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Description
Localization of claudin-3 in tight junctions of the blood-brain barrier is selectively lost during experimental autoimmune encephalomyelitis and human glioblastoma multiforme
Age, injury, disease all of these reduce copper availability, and the enzymes downstream suffer for it

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The weight loss benefits at 1.0 mg are already clinically significant

Understanding this mechanism matters because it explains why most GI side effects are dose-dependent, temporary, and manageable through titration strategies
