INCRETINS: ANTIOBESITY AND ANTIDIABETIC BLOCKBUSTERS
Amit Gangwal*
ABSTRACT
Incretins are a group of specialized hormones secreted in
gastrointestinal tract (usually post - meal) that play crucial role in
feeding behavior directly or indirectly. They stimulate a decrease in
blood glucose levels. Incretins increases insulin release from the beta
cells of the islets of Langerhans of pancreas, post meal so that blood
glucose levels remains in check. They also minimize the rate of
absorption of nutrients into the blood stream by reducing gastric
emptying and may directly reduce food intake by providing a feeling
of satiety. Their gastric emptying delay also causes slower entry of
glucose in blood. They also inhibit glucagon release from the
alphacells of the Islets of Langerhans. Glucagon-like peptide-1 (GLP-1) and gastric inhibitory
peptide (also known as: glucose-dependent insulinotropic polypeptide or GIP) are two major
candidate molecules that fulfill criteria for an incretin. Both GLP-1 and GIP are rapidly
inactivated by enzyme dipeptidyl peptidase- IV (DPP- IV). This led to the concept of DPP -
IV inhibitors as anti diabetic agents. Few insulinotropic activity possessing incretins which
are available in marker for treatment of diabetes are exenatide, liraglutide, exenatide
(extended-release). There are reports of incretins being explored for their role in management
of obesity. This article summarizes potential role of incretins in discovery of antidiabetic and
antiobesity molecule. Article also throws light on recent developments in incretin research.
Keywords: Incretins, GLP-1, Amylin, Exenatide, Gila monster, Diabetes, Obesity, DPP- 4 inhibitors.
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