Norepinephrine Regulation of Ventromedial Hypothalamic Nucleus Astrocyte Glycogen Metabolism.
Animals
Astrocytes
/ drug effects
Carbohydrate Metabolism
/ drug effects
Gene Expression Regulation
Glucose
/ metabolism
Glycogen
/ metabolism
Humans
Neurons
/ metabolism
Norepinephrine
/ metabolism
Receptors, Adrenergic
/ genetics
Rhombencephalon
/ drug effects
Signal Transduction
/ drug effects
Ventromedial Hypothalamic Nucleus
/ drug effects
adrenergic receptor
glycogen phosphorylase brain type
laser-catapult microdissection
norepinephrine
ventromedial hypothalamic nucleus
Journal
International journal of molecular sciences
ISSN: 1422-0067
Titre abrégé: Int J Mol Sci
Pays: Switzerland
ID NLM: 101092791
Informations de publication
Date de publication:
13 Jan 2021
13 Jan 2021
Historique:
received:
08
12
2020
revised:
04
01
2021
accepted:
09
01
2021
entrez:
16
1
2021
pubmed:
17
1
2021
medline:
10
4
2021
Statut:
epublish
Résumé
The catecholamine norepinephrine (NE) links hindbrain metabolic-sensory neurons with key glucostatic control structures in the brain, including the ventromedial hypothalamic nucleus (VMN). In the brain, the glycogen reserve is maintained within the astrocyte cell compartment as an alternative energy source to blood-derived glucose. VMN astrocytes are direct targets for metabolic stimulus-driven noradrenergic signaling due to their adrenergic receptor expression (AR). The current review discusses recent affirmative evidence that neuro-metabolic stability in the VMN may be shaped by NE influence on astrocyte glycogen metabolism and glycogen-derived substrate fuel supply. Noradrenergic modulation of estrogen receptor (ER) control of VMN glycogen phosphorylase (GP) isoform expression supports the interaction of catecholamine and estradiol signals in shaping the physiological stimulus-specific control of astrocyte glycogen mobilization. Sex-dimorphic NE control of glycogen synthase and GP brain versus muscle type proteins may be due, in part, to the dissimilar noradrenergic governance of astrocyte AR and ER variant profiles in males versus females. Forthcoming advances in the understanding of the molecular mechanistic framework for catecholamine stimulus integration with other regulatory inputs to VMN astrocytes will undoubtedly reveal useful new molecular targets in each sex for glycogen mediated defense of neuronal metabolic equilibrium during neuro-glucopenia.
Identifiants
pubmed: 33451134
pii: ijms22020759
doi: 10.3390/ijms22020759
pmc: PMC7828624
pii:
doi:
Substances chimiques
Receptors, Adrenergic
0
Glycogen
9005-79-2
Glucose
IY9XDZ35W2
Norepinephrine
X4W3ENH1CV
Types de publication
Journal Article
Review
Langues
eng
Sous-ensembles de citation
IM
Subventions
Organisme : NIDDK NIH HHS
ID : R01 DK109382
Pays : United States
Organisme : NIH HHS
ID : DK 109382
Pays : United States
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