ABSTRACT
Vascular endothelial growth factor (VEGF) was initially characterized as a potent angiogenic factor based on its activity on the vascular system. However, it is now well established that VEGF also plays a crucial role as a neuroprotective factor in the nervous system. A deficit of VEGF has been related to motoneuronal degeneration, such as that occurring in amyotrophic lateral sclerosis (ALS). Strikingly, motoneurons of the oculomotor system show lesser vulnerability to neurodegeneration in ALS compared to other motoneurons. These motoneurons presented higher amounts of VEGF and its receptor Flk-1 than other brainstem pools. That higher VEGF level could be due to an enhanced retrograde input from their target muscles, but it can also be produced by the motoneurons themselves and act in an autocrine way. By contrast, VEGF's paracrine supply from the vicinity cells, such as glial cells, seems to represent a minor source of VEGF for brainstem motoneurons. In addition, ocular motoneurons experiment an increase in VEGF and Flk-1 level in response to axotomy, not observed in facial or hypoglossal motoneurons. Therefore, in this review, we summarize the differences in VEGF availability that could contribute to the higher resistance of extraocular motoneurons to injury and neurodegenerative diseases.
Subject(s)
Amyotrophic Lateral Sclerosis/metabolism , Brain Stem/metabolism , Motor Neurons/metabolism , Oculomotor Nuclear Complex/metabolism , Vascular Endothelial Growth Factor A/metabolism , Animals , Humans , Neurodegenerative Diseases/metabolism , Neuroprotective Agents/metabolism , Vascular Endothelial Growth Factor Receptor-2/metabolismABSTRACT
Autophagy, the major pathway for protein turnover, is critical to maintain cellular homeostasis and has been implicated in neurodegenerative diseases. The aim of this research was to analyze the expression of autophagy markers in postmortem brains from Machado-Joseph disease (MJD) patients. The expression of autophagy markers in the cerebellum and the oculomotor nucleus from MJD patients and age-matched controls with no signs of neuropathology was inspected postmortem by immunohistochemistry (IHC) and Western blot. Furthermore, autophagy was examined by means of transmission electron microscopy (TEM). Western blot and IHC revealed nuclear accumulation of misfolded ataxin-3 (ATXN3) and the presence of ubiquitin- and p62-positive aggregates in MJD patients as compared to controls. Moreover, the autophagic proteins, autophagy-related gene (Atg) protein (ATG)-7, ATG-12, ATG16L2 and autophagosomal microtubule-associated protein light chain 3 (LC3) were significantly increased in MJD brains relative to controls, while beclin-1 levels were reduced in MJD patients. Increase in the levels of lysosomal-associated membrane protein 2 (LAMP-2) and of the endosomal markers (Rab7 and Rab1A) were observed in MJD patients relatively to controls. In addition, these findings were further confirmed by TEM in brain tissue where large vesicles accumulating electron-dense materials were highly enriched in MJD patients. Postmortem brains with MJD exhibit increased markers of autophagy relative to age-matched control brains, therefore suggesting strong dysregulation of autophagy that may have an important role in the course of MJD pathogenesis.
Subject(s)
Autophagy , Cerebellum/metabolism , Machado-Joseph Disease/metabolism , Oculomotor Nuclear Complex/metabolism , Adult , Ataxin-3/metabolism , Beclin-1/metabolism , Biomarkers/metabolism , Cell Adhesion Molecules, Neuronal/metabolism , Endosomes/metabolism , Female , GPI-Linked Proteins/metabolism , Humans , Lysosomes/metabolism , Male , Microtubule-Associated Proteins/metabolism , Middle Aged , Proto-Oncogene Proteins c-myc/metabolism , Sirolimus/metabolism , Ubiquitin/metabolismABSTRACT
The neuronal input-output function depends on recruitment threshold and gain of the firing frequency-current (f-I) relationship. These two parameters are positively correlated in ocular motoneurons (MNs) recorded in alert preparation and inhibitory inputs could contribute to this correlation. Phasic inhibition mediated by γ-amino butyric acid (GABA) occurs when a high concentration of GABA at the synaptic cleft activates postsynaptic GABAA receptors, allowing neuronal information transfer. In some neuronal populations, low concentrations of GABA activate non-synaptic GABAA receptors and generate a tonic inhibition, which modulates cell excitability. This study determined how ambient GABA concentrations modulate the input-output relationship of rat oculomotor nucleus MNs. Superfusion of brain slices with GABA (100 µm) produced a GABAA receptor-mediated current that reduced the input resistance, increased the recruitment threshold and shifted the f-I relationship rightward without any change in gain. These modifications did not depend on MN size. In absence of exogenous GABA, gabazine (20 µm; antagonist of GABAA receptors) abolished spontaneous inhibitory postsynaptic currents and revealed a tonic current in MNs. Gabazine increased input resistance and decreased recruitment threshold mainly in larger MNs. The f-I relationship shifted to the left, without any change in gain. Gabazine effects were chiefly due to MN tonic inhibition because tonic current amplitude was five-fold greater than phasic. This study demonstrates a tonic inhibition in ocular MNs that modulates cell excitability depending on cell size. We suggest that GABAA tonic inhibition acting concurrently with glutamate receptors activation could reproduce the positive covariation between threshold and gain reported in alert preparation.
Subject(s)
GABA-A Receptor Agonists/pharmacology , GABA-A Receptor Antagonists/pharmacology , Motor Neurons/physiology , Oculomotor Nuclear Complex/physiology , Action Potentials , Animals , Female , Male , Motor Neurons/drug effects , Motor Neurons/metabolism , Oculomotor Nuclear Complex/cytology , Oculomotor Nuclear Complex/metabolism , Pyridazines/pharmacology , Rats , Rats, Wistar , gamma-Aminobutyric Acid/pharmacologyABSTRACT
The distribution of the immunoreactivity for gamma-aminobutyric acid (GABA), choline acetyltransferase (ChAT), calcium-binding proteins (CaBPr) and histochemistry of cytochrome oxidase activity (CO) was studied in turtles (Testudo horsfieldi, Emys orbicularis) isthmal complex of visual nuclei. Magnocellular nucleus (IMc) was shown to reveal mainly the strongly stained GABA-, parvalbumin (PV)-ir neurons and CO-positive cells, as well as variable both in number and degree of intensity of ChAT-, cal- bindin (CB)-, and calretinin (CR)-ir cells. After the local tracer injection into the optic tectum GABA-ir neurons containing also retrograde label were found in IMc. The most caracteristic of the parvocellular nucleus (IPc) was the content of strongly stained ChAT-ir neurons, dense GABA-ir and CO-active terminal fields, as well as the neurons variable by the amount and the degree of immunoreactivity for CaBPr and GABA. Principal similarity in these features in the turtle IMc and IPc and of those in the avian isthmal nuclei of the same name allows suggesting their homology and consequently the same participation in selective processing of the visual information flow. The comparison with lower vertebrates confirms the evolutionary conservatism of visual isthmal complex among vertebrates and the existence of its progressive differentiation in the process of evolution.
Subject(s)
Calcium-Binding Proteins/metabolism , Choline O-Acetyltransferase/metabolism , Electron Transport Complex IV/metabolism , Oculomotor Nuclear Complex/metabolism , Visual Pathways/metabolism , gamma-Aminobutyric Acid/metabolism , Animals , Neurons/metabolism , Oculomotor Nuclear Complex/cytology , Organ Specificity , Species Specificity , Turtles , Visual Pathways/cytologyABSTRACT
Oculomotor deficits, such as insufficiencies in accommodation, convergence, and saccades, are common following traumatic brain injury (TBI). Previous studies in patients with mild TBI attributed these deficits to insufficient activation of subcortical oculomotor nuclei, although the exact mechanism is unknown. A possible cause for neuronal dysfunction in these regions is biomechanically induced plasma membrane permeability. We used our established porcine model of head rotational TBI to investigate whether cell permeability changes occurred in subcortical oculomotor areas following single or repetitive TBI, with repetitive injuries separated by 15 min, 3 days, or 7 days. Swine were subjected to sham conditions or head rotational acceleration in the sagittal plane using a HYGE pneumatic actuator. Two hours prior to the final injury, the cell-impermeant dye Lucifer Yellow was injected into the ventricles to diffuse throughout the interstitial space to assess plasmalemmal permeability. Animals were sacrificed 15 min after the final injury for immunohistological analysis. Brain regions examined for cell membrane permeability included caudate, substantia nigra pars reticulata, superior colliculus, and cranial nerve oculomotor nuclei. We found that the distribution of permeabilized neurons varied depending on the number and spacing of injuries. Repetitive injuries separated by 15 min or 3 days resulted in the most permeability. Many permeabilized cells lost neuron-specific nuclear protein reactivity, although no neuronal loss occurred acutely after injury. Microglia contacted and appeared to begin phagocytosing permeabilized neurons in repetitively injured animals. These pathologies within oculomotor areas may mediate transient dysfunction and/or degeneration that may contribute to oculomotor deficits following diffuse TBI.
Subject(s)
Brain Injuries, Diffuse/pathology , Brain Injuries, Traumatic/pathology , Cell Membrane/pathology , Neurons/pathology , Oculomotor Nuclear Complex/pathology , Animals , Brain/metabolism , Brain/pathology , Brain Injuries, Diffuse/metabolism , Brain Injuries, Traumatic/metabolism , Cell Membrane/metabolism , Female , Neurons/metabolism , Oculomotor Nuclear Complex/metabolism , SwineABSTRACT
Diazoxide (DZX), an anti-hypertonic and anti-hypoglycemic drug, was shown to have anti-inflammatory effects in several injured cell types outside the central nervous system. In the brain, the neuroprotective potential of DZX is well described, however, its anticipated anti-inflammatory effect after acute injury has not been systematically analyzed. To disclose the anti-inflammatory effect of DZX in the central nervous system, an injury was induced in the hypoglossal and facial nuclei and in the oculomotor nucleus by unilateral axonal transection and unilateral target deprivation (enucleation), respectively. On the fourth day after surgery, microglial analysis was performed on tissue in which microglia were DAB-labeled and motoneurons were labeled with immunofluorescence. DZX treatment was given either prophylactically, starting 7 days prior to the injury and continuing until the animals were sacrificed, or postoperatively only, with daily intraperitoneal injections (1.25 mg/kg; in 10 mg/ml dimethyl sulfoxide in distilled water). Prophylactically + postoperatively applied DZX completely eliminated the microglial reaction in each motor nuclei. If DZX was applied only postoperatively, some microglial activation could be detected, but its magnitude was still significantly smaller than the non-DZX-treated controls. The effect of DZX could also be demonstrated through an extended period, as tested in the hypoglossal nucleus on day 7 after the operation. Neuronal counts, determined at day 4 after the operation in the hypoglossal nucleus, demonstrated no loss of motor neurons, however, an increased Feret's diameter of mitochondria could be measured, suggesting increased oxidative stress in the injured cells. The increase of mitochondrial Feret's diameter could also be prevented with DZX treatment.
Subject(s)
Brain Stem/drug effects , Diazoxide/administration & dosage , Gliosis/drug therapy , Microglia/drug effects , Motor Neurons/drug effects , Vasodilator Agents/administration & dosage , Animals , Brain Stem/metabolism , Brain Stem/ultrastructure , Drug Administration Schedule , Facial Nucleus/drug effects , Facial Nucleus/metabolism , Facial Nucleus/ultrastructure , Gliosis/metabolism , Gliosis/pathology , Male , Mice , Mice, Inbred BALB C , Microglia/metabolism , Microglia/ultrastructure , Motor Neurons/metabolism , Motor Neurons/ultrastructure , Oculomotor Nuclear Complex/drug effects , Oculomotor Nuclear Complex/metabolism , Oculomotor Nuclear Complex/ultrastructure , Oxidative Stress/drug effects , Oxidative Stress/physiologyABSTRACT
Several efforts have been made to understand the involvement of rapid eye movement (REM) sleep for cognitive processes. Consolidation or retention of recognition memories is severely disrupted by REM sleep deprivation (REMSD). In this regard, pedunculopontine tegmental nucleus (PPT) and other brainstem nuclei, such as pontine nucleus (Pn) and oculomotor nucleus (OCM), appear to be candidates to take part in this REM sleep circuitry with potential involvement in cognition. Therefore, the objective of this study was to investigate a possible association between the performance of Wistar rats in a declarative memory and PPT, Pn, and OCM activities after different periods of REMSD. We examined c-Fos and choline acetyltransferase (ChaT) expressions as indicators of neuronal activity as well as a familiarity-based memory test. The animals were distributed in groups: control, REMSD, and sleep rebound (REB). At the end of the different REMSD (24, 48, 72, and 96 h) and REB (24 h) time points, the rats were immediately tested in the object recognition test and then the brains were collected. Results indicated that OCM neurons presented an increased activity, due to ChaT-labeling associated with REMSD that negatively correlated (r = -0.32) with the cognitive performance. This suggests the existence of a cholinergic compensatory mechanism within the OCM during REMSD. We also showed that 24 h of REMSD impacted similarly in memory, compared to longer periods of REMSD. These data extend the notion that REM sleep is influenced by areas other than PPT, i.e., Pn and OCM, which could be key players in both sleep processes and cognition.