Evidence map›Paper›PMID 33392718›Full record

ReviewJournal of comparative physiology. A, Neuroethology, sensory, neural, and behavioral physiology2021

Oxygen sensing in crustaceans: functions and mechanisms.

Tábata Martins de Lima, Luiz Eduardo Maia Nery, Fábio Everton Maciel, Hanh Ngo-Vu, Mihika T Kozma, Charles D Derby

Abstract readReview
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In one paragraph

Review in Journal of comparative physiology. A, Neuroethology, sensory, neural, and behavioral physiology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
2.5field-weighted citation impact, top 12% 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

4 citing papers in PubMed, 20 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. 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

6 authors at 2 institutions in 2 countries.

Tábata Martins de LimaPrograma de Pós-Graduação Em Ciências Fisiológicas, Instituto de Ciências Biológicas, Universidade Federal do Rio Grande, FURG, Av. Itália, Km 8, Rio Grande, RS, 96201-300, Brazil. tabatalimafac@gmail.com.ORCID 0000-0003-1641-0146
Luiz Eduardo Maia NeryPrograma de Pós-Graduação Em Ciências Fisiológicas, Instituto de Ciências Biológicas, Universidade Federal do Rio Grande, FURG, Av. Itália, Km 8, Rio Grande, RS, 96201-300, Brazil.
Fábio Everton MacielPrograma de Pós-Graduação Em Ciências Fisiológicas, Instituto de Ciências Biológicas, Universidade Federal do Rio Grande, FURG, Av. Itália, Km 8, Rio Grande, RS, 96201-300, Brazil.
Hanh Ngo-VuNeuroscience Institute, Georgia State University, Atlanta, GA, USA.
Mihika T KozmaNeuroscience Institute, Georgia State University, Atlanta, GA, USA.
Charles D DerbyNeuroscience Institute, Georgia State University, Atlanta, GA, USA.
Georgia State University · USUniversidade Federal do Rio Grande · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Animals that live in changing environments need to adjust their metabolism to maintain body functions, and sensing these changing conditions is essential for mediating the short- and long-term physiological and behavioral responses that make these adjustments. Previous research on nematodes and insects facing changing oxygen levels has shown that these animals rapidly respond using atypical soluble guanylyl cyclases (sGCs) as oxygen sensors connected to downstream cGMP pathways, and they respond more slowly using hypoxia-inducible transcription factors (HIFs) that are further modulated by oxygen-sensing prolyl hydroxylases (PHs). Crustaceans are known to respond in different ways to hypoxia, but the mechanisms responsible for sensing oxygen levels are more poorly understood than in nematodes and insects. Our paper reviews the functions of and mechanisms underlying oxygen sensing in crustaceans. Furthermore, using the oxygen sensing abilities of nematodes and insects as guides in analyzing available crustacean transcriptomes, we identified orthologues of atypical sGCs, HIFs, and PHs in crustaceans, including in their chemosensory organs and neurons. These molecules include atypical sGCs activated by hypoxia (Gyc-88E/GCY-31 and Gyc-89D/GCY-33) but not those activated by hyperoxia (GCY-35, GCY-36), as well as orthologues of HIF-α, HIF-β, and PH. We offer possible directions for future research on oxygen sensing by crustaceans.

Indexed as

AnimalsChemoreceptor CellsCrustaceaNeuronsOxygenOxygenChemoreceptionHypoxia-inducible transcription factorOxygen sensingProlyl hydroxylaseSoluble guanylyl cyclase

Identifiers

PMID33392718
OpenAlexW3119314775

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.