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<p dir="ltr">Papilledema is the swelling of the optic disc resulting from increased cranial pressure. The diagnosis of papilledema is important not only to treat pathologies of the eye, but it also can be an important indicator for underlying brain pathology since the subarachnoid space surrounding the optic nerve is contiguous with the brain. Therefore increased pressure from the brain from pathologies such as hydrocephalus can be transmitted to the posterior eye. To study papilledema, a reproducible post hemorrhagic hydrocephalic rat model was used to study the changes of the retina, optic disc and optic nerve when exposed to high intracranial pressure. Multiple changes were noted in the post hemorrhagic hydrocephalic model including decreased thickness of the ganglion cell complex, decreased retinal thickness in the periphery in females, increased retinal thickness close to the optic nerve in males, increased optic disc width and diameter along with a decrease number of retinal ganglion cells. These findings were similar to findings in human patients with papilledema. Therefore, future studies are indicated using the post hemorrhagic hydrocephalic rat model to further understand the mechanism of papilledema progression and the use of possible therapeutics.</p>

For glutamate and the developing optic pathway, glutamate and its ionotropic receptor subunits are expressed widely in retina and ventral diencephalon, and in cells that are related to the chiasm formation. These studies indicate that glutamate may act as a communicator or attractor to coordinate with other factors to affect the retinal axon pathfinding in the prenatal optic pathway. / Furthermore, for the function of glutamate, AMPARs and KARs in the optic chiasm formation, we did retinal explant culture experiment at E14 in vitro, with application of different concentration of L-glutamate (500muM -1mM), AMPAR antagonists: CP465022 hydrochloride (2-20muM) and GYK15466 dihydrochloride (25-150muM), and KAR antagonists: CNQX (50-500muM) and UBP301 (5-25muM). The results show that L-glutamate promotes retinal axon outgrowth; AMPA receptor antagonists inhibit that; and KAR antagonists have no effect on that. In the presence of different combinations of ionotropic receptor antagonists (including NMDAR antagonist), they suggest that the blockage of glutamate iontroptic receptors displays an obvious effect of inhibiting neurite outgrowth in E14 retinal explants. However, inhibiting kainate receptors show little effect on retinal neurite outgrowth which is different from that of blocking AMPARs. We also did E13 and E15 brain slice culture experiments, and found that blocking of glutamate ionotropic receptors affects crossed axon projection in the midline at early stage, but has no effect to the uncrossed one. / Glutamate is the dominant amino acid neurotransmitter in the central nervous system naturally occurring in the L-form. Glutamate ionotropic receptors can be further a-amino-3-hydroxy-5-methy1-4-isoxazole-propionate divided into three types by their ligand (AMPA, specificities: GluR1-4), N-methyl-D-aspartate (NMDA, NR1-3) and kainate (KA, GluR5-7 and KA1-2) receptors, which function as ligand-gated ion channels. In this study, we focus on the AMPARs and KARs which are expressed in the developing brain. / Here, we used semi-quantitative RT-PCR to analyze mRNA expression levels of AMPAR and KAR subunits in the mouse retina and ventral diencephalons at different developmental stages, and in adult retina. The results show that both AMPAR and KAR subunits can be detected in retina and ventral diencephalon at as early as E13. We also used specific antibodies to investigate glutamate, AMPAR and KAR subunit expression in the mouse retinofugal pathway. We found that: 1) Glutamate is expressed at as early as E13. In retina, it tends to localize in retinal ganglion cells (RGCs) and their axons; in ventral diencephalon, it is most intense in optic stalk, optic chiasm and optic tract. It is also localized with chiasmatic neurons, which are related to the formation of optic chiasm. 2) For the individual AMPAR and KAR subunits, all of them are expressed at as early as E13. The immunoreactive GluRl and GluR5/6/7 are distributed preferentially in the RGCs and their axons; the staining of GluR2/3 and GluR4 are largely found in RGCs and the supporting cells around the pathway, but for GluR4, its staining is weakly detected in optic fibers and strongly in the midline of chiasm. Although the staining patterns of these specific subunits are different, they are all localized in chiasmatic neurons in diencephalon. / Cheng, Xiaojing. / "November 2010." / Adviser: Sun On Chan. / Source: Dissertation Abstracts International, Volume: 73-04, Section: B, page: . / Thesis (Ph.D.)--Chinese University of Hong Kong, 2011. / Includes bibliographical references (leaves 137-152). / Electronic reproduction. Hong Kong : Chinese University of Hong Kong, [2012] System requirements: Adobe Acrobat Reader. Available via World Wide Web. / Electronic reproduction. [Ann Arbor, MI] : ProQuest Information and Learning, [201-] System requirements: Adobe Acrobat Reader. Available via World Wide Web. / Abstract also in Chinese.

[Truncated abstract] There is limited intrinsic potential for repair in the adult human central nervous system (CNS). Dysfunction resulting from CNS injury is persistent and requires prolonged medical treatment and rehabilitation. The retina and optic nerve are CNSderived, and adult retinal ganglion cells (RGCs) and their axons are often used as a model in which to study the mechanisms associated with injury, neuroprotection and regeneration. In this study I investigated the effects of a variety of strategies on promoting RGC survival and axonal regeneration after optic nerve injury, including the use of reconstructed chimeric peripheral nerve (PN) grafts, gene therapy, and intraocular application of pharmacological agents and other factors . . . C3 transferase is an enzyme derived from Clostridium botulinum that inactivates Rho GTPase. Because SC myelin contains MAG and PN also contains CSPGs, I tested the effects of intraocular injection of a modified form of C3 (C3-11), provided by Dr Lisa McKerracher (CONFIDENTIAL data, under IP agreement with Bioaxone Therapeutic, Montreal) on RGC axonal regeneration into PN autografts. My results showed that there was significantly more RGC survival and axonal regeneration in PN autografts after repeated intraocular injection of C3. I also tested whether intraocular injections of CPT-cAMP and/or CNTF can act in concert with the C3 to further increase RGC survival and/or regeneration. Results showed that the effect of C3 and CPT-cAMP plus CNTF were synergistic and partially additive. The use of combination therapies therefore offers the best hope for robust and substantial regeneration. The overall results from my PhD project will help determine how best to reconstruct nerve pathways and use pharmacological interventions in the clinical treatment of CNS injury, hopefully leading to improved functional outcomes after neurotrauma.

A deficiência de ferro é a carência nutricional mais frequente no mundo, uma vez que a população de crianças é uma das que mais sofre com essa condição. É sabido que o desenvolvimento cerebral é determinado não apenas por um plano genético, mas sim por uma forte interação de fatores genéticos e ambientais. Evidências emergentes sugerem que a estimulação precoce pode oferecer grande eficácia terapêutica, uma vez que o cérebro é notavelmente responsivo a essa interação com o ambiente. Dado que a estimulação tátil (TS) tem sido previamente demonstrada ser uma abordagem terapêutica eficaz e com potencial aplicação em seres humanos, o objetivo deste estudo foi verificar se a exposição à estimulação tátil desde o dia pós-natal (P) 1 até P32 durante 3 min/dia, poderia ser utilizada para prevenir alterações estruturais do nervo óptico de ratos mantidos com uma dieta deficiente em ferro durante o desenvolvimento pós-natal. Foram utilizados 72 ratos machos recém-nascidos (Wistar), sendo que as ratas-lactantes foram mantidas com dieta isocalórica com 35mg/Fe por kg de ração (Grupo ANTS) ou com 4mg/Fe por kg de ração (Grupo DNTS) durante todo o período de lactação e os filhotes receberam a dieta de suas respectivas ratas-lactantes após o desmame (P22-32). Metade dos filhotes de cada grupo foi submetida à TS diária (Grupo ATS e DTS), durante todo o período experimental (P01-32). Foram realizadas análises estrutural e ultraestrutural, em 3 diferentes idades, para avaliar a integridade tecidual e também a fim de determinar se as mudanças observadas na citoarquitetura do nervo óptico foram significativamente diferentes entre os grupos e idades. Verificou-se que os animais mantidos com dieta deficiente em ferro apresentaram baixo peso corporal a partir do desmame, revelando uma curva de crescimento menos acentuada. A baixa concentração de hemoglobina e hematócritos indicam que esses animais sofreram com anemia severa em todos os períodos estudados. A análise ultraestrutural qualitativa mostrou que a deficiência de ferro imposta durante o período crítico do desenvolvimento leva a sérios danos as fibras das células ganglionares da retina, com efeitos sobre o envoltório de mielina que frequentemente apresentou afrouxamento lamelar e em idades mais avançadas foram encontradas degenerações mielínicas e axonais. A análise ultraestrutural quantitativa mostrou que a dieta deficiente em ferro leva a um atraso no processo de mielinização que pode ser parcialmente revertido pelo tratamento com estimulação tátil. Além disso, fica claro que as fibras de menor diâmetro são mais sensíveis às lesões geradas pela deficiência de ferro e também ao tratamento, enquanto que as fibras de maior diâmetro são afetadas de forma desproporcional tanto pela deficiência de ferro quanto pela estimulação tátil. As lesões sugerem que a transmissão dos sinais elétricos pode estar prejudicada, interferindo com as funções normais do sistema visual. / Iron deficiency has a critical impact on maturational mechanisms of the brain and the damage related to neuroanatomical parameters is not satisfactorily reversed after iron replacement. However, emerging evidence suggest that enriched early experience may offer great therapeutic efficacy in cases of nutritional disorders postnatally, since the brain is remarkably responsive to its interaction with the environment. Given the fact that tactile stimulation (TS) treatment has been previously shown to be an effective therapeutic approach and with potential application to humans, here we ask whether exposure to TS treatment, from postnatal day (P) 1 to P32 for 3 min/day, could also be employed to prevent neuroanatomical changes in the optic nerve of rats maintained on an iron-deficient diet during brain development. It was verified that the animals maintained with iron deficient diet presented low weight from the weaning, revealing a lower growth curve. The low concentration of hemoglobin and hematocrits indicate that these animals suffered from severe anemia in all studied periods. The qualitative ultrastructural analysis showed that the iron deficiency imposed during the critical period of development leads to serious damage to the fibers from retinal ganglion cells, with effects on the myelin sheath that frequently presented lamellar loosening and myelin degenerations and axonal at more advanced age. Quantitative ultrastructural analysis has shown that the iron deficient diet leads to a delay in the myelination process that can be partially reversed by treatment with tactile stimulation. In addition, it is clear that the smaller diameter fibers are more sensitive to the iron deficiency and also to the treatment, whereas the larger fibers are disproportionately affected by both iron deficiency and tactile stimulation. The lesions suggest that the transmission of electrical signals may be impaired, interfering with the normal functions of the visual system.

Diante da deficiência de ferro que leva a processos degenerativos do sistema nervoso central e da estimulação tátil neonatal como uma estratégia não invasiva e promissora para atenuar os déficits causados pela degeneração, assim, justifica-se comparar em ratos submetidos à dieta deficiente em ferro (A - 4mg/kg) ou dieta adequada em ferro (C - 35mg/kg) os efeitos da estimulação tátil neonatal, em relação aos aspectos morfológicos e morfométricos das células gliais, fibras mielínicas e vasos sanguíneos do nervo óptico, aos 18, 22 e 32 dias de idade. Foram utilizadas 12 ninhadas de ratos Wistar, compostas por 12 ratas-mãe e 72 filhotes machos recém-nascidos, que por sua vez, foram divididos em dois grupos de acordo com a dieta submetida às ratas-mãe (A e C). Metade das ninhadas do grupo A e C foram submetidas à estimulação tátil (E) e a outra metade não recebeu nenhuma forma de estímulo (N). Resultando, portanto, nos seguintes grupos experimentais: grupo controle não estimulado (CN), grupo controle estimulado (CE), grupo anêmico não estimulado (AN), e grupo anêmico estimulado (AE), cada grupo foi composto por 3 ratas-mães e 18 filhotes. Aos 18, 22 e 32 dias de vida, seis animais de cada grupo experimental foram profundamente anestesiados e perfundidos por via transcardíaca. Os nervos ópticos foram cuidadosamente dissecados com o auxílio de um estereomicroscópio (Stemi DRC, Carl Zeiss) e esses fragmentos foram refixados em tetróxido de ósmio a 1% em tampão fosfato e então processados para inclusão em araldite. Na análise dos aspectos morfológicos dos nervos ópticos dos ratos do grupo AN, foi observada grande quantidade de fibras com aumento do diâmetro axônal indicando aumento de líquido intracelular e, por conseguinte edema axônal. Ainda, foram encontradas bainhas de mielina desconfiguradas, caracterizando frouxidão lamelar ou desprendimento da bainha de mielina de seu axônio, além do mais, é notório o aumento de espaços entre as fibras. Os astrócitos e os oligodendrócitos também demonstravam sinais claros de sofrimento celular, apresentando deformidades da membrana nuclear, como invaginação ou irregularidade do envelope nuclear. Os nervos ópticos dos ratos anêmicos e submetidos à estimulação neonatal apresentaram diminuição dos efeitos deletérios da deficiência de ferro. Não houve diferença das características dos nervos ópticos dos grupos CN e CE. De acordo com o resultado de quantificação de células gliais, constata-se que os animais alimentados com dieta inadequada em ferro apresentaram maior quantidade de astrócitos e menor quantidade de oligodendrócitos em todas as idades estudadas e essas medidas não são alteradas pela estimulação tátil neonatal. A quantificação de vasos sanguíneos mostra que a dieta deficiente em ferro não tem qualquer efeito sobre a densidade de vasos, entretanto a estimulação tátil neonatal aumenta significativamente o número de vasos no nervo óptico. A quantificação revelou grande aumento de fibras nervosas mielínicas lesadas nos animais que se alimentaram com dieta deficiente em ferro e também revelou que a estimulação tátil neonatal diminui o número de fibras lesadas. Os dados do presente estudo mostram que animais alimentados com dieta deficiente em ferro sofrem alterações celulares importantes durante o desenvolvimento pós-natal precoce do nervo óptico quando comparados com controle. Também é possível notar que a estimulação tátil neonatal, realizada no período crítico do desenvolvimento do SNC foi eficaz, minimizando a quantidade de fibras mielínicas lesadas e aumentando a quantidade de vasos sanguíneos. / Previous studies showed that iron deficiency leads to degenerative processes in the CNS and neonatal tactile stimulation is a noninvasive and promising strategy to attenuate the deficits caused by the degeneration, it is important to compare in rats, subjected to iron-deficient diet (A - 4mg/kg) or iron-adequate diet (C - 35mg/kg), the effects of neonatal tactile stimulation on the morphometric aspects of the optic nerve, such as the quantification of glial cells, blood vessels and myelinated fibers, at 18, 22 and 32 days of age. A total of twelve litters of Wistar rats was used, consisting of 12 dam and 72 male newborns, which were divided into two groups according to the diet given to the dam (A and C). Half of the litters in group A and C was subjected to tactile stimulation (E) and the other half received no stimulation (N). Finally, resulting in four experimental groups: non-stimulated control group (CN), stimulated control group (CE), the non-stimulated anemic group (AN), and the stimulated anemic group (AE), each group consisted of 3 dam and 18 pups. At 18, 22 and 32 days of life, six pups of each group was anesthetized and sacrificed by transcardiac perfusion. The optic nerve of the pups was dissected and immersed in 1% osmium tetroxide and embedded in araldite. Morphological analysis of the AN group showed that a large amount of fibers with increased axonal diameter which indicates excessive intracellular fluid and therefore axonal swelling. Furthermore, it was found disarranged myelin sheaths, characterized by lamellar loose or myelin detached from its axon. In addition, there was an increase of spaces between the fibers. Astrocytes and oligodendrocytes also showed clear signs of cell suffering, with deformities of the nuclear membrane, such as invagination or irregularity of the nuclear envelope. The analysis of the AE group showed a decrease of the deleterious effects of iron deficiency. There was no difference in the characteristics of the optic nerves of CN and CE groups. According to the result of glial cells quantification, it was found that animals fed with iron-deficient diet had a higher amount of astrocytes and a lower amount of oligodendrocytes at all ages studied, and these numbers were not altered by tactile stimulation. The blood vessels quantification shows that the iron-deficient diet has no effect on the vessel density, however, the neonatal tactile stimulation increased significantly the number of vessels in optic nerve. Morphometry showed a significant increase of the number of damaged fibers on optic nerve of animals that were fed with iron-deficient diet and neonatal tactile stimulation reduced the number of damaged fibers in these animals. The present study showed that animals fed with iron-deficient diet presented significant cellular changes during the early postnatal development of the optic nerve compared with their paired controls. It was also noted that the neonatal tactile stimulation, performed during the critical period of development of the CNS was effective, minimizing the amount of damaged fibers and increasing the amount of blood vessels.

Le récepteur aux hydrocarbures aromatiques (AhR) est un facteur de transcription activé par de nombreux xénobiotiques (molécules étrangères à l’organisme) qui régule l’expression d’enzymes et transporteurs permettant le métabolisme et l’élimination de ces ligands. Cette protéine exprimée dans toutes les cellules chez les vertébrés, joue un rôle majeur dans la détoxication et la protection des organismes vis à vis des molécules toxiques. Des orthologues de celle-ci ont été identifiés chez les invertébrés mais ne semblent pas jouer le même rôle; ils sont exprimés principalement dans des neurones et ne sont pas activés par des polluants. L’absence du AhR chez ces organismes entraîne au niveau cellulaire, des défauts de morphologie dendritique et sur le plan comportemental, des anomalies dans le comportement de nutrition. Malgré ces découvertes, peu de recherches ont été entreprises sur les conséquences d’une invalidation du AhR sur le fonctionnement du système nerveux central chez les vertébrés. Au cours de ma thèse, j’ai étudié ces conséquences au niveau moléculaire, cellulaire et comportemental: les souris AhR KO développent un nystagmus pendulaire horizontal dont l’origine est en partie liée à des défauts structuraux de la gaine de myéline. Au niveau moléculaire, nous avons mis en évidence un changement de la composition lipidique, de l’expression des gènes de la myéline et de l’inflammation, défauts qui sont retrouvés en partie chez des souris dont le AhR a été invalidé spécifiquement dans l’oligodendrocyte, la cellule responsable de la formation de la gaine de myéline. J’ai donc réalisé des études en parallèle sur la lignée murine d’oligodendrocyte, 158N, et montré que l’invalidation du AhR dans cette lignée ainsi que in vivo, modifiait l’expression du gène MAG (Myelin Associated Glycoprotein). Compte tenu du rôle du AhR en tant que récepteur de polluants, nous avons également exposé ou traité nos modèles avec de la TCDD (dioxine de Seveso) et montré que celle-ci modifiait également l’expression du gène MAG. Mes travaux démontrent donc que le AhR joue un rôle au niveau oligodendrocytaire dans la formation de la gaine de myéline. Son rôle connu en tant que récepteur de polluants laisse supposer que certaines contaminations environnementales pourraient jouer un rôle dans l’incidence de pathologies au niveau du système nerveux central, ce qui soulève de nombreuses questions en terme de santé publique. / The aryl hydrocarbon receptor (AhR) is a transcription factor activated by many xenobiotics (foreign molecules) that regulates the expression of enzymes and transporters which allow the metabolism and elimination of these ligands. This protein expressed in all cells in vertebrates, plays a major role in detoxication and protection of the organisms against toxic molecules. Some orthologs have been identified in invertebrates but do not seem to play the same role; they are expressed mainly in neurons and are not activated by pollutants. The absence of the AhR in these organisms causes at the cellular level, defects of the dendritic morphology and behaviourally, abnormalities in the feeding behavior. Despite these findings, little research has been conducted on the consequences of the AhR invalidation in the central nervous system of vertebrates. During my PhD, I studied these consequences at the molecular, cellular and behavioral : the AhR knockout mice develop a horizontal pendular nystagmus whose origin is partly related to structural defects in the myelin sheath. At the molecular level, we have shown modifications in the lipid composition, myelin and inflammation gene expression, defects that are found partly in mice whose AhR was invalidated specifically in the oligodendrocytes, the cells involved in myelin sheath formation. I therefore made parallel studies on the murine oligodendrocyte lineage, 158N, and showed that the invalidation of the AhR in this cell line and in vivo, altered MAG (Myelin Associated Glycoprotein) gene expression. Given the role of the AhR as a receptor of pollutants, we have also exposed or treated our models with TCDD (dioxin of Seveso) and showed that it also changed the expression of MAG gene. My works show that the AhR is involved in oligodendrocyte level in the formation of the myelin sheath. As the AhR is also a receptor of pollutants, some environmental contaminants may play a role in the incidence of diseases in the central nervous system, which raises many issues in terms of public health.

Su Huan Xing. / Thesis (M.Phil.)--Chinese University of Hong Kong, 2002. / Includes bibliographical references (leaves 79-89). / Abstracts in English and Chinese. / Abstract --- p.i / 中文摘要 --- p.iii / Acknowledgements --- p.iv / Abbreviations Frequently Used --- p.v / Table of contents --- p.vi / Chapter Chapter1 --- General Introduction --- p.1 / Chapter Chapter2 --- Effects of an intravitreal optic nerve graft on the sprouting and regeneration of axotomized retinal ganglion cells --- p.17 / Chapter Chapter3 --- Effects of an intravitreal pre-injured optic nerve graft on the sprouting and regeneration of axotomized retinal ganglion cells --- p.44 / Chapter Chapter4 --- Effects of co-transplantation of an optic nerve graft and a peripheral nerve graft into the vitreous body on the sprouting and regeneration of axotomized retinal ganglion cells --- p.60 / Chapter Chapter5 --- General discussion --- p.74 / References --- p.79 / Tables --- p.90

Diante da deficiência de ferro que leva a processos degenerativos do sistema nervoso central e da estimulação tátil neonatal como uma estratégia não invasiva e promissora para atenuar os déficits causados pela degeneração, assim, justifica-se comparar em ratos submetidos à dieta deficiente em ferro (A - 4mg/kg) ou dieta adequada em ferro (C - 35mg/kg) os efeitos da estimulação tátil neonatal, em relação aos aspectos morfológicos e morfométricos das células gliais, fibras mielínicas e vasos sanguíneos do nervo óptico, aos 18, 22 e 32 dias de idade. Foram utilizadas 12 ninhadas de ratos Wistar, compostas por 12 ratas-mãe e 72 filhotes machos recém-nascidos, que por sua vez, foram divididos em dois grupos de acordo com a dieta submetida às ratas-mãe (A e C). Metade das ninhadas do grupo A e C foram submetidas à estimulação tátil (E) e a outra metade não recebeu nenhuma forma de estímulo (N). Resultando, portanto, nos seguintes grupos experimentais: grupo controle não estimulado (CN), grupo controle estimulado (CE), grupo anêmico não estimulado (AN), e grupo anêmico estimulado (AE), cada grupo foi composto por 3 ratas-mães e 18 filhotes. Aos 18, 22 e 32 dias de vida, seis animais de cada grupo experimental foram profundamente anestesiados e perfundidos por via transcardíaca. Os nervos ópticos foram cuidadosamente dissecados com o auxílio de um estereomicroscópio (Stemi DRC, Carl Zeiss) e esses fragmentos foram refixados em tetróxido de ósmio a 1% em tampão fosfato e então processados para inclusão em araldite. Na análise dos aspectos morfológicos dos nervos ópticos dos ratos do grupo AN, foi observada grande quantidade de fibras com aumento do diâmetro axônal indicando aumento de líquido intracelular e, por conseguinte edema axônal. Ainda, foram encontradas bainhas de mielina desconfiguradas, caracterizando frouxidão lamelar ou desprendimento da bainha de mielina de seu axônio, além do mais, é notório o aumento de espaços entre as fibras. Os astrócitos e os oligodendrócitos também demonstravam sinais claros de sofrimento celular, apresentando deformidades da membrana nuclear, como invaginação ou irregularidade do envelope nuclear. Os nervos ópticos dos ratos anêmicos e submetidos à estimulação neonatal apresentaram diminuição dos efeitos deletérios da deficiência de ferro. Não houve diferença das características dos nervos ópticos dos grupos CN e CE. De acordo com o resultado de quantificação de células gliais, constata-se que os animais alimentados com dieta inadequada em ferro apresentaram maior quantidade de astrócitos e menor quantidade de oligodendrócitos em todas as idades estudadas e essas medidas não são alteradas pela estimulação tátil neonatal. A quantificação de vasos sanguíneos mostra que a dieta deficiente em ferro não tem qualquer efeito sobre a densidade de vasos, entretanto a estimulação tátil neonatal aumenta significativamente o número de vasos no nervo óptico. A quantificação revelou grande aumento de fibras nervosas mielínicas lesadas nos animais que se alimentaram com dieta deficiente em ferro e também revelou que a estimulação tátil neonatal diminui o número de fibras lesadas. Os dados do presente estudo mostram que animais alimentados com dieta deficiente em ferro sofrem alterações celulares importantes durante o desenvolvimento pós-natal precoce do nervo óptico quando comparados com controle. Também é possível notar que a estimulação tátil neonatal, realizada no período crítico do desenvolvimento do SNC foi eficaz, minimizando a quantidade de fibras mielínicas lesadas e aumentando a quantidade de vasos sanguíneos. / Previous studies showed that iron deficiency leads to degenerative processes in the CNS and neonatal tactile stimulation is a noninvasive and promising strategy to attenuate the deficits caused by the degeneration, it is important to compare in rats, subjected to iron-deficient diet (A - 4mg/kg) or iron-adequate diet (C - 35mg/kg), the effects of neonatal tactile stimulation on the morphometric aspects of the optic nerve, such as the quantification of glial cells, blood vessels and myelinated fibers, at 18, 22 and 32 days of age. A total of twelve litters of Wistar rats was used, consisting of 12 dam and 72 male newborns, which were divided into two groups according to the diet given to the dam (A and C). Half of the litters in group A and C was subjected to tactile stimulation (E) and the other half received no stimulation (N). Finally, resulting in four experimental groups: non-stimulated control group (CN), stimulated control group (CE), the non-stimulated anemic group (AN), and the stimulated anemic group (AE), each group consisted of 3 dam and 18 pups. At 18, 22 and 32 days of life, six pups of each group was anesthetized and sacrificed by transcardiac perfusion. The optic nerve of the pups was dissected and immersed in 1% osmium tetroxide and embedded in araldite. Morphological analysis of the AN group showed that a large amount of fibers with increased axonal diameter which indicates excessive intracellular fluid and therefore axonal swelling. Furthermore, it was found disarranged myelin sheaths, characterized by lamellar loose or myelin detached from its axon. In addition, there was an increase of spaces between the fibers. Astrocytes and oligodendrocytes also showed clear signs of cell suffering, with deformities of the nuclear membrane, such as invagination or irregularity of the nuclear envelope. The analysis of the AE group showed a decrease of the deleterious effects of iron deficiency. There was no difference in the characteristics of the optic nerves of CN and CE groups. According to the result of glial cells quantification, it was found that animals fed with iron-deficient diet had a higher amount of astrocytes and a lower amount of oligodendrocytes at all ages studied, and these numbers were not altered by tactile stimulation. The blood vessels quantification shows that the iron-deficient diet has no effect on the vessel density, however, the neonatal tactile stimulation increased significantly the number of vessels in optic nerve. Morphometry showed a significant increase of the number of damaged fibers on optic nerve of animals that were fed with iron-deficient diet and neonatal tactile stimulation reduced the number of damaged fibers in these animals. The present study showed that animals fed with iron-deficient diet presented significant cellular changes during the early postnatal development of the optic nerve compared with their paired controls. It was also noted that the neonatal tactile stimulation, performed during the critical period of development of the CNS was effective, minimizing the amount of damaged fibers and increasing the amount of blood vessels.

Durchtrennte Axone adulter retinaler Ganglienzellen (RGZ) können in periphere Nerventransplantate (PNT) einwachsen, die als “bypass” des distalen Sehnervenstumpfes verwendet werden. Das Transplantationsmodell, bei dem der durchtrennte Sehnerv durch ein Ischiasnervsegment ersetzt wird, ist in der Regenerationsforschung ein seit Jahren fest etabliertes Verfahren. In dieser Arbeit soll der Frage nachgegangen werden, ob a) der Ersatz des Sehnervs durch ein peripheres Nervensegment RGZ über einen langen Zeitraum hinweg morphologisch und funktionell stabilisiert, ob b) Unterschiede der Stabilisierung in Abhängigkeit von der Hirnregion, mit der das PNT in Kontakt tritt, zu beobachten sind und c) inwieweit regenerierende RGZ dadurch selbst peripher-nervöse Eigenschaften annehmen. Der Sehnerv adulter Ratten wurde zunächst komplett intraorbital durchtrennt. Der okuläre Stumpf wurde über ein autologes Ischiasnervsegment mit verschiedenen visuellen Zentren (Kortex, Mittelhirn) oder mit Fremdzielgebieten (z. B. Muskel) verbunden. Weitere Kontrollgruppen bestanden in der Quetschung des Sehnervs, der Durchtrennung ohne Transplantation und der Transplantation mit blind endendem Transplantat. Die Netzhautintegrität wurde pupillometrisch und elektroretinographisch regelmäßig überprüft, um eine eventuelle, funktionelle Wiederherstellung der visuellen Bahn zu erfassen. Nach einem, sechs und neun Monaten wurden die regenerierenden bzw. axotomierten oder gequetschten RGZ mit 4-(4-(didecylamino)styryl)-N-methylpyridinium (4-Di-10-ASP) retrograd markiert und morphometrisch quantifiziert (Fluoreszenz-, Konfokal- und Elektronenmikroskopie sowie Differentialinterferenzkontrast). Zusätzlich wurden immunhistochemische und anterograde Markierungsuntersuchungen durchgeführt. Regenerierende Ganglienzellen bleiben bis neun Monate nach der Transplantation am Nervus opticus stabil. Es gibt quantitative sowie morphometrisch erfassbare Unterschiede zwischen den experimentellen Gruppen und den Kontrollen, wobei die wieder verbundenen Ganglienzellen morphologisch am besten zu klassifizieren sind. Quantitativ zeigen die Retinae mit gequetschtem Sehnerv nach sechs Monaten die höchste Überlebensrate der RGZ. Die Effektivität dieses Verfahrens als Modell der zentralen Nervenläsion darf in Folge dieser Ergebnisse in Frage gestellt werden. Nach neun Monaten sind in den Retinae mit Rekonnektion zum Mittelhirn die meisten Ganglienzellen vorhanden. Elektrophysiologisch zeigen die Augen mit Verbindung zum Muskelgewebe die besten funktionellen Ergebnisse. Schlussfolgernd zeigt sich, dass adulte RGZ der Ratte über ein peripher-nervöses Transplantat, welches mit visuellen Zentren in Verbindung steht, über lange Zeit stabilisiert werden können.