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assisted reproduction

 
Dictionary: assisted reproduction

n.
The use of medical techniques, such as drug therapy, artificial insemination, or in vitro fertilization, to enhance fertility.


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Sci-Tech Encyclopedia: Reproductive technology
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Any procedure undertaken to aid in conception, intrauterine development, and birth when natural processes do not function normally. The most common are in vitro fertilization and gamete intrafallopian transfer.

Infertility, which is the inability to conceive during at least 12 months of unprotected intercourse, is an increasingly common problem. Hormonal therapy and microsurgery are used to overcome many hormonal and mechanical forms of infertility, but many types of infertility do not respond to such treatment. See also Infertility.

In vitro fertilization bypasses the Fallopian tubes. Immediately prior to ovulation the mature oocyte is removed from the ovary and placed, together with prepared sperm, in a petri dish for 2–3 days. Fertilization takes place during this time and the fertilized oocyte develops into a two- to eight-cell embryo, which is then transferred into the uterus. In vitro fertilization is useful for females with absent or severely damaged Fallopian tubes; couples in which the female has endometriosis; when the male has severely reduced sperm counts; or when the couple has immunologic or unexplained infertility for a period of 2 or more years. The four principal steps of in vitro fertilization are induction and timing of ovulation, oocyte retrieval, fertilization, and embryo transfer.

Gamete intrafallopian transfer, or GIFT, is similar to in vitro fertilization with a few important distinctions. In gamete intrafallopian tube transfer, the spermatozoa and oocytes are placed into the fimbriated end of the Fallopian tube during the laparoscopy. It is unusual for more than two oocytes to be placed into either Fallopian tube. Indications for gamete intrafallopian transfer include unexplained infertility of two or more years' duration, cervical stenosis, immunologic infertility, oligospermia, and endometriosis. At least one Fallopian tube must appear normal; where there has been severe pelvic adhesions or distorted tubal anatomy from any cause, gamete intrafallopian transfer should not be considered. See also Pregnancy; Reproductive system disorders.


World of the Body: assisted reproduction
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Although techniques like donor insemination and induction of ovulation (stimulation of the ovary to produce eggs) have been used for many years, it was the birth of Louise Brown (the first ‘test-tube baby’) in 1978 that marked the beginning of new methods of assisted reproduction. The success of in vitro fertilization (IVF) showed that eggs and sperm could be manipulated in the laboratory to produce embryos which, when implanted into the uterus, could result in successful pregnancies. The success of IVF opened new horizons in the alleviation of infertility and in the science of embryology. It is now possible to observe the very earliest stages of human development, and with these discoveries came the hope of identifying defects at this very early stage and making it possible to remedy these defects. However, there was unease at the apparent uncontrolled advance of science and the new possibilities for manipulating the early stages of human development. Society was worried.

Because of this concern the UK government set up, in 1982, the Committee of Inquiry into Human Fertilisation and Embryology under the chairmanship of Lady Warnock — it is now commonly known as the Warnock Committee. This committee considered all aspects of assisted reproduction available at the time and made some 63 recommendations. One of the most important of these was that the government should set up a new statutory licensing authority to regulate both research and those infertility services which the committee recommended should be subject to control. Certain activities were to be made a criminal offence, such as the placing of a human embryo in the uterus of another species. The UK government did not act until 1990 when the Human Fertilisation and Embryology Act was passed. This Act set up the Human Fertilisation and Embryology Authority (HFEA), and the main recommendations of the Warnock Committee were incorporated into the Act, which now regulates the use of assisted reproduction in the UK.

In the period between 1984, when the Warnock Committee reported, and the 1990 Act, the Medical Research Council of Great Britain and the Royal College of Obstetricians and Gynaecologists set up a Voluntary Licensing Authority (VLA). This body had no statutory authority but great moral authority and all the centres in the UK using the new techniques were licensed by the Authority after inspection. The VLA set the pattern for the later HFEA, and much of the methodology used by the HFEA derives from the work and experience of the VLA. Unfortunately not all other countries have followed this example. For example, in the USA there is no Federal law relating to embryo research or IVF, and rules tend to be established on a case by case basis. Some other countries have legislated, but what is required is some international agreement to control developments in this area.

IVF was initially instituted to bypass blockage of the Fallopian tubes, but it is now utilized in the treatment of infertility from various causes — male, female, combined or unexplained; also when donor insemination or ovulation induction (see below) have failed.

IVF is carried out in many centres in the UK and elsewhere. The UK centres have all been licensed by the HFEA after inspection by a team from that body. Many centres have evolved specific criteria for inclusion in their programmes. Each couple has to be carefully assessed. Factors like female age and sperm dysfunction affect the success rate considerably. These couples have usually undergone a series of tests before being accepted as suitable for IVF, and this frequently puts a strain on their marriage, so counselling is an important aspect of decision making. IVF treatment should not be used as a panacea for marital or psychosexual disorders but to fulfill the wishes of a well-adjusted couple to have a baby.

In recent years, however, some rather unorthodox requests have been made for IVF. For example a number of lesbian couples have requested IVF using the egg from one of the partners and sperm from a donor. Also, male homosexual couples have requested the use of a donated egg to be fertilized by the sperm from one of them, the resulting embryo to be implanted into the uterus of a woman who would be a surrogate and hand over the baby, when born, to the homosexual male couple. These developments have caused concern to society, as has the use of IVF to enable women past the menopause to have babies. The oldest of such women to date had a successful pregnancy at the age of 63. These new developments require to be reviewed and society must decide what is appropriate and what is not acceptable.

IVF involves the removal of an egg from the ovary and the fertilization of the egg by the partner's sperm in the laboratory. The embryo thus formed is then placed in the woman's uterus, where it will, hopefully, implant resulting in a pregnancy. The incidence of live births resulting from this procedure is on average 20%. Before the egg is removed the ovary is stimulated with drugs (gonadotropins). This results in a number of eggs — maybe 10 or more — being available instead of the usual natural single one. All of them are removed and fertilized, and usually 3 are implanted in the uterus at one time. This number is stipulated as a maximum by the HFEA. This gives a higher pregnancy rate than if only one egg is implanted, but if more than 3 eggs are implanted there is obviously a greater risk of triplets or more. Even when only 3 embryos are implanted the multiple births, usually twins, account for 30% of outcomes, so some centres now replace only 2 embryos to try to avoid this situation, as the loss rate with twins is greater than in single pregnancies. The ‘spare embryos’, as they are called, are frozen and used if the first attempt is not successful. Should a high multiple pregnancy (triplets or above) become evident (and this can be diagnosed early in pregnancy by ultrasound scan) the question of ‘fetal reduction’ has to be considered. The higher the multiple the greater is the risk of miscarriage or preterm birth of a small baby which may be handicapped. Fetal reduction means the injection, under ultrasound control, of a lethal substance into one or more fetuses to reduce the number from, say, four to two. This gives a much greater chance of survival for the remaining two babies. This method has also caused concern to society but it should be discussed with the couple involved and they should be offered this procedure if they so wish. It follows that with all IVF methods the couple must be well informed of the details of the procedures and the possible outcomes. The message is that, with careful evaluation, persistance in IVF can lead to a successful outcome in a large proportion of cases.

Other techniques which can be used include GIFT (gamete intra fallopian transfer) and ZIFT (zygote intra fallopian transfer). In GIFT eggs and sperm are transferred to the fallopian tube where fertilization occurs naturally. This seems to be particularly effective in unexplained infertility. In the case of ZIFT the egg is fertilized in the laboratory and then placed in the fallopian tube, where it passes down the tube in the natural way.

A newer technique that is very successful is called ICSI (intracellular sperm injection). In this method a single sperm is injected into the egg, which is thus fertilized. The advantage of this method is that the doctor can select and use a single sperm that looks normal and is active. This can be done using sperm from men with very low counts and has therefore greatly improved the results and has given hope to many couples when this is the problem

What are the results for the babies born as a result of these methods? The incidence of preterm delivery is high and there is a 4-fold increase in the number of babies of low birth weight. The reason for this is not clear. The rates of perinatal (around birth) and infant deaths are about twice the national average. This is mainly due to the number of multiple births and the age of the mother — IVF mothers are usually older. There is no greater incidence of congenital abnormalities.

Other forms of assisted reproduction include donor insemination (DI) and ovulation induction. In DI the sperm from a donor is used to inseminate the wife of an infertile man. Provided the husband agrees to his wife being inseminated in this manner he is considered in the UK to be the legal father of the child. However, the birth certificate is false because it says that the husband is the father when he is not. While this is of benefit to the child, ethicists are worried about this falsehood.

Sperm can be frozen and stored and now, to avoid the possible transmission of the AIDS virus, donors have to be tested for the virus at the time of donation and again 180 days later. If the tests are negative on both occasions the sperm which has then been frozen for 180 days can be used. Eggs cannot be frozen at the present time so they have to be fertilized at once, forming embryos which can be frozen and stored. The stored embryos come under the same storage regulations as sperm. The storage of sperm and embryos have sometimes caused difficulties when the partners have separated or one or both has died. Therefore when sperm or embryos are frozen and stored the donors of the gametes now have to record what should happen in such eventualities.

Ovulation induction is a method of assistance for women who are not producing eggs. Drugs (gonadotropins) which stimulate the ovary to produce eggs are used. The dose is care-fully monitored by ultrasound scanning of the ovary and the measurement of hormones in the blood.

There are many ethical dilemmas arising out of assisted reproductive methods and the developments therefrom, many of which were not foreseen. Society has to consider which advances are acceptable and which are not. The latest to date is the possibility of ‘cloning’ human beings by taking cells from a human embryo and forming identical human beings. This has been done with animals and it seems likely that it will be done in the human, probably in a country with no restrictions on such a procedure. Assisted reproduction has enabled many couples to have children who would not otherwise have been able to do so. As long as these methods and the developments from them are kept under control they can be of great benefit to mankind.

— Malcolm Macnaughton

Bibliography

  • Harris, J. and Holm, S. (eds) (1998). The future of human reproduction. Clarendon Press, Oxford.
  • Houghton, D. and Houghton, P. (1994). Coping with childlessness. George Allen & Unwin, London.
  • Bellar, F. K. and Weir, R. F. (eds) (1994). The beginning of human life. Kluwer Academic Publishers

See also infertility; pregnancy.

Genetics Encyclopedia: Reproductive Technology
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Successful pregnancy requires ovulation (when an ovary releases an egg into a fallopian tube), transport of the egg partway down the fallopian tube, movement of sperm from the vagina to the fallopian tube, penetration by the sperm of the egg's protective layer, and implantation of the fertilized egg in the uterus.

In the United States, infertility is an issue of great concern to many couples of childbearing age. More than 15 percent of all such couples are estimated to be infertile. In a 1995 study by the Centers for Disease Control and Prevention, 10 percent of 10,847 women interviewed, a percentage that represents 6.1 million women of childbearing age nationwide, reported having experienced some problems getting pregnant or carrying a baby to term. Of this group, about half were fertile themselves but had infertile partners. The number of women seeking professional assistance to deal with infertility problems is increasing every year (600,000 in 1968, 1.35 million in 1988, 2.7 million in 1995), and it is reasonable to believe that this trend will continue unabated well into the twenty-first century.

Pregnancy and Infertility

There are many causes of infertility. Abnormal semen causes the infertility problems of about 30 percent of couples seeking treatment. Tubal disease and endometriosis in the female partner account for another 30 percent. A female partner's failure to ovulate accounts for 15 percent, and the inability of sperm to penetrate the woman's cervical mucus accounts for another 10 percent. The final 15 percent of couples seeking treatment are infertile for reasons that cannot be diagnosed.

Many couples can be helped to overcome infertility through hormonal or surgical interventions. Women experiencing ovulation disorders may benefit from treatment with oral drugs such as clomiphene citrate, or through the injection of gonadotropins, such as follicle-stimulating hormone, which has about a 75 percent success rate. Women with tubal disease can be helped by various types of reconstructive surgery, but the success rate is only about 33 percent.

However, many infertile couples cannot be helped by such standard methods of treatment. Instead, as a last resort, couples that want children must turn to newer techniques that bypass one or more steps in the usual physiological processes of ovulation, fertilization, and implantation. Commonly referred to as "assisted reproductive technology," these techniques include in vitro fertilization (IVF), gamete intrafallopian transfer, zygote intrafallopian transfer, donor insemination, egg donation, embryo cryopreservation, intracytoplasmic sperm injection, tubal embryo stage transfer, and intrauterine insemination.

In Vitro Fertilization

When performed by an experienced practitioner and in an experienced clinic, IVF generally results in pregnancy rates of about 28 percent after one attempt and 51 percent after three. One study has reported the pregnancy rate after six attempts as being 56 percent. Another has reported it as being 66 percent.

Generally, one attempt at IVF is made per menstrual cycle. The IVF process begins when couples are first screened. Clinicians first must rule out infertility in the male partner. If the problem is with the female partner, various courses of treatment may be available. Generally, couples are expected to try to achieve pregnancy for a year after the initial screening before intervention is attempted. However, if a woman is in her late thirties or older, or if she is experiencing irregular menstruation, a clinical investigation may begin earlier.

Especially in older women, the blood level of follicle-stimulating hormone, a hormone that acts on the ovary to stimulate the maturation of viable eggs, is measured. If the hormone's level is found to be elevated early in a woman's menstrual cycle (after the first week of the new cycle), her ovaries may not be responding to it. In that case, hormonal treatment to stimulate ovulation would be ineffective, and assisted reproductive technology would be unable to help achieve pregnancy. Elevated estrogen levels at day three would also indicate that the ovaries are not responding correctly to estrogen or hormones.

In women whose ovaries are capable of generating viable eggs, the first step in IVF is referred to as "superovulation." To increase the chance of success, the woman's ovaries are stimulated to develop many follicles. Normally, only one or perhaps two follicles develop and are released by an ovary during a single menstrual cycle, which is why usually only one or, on rare occasions, two children are born. In superovulation, a doctor forces multiple follicles to develop so that many oocytes can be collected.

To stimulate the ovaries to develop many follicles, the woman undergoes the "long protocol." The action of the pituitary gland is suppressed hormonally, and ten days later the woman is treated with follicle-stimulating hormone. To see how well her ovaries are responding to the hormone, doctors measure estrogen blood levels and observe the ovaries with ultrasound scans. The number and size of the follicles can be visualized. When the doctors judge that the time is right (that is, when the follicle is enlarged to the point that it protrudes above the surface of the ovary), they give the woman human chorionic gonadotropin, wait thirty-six hours, and collect the oocytes from the mature follicles.

In the past, to collect follicles, doctors performed laparoscopy, in which a thin optical tube with a light (called a laproscope) is inserted through a very small incision in the abdominal wall, and the pelvic organs are viewed with fiber optics. Today, the use of a needle guided by ultrasound makes the procedure much faster. The ovary is visualized, mature follicles are located, the needle is inserted, and the follicular fluid that contains the mature oocyte (the unreleased egg) is aspirated. The doctors may collect up to eleven oocytes from a single patient.

Viable sperm are collected from the man and washed in a special solution that activates them so they can fertilize the egg. The process of sperm activation is called "capacitation" and normally occurs when sperm are ejaculated and enter the female reproductive tract. Capacitation involves activating enzymes in the sperm's acrosomal cap, allowing the sperm head, which contains the sperm's genetic material, to penetrate the outer and inner membranes of the egg (zona pellucida and vitelline membrane). For males with azoospermia, microsurgical or aspiration techniques can directly extract sperm from either the epididymis or the testicles. Azoospermia is the most severe form of male infertility, caused by obstructions in the genital tract or by testicular failure.

To allow fertilization to take place, a single egg and about 100,000 sperm are placed together in special culture medium and incubated for about twenty-four hours. Doctors then use a microscope to see if there are two pronuclei (one from the egg and one from the sperm) in the egg, indicating that fertilization occurred. In some cases, the sperm are unable to penetrate the egg. They may be unable to swim correctly, or they may not have been capacitated successfully. In the past, the only solution was to use sperm from another man. Now, however, sperm can be injected directly into the egg's cytoplasm, in a process called microassisted fertilization.

There are three ways used successfully by doctors and researchers to micro-fertilize the egg. The first is "zona drilling," in which a hole is punched into the zona pellucida, letting sperm penetrate the egg. The second method is called "subzonal sperm insertion," in which a sperm is injected directly under the zona pellucida. A third, related method is "intracytoplasmic sperm injection," in which a sperm is injected directly into the egg cytoplasm. The second method is reported to have a higher fertilization success rate (59%) than the third (13%).

The Risks of Ivf

In some women, the drugs used to promote superovulation may cause side effects, including mood swings. Some investigators have suggested that procedures used in assisted reproductive technology may not be safe because of the potential for increased ovarian hyperstimulation syndrome and bone loss from the hormone treatments. Ovarian hyperstimulation syndrome occurs at mild levels in 23 percent of women undergoing the treatments, at moderate levels in 3 percent, and at severe levels in 0.1 percent. Complications also may arise as a result of the surgical procedures involved in egg retrieval and embryo transfer. Such complications include pelvic and other infections, which occur in 0.15 percent to 1.2 percent of women, complications from anesthesia, which occur in 0.2 percent, and internal injuries, which occur in 0.38 percent. Although the incidence of such complications is low, every chemical or surgical intervention is associated with risks, and potential patients should be aware of this.

Other concerns regarding the long-term effects of assisted reproductive technology include the increased incidence of spontaneous abortions, which occur in 20 percent of women, and ectopic and heterotopic pregnancies, which occur in 5.5 and 1.2 percent of women, respectively. In heterotopic pregnancies, an embryo is implanted outside the uterus.

There have been conflicting reports as to whether there is a link between the use of fertility drugs and ovarian cancer. Overall, results from many studies do not seem to support such a connection. Some researchers have suggested that the use of the drugs may increase the risk of ovarian cancer later in life, but this is difficult to prove or disprove because the techniques have not been around long enough to assess long-term effects. There have been no reports of any increase in abnormalities in children born using micro-assisted fertilization, though critics have questioned whether the techniques might increase the incidence of such abnormalities.

Embryo Transfer Techniques

Once the egg is fertilized, the two pronuclei fuse to form the early embryo, or "zygote." The zygotes are placed in culture media, where they undergo cell division, cleaving repeatedly and passing through the two-cell, four-cell, and eight-cell stages. Within seventy-two hours, the zygote develops into the morula, the solid mass of blastomeres formed by the cleavage of the fertilized ovum (egg). After about three to five days in culture, the zygote has become a hollow ball of cells called the blastocyst. During normal embryogenesis, it is the blastocyst that is implanted in the endometrial lining of the uterus.

While the embryos are in culture, problems in their development may become apparent. After embryos with evident problems are discarded, one or more cultured embryos are transferred into the uterus, where, it is hoped, one will become implanted and develop into a healthy, full-term baby. Embryo transfer replaces the natural process in which the embryo passes down the fallopian tube and into the uterus, prior to implantation.

Although this transfer is relatively simple and often takes only a few minutes, the rate of successful implantation is low. Usually, two embryos are transferred, but still only one of five women become pregnant. Most doctors who perform IVF procedures adhere to the limit of two embryos per woman to minimize the risk of multiple pregnancies. In most cases, three embryos are transferred in women older than thirty-five. In the United Kingdom, it is illegal for an IVF doctor to transfer more than three embryos at a time into a woman.

A number of factors play a role in whether embryo transfer leads to a baby being born. Success rate is higher if embryo transfer takes place between forty-eight and seventy-two hours after oocyte collection. When more than one embryo is transferred at the same time, the success rate increases, but so does the chance for multiple pregnancies. As noted above, the maximum number transferred should never exceed three. Probably the single most important factor determining whether or not a successful embryo implantation will take place is the donated egg's age. Embryos formed from eggs donated by younger women have a higher implantation success rate than do embryos formed from eggs donated by older women. The age of the host uterus appears to have little or no effect on outcome.

Gamete Intrafallopian Transfer

An alternative to IVF and intrauterine embryo transfer is gamete intrafallopian transfer (GIFT), introduced more than twenty years ago. In this procedure, the egg and sperm are collected as they would be for IVF procedures. However, instead of allowing fertilization to take place in a culture dish, the egg and sperm are transferred surgically into the woman's fallopian tube. This allows fertilization to occur in the fallopian tube, just as occurs in a natural pregnancy. The transfer can only be performed in women with healthy and functional fallopian tubes, and the sperm used for fertilization must be completely normal and capable of swimming.

After the transfer is made, doctors have no way of knowing if normal fertilization actually takes place until an embryo has implanted in the uterine wall. However, the procedure's success rate (35%) is higher than the success rate for IVF. Another related technique is zygote intrafallopian transfer, in which the egg is fertilized in vitro and the zygote is transferred surgically into the fallopian tube. Other techniques include tubal embryo transfer, in which an embryo already undergoing cleavage is transferred.

Intrauterine Insemination

Intrauterine insemination is used when a couple's inability to conceive a child is caused by the sperm's inability to reach the egg. Sperm must move through the uterus and enter the fallopian tube before they can fertilize the egg. Anything that prevents the sperm from making this trip will block conception. Coital or ejaculatory disorders can limit the sperm's travels, sperm antibodies in the female reproductive tract can kill the sperm, and sperm may be unable to penetrate the cervical mucus.

To help the sperm reach the egg, the female is treated with human chorionic gonadotropin to induce multiple ovulation. The number of follicles that are induced is monitored by ultrasound. Washed sperm from the male partner are injected through the cervical opening, into the uterus. The pregnancy rate using this procedure is about 10 percent.

Donor Insemination and Egg Donation

Donor insemination is used when sperm are incapable of fertilizing the egg. Usually this occurs if the male produces very little or no sperm. Sometimes, donor sperm is used when the male partner is the carrier of a genetic disorder that could be transmitted to the baby. Sperm donors should be between ages eighteen and fifty-five, and all should be screened for genetic disorders, such as cystic fibrosis, and for various types of chromosomal abnormalities and infectious disease, including hepatitis, syphilis, cytomegalovirus, and HIV. As with the use of intrauterine insemination, the female partner undergoes ovarian stimulation to maximize the number of follicles released during ovulation. Pregnancy rates resulting from the use of donor insemination are between 32 percent and 50 percent after ten inseminations.

As with donor insemination, egg donation is used when the woman cannot ovulate or is the carrier of a genetic disease. Egg donors must be younger than thirty-five years and must be screened for the same set of conditions as sperm donors. Donors are treated with drugs to stimulate ovulation, after which the eggs are fertilized with the sperm from the male partner and the embryos are transferred to the uterus of the female partner (other procedures can also be used). Growth and development of the embryos then follow the natural processes.

Surrogacy and Cryopreservation

Surrogacy, in which pregnancy occurs in another woman, can supply a couple with an alternative if the woman partner cannot carry the baby to term in her own uterus. In some cases, if the woman cannot supply the egg, sperm from the male partner can be used to inseminate the surrogate mother, who carries the baby to term. Alternatively, if the female partner can produce her own egg, sperm from the male partner can be used to fertilize the egg, and the resulting pre-embryo can be transferred to the uterus of the surrogate mother to grow and develop. Legal controversies resulting from these arrangements have become common in the last few years, so the arrangements should be carefully reviewed by all parties, along with experts in the field, before any final decisions are made.

Frozen sperm and embryos effectively retain their viability for many years. The use of frozen human blastocysts is associated with a 10 percent successful pregnancy rate. Oocyte freezing is much less successful, possibly because oocytes may be genetically damaged or killed in the freezing and thawing. Embryos produced from such cryopreserved eggs have a high incidence of aneuploidy, and they are slow to cleave and develop even if they appear to be genetically undamaged. Various research groups are trying to solve this problem.

Age As a Factor

Age must be taken into account when couples are considering assisted reproductive technology. In humans, the age of the oocyte, not the age of the uterus, is the main cause of reproductive failure in IVF and embryo transfer techniques. Embryos formed from older oocytes demonstrate an increased incidence of aneuploidy. In some other species, such as in rabbits, an aging uterus can keep an embryo from being implanted. The use of cryopreservation to circumvent reproductive failure in humans, cattle, and horses has already been successfully employed and is likely to be developed further.

Sperm generated by older men are capable of successfully producing normal embryos. However, as sperm age, they are exponentially more likely to contain new gene mutations. Older oocytes, on the other hand, do not appear to be more likely to contain new mutations. Scientists are unsure exactly how age affects oocyte integrity. Oocyte maturation takes place only before birth in the female, so no new oocytes are produced during the entire reproductive life of the female. This is quite different from spermatogenesis, which can continue into old age. Thus, oocytes from older women may be forty or more years old when they are collected and used to form the embryos.

Oocytes must reach full maturity before they can be ovulated normally and before they can be fertilized, even artificially, to form embryos. If immature oocytes could be artificially forced to mature in vitro, follicles could be taken from the ovaries of dying or dead women, or from cancer patients planning on undergoing chemotherapy treatments, which can damage oocytes. Unlike immature oocytes, immature sperm can effectively be used in fertilization. Additional research is needed in this area of assisted reproductive technology.

Legal, Ethical, and Moral Considerations

The use of these powerful techniques to facilitate reproduction in both humans and animals (the techniques can be used in cattle and pigs, and in the conservation of endangered wildlife) must be balanced against legal, ethical, and moral concerns. For example, would it be permissible to revive extinct animal species? Although a Jurassic Park-like scenario to reanimate extinct dinosaurs is not scientifically credible at this time, what if it became possible to use this technology to form embryos and clone an extinct mammoth, or the passenger pigeon? And what if we can do this for extinct humans? Just because we can develop the capability, would it be acceptable? What are the ethics involved?

Other concerns include questions about how long embryos should remain frozen and who owns frozen embryos not used by the parents. What happens if the parents separate, divorce, or die? What about the legal entanglements involved with surrogacy? Already in the media there have been a number of such cases reported. With the expected increase of these procedures in the future, it is likely that such complex questions will only escalate. Finally, there are basic concerns about helping people sidestep the natural birth process to bring into the world a new human.

Bibliography

Ryan, Michael. "Countdown to a Baby." New Yorker (July 21, 2002): 68-77.

Schultz, Richard M., and Carmen J. Williams. "The Science of ART." Science 21 (June 2002): 2188-2190.

—Charles J. Grossman and Robert Baumiller

Wikipedia: Reproductive technology
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Reproductive technology encompasses all current and anticipated uses of technology in human and animal reproduction, including assisted reproductive technology, contraception and others.

Contents

Assisted reproductive technology

Assisted reproductive technology (ART) is the use of reproductive technology to treat infertility. This is today the only application of reproductive technology to increase reproduction that is used routinely. Examples include in vitro fertilization and its possible expansions.

Contraception

Contraception is a form of reproductive technology that enables people to control their fertility.

Others

The following techniques, in contrast to ART, are not yet routinely used. In fact, most of them are even at the developmental stage:

Same-sex procreation

In recent decades, a new possibility for LGBT parenting, same-sex procreation (where two women could have a daughter with equal genetic contributions from both women, or where two men could have a son or daughter with equal genetic contributions from both men), has become a possibility, through the creation of either female sperm or male eggs from the cells of adult women and men. With female sperm and male eggs, lesbian and gay couples wishing to become parents would not have to rely on a third party donor of sperm or egg.

The first significant development occurred in 1991, in a patent application filed by U.Penn. scientists to fix male sperm by extracting some sperm, correcting a genetic defect in vitro, and injecting the sperm back into the male's testicles.[1] While the vast majority of the patent application dealt with male sperm, one line suggested that the procedure would work with XX cells, i.e., cells from an adult woman to make female sperm.

In the two decades that followed, the idea of female sperm became more of a reality. In 1997, scientists partially confirmed such techniques by creating chicken female sperm in a similar manner.[2] They did so by injecting blood stem cells from an adult female chicken into a male chicken's testicles. Some years later, other Japanese scientists created female offspring by combining the eggs of two adult mice, though using a procedure that would not be allowed for humans.

In 2008, a flurry of announcements revealed further developments with human same-sex reproduction, with a patent application filed by an American researcher[3] specifically on methods for creating human female sperm using artificial or natural Y chromosomes and testicular transplantation.[4] A UK-based group, in an interview, predicted they would be able to create human female sperm within five years.[5] Another group at the Butantan Institute in Brazil is working on creating male eggs from embryonic stem cells, and if successful, from adult skin cells, though their current experiments are with mice.[6] All of these developments and more are listed in Timelime of Research in Human Same-sex Procreation.

Ethics

Many issues of reproductive technology have given rise to bioethical issues, since technology often alters the assumptions that lie behind existing systems of sexual and reproductive morality.

Also, ethical issues of human enhancement arise when reproductive technology has evolved to be a potential technology for not only reproductively inhibited people but even for otherwise reproductively healthy people.

See individual subarticles for details

In fiction

  • Science fiction has tackled the themes of creating life through other than the conventional methods since Mary Shelley's Frankenstein. In the twentieth century, Aldous Huxley's Brave New World (1932) was the first major fictional work to anticipate the possible social consequences of reproductive technology. Its largely negative view was reversed when the author revisited the same themes in his utopian final novel, Island (1962).

References

  1. ^ US patent 5858354 Repopulation of testicular Seminiferous tubules with foreign cells, corresponding resultant germ cells, and corresponding resultant animals and progeny
  2. ^ Tagami T, Matsubara Y, Hanada H, Naito M (June 1997). "Differentiation of female chicken primordial germ cells into spermatozoa in male gonads". Dev Growth Differ. 39 (3): 267–71. doi:10.1046/j.1440-169X.1997.t01-2-00002.x. PMID 9227893. 
  3. ^ "Methods for Female Mammalian Spermatogenesis and Male Mammalian Oogenesis Using Synthetic Nanobiology" (PDF). Gregory Aharonian. http://www.samesexprocreation.com/document/femsperm.pdf. 
  4. ^ "Color illustration of female sperm making procress" (PDF). Human Samesex Reproduction Project. http://www.samesexprocreation.com/archive/sprmpict.pdf. 
  5. ^ "Scientists turn bone marrow into sperm". The Courier and Mail (Australia — Feb. 2008). http://www.news.com.au/story/0,23599,23139620-401,00.html. 
  6. ^ "Males Now Unneccesary — Women Create Their Own Sperm". Canada Free Press (Feb. 2008). http://canadafreepress.com/index.php/article/1692. 
  7. ^ chicagotribune.com --> Heartache of infertility shared on stage, screen By Colleen Mastony, Tribune reporter. June 21, 2009

 
 

 

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Dictionary. The American Heritage® Dictionary of the English Language, Fourth Edition Copyright © 2007, 2000 by Houghton Mifflin Company. Updated in 2009. Published by Houghton Mifflin Company. All rights reserved.  Read more
Sci-Tech Encyclopedia. McGraw-Hill Encyclopedia of Science and Technology. Copyright © 2005 by The McGraw-Hill Companies, Inc. All rights reserved.  Read more
World of the Body. The Oxford Companion to the Body. Copyright © 2001, 2003 by Oxford University Press. All rights reserved.  Read more
Genetics Encyclopedia. Genetics. Copyright © 2003 by The Gale Group, Inc. All rights reserved.  Read more
Wikipedia. This article is licensed under the Creative Commons Attribution/Share-Alike License. It uses material from the Wikipedia article "Reproductive technology" Read more