Dantrolene is neuroprotective in Huntington's disease transgenic mouse model
© Chen et al; licensee BioMed Central Ltd. 2011
Received: 5 August 2011
Accepted: 25 November 2011
Published: 25 November 2011
Huntington's disease (HD) is a progressive neurodegenerative disorder caused by a polyglutamine expansion in the Huntingtin protein which results in the selective degeneration of striatal medium spiny neurons (MSNs). Our group has previously demonstrated that calcium (Ca2+) signaling is abnormal in MSNs from the yeast artificial chromosome transgenic mouse model of HD (YAC128). Moreover, we demonstrated that deranged intracellular Ca2+ signaling sensitizes YAC128 MSNs to glutamate-induced excitotoxicity when compared to wild type (WT) MSNs. In previous studies we also observed abnormal neuronal Ca2+ signaling in neurons from spinocerebellar ataxia 2 (SCA2) and spinocerebellar ataxia 3 (SCA3) mouse models and demonstrated that treatment with dantrolene, a ryanodine receptor antagonist and clinically relevant Ca2+ signaling stabilizer, was neuroprotective in experiments with these mouse models. The aim of the current study was to evaluate potential beneficial effects of dantrolene in experiments with YAC128 HD mouse model.
The application of caffeine and glutamate resulted in increased Ca2+ release from intracellular stores in YAC128 MSN cultures when compared to WT MSN cultures. Pre-treatment with dantrolene protected YAC128 MSNs from glutamate excitotoxicty, with an effective concentration of 100 nM and above. Feeding dantrolene (5 mg/kg) twice a week to YAC128 mice between 2 months and 11.5 months of age resulted in significantly improved performance in the beam-walking and gait-walking assays. Neuropathological analysis revealed that long-term dantrolene feeding to YAC128 mice significantly reduced the loss of NeuN-positive striatal neurons and reduced formation of Httexp nuclear aggregates.
Our results support the hypothesis that deranged Ca2+ signaling plays an important role in HD pathology. Our data also implicate the RyanRs as a potential therapeutic target for the treatment of HD and demonstrate that RyanR inhibitors and Ca2+ signaling stabilizers such as dantrolene should be considered as potential therapeutics for the treatment of HD and other polyQ-expansion disorders.
KeywordsHuntington's disease calcium signaling calcium imaging cell death dantrolene ryanodine receptor aggregation neuroprotection
Huntington's disease (HD) is an autosomal-dominant inherited neurological disorder characterized by abnormal involuntary movements (chorea, dystonia and bradykinesia) cognitive dysfunction, and psychiatric disturbance. At the molecular level, the cause of HD is a mutation in the cytosolic huntingtin (Htt) protein resulting in the expansion of a polyglutamine (polyQ)-repeat at the amino-terminus. Experimental evidence indicates that the polyQ expansion in mutant Htt (Httexp) leads to a "toxic gain or loss of function", leading to the progressive and selective death of striatal medium spiny neurons (MSNs) [1, 2]. However, the cellular mechanisms underlying the cause of MSN degeneration are not clear. Our previous studies demonstrated that deranged calcium (Ca2+) release from the endoplasmic reticulum (ER) was caused by a direct association of Httexp with the type 1 inositol 1, 4, 5- trisphosphate receptor (InsP3R1) , leading to apoptosis in MSNs . In addition, over-expression of the cytosolic carboxy-terminus region of InsP3R1 (IC10 fragment) disrupted the Httexp-InsP3R1 interaction and prevented the death of HD MSNs . In more recent studies we demonstrated pathological enhancement of neuronal store-operated Ca2+ entry (SOC) pathway in HD . In addition, increased Ca2+ influx via extrasynaptic NR2B subunit of N-methyl-D-aspartate receptor (NMDAR) was proposed to play an important role in excitotoxic cell death of HD MSN neurons [4, 7–12]. Collectively these data indicate that Ca2+ signaling plays an important role in the pathogenesis of HD [13–16].
The mechanisms of Ca2+ release from intracellular stores involves several pathways, including InsP3-induced Ca2+ release (IICR) mediated by the InsP3Rs and Ca2+-induced Ca2+ release (CICR) triggered by the ryanodine receptors (RyanR). Because Ca2+ release by IICR is often amplified by CICR  and augmented release of Ca2+ from intracellular stores were toxic to HD MSNs [4, 5], we reasoned that inhibiting RyanR-mediated CICR and stabilizing Ca2+ signaling would have neuroprotective effects in YAC128 HD mice. We have shown previously that the RyanR antagonist and clinically relevant intracellular Ca2+ stabilizer, dantrolene, was neuroprotective in mouse models of spinocerebellar ataxia type 2 (SCA2) and type 3 (SCA3) [18, 19], attenuating glutamate-induced apoptosis of cultured SCA2-58Q Purkinje cells. Furthermore, feeding dantrolene to both SCA2-58Q and SCA3-YAC-84Q mice prevented neuronal cell loss and improved motor deficits [18, 19]. In the present study we discovered that dantrolene pre-treatment protected cultured YAC128 MSNs from glutamate-induced apoptosis. In addition, feeding dantrolene to YAC128 mice significantly alleviated age-dependent motor deficits developed by YAC128 mice, reduced the death of NeuN-positive striatal neurons and inhibited nuclear aggregation of Httexp. These results suggest that inhibiting RyanR-mediated CICR is a feasible therapeutic approach for the treatment of HD and that dantrolene is a potential agent that can be used for this purpose.
Caffeine potentiates Ca2+ release induced by glutamate in YAC128 MSNs
Dantrolene pre-treatment protects YAC128 MSNs from glutamate-induced toxicity
Effects of dantrolene on glutamate-induced apoptosis in WT and YAC128 MSN.
WT (% TUNEL-positive)
YAC128 (% TUNEL-positive)
0 μM glutamate
250 μM glutamate
0 μM glutamate
250 μM glutamate
5.20 ± 1.16
32.22 ± 2.66
5.94 ± 1.11
57.45 ± 5.62
7.45 ± 1.08
32.02 ± 2.28
7.13 ± 1.37
52.03 ± 5.45
4.92 ± 1.48
31.36 ± 3.64
5.73 ± 0.87
40.37 ± 3.18*
16.43 ± 1.25
37.43 ± 3.66
17.05 ± 1.18
73.26 ± 3.32
14.05 ± 0.68
37.61 ± 2.75
21.76 ± 2.60
50.45 ± 4.11***
17.22 ± 1.39
34.69 ± 1.86
18.75 ± 1.92
42.79 ± 2.85***
17.94 ± 0.95
38.20 ± 2.21
19.73 ± 1.67
35.85 ± 2.24***
Dantrolene rescues the motor coordination deficiencies in YAC128 mice
Dantrolene can be considered a general Ca2+ signaling stabilizer. The neuroprotective characteristics of dantrolene have been shown in glutamate toxicity assay with YAC128 MSNs (Figure 2, Table 1) and in previously reported experiments with cultured neuronal cells and animal models of excitotoxicity [23–31]. We recently reported that dantrolene was neuroprotective in mouse models of SCA2 and SCA3 [18, 19]. These results lead us to evaluate the potential beneficial effects of dantrolene in the YAC128 HD mouse model. For these studies, 5 mg/kg of dantrolene in phosphate buffered saline (PBS) and corn flour was orally delivered to YAC128 and WT mice twice a week from 2 months of age until all the mice were 11.5 months of age, followed by a washout period of 2 months (13.5 months of age). The control groups of WT and YAC128 mice were fed with PBS and corn flour alone. Behavioral assessment of all four groups of mice was performed using the "beam-walk" assay. Basal beam-walking performance was determined before the initiation of dantrolene feeding at 2 months of age. Beam-walking performance data were collected at 2, 4, 7, 9.5, 11.5, and 13.5 (washout) months of age. As in our previous studies with YAC128 HD mice [5, 32, 33], three kinds of beams (17 mm round, 11 mm round, and 5 mm square) were used for testing. The "latency" and "number of foot slips" were for each mouse determined on each beam.
Dantrolene feeding reduces NeuN-postitive cell loss in striata of YAC128 mice
Brain weight and MSN counts of 14 months old WT and YAC128 mice.
Number of female mice
Brain weight (g)
MSN counts (106)
0.499 ± 0.01
1.27 ± 0.03
0.495 ± 0.01
1.263 ± 0.03
0.437 ± 0.01***
0.997 ± 0.03*
0.461 ± 0.01
1.18 ± 0.030#
Pathological analysis of WT and YAC128 mice tissues following dantrolene trial.
Number of mice analyzed
No. of mice per group with any degree of inflammation
To obtain quantitative information about neuronal loss in the experimental mice, we stained the striatal slices for NeuN, a nuclear-specific marker of mature neurons (Figure 5B), and performed stereological analysis. NeuN-positive neurons in each striatum were counted blindly with respect to the nature of slices (genotype and drug treatment). Consistent with our previous findings [5, 32, 33], we determined that PBS-fed YAC128 mice showed significant neuronal loss in the striatum (p < 0.05) when compared with PBS-fed WT mice (Figure 5C, Table 2). We further found that dantrolene feeding had no significant effect on NeuN-positive counts in the striata of WT mice but significantly increased NeuN-positive counts (p < 0.05) in YAC128 mice (Figure 5C, Table 2). The data show that dantrolene feeding protected against the age-dependent loss of NeuN-positive neurons in the striata of YAC128 mice.
Dantrolene feeding inhibits the aggregation of Httexp in the striata of YAC128 mice
In our previous studies we demonstrated that abnormal neuronal Ca2+ signaling plays a significant role in the pathogenesis of HD and other polyQ expansion disorders [3–6, 18–20, 32, 35]. We have also found that the Ca2+ stabilizer and RyanR antagonist, dantrolene, was neuroprotective in the mouse models of polyQ expansion disorders SCA2 and SCA3 [18, 19]. The data in the present study point to the role of RyanRs in the exaggerated Ca2+ response to glutamate observed in MSNs from the YAC128 model of HD (Figure 1). Furthermore, we demonstrated that the treatment of RyanR inhibitor dantrolene significantly protected cultured YAC128 MSNs from glutamate-induced apoptosis (Figure 2). Consistent with our in vitro findings, we showed that long-term feeding of dantrolene to YAC128 mice significantly (p < 0.05) alleviated age-related motor coordination deficits (Figure 3, 4) and prevented NeuN-positive neuronal loss (p < 0.05) (Figure 5, Table 2) while leaving WT control mice and neurons intact. Finally, dantrolene-fed YAC128 mice showed less Httexp nuclear aggregation in striatal cells compared to control YAC128 mice (Figure 6), further supporting neuroprotective effects of dantrolene treatment. These data provide further support for the significant role of disturbed intracellular Ca2+ signaling in the pathogenesis of polyQ expansion diseases and offer a potential, and clinically relevant, drug for the treatment of HD.
Our laboratory has elucidated the interaction between Httexp and InsP3R1 as well as other Ca2+-related mechanisms relevant to HD (for reviews, see [13–16]). Based on these results we argued that the modulation of intracellular Ca2+ signaling is a viable approach in our pursuit of disease-modifying therapies for HD. We first discovered that Httexp binds directly and specifically to the C-terminus region of InsP3R1 and that this interaction is important for the augmented activity of the receptor in planar lipid bilayers and in cultured MSNs . We then confirmed that MSNs from YAC128 HD mice had disturbed IP3R-mediated Ca2+ signaling which lead to glutamate-induced apoptosis in YAC128 MSNs . In a more recent study we demonstrated pathological enhancement of neuronal store-operated Ca2+ entry (SOC) pathway in HD . In addition, increased Ca2+ influx via extrasynaptic NR2B subunit of NMDAR was proposed to play an important role in excitotoxic cell death of HD MSN neurons [4, 7–12]. The CICR mechanism supported by RyanR can amplify the signal from other Ca2+ sources such as InsP3R1 and NMDARs. Perhaps the effectiveness of dantrolene to reduce or block glutamate-induced apoptosis in YAC128 MSN cultures (Figure 2, Table 1) is attributed to the fact that by inhibiting the RyanRs alone, both glutamate signaling pathways important for inducing toxicity are blunted at the same time, leading to robust neuroprotection. In addition to RyanR, dantrolene may also inhibit neuronal SOC pathway , which may also contribute to neuroprotective effects of dantrolene observed in our experiments .
There are drugs available to help manage the clinical symptoms of HD but currently there is no treatment to stop or reverse the course of the disease. The only drug approved by the US Food and Drug Administration to specifically treat HD is tetrabenazine (TBZ), an inhibitor of the vesicular monoamine transporter that alleviates chorea. Therefore, a notable finding of our study is that long-term feeding of dantrolene to YAC128 mice was able to prevent neurodegeneration in the striatum (Figure 5), reduced accumulation of Httexp muclear aggregates (Figure 6) and significantly improve the motor coordination deficiencies (Figure 3, 4) that are characteristic to this model and HD pathogenesis. In motor coordination assays the benefits of dantrolene feeding to YAC128 mice were similar to the benefits of TBZ feeding that we evaluated previously [32, 33]. Thus, it can be expected that dantrolene or other similar RyanR inhibitors may result in significant clinical benefits for HD patients.
Many studies have brought to light the neuroprotective properties of dantrolene (for recent review, see ). For example, in cultured cortical neurons, dantrolene reduced the glutamate-induced increases in intracellular Ca2+-concentrations by 70% under physiologic conditions, and protected against glutamate-induced neurotoxicity . The short-term delivery of dantrolene has been demonstrated previously to be neuroprotective in acute excitotoxicity paradigms, such as cerebral ischemia [26, 38] and a kainic acid injection model [24, 28, 30]. It has also been demonstrated that dantrolene can prevent apoptosis in neurons by ameliorating poly(ADP-ribose) polymerase (PARP)-related bioenergetic failure during DNA repair in rat brain  and up-regulating anti-apoptosis proteins such as Bcl-2 in different cell lines [40, 41]. We have previously demonstrated the beneficial effects of long-term dantrolene treatment in SCA2 and SCA3 genetic mouse models [18, 19]. Data from such studies has inspired researchers to consider the utility of dantrolene as treatment for many neurodegenerative diseases, including Alzheimer disease (AD) [42, 43], amyotrophic lateral sclerosis , and ataxia [18, 19] (for recent review ). However, in our experiments we found that long-term feeding of dantrolene to a mouse model of AD actually exacerbated the neuropathology related to the disease . Dantrolene has been used safely in the clinic for decades as treatment for malignant hyperthermia, but is also used to manage neuroleptic malignant syndrome, muscle spasticity, 3, 4-methylenedioxy methylamphetamine ("ecstasy") intoxication, serotonin syndrome, and 2, 4-dinitrophenol poisoning . However, dantrolene can also induce significant side effects, ranging from transient muscle weakness to more severe respiratory failure  in both acute and chronic treatment regimens. In our experiments, we saw a neuroprotective effect at 5 mg/kg, which is comparable to the effective dose of 2.4 mg/kg in healthy volunteers who experienced dizziness and muscle weakness . We have not observed significant toxic effects of dantrolene after pathological examination of skeletal mucle, heart and liver of WT and YAC128 mice fed with dantrolene (Table 3).
Obtained results provide further support to the "Ca2+ hypothesis of HD" [13–16] and highlight similarities in the pathogenesis of HD, SCA2 and SCA3 [18, 19, 48, 49]. Our data also implicate RyanRs as a potential therapeutic target for the treatment of these disorders. Moreover, our results indicate that RyanR inhibitors and Ca2+ signaling stabilizers such as dantrolene should be considered as potential therapeutics for the treatment of HD and other polyQ-expansion disorders. It is not clear however if dantrolene has a safety profile that allows for its long-term use in clinic. The effect of chronic low dose administration of dantrolene in humans is not known and further study is required to determine if dantrolene is an appropriate clinical tool for HD and other polyQ expansion disorders.
Primary medium spiny neuron (MSN) cultures
All animal studies were approved by the University of Texas Southwestern Medical Center Animal Care and Use Committee. YAC128 transgenic mice (FVBN/NJ background strain) were obtained from Jackson Labs (stock number 004938) and breeding of YAC128 mice was previously described . Briefly, heterozygous male YAC128 mice were crossed with the wild type (WT) female mice and the resulting litters were collected on postnatal days 1-2. The pups were genotyped by PCR with primers specific for exons 44 and 45 of human HTT and MSN cultures of WT and YAC128 mice were established as described previously [4, 7, 20, 32]. Briefly, cultures were grown on poly-L-lysine (Sigma) coated 12 mm round coverslips (Assistent) in Neurobasal-A medium supplemented with 2% B27, 1 mM L-glutamine and penicillin-streptomycin (Invitrogen). Cultures were incubated at 37°C in a 5% CO2 environment.
Ca2+ imaging experiments
Fura-2 Ca2+ imaging experiments were performed as previously described . The MSN cultures were maintained until 10 days in vitro (DIV) and then loaded with 5 μM Fura-2AM (Invitrogen) in artificial cerebral spinal fluid (aCSF) (140 mM NaCl, 5 mM KCl, 1 mM MgCl2, 2 mM CaCl2 and 10 mM HEPES at pH 7.3) for 45 min at 37°C. For imaging experiments, the coverslips were mounted onto a recording chamber (RC-26G; Warner Instruments) that was maintained at 37°C (PH1; Warner Instruments) and positioned on an Olympus IX-70 inverted microscope. Before measurements were taken, the coverslips were washed extensively with Ca2+-free aCSF (CaCl2 was replaced with 100 μM EGTA). For Ca2+ imaging experiments, the MSN cells were intermittently excited by 340 and 380 nm UV light using DeltaRAM illuminator (Photon Technology International (PTI)), and the 510 nm emitted light was collected by an IC-300 camera (PTI). Images were collected using a 60× UV-grade oil immersion objective (Olympus), then digitized and analyzed by ImageMaster Pro software (PTI). Baseline (1 min) measurements were obtained before bath application of 2.5 μM glutamate and/or 2.5 mM caffeine dissolved in Ca2+-free aCSF. Images at 340 and 380 nm excitation wavelengths were captured every 5 s and shown as 340/380 image ratios at the time points as indicated. Background fluorescence was determined according to the recommendations of the manufacturer (PTI) and subtracted.
In vitro cell death assay
The in vitro cell death assay was performed as described previously for MSN cultures [4, 5, 20]. Dantrolene was added to the 14 DIV MSN cultures at 0.0, 0.1, 1, 10 or 50 μM. After 1 h incubation, 250 μM glutamate in Neurobasal-A was added to the culture medium and MSNs were maintained in a cell culture incubator (humidified 5% CO2, 37°C) for 7 h. Immediately after glutamate treatment, neurons were fixed for 30 min in 4% paraformaldehyde plus 4% sucrose in PBS (pH 7.4), permeabilized for 5 min in 0.25% Triton X-100, and assayed for apoptosis using the DeadEnd Fluorometric TUNEL System (Promega) according to manufacturer's instructions. Nuclei were counterstained with 5 μM propidium iodide (PI) (Molecular Probes). Coverslips were washed with PBS and mounted in Mowiol 4-88 (Polysciences). Fluorescein isothiocyanate (FITC)- and PI-fluorescent images were collected with an Olympus IX70 microscope using a 40× objective, a Cascade: 650 camera (Roper Scientific), and METAFLUOR software (Universal Imaging, Downingtown, PA). Four to six randomly chosen microscopic fields containing 200-300 MSN were captured. The percentage of TUNEL-positive cells was determined by taking the cell number of TUNEL-positive MSNs and dividing by the total number of MSNs (or PI stained neurons) × 100%. The percentage of TUNEL-positive cells was among all the fields per treatment was averaged and presented as the mean ± SE (n = number of fields counted). The nuclei of glial cells, identified by their large size and weak PI staining, were not counted in the analysis.
Drug delivery in mice
Dantrolene was fed to mice as we described previously in a tetrabenzine trial in YAC128 mice  and dantrolene trials in SCA3-YAC-84Q  and SCA2-58Q mice . Briefly, groups of 10 WT mice and 10 YAC128 mice were fed 100 μg of dantrolene suspended in 50 μl of PBS with 2% corn flour resulting in a dosage of 5 mg/kg. The control groups (10 WT and 10 YAC128) were fed with 2% corn flour in PBS. All mice were fed orally twice per week from 2 to 11.5 months of age.
Motor coordination assessments in mice
The motor coordination experiments were performed as we described previously in a tetrabenzine trial in YAC128 mice  and dantrolene trials in SCA3-YAC-84Q  and SCA2-58Q mice . The "beam-walking" assay was performed using a homemade experimental setup. The 17 mm round plastic beam, 11 mm round plastic beam, and 5 mm square wood beam were used in our studies. At each time point, the mice were trained on the beams for 3 consecutive days (four trials per day) to traverse the beam into the enclosed box. Once a stable baseline of performance was obtained, the mice were tested in three consecutive trials on the 17 and 11 mm round plastic beams and the 5 mm square wood beam, progressing from the widest to the narrowest beam. The latency to traverse the middle 80 cm of each beam and the number of times the hind-paws slipped off each beam were recorded for each trial. The mean scores for each beam at a particular time point were used in the analysis. For the footprint test, the forepaws and hindpaws of the mice were coated with purple and green non-toxic paints, respectively. The mice were trained to walk along a paper-covered runway that was 50 cm long, 10 cm wide, with 10 cm high walls into an enclosed box. All the mice were given three runs per day for 3 consecutive days. A fresh sheet of white paper was placed on the floor of the runway for each run. The footprint patterns were assessed quantitatively by the measurements of stride length and fore-paw/hind-paw overlap as we described previously [19, 32].
Neuropathological assessments in mice
The neuropathological assessments were performed as previously described [19, 32]. After all the behavioral tests (14.5 month time point), the mice were terminally anesthetized by ketamine/xylazine and perfused transcardially with PBS then 4% paraformaldehyde in 0.1 M PBS, pH 7.4 as before [19, 32]. All brains were removed, weighed, transferred to post-fixative (4% paraformaldehyde) for 24 h at 4°C, and equilibrated in 20-30% (w/v) sucrose in PBS for 24-48 h 4°C. The brains were processed and cut into 30 μm-thick coronal sections using a SM2000R sliding microtome (Leica, Bannockburn, IL). Coronal sections spaced 360 μm apart throughout the striatum (in the range from +1.70 mm to -2.30 mm relative to bregma) were collected. For the quantification of neuronal loss, sections were stained with anti-NeuN monoclonal antibody (1:1000 dilution; Millipore, Billerica, MA). Biotinylated anti-mouse IgG reagent was used as the secondary antibody (1:250 dilution; M.O.M. kit, Vector Laboratories). Signal was amplified with an ABC Elite kit (Vector Laboratories) and detected with diaminobenzidine (DAB) (Vector Laboratories). For the detection of Httexp protein aggregation, sections were stained with anti-Htt monoclonal antibody (1:200 dilution: Millipore), amplified and detected as before, and counter-stained with cresyl violet. The stained sections were mounted with Dako Glycergel Mounting Medium (Dako) onto the slides. All quantitative stereological analyses were performed blindly with respect to the nature of slices (genotype and drug feeding) using the Stereo Investigator setup and software (MicroBrightField Inc., Williston, VT). All quantitative stereological analyses were performed blindly with respect to the nature of slices (genotype and drug feeding) using Stereo Investigator. The grid size was set to 450 × 450 μm, and the counting frame was set to 50 × 50 μm. The average slice thickness after histological processing was determined to be 22 μm.
Before perfusion, a hind-leg with fresh skeletal muscle was taken from each terminally anesthetized mouse. After perfusion and removal of the brain, the mouse carcasses were fixed in 10% buffered formalin until dissected. Representative sections of the heart, liver, lung and skeletal muscle samples from half of the animals in each group were obtained. Tissue was embedded in paraffin blocks, sectioned at 4 μm thickness, stained with hematoxylin and eosin, and coverslipped for light microscopic evaluation. The presence and degree of lymphocytic infiltrates in the four tissue types was semi-quantitatively graded using the following schema: 0, no inflammation; 1, rare, scattered, small collections of lymphocytes; 2, occasional scattered collections; and 3, frequent large collections.
Statistical data analysis
For comparison between two or more groups, ANOVA with post hoc testing was used to statistically analyze data.
We thank Xia Liang for help with maintaining the YAC128 mouse colony and help with behavioral experiments, Leah Benson for administrative assistance. IB is a holder of the Carl J. and Hortense M. Thomsen Chair in Alzheimer's Disease Research. This project was supported by the CHDI foundation, NINDS R01 NS056224 and R01 NS074376 and by the contracts with the Russian Ministry of Science and Education 14.740.11.0924 and 11.G34.31.0056.
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