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Logo of nihpaAbout Author manuscriptsSubmit a manuscriptHHS Public Access; Author Manuscript; Accepted for publication in peer reviewed journal;
J Neurosci. Author manuscript; available in PMC 2010 August 17.
Published in final edited form as:
PMCID: PMC2830729



Neuronal plasticity deficits underlie many of the neurobehavioral problems seen in Fetal Alcohol Spectrum Disorders (FASD). Recently, we showed that third trimester alcohol exposure lead to a persistent disruption in ocular dominance (OD) plasticity. For instance, few days of monocular deprivation results in a robust reduction of cortical regions responsive to the deprived eye in normal animals, but not in ferrets exposed early to alcohol. This plasticity deficit can be reversed if alcohol-exposed animals are treated with a phosphodiesterase type 1 (PDE1) inhibitor during the period of monocular deprivation. PDE1 inhibition can increase cAMP and cGMP levels, activating transcription factors such as the cAMP response element binding protein (CREB) and the Serum response factor (SRF). SRF is important for many plasticity processes such as LTP, LTD, spine motility and axonal pathfinding. Here we attempt to rescue OD plasticity in alcohol-treated ferrets using a Sindbis viral vector to express a constitutively active form of SRF during the period of monocular deprivation. Using optical imaging of intrinsic signals and single unit recordings we observed that overexpression of a constitutively active form of SRF, but neither its dominant negative nor GFP, restored OD plasticity in alcohol-treated animals. Surprisingly, this restoration was observed throughout the extent of the primary visual cortex and most cells infected by the virus were positive for GFAP rather than NeuN. This finding suggests that overexpression of SRF in astrocytes may reduce the deficits in neuronal plasticity seen in models of FASD.

Keywords: Astrocyte, Sindbis virus, ocular dominance plasticity, visual development, ferret, monocular deprivation, optical imaging, neocortex development, fetal alcohol syndrome


Fetal Alcohol Spectrum Disorders (FASD) is considered the leading cause of mental retardation in the western world with as many as 40,000 cases per year in the United States (Klug and Burde, 2003). The sensory cortex is one of the most affected areas in FASD and children with this condition present altered somatosensory, auditory and visual processing (Rasmussen et al., 2006;Mattson et al., 1996;Uecker and Nadel, 1996;Coles et al., 2002). There is growing evidence indicating that these sensory problems may be related to poor cortical map refinement, organization and plasticity (Margret et al., 2006;Medina et al., 2003;Medina et al., 2005;Rema and Ebner, 1999;Powrozec and Zhou, 2005). We have developed a ferret model of FASD that provides a novel approach to test mechanistically how early alcohol exposure can impair sensory cortex function. We showed that Ferrets exposed to alcohol during the third trimester equivalent of human gestation present disorganization of orientation selectivity columns and impaired ocular dominance (OD) plasticity (Medina et al., 2003;Medina and Ramoa, 2005;Medina et al., 2005;Medina and Krahe, 2008). Importantly, both of these cortical features can be rescued by vinpocetine, a phosphodiesterase type 1 inhibitor, even several weeks after alcohol exposure (Medina et al., 2006;Krahe et al., 2009). The efficacy of vinpocetine can be attributed by an increase in cAMP and cGMP levels, which in turn, would result in activation of the transcription factors cAMP/Ca2+ response element-binding protein (CREB) and Serum response factor (SRF) (Kornhauser et al., 2002;Chai and Tarnawski, 2002). Importantly, while cross talks between the cascades exist it is safe to say the CREB and SRF can be preferentially activated by cAMP and cGMP respectively. Recently, we discovered that, contrary to what was observed with vinpocetine, Rolipram, a PDE type 4 inhibitor failed to restore OD plasticity in the ferret model of FASD (Krahe et al., 2010). Since Rolipram increases only cAMP levels and not cGMP, one may suggest that the restoration of plasticity seen earlier is due to SRF activation. While the association of CREB with neuronal plasticity has been in the spotlight for decades (Silva et al., 1998;Frank and Greenberg, 1994;Lamprecht, 2005;Shaywitz and Greenberg, 1999), much less is known regarding SRF. This is surprising, given that many genes necessary for plasticity-related events require activation of both of these transcription factors (Chai and Tarnawski, 2002;Montminy et al., 1990;Platenik et al., 2000). Recently many studies have shown the importance of SRF for LTP, LTD, spine motility and axonal pathfinding (Alberti et al., 2005;Etkin et al., 2006;Knoll et al., 2006;Ramanan et al., 2005). In fact SRF can mediate the expression of many plasticity-related factors such as neurotrophins, immediate early genes, cytoskeletal proteins and trombospondins (Chai and Tarnawski, 2002;Christopherson et al., 2005;Knoll et al., 2006;Morris et al., 1999;Ramanan et al., 2005;Schratt et al., 2002;Stritt et al., 2009). Here, we use viral-mediated gene transfer to overexpress a constitutively active form of SRF in visual cortex, in order to reverse the OD plasticity deficits seen in a ferret model of FASD.


All procedures described in this paper were approved by the Institutional Animal Care and Use Committee at Virginia Commonwealth University. For a summary of our experimental design see supplemental figure S1. Briefly, ferrets were treated with 3.5 g/kg alcohol i.p. (25% in saline) or saline as control every other day between postnatal day (P) 10 to P30. This alcohol treatment lead to a blood alcohol level of approximately 250 mg/dl for 1–5 hours after injection (Medina et al., 2003). At the peak of critical period of the OD plasticity (P38–P45) animals were injected in V1 with a Sindbis virus carrying a constitutively active form of SRF, or a dominant negative (SRF−), or a control GFP. Viruses were made and kindly provided by Drs Amit Etkin and Eric Kandel (Columbia University). The construct was made by fusing the dimerization and DNA binding domains of SRF (aa 90–222) with the HSV VP16 transactivation domain (aas 363–490). The resulting fused construct was inserted in a Sindibis vector. One day after the viral transfection, animals were monocularly deprived by eye lid suture for 4 days. For the virus injection, a small hole was drilled in the skull and the tip of a 31 gauge Hamilton Syringe (Hamilton Company, Reno, Nevada) containing the Sindbis virus (titer = 4.0 × 107 infectious units/mL) was stereotaxically positioned at an angle of 15–22° from the midline and lowered 1mm into the binocular region of the primary visual cortex. A volume of 2μl was injected at a rate of 0.1μl every 30 seconds. Each animal received two injections ~1mm apart. After the period of monocular deprivation (MD), the animals were anesthetized, the deprived eye opened and either an optical imaging of intrinsic signals or a single unit recording experiment was conducted. Please see supplemental methods for surgical procedures. After the physiology experiments animals were perfused, the visual cortex collected and overexpression of the virus was assessed by immunohistochemistry.

Optical imaging of intrinsic signals

Optical imaging of intrinsic signals was performed with Imager 3001 VSD+ (Optical Imaging System Inc., Germantown, NY) by using imaging methods slightly modified from those described elsewhere (Medina et al., 2003;Medina et al., 2005;Medina et al., 2006;Krahe et al., 2005). An image of the vascular pattern was then obtained by illuminating the cortical surface with a green filter (approximately 550 nm) using a tungsten-halogen light source. Next, images of intrinsic signals were obtained using a red filter (approximately 700 nm). Visual stimulation consisting of high-contrast square wave gratings (8.75° dark phase/1.25° light phase) generated by a 21-inch monitor (Sony Trinitron) using SGT+ graphics board and STIM software. Gratings were presented to each eye at an angle of 0°, 45°, 90° or 135° and drifted (22.5°/sec) in both directions along the axis orthogonal to the orientation of the grating. A single trial consisted of these four gratings and a blank screen presented to each eye for 9 sec in a pseudorandom sequence, with data acquisition during the last 8 sec. A total of 20 trials were performed for each eye and the summed images were used to obtain single condition maps by subtracting responses to each eye from responses to a blank screen. In these images, dark areas correspond to regions that are visually responsive. In addition, differential maps were obtained by subtracting left from right eye single condition maps. In this images dark and light regions correspond to areas responsive to right and left eye stimulation respectively. See supplemental methods for additional information regarding imaging processing.

In vivo electrophysiology

Single-unit recordings were conducted using a glass-coated tungsten microelectrode with a 5 μm exposed tip lowered into the primary visual cortex at approximately 20° to the vertical axis. To minimize sampling bias, single-units used in this study were separated by at least 100 μm along the electrode track. After the isolation of a single-unit, its receptive field was mapped and the optimal stimulus orientation, direction and velocity were determined qualitatively using a moving bar of light projected onto a tangent screen. OD, spontaneous activity and number of spikes per stimulus were then quantitatively determined for each cell by presenting a computer-controlled bar of light to each eye. Each stimulus presentation consisted of the bar of light moving across the receptive field at the optimal orientation in one direction and back across in the opposite direction. To assess OD, the moving bar of light was presented to each eye separately at the optimal orientation. Spikes were collected during the 10 stimulus presentations by a computer using Spike 2 software (Cambridge Electronics Design, Cambridge, UK) and peristimulus histograms were generated. Spontaneous activity was determined by recording activity in the absence of stimulation. At the conclusion of the experiment, ferrets were sacrificed with Euthasol, (0.6 ml/kg, i.p.; Delmarva, Midlothian, VA).

Imunohistochemistry and Confocal microscopy

Ferrets were perfused with cold saline followed by cold 4% paraformadehyde solution. After dissection of the occipital cortex, 50μm sections were obtained with a vibratome. For imunohistochemistry the following primary antibodies were used at a concentration of 1:200: NeuN (Neuronal marker, mouse, Chemicon); GFAP (Astrocytic marker, rabbit, Dako); VP16 (Sindibis/SRF+ expression marker, mouse, Santa Cruz), VP16 (Rabbit, Sigma); Flag (Sindibis/SRF− expression marker). The secondary antibodies were goat anti-rabbit (1:400, alexa fluor 594) and goat anti-mouse (1:200, alexa fluor 488). Tissue sections are alternately stained for VP16/GFAP and VP16/NeuN. Sections were analyzed in a Leica TCS-SP2 AOBS confocal laser scanning microscope (inverted) with a spectrophotometer scan head, a high resolution Märzhäuser MCX-2 motorized XY stage and three confocal detectors. The system has five lasers: blue diode (405 nm), Argon (458, 476, 488, 514 nm), green HeNe (543 nm), orange HeNe (594 nm) and red HeNe (633 nm). Double staining (colocalization) was evaluated by two mutually reinforcing techniques: Particle analysis and Z-Stack counting. To perform particle analysis we first selected the two adjacent sections (VP16/GFAP, VP16/NeuN; one pair of sections for each animal; 3 animals used) that presented the greater number of infected cells. Confocal microscope tile scan images (20 X magnification) were taken and analyzed using the IPLab software. To confirm the results obtained with the particle analysis, two independent observers evaluated 14 Z-Stacks (7 VP16/GFAP; 7 VP16/NeuN) from 3 animals. A typical Z-Stack had the dimensions of x = 170 μm, y = 170 μm, z = 30 μm. The stack was covered by a 10 × 7 grid and each independent observer assessed whether a VP16 positive cell had double labeling (with GFAP or NeuN) or not. The total number of VP16 positive cells in VP16/GFAP and VP16/NeuN Z-Stacks were 433 and 293 respectively.


We investigated whether overexpression of SRF by Sindbis virus would improve OD plasticity in ferrets exposed to alcohol during the third trimester equivalent of human gestation, which is roughly P10–P30 in the ferret (Clancy et al., 2001;Medina et al., 2005). A summary of our experimental design can be seen in Figure 1. After a prolonged alcohol-free period animals were injected with Sindbis/SRF+; Sindibis/GFP or Sindbis/SRF in V1/V2 (Fig. 1B, C). We used optical imaging of intrinsic signals to create differential maps to assess changes in OD after monocular deprivation. Fig. 2A show the left visual cortex of representative cases from each group analyzed. Dark and light areas in OD (differential) maps represent regions that respond preferentially to stimulation of the right and left eye respectively. In Monocular response (single condition) maps, dark regions represent areas that display strong responses to visual stimulation. Note that non deprived animals (both saline and alcohol-treated, Fig. 2A) present the typical contralateral bias observed in ferrets (Issa et al., 1999;Medina et al., 2003;White et al., 1999). As expected, 4 days of MD in saline-treated animals lead to a striking shift in ocular dominance towards the experienced eye (Fig. 2A). Remarkably, after the same period of MD, alcohol-treated animals that received the Sindbis/SRF+ virus presented a similar shift (Fig. 2A), which indicates that OD plasticity was restored. Surprisingly, while the virus infected area was around a radius of approximately 2 mm, the shift in OD was observed along all the caudal extension of the visual cortex (V1, ~6–10 mm medial to lateral, Fig. 2A and Fig. 1B and C). In contrast, alcohol-treated animals that received either Sindbis/GFP or/SRF− presented only a very mild change in OD (Fig. 2A), which confirm our previous findings that early alcohol exposure impairs OD plasticity (Medina et al., 2003;Medina and Ramoa, 2005). To quantify OD (differential) maps we calculated the pixel distribution along a 256 gray scale, divided in five class intervals, where 0–50 and 204–255 correspond to classes containing the darkest and lightest pixels, respectively. Accordingly, non-deprived animals (either saline or ethanol treated) presented histograms skewed to the left, which indicates contralateral eye dominance (Fig. 2B). In contrast, after 4 days of contralateral eye lid suture, saline-treated animals, as well as alcohol-treated animals that received Sindbis/SRF+, presented OD profiles skewed to the right, indicating the dominance of the ipsilateral eye (Fig. 2B). In contrast, alcohol-treated animals that received either Sindbis/GFP or/SRF− presented only modest changes in the OD profile. To further quantify these changes we created a contralateral bias index (CBI, Fig. 1C). This index is defined as follows {(P0–50 − P204–255) − [(P51–101 − P153–253)/2] + 100}/200, where PA–B denotes the percentage of pixels with gray values between A and B. A CBI close to 1.0 indicates a prevalence of darker pixels and right eye dominance. A CBI close to 0.0 indicates a prevalence of lighter pixels and left eye dominance. An ANOVA showed a significant (F = 10.09, df = 2, P = 0.001) effect of treatment (SRF+, GFP or SRF−). Post hoc analysis showed that alcohol-treated animals that received Sindbis/SRF+ had significantly smaller CBIs than animals that received GFP (Bonferroni, P=0.01) or SRF− (Bonferroni, P = 0.004). To further assess the effects of SRF in improving OD plasticity we conducted single unit recordings experiments. The virus injection sites were easily identified in each animal and it was used as a landmark to place the electrode. Successful expression of the virus was confirmed by immunohistochemistry after the experiment. We created an OD index for each cell recorded using the following equation: LE/(LE+RE), where LE and RE stand for number of spikes elicited by stimulation of left and right eye respectively. An OD index of 1.0 indicates a neuron that is responsive only to the left eye whereas an OD index of 0.0 indicates responses only to the right eye. Figure 1D shows the cumulative distributions of neurons from alcohol-treated animals that were injected with Sindbis/SRF+ or/GFP. Note that the curve of SRF+ animals is completely skewed to the right when compared to GFP controls. This finding confirms our results with optical imaging showing that SRF restores OD plasticity in alcohol-treated animals. Interestingly, these results were observed even when recordings were made far from the injection site (Fig. 2E). A dominance of the experienced (ipsilateral) eye was present even when cells were recorded 3.5–5.5 mm from the injection site.

Figure 1
A- Experimental design. Ferrets were exposed to alcohol or saline every other day between P10-P30. After a prolonged alcohol-free period animals were injected with Sindbis/SRF+; Sindibis/GFP or Sindbis/SRF−. One day after virus injection animals ...
Figure 2
Optical imaging of instrinsic signals shows that SRF overexpression restores plasticity in alcohol-exposed animals. A- First column shows ocular dominance maps of representative cases of each experimental group. Dark and light areas represent regions ...

To confirm the expression of the virus we conducted immunohistochemistry in tandem with confocal laser microscopy. Figure 3A shows the typical pattern of expression of the Sindbis/SRF+ virus. Note that cells positive for the VP16 transactivation domain can be seen in both gray and white matter (Fig. 3A). The presence of VP16 positive cells was observed in several sections and we calculated that the virus infection had an average diameter of 2,300 μm (S.E.M. ± 220, n = 3 animals). Interestingly, most VP16 positive cells could be identified as astrocytes due to double labeling with GFAP (Fig. 2B 3B3B and Fig. 3C). Further quantification using two different techniques showed that most infected cells could be identified as astrocytes (Fig. 3D). Surprisingly, only a small proportion of infected cells were positive for NeuN, a typical neuronal marker. One possible explanation for this difference is that the Sindbis virus could have infected and killed neurons during the first days of the infection. However, this possibility is unlikely since a similar pattern of infection (predominance of infected astrocytes rather than neurons) was observed after 24 hours of the virus injection (Supplemental Figure S1). To evaluate the extension of the “plasticity enhancing” effect of SRF we made the virus injection on the contralateral (Right) hemisphere of 3 alcohol-treated animals. After 4 days of MD, optical imaging of intrinsic signals of the left hemisphere was performed to assess changes in OD. In the animal showed in panel A, no change in the typical ferret OD profile was observed. However, the virus injection was not successful as revealed by immunohistochemistry for VP16 (Fig. 4A). In animal B, a partial shift in OD and a moderate virus infection was observed (Fig. 4B). Finally, in animal C, a strong shift in OD and a high degree of infection (in the white matter) was observed (Fig. 4C). These findings indicate a high correlation between Sindbis infection and OD shift, suggesting that overexpression of SRF might improve plasticity in contralateral hemisphere. The higher variability of the virus infection observed in this experiment might be due to the fact that all our equipment had to be adjusted to make the injections on the right hemisphere.

Figure 3
Laser confocal microscopy reveals that a cortical injection of Sindbis-SRF virus leads to successful expression of the transgenes. Most infected cells are astrocytes rather than neurons. A- Typical spread pattern of a Sindbis-SRF virus injection. Staining ...
Figure 4
Effects of Sindibis-SRF injection on contralateral hemisphere in three alcohol-treated animals (A_C). First column shows differential maps obtained with optical imaging of intrinsic signals after 4 days of MD. Second column shows areas of highest virus ...

While it is known that SRF is normally expressed in the brain (Knoll and Nordheim, 2009;Stringer et al., 2002), we decided to assess whether endogenous levels of this transcription factor could be detected in visual cortex. To accomplish that, we used a SRF antibody that tags to an AA sequence (AAs 209–508, see methods) that is not present in our SRF construct (See Fig. 5H and I). Fig. 5A shows strong SRF expression in all cortical layers. While SRF expression was also observed in white matter, staining was drastically reduced. This antibody does not stain our SRF construct, and no colocalization between SRF and VP16 was observed. Endogenous SRF expression was also observed in animals that have not received Sindbis-SRF injection (data not shown). We also confirmed previous observations (Knoll and Nordheim, 2009;Stringer et al., 2002) showing the SRF has a high and low expression in neurons and astrocytes respectively (Fig. 5D–F). Next we wanted to confirm that our Sindbis-SRF virus lead to SRF expression. To accomplish that we used an antibody that tags the AAs around the lysine 99 phosphorylation site (AAs 97–101). This region is present in our SRF construct (Fig. 5H and I). Fig. 5J–L shows a high SRF expression in VP16 positive cells. This finding confirms that our construct induces expression of SRF and supports the use of VP16 as a marker in our previous experiments. As Sindbis virus is well known to infect neurons in rodents (Ehrengruber, 2002), we sought to test whether this preference for astrocytes in ferrets is due to species differences. Confirming previous results in rodents, the typical preference of the Sindbis virus for neurons was observed in cortex and hippocampus (Figure 6).

Figure 5
A. Tile scan of the visual cortex of the ferret using an anti-SRF antibody (Santa Cruz). This antibody attaches to the 209–508 AA sequence of the SRF transactivation domain. B- Imunostaining for VP16 transactivation domain, which indicates cells ...
Figure 6
Cell preference of the Sindibis virus is Species-dependent. A–C. Intraventricular injection of 3μl of the sindibis virus resulted in a massive infection of visual cortex neurons in the mouse. A- NeuN, B- SRF, C- merge. D-F. Hippocampal ...


Here we show that overexpression of SRF by Sindbis virus, long after the period of alcohol exposure, rescues OD plasticity in the ferret model of FASD. In addition to this exciting result, we obtained two intriguing findings: First, in ferrets we did not see the Sindbis preference for neurons that was described for rodents (Ehrengruber, 2002). In fact our results showed that most of the cells infected were astrocytes rather than neurons. The preference for astrocytes seen here is probably due to species differences, since in mice the virus infected mostly neurons Fig. 6. Second, plasticity restoration was observed in almost all V1 rather than being restricted to the area within the infection site. A possible interpretation is that released SRF products may diffuse through the neuropil, or are transported by the blood or CSF. While surprising, the capacity of brain cells to release signaling molecules and affect a large area had been demonstrated before. It was shown by independent groups that implantation of astrocytes overexpressing glial cell line-derived neurotrophic factor (GDNF) provide extensive neuroprotection to dopaminergic neurons (Ericson et al., 2005;Cunningham and Su, 2002). Moreover, the effects observed in these studies were not restricted to the injected site and increased levels of GDNF were observed even in the contralateral hemisphere (Ericson et al., 2005;Cunningham and Su, 2002). Recently, Stritt and colleagues provided evidence that activation of SRF can mediate the release of signaling molecules. They showed that lentiviral-mediated transfer of a constitutively active SRF construct in neurons dramatically affects maturation of oligodendrocytes (Stritt et al., 2009). In our present study, while most of the cells infected by the Sindbis-SRF construct were astrocytes, we observed an effect on neuronal plasticity. This finding suggests the intriguing possibility that activation of SRF in astrocytes may result in the production and release of plasticity-related factors, boosting neuronal plasticity in an extensive cortical area. However, we cannot discard the possibility that the few infected neurons are actually either the major players or significantly contribute to the SRF mediated restoration of ocular dominance plasticity in alcohol-treated animals.

Our understanding of astrocyte function and its relation to neurons has dramatically changed in the last 20 years. Modern neuroscience considers astrocytes major players in brain development and plasticity rather than mere supportive cells, see for review (Fellin, 2009;Stevens, 2008). In addition to producing an intricate pattern of spontaneous and neuronal evoked calcium oscillations, astrocytes can secrete glutamate (Parpura et al., 1994), d-serine (which potentiates the AMPA receptor) (Schell et al., 1995) and a constellation of plasticity related factors. Recently, studies from Ben Barres’ lab provided convincing evidence that astrocytes can secrete molecules that can dramatically affect the establishment of synapses. For instance, this group showed that immature astrocytes can promote synaptogenesis through release of thrombospondins (Christopherson et al., 2005) and refinement of retinogeniculate synapses through secretion of C1q protein (Stevens et al., 2007). Astrocytes may also play an important role in synaptic plasticity. Recently, it was demonstrated that glial release of Tumor Necrosis Factor α (TNα) mediate the compensatory changes in synaptic strength that occur after an increase or decrease in global activity (homeostatic plasticity) (Beattie et al., 2002). In addition, TNFα KO mice have altered OD plasticity (Kaneko et al., 2008)

Astrocytes have also been linked to the establishment of the critical period of ocular dominance plasticity. In a classical study, Christian Muller described that the time of the maturation of astrocytes is coincident with the closure of the critical period. In a subsequent work, Muller showed that implantation of immature astrocytes in the primary visual cortex of adult cats reopen the critical period of ocular dominance plasticity. While these findings strongly indicated a role for astrocytes in the regulation of critical period, the mechanisms that underlie this process were never elucidated. Our findings here suggest that astrocytes may also contribute to the process of ocular dominance plasticity, perhaps trough the release of plasticity-related factors, which could boost plasticity in neurons.

Since early alcohol exposure affects many cascades related to SRF activation (Kalluri and Ticku, 2003;Luo and Miller, 1999;Davis et al., 1999;Tang et al., 2006;Tsuji et al., 2003), as well as the secretory capacity of astrocytes (Tomas et al., 2005), it is plausible that a decrease of astrocytic-released molecules may contribute to the plasticity deficits seen in models of FASD. One possibility is that alcohol causes a reduction in the production and/or release of SRF-mediated molecules and the overexpression of this transcription factor bring these molecules to normal levels. This idea is supported by findings that show that early alcohol exposure can lead to an alteration in pathways that are known to activate SRF such as MAPK (Kalluri and Ticku, 2003;Luo and Miller, 1999;Davis et al., 1999;Tang et al., 2006;Tsuji et al., 2003) and RhoA (Joshi et al., 2006) as well as decrease the secretory capacity of astrocytes (Tomas et al., 2005). Alternatively, SRF function in astrocytes from alcohol-treated animals might be normal, and the beneficial effects of SRF overexpression may be a result of a compensatory boost of plasticity caused by the release of many plasticity-related molecules.

In conclusion we show here that overexpression of SRF leads to a widespread plasticity enhancement in the visual cortex of ferrets early exposed to ethanol. Importantly, our results suggest the intriguing possibility that astrocytes are actually the major players in this restorative effect. Our findings contribute for our understanding of how early alcohol exposure affects astrocyte to neuron signaling and its effects on cortical plasticity. This information may be highly relevant to devise therapeutic interventions that will prevent or alleviate morbidity in FAS.

Supplementary Material



This work was supported by NIH (NIAAA) grant AA-13023 to A.E.M. Microscopy was performed at VCU Department of Anatomy and Neurobiology Microscopy Facility, supported, in part, with funding of the NIH (NINDS) Center core grant (5P30NSD47463-02).

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