Abstract
Endogenous opioid peptides exert multiple modulatory effects in the regulation of cardiovascular function at both central [11] and peripheral sites [49]. A crucial basis for the understanding of the complex mechanisms involved in this regulatory system is the detailed knowledge of the morphological distribution of opioid peptides. The morphological methods appropriate for this purpose require antisera raised against the different opioid peptides and the use of immunohistochemistry. However, difficulties arise from the structural similarities of opioid peptides. To our present knowledge, opioid peptides are cleavage products of three large precursor molecules:
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a)
proopiomelanocortin (POMC) processing results in the production of endorphins,
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b)
prodynorphin is the precursor of neoendorphins and dynorphins, and
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c)
proenkephalin contains one copy of leu-enkephalin (LE) and several opioids sharing the met-enkephalin (ME) sequence at their N-terminus.
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Kummer, W., Reinecke, M., Heym, C., Forssmann, W.G. (1988). Distribution of Opioid Peptides Functionally Related to the Cardiovascular System. In: Stumpe, K.O., Kraft, K., Faden, A.I. (eds) Opioid Peptides and Blood Pressure Control. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-642-73429-8_2
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