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Validation of a radioimmunoassay for measurement of gastrin in equine serum.

Abstract: A commercial radioimmunoassay kit designed for measuring gastrin in human serum was validated for use with equine serum. This nonextraction, double-antibody procedure uses an antiserum with broad specificity for molecular forms of gastrin. Synthetic human gastrin (G17-I) was added to pooled equine serum, and the observed assay values were compared with the mass added. Recovery was 99 to 115% in the gastrin concentration range of 40 to 640 pg/ml. Dilutions of postprandial serum with serum from fasted horses were assayed, and the inhibition curves were compared with those of the human gastrin kit standards, using a log-logit transformation. The slopes of the sample dilution plots were not significantly different from the slopes of the standard curves. Ethylenediamine tetraacetate and heparin adversely affected the assay, resulting in lower assayed gastrin concentration values. The intra-assay coefficient of variation (n = 10) was 3.8%, and the interassay coefficient of variation (n = 6) was 11.2%. The assay sensitivity, as reported by the manufacturer, is 8 pg/ml. Gastrin concentrations in serum from fasted horses ranged from undetectable values (less than 8 pg/ml) to 17.5 pg/ml, and peaked at a mean value (n = 6) of 70 pg/ml 3 hours after feeding. Serum cortisol values monitored during the postprandial blood collection period were in the normal range for horses.
Publication Date: 1988-07-01 PubMed ID: 3421540
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  • Journal Article

Summary

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This research validates the use of a commercially available radioimmunoassay kit initially designed for measuring gastrin levels in human serum for use in horses. The performance of the kit was tested and yielded high accuracy and consistent results, with some considerations around the use of certain substances that may affect results.

Validation of Radioimmunoassay Kit

  • An existing commercial radioimmunoassay kit, created initially for measuring the levels of gastrin in human serum, was tested for validity with equine (horse) serum. Gastrin is a hormone that stimulates the production of gastric acid, which is crucial for digestion.
  • The kit uses a double-antibody procedure, meaning two different antibodies are used in the testing process, enhancing the accuracy and sensitivity of the test.
  • The researchers validated the assay procedure by comparing the assayed gastrin values with the added mass of synthetic gastrin (G17-I) to equine serum, showing a recovery rate of 99 to 115%. This indicates a high level of accuracy in the measurement of gastrin concentration.

Test Outcomes and Variations

  • The behavior of gastrin in postprandial equine serum (serum after feeding) was also tested and yielded consistent results. The dilution plots were comparable to those of the human test gauges.
  • Nonetheless, two substances, ethylenediamine tetraacetate and heparin, were found to adversely affect the assay by decreasing the detected gastrin concentration. These substances should therefore be avoided when using this kit for equine serum gastrin assessment.
  • The assay’s intra-assay coefficient of variation, which shows the degree of variation in the results of several runs of the same sample on the kit, was 3.8%. The interassay coefficient of variation, on the other hand, measuring variations between separate runs of different samples, was 11.2%.

Gastrin Concentration in Fasting and Postprandial Serum

  • The gastrin concentration in serum from fasting horses ranged from undetectable (less than 8 pg/ml) to 17.5 pg/ml, and after feeding, peaked at a mean value of 70 pg/ml. This indicates the utility of the radioimmunoassay for studying the effects of feeding on gastrin levels in horses.
  • During these tests, serum cortisol values were monitored and found to be within the normal range for horses, indicating that the feeding and fasting did not induce undue stress in the test subjects.

Overall, this study confirms the reliability and applicability of this commercially available radioimmunoassay kit for measuring gastrin levels in equine serum, with some considerations around substances that might interfere with the results.

Cite This Article

APA
Young DW, Smyth GB. (1988). Validation of a radioimmunoassay for measurement of gastrin in equine serum. Am J Vet Res, 49(7), 1179-1183.

Publication

ISSN: 0002-9645
NlmUniqueID: 0375011
Country: United States
Language: English
Volume: 49
Issue: 7
Pages: 1179-1183

Researcher Affiliations

Young, D W
  • Department of Physiology and Pharmacology, College of Veterinary Medicine, Auburn University, AL 36849-5522.
Smyth, G B

    MeSH Terms

    • Animals
    • Fasting
    • Gastrins / blood
    • Horses / blood
    • Hydrocortisone / blood
    • Radioimmunoassay / veterinary
    • Reference Values

    Citations

    This article has been cited 4 times.
    1. Clark B, Steel C, Vokes J, Shan JR, Gedye K, Lovett A, Sykes BW. Evaluation of the effects of medium-term (57-day) omeprazole administration and of omeprazole discontinuation on serum gastrin and serum chromogranin A concentrations in the horse. J Vet Intern Med 2023 Jul-Aug;37(4):1537-1543.
      doi: 10.1111/jvim.16795pubmed: 37390114google scholar: lookup
    2. Sandin A, Girma K, Sjöholm B, Lindholm A, Nilsson G. Effects of differently composed feeds and physical stress on plasma gastrin concentration in horses. Acta Vet Scand 1998;39(2):265-72.
      doi: 10.1186/BF03547798pubmed: 9787489google scholar: lookup
    3. Vokes JR, Gedye KR, Lovett AL, de Kantzow MC, Shan R, Steel CM, Sykes BW. Evaluation of Two Commercial ELISA Kits for Measuring Equine Serum Gastrin Compared to Radioimmunoassay. Animals (Basel) 2024 Oct 11;14(20).
      doi: 10.3390/ani14202937pubmed: 39457867google scholar: lookup
    4. Guerrero JLS, Brito PHS, Ferreira MA, Arantes JA, Rusch E, Oliveira BVDS, Velasco-Bolaños J, Carregaro AB, Dória RGS. Evaluation of Gastric pH and Gastrin Concentrations in Horses Subjected to General Inhalation Anesthesia in Dorsal Recumbency. Animals (Basel) 2024 Apr 15;14(8).
      doi: 10.3390/ani14081183pubmed: 38672331google scholar: lookup