Difficulty: Medium
Correct Answer: Albumin
Explanation:
Introduction / Context:Copper absorbed in the small intestine must be trafficked to the liver, where it is incorporated into cuproenzymes and into ceruloplasmin for systemic delivery. Understanding which plasma proteins carry copper at each stage clarifies laboratory findings and disease mechanisms in copper disorders.
Given Data / Assumptions:
Concept / Approach:Distinguish early transport from systemic distribution. The question asks specifically about transport from intestinal cells to the liver, which points to albumin-bound copper rather than ceruloplasmin (a hepatic product for peripheral delivery).
Step-by-Step Solution:
Identify the time point → post-absorption in portal circulation.List plausible carriers → albumin (primary), transcuprein (minor), not transferrin.Select albumin as the dominant carrier to the liver.Verification / Alternative check:Clinical chemistry shows low ceruloplasmin in Wilson’s disease despite copper overload; newly absorbed copper is not ceruloplasmin-bound until processed by the liver.
Why Other Options Are Wrong:
a) Ceruloplasmin is mainly for systemic distribution from the liver, not initial portal transport.b) Secretin is a gastrointestinal hormone, unrelated to metal transport.c) Acrolein is a reactive aldehyde, not a transport protein.e) Transferrin binds Fe3+, not copper, under physiologic conditions.Common Pitfalls:Assuming “ceruloplasmin” for any copper transport question; remember the sequence: albumin in portal blood → liver → ceruloplasmin to tissues.
Final Answer:Albumin.
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