• 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

新型头孢菌素抗生素头孢哌酮的一般药理学(作者译)

[General pharmacology of cefoperazone, a new cephalosporin antibiotic (author's transl)].

作者信息

Takai A, Hirai S, Watanabe I, Hiraiwa T, Abe N, Omori M, Muroda T, Nakajima S, Nakada Y, Tanada K, Senda N, Tanaka K, Makino H

出版信息

Jpn J Antibiot. 1980 Oct;33(10):994-1018.

PMID:6451724
Abstract

General pharmacological properties of cefoperazone (CPZ) were studied in various experimental animals. CPZ showed the following effects with intravenous injection to experimental animals. On the central nervous system, CPZ caused vomiting in dogs at 500 mg/kg, pyrexia and slow waves in electroencephalogram in rabbits at 1,000 mg/kg. On the motor and sensory nervous systems, CPZ enhanced slightly the twitch tension of musculus gastrocnemius induced by electrical stimulation in rats at 500 mg/kg. On the respiratory, cardiovascular and autonomic nervous systems, CPZ increased transiently the respiratory rate and potentiated the depressor response to Ach at 125 mg/kg, increased femoral blood flow, potentiated the pressor response to Adr in dogs and decreased the contraction of nictitating membrane induced by electrical stimulation in cats at 500 mg/kg, and then raised the systolic blood pressure in rabbits at 1,000 mg/kg. On the blood, CPZ decreased ChE activity in rabbit plasma at 250 mg/kg, prolonged bleeding time in mice at 500 mg/kg and prothrombin time in rabbits at 1,000 mg/kg. On the smooth muscle organs, CPZ enhanced slightly gastric motility in rabbits and ileal motility in guinea pigs at 62.5 and 125 mg/kg respectively, and promoted gastrointestinal propulsion of BaSO4 meal in mice at 1,000 mg/kg. On the urinary organ, CPZ increased urine volume and electrolytes excretion in dogs at 500 mg/kg. Subcutaneous injection of CPZ scarcely showed any significant effect in experimental animals under the dose of 2,000 mg/kg. In the in vitro experiments, CPZ enhanced slightly the motility of isolated rabbit gastrointestinal tract at 10(-3) g/ml. Assuming the single clinical dose of CPZ should be 10 approximately 40 mg/kg, it is concluded that the occurrence of pharmacological effects observed in experimental animals seems to be very rare clinically.

摘要

在各种实验动物中研究了头孢哌酮(CPZ)的一般药理学特性。对实验动物静脉注射CPZ后显示出以下效应。在中枢神经系统方面,CPZ在犬中剂量为500mg/kg时引起呕吐,在兔中剂量为1000mg/kg时引起发热和脑电图慢波。在运动和感觉神经系统方面,CPZ在大鼠中剂量为500mg/kg时轻微增强电刺激诱发的腓肠肌抽搐张力。在呼吸、心血管和自主神经系统方面,CPZ在剂量为125mg/kg时短暂增加呼吸频率并增强对乙酰胆碱的降压反应,增加股血流量,在犬中增强对肾上腺素的升压反应,在猫中剂量为500mg/kg时减少电刺激诱发的瞬膜收缩,然后在兔中剂量为1000mg/kg时升高收缩压。在血液方面,CPZ在兔血浆中剂量为250mg/kg时降低胆碱酯酶活性,在小鼠中剂量为500mg/kg时延长出血时间,在兔中剂量为1000mg/kg时延长凝血酶原时间。在平滑肌器官方面,CPZ在兔中剂量为62.5mg/kg、在豚鼠中剂量为125mg/kg时分别轻微增强胃动力和回肠动力,在小鼠中剂量为1000mg/kg时促进硫酸钡餐的胃肠推进。在泌尿器官方面,CPZ在犬中剂量为500mg/kg时增加尿量和电解质排泄。皮下注射CPZ在剂量达2000mg/kg时在实验动物中几乎未显示任何显著效应。在体外实验中,CPZ在浓度为10(-3)g/ml时轻微增强离体兔胃肠道的动力。假设CPZ的单次临床剂量应为约10至40mg/kg,得出结论:在实验动物中观察到的药理学效应在临床上似乎非常罕见。

相似文献

1
[General pharmacology of cefoperazone, a new cephalosporin antibiotic (author's transl)].新型头孢菌素抗生素头孢哌酮的一般药理学(作者译)
Jpn J Antibiot. 1980 Oct;33(10):994-1018.
2
[General pharmacology of T-2588, a new oral cephem antibiotic].新型口服头孢菌素类抗生素T-2588的一般药理学
Jpn J Antibiot. 1986 Apr;39(4):958-78.
3
General pharmacological profile of the new cognition-enhancing agent nefiracetam.新型促认知药物奈非西坦的一般药理学特性
Arzneimittelforschung. 1994 Feb;44(2A):199-210.
4
[General pharmacology of T-1982, a new cephamycin antibiotic].新型头孢霉素抗生素T-1982的一般药理学
Jpn J Antibiot. 1982 Sep;35(9):2139-54.
5
[General pharmacology of aclacinomycin A (author's transl)].阿克拉霉素A的一般药理学(作者译)
Jpn J Antibiot. 1980 Feb;33(2):192-213.
6
[General pharmacology of T-3761, a new oral quinolone antibacterial agent (2). Effect on the respiratory and cardiovascular systems, autonomic nervous system and other functions].
Jpn J Antibiot. 1995 May;48(5):706-32.
7
Pharmacological studies on timiperone, a new neuroleptic drug Part II: General pharmacological properties.新型抗精神病药物替米哌隆的药理学研究 第二部分:一般药理学特性
Arzneimittelforschung. 1981;31(4):707-15.
8
General pharmacology of the new quinolone antibacterial agent levofloxacin.新型喹诺酮类抗菌药物左氧氟沙星的一般药理学
Arzneimittelforschung. 1992 Mar;43(3A):408-18.
9
[General pharmacology of BMY-28100].[BMY - 28100的一般药理学]
Jpn J Antibiot. 1990 Jul;43(7):1289-309.
10
General pharmacology of recombinant human basic fibroblast growth factor.重组人碱性成纤维细胞生长因子的一般药理学
Arzneimittelforschung. 1996 Jul;46(7):727-39.

引用本文的文献

1
Some Pharmacodynamic Aspects of Cefepime.头孢吡肟的一些药效学方面
J Pharm (Cairo). 2013;2013:381910. doi: 10.1155/2013/381910. Epub 2012 Nov 7.
2
Impact of cefoperazone therapy on fecal flora.头孢哌酮治疗对粪便菌群的影响。
Antimicrob Agents Chemother. 1982 Aug;22(2):226-30. doi: 10.1128/AAC.22.2.226.
3
Clinical studies with cefoperazone in the treatment of bacterial infections in surgical practice.头孢哌酮治疗外科手术中细菌感染的临床研究。
Drugs. 1981;22 Suppl 1:87-93. doi: 10.2165/00003495-198100221-00018.