Module F Flashcards

1
Q

List and describe the functions of the 4 hormones produced by the endocrine pancreas

A
  • Insulin: produced by beta cells. Increases glucose uptake, storage, and utilization, lowering blood glucose
  • Glucagon: produced by alpha cells. Inhibits insulin activity and promotes glycogenolysis and gluconeogenesis, increasing blood glucose.
  • Pancreatic polypeptide: facilitates digestive processes, exact functions unclear
  • Amylin: function is unknown
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2
Q

Describe general features of the pathophysiology, onset, and signs/symptoms of type 1 diabetes

A
  • rapid onset (over a few weeks)
  • Ususally juvenile onset, but may be later
  • severe insulin depletion
  • increased circulating glucagon (insulin inhibits glucagon secretion)
  • May cause ketoacidosis
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3
Q

oral hypoglycemics generally ______ (are / are not) effective in management of type 1 NIDDM

A

are not!

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4
Q

Insulin ______ (can / can not) be given orally

A

can not

it is a polypeptide and is hydorlyzed in the GIT

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5
Q

1 unit (u) of insulin is defined as:

A

the amount required to mobilize 10g of dietary carbohydrates

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6
Q

Outline 4 major physiologic effects of insulin

A
  • Inhibits glycogenolyis and promotes glycogenesis in the liver and skeletal muscles
  • Promotes glucose uptake in liver and skeletal muscles by up-regulating GLUT transporters
  • Promotes utilization of glucose for ATP production in skeletal muscle
  • Promotes lipogenesis from glucose in adipose tissue
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7
Q

Compare circulating insulin, glucagon, glucose, and ketone levels in patients with unmanaged type 1 vs type 2 diabetes

A
  • Type 1: Insulin = low, glucagon = high, glucose = high, ketones = high
  • Type 2: Insulin = high, glucagon = low, glucose = high, ketones = low
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8
Q

The 5 classes of insulin analogues are:

A
  • rapid-acting
  • short-acting
  • intermediate-acting
  • long-acting
  • inhaled
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9
Q

The class of insulin analogue used to control post-prandial blood glucose is ________

A

Rapid-acting

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10
Q

Rapid-acting insulins (novolog, humalog), are often combined with a ________

A

long-acting insulin (Glargine/lantus)

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11
Q

The only class of insulin suitable for IV injection during DKA is _______

A

short-acting

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12
Q

short-acting insulin ______ (is / is not) suitable for post-prandial glucose control because:

A

is not, because the onset is too slow and duration too short so it causes post-prandial hyperglycemia followed by reflex hypoglycemia

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13
Q

The cheapest form of insulin preparation is _________. The drawbacks of this formulation are:

A

intermediate acting. Drawbacks are no consistent absorption, and much interpatient variability in activity

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14
Q

Long-acting insulin (glargine/lantus) may be released over a period of ______. It is used to control _____ (basal / post-prandial) insulin levels and is often combined with _____

A

24hrs. Basal insulin levels. A rapid acting insulin

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15
Q

Describe the function and advantages of inhaled insulins

A

used in place of rapid or short-acting insulins. Advantage is that it doesn’t require SC injection and therefore may lead to better patient adherence.

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16
Q

The two classes of insulin secretagogues are:

A

sulfonylureas and meglinitides

17
Q

The mechanism of action of sulfonylurea drugs is:

A

they increase pulsatile (not basal) insulin secretion and decrease glucagon production. They also increase insulin sensitivity somewhat in type 2 DM

18
Q

The major adverse effects of sulfonylurea drugs (glyburide, etc.) are:

A
  • hypoglycemia with increased activity or skipped meals
  • skin rashes, N/V, hematologic effects
  • many drug interactions
19
Q

The drugs of choice in treating type 2 diabetes are:

A

metformin

20
Q

Describe the MOA and administration of meglinitide agents

A

they increase insulin secretion over a 3-4 hour period. They are taken orally pre-prandially

21
Q

The most commonly used oral hypoglycemic is:

A

metformin

22
Q

sulfonylureas _____ (may / may not) be co-administered with a meglinitide. Either insulin secretagogue _____ (may / may not) be combined with metformin

A

may not. May

23
Q

Describe the MOA of metformin

A
  • primarily inhibits liver gluconeogensis
  • Increases insulin sensitivity by promoting insulin-receptor binding and up-regulating GLUT-4 transporter production
  • inhibits glucose absorption from the GIT
24
Q

The first-line therapy for all type 2 diabetes is:

A

diet and lifestyle changes

25
Q

Describe the two major clinical uses of vasopressin

A
  • Used as an antidiuretic to treat states of extreme water excretion such as diabetes insipidus
  • Used as a vasoconstrictor to manage hypotension due to V1 receptor binding in smooth muscle
26
Q

Contrast the effects of V1 and V2 receptor binding by vasopressin

A
  • V1: found in vascular smooth muscle. Binding causes vasoconstriction and increased BP
  • V2: found in renal collecting ducts. Cause aquaporin production on luminal surface of CD, increased water retention and concentration of urine. Leads to increased blood volume and increased BP