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钙通透性AMPA受体拮抗剂IEM1460:对幼鼠的抗惊厥作用?

An antagonist of calcium permeable AMPA receptors, IEM1460: Anticonvulsant action in immature rats?

作者信息

Szczurowska Ewa, Mareš Pavel

机构信息

Department of Developmental Epileptology, Institute of Physiology, Academy of Sciences of the Czech Republic, Videnska 1083, 14220 Prague, Czech Republic.

Department of Developmental Epileptology, Institute of Physiology, Academy of Sciences of the Czech Republic, Videnska 1083, 14220 Prague, Czech Republic.

出版信息

Epilepsy Res. 2015 Jan;109:106-13. doi: 10.1016/j.eplepsyres.2014.10.020. Epub 2014 Nov 6.

Abstract

AMPA receptors lacking GluA2 subunit are widely distributed in developing brain. IEM1460 as a specific antagonist of these receptors might be a potential age-specific anticonvulsant. Possible anticonvulsant action was assessed in two models of epileptic seizures: pentylenetetrazol (PTZ) - induced convulsions and cortical afterdischarges elicited in 12-, 18- and 25-day-old rats. IEM1460 was administered intraperitoneally in doses of 3, 10 and 20mg/kg. Pretreatment with IEM1460 at the dose of 20mg/kg resulted in delayed onset of PTZ-induced minimal clonic seizures in all age groups. PTZ-induced generalized tonic-clonic seizures were suppressed in 18- and 25-day-old rats by 10 and 20mg/kg doses of IEM1460. Duration of cortical afterdischarges progressively increased with repeated stimulations in control 12-day-old rats. The IEM1460 dose of 10mg/kg fully blocked this prolongation and the 20-mg/kg dose partly suppressed it. Administration of IEM1460 had moderate proconvulsant effect on 18- and 25-day-old animals - afterdischarges were prolonged with repeated stimulations. The duration of cortical epileptic afterdischarges in adult (80-day-old) animals was not affected by IEM1460. Effects of IEM1460 are dependent on the model of seizures used, their ictogenic structures and developmental changes in subunit composition of AMPA receptors.

摘要

缺乏GluA2亚基的AMPA受体广泛分布于发育中的大脑。IEM1460作为这些受体的特异性拮抗剂,可能是一种潜在的年龄特异性抗惊厥药物。在两种癫痫发作模型中评估了其可能的抗惊厥作用:戊四氮(PTZ)诱导的惊厥以及在12日龄、18日龄和25日龄大鼠中诱发的皮层后放电。IEM1460以3、10和20mg/kg的剂量腹腔注射。以20mg/kg的剂量预先给予IEM1460可使所有年龄组的PTZ诱导的最小阵挛性发作的发作延迟。10和20mg/kg剂量的IEM1460可抑制18日龄和25日龄大鼠中PTZ诱导的全身强直阵挛性发作。在对照的12日龄大鼠中,随着重复刺激,皮层后放电的持续时间逐渐增加。10mg/kg剂量的IEM1460完全阻断了这种延长,而20mg/kg剂量部分抑制了它。给予IEM1460对18日龄和25日龄动物有中度的促惊厥作用——随着重复刺激,后放电延长。IEM1460对成年(80日龄)动物的皮层癫痫后放电持续时间没有影响。IEM1460的作用取决于所使用的癫痫发作模型、其致痫结构以及AMPA受体亚基组成的发育变化。

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