β-alanine supplementation induces taurine depletion and causes alterations of the retinal nerve fiber layer and axonal transport by retinal ganglion cells.
Animals
Axonal Transport
/ drug effects
Light
/ adverse effects
Nerve Fibers
/ drug effects
Neurofilament Proteins
/ metabolism
Phosphorylation
Rats
Rats, Sprague-Dawley
Retinal Degeneration
/ etiology
Retinal Ganglion Cells
/ drug effects
Taurine
/ blood
Tomography, Optical Coherence
Transcription Factor Brn-3A
/ metabolism
beta-Alanine
/ toxicity
Axonal transport
Light
Phototoxicity
Retinal degeneration
Retinal ganglion cells
Taurine
Journal
Experimental eye research
ISSN: 1096-0007
Titre abrégé: Exp Eye Res
Pays: England
ID NLM: 0370707
Informations de publication
Date de publication:
11 2019
11 2019
Historique:
received:
05
06
2019
revised:
26
08
2019
accepted:
28
08
2019
pubmed:
2
9
2019
medline:
29
2
2020
entrez:
2
9
2019
Statut:
ppublish
Résumé
To study the effect of taurine depletion induced by β-alanine supplementation in the retinal nerve fiber layer (RNFL), and retinal ganglion cell (RGC) survival and axonal transport. Albino Sprague-Dawley rats were divided into two groups: one group received β-alanine supplementation (3%) in the drinking water during 2 months to induce taurine depletion, and the other group received regular water. After one month, half of the rats from each group were exposed to light. Retinas were analyzed in-vivo using Spectral-Domain Optical Coherence Tomography (SD-OCT). Prior to processing, RGCs were retrogradely traced with fluorogold (FG) applied to both superior colliculi, to assess the state of their retrograde axonal transport. Retinas were dissected as wholemounts, surviving RGCs were immunoidentified with Brn3a, and the RNFL with phosphorylated high-molecular-weight subunit of the neurofilament triplet (pNFH) antibodies. β-alanine supplementation decreases significantly taurine plasma levels and causes a significant reduction of the RNFL thickness that is increased after light exposure. An abnormal pNFH immunoreactivity in some RGC bodies, their proximal dendrites and axons, and a further diminution of the mean number of FG-traced RGCs compared with Brn3a
Identifiants
pubmed: 31473259
pii: S0014-4835(19)30412-9
doi: 10.1016/j.exer.2019.107781
pii:
doi:
Substances chimiques
Neurofilament Proteins
0
Transcription Factor Brn-3A
0
neurofilament protein H
108688-71-7
beta-Alanine
11P2JDE17B
Taurine
1EQV5MLY3D
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
107781Informations de copyright
Copyright © 2019 The Authors. Published by Elsevier Ltd.. All rights reserved.