REPRO: Hypothalamic/Pituitary/Gonadal Axis II Flashcards

1
Q

Briefly, describe puberty.

A

Puberty is the transition from the non-reproductive to reproductive state.

The gonads produce mature gametes:

  • the testes make spermatozoa
  • the ovaries develop oocytes

It can also be (clinically) defined as breast development in females, and increased testicular volume in males.

It’s the secondary characteristics that develop, as the primary ones are present from birth.

There are also some profound physiological changes, such as hair patterning, height, and actual body shape, along with some psychological changes.

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2
Q

What are the two endocrine events that occur during puberty?

A
  1. ADRENARCHE (that leads to PUBARCHE)
    • growth of pubic and axillary hair
    • growth in height
  2. GONADARCHE
    • LH leads to steroid synthesis and the development of secondary characteristics
    • FSH stimulates the growth of testes in males and steroid synthesis and follicular genesis in females
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3
Q

Describe adrenarche.

A

It is the change in adrenal androgen secretion due to cellular remodelling of the adrenal.

It is DHEA (dehydroepiandrosterone) and DHEAS (dehydroepiandrosterone sulphate) that change.
There is a gradual increase in their serum levels, starting from the age of 6-15, to a 20-fold increase peaking at 20-25 years of age. It declines thereafter.

It is secreted from the zona reticularis of the adrenal cortex.
There are no known mechanisms for the trigger of adrenarche.

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4
Q

Describe pubarche.

A

It is the appearance of pubic/axillary hair resulting from the adrenal androgen secretion.

It is associated with increased sebum production, which can cause acne. Infection and abnormal keratinisation can also cause acne.

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5
Q

Describe gonadarche.

A

It occurs several years after adrenarche (typically at around 11 years of age).
It is the reactivation of the hypothalamic-pituitary-gonadal axis (because, during foetal development, the HPG axis is in full working order, as it is required for male differentiation).

It is the activation of gonadal steroid production, leading to the production of viable gametes and ability to reproduce.

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6
Q

Describe GnRH.

A

GnRH is synthesised and secreted by specialist hypothalamic centres - the GnRH neurones.

HPG axis is first activated at the 16th gestational week.
The pulsatile GnRH secretion in the foetus occurs until 1-2 years postnatally, then it ceases.
The GnRH neurones are ‘restrained’ during this postnatal period, for about 10 years or more.

At puberty, there is a gradual rise in the pulsatile release of GnRH.

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7
Q

What changes in the pattern of LH secretion occur during puberty?

A

During early to mid-puberty, there is a nocturnal rise of LH secretion, after which the rise normalised throughout the 24 hour period.

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8
Q

What stimulates the onset of puberty?

A

We do not know exactly what causes the onset of puberty.
It’s clear that it is a maturational event within the CNS.

  • the inherent (genetic) maturation of 800-1000 GnRH synthesising neurones?
  • environmental/genetic factors?
  • body fat/nutrition?
  • kisspeptin?
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9
Q

What does nutrition and body fat have to do with puberty?

A

There is a known link between fat metabolism and reproduction (eg. there is metabolic dysfunction in PCOS, a reproductive hormone imbalance syndrome).

Also, in people with anorexia nervosa/ people who undergo physical training, it is found that they have:

  • a reduced response to GnRH
  • decreased gonadotrophin levels
  • amenorrhea
  • ^ that is restored when they are nourished/ they stop exercise
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10
Q

What do mutations in the KISS1R (kisspeptin receptor) cause?

A

Inactivating mutations of KISS1R lead to:

  • hypogonadism
  • failure to enter puberty
  • hypogonadotropic hypogonadism

Activating mutations of KISS1R lead to:
- precocious puberty

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11
Q

What is consonance?

A

Consonance refers to the smooth ordered progression of changes through puberty.

The age of onset, pace and duration of changes are differences that will be large between individuals, but the order that they occur in remains the same.

The average age of menarche onset (in the UK) is 12.5 years, decreased by 2 years over the last 100, and looks to be still decreasing.

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12
Q

Describe the Tanner stages of puberty.

A

It is a scale of physical measurements of development.

There are 5 stages, and it looks at 3 parameters:

  • breasts in females
  • pubic and axillary hair growth
  • male genitalia in males
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13
Q

Describe the physical changes in girls during puberty.

A
  • breasts enlarge (thelarche, the first outward sign of E2 activity)
  • pubic/axillary hair
  • uterus enlarges, cytology changes, secretions occur in response to E2
  • uterine tubes
  • vaginal changes
  • cervical changes
  • height (earlier in boys than girls)
  • body shape (hips widen, etc.)
  • HPG axis activation (increase in ovarian size and follicular growth
  • menarche (not equated with the onset of fertility)
  • fertility (during the first year, around 80% of the menstrual cycles are anovulatory, irregular cycles)
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14
Q

Describe the physical changes in boys during puberty.

A
  • external genitalia (increase in testicular volume, growth of penis, scrotum, scrotal skin changes)
  • vas deferens (lumen increases)
  • seminal vesicles and prostate
  • facial/body hair
  • pubic/axillary hair
  • larynx (androgens cause the enlargements of the larynx, Adam’s apple [projection of thyroid cartilage], voice deepens)
  • height
  • body shape
  • onset of fertility (testosterone from the Leydig cells stimulates meiosis and spermatogenesis in Sertoli cells)
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15
Q

Describe the growth spurt during puberty.

A

It’s a complex interaction, involving:

  • growth hormone
  • oestrogen (boys and girls)

It occurs earlier in females.

There is a biphasic effect of oestrogen on epiphyseal growth:

  • at low levels, it causes linear growth and bone maturation
  • at high levels, it causes epiphyseal fusion
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16
Q

Describe the effect of androgens on the differentiation of pilosebaceous units (PSUs).

A

We can get a sebaceous PCU, which secretes sebum. This can cause infection and, thus, acne.

We can also get a vellous PSU. This can further differentiate into a terminal PSU (beard), or an APO-PSU (pubic and axillary).

17
Q

What are some psychological changes that occur during puberty?

A
  1. an increasing need for independence
  2. an increasing sexual awareness/interest
  3. development of a sexual personality

The later the physical maturation, the better, as it reduces the chances of the disconnect between the physical and psychological changes.

18
Q

Define precocious sexual development.

A

It is the development of any secondary sexual characteristics before the age of 8 in girls and the ages of 9-10 in boys.

Precocious puberty is when pubertal changes (ie. the reawakening of the HPG axis) occur too early , but still in consonance.

19
Q

What are the two ways in which the premature reawakening of the HPG axis can occur?

A
  1. Gonadotrophin-dependent (or central) precocious puberty: maintain consonance
    • excess GnRH secretion - idiopathic or secondary
    • excess gonadotrophin secretion - pituitary tumour
  2. Gonadotrophin-independent precocious puberty: loss of consonance
    • testoxicosis - activating mutation of the LH receptor
    • sex steroid secreting tumour or exogenous steroids
20
Q

How would McCune Albright cause precocious puberty?

A

McCune Albright Syndrome is a result of an α G-subunit activating mutation. This is the hyperactivity of this signalling pathway, thus it will over-produce the hormones that work by this pathway.

LH and FSH work through this pathway, so we would get their overproduction, leading to precocious puberty.

21
Q

Define pubertal delay.

A

It is the absence of secondary sexual maturation by 13 years of age in girls (or absence of menarche by 18 years), or 14 years in boys.

22
Q

What are three ways in which the awakening of the HPG axis is delayed?

A
  1. Constitutional delay
    • affecting growth and puberty
    • 10 times more common in boys
    • secondary to chronic illness (eg. 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 (can occur with normal karyotype, via viral infection eg. mumps)
23
Q

What are some chromosomal abnormalities that can cause gonadal dysgenesis?

A
  • Klinefelter’s Syndrome (an extra X chromosome, XXY)
    would have male genitalia, but also wide hips, long arms and legs, and some breast development
  • Turner’s Syndrome (missing an X chromosome, XO)
    are shorter than usual, have underdeveloped or ‘streak’ ovaries