• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

二氢吡啶类钙通道拮抗剂尼群地平和尼莫地平的抗惊厥作用概况。

Anticonvulsant profile of the dihydropyridine calcium channel antagonists, nitrendipine and nimodipine.

作者信息

Dolin S J, Hunter A B, Halsey M J, Little H J

机构信息

Department of Anaesthesia, Addenbrooke's Hospital, Cambridge, U.K.

出版信息

Eur J Pharmacol. 1988 Jul 26;152(1-2):19-27. doi: 10.1016/0014-2999(88)90831-x.

DOI:10.1016/0014-2999(88)90831-x
PMID:2463174
Abstract

The effects of the dihydropyridine calcium channel antagonists, nitrendipine and nimodipine, on convulsions produced by different mechanisms have been studied in rats. Nitrendipine and nimodipine significantly raised the thresholds to pentylenetetrazol for up to six hours after their injection. The calcium channel agonist, BAY K 8644, lowered the convulsion threshold to pentylenetetrazol and antagonised the effects of nitrendipine. In contrast, the severity of seizures produced by N-methyl-dl-aspartate (NMA) was increased by nitrendipine. BAY K 8644 also slightly increased the effects of NMA. Nimodipine and nitrendipine caused small, but significant, increases in the threshold pressures for the convulsions caused by raising the atmospheric pressure with helium gas. The compounds had no effect on strychnine convulsions. The conclusion is that the calcium channel antagonists are anticonvulsant against only certain types of convulsions, such as pentylenetetrazol and high pressure (and ethanol withdrawal, reported previously). Others may be increased, such as NMA seizures, or unaffected, such as strychnine-induced convulsions.

摘要

在大鼠中研究了二氢吡啶类钙通道拮抗剂尼群地平和尼莫地平对不同机制所致惊厥的影响。尼群地平和尼莫地平在注射后长达6小时显著提高了对戊四氮的惊厥阈值。钙通道激动剂BAY K 8644降低了对戊四氮的惊厥阈值,并拮抗了尼群地平的作用。相反,尼群地平增加了由N-甲基-DL-天冬氨酸(NMA)所致癫痫发作的严重程度。BAY K 8644也轻微增强了NMA的作用。尼莫地平和尼群地平使因用氦气升高大气压所致惊厥的阈值压力有小幅度但显著的升高。这些化合物对士的宁惊厥没有影响。结论是钙通道拮抗剂仅对某些类型的惊厥有抗惊厥作用,如戊四氮和高压(以及先前报道的乙醇戒断)所致惊厥。其他类型的惊厥可能会增加,如NMA所致癫痫发作,或不受影响,如士的宁所致惊厥。

相似文献

1
Anticonvulsant profile of the dihydropyridine calcium channel antagonists, nitrendipine and nimodipine.二氢吡啶类钙通道拮抗剂尼群地平和尼莫地平的抗惊厥作用概况。
Eur J Pharmacol. 1988 Jul 26;152(1-2):19-27. doi: 10.1016/0014-2999(88)90831-x.
2
The effects of dihydropyridine calcium channel modulators on pentylenetetrazole convulsions.二氢吡啶类钙通道调节剂对戊四氮惊厥的影响。
Brain Res Bull. 1990 Jul;25(1):211-4. doi: 10.1016/0361-9230(90)90279-9.
3
Anticonvulsant properties of calcium channel blockers in mice: N-methyl-D-,L-aspartate- and Bay K 8644-induced convulsions are potently blocked by the dihydropyridines.钙通道阻滞剂对小鼠的抗惊厥特性:二氢吡啶类药物可有效阻断N-甲基-D-、L-天冬氨酸和Bay K 8644诱导的惊厥。
Epilepsia. 1993 Mar-Apr;34(2):372-80. doi: 10.1111/j.1528-1157.1993.tb02424.x.
4
Effects of calcium antagonist nimodipine on pentylenetetrazole-induced seizures in rats and rabbits.钙拮抗剂尼莫地平对大鼠和家兔戊四氮诱发癫痫发作的影响。
Arch Int Pharmacodyn Ther. 1988 Mar-Apr;292:58-67.
5
Effects of diltiazem in convulsive states differ from those previously reported for dihydropyridine calcium channel antagonists.地尔硫䓬在惊厥状态下的作用与先前报道的二氢吡啶类钙通道拮抗剂的作用不同。
Psychopharmacology (Berl). 1994 Mar;114(2):321-8. doi: 10.1007/BF02244855.
6
Dihydropyridine antagonists and agonists of calcium channels inhibit the induction of nitric oxide synthase by endotoxin in cultured macrophages.二氢吡啶类钙通道拮抗剂和激动剂可抑制内毒素在培养的巨噬细胞中诱导一氧化氮合酶的产生。
Biochem Biophys Res Commun. 1993 Oct 29;196(2):825-30. doi: 10.1006/bbrc.1993.2323.
7
Effects of dihydropyridine Ca2+ channel blockers on the discriminative stimulus and the motor impairing effects of (+/-)-Bay K 8644.二氢吡啶类钙离子通道阻滞剂对辨别刺激及(±)-Bay K 8644运动损害作用的影响
Eur J Pharmacol. 1997 Oct 8;336(2-3):113-21. doi: 10.1016/s0014-2999(97)01240-5.
8
The effects of chemically and electrically-induced convulsions on [3H]nitrendipine binding in mouse brain.化学诱导和电诱导惊厥对小鼠脑内[3H]尼群地平结合的影响。
Brain Res Bull. 1987 Dec;19(6):673-8. doi: 10.1016/0361-9230(87)90053-0.
9
Anticonvulsant activity of MK-801 and nimodipine alone and in combination against pentylenetetrazole and strychnine.MK-801与尼莫地平单独及联合应用对抗戊四氮和士的宁的抗惊厥活性。
Pharmacol Biochem Behav. 1989 Mar;32(3):595-600. doi: 10.1016/0091-3057(89)90003-8.
10
Effects of dihydropyridine calcium channel antagonists in ethanol withdrawal; doses required, stereospecificity and actions of Bay K 8644.二氢吡啶类钙通道拮抗剂在乙醇戒断中的作用;所需剂量、立体特异性及Bay K 8644的作用
Psychopharmacology (Berl). 1990;100(3):387-92. doi: 10.1007/BF02244612.

引用本文的文献

1
Meta-analysis of initial seizure thresholds in electroconvulsive therapy.电抽搐治疗初始抽搐阈值的荟萃分析。
Eur Arch Psychiatry Clin Neurosci. 2009 Dec;259(8):467-74. doi: 10.1007/s00406-009-0011-7. Epub 2009 Apr 21.
2
Influence of nicardipine, nimodipine and flunarizine on the anticonvulsant efficacy of antiepileptics against pentylenetetrazol in mice.尼卡地平、尼莫地平和氟桂利嗪对小鼠抗癫痫药物抗戊四氮惊厥疗效的影响。
J Neural Transm (Vienna). 1996;103(7):819-31. doi: 10.1007/BF01273360.
3
Interactions between diltiazem and ethanol: differences from those seen with dihydropyridine calcium channel antagonists.
地尔硫䓬与乙醇之间的相互作用:与二氢吡啶类钙通道拮抗剂的相互作用差异。
Psychopharmacology (Berl). 1994 Mar;114(2):329-36. doi: 10.1007/BF02244856.
4
The differential effects of felodipine and nitrendipine on cerebral dihydropyridine binding ex vivo and the ethanol withdrawal syndrome in mice.非洛地平和尼群地平对小鼠大脑二氢吡啶结合体外实验及乙醇戒断综合征的不同作用。
Br J Pharmacol. 1994 Aug;112(4):1017-24. doi: 10.1111/j.1476-5381.1994.tb13184.x.
5
Nitrendipine decreases benzodiazepine withdrawal seizures but not the development of benzodiazepine tolerance or withdrawal signs.尼群地平可减少苯二氮䓬类药物戒断性癫痫发作,但不能减少苯二氮䓬类药物耐受性的形成或戒断症状。
Br J Pharmacol. 1990 Nov;101(3):691-7. doi: 10.1111/j.1476-5381.1990.tb14142.x.
6
Chronic dihydropyridine treatment can reverse the behavioural consequences of and prevent adaptations to, chronic ethanol treatment.慢性二氢吡啶治疗可逆转慢性乙醇治疗的行为后果并防止对其产生适应性变化。
Br J Pharmacol. 1991 Jul;103(3):1669-76. doi: 10.1111/j.1476-5381.1991.tb09845.x.
7
A calcium channel antagonist stereoselectively decreases ethanol withdrawal hyperexcitability but not that due to bicuculline, in hippocampal slices.在海马切片中,一种钙通道拮抗剂能立体选择性地降低乙醇戒断引起的过度兴奋,但对荷包牡丹碱引起的过度兴奋无此作用。
Br J Pharmacol. 1991 Jun;103(2):1313-20. doi: 10.1111/j.1476-5381.1991.tb09786.x.
8
The effects of Ca2+ antagonists and hydralazine on central 5-hydroxytryptamine biochemistry and function in rats and mice.钙通道阻滞剂和肼屈嗪对大鼠和小鼠中枢5-羟色胺生物化学及功能的影响。
Br J Pharmacol. 1990 Jan;99(1):41-6. doi: 10.1111/j.1476-5381.1990.tb14651.x.
9
Effects of dihydropyridine calcium channel antagonists in ethanol withdrawal; doses required, stereospecificity and actions of Bay K 8644.二氢吡啶类钙通道拮抗剂在乙醇戒断中的作用;所需剂量、立体特异性及Bay K 8644的作用
Psychopharmacology (Berl). 1990;100(3):387-92. doi: 10.1007/BF02244612.
10
Cromakalim (BRL 34915) counteracts the epileptiform activity elicited by diltiazem and verapamil in rats.克罗卡林(BRL 34915)可对抗地尔硫卓和维拉帕米在大鼠中引发的癫痫样活动。
Br J Pharmacol. 1991 Dec;104(4):907-13. doi: 10.1111/j.1476-5381.1991.tb12525.x.