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Year 2 - LCRS > Endocrinology > Flashcards

Endocrinology Flashcards

1
Q

What stimulates the production of IGF-1 and where is it made?

A

GH and in the liver

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2
Q

What is the cause of Laron dwarfism?

A

GH receptor defect

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3
Q

Two exaqmples of GnRH deficiency

A

Kallman’s syndrome Prader-Willi

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4
Q

What is the gold standard GH Provocation test?

A

Insulin Tolerance test - Give iv insulin. Should be followed by GH spike

(others = GHRH +Arginine

Glucagon im

Exercise)

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5
Q

What is the replacement hormone for ACTH

A

Hydrocortisone

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6
Q

What is the replacement hormone for GH

A

Recombinant GH = Somatotrophin

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7
Q

What are the symptoms of GH deficiency in adults?

A

Reduced lean mass inc. adiposity inc hip:waist dec. muscle Dec. HDL inc. HDL

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8
Q

What are the drugs of choice in acromegaly

A

Somatostatin analogues such as lanreotide and octreotide are the drugs of choice in acromegaly.

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9
Q

What are the metabollic effects of acromegaly?

A

Gh stimulates an inc. in blood glucose -> inc plasma insulin -> insulin resistance -> impaired glucose tolerance test - > diabetes mellitus

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10
Q

What is the test for GH HYPERsecretion?

A

Glucose induced supression of growth hormone (give glucose -> inhibit GH release. In acromegaly = paradoxical rise in GH)

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11
Q

Name 2 commonly used Dopamine receptor antagonists

A

Bromocriptine (oral) and Cabergoline (oral - longer t1/2)

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12
Q

What is the principle action of vasopressin

A

Antidiuretic

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13
Q

What are the signs and symptoms of Diabetes insipidus ?

A

Lack of vasopressin. Hypo-osmolar polyuria and polydipsia. (peeing large volumes of very dilute water). dehydration if intake not maintained. Electrolyte imbalance

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14
Q

How do you test for diabetes insipidus?

A

Fluid deprivation test?

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15
Q

What results would you expect to see in an individual with DI after a fluid deprivation test?

A

No real change in urine osmolarity

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16
Q

How do you test the difference between nephrogenic and central DI

A

Administer DDAVP (desmopressin). Central DI will be able to concentrate urine and urine osmolarity will rise.

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17
Q

What is SIADH

A

Syndrome of inapropriate ADH

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18
Q

What is the main result of SIADH

A

hyponatraemia due to increased watrer reabsorption diluting the plasma

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19
Q

What are the symptoms of hyponatraemia

A

Generalised weakness Poor mental function Nausea Confusion coma death

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20
Q

What is exogenous Vasopressin called

A

Argipressin

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21
Q

Other than water reabsorption, what other effect does vasopressin have

A

V1 - Vascular smooth muscle - contraction Non- vascular smooth muslce - contraction (gut motility) Liver Platelets CNS - Increased ACTH secretion V2 - Increased VIII and von Willebrand factor production

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22
Q

Name a V2 selection Vasopressin receptor agonist and how is it administered

A

desmopressin (Nasally/orally)

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23
Q

How do you treat nephrogenic DI

A

Thiazides (inhibit Na+/Cl- transport in the distal convoluted tubule).

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24
Q

What is the name given to primary hypothyroidism

A

Myxoedema

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25
Q

What sign and symptoms will you see in myxoedema

A

BMR fall Bradycardia Weakness Cold intolerance Weight gain Constipation

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26
Q

Thyroxine = T4 or T3?

A

T4 = Thyroxine `

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27
Q

What is the normal thyroid hormone replacement therapy ?

A

Levothyroxine Sodium (t4) Rearely T3 is used Liothyronine Sodium

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28
Q
A
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29
Q

What is the binding hormone globulin for T3 +T4 called?

A

TBG (Thyroid Binding Globulin)

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30
Q

What Graves disease?

A

Hyperthyroidism with autoimmune antibodies to the antibodies to the receptor for thyroid-stimulating hormone (TSH)

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31
Q

Smooth goitre = Plummers or Graves?

A

Graves

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32
Q

What is the treatment of hyperthyroid disorders?

A

PTU (Propylthiouracil)

CBZ (Carbimazole)

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33
Q

Why might the clinical effect of Thionamide drugs take weeks to show clinical effects?

A

Large storage in the colloid

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34
Q

What might be a third cause of hyperthyroidism?

A

Viral thyroidistis -(ie de Quervain’s syndrome) Damages the thyroid follicles and all the stored thyroxine gets RELEASED

Patient has thyrotoxicosis but with no uptake of iodine.
Four weeks later, the stored thyroxine will be exhausted so the patient will be hypothyroid.
After another month, the cells will have recovered and will start to produce thyroxine again so they will return to normal

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35
Q

What is the difference between Cushings disease and Cushing’s syndrome

A

Disease = pituitary tumour. Syndrome = all other causes of high cortisol

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36
Q

How do you test for Cushing’s ?

A
  1. 24hr urine collection
  2. Secret midnight blood test - to test for diurnal cortisol levels
  3. Low dose dexamethasone suppression test (GOLD STANDARD)

Dexamethasone = artificial steroid . Someone with Cushing’s Syndrome will have a high level of cortisol even after the low dose dexamethasone suppression test

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37
Q

What is the drug treatment of Cushing’s ?

A

Metyrapone (+Ketoconazole)

Inhibits 11-beta hydroxylase in the zona fasciculata.

(mineralocorticoid effect = hypertension

Increase adrenal androgens can cause hirsiutism)

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38
Q

What is the name given to the syndrome resulting from a benign tumour of zona glomerulosa and waht is the result?

A

Conn’s syndrome

Tumour secretes aldosterone leading to hypertension and Hypokalaemia

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39
Q

What is the treatment give to sufferers of Conn’s syndrome

A

Mineraloocorticoid Receptor Antagonist

eg SPIRONOLACOTNE. However can cause menstrual irregularities (F) and gynaecomastion (M) due to androgen effect

EPLERONONE (fewer progesterone and androgen effects)

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40
Q

What is a phaeochromocytoma?

A

Tumour of the medulla that secretes catecholamines (adrenaline and noradrenaline)

Can cause SUDDEN massive rise in BP, anxiety, panic.

Stroke, sudden death

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41
Q

Fill in the hydroxylases

A
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42
Q

Fill in the missing steroids

A
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43
Q

What are the main causes of adrenocortical failure ?

A

Tuberculous Addisons

Auto immune Addisons

Congenital Adrenal hyperplasia

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44
Q

What are the signs and symptoms of Addisons and why?

A

Lack of aldosterone
Low BP
Na loss in the urine
high plasma K+

No cortisol
Low glucose

High ACTH
hyperpigmentation

Also- Weight loss, anorexia

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45
Q

How do you test for Addison’s?

A

Short synACTHen test

=

  • 250 ug synacthen IM
  • Measure cortisol response
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46
Q

What is the most common cause of congenital adrenal hyperplasia?

A

21-hydroxylase deficiency

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47
Q
A
48
Q

What is the hallmark of 21-hydroxylase deficiency

A

Excess sex-steroids

49
Q

In adrenocortical failure what hormones need to be replaced?

A

Cortisol and aldosterone must be replaced
Androgens do not need to be replaced as the gonads are the main source and they can take over sufficiently

50
Q

What hormones binds to the mineralocorticoid receptor and which has the greatest affiinity?

A

Aldosterone and cortisol
Cortisol has higher affinity

51
Q

Where are glucocorticoid receptors located?

A

Wide distribution in the body

52
Q

Where are mineralocorticoid receptors located?

A

In the kidney

(discrete distribution)

53
Q

What is the principal action of aldosterone?

A

the reabsorption of sodium and excretion of potassium

54
Q

How is cortisol prevented from binding to aldosterone receptors?

A

The enzyem 11βHSD (11β-hydroxysteroid dehydrogenase 2) converts cortisol to cortisone which is inactive

55
Q

Why do patients with Cushing’s syndrome have hypertension and hypokalaemia?

A

High cortisol, eventually 11β-HSD becomes saturated and can’t convert any more cholesterol so the cortisol binds to the mineralocorticoid receptors
= ↑ Na⁺ resorption, ↑ water resorption, ↑ K⁺ excretion
= hypertension, hypokalaemia

56
Q

What is the receptor selectivity of hydrocortisone, prednisolone and dexamethasone?

A

(=Synthetic cortisol)

Hydrocortisone = Glucocorticoid with mineralocorticoid activity at high doses

Prednisolone = Glucocorticoid with weak mineralocorticoid

Dexamethasone = = Glucocorticoid. No mineralocorticoid

57
Q

What is Fludrocortisone?

A

Alodsterone analogue

58
Q

What drugs are used to treat Addison’s disease ie primary adreonocortical failure?

A

Treat with hydrocortisone (replaces cortisol) and fludrocortisone (replaces aldosterone)

59
Q

What drugs are used to treat secondary adreonocortical failure ie ACTH deficiency?

A

Treat with hydrocortisone only (replaces cortisol) everything else is either done by RAS system or gonads

60
Q

How would oyu treat an Addisonian Crisis?

A
  1. IV saline to rehydrate patient, replace salt and restore volume
  2. High-dose hydrocortisone to replace cortisol
  3. 5% dextrose if hypoglycaemic
61
Q

What is therelationship between oestrogen and LH and FSH?

A

At low concentration Oestrogen = negative feedback on FSH and LH

As levels rise = +ve feedback (especially LH)

62
Q

Which hormone stimulates ovulaiton

A

LH Surge

63
Q

What hormone dominate in the luteal phase of the menstrual cycle?

A

Luteal phase is the release of an egg and the subsequent hormonal change. Large progesterone spike (plus oestradiol and inhibin) peaking at the middle of the Luteal phase. As progesterone release decreases it initiates menstration

64
Q

What are the 2 primary reason for infertility?

A

Primary gonadal failure

Hypothalamic/Pituitary disease

65
Q

What investigations are conducted if male hypogonadism is suspected?

A

1) LH, FSH, testosterone
- if all low MRI pituitary
2) Prolactin
3) Sperm count
- Azoospermia = absence of sperm in ejaculate
- Oligospermia = reduced numbers of sperm in ejaculate
4) Chromosomal analysis (Klinefelter’s XXY)

66
Q

What are the products of tissue-specific processing of testosterone? What receptor do these products act on?

A

1) Dihydrotestosterone (DHT)
acts via the androgen receptor
2) 17β-oestradiol
acts via the oestrogen receptor

67
Q

What enzymes process testosterone?

A

5alpha - reductase = DHT
Aromatase (found in brain and adipose tissue) = 17beta-oestradiol

68
Q

What are the causes of Ovarian failure

A
  • premature ovarian failure (eary menopause)
  • ovariectomy
  • chemotherapy
  • ovarian dysgenesis (Turner’s 45 X)
69
Q

What investigations are conducted in a patient with amenorrhoea?

A

Pregnancy test
LH, FSH, oestradiol
Day 21 progesterone
Prolactin, thyroid function tests
Androgens (testosterone, androstenedione, DHEAS)
Chromosomal analysis (Turner’s 45 X)
Ultrasound scan ovaries / uterus

70
Q

What is the criteria to diagnose PCOS?

A

Need 2 of the following:

  • polycystic ovaries on ultrasound scan
  • oligo- / anovulation
  • clinical / biochemical androgen excess
71
Q

What are the clinical features of PCOS

A

1) Hirsuitism
2) Menstrual cycle disturbance
3) Increased BMI

72
Q

What is the treatment for PCOS with regard to fertility?

A
  • *Metformin**
  • *Clomiphene** anti-oestrogen in the hypothalamus pituitary axis. Blocks oestrogen receptors in the hypothalamus so blocks negative feedback which increases secretion of GnRH.
  • *Gonadotrophin therapy as part of IVF treatment**
73
Q

What investigations would be performed on a woman of 30 who has not had a period for 3 months and has a BMI of 18?

A

Pregnancy test
Blood test (prolactin, LH, FSH, oestrogen, hyper/hypothyroid, androgens- PCOS)
High prolactin- pituitary MRI
Low oestrogen, high LH and FSH = something wrong with ovaries

74
Q

What is another name for Addison’s disease?

A

Primary adrenal insufficiency/hypocortisolism. It is a long-term endocrine disorder in which the adrenal glands do not produce enough Cortisol and aldosterone hormones.

75
Q
A
76
Q

Which drugs might cause Hyperprolactinaemia?

A

Metoclopramide (anti-emetic)
Phenothiazines (anti-psychotics)

77
Q

What night be the drug treatment of hyperprolactinoma?

A

Dopamine agonist

  • Bromocriptine
  • Cabergoline
78
Q

What complications are associated with menopause?

A

Osteoporosis: oestrogen deficiency

Cardiovascular disease: women are protected against CVD before menopause, but have the same risk as men by 70 years

79
Q

What are the different types of HRT? When are they used? Give an example of each drug.

A

Oestrogen-only: Used for women who have had a hysterectomy.
e.g. Premarin
Combined: Used to prevent endometrial hyperplasia in all other women.
e.g. PremPro, CEEs and medroxyprogesterone

80
Q

What are the 4 options for HRT formulations

A
  1. Oral estradiol = low bioavailability
  2. Transdermal patch oestradiol
  3. intravaginal
  4. Oral conjugated equine oestrogen = Estrone suphate.
81
Q

What are the different types of SERMs? What do they do? Give examples.

A

Selective oEstrogen Receptor Modulators:

1) Tissue-selective ER antagonist
e. g. tamoxifen
- Antagonises ERs in breast but has oestrogenic activity in bone
- Oestrogenic effects on endometrium limit it’s use in osteoporosis management

2) Tissue selective ER agonist
e. g. raloxifen (further developed for it’s selectivity on bone)
- Oestrogenic activity in bone. Anti-oestrogenic at breast and uterus
- Risks include VTE and stroke

82
Q

How does a combined oral contraceptive work to prevent pregnancy?

A
  • ive feedback actions of progesterone in the hypothalamus and pituitary supresses ovulation.
  • Progesterone thickens cervical mucus which provides hostile environment to sperm
  • Oestrogen up-regulates progesterone receptors, enhancing sensitivity to progesterone
  • Oestrogen counteracts the androgenic effects of synthetic progesterone, preventing masculinisation
  • Oestrogen contributes to negative feedback at hypothalamus and pituitary, by synergising with progesterone
83
Q

What emergency contraception may be taken?

A

Levonogesterel (within 72 hrs)
Ulipristal (up to 120hrs after intercourse)
-delay ovulation by up to 5 days, impairs implantation

84
Q

What hormone controls tubular fluid reabsorption within the male reproductive tract?

A

Oestrogen = increased concentration of sperm

85
Q

What enzyme converts androgens to oestrogens?

A

Aromatase

86
Q

Where is seminal fluid produced?

A

Small contribution from
- Epididymis/testis
Mainly from accessory sex glands
- Seminal vesicle
- Prostate
- also bulbourethral glands

87
Q

What is capacitation of the sperm? What is the process?

A

Maturation of the sperm so it can achieve fertilising capability

  • Loss of glycoprotein coat
  • Change in the surface membrane characteristics
  • Whiplash movements of the tail
88
Q

What hormone is capacitation of sperm dependent on? Where does it occur?

A

Oestrogen-dependent
Takes place in ionic and proteolytic environment of the fallopian tube
Ca²⁺ dependent mechanism

89
Q

What is the acrosome reaction?

A

1) Sperm binds to the ZP3 receptors on the glycoprotein coating of the ovum (zona pellucida)
2) This causes a Ca²⁺ influx into the sperm (stimulated by progesterone)
3) The sperm then releases hyaluronidase and proteolytic enzymes
4) Sperm then penetrates the zona pellucida

90
Q

What is the cortical reaction and what triggers it?

A

It is triggerered by fertilization. Cortical granues release molecules that degrade the zona pellucida , preventing further sperm from binding

91
Q

What are polar bodies?

A

Produced from unequeal division of the ovum, contains only genetic material. No cytoplasm

92
Q

How long can a fertilised ovum survive before implantation as it travels down the fallopian tube? How does it receive nutrients?

A

Can last around 9-10 days
Receives nutrients from uterine secretions

93
Q

What are the 2 phases of implantation ?

A

1) Attachement phase- outer trophoblast cells make contact with the uterine epithelium
2) Decidualizaton process that occurs in the endometrium because of progesterone

94
Q

What molecules are secreted from the secretory glands in the endometrial lining that promote adhesion of the blastocyst?

A

LIF (leukaemia inhibitory factor) -stimulates adhesion of the blastocyst to endometrial cells
IL11 - released into uterine fluid .

95
Q

What changes occur during decidualization of the endometrium ?

A

Glandular epithelium secretion

INcreased glycogen accumulation in stromal cell cytoplams

growth of capillaries

increased vascular permeability

96
Q

What is the first hormone to peak during pregnancy

A

hCG
human chorionic gonadotrophin

97
Q

At what point during pregnancy does the fetoplacental unit take over oestrogen production? and specifically which one

A

From day 40 - mainly oestriol (weaker than eastradiol but produced in greater amounts)

98
Q

What maternal hormones rise during pregnancy (5)

A

ACTH -(pregnant cushings)
Iodothyronines
Prolactin
Adrenal steroids
PTHrp (related peptide)

99
Q

Which hormones fall during pregnancy ?

A

Gonadotrophins
TSH (T4/3 production driven by hCG)
hGH

100
Q

Which hormone stimulates milk synthesis and which stimulates milk ejection?

A

Milk synthesis = Prolactin

Ejection = oxytocin

101
Q

What is the key brain area involved in the regulation of food intake?

A

The arcuate nucleus

102
Q

What are the two neural populations in the arcuate nucleus?

A

1) Stimulatory (of appetite) = (NPY/Agrp neurons)
2) Inhibitory = (POMC neuron)

103
Q

What receptor do these neurons use for signalling?

A

MC4R

(melanocortin 4 receptor)

104
Q

What is the overall effect of MC4R stimulation ?

A

Decrease in food intake

105
Q

How do POMC and Agrp/NPY act on the MC4R?

A

POMC is cleaved to produce α-MSH, an agonist of MC4R = decreases food intake

Agrp = antagonist of MC4R = increased food intake

106
Q

How does a POMC mutation present?

A

Hungry all the time
No cortisol regulation
Pale skin and red hair

107
Q

What effect does Leptin have on POMC/Agrp?

A

Activates POMC, inhibits Agrp

108
Q

What effect does ghrelin have on neurons in the arcuate nucleus?

A
  • Stimulates NPY/Agrp neurons
  • Inhibits POMC neurons
  • Increases appetite
109
Q

Where is Ghrelin released and how is it activated?

A

It is released in the stomach, activated by GOAT

110
Q

What effect does ghrelin have on neurons in the arcuate nucleus?

A
  • Increases appetite, levels go up when fasted. Stimulates NPY/Agrp neurons
  • Inhibits POMC neurons
111
Q

What do L cells secrete?

A

PYY and GLP-1

112
Q

What effect does PYY have on neurons in the arcuate nucleus?

A
  • Inhibits NPY release
  • Stimulates POMC
  • Decreases appetite
113
Q

What does glucagon-like peptide-1 do?

A

Important in stimulating glucose-stimulated insulin release (incretin role) and also reduces food intake

114
Q

What is the synthetic (long-acting) GLP-1-like peptide that is approved for the treatment of obesity?

A

Saxenda

115
Q
A

Year 2 - LCRS (9 decks)

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