IF
we used FSH to pretreat N2a cells, a mouse neuroblastoma cell line expressing FSHR (Fig. S3), and then induced cellular oxidative stress by the addition of hydrogen peroxide to observe the protective effect of FSH on cellular oxidative stress.
IF
The expression of FSHR in depression-related brain regions. a The CA1 region of the mouse hippocampus. b The CA3 region of mouse hippocampus. c The DG of the mouse hippocampus. d The cortex. e The nucleus accumbens. f The amygdala. g The prefrontal cortex. h The bed nucleus of the stria terminalis. i The lateral habenula. FSHR (red), NeuN (green, a marker of neurons), and DAPI (blue) immunofluorescence was detected under a fluorescence microscope
IHC
(A) Immunohistochemical stain of FSHR in mouse hippocampus.
IHC
(A) Immunohistochemical staining of FSHR in the prefrontal cortex.
IF
The expression of FSHR in depression-related brain regions. a The CA1 region of the mouse hippocampus. b The CA3 region of mouse hippocampus. c The DG of the mouse hippocampus. d The cortex. e The nucleus accumbens. f The amygdala. g The prefrontal cortex. h The bed nucleus of the stria terminalis. i The lateral habenula. FSHR (red), NeuN (green, a marker of neurons), and DAPI (blue) immunofluorescence was detected under a fluorescence microscope
IF
The immunofluorescence results showed that FSHR was present in neurons, but not astrocytes (Fig. S1), in multiple depression-related regions, including the hippocampus, cortex, nucleus accumbens, amygdala, and prefrontal cortex (Fig. 1a–g), not in the bed nucleus of the stria terminalis or lateral habenula (Fig. 1h, i).
Previous
IF
Next, we used FSH to pretreat N2a cells, a mouse neuroblastoma cell line expressing FSHR (Fig. S3), and then induced cellular oxidative stress by the addition of hydrogen peroxide to observe the protective effect of FSH on cellular oxidative stress.
Previous
IHC
(A) Immunohistochemical stain of FSHR in mouse hippocampus.
Previous
IHC
(A) Immunohistochemical staining of FSHR in the prefrontal cortex.
Previous