- Research article
- Open Access
Biogenic amines and their metabolites are differentially affected in the Mecp2-deficient mouse brain
BMC Neuroscience volume 12, Article number: 47 (2011)
Rett syndrome (RTT, MIM #312750) is a severe neurological disorder caused by mutations in the X-linked methyl-CpG binding protein 2 (MECP2) gene. Female patients are affected with an incidence of 1/15000 live births and develop normally from birth to 6-18 months of age before the onset of deficits in autonomic, cognitive, motor functions (stereotypic hand movements, impaired locomotion) and autistic features. Studies on Mecp2 mouse models, and specifically null mice, revealed morphological and functional alterations of neurons. Several functions that are regulated by bioaminergic nuclei or peripheral ganglia are impaired in the absence of Mecp2.
Using high performance liquid chromatography, combined with electrochemical detection (HPLC/EC) we found that Mecp2-/y mice exhibit an alteration of DA metabolism in the ponto-bulbar region at 5 weeks followed by a more global alteration of monoamines when the disease progresses (8 weeks). Hypothalamic measurements suggest biphasic disturbances of norepinephrine and serotonin at pathology onset (5 weeks) that were found stabilized later on (8 weeks). Interestingly, the postnatal nigrostriatal dopaminergic deficit identified previously does not parallel the reduction of the other neurotransmitters investigated. Finally, dosage in cortical samples do not suggest modification in the monoaminergic content respectively at 5 and 8 weeks of age.
We have identified that the level of catecholamines and serotonin is differentially affected in Mecp2-/y brain areas in a time-dependent fashion.
Rett syndrome (RTT, MIM #312750) is a severe neurological disorder caused by mutations in the X-linked methyl-CpG binding protein 2 (MECP2) gene . Female patients are affected with an incidence of 1/15000 live births [2, 3] and develop normally from birth to 6-18 months of age before the onset of deficits in autonomic, cognitive, motor functions and autistic features [4, 5]. Several studies shed light on the involvement of catecholaminergic and serotonergic disturbances as a major contributor of the disease in RTT patients and Mecp2 mouse models. Neurochemical analyses of biogenic amines in Mecp2-null male (Mecp2-/y) were previously performed on whole brain homogenates showing that the concentration of dopamine (DA), norepinephrine (NE) and serotonin (5-HT) was reduced after birth [6, 7]. Moreover, the absence of Mecp2 impairs several functions that are regulated by bioaminergic nuclei or peripheral ganglia where such neurochemical deficits occur [8–12]. However, these studies are discordant for several parameters. Here, we evaluated the level of DA, NE and 5-HT and their catabolites homovanillic Acid (HVA), dihydroxyphenylacetic acid (DOPAC) and 5-hydroxyindoleacetic acid (5-HIAA), using high performance liquid chromatography, combined with electrochemical detection (HPLC/EC). We performed our analyses on micropunched brain samples from the cortex, caudate-putamen, hypothalamus, midbrain (Substantia Nigra + Ventral Tegmental Area) and the hindbrain (Brainstem + Pons) (Figure 1) of Mecp2-/y mice and their respective age-matched wild-type (WT) littermates from postnatal day 35 (P35, disease onset) and 55 (P55, severe phenotype).
Neither catecholamines nor serotonin levels are affected in the cortex of Mecp2-/y
Neurochemical analysis performed in the cortex showed no perturbation at P35 for DA, NE and 5-HT levels in Mecp2-/y compared to their WT littermates (p > 0.05). No significant alterations were observed at P55 for DA, NE and 5-HT (p > 0.05). DA measurements in the cortex display great variability possibly masking differences between the two genotypes (Figure 2A). Dopaminergic catabolites HVA and DOPAC were unaffected at P35 and P55 (p > 0.05). The serotonin metabolite 5-HIAA is not different between Mecp2-/y and WT at P35 and P55 (p > 0.05) (Figure 3A). Altogether, these results argue for a preserved biogenic amines metabolism in the cortex of Mecp2-null mice.
The alteration of norepinephrine and serotonin levels in the hypothalamus of Mecp2-/y is postnatal and biphasic
Next, we measured biogenic amines concentrations in the hypothalamus. It was previously reported that a targeted deletion of Mecp2 in Single-minded 1 gene (Sim1)-expressing neurons (located in several hypothalamic nuclei) results in a body of behavioural deficits ranging from feeding disturbances to stress . Increased levels of corticosterone and leptin together with Brain-derived neurotrophic factor (Bdnf) deficits are possible contributors for this phenotype in this mouse. Since catecholamines play a role in hypothalamic nuclei neurotransmission and interplays with leptin and Bdnf [14–17] we wanted to assess deficits in bioamines and their degradation products. Deficits were observed at P35 for NE and 5-HT (p < 0.05). No alteration of DA levels was noticed at this age (p > 0.05). However, the NE and 5-HT decrease identified at P35 was no longer present at P55 and DA levels were normal at P55 (p > 0.05) (Figure 2B). All the tested catabolites were found to be normal in the hypothalamus of Mecp2-/y compared to WT at P35 and P55 (Figure 3B).
Bioaminergic disturbances are global and progressive in pontic and brainstem area of Mecp2-/y
DA, NE and 5-HT contents were evaluated by HPLC using pons and brainstem samples of Mecp2-/y animals and WT animals at P35 and P55 (Figure 2C). DA is reduced both at P35 and at P55 (p < 0.05). NE levels are normal at P35 (p > 0.05) but are clearly reduced at P55 (p < 0.05). For serotonin, we found the same pattern of alteration, with no decrease at P35 (p > 0.05) but a decrease at P55 (p < 0.05). Altogether, our results suggest that Mecp2-/y mice have lower levels of biogenic amines than their WT littermates.
We respectively assessed the level of HVA, DOPAC and 5-HIAA in these samples (Figure 3C). At P35, the only catabolite affected is HVA (p < 0.05) whereas DOPAC and 5-HIAA are normal (p > 0.05). At P55, the levels of HVA, DOPAC and 5-HIAA were all reduced in Mecp2-/y compared to WT samples (p < 0.05).
Mecp2-/y nigrostriatal dopaminergic deficits do not parallel noradrenergic or serotonergic ones
We previously reported a postnatal reduction of DA and HVA but not DOPAC in the caudate-putamen of Mecp2-/y at P35 and P55  (illustrated on Figure 2D and Figure 3D). Here, we observed that at P35, neither NE nor 5-HT contents were affected (p > 0.05). This observation stands true for these neurotransmitters at P55 (p > 0.05). We measured the level of 5-HIAA and found no alteration at P35 (p > 0.05), and P55 (p > 0.05). These results indicate that the noradrenergic and serotonergic neurotransmitters are unaffected in the caudate-putamen of Mecp2-/y compared to their WT littermates at all ages investigated (Figure 2D and Figure 3D).
Our previous work failed to detect changes in the level of DA and DOPAC in the Mecp2-/y midbrain at both P35 and P55. However, we observed a clear reduction of HVA in these dopaminergic neurons at the most advanced age  (illustrated on Figure 2E and Figure 3E). We extended our analysis to NE, 5HT and 5-HIAA at both ages. Our results show that NE is not altered at P35 in Mecp2-deficient midbrain (p > 0.05). 5-HT levels are also preserved compared to WT level at the same age (p > 0.05). Samples obtained from symptomatic mice (P55) do no exhibit any modification of the substrate levels compared to age-matched WT (p > 0.05) (Figure 2E). 5-HIAA values are normal at P35 (p > 0.05) and at P55 (p > 0.05) in Mecp2-/y samples compared to age-matched WT (Figure 3E).
Mecp2-/y cortical neurons exhibit several alterations, ranging from reduced activity to abnormal dendritic spine morphology [18, 19]. These defects are influenced by Bdnf dosage . Bdnf plays a key role in neuronal survival, differentiation and synaptic plasticity . Bdnf metabolism was shown to be involved in the development and function of catecholaminergic neurons, affected in Mecp2-/y [22–25]. Recently, several studies identified NE reductions in the piriform cortex of Mecp2-null mouse at P35  and in the prefrontal and motor cortex at both 3 (P21) and 8 (P56) weeks of age . We were not able to reproduce these findings. One possible explanation for this divergence could be differences in the sampling procedure. We performed micropunches of the motor cortex. Different cortical territories receive monoaminergic inputs from different nuclei, some areas being less densely innervated than others . Serotonergic dosage in Mecp2-/y brains were also reported and discrepancies are existing. Isoda and collaborators did not to identify any modifications of 5-HT and its main catabolite 5-HIAA in the prefrontal cortex from P14 to P56 . However, another laboratory argued for a reduction in the same structure of 5-HT only, at 3 and 8 weeks of age . As Isoda and coauthors measured, we did not found significant reductions of 5-HT or 5-HIAA. Another group reported a 5-HT deficit in whole brain extracts in the same developmental window . Unfortunately, samples used in this study came from pooled 6 to 8 weeks Mecp2-/y animals, two ages that are know to be phenotypically different according to the postnatal development of the Mecp2-/y mouse pathology . These results thus combine 5-HT contents from both mildly and severely affected animals.
It is generally believed that catecholamines play a role in hypothalamic nuclei neurotransmission and that their release is modulated by several factors including Bdnf and leptin . Here, we report a postnatal alteration of hypothalamic NE and 5-HT contents that follows a biphasic scheme. These biogenic amines were found significantly decreased at P35 in Mecp2-/y animals whereas their levels are not significantly different from WT at P55. A recent study showed that specific deletion of Mecp2 in Sim1-positive neurons in the paraventricular nucleus (PVN) of the hypothalamus results in higher serum level of leptin . Since leptin was proposed to lower NE-dependant oxytocin release in the PVN  and to reduce firing of serotonergic neurons  it was tempting to assess the level of bioamines in this brain area. Our results at P35 could reflect a leptin-dependant bioaminergic reduction. However, Fyffe and coauthors did not identify alterations at 6 weeks (P42) but noticed a significant increase 42 weeks. It is important to stress that Mecp2-deletion is not restricted to hypothalamic neurons in the model we used. Moreover, mice used in one study were of mixed 129/FVB genetic background  while we used C57Bl6 Mecp2-/y mice .
In agreement with Taneja and co-workers , we found a reduction of DA and HVA in our hindbrain samples containing both the brainstem and the pons at P35. However, we did not found DOPAC reduction. Taneja et al. used a different Mecp2-/y strain (i.e. generated by Jaenisch laboratory; ). It would be interesting to investigate possible difference in the activity/modulation of DA degradation enzymes in these two models. In the Bird mouse  no difference was found in monoamine oxydase (MAO-A and MAO-B) activity in the cortex . It remains to be determined if MAO and/or catechol-O-methyl transferase (COMT) levels are impaired elsewhere. Interestingly, the caudal structures are the most affected with dopaminergic disturbances at P35 when the Mecp2 animals display a mild phenotype, and a global monoaminergic deficit at P55 affecting DA, NE, 5-HT and their degradation products. This is in good agreement with several studies arguing for a brainstem and pontic basis for the Mecp2-/y phenotype and RTT symptoms in humans [31, 32]. The observed increase in the serotonergic ratio (Table 1) at P55 in the pons and brainstem supports a possible alteration of 5-HT projections innervating this structure and modulating the autonomic functions altered in the absence of Mecp2 .
Mecp2-/y mice display a progressive and postnatal alteration in their motor behavior [11, 34]. Interestingly, mice with a targeted deletion of Mecp2 in Th-expressing neurons show a deficit in motricity among other dysregulations . We recently described in mice harboring a constitutive deletion of Mecp2 progressive alterations of the SNpc and the nigrostriatal dopaminergic pathway, a key component of the brain motor circuitry . Moreover, some of the behaviors impaired were ameliorated by L-Dopa, arguing for a strong, although clearly non-unique, involvement of the DA disturbances in Mecp2-/y motor phenotype. In complement to this previous study, we here pursued our neurochemical investigations for NE and 5-HT in the SNpc and its striatal target. NE, provided from the Locus Coeruleus, A1 and A2 (from brainstem) is implicated in several brain functions and its action on midbrain DA neurons was shown to modulate motivational behaviors [35, 36]. The absence of NE and 5-HT disturbances in the midbrain and the caudate-putamen confirm previous findings [10, 11].
The consequence of Mecp2-deficiency on the integrity of dopaminergic and serotonergic nuclei could be indexed on the HVA + DOPAC/DA and 5-HIAA/5-HT ratios respectively since a toxic alteration of dopaminergic and serotonergic systems induces counteradaptative processes that impact on this values [37, 38]. The calculated ratios are reported in Table 1. Results suggest dopamine turnover was left unaffected in all the structures investigated at both P35 and P55 in Mecp2-/y compared to their WT littermates. Conversely, hypothalamus and caudate-putamen dosage revealed a significant increase of 5-HIAA/5-HT ratio at P35 but not P55. Values from the pons and brainstem indicate a clear increase in the serotonergic turnover in Mecp2-/y at P55. However, this index was not modified in the cortex and the midbrain at P35 and P55. Alteration of the serotonergic innervation lead to an increase in the turnover . Interestingly, a reduction in 5-HT immunoreactive fibers was reported in the hippocampus of Mecp2-/y animals . It remains to be elucidated if such phenomenon contribute to serotonergic deficits described here.
Our results indicate that the level of catecholamines and serotonin is differentially affected in Mecp2-/y brain areas in a time-dependent fashion (Figure 4). Considering behavioral and physiological function altered in the context of Mecp2-deficiency and the positive impact of drugs targeting this system, monoamine neurochemical dosage could help identifying therapeutics resetting central bioaminergic deficits in different brain areas of the Mecp2-deficient mouse.
Experiments were performed on the B6.129P2(c)-Mecp2tm1-1Bird mouse model for RTT . The mice were obtained from the Jackson Laboratories and maintained on a C57Bl/6 background. The experimental procedures were carried out in keeping with the European guidelines for the care and use of laboratory animals (Council Directive 86/609/EEC). Both pre-symptomatic and symptomatic mice were analyzed at different developmental stages. A total number of 15 Mecp2-/y and 18 WT male mice were used in the study. The Mecp2 -/y (null male) and WT (wild-type male) mice were studied at postnatal days 35 (P35; n = 10 WT; n = 6 Mecp2-/y) and 55 (P55; n = 8 WT; n = 9 Mecp2-/y) for neurochemical analysis. Mecp2-deficient mice were compared to their respective WT littermates of the same gender. Breeding and genotyping were performed as previously described .
P35 (n = 10 WT; n = 6 Mecp2-/y) and P55 (n = 8 WT; n = 9 Mecp2-/y) mice were killed by cervical dislocation, and their brains were dissected out within the first 2 min post-mortem. The motor cortex, Caudate-Putamen, Midbrain area (Substantia Nigra + Ventral Tegmental Area) were microdissected using a punching needle (0.5 mm ∅) and kept at -80°C until biochemical analysis. The region containing both the Pons and the Brainstem was dissected under a binocular microscope (Figure 1). Briefly, brain area dissection was performed on cryostat brain sections with the help of a 5× magnifying lens, following their stereotaxic coordinates [39, 40].
Norepinephrine, DHBA, dopamine, DOPAC, HVA, serotonin (5-hydroxytryptamine, 5-HT), 5-hydroxyindole-3-acetic acid (5-HIAA), 1-octanesulfonic acid (OSA), triethylamine and ethylene-diamine-tetra-acetic acid (EDTA) disodium salt were purchased from Sigma, sodium dihydrogen phosphate and citric acid from Merck and methanol from Prolabo. Ultrapure water was obtained with a Milli-Q system (Millipore, Bedford, MA, USA). Standard solutions of each monoamine or metabolite were stored at -20°C at 1 mmol/L as aliquots.
The HPLC system was composed of a Hitachi L-7000 series equipped with a degasser, a L-7100 pump, an L-7200 autosampler thermostated at 10°C and a Decade Intro electrochemical detector fitted with a 3 mm glass carbon working electrode, an Ag/AgCl reference electrode and a 25 μm spacer (Antec, Leyden, The Netherlands). Separations were performed using a 250 mm × 4.6 mm i.d. C18 5 μm Beckman Ultrasphere column equipped with two Phenomenex C18 filters in a security guard system. The mobile phase was pumped at a microflow rate of 0.8 mL/min and composed of 0.7 mol/L sodium phosphate, 0.1 mmol/L EDTA, 1.1 mmol/L OSA, 3.1 mmol/L triethylamine, 14% methanol, pH adjusted to 3.12 with 1 mmol/L citric acid, it was filtered with 0.45 μm cellulose acetate membranes before use. Elutes were detected at an oxidation potential of 700 mV versus reference electrode. The column and the detection cell were housed within the Faraday cage of the electrochemical detector that was set to 25.5°C. The day of the analysis, 35 μL samples were placed in the autosampler and kept at +10°C before injection. The injection volume was 30 μL. The retention times were 7 min, 11 min, 13.5 min, 16.5 min, 21 min, 32 min and 42 min for NE, DHBA, DOPAC, DA, 5-HIAA, HVA, and 5-HT, respectively.
We evaluated whether our data distribution fitted with a Gaussian representation using a K-S Kolmogorov-Smirnov Normality test. If valid, data were statistically analyzed using unpaired Student's t test. If not valid, we used an adapted non-parametric Mann-Whitney test to compare genotypes. The results are reported as mean +/- standard error of the mean (S.E.M). A p-value < 0.05 was considered to be statistically significant.
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This study was supported by Inserm, the Provence-Alpes-Côte d'Azur region, AFSR (Association Française du Syndrome de Rett), the E-rare EuroRett network, the Fondation Jérôme Lejeune and the Dischrom project (FP7). Thanks are due to Dr. Sandrine Parrot and Dr. Luc Denoroy from the NeuroChem facility (Université Claude Bernard, Lyon, France) for technical assistance on high performance liquid chromatography.
LV and JCR conceived and designed the experiment. NP and AG performed the experiments. NP and JCR analyzed the data. NP and JCR wrote the paper. All authors read and approved the final manuscript.