PUBLICATION
Chronic cortisol elevation restricts glucose uptake but not insulin responsiveness in zebrafish skeletal muscle
- Authors
- Antomagesh, F., Jayakumar Rajeswari, J., Vijayan, M.M.
- ID
- ZDB-PUB-230216-34
- Date
- 2023
- Source
- General and comparative endocrinology 336: 114231 (Journal)
- Registered Authors
- Vijayan, Mathilakath
- Keywords
- glucocorticoids, glucose regulation, glucose transporters, insulin signalling, skeletal muscle, stress
- MeSH Terms
-
- Animals
- Blood Glucose/metabolism
- Glucose/metabolism
- Hydrocortisone/metabolism
- Hydrocortisone/pharmacology
- Insulin*/metabolism
- Insulin Resistance*
- Mammals/metabolism
- Muscle, Skeletal/metabolism
- Phosphorylation
- Zebrafish/metabolism
- PubMed
- 36791823 Full text @ Gen. Comp. Endocrinol.
Citation
Antomagesh, F., Jayakumar Rajeswari, J., Vijayan, M.M. (2023) Chronic cortisol elevation restricts glucose uptake but not insulin responsiveness in zebrafish skeletal muscle. General and comparative endocrinology. 336:114231.
Abstract
Although teleosts show an elevated insulin response to hyperglycemia, the circulating glucose levels are not normalized as rapidly as in mammals. While this may suggest a lack of target tissue insulin responsiveness, the underlying mechanisms are unclear. We investigated whether changes in skeletal muscle insulin sensitivity and glucose uptake underlie the cortisol-mediated elevated blood glucose levels. Adult zebrafish (Danio rerio) were exposed to water-borne cortisol for 3 days followed by an intraperitoneal injection of glucose with or without insulin. Cortisol treatment resulted in a temporal delay in the reduction in blood glucose levels, and this corresponded with a reduced glucose uptake capacity and lower glycogen content in the skeletal muscle. The transcript abundance of slc2a1b (which encodes for GLUT1b) and a suite of genes encoding enzymes involved in muscle glycogenesis and glycolysis were upregulated in the cortisol group. Both the control and cortisol groups showed higher whole body insulin expression in response to blood glucose elevation, which also resulted in enhanced insulin-stimulated phosphorylation of Akt in the skeletal muscle. The insulin-mediated phosphorylation of S6 kinase was lower in the cortisol group. Altogether, chronic cortisol stimulation restricts glucose uptake and enhances the glycolytic capacity without affecting insulin responsiveness in zebrafish skeletal muscle.
Genes / Markers
Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Orthology
Engineered Foreign Genes
Mapping