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Article

Motor, Somatosensory, Viscerosensory and Metabolic Impairments in a Heterozygous Female Rat Model of Rett Syndrome

by
Aritra Bhattacherjee
1,2,
Michelle K. Winter
2,
Linda S. Eggimann
2,
Ying Mu
1,2,
Sumedha Gunewardena
1,2,
Zhaohui Liao
1,2,
Julie A. Christianson
2,3 and
Peter G. Smith
1,2,*
1
Department of Molecular and Integrative Physiology, University of Kansas Medical Center, Kansas City, KS 66160, USA
2
Kansas Intellectual and Developmental Disabilities Research Center, University of Kansas Medical Center, Kansas City, KS 66160, USA
3
Department of Anatomy and Cell Biology, University of Kansas Medical Center, Kansas City, KS 66160, USA
*
Author to whom correspondence should be addressed.
Int. J. Mol. Sci. 2018, 19(1), 97; https://doi.org/10.3390/ijms19010097
Submission received: 3 October 2017 / Revised: 19 December 2017 / Accepted: 22 December 2017 / Published: 29 December 2017
(This article belongs to the Section Molecular Pathology, Diagnostics, and Therapeutics)
Browse Figures
Versions Notes

Abstract

:
Rett Syndrome (RTT), an autism-related disorder caused by mutation of the X-linked Methyl CpG-binding Protein 2 (MECP2) gene, is characterized by severe cognitive and intellectual deficits. While cognitive deficits are well-documented in humans and rodent models, impairments of sensory, motor and metabolic functions also occur but remain poorly understood. To better understand non-cognitive deficits in RTT, we studied female rats heterozygous for Mecp2 mutation (Mecp2−/x); unlike commonly used male Mecp2−/y rodent models, this more closely approximates human RTT where males rarely survive. Mecp2−/x rats showed rapid, progressive decline of motor coordination through six months of age as assessed by rotarod performance, accompanied by deficits in gait and posture. Mecp2−/x rats were hyper-responsive to noxious pressure and cold, but showed visceral hyposensitivity when tested by colorectal distension. Mecp2−/x rats ate less, drank more, and had more body fat resulting in increased weight gain. Our findings reveal an array of progressive non-cognitive deficits in this rat model that are likely to contribute to the compromised quality of life that characterizes RTT.

Graphical Abstract

1. Introduction

Autism spectrum disorders (ASDs) and related ASD-like disorders are recognized primarily by cognitive and intellectual deficits. Rett syndrome (RTT) is one of the most severe autism-like disorders affecting, one in 10,000 female births. It is caused by mutation of the X-linked gene MECP2, which is highly expressed in neurons and regulates chromatin organization and global gene transcription [1,2,3]. RTT is associated with severe cognitive, psychomotor and intellectual disabilities [4,5]. Intellectual and cognitive defects in RTT have been extensively studied in humans as well as animal models [6]. Cognitive deficits such as impaired sociability, anxiety, nest building, contextual fear conditioning, memory function and behavioral regression are prominent in rodent models [7,8,9,10,11,12,13,14], and studies using these MECP2 knockout animals have contributed much to our current mechanistic understanding of RTT [15].
RTT subjects are also reported to exhibit profound deficits in a wide range of basic physiological parameters including sensory perception, motor coordination, respiration and GI function, as well as metabolic processes [4,5,16,17,18,19,20]. These dysfunctions contribute to reduced quality of life and health, and frequently aggravate behavioral symptoms. The nature of these dysfunctions and the time course over which they appear, however, remain poorly understood. It has been particularly difficult to document these features in human subjects, given that communication skills are severely compromised by this disability. Unlike other ASDs whose origins involve complex gene–environment interactions or are unidentified, RTT is monogenic and mutation of the MECP2 gene alone in animal models recapitulates many features of the human disease. This provides an opportunity to systematically study onset, nature and progression of non-cognitive dysfunctions [4,6] in RTT.
RTT in humans is essentially a female disorder. While both males and females may harbor Mecp2 mutations of the X chromosome, males born with the mutation typically die within a few months due to severe encephalopathy [4]. Hence, more than 90% of surviving human RTT patients are heterozygous females with Mecp2 mutation (Mecp2−/x) [4]. Females with RTT display mosaicism in the expression of the Mecp2 mutation; X chromosome inactivation leads to normal expression of Mecp2 in some cells while others lack expression. However, animal studies to date have relied predominantly on male hemizygous rodents (Mecp2−/y). Male rodent knockouts (KO) survive after birth but display a more severe phenotype that fails to capture the regressive stages of the disease that occur in humans and show a reduced lifespan of up to 2 months [4,6,15], whereas human females can typically live to middle age. Accordingly, limitations of the standard male rodent model of RTT make it desirable to explore models that may more faithfully capture features of the disorder.
In the current study, we used a heterozygous female rat (Mecp2−/x) that more closely approximates human RTT, and studied longitudinally a wide range of non-cognitive functions.

2. Results

2.1. Motor Function

Motor deficits are one of the most prominent non-cognitive impairments in girls with RTT [4]. We assessed motor coordination by rotarod performance test in Mecp2−/x rats longitudinally over time. Starting at four weeks of age, we measured biweekly the ability of Mecp2−/x and Mecp2x/x rats to remain on the rotarod during a progressively increasing rate of rotation. There was no difference between groups at four weeks, and Mecp2x/x showed consistent performance through 22 weeks (Figure 1A). However, biweekly measurements of Mecp2−/x showed significant declines at 6–10 weeks, plateauing with severely impaired performance at around 16 weeks (Figure 1A and Table 1).
To gain further insight into the mechanics of locomotor dysfunction, we analyzed gait at 22 weeks, after the decline in rotarod performance had reached a stable plateau. DigiGait parameters for gait analysis can be broken down into the major phases of the step cycle, “brake”, “swing” and “propel” [21]. “Brake” is the interval from the first contact with the surface to peak stance, “Propel” is the phase from peak until end of contact, and the transitional phase during which a paw is not in contact and extends forward is referred to as “swing”. In the forepaw step cycle, brake and swing times were increased, whereas time spent in the propel phase was decreased relative to wild type (WT) rats (Figure 1B). In contrast, the hind paw step cycle did not show statistically significant differences (not shown); however, hind limb stance width, which is the distance between the centers of the hind paws at peak stance, was increased, reflecting postural deficits (Figure 1C). Mecp2−/x also showed forepaw ataxia; the ataxia coefficient (maximum stride length minus minimum stride length) in Mecp2x/x = 1.6 ± 0.093, and Mecp2−/x = 1.24 ± 0.129 (p = 0.038).
Because alterations in motor control of stepping could impact ambulation, we assessed free ambulatory behavior of the rats. Measurements over a 24 h period at 22 weeks revealed a moderate decline of diurnal activity. However, there was no difference in nocturnal activity in WT and mutant rats (Figure 1D).

2.2. Sensory Function

Because studies in both humans and male rodent models of RTT suggest that sensory function is altered [16,17,22,23], we studied responses to somatosensory stimuli including mechanical pressure, noxious heat and noxious cold. Behavioral responses to these stimuli were measured longitudinally from four through 22 weeks of age.
Mechanical sensitivity was tested using graded von Frey monofilaments applied to the hind foot paw to determine the threshold for withdrawal response. Thresholds were generally lower in younger rats and no significant difference could be resolved between wild type and heterozygotes at four and six weeks of age. However, while thresholds rose beginning at eight weeks in Mecp2x/x as part of normal developmental course, Mecp2−/x rats remained hypersensitive throughout the adult life with little change of threshold through 22 weeks (Figure 2A and Table 1).
Response to noxious cold was tested by recording the temperature for paw withdrawal on a cold plate. A general tendency toward higher sensitivity to noxious cold existed in Mecp2−/x rats from the beginning; however, significant differences became prominent from eight weeks of age that grew more severe over the subsequent weeks of testing (Figure 2B and Table 1).
Response to noxious heat was tested by using the paw thermal analgesiometer, where a light beam is directed to the Plexiglas surface immediately beneath a hind paw and the latency for foot withdrawal is measured. Both WT and Mecp2-/x rats showed increased response latencies with age, consistent with a developmental diminution in thermal sensitivity. However, unlike mechanical or cold sensitivity, there were no differences in response latencies to noxious heat between the two groups at any age point (Figure 2C).
The gastrointestinal system is imbued with stretch receptors that monitor pressure and elicit reflex contractile responses in the surrounding musculature [24]. Because there are reports that RTT patients show visceral discomfort under certain conditions, we assessed whether responses to colorectal distension [24] are affected in the Mecp2−/x rat. (Figure 3A). In response to applied colorectal pressures from 20 to 80 mm Hg, the visceromotor response (VMR) increased in both WT and Mecp2−/x animals. However, the heterozygous animals showed reduced VMR relative to WT rats at pressures from 40 to 80 mm Hg (Figure 3B and Table 1), consistent with visceral hyposensitivity.

2.3. Metabolic Indicators

Metabolic dysfunction is increasingly associated with autism spectrum disorders [25,26]. We therefore assessed indices of metabolic activity to determine if female rats heterozygous for the Mecp2 mutation showed phenotypes consistent with this type of abnormality. At postnatal weeks 4–6, body weights of Mecp2−/x and Mecp2x/x rats were comparable. Beginning at eight weeks of age, however, Mecp2−/x rats were heavier and the difference increased with time throughout the 22 weeks of the study (Figure 4A).
We assessed the proximate cause of the increased body weight by analyzing body mass composition at 22 weeks using an Echo-MRI. We found no difference in the lean body mass or total body water content between the two groups (Figure 4B,C). However, total body fat was elevated approximately three-fold in the Mecp2−/x relative to the Mecp2x/x rats (Figure 4D).
To assess whether there may be strain-dependent differences in caloric intake, we measured food consumption over a 48-h period in a metabolic chamber. In WT rats, food was consumed in the diurnal phase although nocturnal consumption was significantly greater (Figure 4E). Surprisingly, Mecp2−/x rats ate substantially less food (Figure 4E). Night time consumption was reduced by approximately 1/3, whereas consumption during the daytime was only about 30% of WT controls.
Water intake was also affected by the Mecp2 mutation. WT rats showed similar water consumption in both the diurnal and nocturnal phases (Figure 4F). Daytime drinking in Mecp2−/x rats was similar to WT; however, they drank approximately twice as much water at night relative to WT rats (Figure 4F).
To assess whether changes in metabolic rate may help to explain why Mecp2−/x rats gain weight and fat mass despite lower food consumption, we assessed a range of metabolism-associated parameters (Table 2). Mecp2−/x rats showed consistently lower metabolic values, with a significantly lower respiratory quotient detected during the light phase of the diurnal cycle.

2.4. Inter-Relationships among MECP2 Mosaicism and Behavioral and Metabolic Dysfunctions

Because MECP2 is an X-linked gene, random X-chromosome inactivation means that each RTT female patient (or rat) is a mosaic of MECP2 expressing and null cells, and the degree of mosaicism among different individuals can vary. We reasoned that the degree of mosaicism, or heterozygosity, may correlate with disease severity. We analyzed Mecp2−/x rats for their degree of mosaicism in peripheral blood T-cells as a representative cell population that is easily isolated. Blood samples were drawn from tail veins of the rats and peripheral blood mononuclear cells (PBMNCs) isolated. PBMNCs were fixed and stained for Mecp2 and the T-cell marker CD3. Fluorescence assisted cell sorting (FACS) analysis of these samples revealed the percentage of T-cells expressing Mecp2. We were unable to detect any significant correlation between degree of T-cell mosaicism and behavioral or metabolic dysfunction in any of the measured parameters. Similarly, when we assessed the relationships among different behavioral and metabolic parameters, strong correlations were not evident with the exception of deficits in rotarod performance correlating with a decrease in the swing phase of the step cycle (Table 3).

3. Discussion

This work demonstrates the feasibility of using heterozygous female rats to study progressive non-cognitive pathologies associated with RTT. While homozygous male MECP2 mutant rodents have been used for most RTT animal model studies to date, almost all human patients are heterozygous females. Our observations show that heterozygous female animals develop impairments similar to those seen with homozygous males [22], albeit with later onset, and potentially greater variability that is consistent with human observations. Moreover, the rat has proven advantageous as a model for resolving the longitudinal progression of disease symptoms. Behavioral responses in rat are robust and provide a broad dynamic range to detect regressive changes over time. In fact, before the advent of mouse genetics, the rat was a highly preferred model for study of sensory, motor and cognitive behaviors [27].
Consistent with the human disorder [28], motor impairments emerged as one of the most significant deficits in the Mecp2−/x rats. Motor behavioral deficits have been reported previously in Mecp2−/y mice at up to 60 days post-natal, but the time course is not well established [22,23,29,30]. In the current study, we followed female subjects for longer than five months and found that motor function declines steadily through about four months of age, which may be consistent with the progressive decline with age observed in the late motor deterioration stage in patients with RTT. Interestingly, voluntary ambulatory behavior remained largely preserved throughout the study period; even when Mecp2−/x rats could barely remain on the rotarod, there was no difference of night time voluntary activity and only a moderate decline in diurnal activity, which may suggest that central structures initiating movement may not be affected. On the other hand, poor rotarod performance did correlate significantly with increased swing phase of the step cycle, suggesting that the increased time required to move the foot into the braking position may have led to instability and discoordination.
A curious feature of the motor dysfunction is the rostro-caudal asymmetry of the effect, where the forelimbs are disproportionately affected. This would seem to be consistent with prior reports in heterozygous Mecp2-deficient mice [30]. The Mecp2-308 female mice show defects in purposeful forelimb use as evidenced by impaired handling of nesting material, food and novel environment exploration [31]. Deficient forelimb movement and repetitive patterns is also a key feature of human RTT [32,33,34]. Hence, a greater deficit in forelimb motor function appears to be consistent across male mouse and female rat RTT models as well as in human subjects.
Somatosensory deficits are widespread in ASD [35,36] and abnormal sensory perception as well as indications of pain in RTT patients have been reported by parents and care-givers [16,17]. Nonetheless, it has been challenging to document the exact nature and progression of sensory deficits in patients, which is especially problematic in RTT owing to deficits in verbal communication abilities. Using Mecp2−/y rodent models, we and others found somatosensory deficits associated with Mecp2 mutation which appears to be cell-autonomous to primary sensory neurons of the dorsal root ganglion [22,23]. Hence, deletion of Mecp2 appears to result in altered transcription within the ganglion that directly affects sensory neurons through effects at the levels of the peripheral and central terminals [22]. Consistent with our findings in male Mecp2−/y rats, Mecp2−/x female rats showed marked hypersensitivity to mechanical and noxious cold stimuli [22] although the onset was marginally delayed (eight weeks vs. four weeks in Mecp2−/y) but sustained thereafter. In contrast to Mecp2−/y rats, thermal hypoalgesia was not observed in Mecp2−/x rats.
One question that remains unanswered is whether other behavioral deficits occur secondary to somatosensory disturbances. In light of the increased mechanical sensitivity associated with Mecp2 deletion, it is possible that this could contribute to reduced motor performance. Hence, it is possible that the step cycle may be impacted by ‘guarding’, where animals preferentially spend less time in the propel phase where the increased force associated with propulsion could be perceived as painful. Similarly, while we know that sensory nociceptor [22] and low threshold tactile receptor [23] neuronal functions are altered, it is likely that other types of sensory function may also be disturbed. Accordingly, it is possible that proprioception may also be affected and, if so, this could contribute to alterations in step cycle and posture that occur in these animals. Further investigation will be necessary to elucidate the extent to which motor deficits occur secondary to sensory dysfunction.
This study also provides evidence that visceral perception is disrupted in this female RTT rat model. In human RTT patients, gastrointestinal and bowel related problems are prominent [20,37]. There is strong evidence that patients with RTT experience significant gastrointestinal dysmotility leading to gastroesophageal reflux, constipation, bloating, with resultant distress and frequent abdominal pain [37]. Our findings point to colonic hyposensitivity and/or hyporeflexia as a prominent component of the RTT rat model phenotype. Balloon distension of the colon resulted in a much-diminished abdominal muscular activation, which would be consistent with dysmotility. Visceral function and sensitivity are regulated by complex circuits involving intrinsic enteric neuronal plexuses as well as extrinsic contributions from the autonomic and nervous system and dorsal root ganglia [38,39,40,41,42]. Dysregulation of autonomic functions has been reported in RTT [43,44,45], although Mecp2 is widely expressed in all neuronal and target cells such that the etiology of the visceral dysfunction remains uncertain. Nonetheless, the Mecp2−/x rat should prove to be a useful model in helping to define mechanisms of RTT visceral dysfunction.
Many pervasive developmental disorders including autism are associated with alterations in metabolism [25,26]. However, prior studies using mouse models failed to reveal a systematic trend in metabolic disruption [15]. This may be attributable to the short duration of studies, use of null male mice which are underweight and survive only to two months of age, and/or interactions between the mutation and the genetic background of the different strains. Some studies of Mecp2 mouse models have reported altered body weight, with both increases and decreases observed and occurring in a potentially strain-specific manner [46,47,48]. Mecp2 deletion restricted to the hypothalamus results in increased weight gain in association with increased food intake [46]. Our findings of increased weight gain in association with reduced food intake suggest that possibly other brain regions associated with satiety may be differentially affected in the different models, or that perhaps there is a more profound metabolic disturbance in the heterozygous female rat. Indeed, the Mecp2−/x rat also showed abnormal fat accumulation despite significantly lower food intake and largely comparable activity levels, consistent with severe metabolic dysfunction. This is also consistent with some missense and late truncating Mecp2 mutations that give rise to a RTT variant known as the Zappella, where subjects are overweight [4,49]. Humans with RTT show elevated total cholesterol and LDL levels in plasma [50], and Mecp2−/y mice exhibit defective cholesterol metabolism in brain and liver [51]. It is unclear whether the increased body fat promotes a systemic pro-inflammatory state that may alter sensory neuron thresholds [52,53], thus contributing to the hypersensitivity we see in this model. It is noteworthy that both maternal fostering and genetic modifiers associated with different background strains have been shown to be strong contributors to behavioral and metabolic phenotype [54,55], and interactions with different mutations might also play a prominent role in determining the metabolic outcome. The molecular mechanisms underlying metabolic dysfunctions in RTT remain to be determined.

4. Materials and Methods

4.1. Animals

All animal experiments were conducted on a total of 24 female rats and were approved by the KUMC IACUC. Associated protocols used in this study will be provided upon request. The MECP2 knockout rat was generated by a zinc finger nuclease mediated 71 bp deletion in exon 4 of MECP2 gene (Product# TGRA6090, Sage Labs, Boyertown, PA, USA).

4.2. Timelines for Measurement

Table 4 outlines the frequency and time line (by animal age) for tests and measurements administered in this study.

4.3. Rotarod

Balance and coordination were tested using an accelerating rotarod (Med Associates Inc., St. Albans, Vermont, USA) with an initial speed of 4 rpm ramping to 40 rpm over 300 s. Rats were placed on the 70-mm diameter rod elevated 27 cm above the table. The accelerating program was initiated and the latency to fall off the rod was recorded and averaged from three independent trials at least 5 min apart.

4.4. Gait Analysis

Fully automated gait analysis was conducted with the DigiGait (Mouse Specifics, Framingham, MA, USA) treadmill at a walking speed of 8.5 cm/s. The DigiGait system records foot falls of the subject from the ventral aspect and then automates the analysis of over 40 parameters including brake, propel and stride time, coordination, and ataxia coefficient [21].

4.5. Somatosensory Behavior: Mechanical, Thermal and Cold Sensitivity

Mechanical sensitivity was analyzed using Siemens Weinstein monofilaments of known, graded force. Animals were placed in individual Plexiglas boxes on an elevated mesh table and allowed to acclimate for 20 min. Following acclimation, six monofilaments ranging from 2 to 15 g were applied five times to each hind paw at intervals of not less than 2 min. The number of positive responses, as observed by lifting or biting of the hind paw, was recorded. The calibrated force of the monofilament generating a 50% withdrawal response rate was recorded as the withdrawal threshold.
Thermal sensitivity was measured as withdrawal latency to a fixed 4.85-amp source directed to the paw in a Paw Thermal Stimulator (University of California, San Diego, CA, USA). The glass floor was maintained at 30.0 °C and 20 min of acclimation was allowed prior to testing. Light beam intensity was set at 4.85 amp and withdrawal latency defined as the time from stimulus onset until the automatic sensor turned the light off in response to paw lifting. Thermal withdrawal latencies of each hind paw were measured in triplicate, with a minimum of 3 min between trials, and were averaged.
Cold sensitivity was measured using a Cold Plate Analgesia Meter (IITC Life Science Inc., Los Angeles, CA, USA). Rats were acclimated for five min at 25 °C, and thermal plate temperature was decreased at a ramp rate of 10 °C per min. Upon observing overt nociceptive behavior such as lifting, biting or licking of the hind paws, the thermal plate was immediately returned to 25 °C. Testing was conducted twice with a 5–10 min interval between trials. The average temperature at which nociceptive behaviors were seen is reported as the withdrawal threshold.

4.6. Visceral Sensitivity

Rats were initially anesthetized with 4% inhaled isoflurane followed by continually-administered 1.5–3% inhaled isoflurane to maintain anesthesia. A small, catheterized (0.5 cm × 4 cm) latex or nitrile balloon was inserted into the distal colon. The rat was then put on a 37 °C heating pad under continuous 1.5% isoflurane anesthesia through nose cone and the balloon was distended for 20 s to 20, 40, 60 and 80 mm Hg (each pressure in triplicate with 4 min inter-trial intervals) and the electromyographic activity of the abdominal musculature were measured by thin silver electrode wires implanted acutely into the abdominal muscle on either side of the abdominal midline; the ground was attached to the tail. The VMR was quantified by measuring the area under the curve of the entire distension period divided by the duration of distension and expressed as a percentage of baseline EMG activity [24].

4.7. Food, Water and Activity Monitoring (Metabolic Cage)

Rats were placed in indirect calorimetry home cages (Sable Systems, Las Vegas, NV, USA) and were preconditioned prior to collection of data to eliminate effects of the novel environment. The gas from the cages is sampled each second for O2, CO2, and H2O content. Food, water and animal habitats are placed on weight sensors and movement of the subject is measured with external infrared beams. Fully automated software calculates activity (free ambulation) respiratory quotient, distance traveled, and others.

4.8. Body Mass Composition

Lean and fat mass was analyzed with the EchoMRI Body Composition Analyzer (EchoMRI LLC, Houston, TX, USA). Briefly, unanesthetized rats are placed in the analyzer for approximately 60 s and proprietary NMR-MRI technology is used to calculate fat, lean, free water and total water of the subject.

4.9. PBMNC Isolation, Staining and FACS

About 400–500 µL blood was collected from the tail vein of each Mecp2−/x rat into EDTA coated vials. The blood was diluted 1:1 in sterile PBS layered over Percoll and centrifuged. The buffy coat layer containing the peripheral blood mononuclear cells (PBMNCs) was collected and fixed by adding equal volume of 8% PFA (to make a final 4% concentration). The cells were washed thrice in PBS and then stained for 20–30 min on ice (wrapped in aluminum foil) with FITC conjugated Anti-CD3 antibody at 1:200 (BD Bioscience, San Jose, CA, USA) to label all T-cells. After a wash, primary anti-Mecp2 (rabbit-anti, Cell Signaling Technology, Danvers, MA, USA) was added and incubated for 1 h. After washes, donkey anti-rabbit Cy3 (Jackson Immuno-research, West Grove, PA, USA) at 1:200 and incubated for 30 min. Following three washes, cells were FACS analyzed to determine the percentage of Mecp2 expressing cells within the CD3 positive population.

4.10. Stastical Analysis

The statistical software SigmaPlot (Systat, San Jose, CA, USA) was used to perform analyses reported here. Comparisons of longitudinal measures of behavioral parameters were done by two way repeated measure ANOVA on ranks and using Holms-Sidak for post hoc comparisons. For comparison of two groups and single time point data, unpaired t-tests using Student Newman-Keuls were performed. In all cases p < 0.05 is reported to be significant. All data were reported as Mean ± SEM, unless stated otherwise.

Acknowledgments

We thank Anuradha Chakrabarty for technical guidance, John Thyfault for assistance with the data from metabolic testing, and the staff of the Kansas Intellectual and Developmental Disabilities Research Center. Funding was provided by NICHD RO1HD049615 with core support from NICHD P30 HD002528 and U54 HD090216, and KUMC’s Biomedical Research Training Program.

Author Contributions

Aritra Bhattacherjee and Peter G. Smith conceived and designed the experiments; Aritra Bhattacherjee, Michelle K. Winter, Linda S. Eggimann, Ying Mu and Zhaohui Liao performed the experiments; Aritra Bhattacherjee, Michelle K. Winter and Sumedha Gunewardena analyzed the data; Julie A. Christianson contributed materials and analysis tools; Aritra Bhattacherjee and Peter G. Smith wrote the paper.

Conflicts of Interest

The authors declare no conflict of interest.

Abbreviations

RTTRett Syndrome
ASDAutism spectrum disorder
MECP2Methyl CpG-binding Protein 2
WTWild type
PBMNCPeripheral blood mononuclear cell
EMGElectromyography
VMRVisceromotor reflex

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Figure 1. Motor impairments in RTT. (A) Biweekly measurements of Rota-rod performance in WT Mecp2x/x and Mecp2−/x rats. Two-way repeated measure Analysis of Variance (ANOVA) reveals significant difference at all ages starting from six weeks (p < 0.001); Holm-Sidak post hoc comparisons (n = 10 per group). See Table 1 for statistical details; (B) Forepaw gait analysis using the DigiGait system in WT and Mecp2−/x. Comparison by t-test reveals significant difference between the two groups in Brake (* p = 0.021), Propel (* p = 0.0027) and Swing (* p = 0.024), expressed as percentage of Stride, as measured from the forepaw; (C) Hind paw stance width of the mutant animals was greater (* p = 0.0009, t-test). n: Mecp2x/x =10 and Mecp2−/x = 6 for (B) and (C); 4 Mecp2−/x animals were excluded because they could not stay on the DigiGait treadmill; (D) Difference in distance traveled in a 24-h period by the rats, split between the day and night cycle. Mutant rats are hypoactive during the day (* p = 0.037), but show no difference relative to wildtype at night (p = 0.434) (n = WT = 5 and Mecp2−/x = 10). All graphs represent Mean ± SEM.
Figure 1. Motor impairments in RTT. (A) Biweekly measurements of Rota-rod performance in WT Mecp2x/x and Mecp2−/x rats. Two-way repeated measure Analysis of Variance (ANOVA) reveals significant difference at all ages starting from six weeks (p < 0.001); Holm-Sidak post hoc comparisons (n = 10 per group). See Table 1 for statistical details; (B) Forepaw gait analysis using the DigiGait system in WT and Mecp2−/x. Comparison by t-test reveals significant difference between the two groups in Brake (* p = 0.021), Propel (* p = 0.0027) and Swing (* p = 0.024), expressed as percentage of Stride, as measured from the forepaw; (C) Hind paw stance width of the mutant animals was greater (* p = 0.0009, t-test). n: Mecp2x/x =10 and Mecp2−/x = 6 for (B) and (C); 4 Mecp2−/x animals were excluded because they could not stay on the DigiGait treadmill; (D) Difference in distance traveled in a 24-h period by the rats, split between the day and night cycle. Mutant rats are hypoactive during the day (* p = 0.037), but show no difference relative to wildtype at night (p = 0.434) (n = WT = 5 and Mecp2−/x = 10). All graphs represent Mean ± SEM.
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Figure 2. Somatic sensitivity in the RTT rat model. (A) Biweekly measurements using von Frey monofilaments reveals mechanical hypersensitivity in Mecp2−/x rats at all ages starting from eight weeks (Holm-Sidak post hoc comparisons, p < 0.001 at 8–22 weeks); (B). Biweekly measurements of noxious cold sensitivity using the cold plate reveals hypersensitivity in Mecp2−/x rats at all ages starting from 8 weeks (two-way repeated measure ANOVA, Holm-Sidak post hoc comparisons, p < 0.001); (C) Noxious heat sensitivity tested using the Hargreaves Paw Thermal Analgesiometer. No difference between the two groups registered during the entire testing period. (n: WT = 10, Mecp2−/x = 14). Further details of statistical parameters for (A,B) in Table 1. All graphs represent Mean ± SEM.
Figure 2. Somatic sensitivity in the RTT rat model. (A) Biweekly measurements using von Frey monofilaments reveals mechanical hypersensitivity in Mecp2−/x rats at all ages starting from eight weeks (Holm-Sidak post hoc comparisons, p < 0.001 at 8–22 weeks); (B). Biweekly measurements of noxious cold sensitivity using the cold plate reveals hypersensitivity in Mecp2−/x rats at all ages starting from 8 weeks (two-way repeated measure ANOVA, Holm-Sidak post hoc comparisons, p < 0.001); (C) Noxious heat sensitivity tested using the Hargreaves Paw Thermal Analgesiometer. No difference between the two groups registered during the entire testing period. (n: WT = 10, Mecp2−/x = 14). Further details of statistical parameters for (A,B) in Table 1. All graphs represent Mean ± SEM.
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Figure 3. Visceral sensitivity in the RTT rat model. (A) Representative electromyography (EMG) recordings of visceromotor response in abdominal muscles of Mecp2x/x and Mecp2−/x rats for colorectal distension at 80 mm Hg; (B) Comparison of visceromotor responses expressed as activity per unit time, in 22-week-old rats reveal hyposensitivity to colorectal distension at 40, 60 and 80 mm Hg pressures. EMG/s in Mecp2−/x rats is significantly lower at 60 mm Hg (* p = 0.006) and 80 mm Hg (** p < 0.001) pressures (two-way repeated measure ANOVA, Holm–Sidak Posthoc Analysis; n: WT = 10, Mecp2−/x = 8. See Table 1 for details. Graph represents Mean ± SEM.
Figure 3. Visceral sensitivity in the RTT rat model. (A) Representative electromyography (EMG) recordings of visceromotor response in abdominal muscles of Mecp2x/x and Mecp2−/x rats for colorectal distension at 80 mm Hg; (B) Comparison of visceromotor responses expressed as activity per unit time, in 22-week-old rats reveal hyposensitivity to colorectal distension at 40, 60 and 80 mm Hg pressures. EMG/s in Mecp2−/x rats is significantly lower at 60 mm Hg (* p = 0.006) and 80 mm Hg (** p < 0.001) pressures (two-way repeated measure ANOVA, Holm–Sidak Posthoc Analysis; n: WT = 10, Mecp2−/x = 8. See Table 1 for details. Graph represents Mean ± SEM.
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Figure 4. Abnormal weight gain and calorie intake in the RTT rat model. (A) Biweekly weight measurements from Mecp2x/x and Mecp2−/x rats reveal a significantly increased body weight starting from eight weeks of age (p < 0.001, two-way repeated measure ANOVA with Holmes-Sidak posthoc analysis; see Table 1 for statistical details); (B–D) Comparison of body mass composition between Mecp2x/x and Mecp2−/x rats by Echo-MRI analysis. No difference in lean body mass (B) or total water content (C) detected between the two groups. Body fat levels were highly elevated in the Mecp2−/x; (D) p = 0.0001; (E) Food intake comparison between the two groups revealed lower consumption by the Mecp2−/x rat both during day (p = 0.001) and night (p = 0.044) (t-tests); (F) Water intake compared between the two groups of rats. No diurnal difference, but nocturnal consumption is highly increased in Mecp2−/x rats (p = 0.016, t-test. n: WT = 5, Mecp2−/x = 10). All graphs represent Mean ± SEM.
Figure 4. Abnormal weight gain and calorie intake in the RTT rat model. (A) Biweekly weight measurements from Mecp2x/x and Mecp2−/x rats reveal a significantly increased body weight starting from eight weeks of age (p < 0.001, two-way repeated measure ANOVA with Holmes-Sidak posthoc analysis; see Table 1 for statistical details); (B–D) Comparison of body mass composition between Mecp2x/x and Mecp2−/x rats by Echo-MRI analysis. No difference in lean body mass (B) or total water content (C) detected between the two groups. Body fat levels were highly elevated in the Mecp2−/x; (D) p = 0.0001; (E) Food intake comparison between the two groups revealed lower consumption by the Mecp2−/x rat both during day (p = 0.001) and night (p = 0.044) (t-tests); (F) Water intake compared between the two groups of rats. No diurnal difference, but nocturnal consumption is highly increased in Mecp2−/x rats (p = 0.016, t-test. n: WT = 5, Mecp2−/x = 10). All graphs represent Mean ± SEM.
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Table
Table 1. Summary of statistical analyses for two-way repeated measure ANOVAs.
Table 1. Summary of statistical analyses for two-way repeated measure ANOVAs.
TestSource of VariationDFFP
Body WeightGenotype112.4870.002
Weeks9310.219<0.001
Genotype × Weeks96.613<0.001
RotarodGenotype183.617<0.001
Weeks916.738<0.001
Genotype × Weeks98.143<0.001
Von FreyGenotype121.737<0.001
Weeks93.649<0.001
Genotype × Weeks90.2810.979
Cold PlateGenotype136.002<0.001
Weeks92.2660.021
Genotype × Weeks90.7800.635
VMRGenotype16.5140.021
Pressure333.405<0.001
Genotype x Pressure34.6000.007
Table
Table 2. Metabolic indices measured by calorimetry during light and dark phases over a 48-h test period in wild type (WT) and heterozygous (Het) rats. VO2 = oxygen consumed as O2 mL/min. VCO2 = carbon dioxide produced as mL/min. RQ = Respiratory Quotient obtained as VCO2/VO2. All measurements are from a single rat per cage.
Table 2. Metabolic indices measured by calorimetry during light and dark phases over a 48-h test period in wild type (WT) and heterozygous (Het) rats. VO2 = oxygen consumed as O2 mL/min. VCO2 = carbon dioxide produced as mL/min. RQ = Respiratory Quotient obtained as VCO2/VO2. All measurements are from a single rat per cage.
Light
ParametersWT MeanWT SEMHet MeanHet SEMt-Test p-Value
Average Energy Expenditure1.850.041.670.090.199
Total Energy Expenditure25.960.5623.431.270.199
Average VO26.410.145.880.310.26
Average VCO25.090.164.280.280.073
Average RQ0.790.020.720.020.03
Dark
ParametersWT MeanWT SEMHet MeanHet SEMt-Test p-Value
Average Energy Expenditure2.290.032.010.120.138
Total Energy Expenditure22.850.3120.091.20.138
Average VO27.860.137.010.410.172
Average VCO26.420.115.30.380.064
Average RQ0.820.020.750.020.054
Table
Table 3. Summary of regression analyses performed among behavioral measurements in Mecp2−/x rats.
Table 3. Summary of regression analyses performed among behavioral measurements in Mecp2−/x rats.
Parameters ComparedR2Adjusted R2F-Statistic vs. Constant Modelp-Value
Weight gain rate and day time food intake0.0152−0.1080.1240.734
Weight gain rate and night time food intake0.0522−0.06630.4410.525
Weight gain rate and day time water intake0.0405−0.07940.3380.577
Weight gain rate and night time water intake5.73 × 10−6−0.1254.58 × 10−50.995
von Frey and Brake0.195−0.005720.9720.38
von Frey and Propel0.3070.1341.770.254
von Frey and Swing0.0428−0.1960.1790.694
Sensitivity (% withdrawal) to a 4 mg filament and brake0.5640.4565.180.0851
Sensitivity (% withdrawal) to a 4 mg filament and Propel0.5140.3934.230.109
Sensitivity (% withdrawal) to a 4 mg filament and Swing0.0482−0.190.2020.676
Rotarod and Brake0.2040.004711.020.369
Rotarod and Propel0.0255−0.2180.1050.762
Rotarod and Swing0.7060.6339.620.0362
Table
Table 4. Behavioral testing schedule.
Table 4. Behavioral testing schedule.
TestFrequency of MeasureAge
RotarodBiweeklyWeeks 4–22
DigiGaitOnce Week 18
Somatosensory (mechanical, thermal, cold)BiweeklyWeeks 4–22
Visceral sensitivityOnceWeek 18
Metabolic (food, water, activity)Once Week 18
Body mass compositionOnceWeek 18

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Bhattacherjee, A.; Winter, M.K.; Eggimann, L.S.; Mu, Y.; Gunewardena, S.; Liao, Z.; Christianson, J.A.; Smith, P.G. Motor, Somatosensory, Viscerosensory and Metabolic Impairments in a Heterozygous Female Rat Model of Rett Syndrome. Int. J. Mol. Sci. 2018, 19, 97. https://doi.org/10.3390/ijms19010097

AMA Style

Bhattacherjee A, Winter MK, Eggimann LS, Mu Y, Gunewardena S, Liao Z, Christianson JA, Smith PG. Motor, Somatosensory, Viscerosensory and Metabolic Impairments in a Heterozygous Female Rat Model of Rett Syndrome. International Journal of Molecular Sciences. 2018; 19(1):97. https://doi.org/10.3390/ijms19010097

Chicago/Turabian Style

Bhattacherjee, Aritra, Michelle K. Winter, Linda S. Eggimann, Ying Mu, Sumedha Gunewardena, Zhaohui Liao, Julie A. Christianson, and Peter G. Smith. 2018. "Motor, Somatosensory, Viscerosensory and Metabolic Impairments in a Heterozygous Female Rat Model of Rett Syndrome" International Journal of Molecular Sciences 19, no. 1: 97. https://doi.org/10.3390/ijms19010097

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