TY - JOUR
T1 - Modulation of presynaptic GABA A receptors by endogenous neurosteroids
AU - Kim, B. G.
AU - Cho, J. H.
AU - Choi, I. S.
AU - Lee, M. G.
AU - Jang, I. S.
PY - 2011/11
Y1 - 2011/11
N2 - BACKGROUND AND PURPOSE Although 3α-hydroxy, 5α-reduced pregnane steroids, such as allopregnanolone (AlloP) and tetrahydrodeoxycorticosterone, are endogenous positive modulators of postsynaptic GABA A receptors, the functional roles of endogenous neurosteroids in synaptic transmission are still largely unknown. EXPERIMENTAL APPROACH In this study, the effect of AlloP on spontaneous glutamate release was examined in mechanically isolated dentate gyrus hilar neurons by use of the conventional whole-cell patch-clamp technique. KEY RESULTS AlloP increased the frequency of glutamatergic spontaneous excitatory postsynaptic currents (sEPSCs) in a dose-dependent manner. The AlloP-induced increase in sEPSC frequency was completely blocked by a non-competitive GABA A receptor blocker, tetrodotoxin or Cd 2+, suggesting that AlloP acts on presynaptic GABA A receptors to depolarize presynaptic nerve terminals to increase the probability of spontaneous glutamate release. On the other hand, Iγ-cyclodextrin (Iγ-CD) significantly decreased the basal frequency of sEPSCs. However, Iγ-CD failed to decrease the basal frequency of sEPSCs in the presence of a non-competitive GABA A receptor antagonist or tetrodotoxin. In addition, Iγ-CD failed to decrease the basal frequency of sEPSCs after blocking the synthesis of endogenous 5α-reduced pregnane steroids. Furthermore, Iγ-CD decreased the extent of muscimol-induced increase in sEPSC frequency, suggesting that endogenous neurosteroids can directly activate and/or potentiate presynaptic GABA A receptors to affect spontaneous glutamate release onto hilar neurons. CONCLUSIONS AND IMPLICATIONS The modulation of presynaptic GABA A receptors by endogenous neurosteroids might affect the excitability of the dentate gyrus-hilus-CA3 network, and thus contribute, at least in part, to some pathological conditions, such as catamenial epilepsy and premenstrual dysphoric disorder.
AB - BACKGROUND AND PURPOSE Although 3α-hydroxy, 5α-reduced pregnane steroids, such as allopregnanolone (AlloP) and tetrahydrodeoxycorticosterone, are endogenous positive modulators of postsynaptic GABA A receptors, the functional roles of endogenous neurosteroids in synaptic transmission are still largely unknown. EXPERIMENTAL APPROACH In this study, the effect of AlloP on spontaneous glutamate release was examined in mechanically isolated dentate gyrus hilar neurons by use of the conventional whole-cell patch-clamp technique. KEY RESULTS AlloP increased the frequency of glutamatergic spontaneous excitatory postsynaptic currents (sEPSCs) in a dose-dependent manner. The AlloP-induced increase in sEPSC frequency was completely blocked by a non-competitive GABA A receptor blocker, tetrodotoxin or Cd 2+, suggesting that AlloP acts on presynaptic GABA A receptors to depolarize presynaptic nerve terminals to increase the probability of spontaneous glutamate release. On the other hand, Iγ-cyclodextrin (Iγ-CD) significantly decreased the basal frequency of sEPSCs. However, Iγ-CD failed to decrease the basal frequency of sEPSCs in the presence of a non-competitive GABA A receptor antagonist or tetrodotoxin. In addition, Iγ-CD failed to decrease the basal frequency of sEPSCs after blocking the synthesis of endogenous 5α-reduced pregnane steroids. Furthermore, Iγ-CD decreased the extent of muscimol-induced increase in sEPSC frequency, suggesting that endogenous neurosteroids can directly activate and/or potentiate presynaptic GABA A receptors to affect spontaneous glutamate release onto hilar neurons. CONCLUSIONS AND IMPLICATIONS The modulation of presynaptic GABA A receptors by endogenous neurosteroids might affect the excitability of the dentate gyrus-hilus-CA3 network, and thus contribute, at least in part, to some pathological conditions, such as catamenial epilepsy and premenstrual dysphoric disorder.
KW - allopregnanolone
KW - GABA receptors
KW - hippocampus
KW - neurosteroids
KW - presynaptic modulation
UR - http://www.scopus.com/inward/record.url?scp=80054983077&partnerID=8YFLogxK
U2 - 10.1111/j.1476-5381.2011.01491.x
DO - 10.1111/j.1476-5381.2011.01491.x
M3 - Article
C2 - 21585348
AN - SCOPUS:80054983077
SN - 0007-1188
VL - 164
SP - 1698
EP - 1710
JO - British Journal of Pharmacology
JF - British Journal of Pharmacology
IS - 6
ER -