Abstract
The corticotropin releasing factor (CRF) system in the central amygdala (CeA) has been implicated in the effects of acute ethanol and the development of alcohol dependence. We previously demonstrated that CRF receptor 1 (CRF1) neurons comprise a specific component of the CeA microcircuitry that is selectively engaged by acute ethanol. To investigate the impact of chronic ethanol exposure on inhibitory signaling in CRF1+ CeA neurons, we used CRF1:GFP mice subjected to chronic intermittent ethanol (CIE) inhalation and examined changes in local inhibitory control, the effects of acute ethanol, and the output of these neurons from the CeA. Following CIE, CRF1+ neurons displayed decreased phasic inhibition and a complete loss of tonic inhibition that persisted into withdrawal. CRF1− neurons showed a cell type-specific upregulation of both phasic and tonic signaling with CIE, the latter of which persists into withdrawal and is likely mediated by δ subunit-containing GABAA receptors. The loss of tonic inhibition with CIE was seen in CRF1+ and CRF1− neurons that project out of the CeA and into the bed nucleus of the stria terminalis. CRF1+ projection neurons displayed an increased baseline firing rate and loss of sensitivity to acute ethanol following CIE. These data demonstrate that chronic ethanol exposure produces profound and long-lasting changes in local inhibitory control of the CeA, resulting in an increase in the output of the CeA and the CRF1 receptor system, in particular. These cellular changes could underlie the behavioral manifestations of alcohol dependence and potentially contribute to the pathology of addiction.
SIGNIFICANCE STATEMENT The corticotropin releasing factor (CRF) system in the central amygdala (CeA) has been implicated in the effects of acute and chronic ethanol. We showed previously that CRF receptor 1-expressing (CRF1+) neurons in the CeA are under tonic inhibitory control and are differentially regulated by acute ethanol (Herman et al., 2013). Here we show that the inhibitory control of CRF1+ CeA neurons is lost with chronic ethanol exposure, likely by a functional switch in local tonic signaling. The loss of tonic inhibition is seen in CRF1+ projection neurons, suggesting that a critical consequence of chronic ethanol exposure is an increase in the output of the CeA CRF1 system, a neuroadaptation that may contribute to the behavioral consequences of alcohol dependence.
Introduction
Alcohol dependence is a complex clinical disorder characterized by repeating cycles of intake and withdrawal and a behavioral phenotype that includes the loss of control over consumption and impaired social functioning (Hoffman and Tabakoff, 1996; Eckardt et al., 1998). These behaviors appear to be mediated by adaptations at the cellular level as the brain attempts to overcome the effects of alcohol intake. The central nucleus of the amygdala (CeA) is a component of the extended amygdala, a macrostructure that mediates the negative reinforcing properties of alcohol and drugs of abuse (Alheid and Heimer, 1988). The CeA receives multiple inputs from a number of brain regions and acts as an integrative hub that has been implicated in stress, anxiety, and alcohol use disorders (Gilpin et al., 2015). The CeA is primarily composed of GABA neurons that synapse locally as well as project out of the CeA to regulate the flow of information to downstream brain regions, such as the bed nucleus of the stria terminalis (BNST). Local inhibitory control of CeA neurons includes both phasic and tonic inhibition, both of which are selectively sensitive to the effects of acute ethanol (EtOH; Roberto et al., 2003; Herman et al., 2013). Previous work has identified neuroadaptations in phasic signaling in the CeA following chronic ethanol (Roberto et al., 2004) and in tonic signaling in the rat (Herman and Roberto, 2016), but no studies have used mouse models to selectively examine the changes in tonic conductance in specific components of CeA circuitry.
The transition to alcohol dependence is associated with the recruitment of brain stress systems, most notably the corticotropin releasing factor (CRF) system (Heilig and Koob, 2007). Chronic ethanol exposure and withdrawal is associated with an upregulation of the CRF system in rats (Funk et al., 2007; Roberto et al., 2010) and mice (Eisenhardt et al., 2015). Notably, increased ethanol intake by dependent rats and mice can be reversed by a CRF1 antagonist (Chu et al., 2007; Finn et al., 2007; Funk et al., 2007; Correia et al., 2015), suggesting a critical role of the CRF1 system in the behavioral expression of alcohol dependence. CRF in the CeA has been implicated in the effects of acute ethanol on phasic GABA transmission in naive mice (Nie et al., 2004), after early binge-like ethanol drinking (Lowery-Gionta et al., 2012), and in alterations in GABA transmission in naive and dependent rats (Roberto et al., 2010). However, the impact of chronic ethanol on tonic GABA transmission and CRF1 signaling within the CeA remains unexamined. We showed previously that CRF1-expressing (CRF1+) neurons make up a distinct component of CeA circuitry that is differentially regulated by acute ethanol. CRF1+ neurons are not directly activated by acute ethanol, but instead are engaged via a local microcircuit involving increased inhibition at local CRF1− interneurons that synapse onto CRF1+ neurons (Herman et al., 2013). Based on our previous work on the CRF1 receptor circuitry in the CeA, and the relative sensitivity of specific components of CeA circuitry to acute ethanol, we hypothesized that chronic ethanol exposure would result in significant neuroadaptations in tonic signaling in CRF1+ CeA neurons and that these changes would impact excitability and subsequent output of the CeA network. We used transgenic mice expressing green fluorescent protein (GFP) in CRF1+ neurons to examine the effects of chronic ethanol exposure on (1) inhibitory signaling (phasic and tonic) in CRF1+ CeA neurons, (2) inhibitory signaling (phasic and tonic) in CRF1− CeA neurons, and (3) the excitability of CeA projection neurons and the sensitivity of these neurons to acute ethanol to determine the impact on CeA output to downstream targets in the extended amygdala.
Materials and Methods
Brain slice preparation.
All procedures were approved by the Scripps Research Institutional Animal Care and Use Committee and were consistent with the National Institutes of Health Guide for the Care and Use of Laboratory Animals. We prepared slices from 58 CRF1:GFP transgenic adult male mice (2–6 months, 18–30 g) that express GFP under the control of the promoter of the CRF1 receptor gene (Crhr1). These mice were generated using bacterial artificial chromosome recombination techniques such that the first exon of Crhr1 was replaced with the sequence encoding GFP. For a detailed description of the transgene design and histological validation of these mice, see Justice et al. (2008).
Mice were subjected to brief anesthesia (3–5% isoflurane) followed by rapid decapitation and removal of the brain to an ice-cold high-sucrose solution, pH 7.3–7.4, that contained the following (in mm): 206 sucrose, 2.5 KCl, 0.5 CaCl2, 7.0 MgCl2, 1.2 NaH2PO4, 26 NaHCO3, 5.0 glucose, and 5 HEPES. Brains were cut into transverse sections (300–400 μm) on a vibrating microtome (Leica VT1000S) and placed in an oxygenated (95% O2/5% CO2) artificial CSF (ACSF) solution composed of the following (in mm): 130 NaCl, 3.5 KCl, 1.25 NaH2PO4, 1.5 MgSO4 · 7 H2O, 2.0 CaCl2, 24 NaHCO3, and 10 glucose. Slices were incubated in this solution for 30 min at 35−37°C, followed by 30 min equilibration at room temperature (21–22°C). Following equilibration, a single slice was transferred to a recording chamber mounted on the stage of an upright microscope (Olympus BX50WI).
Electrophysiological recording.
We visualized neurons using infrared differential interference contrast (IR-DIC) optics and an EXi Aqua camera (QImaging). A 60× magnification water-immersion objective (Olympus) was used for identifying and approaching neurons. To avoid photolytic damage, initial exposure to episcopic fluorescence illumination was brief (<2 s). We detected fluorescent neurons using an X-Cite 120Q fluorescent illumination system (Lumen Dynamics) and captured images using QCapture software (QImaging). We made whole-cell (voltage-clamp and current-clamp) and juxtacellular (cell-attached) recordings with patch pipettes (3–5 MΩ; King Precision Glass) coupled to a Multiclamp 700B amplifier (Molecular Devices), low-pass filtered at 2–5 kHz, digitized (Digidata 1440A; Molecular Devices), and stored on a computer using pClamp 10 software (Molecular Devices). All recordings were performed at room temperature. Series resistance was typically <10 MΩ and was continuously monitored with a hyperpolarizing 10 mV pulse. Electrophysiological properties of cells were determined by pClamp 10 Clampex software online during voltage-clamp recording using a 5 mV pulse delivered after breaking into the cell. The resting membrane potential was determined online after breaking into the cell using the zero current (I = 0) recording configuration, and the liquid junction potential was included in the determination.
The intracellular solution used for voltage- and current-clamp recordings was composed of the following (in mm): 145 KCl, 5 EGTA, 5 MgCl2, 10 HEPES, 2 Na-ATP, and 0.2 Na-GTP. The pipette solution for juxtacellular (cell-attached) recordings was ACSF. Drugs were dissolved in ACSF and applied either by Y-tubing application for local perfusion primarily on the neuron of interest or by bath perfusion. To isolate the inhibitory currents mediated by GABAA receptors, all recordings (voltage-clamp and cell-attached) were performed in the presence of the glutamate receptor blockers 6,7-dinitroquinoxaline-2,3-dione (DNQX; 20 μm) and dl-2-amino-5-phosphonovalerate (AP-5; 50 μm) and the GABAB receptor antagonist (2S)-3-[[(1S)-1-(3,4-Dichlorophenyl)ethyl] amino-2-hydroxypropyl](phenylmethyl)phosphinic acid hydrochloride CGP55845A (1 μm). All voltage-clamp and cell-attached recordings were performed in a gap-free acquisition mode with a sampling rate per signal of 10 kHz or a total data throughput equal to 20 kHz (2.29 MB/min). All current-clamp recordings were performed in sweeps with a sampling rate per signal of 10 kHz or a total data throughput equal to 20 kHz (2.29 MB/min) as defined by pClamp 10 Clampex software.
Chronic intermittent ethanol vapor inhalation.
Seven independent cohorts including 30 adult male CRF1:GFP mice were housed in ethanol inhalation chambers (La Jolla Alcohol Research) and exposed to chronic intermittent ethanol (CIE) vapor (16 h) followed by air (8 h) 4 d per week for a period of 4–5 weeks. Before each vapor exposure, CIE mice were injected intraperitoneally with a solution of ethanol (1.5 g/kg) and pyrazole (1 mmol/kg; Sigma), an alcohol dehydrogenase inhibitor, to initiate intoxication and maintain constant blood alcohol levels (BALs). Control mice (n = 28, air) were exposed to room air and received an injection of pyrazole (1 mmol/kg) at the onset of each ethanol vapor exposure. Ethanol drip rate and air flow were adjusted so as to yield BALs averaging 150–275 mg/dl, as determined by regular tail bleedings (one to two times per week). BALs were measured using an Analox GM7 analyzer. Terminal BALs were also determined at the time of death when mice were euthanized immediately after their last ethanol vapor exposure (CIE mice) and averaged 266.6 ± 15.4 mg%. Another group of mice underwent 3–7 d of withdrawal after their last vapor exposure before being euthanized (CIE-WD mice). Air-exposed counterparts were generated for both CIE and CIE-WD groups (i.e., killed 16 h or 4–8 d after their last pyrazole injection, respectively). No statistically significant difference was observed between these two control groups, so data were pooled into a single control group, designated air control (AIR).
Retrograde labeling of CeA neurons.
Adult male mice (n = 14), 3–4 months of age (21–28 g), were anesthetized with a 1–3% isoflurane/oxygen mixture, placed on a warming pad, and mounted in a stereotaxic frame (David Kopf Instruments). A vertical incision was made in the skin overlaying the skull, which was subsequently exposed and cleaned. Head placement was adjusted to a level skull position according to bregma and lambda coordinates. A small hole was drilled over the target brain site [dorsal lateral BNST (dlBNST), AP, 0.0 mm; ML, ±1.1 mm; DV, –4.3 mm] based on the atlas of Franklin and Paxinos (2008). Bilateral 30-gauge stainless-steel injector needles connected to Tygon tubing preloaded with fluorescent microspheres (Lumafluor; 530/590 nm excitation/emission) were lowered to the dorsal lateral BNST. We injected a volume of ∼100 nl of undiluted fluorescent microspheres suspension over a 1–2 min period using a Hamilton microsyringe controlled by a pump (Harvard Apparatus). The injector needles were left in place for an additional 10 min to minimize backflow up the needle track, after which injector needles were removed and the scalp incision was closed. Mice were allowed to recover from surgery for 1 week before beginning chronic intermittent ethanol vapor inhalation.
Drugs and chemicals.
We purchased DNQX, AP-5, and CGP55845A (1 μm) from Tocris Bioscience. We purchased SR-95531 [gabazine (GBZ); 100 μm] and 4,5,6,7-tetrahydroisoxazolo[5,4-c]pyridin-3-ol (THIP; 5 μm) from Sigma.
Statistical analysis.
Frequency, amplitude, and decay of IPSCs were analyzed and visually confirmed using a semiautomated threshold-based mini detection software (Mini Analysis, Synaptosoft). We determined averages of IPSC characteristics from baseline and experimental drug conditions containing a minimum of 60 events (time period of analysis varied as a product of individual event frequency), and we determined decay kinetics using exponential curve fittings and reported them as decay time (in milliseconds). All detected events were used for event frequency analysis, but superimposed events were eliminated for amplitude and decay kinetic analysis. In voltage-clamp recordings, we determined tonic currents using Clampfit 10.2 (Molecular Devices) and a previously described method (Glykys and Mody, 2007b) in which the mean holding current (i.e., the current required to maintain the −60 mV membrane potential) was obtained by a Gaussian fit to an all-points histogram over a 5 s interval. The all-points histogram was constrained to eliminate the contribution of IPSCs to the holding current. We quantified responses as the difference in holding current between baseline and experimental conditions. The frequency of firing discharge in cell-attached recordings was evaluated using threshold-based event detection analysis in Clampfit 10.2 (Molecular Devices). Events were analyzed for independent significance using a one-sample t test and compared using a two-tailed t test for independent samples, a paired two-tailed t test for comparisons made within the same recording, a one-way ANOVA with a Bonferroni post hoc analysis for comparisons made between three or more groups, or a two-way ANOVA with a Bonferroni post hoc analysis for comparisons between there or more groups and multiple independent variables. All statistical analyses were performed using Prism 5.02 (GraphPad). Data are presented as mean ± SE. In all cases, p < 0.05 was the criterion for statistical significance.
Results
Differential membrane properties of CRF1+ and CRF1− CeA neurons are not affected by CIE exposure
GFP-positive CRF1-containing (CRF1+) neurons were identified and differentiated from unlabeled CeA neurons (CRF1−), as described previously (Herman et al., 2013). A coronal section of the CeA with representative sites of CRF1+ neurons detected during live-slice recording is shown in Figure 1A (asterisks). Figure 1B shows CRF1+ CeA neurons from air-exposed, pyrazole-injected control mice (AIR, top) and CIE vapor-exposed mice (bottom) visualized using fluorescent optics (left) and IR-DIC optics (right). CeA neurons were cell typed according to firing properties, as described previously (Chieng et al., 2006; Herman et al., 2013). The majority of CRF1+ neurons were of the low-threshold bursting (LTB) type (Fig. 1C, left), and a smaller proportion were of the regular-spiking (RS) type (Fig. 1C, middle). CRF1− neurons were divided into the late-spiking (LS) type (Fig. 1C, right) and the RS type (Fig. 1C, middle). Importantly, the relative distribution of the cell types was not significantly different between AIR, CIE, and CIE followed by 3–7 d of withdrawal (CIE-WD) groups. Consistent with our previous report (Herman et al., 2013), CRF1+ neurons displayed a significantly smaller membrane capacitance (Cm) and lower time constant (tau) compared to CRF1− neurons, and this difference was consistent between AIR, CIE, and CIE-WD groups (p < 0.05 comparing CRF1+ and CRF1− in each group; Fig. 1D; AIR CRF1+, n = 34; AIR CRF1−, n = 23; CIE CRF1+, n = 25; CIE CRF1−, n = 31; CIE-WD CRF1+, n = 29; CIE-WD CRF1−, n = 35).
Baseline phasic inhibitory transmission is altered in CRF1+ CeA neurons after CIE
Baseline phasic GABAA receptor activity was assessed using whole-cell voltage-clamp recordings of spontaneous IPSCs (sIPSCs). LTB CRF1+ neurons displayed a significantly lower baseline sIPSC frequency and amplitude after CIE (1.1 ± 0.2 Hz, 48.1 ± 4.1 pA; n = 18; Fig. 2A,C) compared to AIR (4.5 ± 0.8 Hz, 76.3 ± 7.4 pA; n = 21; p < 0.05; Fig. 2A,C). The decrease in sIPSC frequency was partially reversed and the decrease in sIPSC amplitude was completely reversed following withdrawal (3.0 ± 0.6 Hz, 74.6 ± 7.1 pA; n = 17; p < 0.05; Fig. 2A,C). RS CRF1+ neurons also displayed a significantly lower baseline sIPSC frequency after CIE (1.7 ± 0.7 Hz; n = 10; Fig. 2D) compared to AIR (4.3 ± 0.7 Hz; n = 13; p < 0.05; Fig. 2D), but the decrease persisted into withdrawal (1.8 ± 0.3 Hz; n = 6; Fig. 2D). No change in sIPSC amplitude was observed in RS CRF1+ neurons after CIE or CIE-WD (Fig. 2D). In contrast to what was observed in CRF1+ neurons, CRF1− neurons displayed cell-type specific changes in sIPSC frequency. LS CRF1− neurons displayed a significantly higher baseline sIPSC frequency after CIE (4.6 ± 0.8 Hz; n = 12; Fig. 2B,E) compared to AIR (2.3 ± 0.4 Hz; n = 18; p < 0.05; Fig. 2B,E), and the increase was reversed by withdrawal (2.7 ± 0.5 Hz; n = 16; p < 0.05; Fig. 2B,E). No change in sIPSC amplitude was observed in LS CRF1− neurons after CIE or CIE-WD (Fig. 2E). RS CRF1− neurons displayed no change in sIPSC frequency or amplitude after CIE or CIE-WD (Fig. 2F). Changes in sIPSC kinetics were also observed in both CRF1+ and CRF1− neurons following CIE and CIE-WD. LTB CRF1+ neurons displayed a small but significant reduction in rise time between the CIE and CIE-WD (2.0 ± 0.2 and 1.4 ± 0.2 ms, respectively; CIE, n = 18; CIE-WD, n = 17; p < 0.05). LS CRF1− neurons displayed a similar reduction in rise time between CIE and CIE-WD (2.0 ± 0.1 and 1.4 ± 0.1 ms, respectively; CIE, n = 19; CIE-WD, n = 12; p < 0.05), and RS CRF1− neurons displayed a significant increase in rise time between AIR and CIE (1.4 ± 0.1 and 2.1 ± 0.1 ms, respectively; AIR, n = 13; CIE, n = 12; p < 0.05). Notably, CIE produced an increase in the decay time of all cell types (CRF1+ and CRF1−) that was reversed in CIE-WD (p < 0.05; Fig. 2G).
Tonic inhibitory transmission is selectively altered in CRF1+ and late-spiking CRF1− CeA neurons after CIE, and this alteration persists into withdrawal
As we reported previously that the tonic conductance in CRF1+ neurons was driven by GABA release (Herman et al., 2013), we hypothesized that the decrease in phasic inhibition in CRF1+ neurons following CIE may also have consequences for tonic conductance. Baseline tonic GABAA receptor activity was assessed using whole-cell voltage-clamp recordings and the GABAA receptor antagonist gabazine. Consistent with our previous report (Herman et al., 2013), gabazine (100 μm) produced a significant reduction in holding current in both RS and LTB CRF1+ neurons from AIR mice (17.0 ± 2.9 pA and 14.2 ± 2.1 pA, respectively; p < 0.05 by one-sample t test; RS, n = 5; LTB, n = 8; Fig. 3A, top trace, C). In contrast, immediately following chronic ethanol exposure gabazine did not significantly alter the holding current in either RS or LTB neurons (1.1 ± 1.0 pA and 2.3 ± 0.9 pA, respectively; RS, n = 4; LTB, n = 7; Fig. 3A, middle trace, C), and this loss of effect persisted in neurons from CIE-WD mice (4.6 ± 0.3 pA and 3.1 ± 1.3 pA, respectively; RS, n = 2; LTB, n = 13; Fig. 3A, bottom trace, C). Two-way ANOVA revealed a significant effect of treatment (F(2,34) = 23.0, p < 0.001; Fig. 3C), but not of cell type (F(1,34) = 0.04, p > 0.05), and no significant interaction (F(2,34) = 0.2, p > 0.05). Gabazine produced no change in holding current in either RS or LS CRF1− neurons from AIR mice (1.2 ± 0.4 pA and 1.1 ± 1.1 pA, respectively; RS, n = 4; LS, n = 8; Fig. 3B, top trace, D). However, in CRF1− neurons from CIE mice, gabazine produced a significant reduction in holding current in LS neurons (11.1 ± 1.3 pA; p < 0.05; n = 6; Fig. 3B, middle trace, D) that was not observed in RS neurons (2.3 ± 1.2 pA; n = 6; Fig. 3D). The significant reduction in holding current produced by gabazine was also observed in LS CRF1− neurons from CIE-WD mice (14.5 ± 2.7 pA; p < 0.05; n = 10; Fig. 3B, bottom trace, D), but not in RS CRF1− neurons from CIE-WD mice (1.6 ± 0.6 pA; n = 8; Fig. 3D). Two-way ANOVA revealed a significant effect of treatment (F(2,36) = 7.05, p < 0.01; Fig. 3D) and of cell type (F(1,36) = 21.82, p < 0.001), as well as a significant interaction (F(2,36) = 6.05, p < 0.01). Based on our previous report showing connectivity between CeA CRF1− and CRF1+ neurons (Herman et al., 2013), these results suggest that chronic ethanol exposure produces an increase in phasic and tonic inhibition specifically in LS CRF1− neurons and a subsequent loss of tonic inhibition in CRF1+ neurons in the CeA.
The relative sensitivity of δ subunit-containing GABAA receptors in CRF1+ and CRF1− neurons is unchanged by CIE and CIE-WD
Based on our previous work demonstrating a tonic conductance that could be stimulated in CRF1− neurons (Herman et al., 2013), we hypothesized that the tonic conductance observed in late-spiking CRF1− was mediated by δ subunit-containing GABAA receptors. To investigate the underlying mechanisms behind the changes in tonic conductance observed in CRF1+ and CRF1− neurons in the CeA, we performed whole-cell voltage-clamp recordings of neurons from AIR, CIE and CIE-WD mice using the δ subunit-preferring agonist gaboxadol (THIP) to assess the relative sensitivity of δ subunit-containing GABAA receptors. THIP (5 μm) increased the holding current in all CRF1− neurons examined; however, in CRF1− neurons from AIR mice, LS CRF1− neurons displayed a significantly greater increase as compared to RS CRF1− neurons (75.9 ± 7.8 pA and 20.9 ± 7.3 pA, respectively; LS, n = 8; RS, n = 5; Fig. 4A,C). The greater increase in holding current in LS CRF1− neurons compared to RS neurons was also observed in neurons from CIE mice (52.4 ± 9.5 pA and 20.1 ± 5.8 pA, respectively; LS, n = 6; RS, n = 6; Fig. 4B,C) and in neurons from CIE-WD mice (58.3 ± 10.4 pA and 23.8 ± 3.6 pA, respectively; LS, n = 9; RS, n = 7; Fig. 4C). Two-way ANOVA revealed a significant effect of cell type (F(1,35) = 34.2, p < 0.001; Fig. 4C), but not of treatment (F(2,35) = 0.8, p > 0.05), and no significant interaction (F(2,35) = 0.9, p > 0.05). THIP produced a small and variable increase in holding current in both RS and LTB CRF1+ neurons, and there was no significant effect of treatment (F(2,22) = 0.2, p > 0.05) or cell type (F(1,22) = 0.06, p > 0.05), and no significant interaction (F(2,22) = 0.5, p > 0.05) in CRF1+ neurons from AIR, CIE, or CIE-WD mice (Fig. 4D). These data suggest that LS CRF1− neurons possess a greater number and/or sensitivity of δ subunit-containing GABAA receptors, which may be the source of the tonic conductance observed in CRF1− neurons from CIE and CIE-WD mice.
The relative sensitivity of CRF1+ and CRF1− neurons to acute ethanol is unchanged by CIE or CIE-WD
Based on the differential sensitivity of CRF1+ and CRF1− neurons to THIP and the role of the δ subunit in the effects of ethanol, we hypothesized that CRF1+ and CRF1− neurons would have a similar relative sensitivity to acute ethanol as what was observed with THIP. To further examine the mechanisms underlying the changes in tonic conductance in CRF1+ and CRF1− neurons following CIE and CIE-WD, we assessed the relative sensitivity of these cells to acute ethanol exposure. Ethanol (44 mm) increased the holding current in all CRF1− neurons from AIR mice, but the increase was significantly greater in LS neurons compared to RS neurons (11.8 ± 2.1 pA and 3.6 ± 1.4 pA, respectively; LS, n = 7; RS, n = 5; Fig. 5A,C). The greater increase in holding current in LS CRF1− neurons compared to RS neurons was also observed in neurons from CIE mice (14.4 ± 2.4 pA and 7.2 ± 1.3 pA, respectively; LS, n = 5; RS, n = 6; Fig. 5B,C) and in neurons from CIE-WD mice (9.9 ± 1.7 pA and 2.7 ± 0.8 pA, respectively; LS, n = 8; RS, n = 4; Fig. 5C). Two-way ANOVA revealed a significant effect of cell type (F(1,29) = 24.6, p < 0.0001; Fig. 5C), but not of treatment (F(2,29) = 3.0, p > 0.05), and no significant interaction (F(2,29) = 0.05, p > 0.05). There was no difference in the sensitivity of sIPSC frequency to acute ethanol between RS and LS CRF1− neurons and no effect of CIE or CIE-WD (Fig. 5D). There was no significant effect of ethanol on sIPSC amplitude in RS or LS CRF1− neurons from AIR, CIE, or CIE-WD mice, either by cell type (F(1,26) = 0.09, p > 0.05) or treatment (F(2,26) = 0.9, p > 0.05), and no significant interaction (F(2,26) = 0.5, p > 0.05). Acute ethanol produced small and variable effects on holding current in both RS and LTB CRF1+ neurons, and there was no significant effect of treatment (F(2,22) = 0.2, p > 0.05) or cell type (F(1,22) = 0.06, p > 0.05) and no significant interaction (F(2,22) = 0.5, p > 0.05) in CRF1+ neurons from AIR, CIE, or CIE-WD mice (Fig. 5E). There was also no difference in the effect of ethanol on sIPSC frequency in RS and LTB CRF1+ neurons between AIR, CIE, and CIE-WD mice (Fig. 5F). There was also no significant effect of ethanol on sIPSC amplitude in RS or LTB CRF1+ neurons from AIR, CIE, or CIE-WD mice, either by cell type (F(1,17) = 0.6, p > 0.05) or by treatment (F(2,17) = 0.3, p > 0.05), and no significant interaction (F(2,17) = 2.3, p > 0.05).
Tonic inhibitory transmission is selectively altered in CeA projection neurons
As we reported previously that CRF1+ neurons make up a subset of neurons that project out of the CeA in to the dlBNST (Herman et al., 2013), we predicted that this subset of CRF1+ neurons would also exhibit a reduced tonic conductance following CIE. To test this hypothesis, we performed whole-cell voltage-clamp recordings in CRF1+ and CRF1− neurons retrogradely labeled with fluorescent microspheres injected into the dlBNST of mice subsequently exposed to AIR, CIE, or CIE-WD. Projection neurons were identified using IR-DIC optics during recording (Fig. 6A, left) and by the presence of red fluorescent microspheres in the cell body (Fig. 6A, right). CRF1+ projection neurons were identified using IR-DIC optics (Fig. 6B, left), by GFP expression (middle), and by red microspheres detected in the cell body (right). CRF1− neurons were exclusively of the RS cell type, and the majority (24 of 30, 80%) of CRF1+ projection neurons were of the LTB cell type. Gabazine (100 μm) produced a significant reduction in holding current in all CRF1+ projection neurons from AIR mice (11.5 ± 2.1 pA; n = 11; Fig. 6C, top trace, D). In contrast, in CRF1+ projection neurons from CIE mice, gabazine produced no change in the holding current (0.6 ± 1.7 pA; p < 0.05 compared to AIR; n = 8; Fig. 6C, middle trace, D), and the same loss of effect was observed in CRF1+ projection neurons from CIE-WD mice (1.5 ± 1.4 pA; p < 0.05 compared to AIR; n = 8; Fig. 6C, bottom trace, D). Similar to what was observed in CRF1+ projection neurons, in CRF1− projection neurons from AIR mice, gabazine produced a significant reduction in holding current (14.5 ± 3.5 pA; n = 8; Fig. 6E) that was not observed in CRF1− projection neurons from CIE mice (−0.4 ± 0.9 pA; p < 0.05 compared to AIR; n = 7; Fig. 6E) or CIE-WD mice (1.7 ± 2.0 pA; n = 6; p < 0.05 compared to AIR; Fig. 6E). The presence of a significant tonic conductance in projecting CRF1− neurons from AIR mice is surprising given the absence of tonic conductance observed in unlabeled CRF1− neurons (Fig. 3D). Although it is possible that microspheres independently alter tonic GABA signaling in neurons in which they are taken up, it is more likely that projection neurons were not included in the neurons examined in the previous groups, as projection neurons make up only a small proportion of CeA CRF1− neurons. These data suggest that all projection neurons (CRF1+ and CRF1−) are under a significant amount of tonic inhibitory control that is lost following chronic ethanol exposure, and that this loss persists into withdrawal.
CRF1+ CeA projection neurons display an increased excitability and loss of sensitivity to acute ethanol following CIE
We predicted that the loss of tonic inhibitory control of CRF1+ CeA projection neurons would impact the excitability of these cells. To test this hypothesis, we performed extracellular cell-attached recordings in microsphere-labeled CRF1+ neurons from AIR and CIE mice. CRF1+ projection neurons from AIR mice displayed a baseline firing rate of 2.9 ± 0.6 Hz (n = 8; Fig. 7A, left, B). CRF1+ projection neurons from CIE mice displayed a baseline firing rate that was significantly higher than that observed in neurons from AIR mice (8.2 ± 2.5 Hz; p < 0.05 compared to AIR; n = 5; Fig. 7A, right, B). To determine how the changes in baseline excitability of CRF1+ CeA projection neurons would impact the effects of acute ethanol on firing discharge, we performed cell-attached recordings during superfusion of acute ethanol in CRF1+ projection neurons from AIR and CIE mice. In AIR mice, ethanol (44 mm) significantly increased the firing rate of CRF1+ projection neurons from 2.9 ± 0.6 Hz to 4.7 ± 0.6 Hz (p < 0.05; n = 8; Fig. 7C, left, D). In contrast, in CRF1+ projection neurons from CIE mice, ethanol did not significantly alter the firing rate (8.2 ± 2.5 Hz compared to 7.1 ± 1.9 Hz; n = 5; Fig. 7C, right, D). When the firing rate of each cell was normalized to baseline firing levels, acute ethanol increased the firing rate of CRF1+ projection neurons to 180.1 ± 21.2% of control (p < 0.05; n = 8) in AIR mice, and this increase was completely lost in CRF1+ projection neurons from CIE mice (96.4 ± 12.5% of control; p < 0.05 compared to AIR; n = 5; Fig. 7E). Together, these data indicate that CRF1+ projection neurons have an increased level of baseline activity after chronic ethanol exposure and can no longer increase their firing rate with acute ethanol exposure. These changes in baseline excitability and sensitivity to acute ethanol likely have significant consequences in the extended amygdala circuitry.
Discussion
This study provides new insight into the functional changes in inhibitory signaling in the CeA CRF1 circuitry following chronic ethanol exposure. Collectively, the data demonstrate that chronic ethanol exposure produces significant decreases in the phasic and tonic inhibition of CRF1+ neurons, regardless of the specific cell type. The loss of tonic inhibition in CRF1+ neurons occurs in parallel with an increase in phasic and tonic signaling in the subpopulation of LS CRF1− neurons. LS CRF1− neurons display an increased sensitivity to the δ subunit-preferring agonist THIP and to acute ethanol as compared to regular-spiking CRF1− neurons, suggesting that the increased tonic signaling is mediated by δ subunit-containing GABAA receptors that are present, but not active in the naive state. The loss of tonic inhibition was also seen in CRF1+ neurons that project into the dlBNST, along with an increase in baseline firing and loss of sensitivity to acute ethanol. Together, these data suggest that chronic ethanol exposure produces a functional switch in tonic signaling in the CeA such that the balance of inhibitory control shifts from CRF1+ projection neurons to LS CRF1− interneurons. This switch results in increased output of the CeA CRF1 system via disinhibition of projection neurons and includes a loss of sensitivity to acute ethanol. Interestingly, many of these changes persist into withdrawal, suggesting that they represent long-term neuroadaptations that could potentially play a role in alcohol dependence behaviors like escalated alcohol intake and the susceptibility to relapse. A schematic of the proposed inhibitory circuitry regulating activity of the CRF1 system in naive mice and the changes in inhibitory signaling that emerge after chronic ethanol exposure is shown in Figure 8.
As the CeA is primarily a GABAergic nucleus (Pitkänen and Amaral, 1994), inhibitory signaling is the predominant neurotransmission, the magnitude and type of which is determined presynaptically by GABA release and postsynaptically by the type and expression pattern of GABA receptor. GABAA receptor inhibition takes two main forms: phasic and tonic. Phasic inhibition mediates fast, point-to-point transmission with a relatively short time scale and rapid deactivation/desensitization. In contrast, tonic inhibition is characterized by a persistent inhibitory tone that dampens excitability (for review, see Glykys and Mody, 2007a; Belelli et al., 2009). Distinct receptor populations with specific GABAA receptor subunit configurations mediate the different types of inhibition and the relative properties of each (Semyanov et al., 2004). We showed previously that the tonic signaling in CRF1+ neurons is driven by action potential-dependent GABA release and is mediated by GABAA receptors containing the α1 subunit (Herman et al., 2013). The loss of tonic signaling in CRF1+ neurons after chronic ethanol could be the result of several (possibly converging) mechanisms. One possibility is that a decrease in presynaptic GABA release removes the input required to stimulate these receptors. This idea is consistent with the decrease in sIPSC frequency in CRF1+ neurons after chronic ethanol. Another possibility is that the GABAA receptors located on CRF1+ neurons are downregulated so that there are fewer receptors to carry a tonic conductance. This interpretation is consistent with an overall downregulation of GABAA receptors as suggested by the decrease in sIPSC amplitude that we observed in CRF1+ neurons after chronic ethanol exposure. However, the decrease in sIPSC amplitude was only observed in LTB CRF1+ neurons, but the loss of tonic conductance was observed in both LTB and RS neurons, suggesting that an overall downregulation of GABAA receptors is not the dominant mechanism behind the loss of tonic inhibition. A third possibility is that the subunit composition and/or or synaptic localization of GABAA receptor subunits is altered in CRF1+ neurons after chronic ethanol, similar to what has been observed in the hippocampus (Liang et al., 2009) and thalamus (Werner et al., 2016) following chronic ethanol treatment. Changes in sIPSC kinetics (rise and decay times) in CRF1+ neurons following chronic ethanol supports the idea that the composition of GABAA receptor subunits is altered in CRF1+ neurons following chronic ethanol. However, while the decrease in sIPSC frequency partially recovered but the loss of tonic conductance persisted into withdrawal, the changes in sIPSC amplitude and decay were restored to control levels in withdrawal, suggesting that they may represent independent neuroadaptations. In addition, changes in sIPSC kinetics were also observed in CRF1− neurons, suggesting that these changes occur independent of changes in tonic conductance.
In contrast to the potential changes in GABAA receptor expression and/or localization in CRF1+ neurons following chronic ethanol, our data suggest that the tonic conductance observed in LS CRF1− neurons following CIE is mediated by GABAA receptors that are present in control conditions. The relative sensitivity of LS CRF1− neurons to the GABAA receptor agonist THIP and to acute ethanol and the lack of effect of chronic ethanol treatment on that relative sensitivity suggest that although δ subunit-containing receptors are present on LS CRF1− neurons in the basal state, they are not occupied. As these receptors are located at extrasynaptic sites (Glykys and Mody, 2007a), they are likely not activated unless ambient GABA levels reach a sufficient threshold, which may not occur in the naive CeA. We have previously reported a rise in ambient GABA levels after chronic ethanol administration (Roberto et al., 2004), which is consistent with the potential for activation of extrasynaptic GABAA receptors containing the δ subunit and the significant increase in tonic signaling that we observed in LS CRF1− neurons. Interestingly, despite the increase in activity of δ subunit-containing GABAA receptors in LS CRF1− neurons following chronic ethanol administration, acute ethanol was still able to stimulate a further increase in tonic signaling, suggesting that the occupation/activation is submaximal.
The CRF system, and particularly CRF1, in the CeA have been implicated in the effects of stress, anxiety, and all stages of alcohol dependence (Koob, 2008; Roberto et al., 2010; Lowery-Gionta et al., 2012). As the CeA is an integrative hub that coordinates internal and external sensory input into behaviorally relevant responses (Gilpin et al., 2015), the CeA CRF1 system represents a common pathway for the convergence of stress, alcohol, and anxiety-related signaling. Activation of CRF1 has been implicated in the development of the negative emotional state associated with dependence, and it has been proposed that alleviation of this negative state drives the motivation to drink (Koob, 2010). Consistent with this view, administration of a CRF1 antagonist has been shown to reduce ethanol consumption in both rat and mouse models of dependence (Chu et al., 2007; Finn et al., 2007; Funk et al., 2007; Correia et al., 2015). The CRF1 system may also play a critical role in stress-related vulnerability to alcohol exposure. Notably, the increased impulsivity and excessive ethanol consumption in rodents subjected to early life stress can be reversed by CRF1 antagonism as well as pharmacological manipulation of GABAA receptor signaling in the CeA (Gondré-Lewis et al., 2016). CRF has been shown to augment GABA transmission in the CeA via actions at CRF1 (Nie et al., 2004; Roberto et al., 2010), and CeA CRF neurons use GABA as a cotransmitter as well as display increased activity after chronic stress (Partridge et al., 2016). It is important to note that the mouse model we used in the present study only reflects neurons that express CRF1 (Justice et al., 2008), and provides no information on CRF peptide actions or circuitry. It is not currently known if the CRF1+ CeA neurons in the CRF1:GFP mouse display any overlap with CRF neurons in the CeA. Although progress has been made with reporter mice (Silberman and Winder, 2015), more sophisticated animal models and/or technological approaches are required to more directly pinpoint the intersection of the CRF and CRF1 systems in the CeA.
The primary focus of this study is CRF1 circuitry in the CeA and the effects of acute and chronic ethanol on local inhibition and the dysregulation of CeA CRF1 output. This information is critical to developing an improved understanding of how specific circuits within the CeA are altered following chronic alcohol exposure. The CeA is a heterogeneous nucleus, but recent studies have begun to characterize distinct cell populations and their role in circuits governing specific behaviors. For example, circuitry-specific changes in CeA processing have been implicated in conditioned fear (Haubensak et al., 2010) and in anxiety (Botta et al., 2015). A common theme of these studies is the importance of local inhibitory signaling in the flow of information through distinct circuits. Specific inhibitory microcircuits in the central amygdala govern different aspects of fear learning (Ciocchi et al., 2010), and extrasynaptic inhibition regulates the changes in excitability underlying the encoding of generalized fear or anxiety (Botta et al., 2015). The mechanism of disinhibition that we report here following chronic ethanol exposure has also been reported for engaging specific aspects of amygdala circuitry in fear learning (Wolff et al., 2014). Disinhibition of projection neurons has been implicated in critical circuitry changes related to learning and memory in various brain regions and systems (Letzkus et al., 2015). If the development of alcohol dependence can be conceptualized as a pathological expression of learning, then it is compelling that both processes would use a similar mechanism of disinhibition for the engagement of specific components of circuitry. This view agrees with the current focus on the role of disease-specific alterations in distinct amygdala circuits as major contributing factors in the development of addiction (Koob and Volkow, 2010) and the commonalities between addiction and anxiety (Lüthi and Lüscher, 2014).
Footnotes
This work was supported by the Pearson Center for Alcoholism and Addiction Research, the Clayton Medical Research Foundation, and NIAAA Grants AA021491, AA023002, AA015566, AA06420, AA017447, AA020913, and AA024198.This is manuscript #29330 from the Scripps Research Institute. We thank Nicholas Justice at the University of Texas Health Science Center at Houston for providing CRF1:GFP breeders.
The authors declare no competing financial interests.
- Correspondence should be addressed to Dr. Melissa A. Herman, The Scripps Research Institute, 10550 North Torrey Pines Road, La Jolla, CA 92037. mherman{at}scripps.edu