1980
DOI: 10.1210/jcem-50-4-744
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Reduced Pancreatic Polypeptide Secretion in Obese Subjects*

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Cited by 57 publications
(27 citation statements)
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“…Our findings of decreased fasting PP levels in obese children are in concordance with most studies in obese adults, [19][20][21] whereas only a few studies consisting of a small number of subjects found no difference between lean and obese subjects. [16][17][18] It could be questioned whether low PP levels may contribute to obesity as circulating PP concentrations decrease appetite in humans.…”
Section: Discussionsupporting
confidence: 91%
See 1 more Smart Citation
“…Our findings of decreased fasting PP levels in obese children are in concordance with most studies in obese adults, [19][20][21] whereas only a few studies consisting of a small number of subjects found no difference between lean and obese subjects. [16][17][18] It could be questioned whether low PP levels may contribute to obesity as circulating PP concentrations decrease appetite in humans.…”
Section: Discussionsupporting
confidence: 91%
“…Some studies found no difference between lean and obese subjects, [16][17][18] whereas other studies demonstrated lower fasting PP levels in obese subjects. [19][20][21] If PP levels are decreased in obese subjects, this could reflect a consequence of overweight or, on the other hand, a cause of overweight as PP affect food intake. To differentiate these two possibilities, long-term studies in obese subjects losing weight are necessary.…”
Section: Introductionmentioning
confidence: 99%
“…Perhaps duration of diabetes or age interacting with diabetes relates to these findings in the older subjects. There was no evidence of an effect of adiposity upon fasting plasma levels of PP [18,19].…”
Section: Discussionmentioning
confidence: 76%
“…[6][7][8][9] In developing such ligands, truncated peptide analogues are becoming increasingly popular. For example, [Nle 30 ]hPP [25][26][27][28][29][30][31][32][33][34][35][36] and [Leu 34 ]pNPY [25][26][27][28][29][30][31][32][33][34][35][36] were found to be Y 4 R selective partial agonists, 10 and a nonapeptide based on the C-terminal fragment of NPY, Ile-Asn-Pro-Ile-Tyr-Arg-Leu-Arg- [28][29][30][31][32][33][34][35][36] ], also known as 1229U91, showed enhanced potency at both receptor subtypes but is in particular the most potent known Y 1 R antagonist.…”
Section: Introductionmentioning
confidence: 99%