Module 5: Hormonal Communication Flashcards

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1
Q

Endocrine glands

A

Produce and secrete hormones directly into the blood.

They have no ducts.

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2
Q

Exocrine glands

A

Do not produce hormones- they secrete molecules into a duct which carries them to where they are needed.

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3
Q

Adrenal medulla

A

Centre of adrenal gland.

Makes and secretes adrenaline and noradrenaline.

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4
Q

Adrenaline causes

A
  • Relaxes smooth muscle in bronchioles
  • Increases stroke volume of heart
  • Increase heart rate
  • Vasoconstriction
  • Glycogen–>Glucose
  • Dilates pupils
  • Increase mental awareness
  • Body hair erection
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5
Q

Noradrenaline

A

Reverse of adrenaline

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6
Q

Function of adrenaline

A

Non-steroid hormone- these cant dissolve in the cell surface membrane of target cells and get inside and must bind to a receptor.

Non-steroid hormones are known as first messengers- they cause an effect on the cell when they bind to a receptor. The binding causes a G-protein to activate adenyl cyclase which converts ATP into cyclic AMP (cAMP) which is the second messenger because it transmits the signal inside the cell and initiates a change inside the cell.

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7
Q

Adrenal cortex

A

Adrenal cortex ‐ uses cholesterol to produce steroid hormones:
3 layers:
‐ Zona Glomerulosa (nearest outside)
secretes mineralocorticoids ‐ help to control sodium and potassium levels in blood and blood pressure
‐ Zona Fasciculata secretes glucocorticoids e.g. cortisol ‐ helps to control metabolism of carbs, fats and protein in liver
‐ Zona Reticularis (nearest medulla) secretes precursors to the sex hormones

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8
Q

Steroid hormones

A

Steroid hormones enter cells by dissolving in the cell surface membrane.
They then bind with a receptor in the cytoplasm, the receptor‐hormone complex enters the nucleus, binds to another receptor on the chromosome. This causes mRNA to be made which then produces proteins.

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9
Q

Using the example of the adrenal glands, describe how different types of hormones are released and take affect on their target cells. (8)

A
  • endocrine glands release hormones
  • hormones travel in blood
  • to target cells
  • adrenal medulla releases non‐steroid hormones/adrenaline
  • (adrenaline) acts as first messenger
  • G‐protein activates adenyl cyclase
  • converts ATP into cyclic AMP (cAMP)
  • cAMP is the second messenger ‐ causes effect in cell
  • adrenal cortex releases steroid hormones
  • dissolve in cell surface membrane (of target cells)
  • bind with a receptor in the cytoplasm
  • receptor‐hormone complex binds to receptor on the chromosome/DNA
  • causes mRNA/proteins to be made
  • AVP: correct reference to Zona Glomerulosa, Zona Fasciculata, Zona Reticularis
  • AVP: ref to complementary shapes
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10
Q

How can hormones travel all around the body in the blood yet still have such specific effects on body tissue?

A

Endocrine glands make and secrete hormones and release them directly into the blood.

Hormones bind to specific complementary receptors on the cell surface membranes of their target cells.

The hormones will not affect cells without these receptors.

Target cells are grouped into target tissues.

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11
Q

Exocrine action of the pancreas

A

The majority of the cells produce digestive enzymes- ‘pancreatic juice’.

These cells form groups (called acini) secrete enzymes into tubules which lead to the pancreatic duct which takes them to the small intestine.

In the ‘juice’:

  • Amylase
  • Trypsinogen
  • Lipase
  • Sodium hydrogen carbonate (alkali)
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12
Q

Endocrine action of the pancreas

A
  • The islets of Langerhans contain alpha and beta cells
  • The cells detect changes in blood glucose levels (normal = 90mg per100cm3)
  • Alpha cells ‐ produce and secrete glucagon (hormone)
  • Beta cells ‐ produce and secrete insulin (hormone)
  • They secrete the hormones directly into closely associated capillaries
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13
Q

Pancreas on a micrograph

A
  • Most cells = exocrine
  • Groups of cells surrounding smallest hollow tubes - acini
  • Slightly larger circular hollow tubes- tubules leading to pancreatic duct
  • Circular patches with different staining- islets of Langerhans
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14
Q

Blood glucose too high

A

1) Beta cells detect rise in blood glucose level.
2) Stimulates production of insulin by beta cells.
3) Glucagon production by alpha cells is inhibited.
4) Insulin secreted into blood.
5) Insulin binds to receptors of target cells (hepatocytes and muscle cells).

6) Causes:
- More glucose channels inserts into plasma membrane
- more glucose enters the cells
- glucose converted to glycogen
- glucose converted to fats
- increased rate of glucose used in respiration.

7) This results in less glucose in the blood This is an example of negative feedback.

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15
Q

Blood glucose too low

A

1) Alpha cells detect fall in blood glucose level.
2) Stimulates production of glucagon by alpha cells
3) Insulin production by beta cells inhibited.
4) Glucagon secreted into blood.
5) Glucagon binds to receptors on target cells (hepatocytes).

6) Causes:
- hydrolysis of glycogen to glucose (glycogenolysis)
- conversion of fats and amino acids to glucose (gluconeogenesis)
- use more fatty acids in respiration

7) The glucose is released into the blood = more glucose in the blood.

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16
Q

Glycogenolysis

A

Glycogen –> Glucose

17
Q

Gluconeogenesis

A

fats/amino acids –> Glucose

  • amino acid have amino group removed
  • creates pyruvate
  • in the presence of enzyme triose phosphate
  • controls condensation reaction into glucose
18
Q

The benefits of storing glucose as glycogen

A
  • Insoluble
  • Un-reactive
  • Compact
  • Can’t diffuse out of cell
  • Easy to convert to glucose
  • Lots of branches for enzymes to work on in hydrolysis
19
Q

Controlling insulin production

A

1) The cell membrane has potassium and calcium ion channels.
2) The potassium channels are normally open so potassium ions flow out.
3) When blood glucose concentration is high, the glucose moves into the cell.
4) Glucose is metabolised to make ATP.
5) The ATP closes the potassium ion channels.
6) The accumulation of potassium ions alters the p.d. across the cell membrane- the inside becomes less negative.
7) The change in p.d. opens the calcium ion channels.
8) Calcium ions cause the vesicles of insulin to fuse with the cell membrane, releasing insulin by exocytosis.

20
Q

Diabetes mellitus

A

A disease where you can’t control blood glucose levels effectively.

21
Q

Hyperglycaemia

A

b.g too high - can lead to organ damage in the long term.

22
Q

Hypoglycaemia

A

b.g too low - not enough glucose to cells, esp. brain - cause tiredness and irritability to brain damage, seizures and death.

23
Q

Type 1 and Type 2 diabetes comparison

A

Type 1:

  • Insulin dependent diabetes.
  • Autoimmune response - attack own B cells and destroys them.
  • Can’t produce sufficient insulin.
  • Can’t store glucose as glycogen - excess glucose remains in blood - hyperglycaemia.
  • When b.g falls - no/little glycogen store to release glucose - causes hypoglycaemia.

Type 2:
- Non-insulin dependent diabetes.
- Receptors on target cells for insulin decline and cells become unresponsive to insulin.
- Can still produce insulin (less though).
-
-
- Risk factors: age, obesity, refined sugar rich diet, certain ethnicities, family history.

24
Q

Treating type 1 diabetes

A

Type 1:

  • Monitor blood glucose levels and insulin injections administered.
  • Insulin pump - permanently pumps insulin at a steady rate into the blood stream.
  • Insulin for injections is made by genetically modified bacteria.
  • Islet/B cell transplant - healthy B cells from dead donor implanted into pancreas of patient.
  • Pancreas transplant.

The future of treating type 1 diabetes:
- Stem cells could be used to grow new islets of Langerhans with B cells which can produce insulin- this would cure type 1 diabetes.

25
Q

Treating type 2 diabetes

A
  • Control of carbohydrates intake, regular exercise.

- Sometimes insulin injections or drugs to slow absorption of glucose.

26
Q

What are the the advantages of obtaining insulin from genetically engineered bacteria? (4 marks)

A

Engineered insulin is cheaper than from pigs.

Much larger amount of product is more readily available as the rate of production is faster.