W4 - Hypothalamic-Pituitary-Gonadal Axis II Flashcards

1
Q

What is Puberty?

A
  • Transition from non-reproductive to reproductive state
  • Gonads produce mature gametes:
  • Testes -> spermatozoa
  • Ovaries -> oocytes (born with full amount for life time. At puberty, gains competence for fertilisation).
  • Breast development in females, and increased testicular volume in males.
  • Secondary characteristics develop (primary are present at birth)
  • Profound physiological changes
  • Profound psychological changes
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2
Q

What is Andrenarche (pubarche)?

A

Caused by secretion of Adrenal androgens.

Growth of pubic
hair, axillary hair
Growth in height
Independently regulated

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3
Q

What is Gonadarche?

A

LH/FSH

LH - steroid synthesis –> secondary sex characteristics
FSH - growth of testis (male)/steroid synthesis/folliculogenesis (female)

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4
Q

What are the mechanisms behind Adrenarche?

A
  • Change in adrenal androgen secretion due to cellular remodelling of adrenal gland:
  • Dehydro-epiandrosterone (DHEA)
  • Dehydro-epiandrosterone sulphate (DHEAS)

Gradual increase 6  15 years
20-fold increase peaking at ̴20-25 years
Declines thereafter

No change in other adrenal steroids
* Secreted from zona reticularis of adrenal cortex
* No known mechanism for trigger of adrenarche

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5
Q

What is the Adrenarche:Pubicarche?

A

This is a consequence of Adrenarche.
* Appearance of pubic / axillary hair resulting from adrenal androgen secretion

  • Associated with:
  • Increased sebum production = acne
  • Infection, abnormal keratinization = acne
  • If before 8 years (girls) or 9 years (boys)
    = PRECOCIOUS
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6
Q

What is the mechanism behind Gonadarche?

A
  • Several years after adrenarche (typically ~11 yrs of age)
  • Reactivation of hypothalamic GnRH
  • Activation of gonadal steroid production -> production of viable
    gametes and ability to reproduce
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7
Q

What is the relationship of GnRH and Gonadarche?

A
  • GnRH is synthesised & secreted by specialist hypothalamic centres – GnRH neurones.
  • HPG axis is first activated at 16th gestational week On the 20th week scan of a baby, you are able to tell the gender because of this.
  • Pulsatile GnRH secretion in foetus until 1-2 years postnatally when ceases
  • Re-activation at ~11 years
  • GnRH neurones ‘restrained’ during postnatal period -> 10 years or more
  • At puberty a gradual rise in pulsatile release of GnRH

In studies, LH secretion is used instead of GnRH because they mimic the same function. This is because GnRH is only present in the hypothalamic circulation - can’t get consent from people.

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8
Q

What stimulates the onset of puberty?

A

Clear that it is maturational event within the CNS

Inherent (genetic) maturation of 800-1000 GnRH synthesising
neurones?
Environmental/genetic factors?
Body fat/nutrition?
Kisspeptin?

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9
Q

How does nutrition and body fat relate to reproduction?

A
  • Link between fat metabolism & reproduction
  • Anorexia nervosa / intensive physical training
  • Reduced response to GnRH
  • ↓gonadotrophin levels
  • Amenorrhea
  • Restored when nourished / exercise stopped
  • Frisch et al.: body fat hypothesis
  • Certain % fat:body weight necessary for
    menarche (17%) & required (22%) to
    maintain female reproductive ability. It makes sense because if you are not at the correct amount of energy reserves, they should not be having a baby.
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10
Q

What is the relationship between nutritional gating and puberty?

A

There are studies that link Ghrelin, the appetising factor and Leptin, the satiety factor to nutritional gating and puberty. Both of these factors link to the Hypothalamus so they influence the activity of Kisspeptin thus GnRH, which in turn affects the onset of puberty.

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11
Q

What is the relationship between Kisspeptin and puberty?

A

Inactivating mutations of KISS1R or the gene coding for kisspeptin
* Hypogonadism
* Failure to enter puberty
* Hypogonadotrophic hypogonadism

Activating mutations of KISS1R
* Precocious puberty

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12
Q

What is Consonance?

A

“Smooth ordered progression of changes”
Order of pubertal changes is uniform
* Age of onset, pace & duration of changes
* Wide inter-individual differences
* Average age of menarche onset (UK) = 12.5 years

For females the onset begins with breast bud and for males with the enlargement of genitals followed by an order of events that leads to full maturity - this order is called consonance.

Studies around the world shows that the onset of puberty begins on average 2 years earlier because we are doing better in terms of nutrition etc globally.

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13
Q

What are the tanner stages of puberty: scale of physical measures of development?

A
  1. Pubic and axillary hair growth (♀♂)
  2. Testicular volume and penile length (♂)
  3. Breast development (♀)
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14
Q

What are the physical changes in girls during puberty?

A
  • Breasts enlarge: thelarche – first outward sign of E2 activity
  • Pubic/axillary hair
  • Uterus enlarges, cytology changes, secretions in response to E2
  • Uterine tubes
  • Vagina
  • Cervical changes
  • Height: earlier onset than boys, peak height velocity (PHV) = 9 cm/y, reached at 12 yrs
  • Body shape
  • HPG axis: increase in ovarian size and follicular growth
  • Menarche: not equated with onset of fertility
  • Fertility: in 1st year ~80% menstrual cycles
    anovulatory, irregular cycles
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15
Q

What are the Physical changes in boys during puberty?

A
  • External genitalia
  • increase in testicular volume >4 ml
  • growth of penis, scrotum, scrotal skin changes
  • Vas deferens
  • lumen increases
  • Seminal vesicles & prostate
  • Facial/body hair
  • Pubic / axillary hair
  • Larynx –
  • androgens  enlarge larynx, Adams apple (projection of thyroid cartilage), voice deepens
  • Height
  • PHV =10.3 cm/y reached at 14 yrs
  • Body shape
  • Onset of fertility
  • testosterone from Leydig cells stimulates meiosis & spermatogenesis in Sertoli cells
  • boys fertile at the beginning of puberty
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16
Q

How does a Growth spurt work?

A

Complex interaction
 Growth hormone
 Oestrogen (boys and girls)

Earlier in girls – approx. 2 years

Biphasic effect of oestrogen on epiphyseal growth
 Low levels  linear growth & bone maturation
 High levels  epiphyseal fusion

17
Q

What are the effects of androgens on the differentiation of pilosebaceous units (PSUs)?

A

We have 2 main types of pilosebaceous units.
1) Sebaceous PSU - produces a lot more sebem. This also causes acne.
2) Vellus PSU - in response to the adrenal androgen, there is a differentiation between Terminal PSU, responsible for beard growth and APO-PSU responsible for pubic and auxiliary hair growth.

18
Q

What are psychological changes that occur with puberty?

A
  1. Increasing need for independence
  2. Increasing sexual awareness/interest
  3. Development of sexual personality
    Later maturation = better adjustment
19
Q

What is Precocious sexual development?

A

Development of any secondary sexual characteristic:

before the age of 8 in girls
before the age of 9-10 in boys

20
Q

How does the Premature activation of HPG axis affect precocious puberty/ sexual development?

A
  1. Gonadotrophin-dependent (or central) precocious puberty – consonance
    – Excess GnRH secretion - idiopathic or secondary
    – Excess gonadotrophin secretion - pituitary tumour
  2. Gonadotrophin-independent precocious puberty - loss of consonance
    – Testotoxicosis - activating mutation of LH receptor
    – Sex steroid secreting tumour or exogenous steroids
21
Q

What is McCune Albright syndrome?

A
  • Café au lait skin pigmentation
  • Autonomous endocrine function – most common
    gonadotrophin- independent precocious puberty
  • Mutations in the GNAS1 gene
    This means that all the pathways in the body that relies on G-protein signalling are activated.
  • Hyperactivity of signalling pathways & over-production of hormones
22
Q

What is Pubertal delay?

A

Absence of secondary sexual maturation by 13yrs in girls (or absence of menarche by 18yr) or 14yrs in boys

23
Q

What might cause Pubertal delay?

A

Delayed HPG axis activation

  1. Constitutional delay
    *affecting both growth and puberty. Approx. 90% of all pubertal delay cases.
    *~10X more common in boys
    *secondary to chronic illness e.g., diabetes, cystic fibrosis.
  2. Hypogonadotrophic hypogonadism (low LH and FSH)
    *Kallman’s syndrome (X-linked KAL1 gene, impaired GnRH migration),
    *Other mutations causing defects in GnRH production
  3. Hypergonadotrophic hypogonadism (high LH and FSH)
    *Gonadal dysgenesis and low sex steroid levels:
    – gonadal dysgenesis with normal karyotype, viral e.g. mumps
24
Q

What is Klinefelter’s syndrome XXY or variants?

A

Occurs due to additional X chromosome in males. They end up with more feminine characteristics and occurs in 1:500 males.
- Frontal baldness absent
- Tendency to grow fewer chest hairs
- Poor beard growth
- Narrow shoulders
- Breast development
- Wide hips
- Female type pubic hair pattern
- Long arms and legs

25
Q

What is Turner’s syndrome XO?

A

This is when females only have one X chromosome.
2 classic symptoms of Turners:
* Being shorter than normal
* Underdeveloped or “streak” ovaries

Affects 1:3000 females.