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  • About
  • The Global ETD Search service is a free service for researchers to find electronic theses and dissertations. This service is provided by the Networked Digital Library of Theses and Dissertations.
    Our metadata is collected from universities around the world. If you manage a university/consortium/country archive and want to be added, details can be found on the NDLTD website.
101

Effects of electrical stimulation and testosterone on regeneration-associated gene expression and functional recovery in a rat model of sciatic nerve crush injury

Meadows, Rena Marie January 2014 (has links)
Indiana University-Purdue University Indianapolis (IUPUI) / Although peripheral motoneurons are phenotypically endowed with robust regenerative capacity, functional recovery is often suboptimal following peripheral nerve injury (PNI). Research to date indicates that the greatest success in achieving full functional recovery will require the use of a combinatorial approach that can simultaneously target different aspects of the post-injury response. In general, the concept of a combinatorial approach to neural repair has been established in the scientific literature but has yet to be successfully applied in the clinical situation. Emerging evidence from animal studies supports the use of electrical stimulation (ES) and testosterone as one type of combinatorial treatment after crush injury to the facial nerve (CN VII). With the facial nerve injury model, we have previously demonstrated that ES and testosterone target different stages of the regeneration process and enhance functional recovery after facial nerve crush injury. What is currently unknown, but critical to determine, is the impact of a combinatorial treatment strategy of ES and testosterone on functional recovery after crush injury to the sciatic nerve, a mixed sensory and motor spinal nerve which is one of the most serious PNI clinical problems. The results of the present study indicate that either treatment alone or in combination positively impact motor recovery. With regard to molecular effects,single and combinatorial treatments differentially alter the expression of regeneration-associated genes following sciatic nerve crush injury relative to facial nerve injury. Thus, our data indicate that not all injuries equally respond to treatment. Furthermore, the results support the importance of treatment strategy development in an injury-dependent manner and based upon the functional characteristics of spinal vs. cranial nerves.
102

Genetische Analyse des Tyrosinkinase-Rezeptors ErbB2

Woldeyesus, Masresha Tsegaye 14 February 2001 (has links)
ErbB2 gehört zu den Klasse I Rezeptor-Tyrosinkinasen und funktioniert als Ko-rezeptor bei der Vermittlung des Neuregulin-Signals. Während der Embryonal-entwicklung wird ErbB2 im Herzen, in den Neuralleistenzellen, im Muskel und in den Epithelien exprimiert (Kokai et al. 1987). Embryonen mit einer Null-Mutation im ErbB2 Gen sterben am Tag 10,5 der Embryonalentwicklung. Die Mutation bewirkt eine morphogenetische Fehlbildung des Herzens, die durch das Fehlen von ventrikulären Trabekeln gekennzeichnet ist (Lee et al. 1995). Weiterhin zeigen diese Embryonen Defekte in den Kranialganglien und in der primären sympathischen Ganglien-Kette, die von Neuralleistenzellen gebildet werden (Lee et al. 1995; Erickson et al. 1997; Britsch et al. 1998). Die herzspezifische Expression von ErbB2 cDNA ermöglicht ErbB2-/- Tieren, sich bis zur Geburt zu entwickeln. Dies erlaubte mir, spätere Funktionen des Rezeptors zu untersuchen. In den geretteten ErbB2-/- Embryonen erfolgte die Bildung der ventrikulären Trabekel, der fingerähnlichen Ausstülpungen des Myokards, zwischen dem 9. und 10. Tag in der Embryonalentwicklung. In den späteren Phasen der intrauterinen Entwicklung war das Herz der geretteten Tiere normal ausgebildet. In den ErbB2-/-R Embryonen fehlten Schwann'sche Zellen entlang der peripheren Nerven. Die Abwesenheit von Schwann'schen Zellen führte zum massiven Absterben von sensorischen und motorischen Neuronen des Rückenmarkes. Dabei zeigten sensorische Neuronen eine frühe Abhängigkeit von neurotrophen Faktoren, die von Schwann'schen Zellen produziert werden, während Motoneuronen diese Faktoren in einer späteren Phase benötigen. Zusätzlich ist bekannt, daß sensorische Neuronen und Motoneuronen neurotrophe Fakten benötigen, die von den Zielorganen, z.B. den Muskeln, produziert werden. Motoneuronen im thorakalen Rückenmark sind nur minimal betroffen, während die Degeneration von Moto-neuronen in den zervikalen und lumbalen Segmenten stark ausgeprägt ist. Verschiedene Motoneuron-Typen unterscheiden sich also in ihrer Abhängigkeit von neurotrophen Signalen. Weiterhin sind die peripheren Nerven der ErbB2-/-R Tiere defaszikuliert und ungeordnet. Der N. phrenicus, der das Diaphragma innerviert, retrahiert und ist am Tag 17 der Entwicklung vollständig degeneriert. Deshalb können die mutanten Tiere bei der Geburt nicht atmen und sterben infolgedessen. Überraschenderweise erfolgt in den geretteten ErbB2-/-R Embryonen die post-synaptische Expression und Aggregation der Acetylcholin-Rezeptoren. Die Phäno-typen der ErbB2-/-R und ErbB3-/- mutanten Tieren sind sehr ähnlich. Dies zeigt, daß ErbB2 eine essentielle Korezeptor-Funktion für ErbB3 in der Vermittlung der Neuregulin-Signale übernimmt. / ErbB2 belongs to class I of receptor tyrosine kinases and functions as a co-receptor by the transduction of the neuregulin signal. During embryonic development the ErbB2 gene is expressed in the heart, neural crest, in muscle and epithelial cells (Kokai et al. 1987). Embryos with null mutation of the ErbB2 gene die at midgestation. The mutation causes a morphogenetic defect that results in the absence of trabecules (Lee et al. 1995). In addition the mutant embryos show defects in cranial ganglia and in the primary sympathetic ganglia chain (Lee et al. 1995; Erickson et al. 1997; Britsch et al. 1998). The heart specific expression of ErbB2 cDNA allowed the mutant animals to survive till birth. This enabels me to study the late function of the receptor. In rescued ErbB2-/- embryos the ventricular trabecules, which are finger-like extensions of the myocardium, form properly between E9 and E10 of embryonic development. At late stages of intrauteral development the hearts of the rescued animals showed an overall normal growth. ErbB2-/- embryos lack Schwann cells along peripheral nerves. The absence of Schwann cells leads to enormous degeneration of sensory and motoneurons. Whereas sensory neurons show an early dependency on neurotrophic factors produced by Schwann cells, motoneurons revealed requirement of these factors during the late phase of their development. Moreover it is known that sensory and motoneurons require neurotrophic factors which are produced by their target tissues such as muscle. Motoneurons at the thoracic level of the spinal cord are minimaly affected, whereas the degeneration of motoneurons at cervical and lumbar segments of the spinal cord are pronounced. This indicates that different motoneuron types differ in their dependency on neurotrophic signals. Furthermore axons of peripheral nerves in ErbB2-/-R (rescued) animals show defasciculation and desorganization. Nervous phrenicus, that innervates the diaphragm muscle retracts and degenerates entirely at E17 of embryonic development. As a result newborn animals can not breath and die shortly after birth. Surprisingly, the expression and aggregation of AchRs (Acetylcholine Receptors) take place in rescued ErbB2-/-R embryos. The overall phenotype of ErbB2-/-R embryos is very similar to that of ErbB3-/- embryos. This substantiates the essential function of ErbB2 as the functional co-receptor for ErbB3 to transmit the neuregulin signal.
103

Modelování Huntingtonovy choroby a bněčná terapie při poškození míchy. / Huntington's disease modeling and stem cell therapy in spinal cord disorders and injury

Hruška-Plocháň, Marián January 2013 (has links)
Neurological disorders affect more than 14% of the population worldwide and together with traumatic brain and spinal cord injuries represent major health, public and economic burden of the society. Incidence of inherited and idiopathic neurodegenerative disorders and acute CNS injuries is growing globally while neuroscience society is being challenged by numerous unanswered questions. Therefore, research of the CNS disorders is essential. Since animal models of the CNS diseases and injuries represent the key step in the conversion of the basic research to the clinics, we focused our work on generation of new animal models and on their use in pre-clinical research. We generated and characterized transgenic minipig model of Huntington's disease (HD) which represents the only successful establishment of a transgenic model of HD in minipig which should be valuable for testing of long term safety of HD therapeutics. Next, we crossed the well characterized R6/2 mouse HD model with the gad mouse model which lacks the expression of UCHL1 which led to results that support the theory of "protective" role of mutant huntingtin aggregates and suggest that UCHL1 function(s) may be affected in HD disturbing certain branches of Ubiquitin Proteasome System. Traumatic spinal cord injury and Amyotrophic Lateral...
104

Optical Analysis of [Ca<sup>2+</sup>]i and Mitochondrial Signaling Pathways: Implications for the Selective Vulnerability of Motoneurons in Amyotrophic Lateral Sclerosis (ALS) / Optische Analysen von [Ca<sup>2+</sup>]i und mitochondrialen Signalwegen: Untersuchungen zur selektiven Verwundbarkeit von Motoneuronen in der amyotrophen Lateralsklerose (ALS)

Jaiswal, Manoj Kumar 23 January 2008 (has links)
No description available.
105

Evaluation neuroprotektiver Strategien am Beispiel ausgewählter neurodegenerativer Erkrankungen: Amyotrophe Lateralsklerose und Alkoholabhängigkeit / Evaluating neuroprotective strategies in neurodegenerative diseases: amyotrophic lateral sclerosis and alcohol dependence

Bartels, Claudia 02 May 2007 (has links)
No description available.

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