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Stimulation of [3H]norepinephrine release from hippocampal slices by excitatory amino acids

  
@article{APS5426,
	author = {Hui-qiu Wu and Annamaria Vezzani and Rosario Samanin},
	title = {Stimulation of [3H]norepinephrine release from hippocampal slices by excitatory amino acids},
	journal = {Acta Pharmacologica Sinica},
	volume = {10},
	number = {3},
	year = {2016},
	keywords = {},
	abstract = {[3H]norepinephrine efflux from preloaded rat hippocampal slices was increased in a dose-dependent manner by excitatory amino acids (EAA) in the following potency order: N-methyl-D-aspartic acid (NMDA) greater than kainic acid greater than L-glutamic acid greater than or equal to D,L-homocysteic acid greater than L-aspartic acid greater than quinolinic acid greater than quisqualic acid. The effect of EAA was blocked by physiological concentration of Mg2+, with the exception of kainic acid. D,L-2-amino-7-phosphonoheptanoic acid (APH) dose-dependently inhibited NMDA effect (IC50 = 69 mumol/L), whereas at 1 mmol/L it was ineffective versus kainic acid. The release of [3H]norepinephrine induced by quinolinic acid was blocked by APH 0.1 mmol/L. gamma-D-glutamylglycine dose-dependently inhibited kainic acid effect with an IC50 = 1.15 mmol/L. Tetrodotoxin 2 mumol/L reduced NMDA and kainic acid effects by 40 and 20%, respectively. The data indicate a possible involvement of central noradrenergic system in the modulation of excitotoxic action of EAA and offer a reliable system for testing new compounds acting at EAA-receptors by measuring norepinephrine release in vitro.},
	issn = {1745-7254},	url = {http://www.chinaphar.com/article/view/5426}
}