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Gonad Hormones : Male Prof.Dr.Gülden Burçak 2011-2012.

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Presentation on theme: "Gonad Hormones : Male Prof.Dr.Gülden Burçak 2011-2012."— Presentation transcript:

1 Gonad Hormones : Male Prof.Dr.Gülden Burçak 2011-2012

2 Testis Testis  male sex hormones  male germ cells

3 Testis : two functional units   Semineferous tubules lined with Sertoli cells and germ cells (spermatogonia) for production and transport of sperm. Sertoli cells provide the environment necessary for germ cell differentiation and maturation   Interstitial cells ( Leydig cells) for production of testosterone.

4 Hypothalamic-Pituitary-Testis Axis Constant pulsatile release of GnRH from the hypothalamus Synthesis, storage and secretion of gonadotropins (FSH and LH) from the anterior pituitary (-)feedback relationship between the androgens and GnRH, FSH, LH secretions Prolonged exposure to LH results in desensitization

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7 In childhood   testosterone and plasma gonadotropin levels are low   HPA is highly sensitive to (-) feedback effects of gonadal steroids Onset of puberty   Bursts of GnRH release   Sleep associated surges in LH secretion and to a lesser extent in FSH secretion Later in puberty pulsatile gonadotropin secretion throughout the day and night and more sustained plasma gonadotropin, testosterone and dihydrotestosterone

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9 For normal testicular function, GnRH pulses occur at a frequency of 3.8 pulses every 6 hours.   At a lower pulse rate FSH release ; at a higher pulse rate LH is more prominent   Circulating half-life : FSH,4 hours ; LH, 30 minutes   Testosterone : diurnal rythmic pattern, highest in the early morning

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11 LH   binds Leydig cells   testosterone synthesis and secretion   secretion is inhibited by both testosterone and estradiol   conversion of testosterone to estradiol in brain, pituitary and testes FSH   binds Sertoli cells   synthesis of androgen binding protein, aromatase enzyme complex, inhibin   secretion is primarily inhibited by inhibin B but also by testosterone

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14 Testosterone biosynthesis Cholesterol   de novo synthesis or from LDL   cholesterol esters storage in cytoplasm (steroidogenic acute regulatory protein (StAR) LH (cAMP) (acute) : esterase activation and cholesterol transport to the inner mitochondrial membrane (steroidogenic acute regulatory protein (StAR) LH (cAMP) (chronic) : steroidogenic enzyme synthesis LH (cAMP) (chronic) : steroidogenic enzyme synthesis

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16 Side chain cleavage and removal of the six-carbon fragment Cytochrome P450 side chain cleavage   Two hydroxylations first at C 22 then at C 20 (O 2 and NADPH)   Cholesterol 20,22- desmolase

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18 5 α-reductase,type I : liver Type II : reproductive tissues and peripheral targets

19 Daily testicular production   5mg testosteron,   50-100μg DHT ; %25 of DHT in circulation   %25 of estradiol (E 2 ) in circulation Testosterone : a circulating precursor of DHT and E 2 DHT (5α-reductase) in liver, kidney, muscle, prostate, external genitalia and genital skin E 2 (aromatase enzyme complex) in muscle, liver, kidney, brain, adipose tissue.

20 50% loosely bound to albumin (> 400 mg /L) 45% bound with high affinity to SHBG 1-2% to CBG < % 4 is free The normal level of SHBG is about 30-50% lower in men than in women SHBG levels may be elevated in testosterone deficient men. A change in the level of SHBG causes a greater change in the free testosterone level than in the free estradiol level.

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22 Effects of androgens Sexual differentiation Spermatogenesis Development of secondary sexual organs Anabolic metabolism and gene regulation Male pattern behaviour   Estradiol : sexual behavior and control of LH secretion

23 Targets for testosterone   Embryonic Wolffian structures, spermatogonia, muscles,bone, kidney and brain Targets for dihydrotestosterone   Prostate, external genitalia and the genital skin   The kidney is a major target tissue of the androgens : general enlargement of the kidney

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25 Excretory metabolites : inactive or less active Oxidation at the 17-position in many tissues, including the liver   17 ketosteroids : androsterone and etiocholanolone   conjugated with glucuronide and sulfate   Androstanediol

26 Pathological States Primary hypogonadism   Genetic disorders : Klinefelter’s syndrome   Androgen receptor defects : Testicular feminization syndrome   Inherited enzyme defects : 20,22-desmolase, 3ß-hydroxydehydrogenase,17α-hydroxylase 17,20 desmolase, 17-ketosteroid reductase   Failure of the pituitary/hypothalamus to respond to low testosterone levels

27 In hypogonadism In hypogonadism Hypothalamus : Low GnRH ; low FSH,LH; low E2 /testosterone Hypothalamus : Low GnRH ; low FSH,LH; low E2 /testosterone Pituitary : High GnRH ; low FSH,LH ; low E2 /testosterone Pituitary : High GnRH ; low FSH,LH ; low E2 /testosterone Gonad : High GnRH ; high FSH,LH ; Gonad : High GnRH ; high FSH,LH ; low E2 /testosterone low E2 /testosterone Hyperprolactinemia is associated with diminished libido and impotence Hyperprolactinemia is associated with diminished libido and impotence

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29 Hypergonadism   Testicular hyperfunction : Testicular tumors (often produce hCG and α- fetoprotein)   Hypothalamic/pituitary hyperactivity usually from a tumor

30   Benign prostatic hypertrophy : extensive and uncontrolled division of prostate cells   Testosterone / dihydrotestosterone + estradiol Erectile dysfunction may occur secondarily to vascular problems associated with diabetes, atherosclerosis Infertility


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