Experiment 3: Investigation of mPFC inputs from vHP GLP-1R expressing neurons

TH Ted M. Hsu
EN Emily E. Noble
CL Clarissa M. Liu
AC Alyssa M. Cortella
VK Vaibhav R. Konanur
AS Andrea N. Suarez
DR David J. Reiner
JH Joel D. Hahn
MH Matthew R. Hayes
SK Scott E. Kanoski
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Rats (n=4) received a unilateral 100nl pressure injection of fluorogold (FG, Fluorochrome LLC; 2% in 0.9 % NaCl) targeting the mPFC. Following a survival period of 10 days, animals were fixation-perfused and tissue was harvested and processed as described in the Methods section. A representative animal with fluorogold back-labeled neurons in the vHP (field CA1) was selected for GLP-1R FISH analyses (See Methods and Supplementary materials). In order to observe separate GLP-1R mRNA in vHP cell bodies (as fluorogold and DAPI autofluoresce in the same channel), the protocol above was repeated in a separate untreated animal where DAPI (ACD, 320851) was placed on the slide prior to coverslipping.

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