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FOLLICLE STIMULATING
HORMONE(FSH), LUTEINIZING
HORMONE(LH) &
TESTOSTERONE
BY: HERMAN NDJAMEN
PREVIEW
1. DEFINITION OF HORMONES
2. BIOCHEMICAL CLASSIFICATION OF HORMONES
3. CASE STUDIED
- Structure & classification
- Origin of production
- Target tissues/organ(s) and functions
- Mechanism of action
- DISEASES
DEFINITION: Hormones are chemical substances synthesized
in small amounts by endocrine tissues and carried by blood
stream to another tissue, where it acts as a messenger to
regulate the function of the target tissue or organ.
CLASSIFICATION OF HORMONES
CLASSES OF HORMONES CHEMICAL COMPOSITION EXAMPLES
AMINO ACIDS DERIVATIVES C, H and N, AMINE GROUP CATECHOLAMINES
POLYPEPTIDES
LONG CHAINS OF AMINO
ACIDS
INSULIN, GLUCAGON
GLYCOPROTEINS
LARGE PROTEINS COMBINED
WITH CARBOHYDRATES
FSH, LH etc
STEROIDS LIPIDS CORTICOIDS, SEX HORMONES
FATTY ACID DERIVATIVES
(EICOSANOIDS)
LONG HYDROCARBON ACID
CHAINS
PROSTAGLANDINS,
LEUKOTRIENES
&THROMBOXANES
CASE STUDY I: FOLLICLE STIMULATING
HORMONE (FSH)
A. STRUCTURE AND CLASSIFICATION.
FSH is a glycoprotein composed of 2
monomeric subunits proteins to which
is attached a sugar. The dimer contains
2 polypeptides; Alpha subunit made up
of 92 amino acids and a beta subunit
made up of 111 amino acids. This beta
subunit confers the hormone its
specific biologic action and is
responsible for interaction with FSH
receptors.
The sugar part of FSH is composed
of fucose, galactose, mannose, galacto
samine, glucosamine, and sialic acid
Normal level: 3mIU/ml – 10mIU/ml
ORIGIN OF PRODUCTION
The hormone is produced in
the pituitary gland(anterior)
under the influence of
Gonadotropic hormone
releasing hormone (GnRH)
produced in the
hypothalamus, inhibited by
inhibin and enhanced by
activin.
FSH is then released to the
blood stream towards the
target tissues.
It has a plasma half life of 3-4
hours
TARGET TISSUES AND FUNCTIONS
• FSH regulates the development, growth, pubertal
maturation, and reproductive processes of the
human body.
• In both males and females, FSH stimulates the
maturation of germ cells.
• In males, FSH induces Sertoli cells to
secrete inhibin and stimulates the formation of
sertoli-sertoli tight junctions (zonula occludens).
• In females, FSH initiates follicular growth,
specifically affecting granulosa cells
MECHANISM OF ACTION
• FSH binds to FSH-R on the cell
membrane.
• This occupied receptor causes
replacement of GDP bound to Gs
protein by GTP, activating this Gs
protein.
• Gs alpha subunit moves to
ADENYLATE CYCLASE. This cyclase
then catalyzes formation of cAMP
(second messenger) from ATP
• The CAMP then activates protein
kinase (third messenger), which in
turn by phosphorylation of cellular
proteins influences on mRNA
synthesis.
DISEASES
1.HIGH LEVELS OF FSH
• Premature menopause also known as Premature
Ovarian Failure
• Poor ovarian reserve also known as Premature
Ovarian Aging
• Gonadal dysgenesis, Turner syndrome (XO)
• Castration
• Swyer syndrome(46XY but externally female)
• Certain forms of CAH
• Testicular failure.
• Klinefelter syndrome(XXY)
2. LOW LEVELS OF FSH
1.Polycystic Ovarian Syndrome
2.Polycystic Ovarian Syndrome + Obesity +
Hirsutism + Infertility
3.Kallmann syndrome (incomplete puberty)
4.Hypothalamic suppression
5.Hypopituitarism
6.Hyperprolactinemia
7.Gonadotropin deficiency
CASE STUDY II: LUTEINIZING
HORMONE(LH)
A.STRUCTURE AND CLASSIFICATION
LH is a heterodimeric glycoprotein.
Each monomeric unit is
a glycoprotein molecule; one alpha and one
beta subunit make the full, functional
protein. The alpha subunit is similar in all
glycoprotein hormones but it’s beta subunit
consists of 120 amino acids, that confers its
specific biologic action and is responsible
for the specificity of the interaction with
the LH receptor. The carbohydrate part
consist of different oligosaccharides
The biologic half-life of LH is 20 minutes.
During the reproductive years, typical levels
of LH are between 1-20 IU/L.
In males over 18 years of age, reference
ranges have been estimated to be 1.8-8.6 IU/L
ORIGIN OF PRODUCTION
LUTEINIZING HORMONE is produced in the
pituitary gland under the regulation of
GONADOTROPIC HORMONE RELEASING
HORMONE(GnRH). It is then released to the
blood stream towards the target tissues
TARGET TISSUES AND FUNCTIONS
In females, LH supports theca cells in the ovaries that
provide androgens and hormonal precursors for estradiol
production.
-"LH surge" triggers ovulation, thereby not only releasing
the egg from the follicle, but also initiating the conversion of
the residual follicle into a corpus luteum that, in turn,
produces progesterone to prepare theendometrium for a
possible implantation.
In the male, LH acts upon the Leydig cells of the testis and
is responsible for the production of testosterone,
an androgen that exerts both endocrine activity and
intratesticular activity on spermatogenesis.
MECHANISM OF ACTION
• The mechanism of action is basically similar to
that seen in FSH and the diseases observed
too.
SWYER SYNDROM:
HIGH FSH AND LH
levels in blood.
HIGH LEVEL OF LH (low level of FSH) in female and male
CASE STUDY III: TESTOSTERONE
STRUCTURE AND CLASSIFICATION
Testosterone is made up of
CYCLOPENTANEPERHYDROPH
ENANTHRENE ring which is a
characteristics of most steroid
hormones.
Therefore testosterone is
considered to be a steroid
hormone with molecular
weigh (MW) = 288,4
ORIGIN OF PRODUCTION
TESTOSTERONE is primarily produced in the
testes by the INTERSTITIAL CELLS OF LEYDIG.
Precursor of testosterone is Progesterone
which is first converted to androstenedione
which is then hydrolyzed to form
testosterone. This is how testosterone is
produced in females.
Testosterone is also produced in small
amount in the zona reticularis of the adrenal
gland.
Testosterone level is regulated by FSH and
LH.
LH stimulates an increase in number of leydig
cells , hence increasing testosterone level, and
vice versa.
Testosterone is transported together with
specific plasma protein binding globulin or
testosterone-estrogen binding globulin
TARGET TISSUES AND FUNCTIONS
Testosterone acts on several tissues of the body
where it carries out the following functions:
1. It is responsible for gonadal development in the male
embryo.
2. This hormone is responsible for "brain masculinization"
in infant boys.
3. It is responsible for secondary sexual characteristics in
male.
4. It increases energy metabolism, thereby helping men to
shed extra pounds, lower their body fat, and acquire a
leaner and fitter physique.
5. Testosterone is also believed to stimulate erythropoeisis
MECHANISM OF ACTION
DISEASES
• LACK OF TESTOSTERONE: this induces
hypogonadism (primary- testicular failure)
• Normal level of testosterone but defective
receptors induces “ testicular feminization” I.e
genotype is XY but phenotype is female (swyer
syndrom).
HYPOGONADISM: Deficient LH activity
THANKS FOR
YOUR
ATTENTION

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FSH, LH & Testosterone

  • 2. PREVIEW 1. DEFINITION OF HORMONES 2. BIOCHEMICAL CLASSIFICATION OF HORMONES 3. CASE STUDIED - Structure & classification - Origin of production - Target tissues/organ(s) and functions - Mechanism of action - DISEASES
  • 3. DEFINITION: Hormones are chemical substances synthesized in small amounts by endocrine tissues and carried by blood stream to another tissue, where it acts as a messenger to regulate the function of the target tissue or organ. CLASSIFICATION OF HORMONES CLASSES OF HORMONES CHEMICAL COMPOSITION EXAMPLES AMINO ACIDS DERIVATIVES C, H and N, AMINE GROUP CATECHOLAMINES POLYPEPTIDES LONG CHAINS OF AMINO ACIDS INSULIN, GLUCAGON GLYCOPROTEINS LARGE PROTEINS COMBINED WITH CARBOHYDRATES FSH, LH etc STEROIDS LIPIDS CORTICOIDS, SEX HORMONES FATTY ACID DERIVATIVES (EICOSANOIDS) LONG HYDROCARBON ACID CHAINS PROSTAGLANDINS, LEUKOTRIENES &THROMBOXANES
  • 4. CASE STUDY I: FOLLICLE STIMULATING HORMONE (FSH) A. STRUCTURE AND CLASSIFICATION. FSH is a glycoprotein composed of 2 monomeric subunits proteins to which is attached a sugar. The dimer contains 2 polypeptides; Alpha subunit made up of 92 amino acids and a beta subunit made up of 111 amino acids. This beta subunit confers the hormone its specific biologic action and is responsible for interaction with FSH receptors. The sugar part of FSH is composed of fucose, galactose, mannose, galacto samine, glucosamine, and sialic acid Normal level: 3mIU/ml – 10mIU/ml
  • 5. ORIGIN OF PRODUCTION The hormone is produced in the pituitary gland(anterior) under the influence of Gonadotropic hormone releasing hormone (GnRH) produced in the hypothalamus, inhibited by inhibin and enhanced by activin. FSH is then released to the blood stream towards the target tissues. It has a plasma half life of 3-4 hours
  • 6. TARGET TISSUES AND FUNCTIONS • FSH regulates the development, growth, pubertal maturation, and reproductive processes of the human body. • In both males and females, FSH stimulates the maturation of germ cells. • In males, FSH induces Sertoli cells to secrete inhibin and stimulates the formation of sertoli-sertoli tight junctions (zonula occludens). • In females, FSH initiates follicular growth, specifically affecting granulosa cells
  • 7. MECHANISM OF ACTION • FSH binds to FSH-R on the cell membrane. • This occupied receptor causes replacement of GDP bound to Gs protein by GTP, activating this Gs protein. • Gs alpha subunit moves to ADENYLATE CYCLASE. This cyclase then catalyzes formation of cAMP (second messenger) from ATP • The CAMP then activates protein kinase (third messenger), which in turn by phosphorylation of cellular proteins influences on mRNA synthesis.
  • 8. DISEASES 1.HIGH LEVELS OF FSH • Premature menopause also known as Premature Ovarian Failure • Poor ovarian reserve also known as Premature Ovarian Aging • Gonadal dysgenesis, Turner syndrome (XO) • Castration • Swyer syndrome(46XY but externally female) • Certain forms of CAH • Testicular failure. • Klinefelter syndrome(XXY)
  • 9. 2. LOW LEVELS OF FSH 1.Polycystic Ovarian Syndrome 2.Polycystic Ovarian Syndrome + Obesity + Hirsutism + Infertility 3.Kallmann syndrome (incomplete puberty) 4.Hypothalamic suppression 5.Hypopituitarism 6.Hyperprolactinemia 7.Gonadotropin deficiency
  • 10. CASE STUDY II: LUTEINIZING HORMONE(LH) A.STRUCTURE AND CLASSIFICATION LH is a heterodimeric glycoprotein. Each monomeric unit is a glycoprotein molecule; one alpha and one beta subunit make the full, functional protein. The alpha subunit is similar in all glycoprotein hormones but it’s beta subunit consists of 120 amino acids, that confers its specific biologic action and is responsible for the specificity of the interaction with the LH receptor. The carbohydrate part consist of different oligosaccharides The biologic half-life of LH is 20 minutes. During the reproductive years, typical levels of LH are between 1-20 IU/L. In males over 18 years of age, reference ranges have been estimated to be 1.8-8.6 IU/L
  • 11. ORIGIN OF PRODUCTION LUTEINIZING HORMONE is produced in the pituitary gland under the regulation of GONADOTROPIC HORMONE RELEASING HORMONE(GnRH). It is then released to the blood stream towards the target tissues
  • 12. TARGET TISSUES AND FUNCTIONS In females, LH supports theca cells in the ovaries that provide androgens and hormonal precursors for estradiol production. -"LH surge" triggers ovulation, thereby not only releasing the egg from the follicle, but also initiating the conversion of the residual follicle into a corpus luteum that, in turn, produces progesterone to prepare theendometrium for a possible implantation. In the male, LH acts upon the Leydig cells of the testis and is responsible for the production of testosterone, an androgen that exerts both endocrine activity and intratesticular activity on spermatogenesis.
  • 13.
  • 14. MECHANISM OF ACTION • The mechanism of action is basically similar to that seen in FSH and the diseases observed too.
  • 15. SWYER SYNDROM: HIGH FSH AND LH levels in blood.
  • 16. HIGH LEVEL OF LH (low level of FSH) in female and male
  • 17. CASE STUDY III: TESTOSTERONE STRUCTURE AND CLASSIFICATION Testosterone is made up of CYCLOPENTANEPERHYDROPH ENANTHRENE ring which is a characteristics of most steroid hormones. Therefore testosterone is considered to be a steroid hormone with molecular weigh (MW) = 288,4
  • 18. ORIGIN OF PRODUCTION TESTOSTERONE is primarily produced in the testes by the INTERSTITIAL CELLS OF LEYDIG. Precursor of testosterone is Progesterone which is first converted to androstenedione which is then hydrolyzed to form testosterone. This is how testosterone is produced in females. Testosterone is also produced in small amount in the zona reticularis of the adrenal gland. Testosterone level is regulated by FSH and LH. LH stimulates an increase in number of leydig cells , hence increasing testosterone level, and vice versa. Testosterone is transported together with specific plasma protein binding globulin or testosterone-estrogen binding globulin
  • 19. TARGET TISSUES AND FUNCTIONS Testosterone acts on several tissues of the body where it carries out the following functions: 1. It is responsible for gonadal development in the male embryo. 2. This hormone is responsible for "brain masculinization" in infant boys. 3. It is responsible for secondary sexual characteristics in male. 4. It increases energy metabolism, thereby helping men to shed extra pounds, lower their body fat, and acquire a leaner and fitter physique. 5. Testosterone is also believed to stimulate erythropoeisis
  • 21. DISEASES • LACK OF TESTOSTERONE: this induces hypogonadism (primary- testicular failure) • Normal level of testosterone but defective receptors induces “ testicular feminization” I.e genotype is XY but phenotype is female (swyer syndrom).

Editor's Notes

  1. Kallmann syndrome is a genetic condition which results in the failure to commence or the non-completion of puberty. It is characterised by hypogonadism and by a total lack of sense of smell (anosmia) or a heavily reduced sense of smell (hyposmia). The term hypogonadism describes a low level of circulating sex related hormones; (testosterone in men and oestrogen and progesterone in women).