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Full Version: Sulfonylurea and meglitinides - 2pac
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Closes K channel on beta cells, depolarize—> calcium influx —-> insulin release

Meg works the same way shorter half life
Meglitinides (glinides) make up a class of drugs used to treat diabetes type 2.[1]

They bind to an ATP-dependent K+ (KATP) channel on the cell membrane of pancreatic beta cells in a similar manner to sulfonylureas but have a weaker binding affinity and faster dissociation from the SUR1 binding site. This increases the concentration of intracellular potassium, which causes the electric potential over the membrane to become more positive. This depolarization opens voltage-gated Ca2+ channels. The rise in intracellular calcium leads to increased fusion of insulin granulae in the cell membrane, and therefore increased secretion of (pro) insulin.
GLINIDES
Glinides, repaglinide and nateglinide, are short acting secretagogues. The short duration of their action means reduced risk of hypoglycemia compared to sulfonylureas. This is an advantage for diabetic subjects with CKD because they belong in the high risk for hypoglycemia group as already mentioned.

Sulfonylureas are contraindicated in ckd!
Hey pac can i get your skype id.I have some questions
Thanks