Sex Differentiation & Reproductive endocrine control (cell bio) Flashcards

1
Q

Embryology

** Totipotent - capable of giving rise to a complete ? **

A - Oocyte
B - Mature Oocyte
- Polar body
C - 2 Cell Zygote
D - 8 cell Embryo
E - 16 cell Embryo
F - Morula
G - Blastocyst
H - Hatching Blastocyst I - Hatched Blastocyst

A
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2
Q

Early embryo development

  • Several ? divisions
  • Early divisions occur without an increase in cell ?
  • “?” (or “Reduction Division”)
  • ? support provided by ? secretions
  • Zygotic protein synthesis begins at 2 to 16-cell stage depending on species (? cells)
A

Early embryo development

  • Several mitotic divisions
  • Early divisions occur without an increase in cell mass
  • “Cleavage” (or “Reduction Division”)
  • metabolic support provided by maternal secretions
  • Zygotic protein synthesis begins at 2 to 16-cell stage depending on species (Totipotent cells)
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3
Q
  • An important event during embryo life is the differentiation from the ? to the blastocyst stage.
  • During the morula stage, the cells differentiate into #? groups of cells
  • Inner cell mass (ICM) – ? cells in the “Blastocyst” that will form the ?
  • Trophoblast – will develop the ? (placenta – ? portion)
  • In addition, the cells from the trophoblast “pump” ? into the intracellular space and because of the osmotic pressure, the embryo is filled with “?”, which forms the “Blastocele or ?”.
  • Blastocele will form the ? that will surround the embryo.
A
  • An important event during embryo life is the differentiation from the morula to the blastocyst stage.
  • During the morula stage, the cells differentiate into 2 groups of cells
  • Inner cell mass (ICM) – polarized cells in the “Blastocyst” that will form the embryo
  • Trophoblast – will develop the chorion (placenta – external portion)
  • In addition, the cells from the trophoblast “pump” sodium into the intracellular space and because of the osmotic pressure, the embryo is filled with “?”, which forms the “Blastocele or ?”.
  • Blastocele will form the cavity that will surround the embryo.
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4
Q

Embryology

The embryo starts as a ? of cells that eventually form layers and will differentiate into the ? proper and ?.

endoderm includes the ?, ?, ?)

mesoderm includes ?, skeleton, ?, reproductive system (MSCR)

ectoderm includes the ? system, skin and ? (HSN)

A

Embryology

The embryo starts as a mass of cells that eventually form layers and will differentiate into the embryo proper and placenta

endoderm includes the digestive system, lungs, endocrine system (endoderm - DLE)

mesoderm includes muscle, skeleton, cardiovascular, reproductive system (MSCR)

ectoderm includes the nervous system, skin and hair (HSN)

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5
Q

PLACENTAL DEVELOPMENT

  • The ? is the external embryonic tissue and gives rise to the placenta.
  • ? mesoderm and trophoblast constitute the (* ? *).
  • Expansion of the allantois forms the ?

Embryology: Sex differentiation
* Initially ? (about 6 weeks in large domestic animals)

** ? ** cells migrate from outside the organism ( ** ? **) into the organism through the hindgut to the undifferentiated gonad just within the dorsal body wall (also known as the * ? *).

A

PLACENTAL DEVELOPMENT

  • The trophoblast is the external embryonic tissue and gives rise to the placenta.
  • extraembryonic mesoderm and trophoblast constitute the (* chorion *).
  • Expansion of the allantois forms the allantochorion

Embryology: Sex differentiation
* Initially indistinguishable (about 6 weeks in large domestic animals)

** primordial germ ** cells migrate from outside the organism ( ** yolk sac **) into the organism through the hindgut to the undifferentiated gonad just within the dorsal body wall (also known as the * genital ridge*).

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6
Q

Embryology: sex differentiation

  • The reproductive system develops at the same time as the ? system

mesonepfric = ? ducts
paramesonephric = ? ducts

A

Embryology: sex differentiation

  • The reproductive system develops at the same time as the renal system

mesonepfric = wolffian ducts
paramesonephric = mullerian ducts

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7
Q

MALE

testes determining factor -> testes develop ->

sertoli cells secrete
1. AMH: causes leydig cells to differentiate
2. Degeneration of paramesonephric duct

AMH: causes Leydig cells to differentiate -> Testosterone -> development of male duct system

AMH causes leydig cells to differentiate -> dihydrotestosterone -> development of penis, scrotum and accessory sex glands

FEMALE

No TDF -> ovaries develop -> no AMH -> ? ducts become the oviducts, the ?, cervix, and part of the vagina -> complete ? tract

A

MALE (XY)

testes determining factor -> testes develop ->

sertoli cells secrete
1. AMH: causes leydig cells to differentiate
2. Degeneration of paramesonephric duct

AMH: causes Leydig cells to differentiate -> Testosterone -> development of male duct system

AMH causes leydig cells to differentiate -> dihydrotestosterone -> development of penis, scrotum and accessory sex glands

FEMALE (XX)

No TDF -> ovaries develop -> no AMH -> paramesonephric ducts become the oviducts, the uterus, cervix, and part of the vagina -> complete female tract

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8
Q

Embryology (MALE XY)

testis determining factor
-> testis development (sertoli cells)

AMH
-> Development of the Leydig cells
- testosterone - male duct system

FEMALE
absence of
- testis determining factor
- AMH
- testosterone

A
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9
Q

Embryology: Sex differentiation

Hypothalamus: Male vs. Female

  • Female hypothalamus contains 2 functional areas for secretion of GnRH
    -> ? (arcuate ventromedial region; ARC) and
    -> ? (preoptic area; POA) centers
  • Hypothalamus is inherently female
    -> testosterone during ? “defeminizes” the brain
    - testosterone crosses blood-? barrier and is converted to ?
    - estradiol defeminizes hypothalamus, ? surge center
    -> fetal ovaries produce estradiol, but this doesn’t cross the blood-brain barrier bc it is bound to alpha-?
A

Embryology: Sex differentiation

Hypothalamus: Male vs. Female

  • Female hypothalamus contains 2 functional areas for secretion of GnRH
    -> tonic (arcuate ventromedial region; ARC) and
    -> surge (preoptic area; POA) centers
  • Hypothalamus is inherently female
    -> testosterone during development “defeminizes” the brain
    - testosterone crosses blood-brain barrier and is converted to estradiol
    - estradiol defeminizes hypothalamus, eliminating surge center
    -> fetal ovaries produce estradiol, but this doesn’t cross the blood-brain barrier bc it is bound to alpha-fetoprotein (@FP)
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10
Q

HORMONES

Chemical messengers
* Most hormones are:
Secreted by an ? gland
Carried by the ?
Affect other organs, ?, or tissues.

Controls ? processes
Signaling molecules produced in the body that regulate the activity of certain ? and ?

A

HORMONES

Chemical messengers
* Most hormones are:
Secreted by an endocrine gland
Carried by the bloodstream
Affect other organs, glands, or tissues.

Controls metabolic processes
Signaling molecules produced in the body that regulate the activity of certain cells and organs

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11
Q

Classification of hormones

Chemical nature:

STEROID:
* Derived from ?
* ? (a male sex hormone like testosterone)
* Metabolized in the ? (first- pass)
* Ex.: Estrogens, ?, progesterone

AMINE HORMONES
* The amino acid-derived hormones are relatively small molecules that are derived from the amino acid ? and ?.
* ? metabolized
* Name of amino acid- derived ends in “-ine”
* Ex.: ?, Epinephrine

PROTEIN/PEPTIDE
* ? proteins or small/medium size peptides (chain of amino acids)
* Much larger than ? and ? hormones
* ?-soluble – membrane ?
* Short peptides – Ex.: ?
* Small proteins – Ex.: ? hormones
* ? – Ex.: FSH, LH

Eicosanoids (not produced by glands so aren’t considered real hormones)
* Derived from ? fatty acids from the cell membrane - usually ? acid (20-carbon)
* Key mediators and regulators of ? and immunity
* autocrine or paracrine?
* Ex.: ?

stomach enzymatic degradation involves:
1. amine hormones
2. protein/peptide hormones (short peptide - oxytocin, small protein - growth hormone)
3. eicosanoids

A

Classification of hormones

Chemical nature:

STEROID:
* Derived from cholestrol
* androgen (a male sex hormone like testosterone)
* Metabolized in the liver (first- pass)
* Ex.: Estrogens, testosterone, progesterone

AMINE HORMONES
* The amino acid-derived hormones are relatively small molecules that are derived from the amino acid tyrosine and tryptophan.
* easily metabolized
* Name of amino acid- derived ends in “-ine”
* Ex.: melatonin, Epinephrine

PROTEIN/PEPTIDE
* larger proteins or small/medium size peptides (chain of amino acids)
* Much larger than steroid and amine hormones
* water-soluble – membrane receptors
* Short peptides – Ex.: oxytocin
* Small proteins – Ex.: growth hormones
* glycoproteins – Ex.: FSH, LH

Eicosanoids (not produced by glands so aren’t considered real hormones)
* Derived from polyunsaturated fatty acids from the cell membrane - usually arachidonic acid (20-carbon)
* Key mediators and regulators of inflammation and immunity
* paracrine
* Ex.: prostaglandins

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12
Q

CLASSIFICATION OF HORMONES

Mechanism of action

Bind to 1. intracellular & 2. cell membrane receptors:

INTRACELLULAR receptors
* Form ?-receptor (H-R) complexes
* Biochemical function mediated by H-R complex
* ?
* Found in the circulation in association with ? proteins
* LONGER OR SHORT half-life (hours or days)
* Ex.: ?

CELL-MEMBRANE receptors
- Hormones bind the cell membrane receptors (?- protein), which induce the release of ? messengers.
- Secondary messengers perform the ? function.
- Hydrophilic or hydrophobic?
- Transported in the ?-form
- Long or Short Half-life (minutes)
Ex.: ? acid derived and ?

A

CLASSIFICATION OF HORMONES

Mechanism of action

Bind to intracellular receptors:

  • Form hormone-receptor (H-R) complexes
  • Biochemical function mediated by H-R complex
  • lipophillic
  • Found in the circulation in association with transport proteins
  • LONGER half-life (hours or days)
  • Ex.: Steroids

CELL-MEMBRANE receptors
- Hormones bind the cell membrane receptors (G- protein), which induce the release of secondary messengers.
- Secondary messengers perform the biochemical function.
- Hydrophilic so
- Transported in the free-form
- Short Half-life (minutes)
Ex.: amino acid derived and eicosanoids

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13
Q

Hormone control: Negative or Positive feedback

  • Most endocrine hormones are regulated by + or - ? feedback loops. Negative feedback keeps the concentration of a hormone within a relatively ? range and maintains ?.
  • Ex.: Testosterone is essential for spermatogenesis. However, excessive concentrations of testosterone cause ? feedback on the anterior pituitary for the release of ?, which will consequently reduce the activity of ? cells for the production of testosterone.
  • Very few endocrine hormones are regulated by ? feedback loops. Positive feedback causes the concentration of a ? to become increasingly higher.
  • Ex.: Estradiol produced by the pre-ovulatory follicle causes ? feedback to the anterior pituitary for the release of LH. The LH will induce the ovulation of the pre-ovulatory ?.
A

Hormone control: Negative or Positive feedback

  • Most endocrine hormones are regulated by negative feedback loops. Negative feedback keeps the concentration of a hormone within a relatively narrow range and maintains homeostasis.
  • Ex.: Testosterone is essential for spermatogenesis. However, excessive concentrations of testosterone cause NEGATIVE feedback on the anterior pituitary for the release of Leydig cells, which will consequently reduce the activity of Leydig cells for the production of testosterone.
    LEYDIG CELLS -> TESTOSTERONE
  • Very few endocrine hormones are regulated by positive feedback loops. Positive feedback causes the concentration of a hormone to become increasingly higher.
  • Ex.: Estradiol produced by the pre-ovulatory follicle causes positive feedback to the anterior pituitary for the release of LH. The LH will induce the ovulation of the pre-ovulatory follicles.
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14
Q

Hormones

Supraphysiological stimulation
* Exceeding what is normally found in healthy individuals
* Hormone becomes ? after long-term use

“?” of hormone receptors
Once the peptide hormones are bound to their receptors on the appropriate ? cells, they are internalized and ? by the process of receptor-mediated endocytosis

Ex.: Prolonged-release, high dose GnRH
Used as a contraceptive in dogs and horses
Physiologically, GnRH is responsible for ? growth and ?

(cells internalize their receptors which means cells can’t respond anymore so the gland stops responding to treatment and stops producing the effect we want

e..g GNRH which is imp. for cycling in females and can induce cyclists in females giving estrogen
too much GnRh then she stops cycling)

A

Hormones

Supraphysiological stimulation
* Exceeding what is normally found in healthy individuals
* Hormone becomes ineffective after long-term use

“ internalization ” of hormone receptors
Once the peptide hormones are bound to their receptors on the appropriate target cells, they are internalized and degraded by the process of receptor-mediated endocytosis

Ex.: Prolonged-release, high dose GnRH
Used as a contraceptive in dogs and horses
Physiologically, GnRH is responsible for follicular growth and ovulation

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15
Q

Hormones

Source of production Hypothalamic-pituitary-gonadal axis

  • Pineal gland: ?
  • Hypothalamus: ?
  • Pituitary Gland: FSH, ?, Prolactin, ?Gonads:
  • Ovary: Follicles - Estradiol, Inhibin, Testosterone; Corpus luteum - Progesterone, Relaxin, Oxytocin
  • Testis: ?, Inhibin, ?
  • Uterus: ? F2 alpha
  • Placenta: ?, ?, hCG , eCG, ?, PGF2α
A

Hormones

Source of production Hypothalamic-pituitary-gonadal axis

  • Pineal gland: melatonin
  • Hypothalamus: GnRH
  • Pituitary Gland: FSH, LH, Prolactin, OxytocinGonads:
  • Ovary: Follicles - Estradiol, Inhibin, Testosterone; Corpus luteum - Progesterone, Relaxin, Oxytocin
  • Testis: testosterone, Inhibin, estradiol
  • Uterus: prostaglandin F2 alpha
  • Placenta: progesterone, estradiol, hCG , eCG, Oxytocin, PGF2α
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16
Q

Hypothalamic-Pituitary Portal System

▪ A system of blood ? in the microcirculation at the ? of the brain, connecting the hypothalamus with the ? pituitary.

▪ Axons of hypothalamic neurons extend to blood vessels of ? system

▪ Function: quickly transport and exchange ? between the hypothalamus ? nucleus and anterior pituitary gland.
▪ Hormones: ?, GHRH (Growth hormone), CRH (corticotrophin), ? (thyrotrophin)

▪ GnRH affects the anterior pituitary ?

▪ Hypothalamic centers (FEMALE*)
▪ ? – Regulates the release of frequent low-amplitude tong GnRH pulses
▪ ? - Only in females – responsive to high levels of estradiol and release of high amplitude GnRH pulse

Regulate by levels of ? - Feedback

A

Hypothalamic-Pituitary Portal System

▪ A system of blood vessels in the microcirculation at the base of the brain, connecting the hypothalamus with the anterior pituitary.

▪ Axons of hypothalamic neurons extend to blood vessels of portal system

▪ Function: quickly transport and exchange hormones between the hypothalamus arcuate nucleus and anterior pituitary gland.
▪ Hormones: GnRH, GHRH (Growth hormone), CRH (corticotrophin), TRH (thyrotrophin)

▪ GnRH affects the anterior pituitary directly

▪ Hypothalamic centers (FEMALE*)
▪ TONIC – Regulates the release of frequent low-amplitude tong GnRH pulses
▪ SURGE - Only in females!! – responsive to high levels of estradiol and release of high amplitude GnRH pulse

Regulate by levels of estrogens - Feedback

adenohypophysis (anterior pituitary - non-neural tissue): release of LH, FSH, ACTH, PRL, GH, TSH

17
Q

Female estrous cycle
* Period from the beginning of one estrus to the beginning of the ? (or from one ovulation to the next)

  • Follicular phase - estrus (? phase in women) - estrogen
  • Luteal phase - diestrus (? phase in women) - ?
  • Quiescent phase – anestrus – ? hormones (when females not cycling; for seasonal animals or females that are sick - too much stress)
  • Estrus is defined behaviorally

Oestrogens:
produced by developing ?
reproductive behaviours
females receptive when oestrogens are high

Progestagens
produced by ? following ovulation
supports conception and ?
females are receptive when progestagens are low (usually)

A

Female estrous cycle
* Period from the beginning of one estrus to the beginning of the next (or from one ovulation to the next)

  • Follicular phase - estrus (proliferative phase in women) - estrogen
  • Luteal phase - diestrus (secretory phase in women) - progestogen
  • Quiescent phase – anestrus – NO hormones (when females not cycling; for seasonal animals or females that are sick - too much stress)
  • Estrus is defined behaviorally

Oestrogens:
produced by developing follicles
reproductive behaviors
females are receptive when oestrogens are high

Progestagens
produced by the corpus luteum following ovulation
supports conception and pregnancy
females are receptive when progestagens are low (usually)

18
Q

Endocrine regulation of estrous cycle Hypothalamo-hypophyseal-ovarian axis

Regulated by:

  • Hypothalamus:
    -> ?
  • Adenohypophysis/anterior pituitary:
    -> ? and ?
  • Ovary:
    -> ? (E2), ? (P4), Inhibin, and ?
  • Uterus:
    -> ? F2α (PGF2α)
A

Endocrine regulation of estrous cycle Hypothalamo-hypophyseal-ovarian axis

Regulated by:

  • Hypothalamus:
    -> GnRH
  • Adenohypophysis/anterior pituitary:
    -> FSH and LH
  • Ovary:
    -> Estradiol (E2), progesterone (P4), Inhibin, and oxytocin
  • Uterus:
    -> prostaglandin F2α (PGF2α)
19
Q

FEMALE ESTROUS CYCLE

Ovary

  • Medulla (intern)
    -> ?, nerves, ? tissue
  • Cortex (extern)
    -> oocytes, ?, CL
A

FEMALE ESTROUS CYCLE

Ovary

  • Medulla (intern)
    -> vasculature, nerves, connective tissue
  • Cortex (extern)
    -> oocytes, follicles, CL
20
Q

Hypothalamo-pituitary-gonadal axis

Diestrus
- progesterone (lack of E2) - no LH
-> FSH doesn’t need ? feedback. Therefore, follicles keep developing

Estrus
- Inhibin - negative feedback for FSH
-> Induce follicular ?
- estradiol - positive feedback for ? (surge center)
-> Induce ?

(estrus -> surge center -> anterior pituitary secrestes estrogen)

A

Hypothalamo-pituitary-gonadal axis

Diestrus
- progesterone (lack of E2) - no LH
-> FSH doesn’t need positive feedback. Therefore, follicles keep developing

Estrus
- Inhibin - negative feedback for FSH
-> Induce follicular regression
- estradiol - positive feedback for LH (surge center)
-> Induce ovulation

(estrus -> surge center -> anterior pituitary secrestes estrogen)

21
Q

FEMALE ESTROUS CYCLE

Follicular dynamics
* Follicular growth occurs in ? or cohorts
- Number varies between and within ?

  • Recruitment
  • Selection
  • Dominance
  • Atresia
A

FEMALE ESTROUS CYCLE

Follicular dynamics
* Follicular growth occurs in waves or cohorts
- Number varies between and within species

  • Recruitment
  • Selection
  • Dominance
  • Atresia

notes:
- 1 estrus cycle is the period between 1 ovulation and the next ovulation
- UNDERSTAND THAT during the estrus cycle is not the one follicle that we develop and ovulate
- in reality, we have a recruitment of follicles so imagine we have one ovulation here so bc of that ovulation that cell will produce progesterone

  • bc of that progesterone the cell doesn’t do much to the hypothalamus or to the anterior pituitary
  • so the anterior pituitary, the tonic center of the hypothalamus they are still working, and then the anterior pituitary produces the hormone called FC follicular stimulating hormone.
  • bc of these FSH the follicles will develop
  • so most of these species will have two or three follicular waves
  • so first many follicles will be recruited.
  • They will develop. And then we have this second phase that’s called SELECTION.
  • During this election, some follicles, they decrease, they go through ATROPHY and the other follicles they still going forward.
  • After that we have 3rd phase called DOMINANCE which happens in the majority of the species that we have only one ovulation, cows, horse, sheep, goats and even humans.
  • so when one follicle reaches dominance means that that follicle will be able to keep growing and other follicles will regress.
  • after that we have ovulation or atresia
  • most of that at the first follicular wave or second these follicles will reach dominance, but won’t ovulate due to absence of estradiol
  • we need enough estradiol for the surge center to work
  • in the 2nd wave everything happens again and one follicle reaches dominance.
  • at this phase (ovulation - big circle on the right of potentially ovulatory) no progesterone left
  • no progesterone being produced in the FSH phase so at this moment lots of estradiol and so this estradiol will cause positive feedback to the surge center
  • and then we have this release of LH by the anterior pituitary and these LH will cause ovulation.
22
Q

Female estrous cycle

FOLLICLES

Primordial follicle
* Oocyte surrounded by a single layer of ? cells

Primary follicle
* Oocyte surrounded by single layer of ? cells

Secondary follicle
* ? surrounded by two or more ?
* Zona ?

Antral follicle
* Fluid accumulates within a cavity formed by ? cells

A

Female estrous cycle

FOLLICLES

Primordial follicle
* Oocyte surrounded by a single layer of squamous cells

Primary follicle
* Oocyte surrounded by a single layer of cuboidal cells

Secondary follicle
* Oocyte surrounded by two or more layers
* Zona pellucida

Antral follicle
* Fluid accumulates within a cavity formed by follicular cells

  • We have the primordial follicles that will be clearly those oocytes that are there resting.
  • they will have only a single layer of hiscamo? cells that can only be seen if u do a histological section of ovary
  • primary follicles when they resume that meiotic division, again, the first meiotic division, and they have a little bit of one layer of cuboid of cells here.
  • similarly secondary follicles have more cells and layers of cells around oocyte but don’t have fluid
  • they all are called PREANTRAL follicles and it means that they can grow and develop even tho we don’t have FSH or LH or gonadotropins so some of them even start developing right before puberty.
  • but if its follicles reach the tertiary follicle stage they start to develop in the antrum which is the fluid-filled cavity inside of the follicle
    and bc of this cavity has been developed at this moment
23
Q

Folliculogenesis

“Resting pool”
* Pool of inactive ? follicles
* ? phase (Prophase I)

Committed follicle (four possibilities)
* Remains ?
* Die
* Begging development and ? later
* Develop and ovulate

Follicle activation is irreversible
* Finite nest

Unknown what triggers the primordial follicle activation
* Intraovarian signaling – oocyte or granulosa cells

Gonadotropin-independent growth
* Follicular development up to the formation of the antrum is independent of FSH or LH

A

Folliculogenesis

“Resting pool”
* Pool of inactive primordial follicles
* Dormant phase (Prophase I)

Committed follicle (four possibilities)
* Remains quiescent
* Die
* Begging development and atresia later
* Develop and ovulate

Follicle activation is irreversible
* Finite nest

Unknown what triggers the primordial follicle activation
* Intraovarian signaling – oocyte or granulosa cells

Gonadotropin-independent growth
* Follicular development up to the formation of the antrum is independent of FSH or LH

  • so first we have resting pools, so all females are born with follicles which get arrested at Prophase one until puberty
  • We don’t know exactly what happens that to make some of these follicles resume that to meiosis while others still resting
  • when they resume meiosis, they finish meiosis I and release their first polar body and at this period are called “pre-antral follicles”
  • it means that these pre-antral follicles are NOT gonadotropin-dependent hormones so they can grow during this pre-antral phase without LH or FSA
  • when they reach antral phase which is when follicles start to develop in this fluid inside of the follicle, they are gonadotropin dependent so they cannot develop anymore without FSH or LH.
  • bc the females have follicles that already started in meiosis these net of follicles is finished
  • that’s why women go through menopause they finish them on some sites so they can’t produce oocytes for ovulation.
  • another imp. thing we talk about those follicular waves, the follicles they start developing and some of them, most of them, they will go to atresia or they will regress.
  • When this follicles start their development, they cannot go back so that follicles will start meiosis I if go back then die The FOLLICLE CANNOT GO BACK, then restart males again.
  • so all those follicles that started will die in one or two or 3 depending on the species
24
Q

Inhibin -> downregulation of FSH secretion

  1. Dominant follicle keeps developing bc it has enough/more receptors for ?
  2. produces estradiol which leads to 3.
  3. induces synthesis of ? which leads to 4.
  4. induces ?

estradiol (when it passes the threshold) -> surge center -> changes to positive feedback, to anterior pituitary to produce LH and also releases GnRH (binds to receptors on follicular wall and cause ovulation)

A

Inhibin -> downregulation of FSH secretion

  1. Dominant follicle keeps developing bc it has enough/more receptors for FSH
  2. produces estradiol which leads to 3.
  3. induces synthesis of LH which leads to 4.
  4. induces ovulation

estradiol (when it passes the threshold) -> surge center -> changes to positive feedback, to anterior pituitary to produce LH and also releases GnRH (binds to receptors on follicular wall and cause ovulation)

25
Q

FEMALE ESTROUS CYCLE

ANTRAL FOLLICLE
* ?-dependent
* Theca externa
* ? tissue
* Theca interna
* Produce ? under LH stimulation
* Granulosa cells
* Produce ?, ?, and follicular fluid
* Responsive to ?

A

FEMALE ESTROUS CYCLE

ANTRAL FOLLICLE
* Gonadotropin-dependent
* Theca externa
* connective tissue
* Theca interna
* Produce androgens under LH stimulation
* Granulosa cells
* Produce estrogen, inhibin and follicular fluid
* Responsive to FSH

26
Q

Female estrous cycle

Other ovarian structures

Corpus hemorrhagic (CH)
* Structure left immediately after ?
* Antrum collapses and is filled with ?

Corpus luteum (CL)
* Theca ? and ? cells proliferate to fill the cavity, and differentiate into ? cells and produce ?
* Large luteal cells (from ?; also secrete ? and Relaxin)
* Small luteal cells (from theca ?)

Corpus albicans
* Remnant of ? corpus luteum (non-functional; doesn’t produce progesterone anymore)

A

Other ovarian structures

Corpus hemorrhagic (CH)
* Structure left immediately after ovulation
* Antrum collapses and is filled with blood

Corpus luteum (CL)
* Theca interna and granulosa cells proliferate to fill the cavity, and differentiate into luteal cells and produce progesterone
* Large luteal cells (from granulosa; also secrete oxytocin and Relaxin)
* Small luteal cells (from theca interna)

Corpus albicans
* Remnant of old corpus luteum (non-functional; doesn’t produce progesterone anymore)

27
Q

if non-pregnant then:

  • produces progesterone
  • FSH release is not affected
  • follicular growth -> produces estradiol -> (around day 14-17 after ovulation) estradiol “open” receptors of oxytocin in the endometrium -> endometrium produces PGF2a by the stimulation of oxytocin
  • CL -> secretion of oxytocin -> also Estradiol “Open” receptors of oxytocin in the endometrium -> endometrium produces PGF2a by the stimulation of oxytocin -> PGF2a causes luteolysis of the CL

(notes: day 14- corpus luteum produces oxytocin (so if pregnant then receptors remain closed) and if receptors in endometrium bind to oxytocin then it produces PGF 2a (eicosanoid hormone)

A
  • if there wasn’t fertilization then at around the day 14 or 17 of this estrus cycle, this female won’t have maternal recognition of pregnancy so this may ovulate and there was a release of the oocyte
  • this here produced progesterone, during this time there is a release of FSH so there is follicular growth as we have the first and second follicular wave
  • at some point these follicles they produce estradiol and bc of production of estradiol there will be some receptors in the endometrium for oxytocin that they will be open
  • the estradiol will open their receptor for oxytocin in the endometrium if this female is not pregnant, if the female is not pregnant,
  • if the female is pregnant, these receptors will remain close and this is imp. bc at this stage around day 14 and day 17 of estrus cycle the corpus luteum starts producing oxytocin
  • if oxytocin binds to receptors in endometirum then the endometrium will produce prostaglandinF2alpha (PGF2a)
  • PGF2a is an eicosanoid hormone (not a real hormone as not produced by glands) and also associated with inflammation?
  • what PGF2a cause in this estrus cycle? this PGF2a will break the corpus luteum, will cause the LUTEOLYSIS of this corpus luteum and with this luteolysis we have a new estrus cycle

summary:
thus, progesterone follicles grow and these follicles produce a lil bit of estrogens and these estrogens will open the oxytocin receptor in the endometrium of a pregnant female.

The CL (corpus luteum) produces oxytocin that will bind the receptors in the endometrium

bc of this endometrium produces prostaglandin. THIS IS THE ESTRUS CYCLE IN FEMALES including HUMANS.

(recall: when prostaglandins break down the corpus luteum, the CL will stop producing progesterone

the CL becomes the corpus albicans and luteolysis is the end of the luteal phase and the beginning of the follicular phase

the day the progesterone drops is the day that there is a rise in the prostaglandins)

28
Q

Male fertility requires

Competent spermatogenesis
* Endocrine regulation
* ?
* Spermatocytogenesis
* Mitosis, meiosis

  • Spermiogenesis
    • ? transformation

Functional delivery system
* ? glands
* ?, ejaculation
* ?

A

Male fertility requires

Competent spermatogenesis
* Endocrine regulation
* thermoregualtion
* Spermatocytogenesis
* Mitosis, meiosis

  • Spermiogenesis
    • morphology transformation

Functional delivery system
* accesory glands
* erection, ejaculation
* libido

(for males, thermoregulation and testosterone is essential for spermatogenesis and we have spermatogenesis divided into spermatogenesis and spermiogenesis

  • for spermatogenesis, we have cell division and for
    spermiogenesis, we have maturation of the sperm losing cytoplasm and become that sperm cell that we all know of.
29
Q

Endocrinology of Male Reproduction

  • Anti-? Hormone (AMH)
  • ?-releasing hormone
  • ? hormone – induce T4 secretion
  • ?-stimulating hormone (FSH)
  • Testosterone (T4) - 100 to 500x higher in the seminiferous tubules
  • ? (E2)
  • ? (INH)

all hormones here are pretty similar to females but remember that testosterone is 100 to 500 higher in concentration inside of the seminiferous tubules than in the bloodstream.

A

Endocrinology of Male Reproduction

  • Anti-mullerian Hormone (AMH)
  • gonadotropin-releasing hormone
  • luteinizing hormone – induce T4 secretion
  • follicle-stimulating hormone (FSH)
  • Testosterone (T4) - 100 to 500x higher in the seminiferous tubules
  • estradiol (E2)
  • inhibition (INH)
30
Q

in the image hypothalamus producing exactly the same hormone, GnRH anterior pituitary/adenohypophysis -> they produce FSH and LH

  • But now NO ovaries instead there are testicles.

IMP remember these things:
- So the LH will affect straight the LEYDIG cells
- FSH affect straight the sertoli cells
- NO surge center present here and only tonic center of the hypothalamus so we have tonic pulls? of GnRH all the time and this hypothalamus only stops working when we have high conc. of testosterone.

  • thus testosterone causes another negative feedback to the hypothalamus. hence why bodybuilder get infertile when they have exogenous testosterone as it sends a negative feeback so no natural testosterone produced from leydig cells so inside testicles/seminiferous tubules become really low.
A
  • the Sertoli cells produce inhibin, when the testosterone is high as well so high testosterone affects Sertoli cells that are inside of the seminiferous tubes,

these Sertoli cells will aromatize testosterone to estradiol and then both produce inhibin

so inhibin and estradiol both cause negative feedback to the anterior pituitary

  • in males only negative feedback, testosterone negative feedback to the hypothalamus, and testosterone going straight to the sertoli cells
  • sertoli cells aromatize testosterone, high levels of estrogens will cause a negative feedback to the anterior pituitary

and bc of these high level of testosterone the sertoli cells also produce inhibin which also cause negative feedback to the anterior pituitary similar as in males - inhibin always causes negative feedback to adenohypophysis so reducing the production of FSH.

31
Q

Hormones Hypothalamic centers

Hypothalamic centers

▪ Tonic (MALES) – Regulates the release of
frequent low amplitude tong ? pulses
▪ Surge - Only in ? – responsive to high levels of ? and release of high amplitude ? pulse

Regulate by levels of ? and ?

A

Hormones Hypothalamic centers

Hypothalamic centers

▪ Tonic (MALES) – Regulates the release of
frequent low amplitude tong GnRH pulses
▪ Surge - Only in females – responsive to high levels of estradiol and release of high amplitude GnRH pulse

Regulate by levels of Testosterone and Estrogens

(- so tonic center here regualted by testosterone, surge center which is present only in females regulated by estradiol and tonic center in females works all the time and no regulation since no testosterone.

If we have a pathological condition with a female producing a lot of testosterone, testosterone will cause downregulation of the tonic center.