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Comparison of (/sup 125/I)somatomedin A and (/sup 125/I)somatomedin C radioreceptor assays for somatomedin peptide content in whole and acid-chromatographed plasma

Journal Article · · J. Clin. Endocrinol. Metab.; (United States)
The placental membrane radioreceptor assay was used to measure the levels of somatomedin (SM) peptides in plasma. Displacement of both (/sup 125/I)somatomedin A ((/sup 125/I)SM-A) and (/sup 125/I)somatomedin C ((/sup 125/I)SM-C) by normal whole plasma, the peptide fraction of acid-chromatographed plasma, and a partially purified, insulin-free SM preparation were compared. The peptide fraction of plasma was isolated by acid chromatography over Sephadex G-50 in 0.25 M formic acid with a yield of greater than or equal to 90%, as determined by bioassay and (/sup 125/I)SM. In the case of (/sup 125/I)SM-A, the dose-response curves for whole plasma, acid-chromatographed plasma, and the standard SM preparation were parallel (P > 0.2). In contrast, for (/sup 125/I)SM-C, the dose-response curves for acid-chromatographed plasma and the purified SM preparation were parallel (P > 0.2), but both differed significantly from that of whole plasma (P < 0.001). In addition, there was less variability in the assay of acid-chromatographed plasma compared to whole plasma. The results indicate that radioreceptor assay of unextracted normal plasma using (/sup 125/I)SM-A is a valid measure of SM peptide concentration, while radioreceptor assay of unextracted normal plasma using (/sup 125/I)SM-C, in our hands, is not. Acid chromatography of plasma before its assay is an uncomplicated procedure which allows valid and precise measurement of SM peptide content using either (/sup 125/I)SM-A or (/sup 125/I)SM-C.
Research Organization:
Stanford Univ. School of Medicine, CA
OSTI ID:
5760864
Journal Information:
J. Clin. Endocrinol. Metab.; (United States), Journal Name: J. Clin. Endocrinol. Metab.; (United States) Vol. 47:6; ISSN JCEMA
Country of Publication:
United States
Language:
English