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Clinical Chemistry, Vol 34, 1579-1584, Copyright © 1988 by American Association for Clinical Chemistry
S Ohgo, J Takemura, Y Oki, F Nishizono, E Ishikawa, T Yoshimi, T Yamamura, Y Seino and S Matsukura
Department of Internal Medicine, Miyazaki Medical College, Japan.
A sensitive and specific radioimmunoassay for cholecystokinin (CCK) has been developed. Synthetic unsulfated carboxy-terminal fragment, CCK-8, was radioiodinated by the conventional Chloramine-T method. Antibodies were raised against sulfated CCK-8 covalently coupled to bovine thyroglobulin via 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide. By purification, highly immunoreactive 125I-labeled CCK-8 was obtained. The antiserum was highly avid, and plasma could be assayed directly. The detection limit of the assay was 5 pmol of sulfated CCK-8 per liter. The assay measured fragments CCK-8, CCK-33, and CCK-39 with equimolar potency. CCK-4, gastrin, and vasoactive intestinal polypeptide were not detected, even at higher concentrations. The concentration of CCK, as the sum of these CCK peptides, in plasma during fasting was low (10.5 +/- 2.1 pmol/L, mean +/- SEM) but still detectable in all normal subjects examined (range, 6.4-20.1 pmol/L). After ingestion of a test meal, CCK in plasma increased rapidly, peaking at 41.3 (SEM 5.7) pmol/L at 40 min and remaining high for 3 h after the meal. This supports the concept that CCK has important roles in digestion and absorption.
The following articles in journals at HighWire Press have cited this article:
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R. A. Liddle On the Measurement of Cholecystokinin Clin. Chem., May 1, 1998; 44(5): 903 - 904. [Full Text] [PDF] |
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J. F. Rehfeld Accurate measurement of cholecystokinin in plasma Clin. Chem., May 1, 1998; 44(5): 991 - 1001. [Abstract] [Full Text] [PDF] |
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