Obesity
|
0.300 |
Biomarker
|
disease |
BEFREE |
A dual incretin receptor agonist designed to co-activate GLP-1 and GIP receptors was recently shown to elicit robust improvements of glycemic control (mean haemoglobin A1c reduction of 1.94%) and massive body weight loss (mean weight loss of 11.3 kg) after 26 weeks of treatment with the highest dose (15 mg once weekly) in a clinical trial including overweight/obese patients with type 2 diabetes.
|
31443356 |
2019 |
Obesity
|
0.300 |
Biomarker
|
disease |
BEFREE |
Ambiguity regarding the role of glucose-dependent insulinotropic polypeptide (GIP) in obesity arises from conflicting reports asserting that both GIP receptor (GIPR) agonism and antagonism are effective strategies for inhibiting weight gain.
|
31447324 |
2019 |
Obesity
|
0.300 |
Biomarker
|
disease |
BEFREE |
Loss or attenuation of GIP receptor (GIPR) action leads to resistance to diet-induced obesity through incompletely understood mechanisms.
|
31451430 |
2019 |
Obesity
|
0.300 |
Biomarker
|
disease |
BEFREE |
Glucose-dependent insulinotropic polypeptide (GIP) receptor (GIPR) is associated with obesity in human genome-wide association studies (GWAS).
|
31511854 |
2020 |
Obesity
|
0.300 |
Biomarker
|
disease |
BEFREE |
Augmentation of glucose mediated insulin release, the incretin effect, was discovered soon after GIP was first isolated and only much later was its important role in the pathogenesis of obesity, through mechanism other than insulin secretion, appreciated.
|
31539554 |
2019 |
Obesity
|
0.300 |
Biomarker
|
disease |
BEFREE |
Lastly, we discuss how dysmetabolic conditions such as obesity and type 2 diabetes may shift the actions of GIP in an atherogenic direction, and we provide a perspective on the therapeutic potential of GIP receptor agonism and antagonism in cardiovascular diseases.
|
31689454 |
2020 |
Obesity
|
0.300 |
Biomarker
|
disease |
BEFREE |
A synthetic monomeric peptide triple receptor agonist, termed "Triagonist" that incorporates glucagon-like peptide-1 (GLP-1), glucose-dependent insulinotropic polypeptide (GIP) and glucagon (Gcg) actions, was previously developed to improve upon metabolic and glucose regulatory benefits of single and dual receptor agonists in rodent models of diet-induced obesity and type 2 diabetes.
|
31730763 |
2020 |
Obesity
|
0.300 |
Biomarker
|
disease |
BEFREE |
As such, blockade of GIP receptor (GIPR) action has been proposed as a means to counter insulin resistance, and improve metabolic status in obesity and related diabetes.
|
31733230 |
2020 |
Obesity
|
0.300 |
GeneticVariation
|
disease |
BEFREE |
This, together with reports on GIP antagonists that may protect against obesity, has revived the interest on the GIP/GIPR axis as a potential anti-diabetic pathway.
|
31751656 |
2020 |
Obesity
|
0.300 |
Biomarker
|
disease |
BEFREE |
GIP analogues and the treatment of obesity-diabetes.
|
31756366 |
2020 |
Obesity
|
0.300 |
Biomarker
|
disease |
BEFREE |
This review will discuss the physiological effects of GIP on fat metabolism in human adipose and other non-adipose tissues such as liver, pancreas, skeletal muscle and heart, describe where the actions of GIP may contribute to the pathophysiology of obesity, T2D and NAFLD and finally describe the therapeutic implications of GIP antagonism and agonism in these conditions.
|
31759125 |
2020 |
Obesity
|
0.300 |
Biomarker
|
disease |
BEFREE |
GIP analogues augment bone strength by modulating bone composition in diet-induced obesity in mice.
|
31765668 |
2020 |
Obesity
|
0.300 |
GeneticVariation
|
disease |
BEFREE |
Nonetheless, interrogation of the GIP/GIPR axis on cardiac function in humans will involve the systemic actions of the GIPR within the myocardium and other systems (e.g. adipose tissue, vasculature), which will influence the long-term future of GIPR modification for the treatment of obesity/T2DM.
|
31812593 |
2020 |
Obesity
|
0.300 |
Biomarker
|
disease |
BEFREE |
Among the gastrointestinal hormones, the incretins: glucose-dependent insulinotropic polypeptide and glucagon-like peptide-1 have attracted interest because of their importance for the development and therapy of type 2 diabetes and obesity.
|
31815785 |
2020 |
Obesity
|
0.300 |
Biomarker
|
disease |
BEFREE |
Recent studies with a GIP receptor antagonist suitable for human studies have confirmed these concepts regarding the actions of endogenous GIP and point to potential beneficial metabolic effects of GIP receptor antagonists rather than agonist in the treatment of obesity and type 2 diabetes.
|
31838219 |
2020 |