Exenatide dosing in alpacas
In order to investigate whether exenatide could be used to stimulate glucose clearance and insulin secretion in alpacas without causing colic signs, six healthy adult alpacas were injected once a day with increasing subcutaneous doses. A follow‐up intravenous glucose injection was given to induce hy...
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Published in | Journal of veterinary pharmacology and therapeutics Vol. 37; no. 4; pp. 417 - 420 |
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Main Authors | , , , |
Format | Journal Article |
Language | English |
Published |
England
Blackwell Science
01.08.2014
Blackwell Publishing Ltd |
Subjects | |
Online Access | Get full text |
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Summary: | In order to investigate whether exenatide could be used to stimulate glucose clearance and insulin secretion in alpacas without causing colic signs, six healthy adult alpacas were injected once a day with increasing subcutaneous doses. A follow‐up intravenous glucose injection was given to induce hyperglycemia, and serial blood samples were collected to measure plasma concentrations of glucose, insulin, triglycerides, beta‐hydroxybutyrate, and nonesterified fatty acids. The exenatide doses used were saline control (no drug), and 0.02, 0.05, or 0.1 mcg/kg injected subcutaneously. Alpacas had significantly lower plasma glucose concentrations and higher insulin concentrations on all treatment days compared with the control day, but the increase in insulin was significantly greater and lasted significantly longer when the alpacas received the two higher dosages. Two of the alpacas developed mild colic signs at the 0.05 mcg/kg dose and were not evaluated at the highest dose. Based on these findings, the 0.05 mcg/kg dose appears to offer the greatest stimulation of insulin secretion and glucose clearance without excessive risk or severity of complications. |
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Bibliography: | http://dx.doi.org/10.1111/jvp.12103 istex:7B1BB384AC2BB00AB8C6F0F42BB04E68BBC34441 Alpaca Research Foundation ark:/67375/WNG-107JJV0L-G ArticleID:JVP12103 ObjectType-Article-2 SourceType-Scholarly Journals-1 ObjectType-Feature-1 content type line 23 |
ISSN: | 0140-7783 1365-2885 |
DOI: | 10.1111/jvp.12103 |