Region-specific interneuron demyelination and heightened anxiety-like behavior induced by adolescent binge alcohol treatment
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Adolescent binge drinking represents a major public health challenge and can lead to persistent neurological and mental conditions, but the underlying pathogenic mechanisms remain poorly understood. Using a mouse model of adolescent binge ethanol treatment (ABET), we found that this treatment induced behavioral changes associated with demyelination in different brain regions. After ABET, adolescent mice exhibited anxiogenic behaviors with no change in locomotion on the elevated plus maze, and impaired spatial memory indicated by a significant reduction in spontaneous alternation in the Y maze test. Both effects persisted into adulthood. Anatomical studies further showed that ABET induced a significant reduction of parvalbumin-positive (PV+) GABAergic interneurons and myelin density in the hippocampus and medial prefrontal cortex (mPFC). While these deficits in PV+ interneurons and myelin persisted into early adulthood in the hippocampus, the myelin density recovered in the mPFC. Moreover, whereas ABET mainly damaged myelin of PV+ axons in the hippocampus, it primarily damaged myelin of PV-negative axons in the mPFC. Thus, our findings reveal that an adolescent binge alcohol treatment regimen disrupts spatial working memory, increases anxiety-like behaviors, and exerts unique temporal and spatial patterns of gray matter demyelination in the hippocampus and mPFC.
KeywordsAdolescent binge ethanol treatment (ABET) Anxiety Gray matter myelin Hippocampus Medial prefrontal cortex (mPFC) Parvalbumin-positive (PV+) GABAergic interneuron
Binge drinking is defined by the National Institute on Alcohol Abuse and Alcoholism as “a pattern of drinking that brings blood alcohol concentration levels to 0.08 g/dL”. This typically occurs after consuming 4–5 standard drinks within a 2 h period. Among all age groups, adolescents are the most likely to binge drink [13, 20]. Meta-analysis showed that approximately 20–40% of adolescents engaged in binge drinking, and in particular, about 10% of 12th graders and 20% of college students who drink alcohol are heavy binge drinkers [28, 41]. Large population studies have found that, across the teenage years, both early age of first use and binge drinking predict increased risk of lifetime alcohol use disorder (AUD) and alcohol-related violence and injuries [20, 41]. Despite the strong association between adolescent binge drinking and AUD, the neural substrates underlying this relationship remain poorly understood.
Alcohol binge drinking can be especially harmful in adolescents, since adolescence is a critical developmental period associated with maturation of cognitive ability, personality, and frontal cortical executive functions. This coincides with gray matter (GM) myelination in different brain regions, including the hippocampus and medial prefrontal cortex (mPFC). GM myelination is a long process that continues into adulthood in both humans and rodents and its disruption can lead to various neurological disorders [1, 2, 30]. Different from white matter (WM) myelin that has been extensively studied, GM myelin often localizes adjacent to neuronal soma, dendrites and synapses. The hippocampus plays a key role in spatial memory and anxiety , and is known as one of the most sensitive targets for the neurotoxic effects of ethanol (EtOH) . The mPFC is involved in planning and decision making, and reciprocally connected to the hippocampus and other regions that mediate positive and negative reinforcement [47, 51]. Alcohol-mediated alterations in mPFC connectivity may lead to loss of control over attention and emotion, and to increased engagement in risky behaviors, such as binge drinking [40, 48]. Chronic EtOH exposure has been shown to reduce myelin protein expression, leading to demyelination in WM that is commonly observed in human alcoholics [6, 25, 32, 36, 53].
Recent studies discovered that the locally-projecting, parvalbumin-positive (PV+) GABAergic interneurons contribute a major portion of myelinated axons within the cortex and hippocampus [29, 42]. These interneurons play a key role in maintaining proper excitatory/inhibitory balance and high-frequency network oscillations via feedback and feedforward inhibition [8, 15, 21]. PV+ interneurons can fire action potential up to 1 kHz and thus they are also called fast-spiking interneurons [19, 21]. They target excitatory neurons, and receive strong excitatory input, as well as inhibition from other PV+ interneurons . PV+ interneuron reduction is associated with cognitive and emotional problems in mice and humans [7, 24, 26]. However, the possible impact of chronic EtOH on GM and interneuron myelin in regions like the hippocampus and mPFC remains unknown.
To address this critical gap in our knowledge, we established a mouse adolescent binge EtOH treatment (aka ABET) model with an on-off-on intermittent temporal pattern . Prior studies revealed that this model led to long-lasting changes in adulthood, including disrupted Barnes Maze reversal learning, volume enlargements in specific brain regions (but no changes in total brain volume) including the orbitofrontal cortex, cerebellum, thalamus, internal capsule and genu of the corpus callosum, and increased expression of extracellular matrix proteins . Other studies have also revealed persistent effects of adolescent alcohol exposure on brain function and structure including increased EtOH intake and risk-taking preference, impaired conditioned discrimination and object recognition [14, 34], and frontal cortical damage . EtOH binge treatment also reduced myelin density in the mPFC in adolescent rats, suggesting that greater severity of PFC WM neuropathology may be correlated with higher levels of relapse-like drinking in adulthood . Thus, ongoing myelination in the adolescent brain may make binge drinkers particularly vulnerable to long-term consequences of chronic alcohol exposure, including cognitive deficits and addiction. However, the mechanism and function of myelin alterations induced by adolescent EtOH binge exposure remain poorly understood.
Using behavioral testing and anatomical analysis, we have found that ABET induces long-lasting behavioral changes associated with differential demyelination in hippocampal and mPFC circuits. Thus, dysregulation of GM myelination in cortical and limbic regions may contribute to maladaptive behavioral phenotypes that develop following adolescent binge alcohol exposure.
Materials and methods
EtOH binge treatment via Intragastric intubation
Mice received either saline or 25% (vol/vol) EtOH (5 g/Kg) via intragastric (i.g.) intubation on days P28, P29, P32, P33, P36, and P37. Previous studies utilizing this EtOH exposure paradigm reported blood EtOH concentrations (BECs) of ~ 300 mg/dL in C57Bl6 mice . To confirm that this EtOH binge model results in a similar level of BECs in our lab, we used the EtOH Assay Kit (Cat. #: ab65343; Abcam, Cambridge, MA, USA) to measure BECs at 1.5 h post i.g. intubation (~ 280 ± 20 mg/dL). Thus, the BECs of this EtOH binge model in our lab are consistent with what was previously reported.
A few days or a month after the final EtOH exposure, mice were subjected to behavioral testing in the following order: Elevated plus maze (EPM), Y-maze spontaneous alternation, and Open Field on consecutive days. All behavioral testing occurred during the light phase. Prior to behavioral testing, mice were acclimated to the procedure room for at least 1 h. Home cages were then moved to an adjacent room and mice were transported to the procedure room for testing one at a time. When testing was complete, mice were returned to their home cage and the apparatus was cleaned using a 70% EtOH solution between trials. Mouse behavior was recorded by a mounted video camera (Sony Corporation, Tokyo, Japan) and stored for offline analysis by hand or using Ethovision XT 12 software (Noldus Information Technology, Wageningen, The Netherlands).
Elevated plus maze
Anxiety-like behavior was measured using the EPM as described previously . EPM testing was carried out on a raised (74 cm) plus-shaped maze with four arms (34 cm long). Two opposite arms were “open” with no walls; the other two arms were “closed” by opaque walls (22 cm high). Mice were placed in the center of the maze at the intersection of the two arms and allowed to explore the maze for 5 min. Total distance traveled, arm entries, and time spent on the four arms were recorded, with percentage time spent in the open arms/(open + closed arms) of the EPM used as a measure of anxiety-like behavior. Time spent in the center was not included in the analysis.
Y-maze spontaneous alternation
Working memory was assessed using the spontaneous alternation Y-maze test as described previously [10, 38]. Mice were placed at the end of one arm of a symmetric Y maze with arms measuring 40 cm long, 8 cm wide, and 20 cm high and allowed 5 min to freely explore the apparatus. The series of arm entries (e.g. ACBCABCBCA) was recorded using an overhead camera. An alteration is counted when the mouse entered the 3 different arms during a triad on overlapping triplet sets (e.g. in the sequence ACBCABCBCA, five alternations were recorded). Spontaneous alternation was measured by counting the number of times the mouse entered each of the 3 arms of the maze in succession divided by the maximum number of possible alternations, where maximum alternations was calculated as the total number of arm entries minus 2.
Locomotor activity was measured using the open field task . Mice were placed in the center of a square arena (40 cm X 40 cm) and behavior was recorded for 10 min. Total distance traveled per 1 min time bins was used as a measure of locomotion, and time spent in the center (25 cm X 25 cm) and perimeter of the arena were also recorded.
Brain tissue preparation
Twenty four hours after the completion of behavioral testing, all mice were deeply anesthetized with avertin (250 mg/kg) and perfused transcardially with 20 ml of PBS followed by 20 ml of a 4% formaldehyde/PBS solution. Brains were removed and post-fixed for 1 h in 4% formaldehyde/PBS solution and then cryoprotected in a 30% sucrose/PBS solution for > 24 h. Tissue blocks were made using optimal cutting temperature (OCT) medium (Braintree Scientific, Braintree, MA, USA) and samples were stored at − 80 °C until being cut using a Microm HM55 cryostat (Thermo Scientific, Waltham, MA, USA). Forty micrometer coronal sections were cut and mounted on Superfrost Plus slides (FisherScientific, Pittsburgh, PA, USA) and stored at − 20 °C.
Antibodies and reagents
The following antibodies were used in the present study: rat monoclonal anti-myelin basic protein (MBP; Cat. #: MAB386; Millipore, Billerica, MA); rabbit anti-parvalbumin (PV; Cat. #: 195002; Synaptic Systems, Gottinggen, Germany); rabbit anti-degraded MBP (dMBP; Cat. #: AB5864; Millipore, Billerica, MA); Cy3-, and Cy5-conjugated secondary antibodies (Jackson ImmunoResearch Laboratories, West Grove, PA, USA). All antibodies were used in a 1:200 dilution. The nuclear dye Hoechst 33342 was purchased from Invitrogen (Cat. #: H3570; Carlsbad, CA, USA).
Mouse brain sections were stained as detailed in previous reports from our laboratory [4, 5, 18, 22, 23]. Sections were permeabilized in 1% Triton X/PBS for 1 h at room temperature (RT) and then blocked with 2.5% normal donkey or goat serum for 1 h at RT. Sections were then incubated overnight at 4 °C with the primary antibodies in blocking buffer. Twenty-four h later, sections were rinsed for 5 min seven times, incubated with the appropriate secondary antibodies in blocking buffer for 3 h at RT, counterstained with Hoechst 33342 for 10 min, and again rinsed for 5 min seven times. Stained slides were coverslipped with tris-buffered Fluoro-Gel mounting media (Electron Microscopy Sciences, Hatfield, PA, USA). Multiple staining rounds were carried out with at least one slide from each experimental group.
Microscopy and image quantification
Fluorescence microscopy and image analyses were carried out as described in previous publications from our laboratory [17, 18, 22, 23, 31, 49]. We focus on the following brain regions, dorsal hippocampus (Bregma between − 1.82 and − 2.30 mm) and mPFC (Bregma between + 1.98 and + 1.78 mm). Low magnification images were captured with a Spot CCD camera RT slider (Diagnostics Instruments, Sterling Heights, MI, USA) on a Zeiss Axiophot upright microscope using a 20X/0.50 Plan Apo objective and saved as 12-bit TIFF files. Exposure times were adjusted to ensure that pixel intensity in targeted tissue samples were below saturation, and exposure time was kept constant across all experimental conditions for each of the specific fluorophores utilized. Representative high magnification images were captured with a Leica TCS SL confocal imaging system (Leica Microsystems, Mannheim, Germany) using a 100X HCX Plan Apo CS oil immersion objective with a numerical aperture of 1.40, or on a Andor Revolution WD spinning disk confocal system (Oxford Instruments, Abingdon-on-Thames, UK) based on a Nikon TiE inverted microscope using a 60X CFI Plan Apo VC water immersion objective with a numerical aperture of 1.40. Z-stack images (8-bit TIFF files) were taken for each region of interest at ~ 0.25 μm steps and flat images were generated using a maximum intensity projection.
Image analyses were performed with NIH ImageJ (Fiji) software on low magnification images captured with 20X0.50 objective. The same staining procedures, imaging exposure times and brain regions were used across the sections from different conditions. PV+ cell counts were carried out by overlaying PV stained sections over the nuclear dye Hoechst stained sections. The number of nuclei that overlapped with PV expression were counted manually and used as a measure of PV+ cells (here, AU = cell number/image field) for subsequent analysis. Each image at 20x is 1200 × 1600 pixels, with a measure of 0.37 μm per pixel. Thus, 1 image field = 444 × 592 μm2 ~ 0.26 mm2. To quantify the density of MBP+/dMBP+ myelin segments and PV+ processes in an image field, each image was thresholded to reveal MBP+ myelin segments or PV+ neuronal processes, and then binarized as previously described [5, 31], for either density quantification (segments or processes/image field) or further quantification of colocalization. In order to determine the extent to which alterations in MBP+ myelin segment density might be related to changes in PV+ processes after ABET, correlations were calculated for overlapping pixels from PV and MBP images. A Pearson’s r was calculated for each set of images, and mean correlation values were compared across treatment conditions. For all dependent measures, at least 3 slides per region of interest per mouse were analyzed from ≥3 mice per experimental condition. The n numbers for analyzed slices are provided in figure legends. All image analysis and quantification have been verified and supported with confocal microscopy.
Results are presented as mean ± SEM. Two-way ANOVAs with condition (Control vs. EtOH) and age (Adolescent vs. Adult) as between-subjects factors were carried out using SigmaPlot 13.0 software (Systat Software Inc., Chicago, IL, USA). Tukey’s post hoc tests were used to compare simple mean effects when following significant interaction effects. One-sample t-test was carried out in the Y maze test to compare each condition with the chance level (50%) as previously reported , and Pearson’s r was calculated for PV/MBP correlation analyses. The Type I error rate was set at 0.05.
ABET induced anxiety-like behaviors that persisted into adulthood
To determine behavioral and brain structural changes associated with adolescent alcohol binge drinking, we used an established mouse model of ABET  with some modifications (Fig. 1). Male C57Bl6 mice received either saline or 25% (vol/vol) EtOH (5 g/kg) via intragastric (i.g.) intubation on days P28, P29, P32, P33, P36, and P37, mimicking human adolescent binge drinking in an on-off-on intermittent temporal pattern (Fig. 1). Right after EtOH intubation, mice transiently displayed moderate sedation and poor coordination, closely resembling some of the physical behavioral characteristics observed in humans after binge drinking. To control for any stress associated with the intubation procedure, control mice received the equivalent volumes of i.g. saline. All mice were subjected to three behavioral assays, including the EPM, Y maze and open-field test, either 3 (Adolescent) or 34 (Adult) days after the final treatment (Fig. 1). We used these three behavioral assays to assess potential acute and long-lasting effects of ABET on general locomotion, cognition and anxiety-like behavior in adolescent mice.
ABET reduced spatial working memory and had no effect in locomotion
ABET induced long-lasting reduction of PV+ neurons and MBP+ myelin density in the hippocampus
ABET caused a marked reduction of PV+ cell density and MBP+ myelin segment density in the hippocampus of both adolescent and adult mice (Fig. 5a–d). Two-way ANOVA revealed a significant main effect for condition [F1,20 = 12.52, p = 0.002], with EtOH exposed (or ABET) mice having reduced PV+ cell body counts across both adolescence and adulthood (Fig. 5c). There were no significant effects of age [F1,20 = 2.52, p = 0.13, two-way ANOVA] and no condition X age interaction [F1,20 = 0.54, p = 0.82, two-way ANOVA] (Fig. 5c). Thus, there was no significant increase of the PV+ cell number between the adolescent and adult mice under our experimental condition. For MBP+ myelin segments, two-way ANOVA revealed that myelin density was significantly reduced in EtOH-exposed mice across both age groups [main effect of condition; F1,64 = 15.54, p < 0.001, two-way ANOVA], and importantly that myelin density was increased in adults regardless of EtOH exposure [main effect of age; F1,64 = 23.75, p < 0.001, two-way ANOVA]. The condition X age interaction was not significant [F1,64 = 0.81, p = 0.37, two-way ANOVA] (Fig. 5d). Therefore, in contrast to PV+ cell body density, the density of myelin segments in the hippocampus significantly increased between adolescence and adulthood.
To estimate how myelin segments of PV+ and PV- axons were impacted by ABET, we performed a correlation of PV and MBP co-localization (Fig. 5e). Pixel-by-pixel intensity was correlated between corresponding PV/MBP images. The average Pearson’s r value was calculated and subjected to a two-way ANOVA (Fig. 5e). This analysis revealed a significant condition X age of testing interaction [F1,32 = 4.57, p = 0.04, two-way ANOVA]. Post hoc pairwise analyses using Tukey’s test found higher PV/MBP correlations in adult control mice compared to adult ABET mice (p = 0.046), but not between the adolescent control and ABET mice (p = 0.35). Furthermore, adult mice demonstrated increased correlation values compared to adolescents for both control (p < 0.001) and ABET (p < 0.05) mice. Since both PV and MBP density were reduced and their correlation did not increase for both adolescent and adult mice after ABET (Fig. 5c–e), a majority of the observed reduction in myelin likely occurred in PV+ axons. This notion was confirmed by confocal microscopy, showing abundant PV+/MBP+ axons in the control (Fig. 5f) and reduced double-positive axons after ABET (Fig. 5g) in adolescent mice. Our results also indicate that there is a higher proportion of myelination on PV+ axons in adult mice compared to adolescent mice, but this increase is blunted by ABET.
In the mPFC ABET caused persistent reduction of PV+ neurons and transient myelin reduction
To determine how myelin segments of PV+ and PV- axons in the mPFC were impacted by ABET, we performed the correlational analysis of PV and MBP co-localization (Fig. 6e). Correlations were carried out for overlaid sets of PV/MBP images. Two-way ANOVA demonstrated significant main effects for condition [F1,32 = 6.53, p = 0.016] and age [F1,32 = 17.04, p < 0.001], while the condition X age interaction failed to reach significance [F1,32 = 0.07, p = 0.79] (Fig. 6e). These results were further confirmed by confocal microscopy. PV+/MBP+ axons were present in the mPFC of control adolescent mice and did not decrease after ABET, although ABET reduced myelin density (Fig. 6f). Taken together, our results suggest that, in sharp contrast to the hippocampus, demyelination mainly occurred for PV- axons in the mPFC immediately after ABET, while the proportion of myelin on PV+ axons significantly increased in early adulthood.
Myelin damage was responsible for myelin density reduction right after ABET
Similar results were found in the mPFC for dMBP expression (Fig. 6f–j). Two-way ANOVA indicated a significant condition x age interaction [F1,24 = 22.39, p < 0.001]. As in the DG, Tukey’s post hoc analyses of the interaction found increased dMBP expression in adolescent EtOH mice compared to controls (p < 0.001) while no significant difference in mPFC dMBP expression between adult control and adult EtOH mice (p = 0.07) (Fig. 7j). The dMBP staining signals also appeared to colocalize with some MBP+ myelin segments after ABET (Fig. 7f–i). Taken together, demyelination is most likely induced by ABET, and accounts for, perhaps not entirely, the reduction in myelin observed shortly after ABET, but it apparently does not persist into early adulthood.
Using the ABET mouse model, we found that this treatment induced a long-lasting increase in anxiety-like behavior, a persistent reduction in working memory, and differentially altered interneuron myelination in the hippocampus and mPFC. Although ABET reduced PV+ neurons and myelin density in both regions, our results show for the first time that there are regional differences in interneuron demyelination caused by this EtOH treatment. Taken together, our findings suggest that brain-region specific alterations of PV+ interneurons and their myelin may play a key role in the maladaptive physiological and behavioral changes induced by adolescent binge drinking.
Our EPM results indicate that after ABET, adolescent mice had significantly less percentage time in the open arms/(open + closed arms), an effect that endured into adulthood (Fig. 2). This result is consistent with prior findings showing that binge alcohol treatment persistently increased anxiety-like behavior using either an open-field test  or a light/dark box exploration test . However, our open-field test (10 min total) failed to detect any significant change in center time caused by ABET (Fig. 4), which is different from the result of the open-field test in the earlier study (2 h total) . This most likely resulted from differences in the durations of the tests being used in these studies. We used a shorter time (10 min) in our open-field assay to primarily examine locomotion (Fig. 4). Actually, our result is likely consistent with the initial period of the long open-field test . Nonetheless, anxiety is a very complex behavior and it is not surprising to see differences between tests, which often reflect different types of anxiety . Importantly, as observed in other studies , we did not observe any ABET-associated changes in locomotor activity (Figs. 3 and 4).
Our result using the Y-maze test shows that ABET significantly reduced spontaneous alternation in adolescent mice, suggesting impaired working memory, and this impairment did persist to some extent into early adulthood (Fig. 3). This seems consistent with a recent study, using the rewarded alternation test, that showed that EtOH binge-treated rats of both sexes displayed spatial working memory deficits . Interestingly, another study using a rat model of alcohol binge drinking showed that heavier drinking predicted worse performance on the T-maze working memory task in adulthood . In mice, adolescent intermittent EtOH did not impact adult Barnes Maze learning, but caused reversal learning deficits in adults . On the other hand, another recent study showed that binge-treated rats were impaired during the first attention set shift on an operant set-shifting task, but displayed no difference in spatial exploration, learning and reversal, or novel object recognition . In DBA/2 J adolescent mice, binge treatment caused long-term memory deficits using the novel object recognition test . These differences most likely result from differences in the tests and animal strains used in these studies. Nonetheless, establishing the specific cognitive deficits caused by alcohol binge drinking likely still requires more extensive investigation.
Since GM myelination is a long process and coincides with periadolescent development, the present study mainly focused on the effects of ABET on GM myelin. Our results show that GM myelin in both the hippocampus and the mPFC was significantly reduced after ABET (Figs. 5 and 6). Notably, the reduced myelin levels appeared to persist into adulthood in the hippocampus, but not the mPFC (Figs. 5 and 6). This appears somewhat different from the conclusion of a recent paper that binge drinking in adolescent male rats reduced myelin density in the mPFC in adulthood . However, it is important to note that in their alcohol dependence protocol, rats were subjected to EtOH vapor exposure before myelin staining in adulthood . Consistent with our results (Fig. 6), right after binge drinking there was a clear reduction of prefrontal myelin . Our results show that reduced myelin in adolescents by ABET returned to control levels in early adulthood, presumably through more robust remyelination, which may be an interesting topic for future instigation.
Recent studies showed that a significant proportion of GM myelination in the cortex and hippocampus of both rodents and humans is localized to the axons of local inhibitory GABAergic interneurons and that almost all myelinated GABAergic axons are from PV+ fast-spiking interneurons [29, 42]. Thus, we performed co-staining for PV and MBP to determine the effect of ABET on interneuron myelination. Interestingly, our results showed that ABET significantly reduced PV+ interneurons in both the hippocampus and the mPFC, and the reduction persisted into adulthood in both regions (Figs. 5 and 6). By using designer receptors exclusively activated by designer drugs (DREADD) technology, a recent study showed that proper control of PV+ interneurons activity in the dentate gyrus of the hippocampus is critical for regulation of the anxiety, social interaction and fear extinction . This is consistent with our results showing persistently reduced PV+ neurons in the hippocampus and persistently heightened anxiety-like behavior following ABET (Figs. 2 and 5). However, it currently remains unclear whether ABET-induced reduction of PV+ cell density resulted from inhibited PV+ cell proliferation during adolescent development and/or PV+ cell death. Moreover, we also cannot exclude the possibility that ABET specifically reduces PV expression without affecting the functions of FS GABAergic interneurons. These possibilities remain to be investigated in future studies.
To the best of our knowledge, the present study is the first report that ABET induces myelin alterations in a region-specific manner. Our results of PV/MBP correlations suggest that, in the hippocampus, ABET reduced myelin primarily on PV+ axons, and this effect persisted into adulthood, whereas PV+ axonal myelination markedly increased in adult control mice (Fig. 5e). In the mPFC, ABET apparently reduced myelin mainly on PV- axons (presumably from excitatory projection neurons), and this effect persisted into adulthood (Fig. 6e). Since overall mPFC myelin recovered while PV+/MBP+ axons increased at the adult time point in ABET mice, PV−/MBP+ axons likely remained low compared to control subjects. Importantly, we found that levels of myelinated PV+ axons are much higher in the hippocampus than that in the mPFC (Figs. 5e and 6e). This varied degree of myelination for PV+ interneurons in different brain regions is actually consistent with the findings of another recent study . Reduced level of myelin, especially at the adult stage, can result from demyelination and/or inhibition of myelination. Our results using dMBP staining clearly showed that ABET-induced acute myelin damage in both the hippocampus and the mPFC (Fig. 7). The dMBP signals returned to normal levels in adult mice, suggesting that differences in the levels of myelin at the adult stage involve altered myelination and/or remyelination processes.
These changes in PV+ interneurons and myelin may have profound effects on the computation of neural networks. For instance, in the hippocampus ABET causes a reduction in PV+ interneurons together with their myelin, which may lead to persistently reduced inhibitory capacity of the neural network. On the other hand, in the mPFC, ABET caused a significant reduction of PV+ interneurons but demyelination was primarily restricted to PV- projection neurons, which may lead to reduced inhibition and synchronization of the neural network. Importantly, reduced density of PV+ interneurons in the PFC and/or hippocampus is associated with cognitive deficits in rodent models [7, 26], and human patients with schizophrenia . Reduced prefrontal and hippocampal myelination during postnatal development may lead to abnormal social interaction, anxiety and working memory [27, 50]. These appear consistent with our findings here. Nonetheless, the exact physiological and behavioral impact of these brain-region specific effects of ABET on interneuron myelination in the hippocampus and mPFC currently remain to be fully elucidated. Of note, adolescent alcohol exposure can persistently impact adult neurobiology, in which different neurotransmission systems have been implicated . Extensive future studies will be needed to fully understand the role of interneuron demyelination of different brain regions (e.g. other regions of cerebral cortex and limbic system, etc) in the pathogenesis associated with adolescent binge drinking. Moreover, it is important to note that the present study has used male mice in the ABET model. Potential gender difference in adolescent binge drinking will be an interesting topic for future investigation.
Taken together, our findings suggest that differential alterations of myelination of PV+ and PV- axons in the hippocampus and mPFC may play a key role in the neuroadaptive changes induced by adolescent binge drinking, and may represent a novel target for the development of new treatment strategies for AUDs
We thank Ms. Farida Eid and Ms. Paula Monsma for technical assistance. This work was supported in part by grants from NIH (R21AA024873 and R01NS093073) to CG, NIAAA center grant (P50AA26117) to JLW, and OSU Neuroscience Core Grant (P30NS104177).
CG designed and supervised the research. JR performed experiments, analyzed data and made figures. LC and JLW provided technical support and consultant. JR and CG wrote the manuscript. All the authors participated in revising the manuscript. All authors read and approved the final manuscript.
The authors declare that they have no competing interests.
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