Short-term fasting differentially regulates PI3K/AkT/mTOR and ERK signalling in the rat hypothalamus.
ERK
Fasting
Hypothalamus
Insulin signaling
Rat
Journal
Mechanisms of ageing and development
ISSN: 1872-6216
Titre abrégé: Mech Ageing Dev
Pays: Ireland
ID NLM: 0347227
Informations de publication
Date de publication:
12 2020
12 2020
Historique:
received:
26
08
2020
revised:
12
09
2020
accepted:
13
09
2020
pubmed:
23
9
2020
medline:
29
10
2021
entrez:
22
9
2020
Statut:
ppublish
Résumé
It is known that insulin secreted by pancreatic β-cells enters the brain by crossing the blood-brain barrier. However, it was demonstrated that insulin expression occurs in various brain regions as well. Albeit the list of insulin actions in the brain is long and it includes control of energy homeostasis, neuronal survival, maintenance of synaptic plasticity and cognition, not much is known about the adaptive significance of insulin synthesis in brain. We previously reported that short-term fasting promotes insulin expression and subsequent activation of insulin receptor in the rat periventricular nucleus. In order to uncover a physiological importance of the fasting-induced insulin expression in hypothalamus, we analyzed the effect of short-term food deprivation on the expression of several participants of PI3K/AKT/mTOR and Ras/MAPK signaling pathways that are typically activated by this hormone. We found that the hypothalamic content of total and activated IRS1, IRS2, PI3K, and mTOR remained unchanged, but phosphorylated AKT1/2/3 was decreased. The levels of activated ERK1/2 were increased after six-hour fasting. Moreover, activated ERK1/2 was co-expressed with activated insulin receptor in the nucleus arcuatus. Our previously published and current findings suggest that the ERK activation in hypothalamus was at least partially initiated by the centrally produced insulin.
Identifiants
pubmed: 32961167
pii: S0047-6374(20)30154-8
doi: 10.1016/j.mad.2020.111358
pii:
doi:
Substances chimiques
Insulin
0
mTOR protein, rat
EC 2.7.1.1
Receptor, Insulin
EC 2.7.10.1
Proto-Oncogene Proteins c-akt
EC 2.7.11.1
TOR Serine-Threonine Kinases
EC 2.7.11.1
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
111358Informations de copyright
Copyright © 2020 Elsevier B.V. All rights reserved.