共 2 条
The Marine Guanidine Alkaloid Crambescidin 816 Induces Calcium Influx and Cytotoxicity in Primary Cultures of Cortical Neurons through Glutamate Receptors
被引:16
|作者:
Mendez, Aida G.
[1
]
Boente Juncal, Andrea
[1
]
Silva, Siguara B. L.
[2
,3
]
Thomas, Olivier P.
[2
,4
]
Martin Vazquez, Victor
[1
]
Alfonso, Amparo
[1
]
Vieytes, Mercedes R.
[5
]
Vale, Carmen
[1
]
Botana, Luis M.
[1
]
机构:
[1] Univ Santiago de Compostela, Fac Vet, Dept Farmacol, Lugo 27002, Spain
[2] Univ Nice Sophia Antipolis, Geoazur, CNRS, UMR,IRD,OCA, F-06560 Valbonne, France
[3] Univ Paris Sud, Fac Pharm, Lab Pharmacognosie, CNRS,UMR 8076,BioCIS,LabEx LERMIT, F-92290 Chatenay Malabry, France
[4] Natl Univ Ireland Galway, Sch Chem, Marine Biodiscovery, Galway, Ireland
[5] Univ Santiago de Compostela, Fac Vet, Dept Fisiol, Lugo 27002, Spain
来源:
ACS CHEMICAL NEUROSCIENCE
|
2017年
/
8卷
/
07期
关键词:
Guanidine alkaloids;
crambescidin;
816;
cortical neurons;
cytosolic Ca2+;
cytotoxicity;
glutamate receptors;
VOLTAGE-GATED SODIUM;
CELL-DEATH;
NEURODEGENERATIVE DISEASES;
ENDOPLASMIC-RETICULUM;
CHANNEL BLOCKER;
IN-VITRO;
APOPTOSIS;
INJURY;
NEUROTOXICITY;
CIGUATOXIN;
D O I:
10.1021/acschemneuro.7b00096
中图分类号:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号:
071010 ;
081704 ;
摘要:
Crambescidin 816 is a guanidine alkaloid produced by the sponge Crambe crambe with known antitumoral activity. While the information describing the effects of this alkaloid in central neurons is scarce, Cramb816 is known to block voltage dependent calcium channels being selective for L-type channels. Moreover, Cramb816 reduced neuronal viability through an unknown mechanism. Here, we aimed to describe the toxic activity of Cramb816 in cortical neurons. Since calcium influx is considered the main mechanism responsible for neuronal cell death, the effects of Cramb816 in the cytosolic calcium concentration of cortical neurons were studied. The alkaloid decreased neuronal viability and induced a dose-dependent increase in cytosolic calcium that was also related to the presence of calcium in the extracellular media. The increase in calcium influx was age dependent, being higher in younger neurons. Moreover, this effect was prevented by glutamate receptor antagonists, which did not fully block the cytotoxic effect of Cramb816 after 24 h of treatment but completely prevented Cramb816 cytotoxicity after 10 min exposure. Therefore, the findings presented herein provide new insights into the cytotoxic effect of Cramb816 in cortical neurons.
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页码:1609 / 1617
页数:9
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