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1.
Neurobiol Dis ; 45(3): 992-8, 2012 Mar.
Article in English | MEDLINE | ID: mdl-22198571

ABSTRACT

Spinal muscular atrophy (SMA) is an autosomal recessive neuromuscular disease, which is the leading genetic cause of mortality in children. To date no effective treatment exists for SMA. The genetic basis for SMA has been well documented as a mutation in the gene for survival of motor neuron (SMN). Because there is an understanding of which gene needs to be replaced (SMN) and where it needs to be replaced (spinal motor systems), SMA is an ideal target for gene replacement via gene therapy. While a variety of animal models for SMA exist, they are either too fulminant to realistically test most gene delivery strategies, or too mild to provide a robust read out of the therapeutic effect. The field, therefore, requires a robust model with a slower symptomatic progression. A conditional knockout of SMN in neuronal cell types, giving a phenotype of functional motor defects, weight loss and reduced life expectancy partially satisfies this need (Frugier, Tiziano et al. 2000). This Cre/LoxP mediated neuron specific model presents an attractive alternative. In the present manuscript, we characterize the functional motor deficits of the model. We observed a decline in locomotor ability, as assessed by open field testing. The finer functions of motor skills such as righting reflex and grip strength were also observed to degenerate in the SMA mice. The decline in motor function that we observed here correlates with the anatomical decline in motor neurons and motor axons presented in the literature (Ferri, Melki et al. 2004). This work adds to our understanding and knowledge base of this Cre/LoxP model and provides a basis from which functional recovery, following interventions can be assessed.


Subject(s)
Disease Models, Animal , Muscular Atrophy, Spinal/pathology , Muscular Atrophy, Spinal/physiopathology , Mutation , Age Factors , Animals , Exploratory Behavior/physiology , Functional Laterality/genetics , Genotype , Hand Strength/physiology , Mice , Mice, Transgenic , Motor Activity/genetics , Motor Neurons/pathology , Muscular Atrophy, Spinal/genetics , Muscular Atrophy, Spinal/mortality , Statistics as Topic , Survival of Motor Neuron 2 Protein/genetics
2.
Stereotact Funct Neurosurg ; 89(5): 275-85, 2011.
Article in English | MEDLINE | ID: mdl-21849811

ABSTRACT

BACKGROUND/AIMS: Expression of the neuropeptide galanin in hippocampal neurons reduces seizures in the kainic acid rodent model of epilepsy. In order to translate these findings into a human clinical trial, the safety and feasibility of hippocampal adeno-associated viral (AAV) vector expression must be demonstrated in a nonhuman primate model. METHODS: The Stealth Frameless Stereotactic System and Navigus Biopsy Appliance (Medtronic) were used to inject self-complementary AAV2 carrying the gene for green fluorescent protein (GFP) into monkey hippocampi. Using a single occipital trajectory per side (n = 8 trajectories), multiple injections spaced by 5 mm were delivered to each hippocampus. RESULTS: GFP was expressed in both neuronal and glial cells. Injections led to nonhomogeneous gene expression, suggesting closer spacing of injections may lead to more gene expression. Increasing injection volumes entailed a general increase in volume of expression, but there was no overlap of expression within the 5-mm injection interval. Efforts to avoid the occipital horn failed to prevent leaking of vector into the ventricle, and resulted in deviation of the trajectory at proximal points from the hippocampus. CONCLUSION: Using the occipital approach, adequate cannulation of the monkey hippocampus will require transventricular trajectories.


Subject(s)
Dependovirus/genetics , Gene Transfer Techniques , Genetic Vectors/genetics , Hippocampus , Neuronavigation/methods , Animals , Gene Transfer Techniques/instrumentation , Genetic Vectors/administration & dosage , Green Fluorescent Proteins/administration & dosage , Green Fluorescent Proteins/genetics , Hippocampus/metabolism , Hippocampus/virology , Macaca mulatta , Male
3.
Amyotroph Lateral Scler ; 12(5): 331-9, 2011 Sep.
Article in English | MEDLINE | ID: mdl-21864053

ABSTRACT

Amyotrophic lateral sclerosis (ALS) is characterized by motor neuron loss leading to paralysis and death. Vascular endothelial growth factor (VEGF) has angiogenic, neurotrophic, and neuroprotective properties, and has preserved neuromuscular function and protected motor neurons in rats engineered to overexpress the human gene coding the mutated G93A form of the superoxide dismutase-1 (SOD1). We assessed the effects of intramuscular administration of a plasmid that encodes a zinc finger protein transcription factor (ZFP-TF) engineered to induce VEGF expression in the SOD1 rat model of ALS. Weekly injections of the plasmid preserved ipsilateral hindlimb grip strength and markedly improved rotarod performance in SOD1 rats compared to the vehicle-treated group. The number of motor neurons and the proportion of innervated neuromuscular junctions were similar in both groups. In conclusion, our data suggest that administration of the VEGF-ZFP-TF may be neuroprotective and has potential as a safe and practical approach for the management of motor disability in ALS.


Subject(s)
Amyotrophic Lateral Sclerosis/therapy , Genetic Therapy , Superoxide Dismutase/genetics , Transcription Factors/administration & dosage , Vascular Endothelial Growth Factor A/administration & dosage , Zinc Fingers , Amyotrophic Lateral Sclerosis/genetics , Amyotrophic Lateral Sclerosis/metabolism , Animals , Disease Models, Animal , Female , Genetic Therapy/methods , Humans , Injections, Intramuscular , Male , Muscle, Skeletal/physiology , Rats , Rats, Transgenic , Superoxide Dismutase/biosynthesis , Superoxide Dismutase/physiology , Superoxide Dismutase-1 , Transcription Factors/genetics , Transcription Factors/physiology , Vascular Endothelial Growth Factor A/genetics , Vascular Endothelial Growth Factor A/physiology , Zinc Fingers/genetics
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