1. The female reproductive system includes the ovaries, fallopian tubes, uterus, and vagina. The ovaries produce eggs and female sex hormones like estrogen and progesterone.
2. During the menstrual cycle, hormones cause an egg to mature and be released from an ovary, changing the uterine lining in preparation for potential pregnancy. If no pregnancy occurs, the uterine lining is shed through menstruation.
3. The major female sex hormones, estrogen and progesterone, regulate the development of female secondary sex characteristics and control the menstrual cycle by stimulating the growth of the uterine lining and changes in cervical mucus. Their levels fluctuate during
Steps of fertilization, where transport of gametes(oocyte and spermatozoon) , illustrated with images.
Differences in characteristics of egg and sperm of fertilization are tabulated.
Capacitation and acrosomal reaction are shown with diagrams to understand.
Barriers protecting female gamete shown with images.
Flowchart has been drawn to show the phases of fertilization and response of egg after entry of the sperm with explanation.
The result of fertilization is highlighted .
Ends
Reproductive and hormonal functions of the male Maryam Fida
Reproductive and hormonal functions of the male 1. Primary Sex Organs
Testes are the primary sex organs or gonads in males.
Accessory Sex Organs
Accessory sex organs in males are:
1. Seminal vesicles 2. Prostate gland
3.Urethra 4. Penis
Testis contain Seminiferous Tubules. Sperms are formed in seminiferous tubules. Testis has two important types of cells. 1.Sertoli cells are the supporting cells in seminiferous tubules. Sertoli cells provide support, protection and nourishment for the spermatogenic cells present in seminiferous tubules. Sertoli cells contain hormone “INHIBIN”. 2. Leydig cells. When stimulated by LH, they secrete:
Testosterone
Androstenedione
Dehydroepiandrosterone (DHEA)
Located outside the abdominal cavity within a pouch called scrotum.
Scrotum provides low temperature required for spermatogenesis.
Each testis is about 4 to 5 cm length and 2 to 3 cm width.
Each testis has about 250 compartments called testicular lobules.
Each lobule contains one to three seminiferous tubules.
Seminiferous tubules lined by male germ cells and Sertoli cells.
Male germ cell undergoes meiosis and produce sperm.
Sertoli cells provide nutrition to the germ cell and the sperm.
In between the seminiferous tubule there is interstitial cell or Leydig
cell.
Leydig cells produce testicular hormones
called androgen (testosteron It is the primary female sex organs that produce the female
gamete (ovum).
It also produces several steroid hormones.
The ovaries located in the lower abdomen.
Each ovary is about 2-4 cm in length.
Connected to the pelvic wall and uterus by ligaments.
Each ovary is covered by thin epithelium which encloses the
ovarian stroma
The ovarian stroma has two zones
A peripheral cortex.
An inner medulla.
Steps of fertilization, where transport of gametes(oocyte and spermatozoon) , illustrated with images.
Differences in characteristics of egg and sperm of fertilization are tabulated.
Capacitation and acrosomal reaction are shown with diagrams to understand.
Barriers protecting female gamete shown with images.
Flowchart has been drawn to show the phases of fertilization and response of egg after entry of the sperm with explanation.
The result of fertilization is highlighted .
Ends
Reproductive and hormonal functions of the male Maryam Fida
Reproductive and hormonal functions of the male 1. Primary Sex Organs
Testes are the primary sex organs or gonads in males.
Accessory Sex Organs
Accessory sex organs in males are:
1. Seminal vesicles 2. Prostate gland
3.Urethra 4. Penis
Testis contain Seminiferous Tubules. Sperms are formed in seminiferous tubules. Testis has two important types of cells. 1.Sertoli cells are the supporting cells in seminiferous tubules. Sertoli cells provide support, protection and nourishment for the spermatogenic cells present in seminiferous tubules. Sertoli cells contain hormone “INHIBIN”. 2. Leydig cells. When stimulated by LH, they secrete:
Testosterone
Androstenedione
Dehydroepiandrosterone (DHEA)
Located outside the abdominal cavity within a pouch called scrotum.
Scrotum provides low temperature required for spermatogenesis.
Each testis is about 4 to 5 cm length and 2 to 3 cm width.
Each testis has about 250 compartments called testicular lobules.
Each lobule contains one to three seminiferous tubules.
Seminiferous tubules lined by male germ cells and Sertoli cells.
Male germ cell undergoes meiosis and produce sperm.
Sertoli cells provide nutrition to the germ cell and the sperm.
In between the seminiferous tubule there is interstitial cell or Leydig
cell.
Leydig cells produce testicular hormones
called androgen (testosteron It is the primary female sex organs that produce the female
gamete (ovum).
It also produces several steroid hormones.
The ovaries located in the lower abdomen.
Each ovary is about 2-4 cm in length.
Connected to the pelvic wall and uterus by ligaments.
Each ovary is covered by thin epithelium which encloses the
ovarian stroma
The ovarian stroma has two zones
A peripheral cortex.
An inner medulla.
Ovary: Structure and hormonal regulationN K Agarwal
Slides describe the structure of ovary, folliculogenesis, hormonal control of female reproductive cycle, mechanism of ovulation, female sex hormones and their function.
Ovarian cycle (the guyton and hall physiology)Maryam Fida
Ovarian cycle
The germ cells that migrate into the ovaries during early embryonic development multiply, so that by about 5 months of gestation (prenatal life) the ovaries contain approximately 6 million to 7 million oogonia.
Most of these oogonia die prenatally through a process of apoptosis.
The production of new oogonia stops at this point and never resumes again.
The oogonia begin meiosis toward the end of gestation, at which time they are called primary oocytes.
Like spermatogenesis in the prenatal male, oogenesis is arrested at prophase I of the first meiotic division.
The primary oocytes are thus still diploidPrimary oocytes decrease in number throughout a woman’s life.
The ovaries of a newborn girl contain about 2 million Primary oocytes—all she will ever have.
Each Primary oocyte is contained within its own hollow ball of single layer of granulosa cells, the Primordial follicle.
By the time a girl reaches puberty, the number of Primary oocytes and follicles has been reduced to 400,000.
Only about 400 of these Primary oocytes will ovulate during the woman’s reproductive years, and the rest will die by apoptosis.
Oogenesis ceases entirely at menopause
Definition:
“Monthly rhythmical changes in the secretion of the female hormones and corresponding physical changes in the ovaries and other sexual organs”.
Duration: The duration of the cycle averages 28 days. It may be as short as 20 days ar as long as 45 days.
PHASES
Follicular Phase (Proliferative Phase) (1-14 Day)
Menstrual Phase (Day 1-5)
Preovulatory Phase. (Day 6-14)
Ovulation (Day 14)
Post Ovulatory Phase (Secretory Phase). (15-28 Day)
Leuteal Phase (Day 15-26)
Premenstrual phase. (Last 2 Day)
Concept of Hypothalamic-Pituitary-ovarian Axis
Overall, the most advanced follicle reduces the FSH supply to other follicles while at the same time it makes itself more sensitive to the FSH that remains.
The less developed, less sensitive follicles undergo atresia, while the most developed follicle attains a diameter of up to 2.5 cm. This follicle, called a mature (graafian) follicle, protrudes from the surface of the ovary like a blister.
As the follicle matures, the primary oocyte completes meiosis I and becomes a secondary oocyte.
This cell begins meiosis II but stops at metaphase II. It is now ready for ovulation.
FSH and estrogen also stimulate the maturing follicle to produce LH receptors, which are important to the next phase of the cycle
All mammalian eggs are surrounded by a relatively thick extracellular coat, the zona pellucida, that plays vital roles during oogenesis, fertilization, and preimplantation development.
The strong membrane that forms around an ovum as it develops in the ovary. The membrane remains in place during the egg's travel through the fallopian tube. To fertilize the egg, a sperm must penetrate the thinning zona pellucida. If fertilization takes place, the zona pellucida disappears, to permit implantation in the uterus.
The topic discussed here is the Anatomy of Female Reproductive system in Human Female, Process of Oogenesis (Gametogenesis). Menstrual Cycle, hormones and its function in Oogenesis. Structure of Ovum, & Oestrous cycle in detail
Ovary: Structure and hormonal regulationN K Agarwal
Slides describe the structure of ovary, folliculogenesis, hormonal control of female reproductive cycle, mechanism of ovulation, female sex hormones and their function.
Ovarian cycle (the guyton and hall physiology)Maryam Fida
Ovarian cycle
The germ cells that migrate into the ovaries during early embryonic development multiply, so that by about 5 months of gestation (prenatal life) the ovaries contain approximately 6 million to 7 million oogonia.
Most of these oogonia die prenatally through a process of apoptosis.
The production of new oogonia stops at this point and never resumes again.
The oogonia begin meiosis toward the end of gestation, at which time they are called primary oocytes.
Like spermatogenesis in the prenatal male, oogenesis is arrested at prophase I of the first meiotic division.
The primary oocytes are thus still diploidPrimary oocytes decrease in number throughout a woman’s life.
The ovaries of a newborn girl contain about 2 million Primary oocytes—all she will ever have.
Each Primary oocyte is contained within its own hollow ball of single layer of granulosa cells, the Primordial follicle.
By the time a girl reaches puberty, the number of Primary oocytes and follicles has been reduced to 400,000.
Only about 400 of these Primary oocytes will ovulate during the woman’s reproductive years, and the rest will die by apoptosis.
Oogenesis ceases entirely at menopause
Definition:
“Monthly rhythmical changes in the secretion of the female hormones and corresponding physical changes in the ovaries and other sexual organs”.
Duration: The duration of the cycle averages 28 days. It may be as short as 20 days ar as long as 45 days.
PHASES
Follicular Phase (Proliferative Phase) (1-14 Day)
Menstrual Phase (Day 1-5)
Preovulatory Phase. (Day 6-14)
Ovulation (Day 14)
Post Ovulatory Phase (Secretory Phase). (15-28 Day)
Leuteal Phase (Day 15-26)
Premenstrual phase. (Last 2 Day)
Concept of Hypothalamic-Pituitary-ovarian Axis
Overall, the most advanced follicle reduces the FSH supply to other follicles while at the same time it makes itself more sensitive to the FSH that remains.
The less developed, less sensitive follicles undergo atresia, while the most developed follicle attains a diameter of up to 2.5 cm. This follicle, called a mature (graafian) follicle, protrudes from the surface of the ovary like a blister.
As the follicle matures, the primary oocyte completes meiosis I and becomes a secondary oocyte.
This cell begins meiosis II but stops at metaphase II. It is now ready for ovulation.
FSH and estrogen also stimulate the maturing follicle to produce LH receptors, which are important to the next phase of the cycle
All mammalian eggs are surrounded by a relatively thick extracellular coat, the zona pellucida, that plays vital roles during oogenesis, fertilization, and preimplantation development.
The strong membrane that forms around an ovum as it develops in the ovary. The membrane remains in place during the egg's travel through the fallopian tube. To fertilize the egg, a sperm must penetrate the thinning zona pellucida. If fertilization takes place, the zona pellucida disappears, to permit implantation in the uterus.
The topic discussed here is the Anatomy of Female Reproductive system in Human Female, Process of Oogenesis (Gametogenesis). Menstrual Cycle, hormones and its function in Oogenesis. Structure of Ovum, & Oestrous cycle in detail
The following power point discusses about how the process of sexual reproduction takes place in Humans. In it, we discuss about the male and female reproductive systems, then we discuss about how the process of fertilisation occurs in humans. Thereafter we discuss about pregnancy. Menstrual Cycle, Ways to control Population growth, STDs etc
Introduction to female reproductive physiology (the guyton and hall physiology)Maryam Fida
Introduction to female reproductive physiology
Formation of female gametes, ova
Reception of male gametes, spermatozoa
Provision of suitable environments for fertilization of the ovum by spermatozoa and development of the resultant fetus
Parturition (childbirth)
Lactation, the production of breast milk, which provides complete nourishment for the baby in its early life
Onset of adult sexual life
Developing of female glands
Enlargement of breasts and erection of nipples
Growth of body hair, most prominently underarm and pubic hair
Greater development of thigh muscles behind the femur, rather than in front of it
Widening of hips
lower waist to hip ratio than adult males
Smaller hands and feet than men
Rounder face
Smaller waist than men
Changed distribution in weight and fat; more subcutaneous fat and fat deposits, mainly around the buttocks, thighs, and hips
Effect of Estrogens on the Uterus and External Female Sex Organs
Enlargement of external genitalia due to fat deposition
Change of Vaginal epithelium from cuboidal to stratified
Increased size of uterus after puberty
Proliferation of endometrial stroma
Effect of Estrogens on the Fallopian Tubes
Glandular tissue proliferation
Number of ciliated epithelial cells increase
Effect of Estrogens on the Breasts
development of the stromal tissues of the breasts
Growth of an extensive ductile system
Deposition of fat in the breasts.
Effect of Estrogens on the Skeleton
Estrogens inhibit osteoclastic activity in the bones stimulating bone growth
uniting of the epiphyses with the shafts of the long bones
Osteoporosis of the Bones Caused by Estrogen deficiency in Old Age
increased osteoclastic activity in the bones
decreased bone matrix
decreased deposition of bone calcium and phosphate
Effect of Estrogens on Protein Deposition
Slight increase in total body protein
BMR increased only1/3rd as compared to testosterone
Increased deposition of fate in:
Subcutaneous tissue
Breasts, buttocks and thighs
Effect of Estrogens on Hair Distribution
No effect
Effect of Estrogens on the Skin
Makes skin soft and smooth
Increased skin vascularity
Effect of Estrogens on Electrolyte Balance
Slight sodium and water reabsorption
This describes in detail about the development of Central nervous System.
https://www.youtube.com/channel/UC1QhJfPiWnmk2WpKVH1fzrQ
Subscribe and share for more topics of Neurophysiology.
This explains in detail about the different nerve potentials like Resting Membrane Potential and Action Potential.
https://www.youtube.com/channel/UC1QhJfPiWnmk2WpKVH1fzrQ
Subscribe and share for more topics of Neurophysiology.
This gives in detail about male reproductive system including Spermatogenesis.
For more Physiology subscribe
https://www.youtube.com/channel/UC1QhJfPiWnmk2WpKVH1fzrQ
The presentation describes in detail the phenomenon of Pregnancy and Parturition.
More details at https://www.youtube.com/channel/UC1QhJfPiWnmk2WpKVH1fzrQ
Factory Supply Best Quality Pmk Oil CAS 28578–16–7 PMK Powder in Stockrebeccabio
Factory Supply Best Quality Pmk Oil CAS 28578–16–7 PMK Powder in Stock
Telegram: bmksupplier
signal: +85264872720
threema: TUD4A6YC
You can contact me on Telegram or Threema
Communicate promptly and reply
Free of customs clearance, Double Clearance 100% pass delivery to USA, Canada, Spain, Germany, Netherland, Poland, Italy, Sweden, UK, Czech Republic, Australia, Mexico, Russia, Ukraine, Kazakhstan.Door to door service
Hot Selling Organic intermediates
These lecture slides, by Dr Sidra Arshad, offer a quick overview of physiological basis of a normal electrocardiogram.
Learning objectives:
1. Define an electrocardiogram (ECG) and electrocardiography
2. Describe how dipoles generated by the heart produce the waveforms of the ECG
3. Describe the components of a normal electrocardiogram of a typical bipolar leads (limb II)
4. Differentiate between intervals and segments
5. Enlist some common indications for obtaining an ECG
Study Resources:
1. Chapter 11, Guyton and Hall Textbook of Medical Physiology, 14th edition
2. Chapter 9, Human Physiology - From Cells to Systems, Lauralee Sherwood, 9th edition
3. Chapter 29, Ganong’s Review of Medical Physiology, 26th edition
4. Electrocardiogram, StatPearls - https://www.ncbi.nlm.nih.gov/books/NBK549803/
5. ECG in Medical Practice by ABM Abdullah, 4th edition
6. ECG Basics, http://www.nataliescasebook.com/tag/e-c-g-basics
These simplified slides by Dr. Sidra Arshad present an overview of the non-respiratory functions of the respiratory tract.
Learning objectives:
1. Enlist the non-respiratory functions of the respiratory tract
2. Briefly explain how these functions are carried out
3. Discuss the significance of dead space
4. Differentiate between minute ventilation and alveolar ventilation
5. Describe the cough and sneeze reflexes
Study Resources:
1. Chapter 39, Guyton and Hall Textbook of Medical Physiology, 14th edition
2. Chapter 34, Ganong’s Review of Medical Physiology, 26th edition
3. Chapter 17, Human Physiology by Lauralee Sherwood, 9th edition
4. Non-respiratory functions of the lungs https://academic.oup.com/bjaed/article/13/3/98/278874
Tom Selleck Health: A Comprehensive Look at the Iconic Actor’s Wellness Journeygreendigital
Tom Selleck, an enduring figure in Hollywood. has captivated audiences for decades with his rugged charm, iconic moustache. and memorable roles in television and film. From his breakout role as Thomas Magnum in Magnum P.I. to his current portrayal of Frank Reagan in Blue Bloods. Selleck's career has spanned over 50 years. But beyond his professional achievements. fans have often been curious about Tom Selleck Health. especially as he has aged in the public eye.
Follow us on: Pinterest
Introduction
Many have been interested in Tom Selleck health. not only because of his enduring presence on screen but also because of the challenges. and lifestyle choices he has faced and made over the years. This article delves into the various aspects of Tom Selleck health. exploring his fitness regimen, diet, mental health. and the challenges he has encountered as he ages. We'll look at how he maintains his well-being. the health issues he has faced, and his approach to ageing .
Early Life and Career
Childhood and Athletic Beginnings
Tom Selleck was born on January 29, 1945, in Detroit, Michigan, and grew up in Sherman Oaks, California. From an early age, he was involved in sports, particularly basketball. which played a significant role in his physical development. His athletic pursuits continued into college. where he attended the University of Southern California (USC) on a basketball scholarship. This early involvement in sports laid a strong foundation for his physical health and disciplined lifestyle.
Transition to Acting
Selleck's transition from an athlete to an actor came with its physical demands. His first significant role in "Magnum P.I." required him to perform various stunts and maintain a fit appearance. This role, which he played from 1980 to 1988. necessitated a rigorous fitness routine to meet the show's demands. setting the stage for his long-term commitment to health and wellness.
Fitness Regimen
Workout Routine
Tom Selleck health and fitness regimen has evolved. adapting to his changing roles and age. During his "Magnum, P.I." days. Selleck's workouts were intense and focused on building and maintaining muscle mass. His routine included weightlifting, cardiovascular exercises. and specific training for the stunts he performed on the show.
Selleck adjusted his fitness routine as he aged to suit his body's needs. Today, his workouts focus on maintaining flexibility, strength, and cardiovascular health. He incorporates low-impact exercises such as swimming, walking, and light weightlifting. This balanced approach helps him stay fit without putting undue strain on his joints and muscles.
Importance of Flexibility and Mobility
In recent years, Selleck has emphasized the importance of flexibility and mobility in his fitness regimen. Understanding the natural decline in muscle mass and joint flexibility with age. he includes stretching and yoga in his routine. These practices help prevent injuries, improve posture, and maintain mobilit
HOT NEW PRODUCT! BIG SALES FAST SHIPPING NOW FROM CHINA!! EU KU DB BK substit...GL Anaacs
Contact us if you are interested:
Email / Skype : kefaya1771@gmail.com
Threema: PXHY5PDH
New BATCH Ku !!! MUCH IN DEMAND FAST SALE EVERY BATCH HAPPY GOOD EFFECT BIG BATCH !
Contact me on Threema or skype to start big business!!
Hot-sale products:
NEW HOT EUTYLONE WHITE CRYSTAL!!
5cl-adba precursor (semi finished )
5cl-adba raw materials
ADBB precursor (semi finished )
ADBB raw materials
APVP powder
5fadb/4f-adb
Jwh018 / Jwh210
Eutylone crystal
Protonitazene (hydrochloride) CAS: 119276-01-6
Flubrotizolam CAS: 57801-95-3
Metonitazene CAS: 14680-51-4
Payment terms: Western Union,MoneyGram,Bitcoin or USDT.
Deliver Time: Usually 7-15days
Shipping method: FedEx, TNT, DHL,UPS etc.Our deliveries are 100% safe, fast, reliable and discreet.
Samples will be sent for your evaluation!If you are interested in, please contact me, let's talk details.
We specializes in exporting high quality Research chemical, medical intermediate, Pharmaceutical chemicals and so on. Products are exported to USA, Canada, France, Korea, Japan,Russia, Southeast Asia and other countries.
Couples presenting to the infertility clinic- Do they really have infertility...Sujoy Dasgupta
Dr Sujoy Dasgupta presented the study on "Couples presenting to the infertility clinic- Do they really have infertility? – The unexplored stories of non-consummation" in the 13th Congress of the Asia Pacific Initiative on Reproduction (ASPIRE 2024) at Manila on 24 May, 2024.
Pulmonary Thromboembolism - etilogy, types, medical- Surgical and nursing man...VarunMahajani
Disruption of blood supply to lung alveoli due to blockage of one or more pulmonary blood vessels is called as Pulmonary thromboembolism. In this presentation we will discuss its causes, types and its management in depth.
Explore natural remedies for syphilis treatment in Singapore. Discover alternative therapies, herbal remedies, and lifestyle changes that may complement conventional treatments. Learn about holistic approaches to managing syphilis symptoms and supporting overall health.
New Directions in Targeted Therapeutic Approaches for Older Adults With Mantl...i3 Health
i3 Health is pleased to make the speaker slides from this activity available for use as a non-accredited self-study or teaching resource.
This slide deck presented by Dr. Kami Maddocks, Professor-Clinical in the Division of Hematology and
Associate Division Director for Ambulatory Operations
The Ohio State University Comprehensive Cancer Center, will provide insight into new directions in targeted therapeutic approaches for older adults with mantle cell lymphoma.
STATEMENT OF NEED
Mantle cell lymphoma (MCL) is a rare, aggressive B-cell non-Hodgkin lymphoma (NHL) accounting for 5% to 7% of all lymphomas. Its prognosis ranges from indolent disease that does not require treatment for years to very aggressive disease, which is associated with poor survival (Silkenstedt et al, 2021). Typically, MCL is diagnosed at advanced stage and in older patients who cannot tolerate intensive therapy (NCCN, 2022). Although recent advances have slightly increased remission rates, recurrence and relapse remain very common, leading to a median overall survival between 3 and 6 years (LLS, 2021). Though there are several effective options, progress is still needed towards establishing an accepted frontline approach for MCL (Castellino et al, 2022). Treatment selection and management of MCL are complicated by the heterogeneity of prognosis, advanced age and comorbidities of patients, and lack of an established standard approach for treatment, making it vital that clinicians be familiar with the latest research and advances in this area. In this activity chaired by Michael Wang, MD, Professor in the Department of Lymphoma & Myeloma at MD Anderson Cancer Center, expert faculty will discuss prognostic factors informing treatment, the promising results of recent trials in new therapeutic approaches, and the implications of treatment resistance in therapeutic selection for MCL.
Target Audience
Hematology/oncology fellows, attending faculty, and other health care professionals involved in the treatment of patients with mantle cell lymphoma (MCL).
Learning Objectives
1.) Identify clinical and biological prognostic factors that can guide treatment decision making for older adults with MCL
2.) Evaluate emerging data on targeted therapeutic approaches for treatment-naive and relapsed/refractory MCL and their applicability to older adults
3.) Assess mechanisms of resistance to targeted therapies for MCL and their implications for treatment selection
6. A developing egg (oocyte) differentiates into a mature egg (ovum) through a series of steps
called oogenesis.
Each primordial ovum then collects around it a layer of spindle cells from the ovarian stroma
(the supporting tissue of the ovary) and causes them to take on epithelioid characteristics;
these epithelioid-like cells are then called granulosa cells.
The ovum surrounded by a single layer of granulosa cells is called a primordial follicle.
7. The oogonia in the embryonic ovary complete mitotic replication and the first stage of meiosis
by the fifth month of fetal development. The germ cell mitosis then ceases and no additional
oocytes are formed. At birth the ovary contains about 1 to 2 million primary oocytes.
During all the reproductive years of adult life, between about 13 and 46 years of age, only 400
to 500 of the primordial follicles develop enough to expel their ova—one each month; the
remainder degenerate (i.e., become atretic).
11. Primordial follicle: The stage all follicles are in within the ovaries of a newborn baby
Primary follicles: A few primordial follicles move into the primary follicle stage every day,
starting in puberty and continuing until menopause
Secondary follicles: Involves the addition of theca cells, which will secrete hormones
Tertiary follicles, also known as antral follicles: Follicles that contain a fluid-filled cavity
called the antrum; follicles at this stage are visible via transvaginal ultrasound
Graafian follicle: A follicle large enough to ovulate; only one or two of the tertiary follicles in
each cycle will mature to ovulation
Corpus luteum: No longer a follicle anymore; develops from the open follicle that released an
egg
16. At time of birth female child is with millions of
primordial follicle.
Throughout childhood granulosa cells
surrounding the ovum provide the
nourishment and secrete oocyte maturation
inhibiting factor, keeping the primordial
follicle arrested in prophase stage of 1st meiotic
dvn.
At Puberty FSH and LH secretion starts,
accelerated growth of primary follicle each
month starts, Theca layers develop and start
secreting Estrogen and Progesterone.
17. Granulosa cells under influence of FSH secretes follicular
fluid present in antrum .
There is accelerated growth of the follicles by the
following mechanisms:
Estrogen in follicle increases FSH receptors leading to
increased pituitary FSH.
Pituitary FSH and estrogen together promote LH
receptors, thus lead to LH surge.
Only one follicle matures rest become atretic.
Ovulation occurs at around 14th days after the onset of
menstrual cycle. Ovum with corona radiata released.
Under the influence of LH, progesterone is secreted by
the theca and granulosa cells.
20. After ovulation, theca interna and
granulosa cell change into luten cells.
Luten cells enlarge and become filled
with lipid process k/a Luetenization
forming Corpus Luteum.
Corpus Luteum secret sex hormones
e.g. Estrogen and Progesterone.
If no fertilization , it gets converted to
Corpus albicans
24. Estrogen makes the cervical
mucus thin and alkaline, fern
pattern of smear.
Progesterone makes it thick,
tenacious and cellular.
Estrogen makes the vaginal
epithelium cornified.
25. Estrogen – Estradiol
Promotes proliferation and growth of specific cells and secondary
sexual characteristics of female
Progestins – Progesterone
Prepares the uterus for pregnancy and the breasts for lactation
26. In nonpregnant female , estrogen is secreted by ovaries.
In pregnant female it is secreted by placenta
Types: β-estradiol, estrone, and estriol
The estrogenic potency of β-estradiol is 12 times that of estrone and 80 times that
of estriol.
27. In nonpregnant female , progesterone is secreted by corpus luteum.
In pregnant female it is secreted by placenta, after 4 months of gestation
Types: Progesterone, 17-α-hydroxyprogesterone
The estrogenic potency of β-estradiol is 12 times that of estrone and 80 times that
of estriol.
28.
29.
30. Estrogens and Progesterone are transported in the Blood Bound to Plasma Proteins.
Metabolism of Estrogen:
The liver conjugates the estrogens to form glucuronides and sulfates, and about one fifth of
these conjugated products is excreted in the bile; most of the remainder is excreted in the
urine.
Liver converts the potent estrogens estradiol and estrone into the almost totally impotent
estrogen estriol.
Diminished liver function increases the activity of estrogens in the body, sometimes causing
hyperestrinism.
31. Within a few minutes after secretion, almost all the progesterone is degraded to other
steroids that have no progestational effect.
Liver is the major site for degradation. The major end product of progesterone
degradation is pregnanediol. About 10 percent of the original progesterone is excreted
in the urine in this form.
32. Development of
female reproductive
system.
Development of
female secondary
sexual
characteristics
Stimulation of
proliferative phase of
endometrium
Estrogens Increase
Body Metabolism
and Fat Deposition
Cardioprotective role
Inhibit osteoclastic
activity in the bones
and stimulates bone
growth
33. The ovaries, fallopian tubes, uterus, and vagina all increase several times in size. External genitalia
enlarge, with deposition of fat in the mons pubis and labia majora and enlargement of the labia
minora.
Estrogens change the vaginal epithelium from a cuboidal into a stratified type, which is considerably
more resistant to trauma and infection than is the prepubertal cuboidal cell epithelium.
Estrogens cause marked proliferation of the endometrial stroma and greatly increased development of
the endometrial glands, which will later aid in providing nutrition to the implanted ovum.
34. Estrogens cause the glandular tissues of mucosal lining of fallopian tube to proliferate.
Increases the number of ciliated epithelial cells that line the fallopian tubes
Also, activity of the cilia is considerably enhanced. These cilia always beat toward the
uterus, which helps propel the fertilized ovum in that direction.
35. Estrogens cause:
1. development of the stromal tissues of the breasts,
2. growth of an extensive ductile system, and
3. deposition of fat in the breasts. The lobules and alveoli of the breast
develop to a slight extent under the influence of estrogens alone, but it is
progesterone and prolactin that cause the ultimate determinative growth
and function of these structures.
36. Estrogens inhibit osteoclastic activity in the bones and therefore stimulate bone
growth.development.
Estrogens cause uniting of the epiphyses with the shafts of the long bones.
After menopause, almost no estrogens are secreted by the ovaries. This estrogen
deficiency leads to:
(1) increased osteoclastic activity in the bones
(2) decreased bone matrix, and
(3) decreased deposition of bone calcium and phosphate
In some women this effect is extremely severe, and the resulting condition is
osteoporosis.
37. Increase the whole-body metabolic rate
Cause deposition of increased quantities of fat in the subcutaneous tissues, addition to
deposition of fat in the breasts and subcutaneous tissues, estrogens cause the deposition of fat
in the buttocks and thighs, which is characteristic of the feminine figure.
Estrogens cause a slight increase in total body protein.
38. ON SKIN
Estrogens cause the skin to develop a texture that is soft and usually smooth.
Estrogens also cause the skin to become more vascular, which is often associated with increased
warmth of the skin and also promotes greater bleeding of cut surfaces than is observed in men.
ON ELECTROLYTE
Estrogens, like aldosterone and some other adrenocortical hormones, cause sodium and water
retention by the kidney tubules.
During pregnancy the tremendous formation of estrogens by the placenta may contribute to body fluid
retention.
39. FUNCTIO
NS OF
PROGEST
ERONE
ON UTERUS
Progesterone Promotes Secretory Changes in the Uterus.
Progesterone decreases the frequency and intensity of uterine
contractions, thereby helping to prevent expulsion of the implanted
ovum.
ON FALLOPIAN TUBE
Promotes increased secretion by the mucosal lining of the fallopian
tubes. These secretions are necessary for nutrition of the fertilized,
dividing ovum as it traverses the fallopian tube before implantation.
ON BREASTS
Progesterone promotes development of the lobules and alveoli of the
breasts, causing the alveolar cells to proliferate, enlarge, and
become secretory.
Progesterone also causes the breasts to swell. Part of this swelling
is due to the secretory development in the lobules and alveoli, but
part also results from increased fluid in the tissue.
43. Describe in detail the physiological functions of Testosterone.
Explain with the help of diagram the feedback mechanism of hypothalamic-
pituitary-gonadal axis.
Discuss in detail the female sex hormones.