Normal sleep homeostasis and lack of epilepsy phenotype in GABA A receptor alpha3 subunit-knockout mice.
Thalamo-cortical networks generate specific patterns of oscillations during distinct vigilance states and epilepsy, well characterized by electroencephalography (EEG). Oscillations depend on recurrent synaptic loops, which are controlled by GABAergic transmission. In particular, GABA A receptors con...
| Main Authors: | , , , , , , , , |
|---|---|
| Format: | Journal article |
| Language: | English |
| Published: |
2008
|
| _version_ | 1797090739891470336 |
|---|---|
| author | Winsky-Sommerer, R Knapman, A Fedele, D Schofield, C Vyazovskiy, V Rudolph, U Huguenard, JR Fritschy, J Tobler, I |
| author_facet | Winsky-Sommerer, R Knapman, A Fedele, D Schofield, C Vyazovskiy, V Rudolph, U Huguenard, JR Fritschy, J Tobler, I |
| author_sort | Winsky-Sommerer, R |
| collection | OXFORD |
| description | Thalamo-cortical networks generate specific patterns of oscillations during distinct vigilance states and epilepsy, well characterized by electroencephalography (EEG). Oscillations depend on recurrent synaptic loops, which are controlled by GABAergic transmission. In particular, GABA A receptors containing the alpha3 subunit are expressed predominantly in cortical layer VI and thalamic reticular nucleus (nRT) and regulate the activity and firing pattern of neurons in relay nuclei. Therefore, ablation of these receptors by gene targeting might profoundly affect thalamo-cortical oscillations. Here, we investigated the role of alpha3-GABA A receptors in regulating vigilance states and seizure activity by analyzing chronic EEG recordings in alpha3 subunit-knockout (alpha3-KO) mice. The presence of postsynaptic alpha3-GABA A receptors/gephyrin clusters in the nRT and GABA A-mediated synaptic currents in acute thalamic slices was also examined. EEG spectral analysis showed no difference between genotypes during non rapid-eye movement (NREM) sleep or at waking-NREM sleep transitions. EEG power in the spindle frequency range (10-15 Hz) was significantly lower at NREM-REM sleep transitions in mutant compared with wild-type mice. Enhancement of sleep pressure by 6 h sleep deprivation did not reveal any differences in the regulation of EEG activities between genotypes. Finally, the waking EEG showed a slightly larger power in the 11-13-Hz band in alpha3-KO mice. However, neither behavior nor the waking EEG showed alterations suggestive of absence seizures. Furthermore, alpha3-KO mice did not differ in seizure susceptibility in a model of temporal lobe epilepsy. Strikingly, despite the disruption of postsynaptic gephyrin clusters, whole-cell patch clamp recordings revealed intact inhibitory synaptic transmission in the nRT of alpha3-KO mice. These findings show that the lack of alpha3-GABA(A) receptors is extensively compensated for to preserve the integrity of thalamo-cortical function in physiological and pathophysiological situations. |
| first_indexed | 2024-03-07T03:23:02Z |
| format | Journal article |
| id | oxford-uuid:b810ae14-2d4b-434d-9a2c-942b0f54108e |
| institution | University of Oxford |
| language | English |
| last_indexed | 2024-03-07T03:23:02Z |
| publishDate | 2008 |
| record_format | dspace |
| spelling | oxford-uuid:b810ae14-2d4b-434d-9a2c-942b0f54108e2022-03-27T04:53:25ZNormal sleep homeostasis and lack of epilepsy phenotype in GABA A receptor alpha3 subunit-knockout mice.Journal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:b810ae14-2d4b-434d-9a2c-942b0f54108eEnglishSymplectic Elements at Oxford2008Winsky-Sommerer, RKnapman, AFedele, DSchofield, CVyazovskiy, VRudolph, UHuguenard, JRFritschy, JTobler, IThalamo-cortical networks generate specific patterns of oscillations during distinct vigilance states and epilepsy, well characterized by electroencephalography (EEG). Oscillations depend on recurrent synaptic loops, which are controlled by GABAergic transmission. In particular, GABA A receptors containing the alpha3 subunit are expressed predominantly in cortical layer VI and thalamic reticular nucleus (nRT) and regulate the activity and firing pattern of neurons in relay nuclei. Therefore, ablation of these receptors by gene targeting might profoundly affect thalamo-cortical oscillations. Here, we investigated the role of alpha3-GABA A receptors in regulating vigilance states and seizure activity by analyzing chronic EEG recordings in alpha3 subunit-knockout (alpha3-KO) mice. The presence of postsynaptic alpha3-GABA A receptors/gephyrin clusters in the nRT and GABA A-mediated synaptic currents in acute thalamic slices was also examined. EEG spectral analysis showed no difference between genotypes during non rapid-eye movement (NREM) sleep or at waking-NREM sleep transitions. EEG power in the spindle frequency range (10-15 Hz) was significantly lower at NREM-REM sleep transitions in mutant compared with wild-type mice. Enhancement of sleep pressure by 6 h sleep deprivation did not reveal any differences in the regulation of EEG activities between genotypes. Finally, the waking EEG showed a slightly larger power in the 11-13-Hz band in alpha3-KO mice. However, neither behavior nor the waking EEG showed alterations suggestive of absence seizures. Furthermore, alpha3-KO mice did not differ in seizure susceptibility in a model of temporal lobe epilepsy. Strikingly, despite the disruption of postsynaptic gephyrin clusters, whole-cell patch clamp recordings revealed intact inhibitory synaptic transmission in the nRT of alpha3-KO mice. These findings show that the lack of alpha3-GABA(A) receptors is extensively compensated for to preserve the integrity of thalamo-cortical function in physiological and pathophysiological situations. |
| spellingShingle | Winsky-Sommerer, R Knapman, A Fedele, D Schofield, C Vyazovskiy, V Rudolph, U Huguenard, JR Fritschy, J Tobler, I Normal sleep homeostasis and lack of epilepsy phenotype in GABA A receptor alpha3 subunit-knockout mice. |
| title | Normal sleep homeostasis and lack of epilepsy phenotype in GABA A receptor alpha3 subunit-knockout mice. |
| title_full | Normal sleep homeostasis and lack of epilepsy phenotype in GABA A receptor alpha3 subunit-knockout mice. |
| title_fullStr | Normal sleep homeostasis and lack of epilepsy phenotype in GABA A receptor alpha3 subunit-knockout mice. |
| title_full_unstemmed | Normal sleep homeostasis and lack of epilepsy phenotype in GABA A receptor alpha3 subunit-knockout mice. |
| title_short | Normal sleep homeostasis and lack of epilepsy phenotype in GABA A receptor alpha3 subunit-knockout mice. |
| title_sort | normal sleep homeostasis and lack of epilepsy phenotype in gaba a receptor alpha3 subunit knockout mice |
| work_keys_str_mv | AT winskysommererr normalsleephomeostasisandlackofepilepsyphenotypeingabaareceptoralpha3subunitknockoutmice AT knapmana normalsleephomeostasisandlackofepilepsyphenotypeingabaareceptoralpha3subunitknockoutmice AT fedeled normalsleephomeostasisandlackofepilepsyphenotypeingabaareceptoralpha3subunitknockoutmice AT schofieldc normalsleephomeostasisandlackofepilepsyphenotypeingabaareceptoralpha3subunitknockoutmice AT vyazovskiyv normalsleephomeostasisandlackofepilepsyphenotypeingabaareceptoralpha3subunitknockoutmice AT rudolphu normalsleephomeostasisandlackofepilepsyphenotypeingabaareceptoralpha3subunitknockoutmice AT huguenardjr normalsleephomeostasisandlackofepilepsyphenotypeingabaareceptoralpha3subunitknockoutmice AT fritschyj normalsleephomeostasisandlackofepilepsyphenotypeingabaareceptoralpha3subunitknockoutmice AT tobleri normalsleephomeostasisandlackofepilepsyphenotypeingabaareceptoralpha3subunitknockoutmice |