Results 191 to 200 of about 64,020 (335)
Effects of Synthetic Human Gastric Inhibitory Polypeptide on Splanchnic Circulation in Dogs
Masafumi Kogire +8 more
openalex +1 more source
Lowering of fasting and food stimulated serum immunoreactive gastric inhibitory polypeptide (GIP) by glucagon. [PDF]
R. Ebert, R. Arnold, W. Creutzfeldt
openalex +1 more source
Gastric Inhibitory Polypeptide Receptor (GIPR) Overexpression Reduces the Tumorigenic Potential of Retinoblastoma Cells. [PDF]
Haase A +5 more
europepmc +1 more source
Central illustration: Pathophysiological mechanisms linking diabetes mellitus and cardiovascular disease. Chronic hyperglycaemia, insulin resistance, and low‐grade inflammation contribute to endothelial dysfunction, myocardial fibrosis, and cardiomyocyte apoptosis.
Lilian Anagnostopoulou +13 more
wiley +1 more source
Tirzepatide as adjunct to insulin in adults with type 1 diabetes and overweight or obesity shows the most consistent signal for body weight reduction, with possible improvements in HbA1c and insulin requirements. However, current evidence remains early, low‐certainty, and insufficient to establish long‐term efficacy or safety.
Giuseppina Alessia Acucella +1 more
wiley +1 more source
Preservation of incretin activity after removal of gastric inhibitory polypeptide (GIP) from rat gut extracts by immunoadsorption [PDF]
R. Ebert, H Unger, W. Creutzfeldt
openalex +1 more source
Natural compounds regulate gut microbiota by improving microbial balance and increasing probiotics, which boost short‐chain fatty acid production to alleviate insulin resistance and inflammation. Additionally, they stimulate appetite‐suppressing hormones through bile acid signaling, while inhibiting pathogenic bacteria to repair intestinal barrier ...
Hongchao Yuan +7 more
wiley +1 more source
Abstract Two Phase 1 open‐label studies were conducted in otherwise healthy participants, with BMI classified as overweight/obesity, to assess the potential of lotiglipron (a glucagon‐like peptide‐1 receptor agonist) as precipitant for pharmacokinetic (PK) drug–drug interactions (DDIs) when co‐administered with substrates of cytochrome P450 (CYP) 3A ...
Carol Cronenberger +11 more
wiley +1 more source

