• 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

尼卡地平对内毒素休克大鼠的影响。

Effects of nicardipine in rats subjected to endotoxic shock.

作者信息

Lee H C, Hardman J M, Lum B K

机构信息

Department of Pharmacology, John A. Burns School of Medicine, University of Hawaii, Honolulu 96822.

出版信息

Gen Pharmacol. 1992 Jan;23(1):71-4. doi: 10.1016/0306-3623(92)90050-t.

DOI:10.1016/0306-3623(92)90050-t
PMID:1592229
Abstract
  1. The calcium channel blocker, nicardipine, produced a dose-dependent reduction in the mortality caused by endotoxin in rats. 2. The drug also reduced most of the hematological and gross pathological manifestations of disseminated intravascular coagulation (DIC) caused by endotoxin. 3. The endotoxin-induced monocytopenia but not the granulocytopenia, lymphocytopenia or thrombocytopenia was inhibited by the drug. 4. The results suggest that the protective action of nicardipine is causally related to prevention of the endotoxin-induced DIC and that an effect of the drug on monocytes may be of importance.
摘要
  1. 钙通道阻滞剂尼卡地平可使大鼠内毒素所致死亡率呈剂量依赖性降低。2. 该药还减轻了内毒素所致弥散性血管内凝血(DIC)的大部分血液学和大体病理学表现。3. 该药可抑制内毒素诱导的单核细胞减少,但对粒细胞减少、淋巴细胞减少或血小板减少无抑制作用。4. 结果提示,尼卡地平的保护作用与预防内毒素诱导的DIC有因果关系,且该药对单核细胞的作用可能很重要。

相似文献

1
Effects of nicardipine in rats subjected to endotoxic shock.尼卡地平对内毒素休克大鼠的影响。
Gen Pharmacol. 1992 Jan;23(1):71-4. doi: 10.1016/0306-3623(92)90050-t.
2
Protective effect of gabexate mesilate against experimental disseminated intravascular coagulation in rats.甲磺酸加贝酯对大鼠实验性弥散性血管内凝血的保护作用。
Haemostasis. 1983;13(4):262-7. doi: 10.1159/000214758.
3
Prevention by methylprednisolone of disseminated intravascular coagulation induced by sustained infusion of endotoxin in rats.甲基强的松龙对大鼠持续输注内毒素诱导的弥散性血管内凝血的预防作用。
Haemostasis. 1983;13(4):268-73. doi: 10.1159/000214759.
4
Effects of slow intravenous administration of endotoxin on blood cells and coagulation in dogs.缓慢静脉注射内毒素对犬血细胞及凝血的影响。
Eur Surg Res. 1978;10(3):194-205. doi: 10.1159/000128008.
5
Effects of superoxide dismutase and catalase on disseminated intravascular coagulation in rats.超氧化物歧化酶和过氧化氢酶对大鼠弥散性血管内凝血的影响。
Thromb Haemost. 1983 Dec 30;50(4):869-72.
6
The effects of the calcium entry blockers, nilvadipine and nitrendipine, on endotoxin-induced disseminated intravascular coagulation.钙通道阻滞剂尼伐地平与尼群地平对内毒素诱导的弥散性血管内凝血的影响。
Life Sci. 1989;45(10):877-83. doi: 10.1016/0024-3205(89)90201-4.
7
Prednisolone inhibits endotoxin-induced disseminated intravascular coagulation and improves mortality in rats: importance of inflammatory cytokine suppression.泼尼松龙可抑制内毒素诱导的大鼠弥散性血管内凝血并提高其存活率:抑制炎性细胞因子的重要性。
Blood Coagul Fibrinolysis. 1999 Sep;10(6):321-30. doi: 10.1097/00001721-199909000-00002.
8
Monophosphoryl lipid A protects against endotoxic shock via inhibiting neutrophil infiltration and preventing disseminated intravascular coagulation.单磷酰脂质A通过抑制中性粒细胞浸润和预防弥散性血管内凝血来预防内毒素休克。
Circ Shock. 1994 Jul;43(3):107-14.
9
Effect of dipyridamole on experimental disseminated intravascular coagulation in rats.双嘧达莫对大鼠实验性弥散性血管内凝血的影响。
Thromb Res. 1983 Mar 15;29(6):619-25. doi: 10.1016/0049-3848(83)90216-5.
10
Effect of vitamin E on endotoxin-induced disseminated intravascular coagulation in rats.维生素E对大鼠内毒素诱导的弥散性血管内凝血的影响。
Thromb Haemost. 1982 Oct 29;48(2):235-7.

引用本文的文献

1
Altered L-type Ca2+ channel activity contributes to exacerbated hypoperfusion and mortality in smooth muscle cell BK channel-deficient septic mice.平滑肌细胞 BK 通道缺陷型脓毒症小鼠中 L 型钙通道活性改变导致灌注不足和死亡率增加。
Am J Physiol Regul Integr Comp Physiol. 2014 Jul 15;307(2):R138-48. doi: 10.1152/ajpregu.00117.2014.
2
Vascular BK channel deficiency exacerbates organ damage and mortality in endotoxemic mice.血管 BK 通道缺陷可加重内毒素血症小鼠的器官损伤和死亡。
J Cardiovasc Pharmacol. 2012 Mar;59(3):207-14. doi: 10.1097/FJC.0b013e31823b493b.