• 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

一种自由基清除剂在预防犬阿霉素诱导的心力衰竭中的效用。

Usefulness of a free radical scavenger in preventing doxorubicin-induced heart failure in dogs.

作者信息

Unverferth D V, Leier C V, Balcerzak S P, Hamlin R L

出版信息

Am J Cardiol. 1985 Jul 1;56(1):157-61. doi: 10.1016/0002-9149(85)90585-5.

DOI:10.1016/0002-9149(85)90585-5
PMID:4014022
Abstract

This study was designed to investigate whether either of 2 dosage schedules of N-acetylcysteine (NAC) was effective in preventing chronic doxorubicin-induced heart failure in dogs. Thirty-eight dogs were randomly assigned to 1 of 4 groups: controls, 10 dogs; doxorubicin only, 12 dogs; doxorubicin + low dose NAC, 8 dogs; and doxorubicin + high dose NAC, 8 dogs. All dogs except the controls received 1 mg/kg of doxorubicin weekly for 8 weeks and then every other week for 8 weeks. The doxorubicin + low-dose NAC group received 140 mg/kg of NAC 30 minutes before each dose of doxorubicin. The doxorubicin + high-dose NAC group received NAC before and then twice a day for 5 days. Systolic time intervals and echocardiograms were obtained weekly; cardiac catheterization was performed at the conclusion of the study. Of the 38 dogs in the study, 9 died; all deaths were in the doxorubicin treatment groups. The incidence of death was not different between the doxorubicin-only, the doxorubicin + low-dose and the doxorubicin + high-dose NAC groups. The noninvasive and the invasive and the catheterization data generally revealed poorer cardiac function of the doxorubicin treatment groups than in controls. However, no significant differences existed between the doxorubicin-only and doxorubicin + low-dose and doxorubicin + high-dose NAC groups. In conclusion, NAC in a low- or high-dose regimen did not significantly ameliorate doxorubicin cardiac toxicity. Because NAC is a free radical scavenger, perhaps doxorubicin cardiac toxicity is not a result of free radical generation.

摘要

本研究旨在调查两种剂量方案的N-乙酰半胱氨酸(NAC)是否能有效预防犬慢性阿霉素诱导的心力衰竭。38只犬被随机分为4组中的1组:对照组,10只犬;仅阿霉素组,12只犬;阿霉素+低剂量NAC组,8只犬;阿霉素+高剂量NAC组,8只犬。除对照组外,所有犬每周接受1mg/kg阿霉素,共8周,然后每两周接受一次,共8周。阿霉素+低剂量NAC组在每次阿霉素给药前30分钟接受140mg/kg NAC。阿霉素+高剂量NAC组在阿霉素给药前接受NAC,然后每天两次,共5天。每周获取收缩期时间间隔和超声心动图;在研究结束时进行心脏导管插入术。研究中的38只犬中有9只死亡;所有死亡均发生在阿霉素治疗组。仅阿霉素组、阿霉素+低剂量组和阿霉素+高剂量NAC组之间的死亡率没有差异。非侵入性、侵入性和导管插入术数据总体显示,阿霉素治疗组的心脏功能比对照组差。然而,仅阿霉素组与阿霉素+低剂量组和阿霉素+高剂量NAC组之间没有显著差异。总之,低剂量或高剂量方案的NAC并不能显著改善阿霉素的心脏毒性。由于NAC是一种自由基清除剂,或许阿霉素的心脏毒性不是自由基生成的结果。

相似文献

1
Usefulness of a free radical scavenger in preventing doxorubicin-induced heart failure in dogs.一种自由基清除剂在预防犬阿霉素诱导的心力衰竭中的效用。
Am J Cardiol. 1985 Jul 1;56(1):157-61. doi: 10.1016/0002-9149(85)90585-5.
2
Comparison of the effectiveness of (+/-)-1,2-bis(3,5-dioxopiperazinyl-1-yl)propane (ICRF-187) and N-acetylcysteine in preventing chronic doxorubicin cardiotoxicity in beagles.(±)-1,2-双(3,5-二氧代哌嗪基-1-基)丙烷(ICRF-187)与N-乙酰半胱氨酸预防比格犬慢性阿霉素心脏毒性的效果比较
Cancer Res. 1985 Jan;45(1):276-81.
3
Prospective randomized study of the role of N-acetyl cysteine in reversing doxorubicin-induced cardiomyopathy.N-乙酰半胱氨酸对阿霉素诱导的心肌病逆转作用的前瞻性随机研究。
Am J Clin Oncol. 1982 Dec;5(6):657-63. doi: 10.1097/00000421-198212000-00015.
4
Free radical involvement in doxorubicin-induced electrophysiological alterations in rat papillary muscle fibres.自由基参与阿霉素诱导的大鼠乳头肌纤维电生理改变。
Cardiovasc Res. 1998 Jun;38(3):695-702. doi: 10.1016/s0008-6363(98)00034-0.
5
N-acetylcysteine prevents doxorubucine-induced cardiotoxicity in rats.N-乙酰半胱氨酸可预防阿霉素引起的大鼠心脏毒性。
Hum Exp Toxicol. 2013 Jun;32(6):655-61. doi: 10.1177/0960327112467043. Epub 2013 Feb 19.
6
Doxorubicin-induced canine CHF: advantages and disadvantages.
J Card Surg. 2003 Jul-Aug;18(4):301-6. doi: 10.1046/j.1540-8191.2003.02032.x.
7
Protective effect of N-acetylcysteine, caffeic acid and vitamin E on doxorubicin hepatotoxicity.N-乙酰半胱氨酸、咖啡酸和维生素E对阿霉素肝毒性的保护作用。
Hum Exp Toxicol. 2007 Jun;26(6):519-25. doi: 10.1177/0960327107076885.
8
Lower incidence of doxorubicin-induced cardiomyopathy by once-a-week low-dose administration.每周一次低剂量给药降低阿霉素诱导的心肌病发生率。
Am Heart J. 1986 Apr;111(4):755-9. doi: 10.1016/0002-8703(86)90112-2.
9
Inhibition by oral N-acetylcysteine of doxorubicin-induced clastogenicity and alopecia, and prevention of primary tumors and lung micrometastases in mice.口服N-乙酰半胱氨酸对阿霉素诱导的染色体断裂及脱发的抑制作用,以及对小鼠原发性肿瘤和肺微转移的预防作用。
Int J Oncol. 1998 Aug;13(2):217-24. doi: 10.3892/ijo.13.2.217.
10
Doxorubicin-induced cardiotoxicosis. Clinical features in 32 dogs.阿霉素诱导的心脏中毒。32只犬的临床特征
J Vet Intern Med. 1992 Mar-Apr;6(2):82-8. doi: 10.1111/j.1939-1676.1992.tb03156.x.

引用本文的文献

1
Impact of Doxorubicin on Cardiac Function in Dogs: Ejection Fraction Changes and Heart Failure Risk.阿霉素对犬心脏功能的影响:射血分数变化及心力衰竭风险
Vet Med Sci. 2025 Sep;11(5):e70497. doi: 10.1002/vms3.70497.
2
Novel Therapeutics for Anthracycline Induced Cardiotoxicity.蒽环类药物所致心脏毒性的新型治疗方法
Front Cardiovasc Med. 2022 Apr 22;9:863314. doi: 10.3389/fcvm.2022.863314. eCollection 2022.
3
Arachidonic Acid Metabolism by Human Cardiovascular CYP2J2 Is Modulated by Doxorubicin.多柔比星对人心血管CYP2J2介导的花生四烯酸代谢有调节作用。
Biochemistry. 2017 Dec 26;56(51):6700-6712. doi: 10.1021/acs.biochem.7b01025. Epub 2017 Dec 12.
4
Mitochondrial topoisomerase I (top1mt) is a novel limiting factor of doxorubicin cardiotoxicity.线粒体拓扑异构酶I(top1mt)是阿霉素心脏毒性的一种新型限制因素。
Clin Cancer Res. 2014 Sep 15;20(18):4873-81. doi: 10.1158/1078-0432.CCR-13-3373. Epub 2014 Apr 8.
5
Oxidative stress, redox signaling, and metal chelation in anthracycline cardiotoxicity and pharmacological cardioprotection.蒽环类药物心脏毒性的氧化应激、氧化还原信号和金属螯合作用及药理学心脏保护作用。
Antioxid Redox Signal. 2013 Mar 10;18(8):899-929. doi: 10.1089/ars.2012.4795. Epub 2012 Oct 12.
6
Myocardial diseases of animals.动物的心肌疾病
Am J Pathol. 1986 Jul;124(1):98-178.
7
Anthracycline antitumour agents. A review of physicochemical, analytical and stability properties.蒽环类抗肿瘤药物。物理化学、分析及稳定性性质综述。
Pharm Weekbl Sci. 1986 Apr 25;8(2):109-33. doi: 10.1007/BF02086146.
8
Doxorubicin cardiotoxicity may be caused by its metabolite, doxorubicinol.阿霉素心脏毒性可能由其代谢产物阿霉素醇引起。
Proc Natl Acad Sci U S A. 1988 May;85(10):3585-9. doi: 10.1073/pnas.85.10.3585.
9
Reducing doxorubicin cardiotoxicity in the rat using deferred treatment with ADR-529.
Cancer Chemother Pharmacol. 1992;30(2):95-9. doi: 10.1007/BF00686399.