Effects of crowding on the three main proteolytic mechanisms of skeletal muscle in rainbow trout (Oncorhynchus mykiss).
Animals
Aquaculture
/ methods
Autophagy
Body Weight
Calcium-Binding Proteins
/ metabolism
Calpain
/ metabolism
Crowding
Hydrocortisone
/ blood
Lysosomes
/ metabolism
Muscle, Skeletal
/ metabolism
Oncorhynchus mykiss
/ metabolism
Proteasome Endopeptidase Complex
/ metabolism
Proteolysis
RNA, Messenger
Stress, Physiological
/ genetics
Ubiquitin
/ metabolism
Autophagy
Calpain/calpastatin
Fish
Stress response
Ubiquitin-proteasome
Journal
BMC veterinary research
ISSN: 1746-6148
Titre abrégé: BMC Vet Res
Pays: England
ID NLM: 101249759
Informations de publication
Date de publication:
17 Aug 2020
17 Aug 2020
Historique:
received:
23
05
2019
accepted:
07
08
2020
entrez:
18
8
2020
pubmed:
18
8
2020
medline:
10
4
2021
Statut:
epublish
Résumé
Skeletal muscle is one of the tissues most affected by stress conditions. The protein degradation in this tissue is vital for the supply of energy mediated by different proteolytic pathways such as the ubiquitin-proteasome (UPS), autophagy-lysosome (ALS) and the calpain/calpastatin system (CCS). Nevertheless, the regulation of this proteolytic axis under stress conditions is not yet completely clear. Chile is the main producer of rainbow trout (Oncorhynchus mykiss) in the world. This intensive fish farming has resulted in growing problems as crowding and stress are one of the major problems in the freshwater stage. In this context, we evaluated the crowding effect in juvenile rainbow trout kept in high stocking density (30 kg/m Plasmatic cortisol and glucose were evaluated by enzyme immunoassay. The mRNA levels of stress-related genes (gr1, gr2, mr, hsp70, klf15 and redd1), markers of the UPS (atrogin1 and murf1) and CCS (capn1, capn1, cast-l and cast-s) were evaluated using qPCR. ALS (LC3-I/II and P62/SQSTM1) and growth markers (4E-BP1 and ERK) were measured by Western blot analysis. The cortisol levels increased concomitantly with weight loss at 45 days of crowding. The UPS alone was upregulated at 15 days of high stocking density, while ALS activation was observed at 60 days. However, the CCS was inactivated during the entire trial. All these data suggest that stress conditions, such as crowding, promote muscle degradation in a time-dependent manner through the upregulation of the UPS at early stages of chronic stress and activation of the ALS in long-term stress, while the CCS is strongly inhibited by stress conditions in the rainbow trout muscle farmed during freshwater stage. Our descriptive study will allow perform functional analysis to determine, in a more detailed way, the effect of stress on skeletal muscle physiology as well as in the animal welfare in rainbow trout. Moreover, it is the first step to elucidate the optimal crop density in the freshwater stage and improve the standards of Chilean aquaculture.
Sections du résumé
BACKGROUND
BACKGROUND
Skeletal muscle is one of the tissues most affected by stress conditions. The protein degradation in this tissue is vital for the supply of energy mediated by different proteolytic pathways such as the ubiquitin-proteasome (UPS), autophagy-lysosome (ALS) and the calpain/calpastatin system (CCS). Nevertheless, the regulation of this proteolytic axis under stress conditions is not yet completely clear. Chile is the main producer of rainbow trout (Oncorhynchus mykiss) in the world. This intensive fish farming has resulted in growing problems as crowding and stress are one of the major problems in the freshwater stage. In this context, we evaluated the crowding effect in juvenile rainbow trout kept in high stocking density (30 kg/m
RESULTS
RESULTS
Plasmatic cortisol and glucose were evaluated by enzyme immunoassay. The mRNA levels of stress-related genes (gr1, gr2, mr, hsp70, klf15 and redd1), markers of the UPS (atrogin1 and murf1) and CCS (capn1, capn1, cast-l and cast-s) were evaluated using qPCR. ALS (LC3-I/II and P62/SQSTM1) and growth markers (4E-BP1 and ERK) were measured by Western blot analysis. The cortisol levels increased concomitantly with weight loss at 45 days of crowding. The UPS alone was upregulated at 15 days of high stocking density, while ALS activation was observed at 60 days. However, the CCS was inactivated during the entire trial.
CONCLUSION
CONCLUSIONS
All these data suggest that stress conditions, such as crowding, promote muscle degradation in a time-dependent manner through the upregulation of the UPS at early stages of chronic stress and activation of the ALS in long-term stress, while the CCS is strongly inhibited by stress conditions in the rainbow trout muscle farmed during freshwater stage. Our descriptive study will allow perform functional analysis to determine, in a more detailed way, the effect of stress on skeletal muscle physiology as well as in the animal welfare in rainbow trout. Moreover, it is the first step to elucidate the optimal crop density in the freshwater stage and improve the standards of Chilean aquaculture.
Identifiants
pubmed: 32799856
doi: 10.1186/s12917-020-02518-w
pii: 10.1186/s12917-020-02518-w
pmc: PMC7429773
doi:
Substances chimiques
Calcium-Binding Proteins
0
RNA, Messenger
0
Ubiquitin
0
calpastatin
79079-11-1
Calpain
EC 3.4.22.-
Proteasome Endopeptidase Complex
EC 3.4.25.1
Hydrocortisone
WI4X0X7BPJ
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
294Subventions
Organisme : Fondo Nacional de Desarrollo Científico y Tecnológico
ID : 1171307
Organisme : Fondo Nacional de Desarrollo Científico y Tecnológico
ID : 1171318
Organisme : Fondo de Financiamiento de Centros de Investigación en Áreas Prioritarias INCAR
ID : 15110027
Références
Ontogenez. 2016 Jul-Aug;47(4):197-208
pubmed: 30272394
Front Physiol. 2018 Jul 05;9:837
pubmed: 30026700
Fish Shellfish Immunol. 2019 Mar;86:436-448
pubmed: 30502466
FEBS Lett. 2010 Apr 2;584(7):1411-6
pubmed: 20132819
Int J Biochem Cell Biol. 2005 Oct;37(10):2134-46
pubmed: 15893952
Skelet Muscle. 2016 Apr 06;6:16
pubmed: 27054028
Mol Cancer Res. 2014 Jun;12(6):867-77
pubmed: 24615339
Comp Biochem Physiol B Biochem Mol Biol. 2005 Aug;141(4):488-97
pubmed: 15990347
Acta Histochem. 2014 Oct;116(8):1337-41
pubmed: 25190107
Cell Metab. 2011 Feb 2;13(2):170-82
pubmed: 21284984
Annu Rev Genet. 2009;43:67-93
pubmed: 19653858
Methods Mol Biol. 2019;1928:149-173
pubmed: 30725456
Mar Biotechnol (NY). 2013 Feb;15(1):104-14
pubmed: 22777624
Integr Comp Biol. 2002 Jul;42(3):517-25
pubmed: 21708747
J Exp Biol. 2016 Dec 1;219(Pt 23):3712-3718
pubmed: 27618858
Comp Biochem Physiol A Mol Integr Physiol. 2013 Mar;164(3):506-11
pubmed: 23277222
PLoS One. 2017 Dec 20;12(12):e0187339
pubmed: 29261652
Physiol Rev. 2003 Jul;83(3):731-801
pubmed: 12843408
Scand J Med Sci Sports. 2018 Mar;28(3):772-781
pubmed: 28685860
Methods Mol Biol. 2008;445:77-88
pubmed: 18425443
J Nutr. 2009 May;139(5):828-34
pubmed: 19297425
Dis Model Mech. 2013 Jan;6(1):25-39
pubmed: 23268536
Am J Physiol Regul Integr Comp Physiol. 2018 Jan 1;314(1):R102-R113
pubmed: 28978511
Fish Shellfish Immunol. 2016 Jan;48:43-53
pubmed: 26549176
BMC Genomics. 2015 Dec 01;16:1024
pubmed: 26626593
PLoS One. 2013 Aug 19;8(8):e71421
pubmed: 23990952
J Physiol. 2019 Mar;597(6):1585-1603
pubmed: 30615194
Trends Endocrinol Metab. 2013 Dec;24(12):635-43
pubmed: 24182456
Annu Rev Physiol. 2005;67:259-84
pubmed: 15709959
J Exp Biol. 2011 May 15;214(Pt 10):1617-28
pubmed: 21525308
Am J Physiol Regul Integr Comp Physiol. 2011 Jun;300(6):R1532-42
pubmed: 21389330
Dev Comp Immunol. 2015 Nov;53(1):145-57
pubmed: 26165160
Cell Cycle. 2014;13(14):2281-95
pubmed: 24897381
Gen Comp Endocrinol. 2007 Aug-Sep;153(1-3):47-56
pubmed: 17470371
Science. 2001 Nov 23;294(5547):1704-8
pubmed: 11679633
Am J Physiol Regul Integr Comp Physiol. 2014 Dec 1;307(11):R1330-7
pubmed: 25274907
Drug Discov Today Technol. 2017 Dec;26:25-31
pubmed: 29249239
Int J Mol Sci. 2017 Aug 28;18(9):
pubmed: 28846632
Comp Biochem Physiol B Biochem Mol Biol. 2017 Sep;211:22-28
pubmed: 28499850
J Exp Biol. 2018 Jan 25;221(Pt 2):
pubmed: 29212844
Domest Anim Endocrinol. 2014 Jan;46:26-36
pubmed: 24411181