Korean, Edit

Chapter 31. Reproductive System

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1. Overview

2. Gonad Hormones

3. Development of the Reproductive System: Embryonic Duct

4. Male Reproductive System

5. Female Reproductive System

6. Menstrual Cycle

7. Fertilization

8. Pregnancy and Childbirth


a. Reproductive System Problem Sets



1. Overview

⑴ Cell Division

① Mitosis: Somatic Cell Division

② Meiosis: Germ Cell Division (Diploid → Haploid)

○ Occurs in the Gonads

○ Prevents doubling of genetic material in each generation

⑵ Gametes and Zygotes

① Gametes: Haploid cells (n)

② Zygote: Formed by fusion of two gametes, Diploid (2n)

③ Fertilization: Fusion of Sperm and Egg

○ Sperm: Motile gamete

○ Egg: Non-motile gamete

○ Female: Organism producing larger gamete (egg)

○ Male: Organism producing smaller gamete (sperm)

④ Gonads: Organs that produce gametes, i.e., testes and ovaries

⑤ Methods of Fertilization

○ Internal Fertilization: Fertilization within reproductive tract through copulation. Mammals, birds, reptiles, sharks, etc.

○ External Fertilization: Female releases eggs into the water, and males release sperm. Fish, amphibians, etc.

⑶ Reproduction

① Asexual Reproduction: Involves only mitosis, producing genetically identical offspring

○ Division: Separation into two identical cells through mitosis; e.g., sea anemone.

○ Budding: A portion of a somatic cell detaches and develops into a new individual; e.g., hydra.

○ Regeneration: In cases of whole-body regeneration, it is considered a form of reproduction; e.g., starfish, flatworms.

○ Parthenogenesis: Development of an unfertilized egg; e.g., aphids (female and male), bees (male).

② Sexual Reproduction: Involves meiosis, ensuring genetic diversity for evolution

○ Gametogenesis → Mating → Fertilization

○ Chromosomal recombination creates diverse offspring for adaptation to various environments

○ Hermaphroditism and Gonochorism



2. Gonad Hormones

⑴ Overview

① Most gonad hormones are steroids, except for LH, FSH.

⑵ GnRH (Gonadotropin-Releasing Hormone)

① Function 1. Stimulates secretion of LH and FSH from anterior pituitary

⑶ Follicle-Stimulating Hormone (FSH): Peptide hormone

① Male

○ Function 1. Stimulates Sertoli cells along with testosterone production → Sperm production

② Female

○ Function 1. Stimulates granule cells in ovarian follicles, promoting aromatase enzyme secretion

○ Function 2. Early Maturation: Follicular maturation

⑷ Luteinizing Hormone (LH): Peptide hormone from anterior pituitary

① Male

○ Function 1. Stimulates Leydig cells for testosterone secretion

○ Function 2. Testosterone stimulates Sertoli cells along with FSH

② Female

○ Function 1. Stimulates granule cells for testosterone secretion

○ **Function 2. Late Maturation: Ovulation induction

○ Function 3. Promotes the secretion of other androgens

○ Testosterone is converted to estrogen by aromatase enzyme secreted by granule cells

⑸ Androgen: A collective term for testosterone, androsterone, and DHA.

① Function: Important steroid hormones for male reproduction

○ Function 1. Sperm production

○ Function 2. Male secondary sexual characteristics: development of male reproductive organs, hair thickness and distribution, muscle mass increase, low voice

○ Function 3. Inhibits breast growth by estrogen

○ Function 4. Initiates and maintains sperm formation through Sertoli cells

○ Function 5. Negative feedback on LH, inhibiting GnRH release via hypothalamus and LH secretion from anterior pituitary

○ Function 6. Induces and maintains accessory reproductive organ differentiation and function

○ Function 7. Promotes bone growth (adolescence) and halts bone growth (late adolescence)

○ Function 8. Sexual desire and aggressive behavior

○ Function 9. Stimulation of erythropoietin secretion in the kidneys

② Women also produce small amounts in ovaries and adrenal cortex

③ Type 1: Testosterone

○ Very similar to estrone and estradiol, differing mainly in methylation, double bonds, and ketone groups

○ About 95% of testosterone in males is secreted by testes, 5% by adrenal cortex

④ Type 2: Androsterone

⑤ Type 3: DHEA (Dehydroepiandrosterone): DHT is the most representative

⑥ Type 3-1: DHT (Dehydrotestosterone)

○ Testosterone is converted to DHT by 5α-reductase in peripheral tissues

○ Prostate cancer and prostatic hyperplasia: Cancer cells are stimulated by DHT. Treatment involves inhibiting 5α-reductase to suppress DHT.

○ Congenital Adrenal Hyperplasia (CAH), Adrenogenital Syndrome

○ Cholesterol is converted to sexual hormones due to 21-α-hydroxylase deficiency, enhancing DHT function

○ Corticosterone, cortisol, aldosterone deficiency results in masculinization of females

○ Cortisol and aldosterone prescription can alleviate CAH

⑦ Brain: Testosterone is converted to estrogen by aromatase enzyme

⑧ Eunuch: Removal of testes. All accessory reproductive ducts regress. Used during Chosun Dynasty

⑹ Estrogen: A collective term for estrone, estradiol, and estriol.

① Structure


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Figure 1. Functional Domains of Estrogen Receptor


○ AF: Activation Factor

○ DBD: DNA-Binding Domain

○ D: Heat Shock Proteins Binding Domain

○ F: C-Terminal Domain

② Mechanism

○ Genomic pathway: Estrogen binds to ERα or ERβ and then acts on ERE or AP-1 within the target DNA to activate transcription.

○ Nongenomic pathway: Estrogen + ERα/ERβ or estrogen + GPR30 activates signaling pathways, including MAPK and cAMP.

③ Functions: Essential steroid hormones in female reproduction.

○ Function 1. Secondary Sexual Characteristics: External genitalia development, breast growth, body fat accumulation, sebaceous gland secretion, narrow shoulders, pelvic widening, pubic hair development, bone growth, epiphyseal plate closure.

○ Function 2. Reproductive Cycle: Endometrial creation, uterine wall development, oocyte maturation, follicular growth, increase in uterine progesterone receptors.

○ Function 3. During Fertilization: Stimulates transparent thin cervical mucus secretion (affects sperm movement).

○ Function 4. During Pregnancy: Increase in oxytocin receptors, uterine wall contractions, increased ciliary movement, promotion of milk ejection.

○ Function 5. Pre-partum: Promotes breast development via prolactin secretion, inhibits milk secretion.

○ Function 6. Post-partum: Decreased estrogen and progesterone levels enhance milk secretion.

○ Function 7. Inhibits atherosclerosis by affecting plasma cholesterol, blood vessels, and blood coagulation.

○ Function 8. When estrogen is deficient, the risk of developing osteoporosis, a menopausal disorder, increases.

○ Function 9. Affects brain neurons, enhancing learning and memory.

○ Function 10. Hypothalamic and pituitary feedback.

○ Function 11. Menopause regulation.

○ Function 12. Slightly lowers body temperature.

④ Synthesis: After testosterone is produced, it is converted into estrogen by the enzyme aromatase.

○ In males, testosterone is converted to estrogen in the brain, skin, liver, and adipose tissue.

○ Aromatase in turtle is less active at 25°C, resulting in male birth.

○ Aromatase in turtle is more active at 32°C, resulting in female birth.

⑤ Also produced in small amounts in males.

○ Excess estrogen in males can lead to gynecomastia.

○ In male aquatic animals, the testes may become feminized and produce eggs.

⑥ Types

○ Estrone, estradiol, and estriol are included.

○ Estradiol: The most potent hormone among the estrogens.

○ Estrogen mainly exists in the form of 17β-estradiol, but after menopause, it is present primarily as estrone.

⑺ Luteal hormone (progesterone): A steroid hormone

① Production Sites: Corpus luteum (yellow body), placenta.

○ During pregnancy, luteal hormone is produced in the placenta.

② Hypothalamic and Pituitary Feedback.

③ Function 1. GnRH Regulation

○ In small amounts: Stimulates GnRH → Stimulates FSH, LH.

○ In excess: Strongly inhibits GnRH → Inhibits FSH, LH → Prevents new follicle development.

④ Function 2. Pregnancy Preparation

○ Secretion of thick mucus from the cervix: Maintains the thickened uterine lining.

○ Activates MPF for oocyte cell division resumption.

○ Converts uterine lining to suitable secretion tissue for embryo implantation.

○ Inhibits contractions in fallopian tubes and uterine muscles.

○ Inhibits proliferation of vaginal epithelial cells.

○ Promotes breast development.

○ Suppresses prolactin’s lactogenic effects.

⑤ Function 3. Raises set point, so slightly increases body temperature.

⑥ Function 4. Increases blood vessels and promotes glycogen storage.

⑦ Cervical mucus changes and body temperature variations: Indicators of ovulation.

⑻ Anti-Müllerian Hormone: Glycoprotein.

⑼ Inhibin: Peptide hormone.

① Production: Secreted by Sertoli cells in the testes of males, and by granule cells of ovarian follicles in females.

○ The only peptide hormone in the ovary.

② Suppression of GnRH and FSH: Selectively inhibits FSH, thereby preventing the maturation of additional follicles during the reproductive cycle.

⑽ Activin: Peptide hormone.

① Present in the pituitary gland, testes, and follicular fluid.

② Also involved in developmental processes: located at the vegetal pole.


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Figure 2. Activin and Differentiation Experiment


⑾ Human Chorionic Gonadotropin (hCG)

① Secreted when fertilized egg is implanted.

② Acts similar to LH, stimulates excess secretion of estrogen, progesterone, maintains corpus luteum, and inhibits ovarian cycle.

③ hCG concentration is maintained during 2-3 months of pregnancy, then decreases.

④ Corpus luteum regresses after 5 weeks of pregnancy, and placenta takes over hCG’s role.

⑤ Pregnancy Test Kit: Detects hCG.



3. Development of the Reproductive System: Embryonic Duct

⑴ Bipotential (indifferent) gonad

① The reproductive structures do not begin differentiation until the 7th week of development.

② When developmental signals are delivered, the medulla differentiates into the testes, forming the male reproductive system.

③ In the absence of developmental signals, the cortex differentiates into the ovaries, forming the female reproductive system.

④ Bipotential internal genitalia: Derived from the embryonic kidney, consisting of the Wolffian duct and the Müllerian duct.

○ As development proceeds, one pair of ducts develops while the other regresses.

⑤ Bipotential external genitalia: Composed of the genital tubercle, urogenital folds, urethral groove, penis/clitoris, and scrotum/labia.

⑵ SRY (sex-determining region of the Y chromosome): the sex-determining locus on the male Y chromosome

① SRY induces differentiation of the gonadal medulla into testes and stimulates Leydig and Sertoli cells.

② Leydig cells: under SRY influence, secrete testosterone and its derivative DHT (dihydrotestosterone)

○ Testosterone: promotes Wolffian duct differentiation and contributes to the descent of the testes from the abdomen into the scrotum

○ DHT: regulates differentiation of the external genitalia and other male secondary sex characteristics

③ Sertoli cells: under SRY influence, secrete anti-Müllerian hormone (AMH)

⑶ Male: Wolffian duct → vas (ductus) deferens, epididymis, seminal vesicles

① Testosterone secreted by Leydig cells actively promotes development of the Wolffian ducts.

② AMH secreted by Sertoli cells actively causes regression of the Müllerian ducts.

③ Pseudohermaphroditism

○ Males inherit 5α-reductase, the enzyme that converts testosterone to DHT.

○ In patients deficient in this enzyme, DHT is not produced, so the external genitalia appear female at birth.

○ For example, the male external genitalia and prostate fail to develop adequately during fetal development.

○ At puberty, renewed testicular testosterone secretion often leads to spontaneous masculinization.

④ Cryptorchidism

○ If the testes remain in the abdominal cavity, the elevated temperature can impair spermatogenesis and cause infertility.

⑷ Female: Müllerian duct → upper vagina, oviducts/uterine (fallopian) tubes, uterus, cervix, vagina

① Because Leydig cells do not secrete significant testosterone, the Wolffian ducts regress.

② In the absence of DHT, the external genitalia develop female characteristics.

③ Because Sertoli cells do not secrete AMH, the Müllerian ducts develop naturally.


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Figure 3. Embryonic Ducts in Males and Females



4. Male Reproductive System

⑴ Reproductive organs

① From the Wolffian (mesonephric) duct, the epididymis and seminal vesicles are formed.

② Testis (testes): produces sperm and hormones; a relatively low temperature is required for normal spermatogenesis.

○ Around the 7th fetal month, the testes descend from the abdominal cavity into the scrotum.

○ 1–3% of newborns have incomplete descent.

○ About 80% descend spontaneously with growth.

○ Spermatogenesis requires a temperature 4–5 °C below core body temperature; at ≥35 °C smooth muscle relaxes.

③ Epididymis: stores and concentrates sperm; confers motility (i.e., sperm maturation); transports sperm by peristalsis during ejaculation.

④ Prostate: secretes a thin fluid containing prostaglandins, nutrients, and alkaline substances, enhancing motility.

○ Prostaglandins, 60% of semen, promote sperm motility and the motility of the female reproductive tract.

○ Benign prostatic hyperplasia (BPH): causes urinary frequency and a sense of incomplete emptying; evaluated with the prostate-specific antigen (PSA) test.

⑤ Seminal vesicle: secretes most components of seminal fluid.

○ Produces a viscous secretion containing glucose and fructose.

○ Alkaline, protecting sperm from acidic secretions in the female tract.

○ Fructose provides most of the energy used by sperm.

⑥ Cowper’s (bulbourethral) gland: secretes a clear, mucous, alkaline pre-ejaculatory fluid → neutralizes urinary acidity and clears the urethra prior to ejaculation.

○ Also secretes a small amount of lubricating mucus.

⑦ Urethra

○ The reproductive tract (ejaculatory ducts) and urinary tract share the urethra.

○ The ejaculatory duct forms when the duct from the seminal vesicle joins a duct passing through the prostate, then connects to the urethra.

○ The ducts from the bulbourethral (Cowper’s) glands connect separately.

⑧ Glans (glans penis)

○ Circumcision: removal of the prepuce. Associated with reduced risks of penile cancer, certain STIs, and cervical infections; related to the religious rite of circumcision.

⑵ Testis

① Basement membrane: prevents intrusion of foreign substances; forms part of the blood–testis barrier to regulate molecular transport.

② Seminiferous tubules

○ Site of spermatogenesis.

○ Include Sertoli cells and Leydig cells.

○ Total combined length is about 250 m.

③ Leydig cells

○ Located in the interstitial spaces between seminiferous tubules.

○ Hormonal stimulation: under LH stimulation, secrete testosterone and other androgens.

○ Hormone secretion: testosterone.

④ Sertoli cells

○ Embedded in the wall of the seminiferous tubules; provide extensive support for the production and development of sperm cells.

○ Hormonal stimulation: in response to testosterone and FSH, secrete paracrine factors that promote spermatogenesis.

○ Hormone secretion: anti-Müllerian hormone (AMH), androgen-binding protein (ABP), inhibin.

○ Provide nutritional support.

○ Form the blood–testis barrier, protecting sperm cells from immune attack.

○ Phagocytose residual cytoplasm from developing spermatids.

⑶ Spermatozoon

① Haploid nucleus.

② Acrosome: derived from the Golgi apparatus; contains hydrolytic enzymes for penetration of the ovum; the Golgi apparatus is involved in forming the acrosome required for the acrosome reaction.

③ Flagellum (midpiece): contains numerous mitochondria; generates ATP.

④ Tail: flagellar motility; speed 1–4 mm/min.

⑤ Must be exposed to the chemical environment of the female reproductive tract to acquire fertilizing capacity (capacitation).


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Figure 4. Structure of the testis


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Figure 5. Hormonal relationships in the male reproductive system


⑷ Sperm Production

① From puberty to adulthood, sperm production continues in the seminiferous tubules.

② Duration: 65 days

③ Daily production: 30 million

④ Lifetime production: 1012 to 1013 sperms

⑤ Ejaculate: 100-300 million sperm

⑸ 1st. Spermatogonia generated from primitive germ cells

⑹ 2nd. No change from birth to puberty

⑺ 3rd. Endocrine changes during puberty

① 3rd - 1st. GnRH secretion ↑ → FSH and LH secretion from the anterior pituitary

② 3rd - 2nd. LH → Stimulates Leydig cells → Increases testosterone secretion

③ 3rd - 3rd. FSH → Stimulates Sertoli cells → GPCR → Androgen binding protein (ABP) secretion ↑

④ 3rd - 4th. Testosterone + ABP → Stimulates Sertoli cell in a way of positive feedback control.

○ Spermatocytes do not possess testosterone receptors, so they cannot respond to testosterone directly.

○ However, spermatocytes do have receptors for androgen-binding protein (ABP), allowing them to respond to testosterone.

⑤ 3rd - 5th. Morphological change of Sertoli cells: Sertoli cells that were connected by tight junction undergo separation

⑻ 4th. As spermatogonia migrate between Sertoli cells from the cortical region of the seminiferous tubules toward the medullary region, they undergo differentiation.

① 4th - 1st. Accumulation of cytoplasm in spermatogonia and DNA replication leads to the formation of Primary Spermatocyte (2n)

○ A primary spermatocyte is a cell corresponding to prophase I of meiosis.

○ Males are born with spermatogonia, whereas females are not born with oogonia.

② 4th - 2nd. Primary spermatocytes undergo the first meiotic division to generate 2 Secondary Spermatocytes (n)

○ A secondary spermatocyte is a cell corresponding to metaphase II of meiosis.

③ 4th - 3rd. Two secondary spermatocytes undergo the second meiotic division to produce 4 Spermatids (n)

④ 4th - 4th. Cytoplasmic connections between spermatids are maintained until the completion of meiosis, with Sertoli cells playing a role in this process.

⑤ 4th - 5th. Spermatids differentiate into sperm cells

○ Most of the cellular organelles of spermatids are lost as they differentiate into sperm cells

○ Exception: Golgi apparatus for acrosome reaction

⑥ 4th - 6th. Mature sperm cells are released into the lumen of the seminiferous tubule

⑼ 5th. Epididymis and vas deferens

① Until reaching the epididymis, sperm are non-motile and are carried along by secretions from Sertoli cells.

② Sperm mature in the epididymis (acquiring motility), become highly concentrated, are stored until ejaculation, and are transported by peristaltic contractions.

③ After vasectomy (ligation of the ductus deferens), the small number of sperm present are degraded and reabsorbed by the surrounding tissues.



5. Female Reproductive System

⑴ Reproductive organs

① External genitalia: labia majora, labia minora, clitoris

② Ovary: site of oocyte maturation

○ One on each side high in the pelvic cavity; roughly almond-sized

○ Cortex: connective tissue layer

○ Medulla: follicular cells, granulosa cells, thecal layers

○ Follicular cells: produce androgens (mainly androstenedione)

○ Granulosa cells: produce aromatase and convert those androgens to estrogens

③ Uterus: thick-walled muscular organ; site of embryo implantation

④ Oviduct/uterine tube (Fallopian tube): ciliated epithelium transports the fertilized ovum

○ Opens into the peritoneal cavity adjacent to the ovary—the only natural passage

⑤ Cervix: part of the birth canal; regulates the passage of sperm

⑥ Vagina: birth canal; site of intercourse

⑦ The reproductive tract and urinary tract are completely separate.

⑵ Development of female gametes

① 1st. Oogonia generated from primordial germ cells

② 2nd. Oogonia undergo mitosis during embryo stage

③ 3rd. A primary oocyte is an oogonium that has entered meiosis and then arrested in prophase I (atresia state).

○ A primary oocyte contains 46 chromosomes.

○ A primary oocyte together with surrounding granulosa cells is collectively called a primordial follicle.

○ A primary oocyte is produced by meiosis, whereas a primary spermatocyte is produced by mitosis.

④ 4th. Birth to puberty

○ Fetus: Has around 7 million primary oocytes

○ After birth: Has around 1 million primary oocytes

○ Childhood: Has around 400,000 primary oocytes

○ Puberty: Has around 200,000 to 400,000 primary oocytes

⑤ 5th. At puberty, GnRH stimulates FSH secretion from the anterior pituitary

⑥ 6th. FSH promotes the maturation of primary follicles; through estrogen’s negative feedback and inhibin secretion from the earliest maturing (dominant) follicle, only one or two follicles are selected.

○ Primary follicle: the follicle enlarges; ribosomes, mRNA, cellular organelles, and energy reserves accumulate.

○ Under FSH stimulation, the primary follicle begins to produce estrogens.

⑦ 7th. Unequal cytoplasmic division: Stimulated primary oocyte undergoes the first meiotic division to form primary polar body and larger daughter cell

⑧ 8th. Secondary Oocyte: The larger daughter cell of the primary oocyte arrests in Metaphase II of the second meiotic division. 23 chromosomes.

○ Approximately 8-9 days of the menstrual cycle

⑨ 9th. Secondary oocyte is released from the mature follicle through ovulation

○ Secondary oocyte is around 500 μm during ovulation

○ Around day 14 of the menstrual cycle

⑩ 10th. Activation of MPF by progesterone at ovulation

⑪ 11th. Sperm meets secondary oocyte in the fallopian tube and resumes the second meiotic division of the ovum

⑫ 12th. Through unequal cytokinesis, a second polar body and the ovum (egg cell) are produced.

○ The first polar body may resume meiosis II and divide to yield two second polar bodies.

○ However, the first polar body may also fail to divide.

○ Polar bodies eventually degenerate.

⑶ Follicular development

① Follicle: a saclike cluster of cells within the ovarian endocrine tissue, composed of theca cells and granulosa cells.



6. Menstrual Cycle


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Figure 6. Menstrual cycle


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Figure 7. Hormonal Relationship of the Female Reproductive System


⑴ Overview

① The reproductive cycle occurs every 28 days, with ovulation around day 14 and menstruation around day 28.

② Pre-ovulation is called the follicular phase, and post-ovulation is called the luteal phase.

③ The reproductive cycle progresses simultaneously with the development of female gametes: the 5th to the 10th aforementioned steps.

⑵ 1st. Maturation of Follicles

① 1st. After the dissolution of the corpus luteum that strongly inhibits GnRH, there is a slight increase in FSH and LH secretion.

② 1st - 2nd. Negative feedback: Small amounts of estrogen inhibit GnRH, thereby inhibiting FSH and LH.

○ Estrogen gradually increases.

③ 1st - 3rd. Early maturation (secondary follicles): A few among numerous follicles undergo early maturation first.

○ Secondary follicles possess secondary oocytes and secrete estrogen and a small amount of luteal hormone.

○ Early maturation is relatively easy due to the lack of inhibitory effects from inhibin.

○ Theca cells, the zona pellucida, and the follicular antrum appear.

○ Theca cells: surround the follicular (granulosa) cells.

○ Zona pellucida: surrounds the germ cell (oocyte).

④ 1st - 4th. Late maturation: As the follicles mature, the granulosa cell layer proliferates, and LH receptors are expressed on the layer cells.

⑤ 1st - 5th. Follicle competition: During follicle maturation, several follicles within the ovary mature, but ultimately only one or two 3rd-stage follicles mature for ovulation.

○ 1st - 5th - 1st. The inhibin secreted by the first mature follicle suppresses FSH, which is involved in early maturation.

○ 1st - 5th - 2nd. Low estrogen levels inhibit FSH and LH, preventing the maturation of other follicles.

○ Moderately mature follicles undergo atresia.

○ 3rd-stage follicle (Graafian follicle) is characterized by a large antrum and is responsible for secreting estrogen.

⑶ 2nd. Development of Uterine Endometrium

① 2nd - 1st. The earliest maturing (dominant) follicle persists in producing aromatase and testosterone despite low estrogen levels.

○ 2nd - 1st - 1st. FSH: stimulates granulosa cells of the follicle to promote secretion of aromatase.

○ 2nd - 1st - 2nd. LH: stimulates granulosa cells of the follicle to promote secretion of testosterone.

○ 2nd - 1st - 3rd. Testosterone is converted to estradiol (estrogen) by aromatase.

② 2nd - 2nd. Because of the “uncooperative” earliest maturing (dominant) follicle, estrogen levels rise gradually.

○ At low concentrations, estrogen exerts strong negative feedback, so the increase takes time—on the order of a full ovarian (menstrual) cycle.

③ 2nd - 3rd. Estrogen thickens the uterine endometrium.

⑷ 3rd. Estrogen Surge

① 3rd - 1st. When estrogen levels exceed a threshold, GnRH is stimulated, promoting FSH and LH secretion.

② 3rd - 2nd. Positive feedback: Increased FSH and LH due to estrogen further elevates estrogen concentration.

③ 3rd - 3rd. FSH and LH dramatically increase, with FSH’s increase being moderate due to inhibin.

○ Inhibin selectively suppresses FSH, preventing an FSH surge comparable to that of LH.

○ If FSH secretion were to rise as much as LH, the FSH that drives early maturation would initiate maturation of new follicles.

⑸ 4th. Ovulation: 14 days after menstruation

① 4th - 1st. As LH responsible for late maturation (including ovulation) dramatically increases, it promotes the secretion of prostaglandins, causing follicle rupture.

② 4th - 2nd. When the follicle ruptures, the antral cavity (follicular antrum) releases its follicular cells.

③ 4th - 3rd. The follicle from which the oocyte has been released becomes the corpus luteum and secretes luteal hormones (primarily progesterone).

○ Prostaglandins promote the transformation of the follicle into the corpus luteum (luteinization).

○ The abrupt hormonal changes at ovulation can cause ovulatory pain (mittelschmerz) and ovulatory spotting/bleeding.

④ Over a lifetime, approximately 400–500 ovulations occur.

⑹ 5th. Corpus Luteum Development

① 5th - 1st. After ovulation, due to the absence of follicles that would secrete estrogen, estrogen decreases.

② 5th - 2nd. As the corpus luteum develops, testosterone and progesterone secretion increases.

③ 5th - 3rd. Negative feedback: Excessive progesterone inhibits GnRH, leading to FSH and LH inhibition.

○ Inhibits FSH involved in early maturation, thus inhibiting maturation of new follicles and ovulation.

○ A small amount of progesterone stimulates GnRH, leading to FSH and LH stimulation.

④ 5th - 4th. Testosterone and progesterone contribute to the development of the uterine endometrium.

○ Estrogen: Continues to thicken the uterine endometrium.

○ Progesterone: Maintains the thickness of the uterine endometrium.

⑺ 6th - 1st. In case the fertilized oocyte does not implant

① 6th - 1st - 1st. The corpus luteum increases cholesterol and fats, leading to its degeneration into the corpus albicans (fibrous tissue) with a lifespan of 2 weeks.

② 6th - 1st - 2nd. Menstruation: Due to the cessation of LH and progesterone secretion, the thickened uterine endometrium collapses.

○ During menopause, when menstruation ceases, no primary oocytes remain.

③ 6th - 1st - 3rd. Returns to step ⑵.

⑻ 6th - 2nd. In case the fertilized oocyte implants

① 6th - 2nd - 1st. Fertilized egg implants in the uterus.

② 6th - 2nd - 2nd. Progesterone activates MPF, thereby resuming oocyte cell division.

③ 6th - 2nd - 3rd. Implantation signals stimulate the secretion of human chorionic gonadotropin (hCG).

④ 6th - 2nd - 4th. hCG prevents the decline of the corpus luteum, which has a lifespan of only 2 weeks.

⑤ 6th - 2nd - 5th. The corpus luteum’s function is maintained, preventing new follicle maturation and menstruation.



7. Fertilization

⑴ Fertilization Process of Sea Urchin: Sea urchins are frequently used as models for fertilization.

① 1st. Attraction (chemoattraction): this step shows no species specificity.

○ 1st - 1st. Oocyte releases resact molecules into its surroundings.

○ 1st - 2nd. Resact molecules react with sperm, enhancing sperm motility.

○ 1st - 3rd. Sperm randomly moving becomes faster in the direction of the oocyte, facilitating movement towards the oocyte.

② 2nd. Contact

○ 2nd - 1st. Sperm cell contacts the jelly layer of the oocyte.

○ 2nd - 2nd. Exocytosis occurs from the acrosome of the sperm.

○ Sea urchin oocyte structure: jelly layer (no receptors) – vitelline envelope (receptors present) – plasma membrane (receptors present).

○ Mammalian oocyte structure: cumulus cell layer – zona pellucida – vitelline membrane – plasma membrane.

③ 3rd. Acrosomal reaction

○ 3rd - 1st. Hydrolytic enzymes released from the sperm acrosome create pores in the jelly layer (involving numerous Golgi-derived vesicles).

○ 3rd - 2nd. A large amount of Ca2+ is released from the smooth endoplasmic reticulum, and growing actin filaments form the acrosomal process.

○ 3rd - 3rd. Bindin on the acrosomal process protruding from the sperm head binds to bindin receptors on the egg’s vitelline envelope.

○ Bindin-mediated binding is species-specific.

④ 4th. Formation of holes in the vitelline envelope → Fusion of sperm and egg cell membranes → Insertion of sperm nucleus into egg cytoplasm

⑤ 5th. Fast block to polyspermy: sea urchins only

○ 5th - 1st. Na+ and Ca2+ ions enter the zygote together with the sperm.

○ 5th - 2nd. Depolarization of the membrane

○ 5th - 3rd. Anions surround the depolarized membrane.

○ 5th - 4th. Anion-enveloped membrane limits the secondary fertilization of negatively charged sperm

⑥ 6th. Slow block to polyspermy (cortical reaction) occurs about a minute after sperm-egg fusion

○ 6th - 1st. Separation of the vitelline envelope from the plasma membrane: an absolute blockade of the zygote’s plasma membrane to additional sperm (polyspermy block).

○ 6th - 1st - 1st. Ca2+ is released from the zygote’s smooth endoplasmic reticulum.

○ As with neurotransmitter release, Ca2+ is always involved in vesicle exocytosis.

○ 6th - 1st - 2nd. Ca2+ wave: the released Ca2+ actively propagates toward vesicle-rich sites (not merely by diffusion).

○ When two sperm are experimentally bound to a single egg, distinct Ca2+ waves occur for each.

○ A23187: an ionophore that transports Ca2+ across the phospholipid bilayer.

○ Treatment with A23187 induces formation of the fertilization envelope without fertilization, whereas the Ca²⁺ chelator BAPTA inhibits fertilization-envelope formation.

○ 6th - 1st - 3rd. The egg’s cortical granules (oligosaccharide-containing vesicles) are exocytosed into the space between the plasma membrane and the vitelline envelope.

○ 6th - 1st - 4th. Because cortical granules are highly osmotic, water influx occurs.

○ 6th - 1st - 5th. A perivitelline space forms between the vitelline envelope and the cell membrane.

○ 6th - 2nd. Removal of plasma-membrane receptors: substances from the cortical granules cleave the membrane receptors that bind sperm.

○ 6th - 3rd. Fertilization envelope formation: enzymes from the cortical granules harden the vitelline envelope, forming the fertilization envelope.

⑦ 7th. Cleavage

⑵ Fertilization in mammals

① Overview

○ In mammals, fertilization of the oocyte by sperm occurs in the oviduct (Fallopian tube).

○ Of roughly 300 million sperm, only about 200 reach the oocyte in the oviduct.

○ Many sperm fail to survive the acidic conditions in the upper vagina.

○ It takes about 30 minutes for sperm to travel from the upper vagina to the oviduct.

② 1st. The sperm penetrates the cumulus (follicular) cell layer.

③ 2nd. The sperm head binds to the species-specific zona pellucida glycoprotein ZP3.

④ 3rd. Acrosomal enzymes are released, digesting the zona pellucida and forming a tunnel.

⑤ 4th. The oocyte and sperm membranes fuse.

⑥ 5th. The sperm nucleus enters the oocyte.

⑦ 6th. The oocyte nucleus, having completed meiosis II, fuses with the sperm nucleus.

⑧ 7th. The zygote begins cleavage.


스크린샷 2026-08-18 오후 10 14 20

Figure 8. Mammalian Fertilization



8. Pregnancy and Childbirth

⑴ Early Development of the Zygote

① Fertilization in mammals

② Cleavage

○ Mammalian cleavage is the slowest in the animal kingdom.

○ During cleavage, the embryo is transported to the uterus by the cilia of the oviduct (Fallopian tube).

○ About one week after fertilization, the zygote reaches the blastocyst stage (the mammalian form of the blastula).

③ Embryonic gene expression

○ In sea urchins, embryonic gene expression begins at the mid-blastula stage.

○ In mammals, embryonic gene expression begins at the 2-cell or 4-cell stage.

④ Implantation

○ Implantation occurs about one week after fertilization.

○ A few days after the blastocyst stage, implantation occurs in the endometrium.

○ The embryo implants in the uterus under the influence of progesterone.


스크린샷 2026-08-18 오후 10 14 35 스크린샷 2026-08-18 오후 10 15 00

Figure 9. Process of Oocyte Formation and Early Zygote Development in Humans

A: 2-cell embryo, B: 1st polar body, C: 2nd polar body


⑵ Pregnancy

① Definition

○ Presence of one or more embryos in the uterus.

○ Dating: fertilization day → ~266 days after fertilization, or LMP → ~280 days.

○ Signs: amenorrhea plus nausea/vomiting.

○ Tests: detection of hCG in urine; ultrasound exam.

② First trimester (~12 weeks): the period of most rapid change for both mother and embryo

○ Uterine enlargement compresses the bladder → frequent urination.

○ Blastocyst growth: after implantation in the endometrium, the blastocyst grows and embryonic body structures begin to differentiate.

○ Early development (weeks 2–4): the embryo obtains nutrients directly from the endometrium; the trophoblast expands and contributes to placental formation.

○ ~4 weeks: heartbeat; ~8 weeks: limb formation begins.

○ Organogenesis

○ By 8 weeks after fertilization, the major organs are formed.

○ By the end of the first trimester, most organs have begun to form.

○ hCG maintains the corpus luteum until about the 4th month.

③ Second trimester (13–26 weeks)

○ Fetal mass up to ~600 g.

○ Lower abdomen enlarges; breasts enlarge; colostrum is secreted.

○ Fetal movement felt at ~16 weeks; by late 2nd trimester the fetus sucks its thumb.

○ hCG secretion decreases → corpus luteum regresses.

○ Placenta secretes progesterone to maintain pregnancy.

○ High progesterone: forms a protective cervical mucus plug; promotes growth of the maternal portion of the placenta; enlarges the uterus; suppresses the ovarian cycle.

④ Third trimester (27–40 weeks)

○ Fetal size increases; fetal movements decrease.

○ Uterine enlargement compresses abdominal organs → maternal dyspnea, indigestion, constipation, frequent urination, muscle stiffness, edema of leg joints; fetal pressure on maternal organs.

○ Fetal physiology: begins digestion, stores glycogen, produces urine, and shows periodic sleep–wake cycles.

○ Estrogen: stimulates prolactin secretion, but suppresses milk release before birth.

○ Prolactin: promotes breast growth; strengthens the milk-producing apparatus of the mammary glands.

○ Prostaglandins: secreted by the placenta; induce contraction of the uterine wall.

○ Oxytocin: promotes labor by inducing uterine smooth-muscle contractions via positive feedback.

⑤ Maternal–fetal exchange at the placenta

○ Maternal and fetal blood do not mix directly across the placenta, preventing antigen–antibody reactions and blood-type agglutination.

○ Umbilical arteries: high in CO₂ and wastes.

○ Mother → fetus: oxygen and nutrients.

○ Fetus → mother: carbon dioxide and wastes.

○ Umbilical vein: high in oxygen and nutrients.

○ Amniotic fluid: prevents fetal drying and cushions external shocks.

○ Countercurrent exchange increases the efficiency of transfer.

⑥ Morning sickness

○ hCG hypothesis: morning sickness peaks around weeks 6–7, coinciding with rising hCG levels.

○ Newer view: protective response against toxicity from excessive animal-protein intake; vegetarians are said not to experience morning sickness.

⑶ Childbirth: the process in which the fetus emerges from the mother, occurring 280 days after ovulation or 266 days after fertilization.

① Promotion of uterine contractions during labor: estrogen, oxytocin (positive feedback)

○ Stage 1: cervical dilation (1 mm → 10 cm)

○ Stage 2: delivery of the baby

○ Stage 3: delivery of the placenta

② After delivery, once the placenta is expelled, estrogen and progesterone are no longer secreted.

③ The decrease in estrogen secretion initiates milk production.

④ Positive feedback: when the infant suckles after birth, prolactin secretion from the anterior pituitary is stimulated.

⑤ Ovulation resumes as the frequency of breastfeeding decreases.

○ For about two months postpartum, estrogen and progesterone levels are low, so ovulation and menstruation do not occur.

⑷ Twins

① Dizygotic twins: fertilization of two ova by two sperm within the same uterus.

○ In a single reproductive cycle, two follicles independently develop into embryos and implant.

② Monozygotic twins

○ Separation before implantation (within 5 days after fertilization): two chorions and two amnions.

○ Separation 5–10 days after fertilization: two amniotic sacs within a single chorion.

○ Separation 10–14 days after fertilization: one chorion and one amnion; rare (4–6%). Conjoined twins can only occur in this way.

○ If the embryo is separated during the first month of development, monozygotic twins can result.


스크린샷 2026-08-18 오후 10 15 00

Figure 10. Three Ways Identical Twins Are Formed

Only Siamese twins can be produced through the right method


⑸ Contraception

① Withdrawal (coitus interruptus)

② Rhythm method (natural family planning)

○ The rhythm method is the only contraceptive method recognized by the Roman Catholic Church.

○ Ovulation around day 14 ± 1 of the cycle.

○ Ovum survives ~2 days; sperm ~5 days.

○ Fertile window: from 5 days before ovulation to 2 days after ovulation.

③ Basal body temperature method: predict ovulation by measuring body temperature.

④ Cervical mucus method: predict ovulation by the turbidity and viscosity of cervical mucus.

⑤ Contraceptive pills

○ Commonly used: oral contraceptives combining progestin and estrogen at a 2:1 ratio.

○ Effect 1: Suppresses the hypothalamus, inhibiting GnRH secretion and ovulation (effectiveness 95%).

○ Effect 2: Thickens cervical mucus and hinders sperm motility (effectiveness 95%).

○ Effect 3: Prevents implantation of the ovum (emergency contraception) (effectiveness 80%).

○ Types include combined pills, the mini-pill, and emergency (morning-after) pills.

○ Side effects: menstrual cycle disturbances, fetal blood coagulation, breast cancer, uterine and ovarian cancer, ovarian cysts, nausea, vomiting, abdominal pain, fatigue, headache.

⑥ Vaginal ring: inserted into the vagina; supplies progestin and estrogen to prevent ovulation and thicken cervical mucus (effectiveness 99%).

⑦ Cervical cap, diaphragm (pessary), sponge, female condom, male condom.

⑧ Spermicides: inserted into the vagina one hour before intercourse; kill sperm.

⑨ Intrauterine device (IUD): a plastic device inserted into the uterus; increased risk of pelvic inflammatory disease.

⑩ Female sterilization (tubal surgery): permanently occludes the fallopian tubes by tightly twisting them (effectiveness 99.5%).

⑪ Male sterilization (vasectomy): ligates the vas deferens to prevent sperm from being ejaculated in semen (effectiveness 99.9%).

⑹ Infertility

① Definition: Failure to achieve pregnancy after at least 1 year of sexual activity.

② Cause 1. Male infertility (90%)

○ Low sperm count, poor sperm motility, or abnormal sperm morphology (e.g., enlarged or small head, two heads, two tails).

○ In healthy individuals, about 25% of the 200–300 million sperm are morphologically abnormal.

○ Abnormal sperm are eliminated in the competition to reach the fallopian tubes.

○ Atrazine: a pesticide component; decreases sperm viability.

○ Trichloroethylene: a degreasing/cleaning solvent; leads to production of abnormal sperm.

③ Cause 2. Female infertility

○ Endometriosis: a condition in which tissue lining the uterus grows on the ovaries and fallopian tubes and responds to hormones.

○ Cause 1. Retrograde menstruation (main cause).

○ Cause 2. Possible family history.

○ Cause 3. Excess female hormones.

○ Cause 4. Menstrual cycles of 27 days or fewer, or menstruation lasting 7 days or more.

○ Cause 5. Early menarche.

○ Cause 6. Few childbirths.

○ Creates scarring in ovarian tissue and disrupts ovulation.

○ Occurs in 3–10% of women of reproductive age and in 25% of infertile women.

○ Scarring from infections and sexually transmitted diseases can block tubular structures and cause infertility.

○ DEHP: an endocrine disruptor and carcinogenic substance.

⑺ Sexually Transmitted Diseases (STDs)



Input: 2019.01.26 20:13

Last Updated: 2022.06.06 22:30

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