Circulating concentrations of glucagon-like peptide 1, glucose-dependent insulinotropic peptide, peptide YY, and insulin in client-owned lean, overweight, and diabetic cats

Our objectives were to measure plasma concentrations of glucagon-like peptide 1 (GLP-1), glucose-dependent insulinotropic peptide (GIP), and peptide YY (PYY) in client-owned newly diagnosed diabetic cats and nondiabetic lean or overweight cats and to determine whether circulating concentrations of t...

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Veröffentlicht in:Domestic animal endocrinology 2016-01, Vol.54, p.85-94
Hauptverfasser: McMillan, C.J., Zapata, R.C., Chelikani, P.K., Snead, E.C.R., Cosford, K.
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container_end_page 94
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container_start_page 85
container_title Domestic animal endocrinology
container_volume 54
creator McMillan, C.J.
Zapata, R.C.
Chelikani, P.K.
Snead, E.C.R.
Cosford, K.
description Our objectives were to measure plasma concentrations of glucagon-like peptide 1 (GLP-1), glucose-dependent insulinotropic peptide (GIP), and peptide YY (PYY) in client-owned newly diagnosed diabetic cats and nondiabetic lean or overweight cats and to determine whether circulating concentrations of these hormones differed between study groups and if they increased postprandially as seen in other species. A total of 31 cats were recruited and placed into 1 of 3 study groups: lean (body condition score 4–5 on a scale of 1–9; n = 10), overweight (body condition score 6–8; n = 11), or diabetic (n = 10). Diabetics were newly diagnosed and had not had prior insulin therapy. Preprandial (fasting) and postprandial (60 min after meal) plasma hormone and glucose concentrations were measured at baseline and 2 and 4 wk. All cats were exclusively fed a commercially available high-protein and low-carbohydrate diet commonly prescribed to feline diabetic patients for 2 wk before the 2-wk assessment and continued through the 4-wk assessment. Results showed that plasma concentrations of GLP-1, GIP, PYY, and insulin increased in general after a meal in all study groups. Plasma PYY concentrations did not differ (P > 0.10) between study groups. Diabetics had greater plasma concentrations of GLP-1 and GIP compared with the other study groups at baseline (P < 0.05), and greater preprandial and postprandial GLP-1 concentrations than lean cats at 2 and 4 wk (P < 0.05). Preprandial plasma GIP concentrations were greater in diabetics than obese and lean (P < 0.05) cats at week 4. Postprandial plasma GIP concentrations in diabetics were greater than lean (P < 0.05) at week 2 and obese and lean cats (P < 0.05) at week 4. Together, our findings suggest that diabetic status is an important determinant of circulating concentrations of GLP-1 and GIP, but not PYY, in cats. The role of GLP-1, GIP, and PYY in the pathophysiology of feline obesity and diabetes remains to be determined. •Diabetics had greater concentrations of GLP-1 and GIP than lean cats.•Diabetics had greater GIP concentrations than overweight cats.•GLP-1, GIP, and PYY increase postprandially in diabetic, lean and overweight cats.•Plasma PYY concentrations did not differ between study groups.•Diabetes is a determinant of GLP-1 and GIP, but not PYY concentrations, in cats.
doi_str_mv 10.1016/j.domaniend.2015.10.001
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A total of 31 cats were recruited and placed into 1 of 3 study groups: lean (body condition score 4–5 on a scale of 1–9; n = 10), overweight (body condition score 6–8; n = 11), or diabetic (n = 10). Diabetics were newly diagnosed and had not had prior insulin therapy. Preprandial (fasting) and postprandial (60 min after meal) plasma hormone and glucose concentrations were measured at baseline and 2 and 4 wk. All cats were exclusively fed a commercially available high-protein and low-carbohydrate diet commonly prescribed to feline diabetic patients for 2 wk before the 2-wk assessment and continued through the 4-wk assessment. Results showed that plasma concentrations of GLP-1, GIP, PYY, and insulin increased in general after a meal in all study groups. Plasma PYY concentrations did not differ (P &gt; 0.10) between study groups. Diabetics had greater plasma concentrations of GLP-1 and GIP compared with the other study groups at baseline (P &lt; 0.05), and greater preprandial and postprandial GLP-1 concentrations than lean cats at 2 and 4 wk (P &lt; 0.05). Preprandial plasma GIP concentrations were greater in diabetics than obese and lean (P &lt; 0.05) cats at week 4. Postprandial plasma GIP concentrations in diabetics were greater than lean (P &lt; 0.05) at week 2 and obese and lean cats (P &lt; 0.05) at week 4. Together, our findings suggest that diabetic status is an important determinant of circulating concentrations of GLP-1 and GIP, but not PYY, in cats. 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A total of 31 cats were recruited and placed into 1 of 3 study groups: lean (body condition score 4–5 on a scale of 1–9; n = 10), overweight (body condition score 6–8; n = 11), or diabetic (n = 10). Diabetics were newly diagnosed and had not had prior insulin therapy. Preprandial (fasting) and postprandial (60 min after meal) plasma hormone and glucose concentrations were measured at baseline and 2 and 4 wk. All cats were exclusively fed a commercially available high-protein and low-carbohydrate diet commonly prescribed to feline diabetic patients for 2 wk before the 2-wk assessment and continued through the 4-wk assessment. Results showed that plasma concentrations of GLP-1, GIP, PYY, and insulin increased in general after a meal in all study groups. Plasma PYY concentrations did not differ (P &gt; 0.10) between study groups. Diabetics had greater plasma concentrations of GLP-1 and GIP compared with the other study groups at baseline (P &lt; 0.05), and greater preprandial and postprandial GLP-1 concentrations than lean cats at 2 and 4 wk (P &lt; 0.05). Preprandial plasma GIP concentrations were greater in diabetics than obese and lean (P &lt; 0.05) cats at week 4. Postprandial plasma GIP concentrations in diabetics were greater than lean (P &lt; 0.05) at week 2 and obese and lean cats (P &lt; 0.05) at week 4. Together, our findings suggest that diabetic status is an important determinant of circulating concentrations of GLP-1 and GIP, but not PYY, in cats. The role of GLP-1, GIP, and PYY in the pathophysiology of feline obesity and diabetes remains to be determined. •Diabetics had greater concentrations of GLP-1 and GIP than lean cats.•Diabetics had greater GIP concentrations than overweight cats.•GLP-1, GIP, and PYY increase postprandially in diabetic, lean and overweight cats.•Plasma PYY concentrations did not differ between study groups.•Diabetes is a determinant of GLP-1 and GIP, but not PYY concentrations, in cats.</description><subject>Animals</subject><subject>Cat Diseases - blood</subject><subject>Cats</subject><subject>Diabetes</subject><subject>Diabetes Mellitus - blood</subject><subject>Diabetes Mellitus - veterinary</subject><subject>Enteroendocrine hormone</subject><subject>Fasting</subject><subject>Feline</subject><subject>Gastric Inhibitory Polypeptide - blood</subject><subject>Glucagon-Like Peptide 1 - blood</subject><subject>Insulin - blood</subject><subject>Obesity - blood</subject><subject>Obesity - veterinary</subject><subject>Overweight - blood</subject><subject>Overweight - veterinary</subject><subject>Peptide YY - blood</subject><subject>Postprandial Period</subject><issn>0739-7240</issn><issn>1879-0054</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkc9uGyEQxlHVqHGTvELLsQevC-wueI-R1X9SpF6aQ06IhcHFxbAFNlHfqQ9ZHMe-9jSC-X3fzOhD6D0lK0oo_7hbmbhXwUEwK0ZoX39XhNBXaEHXYmgI6bvXaEFEOzSCdeQSvc15RwgRVf0GXTLOydBzsUB_Ny7p2aviwhbrGDSEkuorhoyjxVs_a7WNofHuF-AJpuIMYLp8bsQMjYGp7lBF2IU8exdiSXFy-sQuz6KHhyVWwZy4WrH29YDSxKcABntQYYnjI6QncNuf5Ugbp0Yo1U-rkq_RhVU-w81LvUL3nz_92Hxt7r5_-ba5vWt014rSMBCKt_2oW06Y4QzWw6g4HwRldN12THQWRmCcjWsYOPTUWs2MZr0l1pKBtVfow9F3SvH3DLnIvcsavFcB4pwlFT3p2qF7RsUR1SnmnMDKKbm9Sn8kJfIQldzJc1TyENWhUaOqyncvQ-ZxD-asO2VTgdsjAPXURwdJZl1dNBiXQJdq6_475B_HGazQ</recordid><startdate>201601</startdate><enddate>201601</enddate><creator>McMillan, C.J.</creator><creator>Zapata, R.C.</creator><creator>Chelikani, P.K.</creator><creator>Snead, E.C.R.</creator><creator>Cosford, K.</creator><general>Elsevier Inc</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>201601</creationdate><title>Circulating concentrations of glucagon-like peptide 1, glucose-dependent insulinotropic peptide, peptide YY, and insulin in client-owned lean, overweight, and diabetic cats</title><author>McMillan, C.J. ; 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A total of 31 cats were recruited and placed into 1 of 3 study groups: lean (body condition score 4–5 on a scale of 1–9; n = 10), overweight (body condition score 6–8; n = 11), or diabetic (n = 10). Diabetics were newly diagnosed and had not had prior insulin therapy. Preprandial (fasting) and postprandial (60 min after meal) plasma hormone and glucose concentrations were measured at baseline and 2 and 4 wk. All cats were exclusively fed a commercially available high-protein and low-carbohydrate diet commonly prescribed to feline diabetic patients for 2 wk before the 2-wk assessment and continued through the 4-wk assessment. Results showed that plasma concentrations of GLP-1, GIP, PYY, and insulin increased in general after a meal in all study groups. Plasma PYY concentrations did not differ (P &gt; 0.10) between study groups. Diabetics had greater plasma concentrations of GLP-1 and GIP compared with the other study groups at baseline (P &lt; 0.05), and greater preprandial and postprandial GLP-1 concentrations than lean cats at 2 and 4 wk (P &lt; 0.05). Preprandial plasma GIP concentrations were greater in diabetics than obese and lean (P &lt; 0.05) cats at week 4. Postprandial plasma GIP concentrations in diabetics were greater than lean (P &lt; 0.05) at week 2 and obese and lean cats (P &lt; 0.05) at week 4. Together, our findings suggest that diabetic status is an important determinant of circulating concentrations of GLP-1 and GIP, but not PYY, in cats. The role of GLP-1, GIP, and PYY in the pathophysiology of feline obesity and diabetes remains to be determined. •Diabetics had greater concentrations of GLP-1 and GIP than lean cats.•Diabetics had greater GIP concentrations than overweight cats.•GLP-1, GIP, and PYY increase postprandially in diabetic, lean and overweight cats.•Plasma PYY concentrations did not differ between study groups.•Diabetes is a determinant of GLP-1 and GIP, but not PYY concentrations, in cats.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>26609567</pmid><doi>10.1016/j.domaniend.2015.10.001</doi><tpages>10</tpages></addata></record>
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source MEDLINE; Elsevier ScienceDirect Journals
subjects Animals
Cat Diseases - blood
Cats
Diabetes
Diabetes Mellitus - blood
Diabetes Mellitus - veterinary
Enteroendocrine hormone
Fasting
Feline
Gastric Inhibitory Polypeptide - blood
Glucagon-Like Peptide 1 - blood
Insulin - blood
Obesity - blood
Obesity - veterinary
Overweight - blood
Overweight - veterinary
Peptide YY - blood
Postprandial Period
title Circulating concentrations of glucagon-like peptide 1, glucose-dependent insulinotropic peptide, peptide YY, and insulin in client-owned lean, overweight, and diabetic cats
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