The Journal of Clinical Endocrinology & Metabolism · 1957 · 63 citations · 14 references
Life SciencesBiochemistryEndocrinologyBiochemical PharmacologyHormone BiochemistrySteroid BiochemistryAdrenal EndocrinologyAdrenal HormonesAdrenal Steroid HormonesSteroid BiosynthesisSteroid Hormone BiochemistrySteroid MetabolismAdrenal Steroid MetabolismAdrenocortical SecretionEndogenous Steroid MarkersPlasma Steroid ProfilingUrinary Steroid Analysis
IN 1950 Porter and Silber (1) observed that a color reaction occurred if 17,21-dihydroxy-20-ketosteroids were exposed to a phenylhydrazinesulfuric acid solution. Utilizing this color reaction, Nelson and Samuels (2), Glenn and Nelson (3) and Reddy et al. (4) have published methods for the determination of adrenal steroids having a 17,21-dihydroxy-20-keto configuration. Since then, numerous publications have appeared dealing with adrenocortical physiology and pathology, using levels of 17-hydroxycorticosteroids as an index for these conditions. Marks and Leftin (5), however, were able to find butanol-extractable substances in human urine which gave rise to a positive Porter-Silber reaction without fulfilling the 17,21-dihydroxy-20-keto qualification. These findings raise an essential point of methodology: How much of the Porter-Silber chromogen in plasma or urine estimated by the simpler techniques may be ascribed to nonsteroidal material? Even with the Nelson and Samuels method as originally described, the Porter-Silber chromogen in blood plasma from normal subjects seldom exhibits a peak absorbancy at 410 mμ, whereas crystalline cortisol, even when extracted from water with chloroform and subjected to chromatographic treatment on Florisil columns, exhibits such a peak.
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