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Blood Glucose and Insulin Concentrations after Octreotide Administration in Horses With Insulin Dysregulation

BACKGROUND: Octreotide is a somatostatin analog that suppresses insulin secretion. HYPOTHESIS: We hypothesized that octreotide would suppress insulin concentrations in horses and that normal (N) horses and those with insulin dysregulation (ID) would differ significantly in their plasma glucose and i...

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Autores principales: Frank, N., Hermida, P., Sanchez‐Londoño, A., Singh, R., Gradil, C.M., Uricchio, C.K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5508354/
https://www.ncbi.nlm.nih.gov/pubmed/28503791
http://dx.doi.org/10.1111/jvim.14718
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author Frank, N.
Hermida, P.
Sanchez‐Londoño, A.
Singh, R.
Gradil, C.M.
Uricchio, C.K.
author_facet Frank, N.
Hermida, P.
Sanchez‐Londoño, A.
Singh, R.
Gradil, C.M.
Uricchio, C.K.
author_sort Frank, N.
collection PubMed
description BACKGROUND: Octreotide is a somatostatin analog that suppresses insulin secretion. HYPOTHESIS: We hypothesized that octreotide would suppress insulin concentrations in horses and that normal (N) horses and those with insulin dysregulation (ID) would differ significantly in their plasma glucose and insulin responses to administration of octreotide. ANIMALS: Twelve horses, N = 5, ID = 7. METHODS: Prospective study. An oral sugar test was performed to assign horses to N and ID groups. Octreotide (1.0 μg/kg IV) was then administered, and blood was collected at 0, 5, 10, 15, 20, 25, 30, 45, 60, 75, and 90 minute, and 2, 3, 4, 6, 8, 12, and 24 hour for measurement of glucose and insulin concentrations. Area under the curve (AUC) values were calculated. RESULTS: Mean AUC values for glucose and insulin did not differ between normal (n = 5) and ID (n = 7) groups after octreotide injection. Significant time (P < .001) effects were detected for glucose and insulin concentrations. A group × time interaction (P = .091) was detected for insulin concentrations after administration of octreotide, but the group (P = .33) effect was not significant. CONCLUSIONS AND CLINICAL IMPORTANCE: Octreotide suppresses insulin secretion, resulting in hyperglycemia, and then concentrations increase above baseline as glycemic control is restored. Our hypothesis that octreotide causes insulin concentrations to decrease in horses was supported, but differences between N and ID groups did not reach statistical significance when blood glucose and insulin responses were compared. The utility of an octreotide response test remains to be determined.
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spelling pubmed-55083542017-07-14 Blood Glucose and Insulin Concentrations after Octreotide Administration in Horses With Insulin Dysregulation Frank, N. Hermida, P. Sanchez‐Londoño, A. Singh, R. Gradil, C.M. Uricchio, C.K. J Vet Intern Med EQUID BACKGROUND: Octreotide is a somatostatin analog that suppresses insulin secretion. HYPOTHESIS: We hypothesized that octreotide would suppress insulin concentrations in horses and that normal (N) horses and those with insulin dysregulation (ID) would differ significantly in their plasma glucose and insulin responses to administration of octreotide. ANIMALS: Twelve horses, N = 5, ID = 7. METHODS: Prospective study. An oral sugar test was performed to assign horses to N and ID groups. Octreotide (1.0 μg/kg IV) was then administered, and blood was collected at 0, 5, 10, 15, 20, 25, 30, 45, 60, 75, and 90 minute, and 2, 3, 4, 6, 8, 12, and 24 hour for measurement of glucose and insulin concentrations. Area under the curve (AUC) values were calculated. RESULTS: Mean AUC values for glucose and insulin did not differ between normal (n = 5) and ID (n = 7) groups after octreotide injection. Significant time (P < .001) effects were detected for glucose and insulin concentrations. A group × time interaction (P = .091) was detected for insulin concentrations after administration of octreotide, but the group (P = .33) effect was not significant. CONCLUSIONS AND CLINICAL IMPORTANCE: Octreotide suppresses insulin secretion, resulting in hyperglycemia, and then concentrations increase above baseline as glycemic control is restored. Our hypothesis that octreotide causes insulin concentrations to decrease in horses was supported, but differences between N and ID groups did not reach statistical significance when blood glucose and insulin responses were compared. The utility of an octreotide response test remains to be determined. John Wiley and Sons Inc. 2017-05-15 2017 /pmc/articles/PMC5508354/ /pubmed/28503791 http://dx.doi.org/10.1111/jvim.14718 Text en Copyright © 2017 The Authors. Journal of Veterinary Internal Medicine published by Wiley Periodicals, Inc. on behalf of the American College of Veterinary Internal Medicine. This is an open access article under the terms of the Creative Commons Attribution‐NonCommercial (http://creativecommons.org/licenses/by-nc/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
spellingShingle EQUID
Frank, N.
Hermida, P.
Sanchez‐Londoño, A.
Singh, R.
Gradil, C.M.
Uricchio, C.K.
Blood Glucose and Insulin Concentrations after Octreotide Administration in Horses With Insulin Dysregulation
title Blood Glucose and Insulin Concentrations after Octreotide Administration in Horses With Insulin Dysregulation
title_full Blood Glucose and Insulin Concentrations after Octreotide Administration in Horses With Insulin Dysregulation
title_fullStr Blood Glucose and Insulin Concentrations after Octreotide Administration in Horses With Insulin Dysregulation
title_full_unstemmed Blood Glucose and Insulin Concentrations after Octreotide Administration in Horses With Insulin Dysregulation
title_short Blood Glucose and Insulin Concentrations after Octreotide Administration in Horses With Insulin Dysregulation
title_sort blood glucose and insulin concentrations after octreotide administration in horses with insulin dysregulation
topic EQUID
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5508354/
https://www.ncbi.nlm.nih.gov/pubmed/28503791
http://dx.doi.org/10.1111/jvim.14718
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