Unit 2: Endocrine control of sexual maturity Flashcards
1
Q
Biological changes in puberty
A
- neurosecretory factors and/or hormones
- modulation of somatic growth
- initiation of the development of sexual organs
2
Q
The role of hypothalamic-pituitary-gonadal axis in puberty
A
- activated in puberty
- induce ovarian and testicular sex hormone secretion
- results in biological, morphological and physiological changes in puberty
- increase in GnRH release increases pituitary responsiveness to GnRH (up regulation) which results in FSH and LH release and ultimately sex steroid relase from gonads. Secondary sexual characteristics develop
3
Q
Effects of sex steroid production in puberty
A
- appearance and maintenance of secondary sexual characteristics
- attaining capacity of reproduction
4
Q
Periods of life when the hypothalamic-pituitary-gonadal axis is activated
A
- mid trimester of foetal life - testosterone masculinises the brain and FSH causes folliculogenesis
- early neonatal period - due to the decrease in steroid hormones after birth (disinhibition effect)
- puberty to reproductive years - pulsatile release at first, later throughout the day
5
Q
Factors that initiate puberty
A
- exact cause unknown, but few postulations
1. Leptin - caused by the change in adiposity in girls. Leptin stimulates hypothalamus to release GnRH
2. Melatonin - anti-gonadotropic. In adolescents secretion decrease at night, correlates to when GnRh is released
6
Q
Explain the brain-testicular axis
A
FSH:
1. FSH stimulates the secretion of ABP (androgen binding protein) by the sertoli cells
- ABP prompts spermatogenic cells to bind and concentrate testosterone
- Locally, ABP and testosterone = final trigger to spermatogenesis
- FSH indirectly makes sertoli cells more receptive to the stimulatory effects of testosterone
- High sperm count causes the release of inhibit by sertoli cells. Inhibin negatively feeds back on the pituitary to decrease FSH release.
LH:
- LH binds to Leydig (interstitial cells) and stimulates testosterone production
- testosterone negatively feeds back on hypothalamus and pituitary to inhibit LH release.
a) Act directly on hypothalamus
b) Reduce LH producing cells’ responsiveness to GnRH & exert inhibitory effects on FSH and LH producing cells
7
Q
General effects of testosterone
A
- initiates spermatogenesis
- development of secondary sexual characteristics
- synthesised from cholesterol
- 98% are circulating in blood, bound to SHBG (44%) and serum albumin (54%)
- activates genes
- targets accessory reproductive organs, causes them to grow and assume adult size and function.
- in adult males, plasma concentration of testosterone is responsible for the maintenance of accessory reproductive organs.
8
Q
Deficiency of testosterone
A
- accessory organs atrophy
- semen volume decline
- erection and ejaculation impaired
- sterility and impotence
9
Q
Secondary sexual characteristics in males
A
- pubic, axillary and facial hair
- hair growth in chest and other areas
- larynx enlarge
- skin thicken and become coarser
10
Q
Somatic effects of testosterone
A
- thicken and lengthening of bones
- skeletal muscle mass and size increase
- epiphyseal plate closure occur late in puberty
11
Q
Metabolic effects of testosterone
A
- anabolic
- increased haematopoeisis
- increased basal metabolic rate
12
Q
Neural effects of testosterone
A
- increased libido
- masculinises brain (brain areas responsible for sexual arousal)
- agressiveness