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Imaging Biotin Trafficking In Vivo with Positron Emission Tomography

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posted on 24.07.2020, 19:03 by Salvatore Bongarzone, Teresa Sementa, Joel Dunn, Jayanta Bordoloi, Kavitha Sunassee, Philip J. Blower, Antony Gee
The water-soluble vitamin biotin is essential for cellular growth, development, and well-being, but its absorption, distribution, metabolism, and excretion are poorly understood. This paper describes the radiolabeling of biotin with the positron emission tomography (PET) radionuclide carbon-11 ([11C]­biotin) to enable the quantitative study of biotin trafficking in vivo. We show that intravenously administered [11C]­biotin is quickly distributed to the liver, kidneys, retina, heart, and brain in rodentsconsistent with the known expression of the biotin transporterand there is a surprising accumulation in the brown adipose tissue (BAT). Orally administered [11C]­biotin was rapidly absorbed in the small intestine and swiftly distributed to the same organs. Preadministration of nonradioactive biotin inhibited organ uptake and increased excretion. [11C]­Biotin PET imaging therefore provides a dynamic in vivo map of transporter-mediated biotin trafficking in healthy rodents. This technique will enable the exploration of biotin trafficking in humans and its use as a research tool for diagnostic imaging of obesity/diabetes, bacterial infection, and cancer.

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