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what are the 2 classes of anti diabetic drugs that act at targets involved in the absorption of glucose in the GIT and reabsorption of glucose in the kidney, thus affecting glucose homeostasis
sodium glucose co-transport 2 (SGLT-2) inhibitors e.g. dapagliflozin
alpha-glucosidase inhibitors e.g. acarbose
what does dapagliflozin affect
the reabsorption of glucose
what does acarbose reduce
absorption in the gut
what do neither mechanisms of SGLT-2 inhibitors and alpha-glucosidase inhibitors directly involve
insulin
what is the pharmacological target of SGLT-2 inhibitors
SGLT-2
what is SGLT-2
a major transporter that mediates the reabsorption of glucose in the kidney
what will inhibitors of SGLT-2 do
reduce reabsorption and therefore increase excretion of glucose in the urin
hence plasma conc. of glucose is reduced
where is SGLT-2 found and what can you say about its affinity and capacity
proximal convoluted tubule
low affinity, high capacity
means majority of glucose reabsorbed
where is SGLT-1 found and what can you say about its affinity and capacity
proximal straight tubule
high affinity, low capacity
what is the main isoform in the gut between SGLT-2 and SGLT-1
SGLT-1
why do we still absorb some glucose even with an SGLT-2 inhibitor
SGLT-1 can still reabsorb glucose
what is the pharmacological target of alpha-glucosidase inhibitors
alpha-glucosidase (maltase)
what is alpha-glucosidase and what does it do
an enzyme
breaks down short-chain oligosaccharides including maltose to glucose in the GIT
what is required before glucose can be absorbed from the gut into the blood stream
alpha-glucosidase
what would inhibition of alpha-glucosidase do
decrease glucose absorption after a mela
what does acarbose inhibit
alpha-glucosidase
therefore reducing glucose absorption and therefore decreasing post-prandial blood glucose concentration.