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Comparison of L- and D-Amino Acids for Bacterial Imaging in Lung Infection Mouse Model

The effectiveness of L- and D-amino acids for detecting the early stage of infection in bacterial imaging was compared. We evaluated the accumulation of (3)H-L-methionine (Met), (3)H-D-Met, (3)H-L-alanine (Ala), and (3)H-D-Ala in E. coli EC-14 and HaCaT cells. Biological distribution was assessed in...

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Detalles Bibliográficos
Autores principales: Muranaka, Yuka, Mizutani, Asuka, Kobayashi, Masato, Nakamoto, Koya, Matsue, Miki, Nishi, Kodai, Yamazaki, Kana, Nishii, Ryuichi, Shikano, Naoto, Okamoto, Shigefumi, Kawai, Keiichi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8910731/
https://www.ncbi.nlm.nih.gov/pubmed/35269610
http://dx.doi.org/10.3390/ijms23052467
Descripción
Sumario:The effectiveness of L- and D-amino acids for detecting the early stage of infection in bacterial imaging was compared. We evaluated the accumulation of (3)H-L-methionine (Met), (3)H-D-Met, (3)H-L-alanine (Ala), and (3)H-D-Ala in E. coli EC-14 and HaCaT cells. Biological distribution was assessed in control and lung-infection-model mice with EC-14 using (3)H-L- and D-Met, and (18)F-FDG. A maximum accumulation of (3)H-L- and D-Met, and (3)H-L- and D-Ala occurred in the growth phase of EC-14 in vitro. The accumulation of (3)H-L-Met and L-Ala was greater than that of (3)H-D-Met and D-Ala in both EC-14 and HaCaT cells. For all radiotracers, the accumulation was greater in EC-14 than in HaCaT cells at early time points. The accumulation was identified at 5 min after injection in EC-14, whereas the accumulation gradually increased in HaCaT cells over time. There was little difference in biodistribution between (3)H-L-and D-Met except in the brain. (3)H-L- and D-Met were sensitive for detecting areas of infection after the spread of bacteria throughout the body, whereas (18)F-FDG mainly detected primary infection areas. Therefore, (11)C-L- and D-Met, radioisotopes that differ only in terms of (3)H labeling, could be superior to (18)F-FDG for detecting bacterial infection in lung-infection-model mice.