|
![]() |
|||
|
||||
OverviewThis dissertation, The Plasticity of Hypothalamic Magnocellular System Following Axonal Damage by Hypophysectomy in Developing and Adult Rats by Qiuju, Yuan, 袁秋菊, was obtained from The University of Hong Kong (Pokfulam, Hong Kong) and is being sold pursuant to Creative Commons: Attribution 3.0 Hong Kong License. The content of this dissertation has not been altered in any way. We have altered the formatting in order to facilitate the ease of printing and reading of the dissertation. All rights not granted by the above license are retained by the author. Abstract: Abstract Axonal transection provides very useful paradigms to study cellular responses to injury, mechanisms of plasticity and the processes that lead to nerve cell degeneration. The outcome of axonal injury depends on many parameters including the location and nature of the lesion, age of animal and etc. Hypophysectomy axotomizes the magnocellular neurons in the supraoptic (SON) and paraventricular (PVN) nuclei of the hypothalamo-neurohypophyseal system (HNS). In the adult mammal, the HNS shows a remarkable ability to recover function despite substantial neuronal degeneration following hypophysectomy. The mechanisms underlying this recovery are completely unknown, but it has been hypothesized that the neuronal regeneration may be due to, at least in part, upregulation of nitric oxide synthase, increased neuronal activity, or special microenvironment. There is little data regarding how hypophysectomy influences HNS in immature animals. The retrograde reactions induced by axonal injury also involve in the cellular elements of the local microenvironment of those neurons, surrounding nonneuronal cells. These changes are likely to play a critical role in the attempt of the injured neuron to survive and achieve functional repair. Though these various cellular processes have been well documented by many groups over the last few decades, few have directly addressed the perineuronal glial reaction of magnocellular neurons of the HNS and the role of the glial reaction in the post-injury remodeling of the HNS. The present study was undertaken to examine 1) the response of magnocellular neurons of oxytocin (OT) and arginine vasopressin (AVP) neuron to hypophysectomy including survival, regeneration, expression of nitric oxide synthase and c-fos in adult and developing rats; 2) the role of NOS on survival and regeneration after hypophysectomy by use of the NOS blocker, L-NAME; 3) the glial reaction to hypophysectomy in adult and developing rats. In the present study we found that, in contrast to a striking age-dependent alteration in nNOS expression and regeneration, hypophysectomy induced substantial degeneration of magnocellular neurons of HNS in both immature and adult rats and there was no obvious difference in neuronal survival after the same injury between immature and adult rats. Moreover, L-NAME, could inhibit neural regeneration but had no effect on magnocellular neuronal survival. These results suggested that 1) difference in vulnerability to axotomy between immature and mature neurons is not a general feature; 2) induced increase of NOS expression is involved in the regeneration of magnocellular neurons of HNS; 3) the magnocellular neurons are resistant to induced NO. Secondly, we demonstrated that there were qualitative as well as quantitative differences in induced c-fos expression between the newborn and the adult hypophysectomized SON and PVN. Following the hypothesis that the expression c-fos protein is induced by the cellular demands for acceleration of the gene transcription, we suggest that different pattern of c-fos expression between immature and adult rats may regulate different gene expression in response to hypophysectomy. Furthermore, hypophysectomy also induced different responses of astrocytes surrounding the affected neuronal perikaya in immature rats and adult rats. Following hypophysectomy in the adult, reactive astrocytes re-ex Full Product DetailsAuthor: Qiuju Yuan , 袁秋菊Publisher: Open Dissertation Press Imprint: Open Dissertation Press Dimensions: Width: 21.60cm , Height: 1.40cm , Length: 27.90cm Weight: 0.807kg ISBN: 9781374719477ISBN 10: 1374719471 Publication Date: 27 January 2017 Audience: General/trade , General Format: Hardback Publisher's Status: Active Availability: Temporarily unavailable ![]() The supplier advises that this item is temporarily unavailable. It will be ordered for you and placed on backorder. Once it does come back in stock, we will ship it out to you. Table of ContentsReviewsAuthor InformationTab Content 6Author Website:Countries AvailableAll regions |