Hormonal Control Of Spermatogenesis Essay

Spermatogenesis is the process by which haploidspermatozoa develop from germ cells in the seminiferous tubules of the testis. This process starts with the mitotic division of the stem cells located close to the basement membrane of the tubules. These cells are called spermatogonial stem cells. The mitotic division of these produces two types of cells. Type A cells replenish the stem cells, and type B cells differentiate into spermatocytes. The primary spermatocyte divides meiotically (Meiosis I) into two secondary spermatocytes; each secondary spermatocyte divides into two spermatids by Meiosis II. These develop into mature spermatozoa, also known as sperm cells.[1] Thus, the primary spermatocyte gives rise to two cells, the secondary spermatocytes, and the two secondary spermatocytes by their subdivision produce four spermatozoa.[2]

Spermatozoa are the mature male gametes in many sexually reproducing organisms. Thus, spermatogenesis is the male version of gametogenesis, of which the female equivalent is oogenesis. In mammals it occurs in the seminiferous tubules of the male testes in a stepwise fashion. Spermatogenesis is highly dependent upon optimal conditions for the process to occur correctly, and is essential for sexual reproduction. DNA methylation and histone modification have been implicated in the regulation of this process.[3] It starts at puberty and usually continues uninterrupted until death, although a slight decrease can be discerned in the quantity of produced sperm with increase in age (see Male infertility).


Spermatogenesis produces mature male gametes, commonly called sperm but more specifically known as spermatozoa, which are able to fertilize the counterpart female gamete, the oocyte, during conception to produce a single-celled individual known as a zygote. This is the cornerstone of sexual reproduction and involves the two gametes both contributing half the normal set of chromosomes (haploid) to result in a chromosomally normal (diploid) zygote.

To preserve the number of chromosomes in the offspring – which differs between species – each gamete must have half the usual number of chromosomes present in other body cells. Otherwise, the offspring will have twice the normal number of chromosomes, and serious abnormalities may result. In humans, chromosomal abnormalities arising from incorrect spermatogenesis results in congenital defects and abnormal birth defects (Down Syndrome, Klinefelter's Syndrome) and in most cases, spontaneous abortion of the developing foetus.

Location in humans[edit]

Spermatogenesis takes place within several structures of the male reproductive system. The initial stages occur within the testes and progress to the epididymis where the developing gametes mature and are stored until ejaculation. The seminiferous tubules of the testes are the starting point for the process, where spermatogonial stem cells adjacent to the inner tubule wall divide in a centripetal direction—beginning at the walls and proceeding into the innermost part, or lumen—to produce immature sperm.[1] Maturation occurs in the epididymis. The location [Testes/Scrotum] is specifically important as the process of spermatogenesis requires a lower temperature to produce viable sperm, specifically 1°-8 °C lower than normal body temperature of 37 °C (98.6 °F).[4] Clinically, small fluctuations in temperature such as from an athletic support strap, causes no impairment in sperm viability or count.[5]


For humans, the entire process of spermatogenesis is variously estimated as taking 74 days[6][7] (according to tritium-labelled biopsies) and approximately 120 days[8] (according to DNA clock measurements). Including the transport on ductal system, it takes 3 months. Testes produce 200 to 300 million spermatozoa daily.[9] However, only about half or 100 million of these become viable sperm.[10]


The entire process of spermatogenesis can be broken up into several distinct stages, each corresponding to a particular type of cell in humans. In the following table, ploidy, copy number and chromosome/chromatid counts are for one cell, generally prior to DNA synthesis and division (in G1 if applicable). The primary spermatocyte is arrested after DNA synthesis and prior to division.


Main article: Spermatocytogenesis

Spermatocytogenesis is the male form of gametocytogenesis and results in the formation of spermatocytes possessing half the normal complement of genetic material. In spermatocytogenesis, a diploid spermatogonium, which resides in the basal compartment of the seminiferous tubules, divides mitotically, producing two diploid intermediate cells called primary spermatocytes. Each primary spermatocyte then moves into the adluminal compartment of the seminiferous tubules and duplicates its DNA and subsequently undergoes meiosis I to produce two haploid secondary spermatocytes, which will later divide once more into haploidspermatids. This division implicates sources of genetic variation, such as random inclusion of either parental chromosomes, and chromosomal crossover, to increase the genetic variability of the gamete.

Each cell division from a spermatogonium to a spermatid is incomplete; the cells remain connected to one another by bridges of cytoplasm to allow synchronous development. It should also be noted that not all spermatogonia divide to produce spermatocytes; otherwise, the supply of spermatogonia would run out. Instead, spermatogonial stem cells divide mitotically to produce copies of themselves, ensuring a constant supply of spermatogonia to fuel spermatogenesis.[11]


Main article: Spermatidogenesis

Spermatidogenesis is the creation of spermatids from secondary spermatocytes. Secondary spermatocytes produced earlier rapidly enter meiosis II and divide to produce haploid spermatids. The brevity of this stage means that secondary spermatocytes are rarely seen in histological studies.


Main article: Spermiogenesis

During spermiogenesis, the spermatids begin to form a tail by growing microtubules on one of the centrioles, which turns into basal body. These microtubules form an axoneme. Later the centriole is modified in the process of centrosome reduction.[12] The anterior part of the tail (called midpiece) thickens because mitochondria are arranged around the axoneme to ensure energy supply. Spermatid DNA also undergoes packaging, becoming highly condensed. The DNA is packaged firstly with specific nuclear basic proteins, which are subsequently replaced with protamines during spermatid elongation. The resultant tightly packed chromatin is transcriptionally inactive. The Golgi apparatus surrounds the now condensed nucleus, becoming the acrosome.

Maturation then takes place under the influence of testosterone, which removes the remaining unnecessary cytoplasm and organelles. The excess cytoplasm, known as residual bodies, is phagocytosed by surrounding Sertoli cells in the testes. The resulting spermatozoa are now mature but lack motility, rendering them sterile. The mature spermatozoa are released from the protective Sertoli cells into the lumen of the seminiferous tubule in a process called spermiation.

The non-motile spermatozoa are transported to the epididymis in testicular fluid secreted by the Sertoli cells with the aid of peristaltic contraction. While in the epididymis the spermatozoa gain motility and become capable of fertilization. However, transport of the mature spermatozoa through the remainder of the male reproductive system is achieved via muscle contraction rather than the spermatozoon's recently acquired motility.

Role of Sertoli cells[edit]

Main article: Sertoli cell

At all stages of differentiation, the spermatogenic cells are in close contact with Sertoli cells which are thought to provide structural and metabolic support to the developing sperm cells. A single Sertoli cell extends from the basement membrane to the lumen of the seminiferous tubule, although the cytoplasmic processes are difficult to distinguish at the light microscopic level.

Sertoli cells serve a number of functions during spermatogenesis, they support the developing gametes in the following ways:

  • Maintain the environment necessary for development and maturation, via the blood-testis barrier
  • Secrete substances initiating meiosis
  • Secrete supporting testicular fluid
  • Secrete androgen-binding protein (ABP), which concentrates testosterone in close proximity to the developing gametes
    • Testosterone is needed in very high quantities for maintenance of the reproductive tract, and ABP allows a much higher level of fertility
  • Secrete hormones affecting pituitary gland control of spermatogenesis, particularly the polypeptide hormone, inhibin
  • Phagocytose residual cytoplasm left over from spermiogenesis
  • Secretion of anti-Müllerian hormone causes deterioration of the Müllerian duct[13]
  • Protect spermatids from the immune system of the male, via the blood-testis barrier
  • Contribute to the spermatogonial stem cell niche

The intercellular adhesion moleculesICAM-1 and soluble ICAM-1 have antagonistic effects on the tight junctions forming the blood-testis barrier.[14]ICAM-2 molecules regulate spermatid adhesion on the apical side of the barrier (towards the lumen).[14]

Influencing factors[edit]

The process of spermatogenesis is highly sensitive to fluctuations in the environment, particularly hormones and temperature. Testosterone is required in large local concentrations to maintain the process, which is achieved via the binding of testosterone by androgen binding protein present in the seminiferous tubules. Testosterone is produced by interstitial cells, also known as Leydig cells, which reside adjacent to the seminiferous tubules.

Seminiferous epithelium is sensitive to elevated temperature in humans and some other species, and will be adversely affected by temperatures as high as normal body temperature. Consequently, the testes are located outside the body in a sack of skin called the scrotum. The optimal temperature is maintained at 2 °C (man)–8 °C (mouse) below body temperature. This is achieved by regulation of blood flow[15] and positioning towards and away from the heat of the body by the cremasteric muscle and the dartos smooth muscle in the scrotum.

Dietary deficiencies (such as vitamins B, E and A), anabolic steroids, metals (cadmium and lead), x-ray exposure, dioxin, alcohol, and infectious diseases will also adversely affect the rate of spermatogenesis.[citation needed] In addition, the male germ line is susceptible to DNA damage caused by oxidative stress, and this damage likely has a significant impact on fertilization and pregnancy.[16] Exposure to pesticides also affects spermatogenesis.[17]

Hormonal control[edit]

Hormonal control of spermatogenesis varies among species. In humans the mechanism is not completely understood; however it is known that initiation of spermatogenesis occurs at puberty due to the interaction of the hypothalamus, pituitary gland and Leydig cells. If the pituitary gland is removed, spermatogenesis can still be initiated by follicle stimulating hormone (FSH) and testosterone.[18] In contrast to FSH, LH appears to have little role in spermatogenesis outside of inducing gonadal testosterone production.[18][19]

FSH stimulates both the production of androgen binding protein (ABP) by Sertoli cells, and the formation of the blood-testis barrier. ABP is essential to concentrating testosterone in levels high enough to initiate and maintain spermatogenesis. Intratesticular testosterone levels are 20–100 or 50–200 times higher than the concentration found in blood, although there is variation over a 5- to 10-fold range amongst healthy men.[20][21] FSH may initiate the sequestering of testosterone in the testes, but once developed only testosterone is required to maintain spermatogenesis.[18] However, increasing the levels of FSH will increase the production of spermatozoa by preventing the apoptosis of type A spermatogonia. The hormone inhibin acts to decrease the levels of FSH. Studies from rodent models suggest that gonadotropins (both LH and FSH) support the process of spermatogenesis by suppressing the proapoptotic signals and therefore promote spermatogenic cell survival.[22]

The Sertoli cells themselves mediate parts of spermatogenesis through hormone production. They are capable of producing the hormones estradiol and inhibin. The Leydig cells are also capable of producing estradiol in addition to their main product testosterone. Estrogen has been found to be essential for spermatogenesis in animals.[23][24] However, a man with estrogen insensitivity syndrome (a defective ERα) was found produce sperm with a normal sperm count, albeit abnormally low sperm viability; whether he was sterile or not is unclear.[25] Levels of estrogen that are too high can be detrimental to spermatogenesis due to suppression of gonadotropin secretion and by extension intratesticular testosterone production.[26]Prolactin also appears to be important for spermatogenesis.[19]

See also[edit]


Further reading[edit]

  • "The testes and spermatogenesis". University of Wisconsin. 1998. Retrieved 2006-11-27. [permanent dead link]
  • Johnson, L.; Blanchard, T.L.; Varner, D.D.; Scrutchfield, W.L. (1997). "Factors affecting spermatogenesis in the stallion". Theriogenology. 48 (7): 1199–216. doi:10.1016/S0093-691X(97)00353-1. PMID 16728209. 
  • Bardin, C.W. (1991). "Pituitary-testicular axis". In Yen, S.S.C.; Jaffee, R.B. Reproductive Endocrinology (3rd ed.). Philadelphia: WB Saunders. ISBN 0721632068. 
  • Chambers, CV; Shafer, MA; Adger, H; Ohm-Smith, M; Millstein, SG; Irwin Jr, CE; Schachter, J; Sweet, R (1987). "Microflora of the urethra in adolescent boys: Relationships to sexual activity and nongonococcal urethritis". The Journal of Pediatrics. 110 (2): 314–21. doi:10.1016/S0022-3476(87)80180-4. PMID 3100755. 
  • Czyba, J.C.; Girod, C. (1980). "Development of normal testis". In Hafez, E.S.E. Descended and Cryptorchid Testis. The Hague: Martinus Nijhoff. ISBN 9024723337. 
  • Whitmore Wf, 3rd; Karsh, L; Gittes, RF (1985). "The role of germinal epithelium and spermatogenesis in the privileged survival of intratesticular grafts". The Journal of Urology. 134 (4): 782–6. PMID 2863395. 

External links[edit]

The process of spermatogenesis as the cells progress from primary spermatocytes, to secondary spermatocytes, to spermatids, to Sperm
Schematic diagram of Spermatocytogenesis
Labelled diagram of the organisation of Sertoli cells (red) and spermatocytes (blue) in the testis. Spermatids which have not yet undergone spermination are attached to the lumenal apex of the cell
  1. ^ abSharma S, Hanukoglu A, Hanukoglu I (2018). "Localization of epithelial sodium channel (ENaC) and CFTR in the germinal epithelium of the testis, Sertoli cells, and spermatozoa". Journal of Molecular Histology. 49 (2): 195–208. doi:10.1007/s10735-018-9759-2. PMID 29453757. 
  2. ^"The Spermatozoön, in Gray's Anatomy". Retrieved 2010-10-07. 
  3. ^Song, Ning; Liu, Jie; An, Shucai; Nishino, Tomoya; Hishikawa, Yoshitaka; Koji, Takehiko (2011). "Immunohistochemical Analysis of Histone H3 Modifications in Germ Cells during Mouse Spermatogenesis". Acta Histochemica et Cytochemica. 44 (4): 183–90. doi:10.1267/ahc.11027. PMC 3168764. PMID 21927517. 
  4. ^"scrotum". Encyclopædia Britannica. Encyclopædia Britannica Online. Encyclopædia Britannica Inc., 2015. Web. 14 Jan. 2015 <http://www.britannica.com/EBchecked/topic/530078/scrotum>.
  5. ^Wang C, McDonald V, Leung A, Superlano L, Berman N, Hull L, Swerdloff RS (1997). "Effect of increased scrotal temperature on sperm production in normal men". Fertil. Steril. 68 (2): 334–9. doi:10.1016/s0015-0282(97)81525-7. PMID 9240266. 
  6. ^Heller CG, Clermont Y (1964). "Kinetics of the germinal epithelium in man". Recent Prog Horm Res. 20: 545–571. 
  7. ^Amann RP (2008). "The cycle of the seminiferous epithelium in humans: a need to revisit?". J Androl. 29 (5): 469–487. doi:10.2164/jandrol.107.004655. PMID 18497337. 
  8. ^Forster P, Hohoff C, Dunkelmann B, Schürenkamp M, Pfeiffer H, Neuhuber F, Brinkmann B (2015). "Elevated germline mutation rate in teenage fathers". Proc R Soc B. 282: 20142898. doi:10.1098/rspb.2014.2898. PMC 4345458. PMID 25694621. 
  9. ^Padubidri, VG; Daftary, SN, eds. (2011). Shaw's Textbook of Gynaecology (15th ed.). p. 201. ISBN 978-81-312-2548-6. 
  10. ^Johnson L, Petty CS, Neaves WB (1983). "Further quantification of human spermatogenesis: germ cell loss during postprophase of meiosis and its relationship to daily sperm production". Biol. Reprod. 29 (1): 207–15. doi:10.1095/biolreprod29.1.207. PMID 6615966. 
  11. ^Fishelson, Lev; Gon, Ofer; Holdengreber, Vered; Delarea, Yakob (2007). "Comparative spermatogenesis, spermatocytogenesis, and spermato-zeugmata formation in males of viviparous species of clinid fishes (Teleostei: Clinidae, Blennioidei)". The Anatomical Record. 290 (3): 311–23. doi:10.1002/ar.20412. PMID 17525946. 
  12. ^Atypical centrioles during sexual reproduction Tomer Avidor-Reiss*, Atul Khire, Emily L. Fishman and Kyoung H. Jo Curr Biol. 2015 Nov 16;25(22):2956-63. doi: 10.1016/j.cub.2015.09.045. Epub 2015 Oct 17. http://journal.frontiersin.org/article/10.3389/fcell.2015.00021/full
  13. ^Hadley, Mac E.; Levine, Jon E. (2007). Endocrinology (6th ed.). Upper Saddle River, NJ: Prentice Hall. p. 369. ISBN 0-13-187606-6. 
  14. ^ abXiao, X.; Mruk, D. D.; Cheng, C. Y. (2013). "Intercellular adhesion molecules (ICAMs) and spermatogenesis". Human Reproduction Update. 19 (2): 167–86. doi:10.1093/humupd/dms049. PMC 3576004. PMID 23287428. 
  15. ^Harrison, RG; Weiner, JS (1949). "Vascular patterns of the mammalian testis and their functional significance". The Journal of Experimental Biology. 26 (3): 304–16, 2 pl. PMID 15407652. 
  16. ^Lewis, SE; Aitken, RJ (2005). "DNA damage to spermatozoa has impacts on fertilization and pregnancy". Cell and Tissue Research. 322 (1): 33–41. doi:10.1007/s00441-005-1097-5. PMID 15912407. 
  17. ^Mehrpour, O; Karrari P (2014). "Occupational exposure to pesticides and consequences on male semen and fertility: A review". Toxicol Lett. 230: 146–156. doi:10.1016/j.toxlet.2014.01.029. PMID 24487096. 
  18. ^ abcWilliam J. Kraemer; A. D. Rogol (15 April 2008). The Encyclopaedia of Sports Medicine: An IOC Medical Commission Publication, The Endocrine System in Sports and Exercise. John Wiley & Sons. pp. 286–. ISBN 978-0-470-75780-2. 
  19. ^ abFody EP, Walker EM (1985). "Effects of drugs on the male and female reproductive systems". Ann. Clin. Lab. Sci. 15 (6): 451–8. PMID 4062226. 
  20. ^Wolf-Bernhard Schill; Frank H. Comhaire; Timothy B. Hargreave (26 August 2006). Andrology for the Clinician. Springer Science & Business Media. pp. 76–. ISBN 978-3-540-33713-3. 
  21. ^Eberhard Nieschlag; Hermann M. Behre; Susan Nieschlag (26 July 2012). Testosterone: Action, Deficiency, Substitution. Cambridge University Press. pp. 130–. ISBN 978-1-107-01290-5. 
  22. ^Pareek, Tej K.; Joshi, Ayesha R.; Sanyal, Amartya; Dighe, Rajan R. (2007). "Insights into male germ cell apoptosis due to depletion of gonadotropins caused by GnRH antagonists". Apoptosis. 12 (6): 1085–100. doi:10.1007/s10495-006-0039-3. PMID 17268770. 
  23. ^O'Donnell L, Robertson KM, Jones ME, Simpson ER (2001). "Estrogen and spermatogenesis". Endocr. Rev. 22 (3): 289–318. doi:10.1210/edrv.22.3.0431. PMID 11399746. 
  24. ^Carreau S, Bouraima-Lelong H, Delalande C (2012). "Role of estrogens in spermatogenesis". Front Biosci. 4: 1–11. PMID 22201851. 
  25. ^Smith, Eric P.; Boyd, Jeff; Frank, Graeme R.; Takahashi, Hiroyuki; Cohen, Robert M.; Specker, Bonny; Williams, Timothy C.; Lubahn, Dennis B.; Korach, Kenneth S. (1994). "Estrogen Resistance Caused by a Mutation in the Estrogen-Receptor Gene in a Man". New England Journal of Medicine. 331 (16): 1056–1061. doi:10.1056/NEJM199410203311604. ISSN 0028-4793. PMID 8090165. 
  26. ^Edmund S. Sabanegh, Jr. (20 October 2010). Male Infertility: Problems and Solutions. Springer Science & Business Media. pp. 83–. ISBN 978-1-60761-193-6. 

The Reproductive System Essay

The Reproductive System

The reproductive system occurs in both male and female.

Like in plants it is the male gamete that needs to be transferred to
the female gamete. The female gamete is fertilised and develops inside
the mother’s body so the reproductive systems of both males and
females are highly adapted for this.

Production of sperm is called spermatogenesis.

It occurs at puberty and for the rest of there life.

It takes place in the gonads of the male - the testes. Over 100
million can be made in one day!

Each testis is composed of numerous tiny tubes called seminiferous
tubules. It is in the walls of these tubules that sperm production
actually takes place.

Development begins in the outer side of the wall in a layer of cells
called the germinal epithelium. As the immature sperm cells become
more mature they move to the inner side and break way into the lumen
of the tubule to be carried away to the epididymis for storage. The
process of this production is shown in the next two diagrams.

In between the tubules, inside the testes, are interstitial cells
called Leydig cells. These secrete the hormone testosterone.

There are also blood vessels in close proximity, delivering nutrients
and carrying away some testosterone to other target cells for the
development and maintenance of secondary sexual characteristics, e.g.
facial and pubic hair, deepening of the voice. The testosterone also
stimulates the cells inside the testis involved in spermatogenesis.

Hormonal control of spermatogenesis

The control centres are the pituitary gland and the hypothalamus in
the brain.

The hypothalamus secretes GnRH (gonadotrophin releasing hormone). This
is released into the blood and stimulates the anterior lobe of the
pituitary gland.

The anterior lobe of the pituitary gland secretes ICSH (interstitial
cell stimulating hormone).

ICSH: this stimulates the leydig cells that produce testosterone.

FSH: this stimulates the seminiferous tubules, including the Sertoli
cells. They produce sperm in response.

Note: Testosterone also acts on the seminiferous tubules and
stimulates sperm production.

The testosterone feeds back to the hypothalamus and pituitary gland to
switch off GnRH and ICSH release.

The Sertoli cells produce a hormone called inhibin that feeds back to
the pituitary gland to switch off FSH release.

Since the action of the interstitial cells and Sertoli cells are
inhibited, less testosterone and inhibin are released as a result. The
inhibition of the hypothalamus and pituitary is lifted and the process
can start again. Due to the levels of the hormones and their effects,
the process is not noticeably cyclical – there aren’t noticeable peaks
and troughs in the levels of the hormones.


The production of eggs is called...

Loading: Checking Spelling


Read more

Practical Report on human sexual reproduction.

764 words - 3 pages BIOLOGY 2: PRACTICAL REPORTHUMAN SEXUAL REPRODUCTIONReproduction is the generation of new individuals of the same species. In asexual reproduction individuals are derived from one parent and no special reproductive structures are involved. The simplest form is fission, occurring mostly in unicellular organisms. Simple multicellular...

Endocrine Disruptors Essay

1726 words - 7 pages Endocrine Disruptors During recent years, numerous newspaper and magazine articles have suggested that humans may be at risk because small amounts of well known environmental contaminants, such as dioxin, PCBs and DDT, can affect hormone levels. Hormones are produced by the endocrine system as regulators of biological function in target organs. Because hormones play a critical role in early development, toxicological effects on the endocrine...

RH Law in the Philippines

3836 words - 15 pages Are the guiding principles found in Responsible Parenthood, Reproductive Health and Population and Development Bill based on Christianity's Natural Law or on social conventions during the time the bill was made?The Responsible Parenthood, Reproductive Health and Population and Development Bill has become a big issue in the Philippines. It has been debated by different groups and institutions that created the two...


2540 words - 10 pages As years pass, more and more gadgets, machines, forms of transportation and foods are being improved because of the technological advancements. Even the life of humans is improved by the years, where the life expectancy is increasing because of the developed medical research, medicines, and medical equipment. However, developed biomedical methods such as cloning are controversial, and in fact 93% of all Americans oppose cloning. Because of the...

Frog Body Parts and Functions

623 words - 2 pages Frog Body Parts and Functions Anatomy of a Frog's Head External Anatomy of the Frog Functions of the External Anatomy of the Frog • Nictitating Membrane - A transparent part of a frog's lower eyelid that moves over the eye to clean it and protect it. • Cloacal Opening - Opening of cloaca...

The Presence of the Human Vomeronasal Organ (VNO) and Its Function

2476 words - 10 pages The presence of the human Vomeronasal Organ (VNO) and its function The vomeronasal organ (VNO), also known as Jacobson’s organ, is an auxiliary olfactory sense organ found in many animals. It is also the first stage of their accessory olfaction systems and is the sense organ involved in the Flehman response. In many mammalian species, a portion of the olfactory neuroepithelium is discretely organized into a VNO [1]. Animals use their...

Government Control of the Female Body

1896 words - 8 pages Government Control of the Female Body Internationally, issues revolving around the female body and reproduction are extremely controversial. For a woman, her body is a very private matter. At the same time, however, a woman's body and her reproduction rights are the center of attention in many public debates. Several questions regarding women's reproductive rights remain unanswered. How much control do women have over their bodies? What...

A Disease of Concern for Females - Pelvic Inflammatory Disease

837 words - 3 pages As females we are taught to maintain a healthy body by eating the right foods, exercising and scheduling regular checkups with the doctor. However, there are several diseases that affect the human female body. Pelvic inflammatory disease is one of many diseases that affect the female reproductive system, and it is a disease women should be concerned with. Pelvic inflammatory disease is an infectious disease that invades the female reproductive...

Cyborg M(others): Feminism and the New Reproductive Technologies

3068 words - 12 pages The technological regulation of bodies and the control of reproduction are central issues within the sociology of the body. The existence of such technologies has changed and transformed the way we understand the physical body, and has in turn created spaces where new truths about the body have arisen. As such, the issues raised by reproductive technologies are central to any consideration of the sociology of the body. However, it is not the...


1549 words - 6 pages Over the last thirty years, abortion policies have been the most controversial of all political and legal issues in the United States. Each state has its own laws and regulations concerning abortion. These laws mainly refer to the conditions in which abortion is legal, the requirements for minors who make the decision of having an abortion, and the government's funding for people having an abortion. The United States government has played a...

Earthworm Lab Report

1504 words - 6 pages ~General Information~ Worms are the most complex animals that I have studied. They are classified into three different phyla. There is a small number of species(20,000) of worms but there are a large number of worms. All worms have three layers of cells. They also have true organs and organ systems, and a complex nervous system.The Lumbricus terrestris earthworm is a segmented worm in the

0 Replies to “Hormonal Control Of Spermatogenesis Essay”

Lascia un Commento

L'indirizzo email non verrà pubblicato. I campi obbligatori sono contrassegnati *