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Related Concept Videos

Drug Excretion: Miscellaneous Routes01:10

Drug Excretion: Miscellaneous Routes

Drug excretion involves various organs, including the liver, intestines, skin, and eyes. In the case of drugs or toxins, they can be actively secreted into bile by transporters in the hepatocyte's canalicular membrane. These substances enter the GI tract during digestion and may be reabsorbed into the body from the intestine. This process, known as enterohepatic recycling, can significantly prolong the presence and effects of a substance in the body. To interrupt this cycle, specific substances...
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Microbes and Other Elemental Cycles

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Drug Elimination: Non-Renal Routes01:23

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Updated: Jun 19, 2026

Quantitating Iron Transport Across the Mouse Placenta In Vivo Using Nonradioactive Iron Isotopes
08:45

Quantitating Iron Transport Across the Mouse Placenta In Vivo Using Nonradioactive Iron Isotopes

Published on: May 10, 2022

RADIOACTIVE IRON AND ITS EXCRETION IN URINE, BILE, AND FECES.

P F Hahn1, W F Bale, R A Hettig

  • 1Departments of Pathology and Medicine (Radiology), The University of Rochester School of Medicine and Dentistry, Rochester, New York, and The Radiation Laboratory, The University of California, Berkeley, California.

The Journal of Experimental Medicine
|October 30, 2009
PubMed
Summary
This summary is machine-generated.

This study shows that dogs struggle to excrete iron, primarily through bile and the gastrointestinal tract. Initial iron injections lead to a small, temporary increase in excretion, but overall elimination is very limited.

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Area of Science:

  • Physiology
  • Biochemistry

Background:

  • Iron homeostasis is critical for cellular function.
  • Understanding iron excretion mechanisms is key to managing iron overload disorders.

Purpose of the Study:

  • To investigate the routes and efficiency of iron excretion in dogs using radioactive iron.
  • To determine the body's capacity to eliminate excess iron.

Main Methods:

  • Administration of radioactive iron (ferrous gluconate) intravenously to dogs.
  • Quantification of radio-iron excretion in urine, bile, and feces over time.
  • Induction of blood destruction to assess iron excretion response.

Main Results:

  • An initial, transient increase (2-8%) in urinary and fecal radio-iron excretion occurred post-injection.
  • Urinary excretion rapidly decreased to negligible levels.
  • Fecal excretion stabilized at 0.05-0.4 mg/day, increasing to 0.1-1.0 mg/day with induced hemolysis.
  • Bile contributed minimally to iron excretion under normal conditions.

Conclusions:

  • Dogs exhibit limited capacity for iron excretion, primarily via the gastrointestinal and biliary tracts.
  • Iron regulation in dogs relies heavily on absorption control rather than efficient elimination.
  • The study highlights the challenges in managing iron overload in canines.