<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Kemp KL</submitter><funding>The University of Queensland Graduate School Research Training Program (RTP) Scholarship</funding><funding>Morris Animal Foundation</funding><funding>Destination Australia Scholarship</funding><pagination>1177-1184</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC10937495</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>38(2)</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>Phenylbutazone is often prescribed to manage pain caused by hyperinsulinemia-associated laminitis, but in diabetic people nonsteroidal anti-inflammatory drugs increase insulin secretion and pancreatic activity.&lt;h4>Hypothesis/objectives&lt;/h4>Investigate the effect of phenylbutazone administration on insulin secretion in horses. It was hypothesized that phenylbutazone will increase insulin secretion in horses with insulin dysregulation (ID).&lt;h4>Animals&lt;/h4>Sixteen light breed horses, including 7 with ID.&lt;h4>Methods&lt;/h4>Randomized cross-over study design. Horses underwent an oral glucose test (OGT) after 9 days of treatment with phenylbutazone (4.4 mg/kg IV q24h) or placebo (5 mL 0.9% saline). After a 10-day washout period, horses received the alternative treatment, and a second OGT was performed. Insulin and glucose responses were compared between groups (ID or controls) and treatments using paired t test and analyses of variance with P &lt; .05 considered significant.&lt;h4>Results&lt;/h4>In horses with ID, phenylbutazone treatment significantly decreased glucose concentration (P = .02), glucose area under the curve (2429 ± 501.5 vs 2847 ± 486.1 mmol/L × min, P = .02), insulin concentration (P = .03) and insulin area under the curve (17 710 ± 6676 vs 22 930 ± 8788 μIU/mL × min, P = .03) in response to an OGT. No significant effect was detected in control horses.&lt;h4>Conclusion and clinical importance&lt;/h4>Phenylbutazone administration in horses with ID decreases glucose and insulin concentrations in response to an OGT warranting further investigation of a therapeutic potential of phenylbutazone in the management of hyperinsulinemia-associated laminitis beyond analgesia.</pubmed_abstract><journal>Journal of veterinary internal medicine</journal><pubmed_title>Effect of phenylbutazone on insulin secretion in horses with insulin dysregulation.</pubmed_title><pmcid>PMC10937495</pmcid><funding_grant_id>D19‐EQ‐302</funding_grant_id><funding_grant_id>D19-EQ-302</funding_grant_id><pubmed_authors>Kemp KL</pubmed_authors><pubmed_authors>Skinner JE</pubmed_authors><pubmed_authors>Bertin FR</pubmed_authors></additional><is_claimable>false</is_claimable><name>Effect of phenylbutazone on insulin secretion in horses with insulin dysregulation.</name><description>&lt;h4>Background&lt;/h4>Phenylbutazone is often prescribed to manage pain caused by hyperinsulinemia-associated laminitis, but in diabetic people nonsteroidal anti-inflammatory drugs increase insulin secretion and pancreatic activity.&lt;h4>Hypothesis/objectives&lt;/h4>Investigate the effect of phenylbutazone administration on insulin secretion in horses. It was hypothesized that phenylbutazone will increase insulin secretion in horses with insulin dysregulation (ID).&lt;h4>Animals&lt;/h4>Sixteen light breed horses, including 7 with ID.&lt;h4>Methods&lt;/h4>Randomized cross-over study design. Horses underwent an oral glucose test (OGT) after 9 days of treatment with phenylbutazone (4.4 mg/kg IV q24h) or placebo (5 mL 0.9% saline). After a 10-day washout period, horses received the alternative treatment, and a second OGT was performed. Insulin and glucose responses were compared between groups (ID or controls) and treatments using paired t test and analyses of variance with P &lt; .05 considered significant.&lt;h4>Results&lt;/h4>In horses with ID, phenylbutazone treatment significantly decreased glucose concentration (P = .02), glucose area under the curve (2429 ± 501.5 vs 2847 ± 486.1 mmol/L × min, P = .02), insulin concentration (P = .03) and insulin area under the curve (17 710 ± 6676 vs 22 930 ± 8788 μIU/mL × min, P = .03) in response to an OGT. No significant effect was detected in control horses.&lt;h4>Conclusion and clinical importance&lt;/h4>Phenylbutazone administration in horses with ID decreases glucose and insulin concentrations in response to an OGT warranting further investigation of a therapeutic potential of phenylbutazone in the management of hyperinsulinemia-associated laminitis beyond analgesia.</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Mar-Apr</publication><modification>2026-06-24T03:08:32.473Z</modification><creation>2026-06-24T03:06:03.41Z</creation></dates><accession>S-EPMC10937495</accession><cross_references><pubmed>38363029</pubmed><doi>10.1111/jvim.17013</doi></cross_references></HashMap>