Abstract
Parkinson’s disease is one of the most common disorders that affect the nigrostriatal system in human. Loss of neurons in the substantia nigra and severe depletion of dopamine (DA) in the corpus striatum are the hallmarks of this condition. The most effective treatment of Parkinson’s disease, particularly in its early phase, is the administration of both the L-isomer of 3,4-dihydroxyphenylalanine (L-DOPA) and dopamine-receptor agonists. However, it is clear that L-DOPA and the receptor agonists provide only limited ameliorable treatment and that most patients inexorably become progressively debilitated regardless of the type of therapy. On the other hand, an alternative approach in the therapeutic management of Parkinson’s disease is surgical implantation of either DA neurons or adrenal chromaffin cells that have the ability to release DA.1
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© 1990 Plenum Press, New York
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Shimizu, K., Yamada, M., Matsui, Y., Tamura, K., Moriuchi, S., Mogami, H. (1990). Investigation of MHC Antigens on Neural Graft in Mouse Parkinson’s Models. In: Nagatsu, T., Fisher, A., Yoshida, M. (eds) Basic, Clinical, and Therapeutic Aspects of Alzheimer’s and Parkinson’s Diseases. Advances in Behavioral Biology, vol 38A. Springer, Boston, MA. https://doi.org/10.1007/978-1-4684-5844-2_161
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DOI: https://doi.org/10.1007/978-1-4684-5844-2_161
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