Long-acting CCK analogue NN9056 lowers food intake and body weight in obese Göttingen Minipigs

Background/Objectives Cholecystokinin (CCK) is a regulator of appetite and energy intake in man. The aim of this study was to determine the effect of NN9056, a long-acting CCK-1 receptor-selective CCK analogue, on food intake and body weight (BW) in obese Göttingen Minipigs. Subjects/Methods Tolerab...

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Veröffentlicht in:International Journal of Obesity 2020-02, Vol.44 (2), p.447-456
Hauptverfasser: Christoffersen, Berit Ø., Skyggebjerg, Rikke Bjerring, Bugge, Anne, Kirk, Rikke Kaae, Vestergaard, Bill, Uldam, Henriette Kold, Fels, Johannes Josef, Pyke, Charles, Sensfuss, Ulrich, Sanfridson, Annika, Clausen, Trine Ryberg
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Sprache:eng
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Zusammenfassung:Background/Objectives Cholecystokinin (CCK) is a regulator of appetite and energy intake in man. The aim of this study was to determine the effect of NN9056, a long-acting CCK-1 receptor-selective CCK analogue, on food intake and body weight (BW) in obese Göttingen Minipigs. Subjects/Methods Tolerability of NN9056 and acute effects on food intake, pancreas histology, amylase and lipase levels were assessed in lean domestic pigs in doses up to 100 nmol/kg ( n  = 3–4). Subsequently, obese Göttingen Minipigs were treated subcutaneously (s.c.) once daily for 13 weeks with vehicle, NN9056 low dose (regulated from 5 to 2 nmol/kg) or NN9056 high dose (10 nmol/kg) ( n  = 7–8). Food intake was measured daily and BW twice weekly. At the end of the treatment period, an intravenous glucose tolerance test (IVGTT) and a 24-h exposure profile was obtained. Data are mean ± SD. Results The acute studies in domestic pigs showed significant and dose-dependent effect of NN9056 on food intake, acceptable tolerability and no histopathological signs of pancreatitis. Sub-chronic treatment in obese Göttingen Minipigs was also well tolerated and accumulated food intake was significantly lower in both treated groups compared to vehicle, with no significant difference between the dose levels of NN9056 (41.8 ± 12.6, 51.5 ± 13.8 and 86.5 ± 19.5 kg in high-dose, low-dose and vehicle groups, respectively, p  = 0.012 and p  
ISSN:0307-0565
1476-5497
DOI:10.1038/s41366-019-0386-0