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   <dc:title>Efficacy of the fluorescent dyes Fast Blue, Fluoro-Gold, and Diamidino Yellow for retrograde tracing to dorsal root ganglia after subcutaneous injection</dc:title>
   <dc:creator>Puigdellívol Sánchez, Anna</dc:creator>
   <dc:creator>Prats Galino, Alberto</dc:creator>
   <dc:creator>Ruano Gil, Domingo</dc:creator>
   <dc:creator>Molander, Carl</dc:creator>
   <dc:subject>Transport biològic</dc:subject>
   <dc:subject>Nervis espinals</dc:subject>
   <dc:subject>Pell</dc:subject>
   <dc:subject>Rates (Animals de laboratori)</dc:subject>
   <dc:subject>Biological transport</dc:subject>
   <dc:subject>Spinal nerves</dc:subject>
   <dc:subject>Skin</dc:subject>
   <dc:subject>Rats as laboratory animals</dc:subject>
   <dc:description>The present study was designed to investigate the efficacy of the fluorescent dyes Fast Blue (FB), Fluoro-Gold (FG), and Diamidino Yellow (DY) for retrograde tracing of lumbar dorsal root ganglia after their subcutaneous injection into different hindlimb digits. Injection of equal volumes (0.5 mu l) of 5% FB or 2% FG resulted in similar mean numbers of sensory neurones labelled by each tracer. Injection of equal volumes (0.5 mu l) of FB or FG in a single digit followed 10 days later by a second injection of the same volume of 5% DY into the same digit resulted in similar mean numbers of labelled sensory neurones for each of the three tracers. Furthermore, on average, 75% of all the FB-labelled cells and 74% of all FC-labelled cells also contained DY. Repeating the same experiment with an increased volume of DY (1.5 mu l) resulted in an increase in the mean number of double-labelled profiles to 82 and 84% for FB and FG, respectively. The results show that FB, FG and DY label similar numbers of cutaneous afferents and that a high level of double labelling may be obtained after sequential injections in digits. These properties make them suitable candidates in investigations where a combination of tracers with similar labelling efficacies is needed.</dc:description>
   <dc:date>2014-09-05T09:51:42Z</dc:date>
   <dc:date>2014-09-05T09:51:42Z</dc:date>
   <dc:date>1998-12-15</dc:date>
   <dc:date>2014-09-05T09:51:42Z</dc:date>
   <dc:type>info:eu-repo/semantics/article</dc:type>
   <dc:type>info:eu-repo/semantics/acceptedVersion</dc:type>
   <dc:identifier>0165-0270</dc:identifier>
   <dc:identifier>https://hdl.handle.net/2445/56744</dc:identifier>
   <dc:identifier>502145</dc:identifier>
   <dc:identifier>9894781</dc:identifier>
   <dc:language>eng</dc:language>
   <dc:relation>Versió postprint del document publicat a: http://dx.doi.org/10.1016/S0165-0270(98)00137-X</dc:relation>
   <dc:relation>Journal of Neuroscience Methods, 1998, vol. 86, num. 1, p. 7-16</dc:relation>
   <dc:relation>http://dx.doi.org/10.1016/S0165-0270(98)00137-X</dc:relation>
   <dc:rights>(c) Elsevier B.V., 1998</dc:rights>
   <dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
   <dc:format>23 p.</dc:format>
   <dc:format>application/pdf</dc:format>
   <dc:publisher>Elsevier B.V.</dc:publisher>
   <dc:source>Articles publicats en revistes (Fonaments Clínics)</dc:source>
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