeneration: A novel Drosophila modelR15NS078728 · NINDS · UNIVERSITY OF ALABAMA IN TUSCALOOSA · PI O'DONNELL, JANIS · 2012 to 2012
$406k
NINDS NIH HHS R15 NS078728
6 · The paper itself

Abstract

The impact of mutations in four essential genes involved in dopamine (DA) synthesis and transport on longevity, motor behavior, and resistance to oxidative stress was monitored in Drosophila melanogaster. The fly lines used for this study were: (i) a loss of function mutation in Catecholamines up (Catsup(26)), which is a negative regulator of the rate limiting enzyme for DA synthesis, (ii) a mutant for the gene pale (ple(2)) that encodes for the rate limiting enzyme tyrosine hydroxylase (TH), (iii) a mutant for the gene Punch (Pu(Z22)) that encodes guanosine triphosphate cyclohydrolase, required for TH activity, and (iv) a mutant in the vesicular monoamine transporter (VMAT(Δ14)), which is required for packaging of DA as vesicles inside DA neurons. Median lifespans of ple(2), Pu(Z22) and VMAT(Δ14) mutants were significantly decreased compared to Catsup(26) and wild type controls that did not significantly differ between each other. Catsup(26) flies survived longer when exposed to hydrogen peroxide (80 μM) or paraquat (10mM) compared to ple(2), Pu(Z22) or VMAT(Δ14) and controls. These flies also exhibited significantly higher negative geotaxis activity compared to ple(2), Pu(Z22), VMAT(Δ14) and controls. All mutant flies demonstrated rhythmic circadian locomotor activity in general, albeit Catsup(26) and VMAT(Δ14) flies had slightly weaker rhythms. Expression analysis of some key antioxidant genes revealed that glutathione S-transferase Omega-1 (GSTO1) expression was significantly up-regulated in all DA synthesis pathway mutants and especially in Catsup(26) and VMAT(Δ14) flies at both mRNA and protein levels. Taken together, we hypothesize that DA could directly influence GSTO1 transcription and thus play a significant role in the regulation of response to oxidative stress. Additionally, perturbations in DA synthesis do not appear to have a significant impact on circadian locomotor activity rhythms per se, but do have an influence on general locomotor activity levels.

Indexed as

AnimalsAnimals, Genetically ModifiedAntioxidantsBiomarkersCircadian RhythmDopamineDrosophila melanogasterGenes, InsectGenetic MarkersGlutathione TransferaseMaleMotor ActivityMutationOxidative StressRandom AllocationAntioxidantsBiomarkersDopamineGenetic MarkersGlutathione TransferaseCatecholamineCircadianDopamineDrosophilaGlutathione-S-transferaseOxidative stress

Identifiers

PMID25585352
PMCPMC4699656
OpenAlexW1966797442

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.