By Prof. Dr. U. Trendelenburg (auth.), Prof. Dr. Peter Riederer, Prof. Dr. Moussa B. H. Youdim (eds.)
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Additional info for Amine Oxidases and Their Impact on Neurobiology: Proceedings of the 4th International Amine Oxidases Workshop, Wurzburg, Federal Republic of Germany, July 7–10, 1990
These observations provide convincing evidence that the labelled amine is taken up selectively and stored in sympathetic nerve terminals in the heart. , 1990). , 1990). This llC-labelled compound was obtained with sufficiently high specific activity to circumvent pharmacological effects and appears to be a promising new approach for PET imaging of neuronal amine uptake and storage and thus integrity of sympathetic nerve terminals. The metabolic stability and avid uptake which enhance the value of metaraminol and its derivatives for assessing Uptake l may, however, limit their ability to reflect the turnover rate of endogenous norepinephrine.
The isotopes must be produced within a reasonable distance from the site at which they are to be used. The positron-emitting isotopes that would be most useful for labelling endogenous substances have very short half-lives 50 has a half-life of about 2 min, l3N about 10 min, and llC about 20 min). , H/ 80), but use of llC is possible because there are available methods for rapid production of several llC-labelled compounds, particularly those which can be produced using llC-methyl iodide. Labelling compounds with l8F (half-life of about 2 hours) is more attractive but the biological behavior of the fluorinated analogue must be examined to ensure that it adequately reflects the process being studied.
A selective, quantitative and high resolution technique (in vitro and in vivo enzyme radioautography) has been used to reveal the tissue distribution and abundance of MAO-A and MAO-B in the central nervous system and peripheral organs in the rat. The in vitro approach was also used to map the enzymes in human post-mortem brain. Furthermore, using in situ hybridization histochemistry, locus coeruleus and raphe neurons in the human brain were found to code for MAO-A and MAO-B respectively and not vice versa.