Примери за използване на Glucagon secretion на Английски и техните преводи на Български
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Glucagon secretion.
In parallel, glucagon secretion is suppressed.
In case of hypoglycaemia, the rescue mechanism of glucagon secretion is preserved.
Exenatide suppresses glucagon secretion which is known to be inappropriately elevated in type 2 diabetes.
Simultaneously, liraglutide lowers inappropriately high glucagon secretion, also in a glucose-dependent manner.
Conversely, during hypoglycaemia liraglutide diminishes insulin secretion and does not impair glucagon secretion.
In addition, GLP-1 lowers glucagon secretion from pancreatic alpha cells.
Thus, when blood glucose is high,insulin secretion is stimulated and glucagon secretion is inhibited.
In addition, GLP-1 lowers glucagon secretion from pancreatic alpha cells.
When blood glucose levels are low,insulin release is not enhanced and glucagon secretion is not suppressed.
Dulaglutide suppresses glucagon secretion which is known to be inappropriately elevated in patients with type 2 diabetes.
Liraglutide stimulates insulin secretion andlowers inappropriately high glucagon secretion in a glucose-dependent manner.
GLP-1 also lowers glucagon secretion from pancreatic alpha cells, leading to reduced hepatic glucose production.
Semaglutide reduces blood glucose in a glucose dependent manner by stimulating insulin secretion and lowering glucagon secretion when blood glucose is high.
Furthermore GLP-1 also reduces glucagon secretion from pancreatic alpha cells, resulting in a reduction in hepatic glucose output.
Semaglutide lowered high blood glucose concentrations by stimulating insulin secretion and lowering glucagon secretion in a glucose dependent manner.
Liraglutide stimulates insulin secretion and lowers glucagon secretion in a glucose-dependent manner which results in a lowering of fasting and post-prandial glucose.
At a low blood glucose concentration, the listed effects of incretins on the release of insulin and the decrease in glucagon secretion are not observed.
It encourages inulin secretion, blocks glucagon secretion, and increases feelings of fullness.
By increasing endogenous GLP-1 levels, vildagliptin also enhances the sensitivity ofalpha cells to glucose, resulting in more glucose-appropriate glucagon secretion.
Linagliptin glucose-dependently increases insulin secretion and lowers glucagon secretion thus resulting in an overall improvement in the glucose homeostasis.
By increasing the concentration of endogenous GLP-1, vildagliptin increases the sensitivity of α-cells to glucose,which leads to an improvement in glucose-dependent regulation of glucagon secretion.
Semaglutide is a once-weekly analogue of human glucagon-like peptide-1(GLP-1)that stimulates insulin and suppresses glucagon secretion in a glucose-dependent manner, while decreasing appetite and food intake.
By increasing the concentration of endogenous GLP-1, vildagliptin increases the sensitivity of α-cells to glucose,which leads to an improvement in glucose-dependent regulation of glucagon secretion.
GLP-1 and GIP increases insulin biosynthesis and secretion from pancreatic beta cells,while GLP-1 also inhibits glucagon secretion and hepatic glucose production.
The effects of GLP-1 and GIP are glucose-dependent such that when blood glucose concentrations are low,stimulation of insulin release and suppression of glucagon secretion by GLP-1 are not observed.
With a lack of energy andthe hormone insulin, the secretion of glucagon, cortisol and somatotropin is inhibited.
The GLP-1 receptor is the target for native GLP-1,an endogenous incretin hormone that potentiates glucose-dependent insulin secretion from beta cells and suppresses glucagon from alpha cells in the pancreas.
The introduction of glucagon at a dose of 1 mg increases the secretion of HGH 1.5 times.