(e National Brain Program of the Hungarian Academy of Sciences 2022 (NAP3))
(TKP 2021)
(K134221)
Glucagon-like peptide-1 (GLP-1) receptor (GLP-1R) agonists have been approved for
the treatment of type 2 diabetes mellitus (T2DM); however, the brain actions of these
drugs are not properly established. We used post mortem microdissected human hypothalamic
samples for RT-qPCR and Western blotting. For in situ hybridization histochemistry
and immunolabelling, parallel cryosections were prepared from the hypothalamus. We
developed in situ hybridization probes for human GLP-1R and oxytocin. In addition,
GLP-1 and oxytocin were visualized by immunohistochemistry. Radioactive in situ hybridization
histochemistry revealed abundant GLP-1R labelling in the human paraventricular hypothalamic
nucleus (PVN), particularly in its magnocellular subdivision (PVNmc). Quantitative
analysis of the mRNA signal demonstrated increased GLP-1R expression in the PVNmc
in post mortem hypothalamic samples from T2DM subjects as compared to controls, while
there was no difference in the expression level of GLP-1R in the other subdivisions
of the PVN, the hypothalamic dorsomedial and infundibular nuclei. Our results in the
PVN were confirmed by RT-qPCR. Furthermore, we demonstrated by Western blot technique
that the GLP-1R protein level was also elevated in the PVN of T2DM patients. GLP-1
fibre terminals were also observed in the PVNmc closely apposing oxytocin neurons
using immunohistochemistry. The data suggest that GLP-1 activates GLP-1Rs in the PVNmc
and that GLP-1R is elevated in T2DM patients, which may be related to the dysregulation
of feeding behaviour and glucose homeostasis in T2DM.