Cryptotanshinone enhances neurite outgrowth and memory via extracellular signal-regulated kinase 1/2 signaling.
Animals
Cell Differentiation
/ drug effects
Cell Line, Tumor
Cell Proliferation
/ drug effects
Female
Hippocampus
/ metabolism
Learning
/ drug effects
MAP Kinase Signaling System
/ drug effects
Male
Memory
/ drug effects
Mice
Mitogen-Activated Protein Kinase 3
/ metabolism
Neuronal Outgrowth
/ drug effects
Phenanthrenes
/ pharmacology
Phosphorylation
/ drug effects
Cryptotanshinone
ERK1/2
Memory
Neurite outgrowth
Neuro2a cell
Passive avoidance test
Journal
Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association
ISSN: 1873-6351
Titre abrégé: Food Chem Toxicol
Pays: England
ID NLM: 8207483
Informations de publication
Date de publication:
Feb 2020
Feb 2020
Historique:
received:
18
07
2019
revised:
27
11
2019
accepted:
29
11
2019
pubmed:
4
12
2019
medline:
23
7
2020
entrez:
3
12
2019
Statut:
ppublish
Résumé
Neurite outgrowth is important process in synaptic formation and neuronal development. Many previous studies reported that natural compounds as well as neurotrophins induce neurite outgrowth through various signaling pathways. In this study, we tested the effect of cryptotanshinone (CPT), a constituent of Salvia miltiorrhiza Bunge, on neurite outgrowth using neuro2a cell line, a mouse neuroblastoma cell line. And then, we examined the effect of CPT on learning and memory. We first found that CPT facilitated neurite outgrowth in a concentration-dependent manner. Although CPT induced MTT reduction, CPT did not induce LDH release. Moreover, CPT suppressed cell proliferation. CPT increased ERK1/2 phosphorylation and ERK1/2 inhibitor blocked CPT-facilitated neurite outgrowth. CPT also enhanced learning and memory without affecting basal sensory conditions and increased ERK1/2 phosphorylation in the hippocampus in a dose-dependent manner. These results demonstrate that CPT facilitates neurite outgrowth and enhances learning and memory, which may be mediated by facilitating ERK1/2 signal.
Identifiants
pubmed: 31790773
pii: S0278-6915(19)30801-4
doi: 10.1016/j.fct.2019.111011
pii:
doi:
Substances chimiques
Phenanthrenes
0
cryptotanshinone
5E9SXT166N
Mitogen-Activated Protein Kinase 3
EC 2.7.11.24
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
111011Informations de copyright
Copyright © 2019 Elsevier Ltd. All rights reserved.
Déclaration de conflit d'intérêts
Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.