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GONADS
Are
ANDROGENS
Major
androgens in
order of
potency
Testosterone
Androstenedio
ne
Dehydroepiand
rosterone
(DHEA)
Produced in the
following
organs:
Adrenal
Ovaries
Testes
Liver
Testes
1.
2.
Production of sperm
Production of reproductive steroid
hormones
Testes
cord
- it has the ability to retract the testicles
into the inguinal canal in instances of
threatened injury
a.
Seminiferous tubules
- contain germ cells and Sertoli cells and
are responsible for sperm production
Physiology
Spermatogenesis
spermatogonia are sperm formed from
stem cells
Spermatogonia undergo mitosis and
meiosis
Haploid cells then transform to form
mature sperm.
Sertoli cells are polyfunctional cells that
aid in the development and maturation
of sperm
Physiology
Hormogenesis
- testosterone, the predominant hormone
secreted by the testes
Cellular mechanism of
testosterone action
Testosterone
converts to
dihydrotestorone(DHT).DHT
complexes with an inrtracellular
receptor protein and this complex
binds to the nuclear receptor
effecting proteinsynthesis cell
growth.
Postnatal development
Testicular
function
Effects of
spermatogenesis
Stimulation
Hypergonadotropic Hypogonadism
( low testosterone, elevated FSH or LH levels and impaired production of sperm)
Klinefelters syndrome
caused by an extra chromosome; men with
this syndrome have small (<2.5cm), firm
testicles, Gynecomastia (enlargement of the
male breast).
2. Testicular Feminization Syndrome
most severe form of androgen-resistant
syndrome; no response to administration of
exogenous testosterone.
3. 5a-Reductase deficiency
the genotype is XY. A reduction of this enyme
results in reduction of testosterone level.
1.
Hypergonadotropic Hypogonadism
( low testosterone, elevated FSH or LH levels and impaired production of sperm)
4. Myotonic Dystrophy
autosomal dominantly inherited condition that
presents with hypogonadism, muscle weakness,
frontal balding, diabetes and muscle dystonia.
5. Testicular injury and infection
mumps orchitis (swelling of the testes due to
mumps),
HIV infection, radiation and chemotherapy can also
damage the testes.
6. Sertoli-cell-only-syndrome
characterized by lack of germ cells.
Hypogonadotropic Hypogonadism
(low testosterone, low or inappropriately normal FSH and LH)
1. Kallmans syndrome
inherited, x-linked recessive trait that
manifests
as hypogonadism during puberty. Associated
defects are anosmia (inability to smell) and
midline
defects (cleft palate and lip), red-green color
blindness and congenital deafness.
2. Hyperprolactinemia
3. Pituitary Disease.
PROGESTERONE
Produced
in the ovaries
Induces secretory activity of the
endometrial glands that have been
primed by estrogen which readies
the endometrium for embryo
implantation.
Dominant hormone responsible for
the luteal phase of cycle.
PROGESTERONE
Progesterone
PROGESTERONE
Progesterone
However,
the source of
progesterone and estrogen
during most of pregnancy is the
placenta, not the ovaries.
As
Most
abundant
principal
No
CLINICAL SIGNIFICANCE
1. Hyperestrenism- causes exceptionally
early puberty in female child, feminization
of male, irregular menses in female adult.
Pregnancy estrogen very high without
monthly fluctuation.
Polycystic ovary disease increase estrogen
stimulates LH but does not suppress FSH.
Oral Contraceptives with increased estrogen
prevent release of FSH and LH, prevent LH
surge, preventing ovulation.
CLINICAL SIGNIFICANCE
2. Hypoestronism