Postingestional effects of a high-protein diet on the regulation of food intake in monkeys

1990 ◽  
Vol 52 (2) ◽  
pp. 320-325 ◽  
Author(s):  
J S Hannah ◽  
A K Dubey ◽  
B C Hansen
PLoS ONE ◽  
2011 ◽  
Vol 6 (10) ◽  
pp. e26407 ◽  
Author(s):  
Anna-Maria Nässl ◽  
Isabel Rubio-Aliaga ◽  
Manuela Sailer ◽  
Hannelore Daniel

Nutrients ◽  
2017 ◽  
Vol 9 (6) ◽  
pp. 587 ◽  
Author(s):  
William French ◽  
Sami Dridi ◽  
Stephanie Shouse ◽  
Hexirui Wu ◽  
Aubree Hawley ◽  
...  

2013 ◽  
Vol 27 (S1) ◽  
Author(s):  
Katrina Pioli ◽  
Chiara Barbieri ◽  
Isaac Cann ◽  
Roderick Mackie ◽  
Joseph Beverly

1986 ◽  
Vol 251 (1) ◽  
pp. G70-G74 ◽  
Author(s):  
G. M. Green ◽  
V. H. Levan ◽  
R. A. Liddle

The relationship among plasma cholecystokinin (CCK), pancreatic growth, and food intake was studied in rats over a 2-wk period of adaptation from a very low-protein to a very high-protein diet. Rats adapted to a control diet (5% casein) were killed at 0900 (without fasting) at 0 h, 12 h, 24 h, 48 h, 7 days, or 14 days after transfer to a high-protein diet (75% casein). CCK was measured by bioassay using isolated pancreatic acini. Plasma CCK in high protein-fed rats was increased approximately threefold in the first 24 h, but returned to control (approximately 2.5 pM) values by day 7. Pancreatic weight, DNA, protein, and chymotrypsin(ogen) significantly increased to maximal values by day 7 in high protein-fed rats. Food intake in high protein-fed rats was inhibited by 47% after 24 h but returned to control values by day 7. The results indicate that high-protein diets initially increase CCK release and increase pancreatic protease secretory capacity and that, when pancreatic protease secretion is sufficient to match protein digestive requirements, the stimulus for CCK secretion is reduced and plasma CCK returns to normal. The pronounced but transient inhibition of food intake in high protein-fed rats is consistent with a role for CCK in regulation of food intake.


2003 ◽  
Vol 133 (8) ◽  
pp. 2639-2642 ◽  
Author(s):  
Diane L'Heureux-Bouron ◽  
Daniel Tomé ◽  
Olivier Rampin ◽  
Patrick C. Even ◽  
Christiane Larue-Achagiotis ◽  
...  

PROTEOMICS ◽  
2010 ◽  
Vol 10 (14) ◽  
pp. 2573-2588 ◽  
Author(s):  
Björn Kuhla ◽  
Marzena Kucia ◽  
Solvig Görs ◽  
Dirk Albrecht ◽  
Martina Langhammer ◽  
...  

2017 ◽  
Vol 313 (4) ◽  
pp. R473-R486 ◽  
Author(s):  
Lixin Wang ◽  
Jonathan P. Jacobs ◽  
Venu Lagishetty ◽  
Pu-Qing Yuan ◽  
Shuping V. Wu ◽  
...  

High-protein diet (HPD) curtails obesity and/or fat mass, but it is unknown whether it reverses neuroinflammation or alters glucose levels, CCK sensitivity, and gut microbiome in rats fed a Western diet (WD)-induced obesity (DIO). Male rats fed a WD (high fat and sugar) for 12 wk were switched to a HPD for 6 wk. Body composition, food intake, meal pattern, sensitivity to intraperitoneal CCK-8S, blood glucose, brain signaling, and cecal microbiota were assessed. When compared with a normal diet, WD increased body weight (9.3%) and fat mass (73.4%). CCK-8S (1.8 or 5.2 nmol/kg) did not alter food intake and meal pattern in DIO rats. Switching to a HPD for 6 wk reduced fat mass (15.7%) with a nonsignificantly reduced body weight gain, normalized blood glucose, and decreased feeding after CCK-8S. DIO rats on the WD or switched to a HPD showed comparable microbial diversity. However, in HPD versus WD rats, there was enrichment of 114 operational taxonomic units (OTUs) and depletion of 188 OTUs. Of those, Akkermansia muciniphila (enriched on a HPD), an unclassified Clostridiales, a member of the RF39 order, and a Phascolarctobacterium were significantly associated with fat mass. The WD increased cytokine expression in the hypothalamus and dorsal medulla that was unchanged by switching to HPD. These data indicate that HPD reduces body fat and restores glucose homeostasis and CCK sensitivity, while not modifying brain inflammation. In addition, expansion of cecal Akkermansia muciniphila correlated to fat mass loss may represent a potential peripheral mechanism of HPD beneficial effects.


1998 ◽  
Vol 38 (2) ◽  
pp. 199-199
Author(s):  
C. Jean ◽  
G. Fromentin ◽  
J.-F. Huneau ◽  
V. Mathe ◽  
D. Tome

1974 ◽  
Vol 104 (8) ◽  
pp. 1008-1017 ◽  
Author(s):  
Yeh-Shan Peng ◽  
Larry L. Meliza ◽  
Mitchell G. Vavich ◽  
Arthur R. Kemmerer

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