• 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

睾酮或雌二醇对未成熟肉种鸡公鸡中三邻甲苯磷酸酯诱导的迟发性神经毒性发育的影响。

The effect of testosterone or estradiol on the development of TOCP-induced delayed neurotoxicity in immature broiler-breed cockerels.

作者信息

Fathy F A, Bursian S

机构信息

Department of Animal Science, Michigan State University, East Lansing 48824.

出版信息

Vet Hum Toxicol. 1990 Oct;32(5):416-8.

PMID:2238435
Abstract

Immature cockerels were susceptible to OPIDN when dosed with TOCP. Using 30 broiler-breed cockerels, 6 w old, 10 birds each received 28 daily im injections of either 50 mg estradiol, 100 mg testosterone or 0.1 ml of vehicle. At 7 w of age, 5 birds in each of the 3 groups received a single oral dose of 500 mg TOCP/kg body weight, while the remaining 5 birds/groups were given corn oil. The birds were observed daily for 14 d beginning on day 8 post-TOCP exposure for the development of clinical signs characteristic of OPIDN. At 21 d post-TOCP, all birds were killed and the adrenal gland and testes were prepared for histopathology of the birds that received TOCP, 1 of 5 that were given testosterone and 2 of 5 that received estradiol had signs typical of OPIDN. All of the 5 birds that received TOCP alone showed OPIDN signs. The testes of the TOCP-exposed birds that showed clinical signs had reductions in the size of the seminiferous tubules and no evidence of spermatogenic activity. This study demonstrated that sex hormones can modulate the clinical effects of TOCP in immature cockerels through unknown mechanisms that are similar to those reported for corticosterone in adult chickens.

摘要

未成熟的小公鸡经三邻甲苯磷酸酯(TOCP)给药后易患迟发性神经病变(OPIDN)。选用30只6周龄的肉用种小公鸡,每组10只,分别每日肌肉注射28次,每次剂量为50毫克雌二醇、100毫克睾酮或0.1毫升赋形剂。7周龄时,3组中的每组5只鸡口服单剂量500毫克TOCP/千克体重,其余每组5只鸡给予玉米油。从TOCP暴露后第8天开始,每天观察鸡14天,观察OPIDN特征性临床症状的发展情况。TOCP给药后21天,所有鸡均处死后,对接受TOCP的鸡的肾上腺和睾丸进行组织病理学检查,接受睾酮的5只中有1只、接受雌二醇的5只中有2只出现OPIDN典型症状。仅接受TOCP的5只鸡均出现OPIDN症状。出现临床症状的TOCP暴露鸡的睾丸生精小管大小减小,且无生精活性迹象。本研究表明,性激素可通过未知机制调节TOCP对未成熟小公鸡的临床作用,这些机制与成年鸡中报道的皮质酮的机制相似。

相似文献

1
The effect of testosterone or estradiol on the development of TOCP-induced delayed neurotoxicity in immature broiler-breed cockerels.睾酮或雌二醇对未成熟肉种鸡公鸡中三邻甲苯磷酸酯诱导的迟发性神经毒性发育的影响。
Vet Hum Toxicol. 1990 Oct;32(5):416-8.
2
Time-dependent changes of lipid peroxidation and antioxidative status in nerve tissues of hens treated with tri-ortho-cresyl phosphate (TOCP).用磷酸三邻甲苯酯(TOCP)处理的母鸡神经组织中脂质过氧化和抗氧化状态的时间依赖性变化。
Toxicology. 2007 Sep 24;239(1-2):45-52. doi: 10.1016/j.tox.2007.06.091. Epub 2007 Jun 27.
3
Effect of route of administration on the development of organophosphate-induced delayed neurotoxicity in 4-week-old chicks.给药途径对4周龄雏鸡有机磷酸酯诱导的迟发性神经毒性发展的影响。
J Toxicol Environ Health. 1988;23(4):499-505. doi: 10.1080/15287398809531131.
4
Histopathological assessment of triphenyl phosphite neurotoxicity in the hen.亚磷酸三苯酯对母鸡神经毒性的组织病理学评估
Neurotoxicology. 1988 Summer;9(2):223-33.
5
Testicular toxicity following oral administration of tri-o-cresyl phosphate (TOCP) in roosters.公鸡口服磷酸三邻甲苯酯(TOCP)后的睾丸毒性。
Toxicol Lett. 1987 Aug;37(3):279-90. doi: 10.1016/0378-4274(87)90143-3.
6
Changes of mitochondrial ultrastructures and function in central nervous tissue of hens treated with tri-ortho-cresyl phosphate (TOCP).三邻甲苯磷酸酯(TOCP)处理母鸡中枢神经组织中线粒体超微结构和功能的变化。
Hum Exp Toxicol. 2011 Aug;30(8):1062-72. doi: 10.1177/0960327110386815. Epub 2010 Oct 21.
7
Phenylmethylsulfonyl fluoride protects against the degradation of neurofilaments in tri-ortho-cresyl phosphate (TOCP) induced delayed neuropathy.苯甲基磺酰氟可防止磷酸三邻甲苯酯(TOCP)诱导的迟发性神经病中神经丝的降解。
Toxicology. 2009 Aug 21;262(3):258-64. doi: 10.1016/j.tox.2009.06.018. Epub 2009 Jun 30.
8
Organophosphate-induced delayed neurotoxicity of triarylphosphates.
Neurotoxicology. 1999 Aug;20(4):653-73.
9
Characterization of delayed neurotoxicity in the mouse following chronic oral administration of tri-o-cresyl phosphate.慢性口服磷酸三邻甲苯酯后小鼠迟发性神经毒性的特征
Toxicol Appl Pharmacol. 1985 Jun 15;79(1):83-90. doi: 10.1016/0041-008x(85)90370-9.
10
Expression changes of neurofilament subunits in the central nervous system of hens treated with tri-ortho-cresyl phosphate (TOCP).三邻甲苯基磷酸酯(TOCP)处理母鸡中枢神经系统中神经丝亚基的表达变化
Toxicology. 2006 Jun 1;223(1-2):127-35. doi: 10.1016/j.tox.2006.03.008. Epub 2006 Mar 22.