首页> 外文期刊>European Journal of Pharmacology: An International Journal >T-477, a novel Ca(2+)- and Na(+) channel blocker, prevents veratridine-induced neuronal injury.
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T-477, a novel Ca(2+)- and Na(+) channel blocker, prevents veratridine-induced neuronal injury.

机译:T-477,一种新型的Ca(2 +)-和Na(+)通道阻滞剂,防止了维甲酸对神经元的伤害。

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摘要

To evaluate the effect of (R)-(+)-2-(4-chlorophenyl)-2, 3-dihydro-4-diethyl aminoacetyl-4H-1,4-benzothiazine hydrochloride (T-477), a novel Na(+)- and Ca(2+) channel blocker, on neuronal injury in vitro, we studied veratridine-induced injury in cultured rat hippocampal neurons. Neurons swelled extensively 10 min after the addition of veratridine, and returned to their initial size within 2 h. Intracellular Na(+) and Ca(2+) concentrations and amino acid release from the cells, in particular, that of glutamate, increased after the treatment with veratridine. Approximately 70% of neurons died within 24 h. T-477 inhibited both veratridine-induced swelling and death in a concentration-dependent manner. Moreover, T-477 concentration dependently reduced the increases in Na(+) and Ca(2+) influx and amino acid release. These results suggest that T-477 prevented the veratridine-induced influx of Na(+) and, thereby, reduced neuronal swelling. This, combined with the effects of T-477 on the inhibition of Ca(2+) influx and glutamate release, possibly by the blockade of Na(+) channels, may be the mechanism by which T-477 protects neurons from death induced by veratridine.
机译:为了评估(R)-(+)-2-(4-氯苯基)-2,3-二氢-4-二乙基氨基乙酰基-4H-1,4-苯并噻嗪盐酸盐(T-477)的作用,一种新型的Na( +)-和Ca(2+)通道阻滞剂,对体外神经元损伤,我们研究了维拉替丁在培养的大鼠海马神经元中诱导的损伤。加入藜芦定后10分钟,神经元大量肿胀,并在2小时内恢复到初始大小。维拉替丁处理后,细胞内Na(+)和Ca(2+)的浓度以及从细胞释放的氨基酸,特别是谷氨酸的释放增加。约70%的神经元在24小时内死亡。 T-477以浓度依赖的方式抑制维拉替丁诱导的肿胀和死亡。此外,T-477浓度依赖性地减少了Na(+)和Ca(2+)内流和氨基酸释放的增加。这些结果表明,T-477预防了Verrrridine诱导的Na(+)流入,从而减少了神经元肿胀。结合T-477对Ca(2+)内流和谷氨酸释放的抑制作用(可能是通过Na(+)通道的阻滞)相结合的,可能是T-477保护神经元免受由N诱导的死亡的机制。维拉替丁。

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