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Laboratoire dImmunotoxicologie-UER de Pharmacie (E.G., C.B.) 92296 Chatenay-Malabry, France
Département de Biobgie Clinique-Institut Gustave-Roussy (E.C.) 94805 Villejuif Cedex, France
Address requests for reprints to: E. Comoy, Départment de Biologie Clinique, 94805 Villejuif Cedex, France.
In order to develop an immunoradiometric assay for human neuropeptide (hNPY), a recently discovered and potent vasoconstrictor 36-amino-acid peptide, we used hNPY and some of its subpeptides to prepare monoclonal anti-NPY antibodies. Two monoclonal antibodies with high affinity for hNPY, that is affinity constants in the range of 1010 mol/L–1, which respectively, reacted with the 9–18 portion and the 32–36 portion of hNPY were used in the immunoradiometric system. The assay was highly specific, NPY-related peptides such as pancreatic polypeptide and peptide YY not being detected. The lower limit of sensitivity was 0.5 pmol/L. In 303 normal subjects, plasma NPY concentrations were less than 0.5 pmol/L in 67%, 0.5 to 5.0 pmol/L in 25%, and 5.1 to 30 pmol/L in the remaining 8%. A value of 7.5 pmol/L (95th percentile value in the normal group) was considered as the upper limit of normal. Among 111 patients with various neuroendocrine tumors, elevated plasma NPY concentrations were found in patients with pheochromocytomas and neuroblastomas, the highest plasma levels being found in patients with malignant pheochromocytomas. We conclude that patients with neuroendocrine tumors, especially secreting and or malignant tumors of the sympathochromaffin system, often have elevated plasma NPY concentrations. (J Clin Endocrinol Metab 64: 808, 1989)
Received June 6, 1988.
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