Evidence map›Paper›PMID 29753728›Full record

ArticleExperimental eye research2018

Retinal adaptation to dim light vision in spectacled caimans (Caiman crocodilus fuscus): Analysis of retinal ultrastructure.

Anett Karl, Silke Agte, Astrid Zayas-Santiago, Felix N Makarov, Yomarie Rivera, Jan Benedikt, Mike Francke, Andreas Reichenbach, Serguei N Skatchkov, Andreas Bringmann

Open access · greenAbstract read
In one paragraph

Article in Experimental eye research, 2018. 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
0.9field-weighted citation impact, top 26% 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, 15 citations in OpenAlex.

  1. Article
  2. Tissue Transparency In Vivo.Molecules (Basel, Switzerland) · 2019
    Review
  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

10 authors at 4 institutions in 3 countries.

Anett KarlPaul Flechsig Institute for Brain Research, University of Leipzig, Leipzig, Germany; Carl Ludwig Institute for Physiology, University of Leipzig, Leipzig, Germany. Electronic address: Anett.Karl@medizin.uni-leipzig.de.
Silke AgtePaul Flechsig Institute for Brain Research, University of Leipzig, Leipzig, Germany.
Astrid Zayas-SantiagoDepartment of Pathology and Laboratory Medicine, Universidad Central Del Caribe, Bayamón, Puerto Rico, USA.
Felix N MakarovLaboratory of Neuromorphology, Pavlov Institute of Physiology, Russian Academy of Sciences, Saint Petersburg, Russia.
Yomarie RiveraDepartment of Physiology, Universidad Central Del Caribe, Bayamón, Puerto Rico, USA.
Jan BenediktDepartment of Physiology, Universidad Central Del Caribe, Bayamón, Puerto Rico, USA.
Mike FranckePaul Flechsig Institute for Brain Research, University of Leipzig, Leipzig, Germany; Saxonian Incubator for Clinical Translation (SIKT), University of Leipzig, Leipzig, Germany.
Andreas ReichenbachPaul Flechsig Institute for Brain Research, University of Leipzig, Leipzig, Germany.
Serguei N SkatchkovDepartment of Biochemistry, Universidad Central Del Caribe, Bayamón, Puerto Rico, USA; Department of Physiology, Universidad Central Del Caribe, Bayamón, Puerto Rico, USA.
Andreas BringmannDepartment of Ophthalmology and Eye Hospital, University of Leipzig, Leipzig, Germany.
Central University of the Caribbean · PRLeipzig University · DEPavlov Institute of Physiology of the Russian Academy of Sciences · RUUniversity Hospital Leipzig · DE

Funding

UNIVERSITY MEDICAL RESEARCH CENTERG12RR003035 · NCRR · UNIVERSIDAD CENTRAL DEL CARIBE · PI ROJAS, LEGIER V · 1986 to 2011
$26.7M
UNIVERSIDAD CENTRAL DEL CARIBE BIOMEDICAL RESEARCH CENTERSG12MD007583 · NIMHD · UNIVERSIDAD CENTRAL DEL CARIBE · PI RODRIGUEZ, JOSE GINEL · 2012 to 2016
$8.4M
Polyamines and Brain SignalingR01NS065201 · NINDS · UNIVERSIDAD CENTRAL DEL CARIBE · PI SKATCHKOV, SERGUEI N · 2010 to 2013
$1.3M
NCRR NIH HHS G12 RR003035NIMHD NIH HHS G12 MD007583NINDS NIH HHS R01 NS065201
6 · The paper itself

Abstract

It has been shown that mammalian retinal glial (Müller) cells act as living optical fibers that guide the light through the retinal tissue to the photoreceptor cells (Agte et al., 2011; Franze et al., 2007). However, for nonmammalian species it is unclear whether Müller cells also improve the transretinal light transmission. Furthermore, for nonmammalian species there is a lack of ultrastructural data of the retinal cells, which, in general, delivers fundamental information of the retinal function, i.e. the vision of the species. A detailed study of the cellular ultrastructure provides a basic approach of the research. Thus, the aim of the present study was to investigate the retina of the spectacled caimans at electron and light microscopical levels to describe the structural features. For electron microscopy, we used a superfast microwave fixation procedure in order to achieve more precise ultrastructural information than common fixation techniques. As result, our detailed ultrastructural study of all retinal parts shows structural features which strongly indicate that the caiman retina is adapted to dim light and night vision. Various structural characteristics of Müller cells suppose that the Müller cell may increase the light intensity along the path of light through the neuroretina and, thus, increase the sensitivity of the scotopic vision of spectacled caimans. Müller cells traverse the whole thickness of the neuroretina and thus may guide the light from the inner retinal surface to the photoreceptor cell perikarya and the Müller cell microvilli between the photoreceptor segments. Thick Müller cell trunks/processes traverse the layers which contain light-scattering structures, i.e., nerve fibers and synapses. Large Müller cell somata run through the inner nuclear layer and contain flattened, elongated Müller cell nuclei which are arranged along the light path and, thus, may reduce the loss of the light intensity along the retinal light path. The oblique arrangement of many Müller cell trunks/processes in the inner plexiform layer and the large Müller cell somata in the inner nuclear layer may suggest that light guidance through Müller cells increases the visual sensitivity. Furthermore, an adaptation of the caiman retina to low light levels is strongly supported by detailed ultrastructural data of other retinal parts, e.g. by (i) the presence of a guanine-based retinal tapetum, (ii) the rod dominance of the retina, (iii) the presence of photoreceptor cell nuclei, which penetrate the outer limiting membrane, (iv) the relatively low densities of photoreceptor and neuronal cells which is compensated by (v) the presence of rods with long and thick outer segments, that may increase the probability of photon absorption. According to a cell number analysis, the central and temporal areas of the dorsal tapetal retina, which supports downward prey detection in darker water, are the sites of the highest diurnal contrast/color vision, i.e. cone vision and of the highest retinal light sensitivity, i.e. rod vision.

Indexed as

Alligators and CrocodilesAdaptation, OcularAnimalsCell CountFemaleMaleMicroscopy, ElectronNight VisionPhotoreceptor Cells, VertebrateRetinaRetinal Pigment EpitheliumCaimanGliaMüller cellPhotoreceptorRetinaTapetum lucidum

Identifiers

PMID29753728
PMCPMC9930524
OpenAlexW2803297368

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.