Morphological changes of cortical pyramidal neurons in hepatic encephalopathy
© Chen et al.; licensee BioMed Central Ltd. 2014
Received: 2 October 2013
Accepted: 13 January 2014
Published: 17 January 2014
Hepatic encephalopathy (HE) is a reversible neuropsychiatric syndrome associated with acute and chronic liver diseases. It includes a number of neuropsychiatric disturbances including impaired motor activity and coordination, intellectual and cognitive function.
In the present study, we used a chronic rat HE model by ligation of the bile duct (BDL) for 4 weeks. These rats showed increased plasma ammonia level, bile duct hyperplasia and impaired spatial learning memory and motor coordination when tested with Rota-rod and Morris water maze tests, respectively. By immunohistochemistry, the cerebral cortex showed swelling of astrocytes and microglia activation. To gain a better understanding of the effect of HE on the brain, the dendritic arbors of layer V cortical pyramidal neurons and hippocampal CA1 pyramidal neurons were revealed by an intracellular dye injection combined with a 3-dimensional reconstruction. Although the dendritic arbors remained unaltered, the dendritic spine density on these neurons was significantly reduced. It was suggested that the reduction of dendritic spines may be the underlying cause for increased motor evoked potential threshold and prolonged central motor conduction time in clinical finding in cirrhosis.
We found that HE perturbs CNS functions by altering the dendritic morphology of cortical and hippocampal pyramidal neurons, which may be the underlying cause for the motor and intellectual impairments associated with HE patients.
KeywordsPrimary sensorimotor cortex Hippocampus Pyramidal neuron Dendritic spine Liver failure Bile duct ligation
Hepatic encephalopathy is a common disease caused by the liver failure. The consequential disorders of the liver include the cirrhosis, hepatitis, urea cycle defect or lack of blood circulation to the liver . The exact cause of hepatic encephalopathy is still unclear, but ammonia [the term “ammonia” refers to total ammonia:gas (NH3) + ion (NH4+)] may be involved . Ammonia is a metabolite which is mostly produced within the gut during protein digestion and deamination. It can diffuse into the capillaries of gut, and thence transferred to the hepatocytes for urea cycle . The liver maintains the concentration of ammonia in the systemic circulation . Hyperammonaemia develops if the urea cycle cannot control the ammonia overload. Ammonia crosses the blood-brain barrier readily, and it enters the brain from blood by diffusion rather than via a saturable transport system. The brain uptake index for ammonia is independent of arterial ammonia levels over a wide range of concentrations. It is known that the brain has a highly integrated system whose astrocytes are endowed with glutamine synthetase that protect it against serum derived toxicity. The ammonia is detoxified temporarily by its incorporation into the non-toxic amino acid glutamine, but continual hyperammonemic assault would induce glutamine accumulation in the cytoplasm and mitochondria. The glutamine in mitochondria is subsequently hydrolyzed leading to high levels of ammonia. This triggers oxidative and nitrosative stress, the mitochondrial permeability transition and mitochondrial injury, a sequence of events that have been termed as the Trojan horse hypothesis of HE [5, 6].
HE has a lot of symptoms, and most of them are closely related to the functions of the central nervous system. These comprise brain edema, intracranial hypertension and a number of neuropsychiatric disturbances such as somnolence, confusion, sleep-wake inversions, impairments of sensory-motor integration, cognitive performance, attention and memory, or even coma [2, 7]. High ammonia level is believed to be the cause for neuropsychiatric disturbances . Brain imaging confirms that hyperammonemic neonates and infants show cortical atrophy, ventricular enlargement, demyelination or gray and white matter hypodensities [8–10]. Some structural alterations have been associated with the deleterious effects of hyperammonemia. Astrocytes which are metabolically hyperactive, appeared to undergo histological changes in hyperammonemic brain [11, 12]. Some studies have reported that the inhibitory and excitatory neurotransmission might be directly affected by ammonia toxicity. The excitotoxicity induced by hyperammonemia would further trigger the production of nitric oxide synthases (NOS), increase in oxidative stress such as increased production of reactive oxygen and nitrogen oxide species (ROS/RNOS). Thus, in HE model, there is evidence of over-expression of nNOS in the cerebral cortex , cerebellum [14, 15] and striatum . However, the effects of ammonia on central neurons have remained elusive. In view of this, we have used an intracellular dye injection technique along with behavioral tests to investigate whether the behavioral defects in bile duct ligation-induced HE model might be correlated with the changes of dendritic structures of cortical pyramidal neurons.
Thirty male Sprague-Dawley (SD) rats weighing 250-350 g were used for the study. The rats were divided into three groups. Of these, 20 of them were subjected to the common bile duct ligation to induce liver fibrosis and they were allowed to survive for 4 weeks. The surgery of common bile duct ligation followed previous protocol . Briefly, the rats were operated under deep anaesthesia with ketamine and xylazine (8 mg ketamine and 1 mg xylazine/100 g body weight) and a double surgical ligation was placed (2 silk knots proximal to bifurcation were tied on common duct) and the common bile duct was sectioned between both knots. The surgical rats were divided into two groups. Firstly, half of the rats were fed with normal diet for 4 weeks (BDL, n = 10). As in previous article , feeding ammonium acetate could increase blood ammonia level, so some BDL rats in our study were fed with diet containing ammonium acetate (BDLHD, 10% w/w) for last 2 weeks (n = 10) to exacerbate the liver dysfunction. Ten rats served as sham-operated controls. Rats were caged individually with water ad libitum in a temperature (24 ± 1°C) and humidity-controlled room with 12-hour on, 12-hour off lighting schedule. All experimental procedures were approved by the Animal Care and Use Committee of the National Chung-Hsing University under guidelines of the National Science Council of Taiwan.
The protocols were modified from Jones and Roberts  and Chen et al.  to evaluate the motor coordination and spatial learning memory performance of the rats. All rats were subjected to rotarod and Morris water maze tasks before been scheduled for surgical operation and sacrifice.
The motor coordination of HE rats was assessed with an accelerating rotarod apparatus (Ugo Basile, Comerio, Italy) . Rats were trained twice a day for two consecutive days prior to testing. Training sessions consisted of maintaining the rats on the rod for 3 min at the speed (12 rpm). In the test, the rats were evaluated for 3 min in the session, in which the rotation rate increases constantly to reach 12 rpm and the direction of rotation was reversed with each 12 seconds. The mean latency to fall off the rotarod was recorded as the mean of three trials for each rat.
Morris water maze task
Animal performance was recorded with a video camera for subsequent analysis of the path and swimming speed. The maze apparatus consisted of a circular pool 200 cm in diameter and 60 cm deep. The pool was filled with water at approximately 23°C to a height of 50 cm. A transparent platform (diameter 15 cm) was placed at a constant position 2-3 cm below the surface of the water. The visual cues arrayed around the room were made available for the rats to learn the location of the hidden platform. The rats were tested for 3 consecutive days with two trials per day. Rats were allowed to remain on the platform for 20 s if escaped within 180 s, or alternatively placed on the platform and remained there for 20 s if failed to locate the underwater platform within 180 s. A recovery period of 10 minutes was allowed between the two trials. The escape times of the two trials conducted each day were recorded and averaged.
At the end of the survival period the rats in each group were divided into two subgroups. One (N = 5) is decapitated and processed for ammonia level measuring of cerebral cortex as described below. The other (N = 5) is sacrified and processed for intracellular dye injection and immunohistochemical staining as described previously . Briefly, the rats were deeply anaesthetized and perfused with 2% paraformaldehyde in 0.1 M phosphate buffer (PB), pH 7.3, at room temperature for 30 min. Immediately following the perfusion, the whole brain was carefully removed and sectioned with a vibratome (Technical Products International, St. Louis, MO) into 350-μm-thick coronal slices. Half of the thick slices collected were processed by an intracellular dye injection to reveal the dendritic arbor of selective individual neurons. The remaining tissue slices were postfixed in 4% paraformaldehyde in 0.1 M PB for 2 days. They were then cryoprotected and resectioned into 20-μm sections  for studying the cytoarchitecture as described below.
Intracellular dye injection and subsequent immunoconversion of the injected dye
The cerebral neurons whose cell nuclei emitting fluorescence with 10-7 M 4′, 6-diamidino-2-phenyl-indole (DAPI; Sigma-Aldrich, St. Louis, MO) under the filter set were visualized by an intracellular injection of Lucifer yellow (LY, Sigma-Aldrich) which emitted a yellow fluorescence [21, 22]. For this purpose, the brain slice was placed in a chamber on the stage of a fixed-stage fluorescence microscope (Olympus BX51) and covered with 0.1 M PB. A glass micropipette filled with 4% LY in water was steadily positioned with a three-axial hydraulic micromanipulator (Narishige, Tokyo, Japan) for dye injection. The intracellular amplifier (Axoclamp–IIB) was used to generate injection current. When the dye injection was completed, the brain slice were rinsed with 0.1 M PB and postfixed in 4% paraformaldehyde. The brain slices given dye injection were then cryoprotected and sectioned into 60-μm-thick serial sections for subsequent immunoconversion.
The sections derived from above were first incubated with 1% H2O2 in PB for 30 min and then incubated in PBS containing 2% Bovine Serum Albumin (Sigma-Aldrich) and 1% Triton X-100. Sections were then treated with biotinylated rabbit anti-LY (1:200; Molecular Probes, Eugene, OR) in PBS for 18 hours at 4°C and then with standard avidin-biotin HRP reagent (Vector, Burlingame, CA) for 1 hour at room temperature. They were then reacted with 0.05% 3-3′-diaminobenzidine tetrahydrochloride (DAB, Sigma) and 0.01% H2O2 in 0.05 M Tris buffer. Reacted sections were mounted on subbed slides, air-dried, and coverslipped in Permount for 3-dimensional reconstruction.
Some brain sections were stained with Cresyl violet for cell density and soma area evaluation of cortical pyramidal neurons. To reveal microglia, astrocytes or nNOS + cells, sections were reacted with goat antibodies to Iba1 (Abcam, 1:2000, Cambridge, UK), rabbit polyclonal antibodies to glial fibrillary acidic protein (GFAP, 1:400, Merck Millipore, Temecula, California) or monoclonal antibody to the nNOS (1:1000, Santa Cruz Biotechnology, Santa Cruz, California), respectively, for 18 h at 4°C. Biotinylated rabbit anti-goat (1:200), goat anti-rabbit (1:200) and horse anti-mouse (1:200) immunoglobulins were used as the secondary antibodies, respectively. Subsequent DAB reaction process followed that described previously .
Serum biochemical measurement
Blood samples (1.5 ml) were collected via the inferior vena cava when sacrificing the animals (9:00 AM). The sample was centrifuged (3000 × g, 15 min, 4°C) before measurement. Levels of alanine aminotransferase (ALT) and aspartate aminotransferase (AST) were assayed with an ADVIA 1800 analyzer (Siemens Medical Solutions Diagnostics Pte Ltd., Swords, Ireland) with alanine aminotransferase (P/N 03036926, Bayer Siemens) and aspartate aminotransferase (P/N 03039631, Bayer Siemens) reagents commissioned by a clinical laboratory (UM Clinical Laboratory, Taichung, Taiwan).
Ammonia colorimetric assay
The blood sample and homogenized cortex were collected and centrifuged with spin filter (ab93349, Abcam) to remove excessive proteins. After centrifugation, the assays were performed according to the manufacturer’s specifications (K370-100, BioVision) using a Microplate Reader (Infinite F50, Tecan Co., Mannedorf, Switzerland) to detect the level of ammonium ion.
The cell density of microglia, nNOS + and pyramidal neurons in primary sensorimotor cortex was randomly counted twice in each section per 3402, 13902 and 502 μm2, respectively. Ten sections of each rat were analyzed. The soma area of layer V pyramidal neurons and astrocytes in primary sensorimotor cortex was reconstructed using a Camera lucida drawing tube at 100× oil-objective lens in two-dimensional plane. Fifty pyramidal neurons or astrocytes of each rat were randomly chosen from section to analyze their soma size. The astrocytes with a clear cell border and all-around processes were chosen to draw their outline of cell body. In astrocyte end-feet analysis, ten astrocytes of each rat were analyzed. All terminal boutons in the process end within a radius of 50 μm around an astrocyte were counted. The demarcation between soma and process was taken as the point where the convex curvature of the soma became concave . To study the changes of dendritic arbor and length of layer III and layer V pyramidal neurons, the complete dendritic arbors of 5 neurons in each rat were reconstructed 3-dimensionally with Neurolucida (MicroBrightField, Williston, VT). To determine the density of dendritic spines, 5 representative CA1 and layer V pyramidal neurons each from each rat from the respective treatment groups were randomly analyzed. Dendrites of the studied CA1 and layer V pyramidal neurons were divided into proximal and distal segments of the apical and basal dendrites following the criteria described before [20, 21]. Briefly, for layer V pyramidal neurons, proximal and distal basal dendrites were defined as the segments 50–100 μm (around the first to second branch), and 150–200 μm (around the last one or two branches) from where they originate from the soma, respectively. Proximal apical dendrites were the first or second branch of the apical trunk and distal apical dendrites were the terminal dendrites after the last branch point in V pyramidal neurons. For hippocampal CA1 pyramidal neurons, basal dendrites were defined as those in the stratum oriens while apical dendrites were on the other side of the cell body layer with the proximal segment in the stratum radiatum and distal segment in the stratum lacunosum-moleculare as the criteria described before . Data was expressed as mean ± SE unless otherwise indicated. Statistical significance was tested with one-way analysis of variance (ANOVA) followed by the Newman-Keuls test to find out any difference between treatment groups.
Biochemical and behavioral changes of HE rats
For hippocampus-related functions, we assessed the spatial memory with the water maze task. The BDL and BDLHD rats utilized longer duration, an increase by 2.6 and 4.6 folds, respectively, to locate the hidden platform than the control rats (Figure 3B). This was accompanied by a tripling of the swimming path (Figure 3C). The swimming speed in BDL and BDLHD rats was decreased compared with control rats but the reduction was not statistically significant.
Morphological changes of cerebral cortex in HE rats
Alteration of dendritic structures on sensorimotor cortical pyramidal neurons in HE rats
For the spatial learning memory functions, we focused on the hippocampal CA1 pyramidal neurons to explore possible morphological changes induced by hyperammonemia. As in the layer V pyramidal neurons of sensorimotor cortex, hyperammonemia also had no effect on the dendritic arbor of hippocampal CA1 pyramidal neurons (Figure 6D-F, 7C and 7D). The spine density on the basal dendrite and proximal and distal segments of the apical dendrites of CA1 pyramidal neurons was significantly reduced by 27-47% and 24-40% in BDL and BDLHD rats, respectively, (Figure 8B and D).
This study has succeeded in establishing a HE model in rats through ligation of the common bile duct followed by feeding the rats with diet containing ammonium acetate which results in hyperammonemia. More importantly, we have shown that the induced hyperammonemia compromised the sensorimotor integration and spatial learning memory. Moreover, at the cellular level, the astrocytes increased in cell size by 55-65%. The total microglial number was not significantly increased but the frequency of activated microglia was increased by 79-109%. Very interestingly, the dendritic arbors of layer V and CA1 pyramidal neurons in the primary sensorimotor cortex and hippocampus were not affected. A striking change, however, occurred at the dendritic spines whose density was significantly decreased in HE rats. These changes were consistently observed on all segments of the basal and apical dendrites. On the other hand, changes in dendritic structures were revealed in sparse-fur mice, which are deficient in ornithine transcarbamylase. In this congenital metabolic deficiency, the layer V pyramidal neurons in frontoparietal cortex displayed retraction of basal dendritic arbor and decrease in spine density of dendritic terminal . The reduced complexity in basal dendritic arbor in spf/Y mice may have the following explanations. Firstly, ornithine transcarbamylase deficiency might affect the dendritic maturation of cortical pyramidal neurons. In general, dendrite arbors on central neurons reach their normal mature size during 3rd~4th postnatal weeks, and the synaptic transmission is pivotal to the proper development of mature central neuronal architecture [24, 25]. It is speculated that in spf/Y mice, the dendritic arbors of cortical pyramidal neurons might not reach their full maturation. Secondly, in our HE model, the duration of ammonia influence is less than one month. This may be another possible explanation for the discrepancy in results between that of the above authors and ours. In addition, the above authors had used Golgi-Kopsch method to reveal the basilar dendritic tree of layer V pyramidal cells in frontoparietal cortex. The Golgi labels neurons capriciously and often results in overlapping and incomplete dendritic arbors in sections to impede analysis . In the present study, we employed intracellular dye injection [20–22, 27, 28] to reveal the dendritic arbors of the studied pyramidal neurons. This allowed us to study specifically identified layer V and CA1 pyramidal neurons. Neurons, well-spaced apart, could be individually filled with no time constraint. With proper orientation, we were able to preserve most of the dendritic arbors for instance of the relatively large layer V and CA1 pyramidal neurons close to completeness in a 350 μm-thick brain slice.
Unlike dendritic arbors, dendritic spines are highly motile structures that have been shown to be swiftly and dynamically modulated by many factors such as changes in environment , gonadal hormones [27, 28, 30], physical compression and decompression [21, 22], fatigue , insults such as axonal injury , deafferentation , and aging . Here, we have shown that hyperammonemia significantly decreased the spine density in layer V sensorimotor cortical neurons (23-46%) and in hippocampal CA1 pyramidal neurons (24-47%). The dendritic spines of layer V pyramidal neurons in frontoparietal cortex displayed more than 60% loss in sparse-fur mice . In the clinic, threshold to evoke peripheral motor responses to transcranial magnetic stimulation of the primary cortical motor area was increased in the presence of hepatic encephalopathy, and this might be attributed to an ammonia induced loss of glutamatergic excitatory synaptic inputs to cortical pyramidal neurons [34, 35]. Because there was no significant change in cell density, soma size of layer V pyramidal neurons as well as there was no evidence of neuronal death in the sensorimotor cortex, it is suggested that the significant reduction in spine density of cortical pyramidal neurons had contributed to the behavioral dysfunction as observed in the present HE rats.
As far as can be ascertained, there is no defined mechanism to explain the spine loss of cortical pyramidal neurons in HE model rats. It is speculated that this may be multifactorial. Thus, the possibility of involvement of neuroglia activation or oxidative stress is considered. Microglia was robustly activated and underwent proliferation in hyperammonemia [36, 37]. The microglia proliferation and astrocytes swelling might further increase the surrounding pressure which could decrease the dendritic spines of cortical pyramidal neurons . Recent studies have shown that interaction of microglia with synapses contributes to synaptic remodeling during development  and adult . The oxidative stress might be another factor causing decrease in the dendritic spines of cortical pyramidal neurons. There is evidence that hyperammonemia could enhance the production of ROS/RNOS in astrocytes [36, 40]. Excessive ammonia in synaptic cleft may be mediated by an excitotoxic mechanism, oxidative stress and nitric oxide (NO) production in cortical neurons . These oxidative stresses further inhibit the synaptic transmission and promote the synaptic remodeling. Our ongoing studies also found that high oxidative stress, induced by D-galactose, significantly decreases the spine density of layer V sensorimotor cortical neurons and hippocampal CA1 pyramidal neurons, and, remarkably, exogenous antioxidant can fully restore it (unpublished data).
In HE rats, the astrocytes showed enhanced GFAP immunoreactivity, increase in soma size and swollen end-feet. Similar results of astrocyte swelling were observed in vivo  and in vitro [42, 43] in rats. Astrocytic reaction is a hallmark feature of brain edema and its complications (intracranial hypertension, brain herniation) in HE patients . Astrocyte swelling may be caused by over-expression of aquaporin-4 protein [42, 45], or an auto-amplificatory loop between ROS/RNOS formation and astrocyte swelling [36, 40]. Hyperammonemia is also frequently complicated by systemic inflammation including increasing systemic and cerebral levels of vascular endothelial growth factor (VEGF), Tumor Necrosis Factor (TNF)-alpha and the interleukins (IL)-1beta and IL-6 . The VEGF may stimulate liver regeneration but it can also be pro-inflammatory, activating endothelial cells and increasing permeability, actions mediated through Src kinase signaling . These proinflammatory cytokines progress in parallel with the severity of astrocyte swelling . The alterations in blood-brain barrier remain unclear although some studies have shown disruption of tight junction proteins indicative of involvement of blood-brain barrier in cellular swelling [48, 49]. Hypertrophy of end-feet of astrocytes was evident after BDL surgery, but there was no noticeable difference between the BDL and BDLHD rats. More studies are desirable to confirm whether the enlarged end-feet may be correlated with the blood-brain barrier damage in BDL rat model. A feature worthy of note is that hyperammonemia promotes the astrocyte swelling but has no affect on soma area of layer III and Layer V pyramidal neurons in sensorimotor cortex. In vitro culture study showed that NH4Cl could promote the swelling of culture astrocytes and microglia in a glutamine-synthesis dependent way but has no effect on cell volume of cultured neurons .
Hyperammonemia, in addition to affecting peripheral organs, also alters the structure of astrocytes and central neurons. It enhances the astrocyte swelling and microglia activation; moreover, it significantly decreases the spine density of layer V sensorimotor cortical neurons and hippocampal CA1 pyramidal neurons, which may be the underlying cause for the motor and intellectual impairments associated with HE patients.
Nitric oxide synthases
Reactive oxygen and nitrogen oxide species
Bile duct ligation
BDL rats feed with diet containing ammonium acetate
Glial fibrillary acidic protein
Analysis of variance
Vascular endothelial growth factor
Tumor necrosis factor
This work was supported by research grants from the National Science Council of Taiwan to Chen, J-R (NSC102-2320-B-005-001-MY3), Wang, T-J (NSC-95-2320-B-438-001), Wang, Y-J (NSC100-2320-B-320-002) and Tseng, G-F (NSC101-2320- B-320-001) and grants from the Tzu-Chi University to Wang, Y-J and Tseng, G-F (TCIRP98006).
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