National Research, Development and Innovation Office(K_119742)
(2017-1.2.1-NKP-2017-00002)
(EFOP-3.6.3-VEKOP-16-2017-00009)
Intramural Research Program
GABAergic neurons are key circuit elements in cortical networks. Despite growing evidence
showing that inhibitory cells play a critical role in the lateral (LA) and basal (BA)
amygdala functions, neither the number of GABAergic neurons nor the ratio of their
distinct types has been determined in these amygdalar nuclei. Using unbiased stereology,
we found that the ratio of GABAergic neurons in the BA (22%) is significantly higher
than in the LA (16%) in both male and female mice. No difference was observed between
the right and left hemispheres in either sex. In addition, we assessed the ratio of
the major inhibitory cell types in both amygdalar nuclei. Using transgenic mice and
a viral strategy for visualizing inhibitory cells combined with immunocytochemistry,
we estimated that the following cell types together compose the vast majority of GABAergic
cells in the LA and BA: axo-axonic cells (5.5%-6%), basket cells expressing parvalbumin
(17%-20%) or cholecystokinin (7%-9%), dendrite-targeting inhibitory cells expressing
somatostatin (10%-16%), NPY-containing neurogliaform cells (14%-15%), VIP and/or calretinin-expressing
interneuron-selective interneurons (29%-38%), and GABAergic projection neurons expressing
somatostatin and neuronal nitric oxide synthase (5.5%-8%). Our results show that these
amygdalar nuclei contain all major GABAergic neuron types as found in other cortical
regions. Furthermore, our data offer an essential reference for future studies aiming
to reveal changes in GABAergic cell number and in inhibitory cell types typically
observed under different pathologic conditions, and to model functioning amygdalar
networks in health and disease.SIGNIFICANCE STATEMENTGABAergic
cells in cortical structures, as in the lateral and basal nucleus of the amygdala,
have a determinant role in controlling circuit operation. In this study, we provide
the first estimate for the total number of inhibitory cells in these two amygdalar
nuclei. In addition, our study is the first to define the ratio of the major GABAergic
cell types present in these cortical networks. Taking into account that hyperexcitability
in the amygdala, arising from the imbalance between excitation and inhibition typifies
many altered brain functions, including anxiety, post-traumatic stress disorder, schizophrenia,
and autism, uncovering the number and ratio of distinct amygdalar inhibitory cell
types offers a solid base for comparing the changes in inhibition in pathologic brain
states.