• 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

Dietary iron loading does not influence biliary iron excretion in rats.

作者信息

Yu S, Beynen A C

机构信息

Department of Large Animal Medicine and Nutrition, State University, Utrecht, The Netherlands.

出版信息

Biol Trace Elem Res. 1992 Oct;35(1):73-5. doi: 10.1007/BF02786239.

DOI:10.1007/BF02786239
PMID:1384629
Abstract

The effect of dietary iron loading on biliary iron excretion was investigated with male Wistar rats aged 6 wk. The rats were fed purified diets with either 174 or 1740 mg FeSO4. 7H2O/kg diet and demineralized water for 6 wk. Blood haemoglobin, hematocrit, and iron concentrations in kidney and heart were not affected and iron concentrations in liver, spleen, and tibia were significantly raised after feeding the high-iron diet. The high-iron diet did not raise biliary iron excretion, suggesting that biliary iron excretion does not play an important role in regulating iron metabolism in rat after dietary iron loading.

摘要

相似文献

1
Dietary iron loading does not influence biliary iron excretion in rats.
Biol Trace Elem Res. 1992 Oct;35(1):73-5. doi: 10.1007/BF02786239.
2
Iron and copper interact during their uptake and deposition in the brain and other organs of developing rats exposed to dietary excess of the two metals.
J Nutr. 1996 Jan;126(1):183-94. doi: 10.1093/jn/126.1.183.
3
High intakes of tin lower iron status in rats.
Biol Trace Elem Res. 1992 Oct;35(1):85-8. doi: 10.1007/BF02786242.
4
Increasing intakes of iron reduce status, absorption and biliary excretion of copper in rats.大鼠体内铁摄入量的增加会降低铜的状态、吸收及胆汁排泄。
Br J Nutr. 1994 Jun;71(6):887-95. doi: 10.1079/bjn19940194.
5
Impaired iron status in rats as induced by copper deficiency.
Biol Trace Elem Res. 1992 Oct;35(1):77-9. doi: 10.1007/BF02786240.
6
Dietary fructose vs glucose does not influence iron status in rats.
Biol Trace Elem Res. 1992 Oct;35(1):89-92. doi: 10.1007/BF02786243.
7
Influence of nutritional iron deficiency development on some aspects of iron, copper and zinc metabolism.营养性缺铁的发展对铁、铜和锌代谢某些方面的影响。
Lab Anim. 1998 Jul;32(3):298-306. doi: 10.1258/002367798780559248.
8
Iron status in rats fed a purified diet without vitamin A.喂食不含维生素A的纯化日粮的大鼠的铁状态
Biol Trace Elem Res. 1992 Oct;35(1):81-4. doi: 10.1007/BF02786241.
9
Iron supplementation by intraperitoneal injection eliminates the accumulation of hepatic copper induced by excess calcium in rats.通过腹腔注射补充铁可消除大鼠体内因钙过量而导致的肝脏铜蓄积。
Br J Nutr. 2009 Jul;102(2):258-63. doi: 10.1017/S0007114508184707. Epub 2009 Jan 13.
10
Biliary excretion of iron from hepatocyte lysosomes in the rat. A major excretory pathway in experimental iron overload.大鼠肝细胞溶酶体中铁的胆汁排泄。实验性铁过载中的一条主要排泄途径。
J Clin Invest. 1986 Jan;77(1):90-7. doi: 10.1172/JCI112307.

引用本文的文献

1
Bile from the hemojuvelin-deficient mouse model of iron excess is enriched in iron and ferritin.铁过量的hemojuvelin 缺陷型小鼠模型的胆汁中铁和铁蛋白含量丰富。
Metallomics. 2024 Oct 4;16(10). doi: 10.1093/mtomcs/mfae043.

本文引用的文献

1
Biliary iron excretion in rats following pyridoxal isonicotinoyl hydrazone.大鼠服用异烟腙后胆汁中铁的排泄情况
Br J Haematol. 1980 Jun;45(2):275-83. doi: 10.1111/j.1365-2141.1980.tb07147.x.
2
Effect of aluminum and deferoxamine on biliary iron elimination in the rat.铝和去铁胺对大鼠胆汁铁排泄的影响。
Proc Soc Exp Biol Med. 1988 Sep;188(4):471-3. doi: 10.3181/00379727-188-42762.
3
Influence of xenobiotics on bile flow and bile composition in rats--methodological approach.异生物素对大鼠胆汁流量和胆汁成分的影响——方法学探讨
Exp Pathol. 1990;39(3-4):175-85. doi: 10.1016/s0232-1513(11)80181-7.
4
Dietary fluoride prevents phosphorus-induced nephrocalcinosis in female rats.膳食氟可预防雌性大鼠因磷诱导的肾钙质沉着症。
Biol Trace Elem Res. 1991 May;29(2):147-55. doi: 10.1007/BF03032692.