• 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

Effects of treatment with nilvadipine on cerebral ischemia in rats.

作者信息

Kawamura S, Li Y, Shirasawa M, Yasui N, Fukasawa H

机构信息

Department of Surgical Neurology, Research Institute for Brain and Blood Vessels-AKITA, Japan.

出版信息

Tohoku J Exp Med. 1998 Aug;185(4):239-46. doi: 10.1620/tjem.185.239.

DOI:10.1620/tjem.185.239
PMID:9865470
Abstract

The protective effects of a Ca2+ antagonist, nilvadipine, on focal cerebral ischemia were studied in male spontaneously hypertensive rats. The animals received either nilvadipine (3mg x kg(-1) x day(-1)) or a vehicle subcutaneously. Group 1 (n=11) was treated for 7 days, and Group 2 (n=11) for 14 days. The middle cerebral artery was occluded on the 6th (Group 1) or 13th (Group 2) day of the treatment, and neuropathological outcomes were quantified 24 hours later. The mean arterial blood pressure was significantly reduced with nilvadipine to normal levels. The % infarct volumes of Groups 1 (37+/-2) and 2 (34+/-3) were significantly less than those of their controls (39+/-3 [n=11] and 40+/-4 [n=12], respectively), although the difference between Groups 1 and 2 was not significant. When infarct areas were compared in each of 8 coronal sections, the infarct size had decreased in the 5 posterior sections in Group 2, but only in 2 sections of Group 1. A significant decrease in the edema volumes was observed in Group 2, but not in Group 1. Thus, nilvadipine provided protective effects against cerebral ischemia in rats having chronic hypertension, and the effects were dependent on the duration of treatment.

摘要

相似文献

1
Effects of treatment with nilvadipine on cerebral ischemia in rats.
Tohoku J Exp Med. 1998 Aug;185(4):239-46. doi: 10.1620/tjem.185.239.
2
Protective effect of nilvadipine on focal cerebral ischemia in spontaneously hypertensive rats.
Neurol Med Chir (Tokyo). 1996 Mar;36(3):151-5. doi: 10.2176/nmc.36.151.
3
Therapeutic effects of nilvadipine on rat focal cerebral ischemia.
Exp Brain Res. 1994;99(1):1-6. doi: 10.1007/BF00241406.
4
Effects of a Ca2+ entry blocker (nilvadipine) on acute focal cerebral ischemia in rats.
Exp Brain Res. 1991;83(2):434-8. doi: 10.1007/BF00231169.
5
Effects of the calcium antagonist nilvadipine on focal cerebral ischemia in spontaneously hypertensive rats.
Surg Neurol. 1991 Feb;35(2):105-10. doi: 10.1016/0090-3019(91)90259-c.
6
Attenuated neuropathology by nilvadipine after middle cerebral artery occlusion in rats.
Stroke. 1991 Jan;22(1):51-5. doi: 10.1161/01.str.22.1.51.
7
[Ca++ antagonist and acute brain ischemia: effects of nilvadipine and nicardipine on middle cerebral artery occlusion in rats].
Nihon Geka Hokan. 1991 Jan 1;60(1):38-44.
8
Nilvadipine, a new calcium channel blocker, reduces ischemic brain injury in rats.新型钙通道阻滞剂尼伐地平可减轻大鼠的缺血性脑损伤。
Jpn J Pharmacol. 1991 Aug;56(4):547-50. doi: 10.1254/jjp.56.547.
9
Effect of nilvadipine on the development of neurological deficits in stroke-prone spontaneously hypertensive rats.尼伐地平对易卒中型自发性高血压大鼠神经功能缺损发展的影响。
Stroke. 1994 Mar;25(3):677-82; discussion 682-3. doi: 10.1161/01.str.25.3.677.
10
Effects of nilvadipine (a dihydropyridine-type calcium entry blocker) on cerebral blood flow in acute experimental brain ischemia in rats.
Neurol Res. 1996 Aug;18(4):325-8. doi: 10.1080/01616412.1996.11740430.

引用本文的文献

1
Examining the therapeutic potential and side effects of calcium channel blockers in mortality and morbidity of patients with stroke: A systematic review of pre-clinical and clinical studies.研究钙通道阻滞剂对中风患者死亡率和发病率的治疗潜力及副作用:临床前和临床研究的系统评价
IBRO Neurosci Rep. 2025 Jan 8;18:222-243. doi: 10.1016/j.ibneur.2025.01.002. eCollection 2025 Jun.