• 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

[氢化可的松17 - 丁酸酯21 - 丙酸酯的毒性研究 - 4. 大鼠皮下注射的慢性毒性(作者译)]

[Studies on toxicity of hydrocortisone 17-butyrate 21-propionate -4. Chronic toxicity in rats by subcutaneous administration (author's transl)].

作者信息

Tarumoto Y, Tokado H, Kimura M, Kasai A, Iwamatsu Y, Tsuchida T, Noda K, Nakane S, Sasajima M, Ohzeki M

出版信息

J Toxicol Sci. 1981 Jul;6 Suppl:67-96. doi: 10.2131/jts.6.supplement_67.

DOI:10.2131/jts.6.supplement_67
PMID:7310934
Abstract

Chronic toxicity of hydrocortisone 17-butyrate 21-propionate (HBP), a new synthetic corticosteroid, was studied in rats. HBP was subcutaneously injected to rats as the daily doses of 0.001, 0.01, 0.01, 1.0 and 3.0 mg/kg for 6 months, and the following recovery test was carried out for 4 weeks. Hydrocortisone 17-butyrate (HB) and betamethasone 17-valerate (BV) were used as the reference drugs at the doses of 0.1, 1.0 and 3.0 mg/kg. The suppression of body weight gain by the administration of HBP was observed at the doses more than 1.0 mg/kg in male and more than 0.1 mg/kg in female, and the dead animals were sent at the highest dose of HB and BV. Mainly at the doses more than 0.1 mg/kg HBP induced the dose-dependent symptoms such as decrease in the number of white blood cells and total protein level in serum, and increase in total cholesterol, GOT and GPT level in serum, and atrophic changes of adrenals, lymphatic tissues, skin and subsexual organs. No usual abnormality was recognized at the doses less than 0.01 mg/kg of HBP. These symptoms were more toxic in male, and the strength of toxicity was in the order of BV greater than HB greater than HBP. Many of these findings have known as common effects of corticosteroids. The changes observed in this study were almost recovered after withdrawal of HBP at the doses less than 0.1 mg/kg. As the result, it was suggested that the maximum non-toxic dose of HBP was 0.001 mg/kg.

摘要

对一种新型合成皮质类固醇17 - 丁酸氢化可的松21 - 丙酸酯(HBP)进行了大鼠慢性毒性研究。将HBP以每日0.001、0.01、0.1、1.0和3.0 mg/kg的剂量皮下注射给大鼠,持续6个月,随后进行4周的恢复试验。以0.1、1.0和3.0 mg/kg的剂量使用17 - 丁酸氢化可的松(HB)和17 - 戊酸倍他米松(BV)作为参比药物。在雄性大鼠中,剂量超过1.0 mg/kg以及雌性大鼠中剂量超过0.1 mg/kg时,观察到HBP给药对体重增加有抑制作用,且在HB和BV的最高剂量组有动物死亡。主要在剂量超过0.1 mg/kg时,HBP诱导出现剂量依赖性症状,如白细胞数量减少、血清总蛋白水平降低、血清总胆固醇、谷草转氨酶(GOT)和谷丙转氨酶(GPT)水平升高,以及肾上腺、淋巴组织、皮肤和副性器官的萎缩性变化。在HBP剂量低于0.01 mg/kg时未发现常见异常。这些症状在雄性中更具毒性,毒性强度顺序为BV大于HB大于HBP。这些发现中的许多已被认为是皮质类固醇的常见作用。在本研究中观察到的变化在低于0.1 mg/kg剂量的HBP撤药后几乎完全恢复。结果表明,HBP的最大无毒剂量为0.001 mg/kg。

相似文献

1
[Studies on toxicity of hydrocortisone 17-butyrate 21-propionate -4. Chronic toxicity in rats by subcutaneous administration (author's transl)].[氢化可的松17 - 丁酸酯21 - 丙酸酯的毒性研究 - 4. 大鼠皮下注射的慢性毒性(作者译)]
J Toxicol Sci. 1981 Jul;6 Suppl:67-96. doi: 10.2131/jts.6.supplement_67.
2
[Studies on toxicity of hydrocortisone 17-butyrate 21-propionate -2. Subacute toxicity in rats by subcutaneous administration (author's transl)].17-丁酸氢化可的松21-丙酸酯的毒性研究 -2. 大鼠皮下注射的亚急性毒性(作者译)
J Toxicol Sci. 1981 Jul;6 Suppl:17-46. doi: 10.2131/jts.6.supplement_17.
3
[Studies of toxicity of hydrocortisone 17-butyrate 21-propionate -5. Chronic toxicity in rats by percutaneous administration (author's transl)].17-丁酸-21-丙酸氢化可的松的毒性研究-5. 经皮给药对大鼠的慢性毒性(作者译)
J Toxicol Sci. 1981 Jul;6 Suppl:97-120. doi: 10.2131/jts.6.supplement_97.
4
[Studies on toxicity of hydrocortisone 17-butyrate 21-propionate -3. Subacute toxicity in rats by percutaneous administration (author's transl)].[17-丁酸-21-丙酸氢化可的松的毒性研究-3. 经皮给药对大鼠的亚急性毒性(作者译)]
J Toxicol Sci. 1981 Jul;6 Suppl:47-66. doi: 10.2131/jts.6.supplement_47.
5
[Studies on toxicity of hydrocortisone 17-butyrate 21-propionate -1. Acute toxicity of hydrocortisone 17-butyrate 21-propionate and its analogues in mice, rats and dogs (author's transl)].氢化可的松17-丁酸酯21-丙酸酯的毒性研究 - 1. 氢化可的松17-丁酸酯21-丙酸酯及其类似物对小鼠、大鼠和犬的急性毒性(作者译)
J Toxicol Sci. 1981 Jul;6 Suppl:1-16. doi: 10.2131/jts.6.supplement_1.
6
[Studies on toxicity of hydrocortisone 17-butyrate 21-propionate -6. Subacute toxicity in dogs by percutaneous administration (author's transl)].[氢化可的松17 - 丁酸酯21 - 丙酸酯的毒性研究 - 6. 经皮给药对犬的亚急性毒性(作者译)]
J Toxicol Sci. 1981 Jul;6 Suppl:121-40. doi: 10.2131/jts.6.supplement_121.
7
Comparative toxicity study of hydrocortisone 17-butyrate 21-propionate (HBP) ointment and other topical corticosteroids in rats.大鼠中氢化可的松17-丁酸酯21-丙酸酯(HBP)软膏与其他外用皮质类固醇的比较毒性研究。
Drugs Exp Clin Res. 1986;12(8):643-52.
8
[Studies on antigenicity, phototoxicity and other specific toxicities of hydrocortisone 17-butyrate 21-propionate (HBP) (author's transl)].[氢化可的松17 - 丁酸酯21 - 丙酸酯(HBP)的抗原性、光毒性及其他特殊毒性研究(作者译)]
J Toxicol Sci. 1981 Jul;6 Suppl:159-78. doi: 10.2131/jts.6.supplement_159.
9
[Pharmacological study on hydrocortisone 17-butyrate 21-propionate (author's transl)].
Nihon Yakurigaku Zasshi. 1981 Dec;78(6):647-58. doi: 10.1254/fpj.78.647.
10
[Influence of hydrocortisone 17-butyrate 21-propionate on the visual and the auditory organs (author's transl)].17-丁酸-21-丙酸氢化可的松对视觉和听觉器官的影响(作者译)
J Toxicol Sci. 1981 Jul;6 Suppl:141-58. doi: 10.2131/jts.6.supplement_141.