Pharmacology of Insulin Flashcards

1
Q

When is insulin produced?

A

Basally and in response to nutrient intake by beta cells in the islets of langherhans
- With meals, incretins produced by the intestine further enhance insulin secretion.

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2
Q

Where are the insulin producing cells located (islets of langerhans)?

A

The insulin-producing b-cells (in blue) are in the center close to the blood supply. They are surrounded by the glucagon-producing α-cells (in orange). The delta (δ) cells (in yellow) make somatostatin, and the PP cells (in green) make pancreatic polypeptide.

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3
Q

Where does insulin travel upon secretion by the pancreas?

A

Upon secretion by the pancreas, insulin travels to the liver via the portal system, and then to the periphery

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4
Q

What are insulin’s target tissues?

A

Insulin target tissues are liver, muscle, and fat.

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5
Q

Where is insulin degraded?

A

1) About half of the insulin secreted by the pancreas is degraded in the liver.
- This organ is therefore normally exposed to a higher concentration of insulin than are peripheral target tissues.
2) Insulin is also rapidly degraded in the periphery.

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6
Q

Where in pancreatic beta cells is insulin produced?

A

Insulin in the pancreatic beta cells is stored in secretory granules in a complex with zinc.

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7
Q

How is insulin released by beta cells?

A

Insulin can be rapidly released by fusion of the secretory granules with the cell membrane.
- Secretion occurs by exocytosis of the secretory granules from pancreatic Beta cells.

  • Exocytosis is triggered through an increase in ATP (e.g., stimulated by glucose).
  • This increase causes a potassium (K+) channel to close, which prevents K+ exit and causes depolarization of the cell.
  • This in turn causes a Ca++ channel to open, and Ca++ promotes exocytosis.

[Continued insulin production can result in a second phase of sustained release.]

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8
Q

Describe the protein organization/formation of insulin.

A

Mature insulin is composed of two polypeptide chains (the A + B chains) connected by disulfide links.

  • Insulin is initially synthesized as preproinsulin.
  • Removal of the pre-sequence yields proinsulin.
  • Proinsulin is then cleaved to form mature insulin plus C‑peptide (connecting peptide).
  • *- C-peptide is present in the granules and is released along with the insulin.**
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9
Q

How does insulin exert it cellular effects?

A

Insulin exerts its effects by binding to the insulin receptor on the surface of target cells.

  • This receptor consists of 2 alpha subunits and 2 beta subunits.
    • The alpha subunits contain the insulin binding domains and the beta subunits have **tyrosine kinase activity. **

** - Binding of insulin to the alpha subunits promotes autophosphorylation of the beta subunits. **

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10
Q

What is the glucose transporter of muscle and fat cells?

A

Glut 4: Muscle and fat cells contain preformed vesicles with glucose transporters

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11
Q

What are the global actions of insulin?

A

1) Insulin promotes the storage of glucose as glycogen, amino acids as proteins, and fatty acids as triglycerides.
2) Insulin inhibits the breakdown of glycogen, proteins, and fats.
* * - Thus, insulin promotes the build-up and storage of cellular nutrients, and inhibits their breakdown (can do this at the gene transcription/inhibitor level)**

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12
Q

What proteins in the insulin cascade activate (de)phosphorylation?

A

**IRS proteins: **The insulin receptor phosphorylates target proteins, including IRS proteins (Insulin Receptor Substrates). These activate phosphorylation and dephosphorylation.

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13
Q

Who is insulin given to?

A

1) Insulin is a necessary drug for patients with Type 1 diabetes.
2) Insulin can also be used for Type 2 diabetes not controlled by other measures such as diet, exercise, weight loss, and oral agents.

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14
Q

How is insulin administered?

A

Insulin is a protein and would be subject to degradation upon oral administration. It is generally administered subcutaneously.

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15
Q

How are the levels of insulin different in an insulin controlled diabetic and non-diabetic patients?

A

1) In a non-diabetic where insulin is secreted via the portal system, the liver is exposed to a higher concentration than are other target tissues.
2) However, when insulin is administered subcutaneously to a diabetic patient, the liver is not exposed to a higher concentration than other target tissues. **It may therefore be necessary to maintain higher than normal blood levels of insulin in these patients to appropriately suppress hepatic glucose output. **

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16
Q

Describe the time course of various types of insulin.

A

Rapid acting: Insulin Lispro

Short acting: Regular insulin; solution/dissolved (can be given IV)

Intermediate acting: NPH (Neutral Protamine Hagedorn); precipitated

Long acting: Insulin detemir and Insulin glargine

17
Q

What is NPH?

A

Precipitation of insulin with protamine produces NPH insulin (Neutral Protamine Hagedorn).

  • Insulin is present in a precipitated form in this preparation
  • It is not absorbed as rapidly as regular insulin after subcutaneous administration. (This is because of the time required for the insulin to dissolve into solution in order to be absorbed.)
  • **- Because of its slower absorption, NPH insulin has a delayed onset and a longer duration of action than regular insulin. ***
18
Q

What is insulin lispro?

A

In Insulin Lispro, Lys and Pro are reversed at amino acid positions at 28 and 29 of the B chain.

  • Regular insulin forms aggregates (e.g. hexamers in a complex with zinc), which require time for disaggregation and absorption.
  • Insulin Lispro aggregates less, which allows for more rapid absorption.

** - The rapid absorption of Insulin Lispro helps decrease hyperglycemia after the meal. **

19
Q

What are the advantages of insulin lispro?

A
  • Insulin Lispro aggregates less, which allows for more rapid absorption.
  • Regular insulin is taken 30-60 minutes before a meal, to insure that it is present when the meal is eaten.
      • Insulin Lispro is taken 0‑15 minutes before a meal.**
  • ** - The rapid absorption of Insulin Lispro helps decrease hyperglycemia after the meal. ***
20
Q

What is insulin glargine?

A

The modifications made in Insulin glargine cause it to precipitate at the pH present subcutaneously. It is called a “peakless” insulin because it is absorbed very slowly over time such that there is no distinct peak in insulin level.
- long acting insulin

21
Q

What is insulin detemir?

A
  • Insulin Detemir is a long-acting insulin.
  • It contains a fatty acid added to amino acid residue 29 of the B chain among other changes.
  • It binds to albumin in the blood, which prolongs its action.
22
Q

What approach is used to normalize glucose levels in diabetics?

A

This objective can be approached by using a “basal-bolus” approach to provide a basal level of insulin (to suppress hepatic glucose output) **plus additional insulin with meals. **

  • This often involves the use of an intermediate- or long-acting insulin plus a rapid- or short-acting insulin.

[insulin pumps achieve this same effect]

23
Q

What is the benefit of intensive/tight insulin control?

A

Less immediate and long term effects of diabetes

24
Q

What is the potential adverse side effect of intensive insulin therapy?

A

hypoglycemia