TY - JOUR
T1 - Determining the effects of combined liraglutide and phentermine on metabolic parameters, blood pressure, and heart rate in lean and obese Male mice
AU - Simonds, Stephanie E.
AU - Pryor, Jack T.
AU - Koegler, Frank H.
AU - Buch-Rasmussen, Alberte S.
AU - Kelly, Lauren E.
AU - Grove, Kevin L.
AU - Cowley, Michael A.
N1 - Funding Information:
Funding. This work was supported by the National Heart Foundation of Australia (S.E.S.) and the National Health and Medical Research Council of Australia (S.E.S. and M.A.C.). Duality of Interest. This study was supported by Novo Nordisk Research Center Seattle (S.E.S. and M.A.C.). S.E.S., J.T.P., L.E.K., and M.A.C. are shareholders in Integrated Physiology Services, which provides services to Novo Nordisk. F.H.K. and K.L.G. are employees of Novo Nordisk Research Center Seattle. M.A.C. is a consultant to Novo Nordisk and Valeant/iNova, which market liraglutide and phentermine, respectively, in Australia. No other potential conflicts of interest relevant to this article were reported. Author Contributions. S.E.S. designed and conducted experiments, contributed reagents/animals, analyzed data, and prepared the manuscript. J.T.P. analyzed data and prepared the manuscript. F.H.K. designed experiments and contributed reagents/animals. A.S.B.-R. conducted experiments. L.E.K. prepared the manuscript. K.L.G. and M.A.C. designed experiments, contributed reagents/animals, and prepared the manuscript. M.A.C. is the guarantor of this work and, as such, had full access to all the data in the study and takes responsibility for the integrity of the data and the accuracy of the data analysis.
Publisher Copyright:
© 2019 by the American Diabetes Association.
PY - 2019/4/1
Y1 - 2019/4/1
N2 - Liraglutide, a glucagon-like peptide 1 (GLP-1) receptor agonist, and phentermine, a psychostimulant structurally related to amphetamine, are drugs approved for the treatment of obesity and hyperphagia. There is significant interest in combination use of liraglutide and phentermine for weight loss; however, both drugs have been reported to induce systemic hemodynamic changes, and as such the therapeutic window for this drug combination needs to be determined. To understand their impact on metabolic and cardiovascular physiology, we tested the effects of these drugs alone and in combination for 21 days in lean and obese male mice. The combination of liraglutide and phentermine, at 100 mg/kg/day and 10 mg/kg/day, respectively, produced the largest reduction in body weight in both lean and diet-induced obese (DIO) mice, when compared with both vehicle and monotherapy-treated mice. In lean mice, combination treatment at the aforementioned doses significantly increased heart rate and reduced blood pressure, whereas in DIO mice, combination therapy induced a transient increase in heart rate and decreased blood pressure. These studies demonstrate that in obese mice, the combination of liraglutide and phentermine may reduce body weight but only induce modest improvements in cardiovascular functions. Conversely, in lean mice, the additional weight loss from combination therapy does not improve cardiovascular parameters.
AB - Liraglutide, a glucagon-like peptide 1 (GLP-1) receptor agonist, and phentermine, a psychostimulant structurally related to amphetamine, are drugs approved for the treatment of obesity and hyperphagia. There is significant interest in combination use of liraglutide and phentermine for weight loss; however, both drugs have been reported to induce systemic hemodynamic changes, and as such the therapeutic window for this drug combination needs to be determined. To understand their impact on metabolic and cardiovascular physiology, we tested the effects of these drugs alone and in combination for 21 days in lean and obese male mice. The combination of liraglutide and phentermine, at 100 mg/kg/day and 10 mg/kg/day, respectively, produced the largest reduction in body weight in both lean and diet-induced obese (DIO) mice, when compared with both vehicle and monotherapy-treated mice. In lean mice, combination treatment at the aforementioned doses significantly increased heart rate and reduced blood pressure, whereas in DIO mice, combination therapy induced a transient increase in heart rate and decreased blood pressure. These studies demonstrate that in obese mice, the combination of liraglutide and phentermine may reduce body weight but only induce modest improvements in cardiovascular functions. Conversely, in lean mice, the additional weight loss from combination therapy does not improve cardiovascular parameters.
UR - http://www.scopus.com/inward/record.url?scp=85063611777&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85063611777&partnerID=8YFLogxK
U2 - 10.2337/db18-1149
DO - 10.2337/db18-1149
M3 - Article
C2 - 30674622
AN - SCOPUS:85063611777
SN - 0012-1797
VL - 68
SP - 683
EP - 695
JO - Diabetes
JF - Diabetes
IS - 4
ER -