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Note: it is to be noted that in studies involving drug administration or genetic modifications where the larval feed uptake may vary as a response, control feeding assays should be performed in the animals for rational validation. Various researches have utilized fluorescently labeled viable paramecia such as 4-10-Di-ASP-labeled paramecia, fish food coated fluorescent microspheres or fluorescent Tetrahymena to evaluate the feed intake, especially in larvae, in view of their transparent body ( Shimada et al., 2012 ) ( Boyer et al., 2013 ) ( Hsieh et al., 2021 ) ( Hsieh et al., 2021 ). For appropriate HFD controls in hyperlipidemic studies, high fat feed serves are fluorescently (NBD- and BODIPY-Cholesterol) or radioactively labeled (14C-labeled lipids) to monitor lipid trafficking in live larvae, which can be used to indirectly measure lipid (feed) uptake ( Sæle et al., 2018 ) ( Anderson et al., 2016 ).…”
Note: it is to be noted that in studies involving drug administration or genetic modifications where the larval feed uptake may vary as a response, control feeding assays should be performed in the animals for rational validation. Various researches have utilized fluorescently labeled viable paramecia such as 4-10-Di-ASP-labeled paramecia, fish food coated fluorescent microspheres or fluorescent Tetrahymena to evaluate the feed intake, especially in larvae, in view of their transparent body ( Shimada et al., 2012 ) ( Boyer et al., 2013 ) ( Hsieh et al., 2021 ) ( Hsieh et al., 2021 ). For appropriate HFD controls in hyperlipidemic studies, high fat feed serves are fluorescently (NBD- and BODIPY-Cholesterol) or radioactively labeled (14C-labeled lipids) to monitor lipid trafficking in live larvae, which can be used to indirectly measure lipid (feed) uptake ( Sæle et al., 2018 ) ( Anderson et al., 2016 ).…”