Glucosamine Enhancement of BDNF Expression and Animal Cognitive Function.
Animals
Brain-Derived Neurotrophic Factor
/ biosynthesis
Cognition
/ drug effects
Cyclic AMP
/ metabolism
Cyclic AMP Response Element-Binding Protein
/ metabolism
Cyclic AMP-Dependent Protein Kinases
/ metabolism
Glucosamine
/ pharmacology
Male
Membrane Glycoproteins
/ metabolism
Mice
Phosphorylation
/ drug effects
Protein-Tyrosine Kinases
/ metabolism
Up-Regulation
/ drug effects
BDNF
PKA
cognition
glucosamine
Journal
Molecules (Basel, Switzerland)
ISSN: 1420-3049
Titre abrégé: Molecules
Pays: Switzerland
ID NLM: 100964009
Informations de publication
Date de publication:
12 Aug 2020
12 Aug 2020
Historique:
received:
22
07
2020
revised:
10
08
2020
accepted:
11
08
2020
entrez:
19
8
2020
pubmed:
19
8
2020
medline:
6
3
2021
Statut:
epublish
Résumé
Brain-derived neurotrophic factor (BDNF) is an important factor for memory consolidation and cognitive function. Protein kinase A (PKA) signaling interacts significantly with BDNF-provoked downstream signaling. Glucosamine (GLN), a common dietary supplement, has been demonstrated to perform a variety of beneficial physiological functions. In the current study, an in vivo model of 7-week-old C57BL/6 mice receiving daily intraperitoneal injection of GLN (0, 3, 10 and 30 mg/animal) was subjected to the novel object recognition test in order to determine cognitive performance. GLN significantly increased cognitive function. In the hippocampus GLN elevated tissue cAMP concentrations and CREB phosphorylation, and upregulated the expression of BDNF, CREB5 and the BDNF receptor TrkB, but it reduced PDE4B expression. With the in vitro model in the HT22 hippocampal cell line, GLN exposure significantly increased protein and mRNA levels of BDNF and CREB5 and induced cAMP responsive element (CRE) reporter activity; the GLN-mediated BDNF expression and CRE reporter induction were suppressed by PKA inhibitor H89. Our current findings suggest that GLN can exert a cognition-enhancing function and this may act at least in part by upregulating the BDNF levels via a cAMP/PKA/CREB-dependent pathway.
Identifiants
pubmed: 32806562
pii: molecules25163667
doi: 10.3390/molecules25163667
pmc: PMC7465318
pii:
doi:
Substances chimiques
Bdnf protein, mouse
0
Brain-Derived Neurotrophic Factor
0
Creb1 protein, mouse
0
Cyclic AMP Response Element-Binding Protein
0
Membrane Glycoproteins
0
Cyclic AMP
E0399OZS9N
Ntrk2 protein, mouse
EC 2.7.10.1
Protein-Tyrosine Kinases
EC 2.7.10.1
Cyclic AMP-Dependent Protein Kinases
EC 2.7.11.11
Glucosamine
N08U5BOQ1K
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Subventions
Organisme : Ministry of Science and Technology, Taiwan
ID : MOST 105-2320-B-010-026-MY3; MOST 108-2320-B-010-025
Références
Nat Neurosci. 2002 May;5(5):405-14
pubmed: 11953750
FEBS Lett. 2002 Jul 31;524(1-3):199-203
pubmed: 12135767
Nat Rev Neurol. 2009 Jun;5(6):311-22
pubmed: 19498435
Proc Natl Acad Sci U S A. 1998 Jun 23;95(13):7748-53
pubmed: 9636222
Otol Neurotol. 2018 Mar;39(3):e173-e180
pubmed: 29342042
Prog Mol Biol Transl Sci. 2014;122:169-92
pubmed: 24484701
J Neurophysiol. 2002 Aug;88(2):1005-15
pubmed: 12163549
J Neurosci. 2005 Feb 2;25(5):1089-94
pubmed: 15689544
Cell Metab. 2014 Aug 5;20(2):208-13
pubmed: 25100062
Front Cell Neurosci. 2019 Aug 07;13:363
pubmed: 31440144
Pharmacol Biochem Behav. 2010 Feb;94(4):588-94
pubmed: 19969016
Food Chem Toxicol. 2019 Dec;134:110822
pubmed: 31536753
F1000Res. 2019 Jul 31;8:
pubmed: 31448084
Biochem Biophys Res Commun. 2011 Jun 24;410(1):7-12
pubmed: 21621509
Curr Neuropharmacol. 2018;16(10):1455-1465
pubmed: 29651949
Cell Mol Life Sci. 2017 Oct;74(20):3667-3686
pubmed: 28534084
J Neurosci. 2019 Oct 16;39(42):8259-8266
pubmed: 31619495
Mol Brain. 2012 May 14;5:14
pubmed: 22583753
Front Biol (Beijing). 2016 Oct;11(5):376-386
pubmed: 28974957
Food Chem Toxicol. 2005 Feb;43(2):187-201
pubmed: 15621331
J Neurochem. 2018 Jan;144(1):7-34
pubmed: 29049853
Front Neurosci. 2018 Jun 26;12:427
pubmed: 29997473
Arzneimittelforschung. 2001 Sep;51(9):699-725
pubmed: 11642003
Trends Pharmacol Sci. 2019 Dec;40(12):971-985
pubmed: 31704172
Nat Rev Neurosci. 2013 Jan;14(1):7-23
pubmed: 23254191
ACS Chem Neurosci. 2019 May 15;10(5):2209-2221
pubmed: 30985105
Med Hypotheses. 1994 May;42(5):323-7
pubmed: 7935075
Endocr Regul. 2014 Jan;48(1):35-48
pubmed: 24524374
Biomed Biochim Acta. 1985;44(4):611-22
pubmed: 4026816
J Neurosci. 2020 Feb 12;40(7):1405-1426
pubmed: 31915257
J Neural Transm (Vienna). 2013 Oct;120(10):1397-409
pubmed: 23588349
Neuron. 2015 Oct 7;88(1):33-46
pubmed: 26447571
F1000Res. 2019 Sep 19;8:
pubmed: 31583078
J Cereb Blood Flow Metab. 2015 Jan;35(1):74-85
pubmed: 25294126