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Programming and Assisted Reproductive Technologies Modules 18 and 19

Programming and Assisted Reproductive Technologies Modules 18 and 19. AnS 536 Spring 2014. Fetal Programming. Hypothesis The developing fetus responds to nutritional and oxygen shortages by diverting resources from other organs to the brain Potential adverse affects may occur later in life

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Programming and Assisted Reproductive Technologies Modules 18 and 19

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  1. Programming and Assisted Reproductive TechnologiesModules 18 and 19 AnS 536 Spring 2014

  2. Fetal Programming • Hypothesis • The developing fetus responds to nutritional and oxygen shortages by diverting resources from other organs to the brain • Potential adverse affects may occur later in life • Adaptations include: • Vascular response • Metabolic response • Endocrine response

  3. Fetal Programming • Exogenous maternal malnutrition during pregnancy • May cause lifelong, persisting adaptation to the fetus • Low birth weight • ↑ Cardiovascular risk • Non-insulin dependent diabetes • Critical periods of vulnerability to suboptimal conditions during development • Vulnerable periods occur at different times for various tissues • Greatest risk: rapidly dividing cells

  4. Fetal Programming • ‘Fetal origins’ hypothesis • Poor in utero environment induced by maternal dietary or placental insufficiency may program susceptibility later in fetal development and life • ‘Thrifty phenotype hypothesis’ • If in utero nutrition is poor, then predictive adaptive responses are made by the fetus to maximize uptake and conservation of any nutrients available, resulting in a conservative metabolism • Problems occur when postnatal diet is adequate and plentiful and exceeds the range of predicted adaptive response

  5. Fetal Programming • Prevalent in developed and developing countries • Dutch famine (limited intake of 1680-3360 kJ) • During late gestation was associated with increased adult obesity and glucose intolerance • During early gestation resulted in hypertension • Disadvantageous populations in USA, South Africa, the Caribbean, India, and Australia • Shown cardiovascular risk to be greater in populations suffering from poor in utero nutrition

  6. Fetal Programming • Permanent affects of programming • Modifies susceptibility to disease • Structural changes to organs • Might pass across generations • Different effects on males and females • Placental effects • Fetus will attempt to compensate for womb deficiencies

  7. Metabolic Syndrome • Cluster of abnormalities occurring together, increase your risk of heart disease, stroke, and diabetes • Largely attributed to altered dietary and lifestyle factors favoring central obesity • Characterized by a group of metabolic risk factors in a person • Abdominal obesity • Atherogenic dyslipidemia • Elevated blood pressure • Insulin resistance • Proinflammatory states • Prothrombotic states

  8. Metabolic Syndrome • Abdominal obesity • Strongly associated with metabolic syndrome • Atherogenic dyslipidemia • ↑ triglycerides, ↓ concentrations of HDL cholesterol, ↑ remnant lipoproteins, ↑ apolipoprotein B, small LDL particles nad small HDL particles

  9. Metabolic Syndrome • Elevated blood pressure • Strongly associated with obesity • Commonly occurs in insulin-resistant individuals • Insulin resistance • Commonly associated with metabolic syndrome • Usually leads to glucose intolerance  diabetic-level hyperglycemia • Independent risk factor for cardiovascular disease

  10. Metabolic Syndrome • Proinflammatory states • ↑ levels of C-reactive protein • Excess adipose tissue release inflammatory cytokines • Multiple mechanisms contribute to inflammatory state • Prothrombotic states • ↑ Plasma plasminogen activator inhibitor-1 • ↑ fibrinogen • Rises in response to a high cytokine state • Acute phase reactant • Proinglammatory and prothrombotic states are interconnected

  11. Metabolic Syndrome • Underlying risk factors for this condition: • Abdominal obesity • Insulin resistance • Physical inactivity • Aging • Hormonal imbalance • Genetic predisposition • Fetal environment

  12. Non-genomic Intergenerational Effects • Significant evidence that programmed phenomena can be disturbed in later generations • Offspring exposed to a poor uterine environment • Prenatal programming by nutrition or exercise (animal models) • Postnatal programming by nutrition or handling (animal models) • Effects: • Birth weight • Glucose tolerance • Hypothalamic-pituitary axis in subsequent generations

  13. Non-genomic Intergenerational Effects • Effects on birth weight • Black and white hooded rats (Steward, 1975) • Continued poor maternal nutrition produced amplified effects on birth weight through a number of generations • Accidental introduction of less-palatable food in control animals resulted in a period of self-imposed calorie restriction • Evidence that poor nutrition in one generation can produce effects on birth weight in subsequent generations

  14. Non-genomic Intergenerational Effects • Effects on birth weight, cont… • First generation pups (Pinto and Shetty, 1995) • Exercise during pregnancy resulted in low birth weigh first generation pups • First generation offspring were sedentary during pregnancy and second generation offspring were also found to be growth retarded • Suggesting adverse intergenerational influence of maternal exercise stress on fetal growth

  15. Non-genomic Intergenerational Effects • Metabolic parameters and blood pressure • Female rabbits with surgically induced hypertension were mated with normotensive males • Female offspring had increased blood pressure as adults when compared to the offspring of sham-operated females • Blood pressure in male offspring was unaffected

  16. Non-genomic Intergenerational Effects • Postnatal effects • Second generational alterations on glucose homeostasis has been seen when overfeeding takes place in the neonatal period • In rodents, naturally occurring variations in maternal behavior is associated with different hypothalamic-pituitary-adrenal stress responsiveness in offspring • Postnatal environmental manipulations to the hypothalamic-pituitary-adrenal axis stress response may produce intergenerational effects

  17. Assisted Reproductive Technologies (ART) • Artificial insemination (AI) • Sexed semen and embryo sexing • Embryo transfer (ET) • In vitro fertilization (IVF) • Intracytoplasmic sperm injection (ICSI) • Gamete intrafallopian transfer (GIFT) • Zygote intrafallopian transfer (ZIFT) • Donor egg, sperm or embryo • Cloning (SCNT)

  18. Artificial Insemination (AI) • Used commonly in livestock • Method of banking semen (genetics) without keeping a sire on site (cryopreservation) • Challenges • Difficulty passing AI gun through cervix • Potentially reduced pregnancy rates • Breeding when animal is in estrus • Damage to reproductive tract • Reduced fertility with cryopreserved sperm

  19. Artificial Insemination (AI) • Management approaches • Goal is to increase conception rates • Implementing appropriate methods of heat detection • Skilled technician in AI • Time of year, time of day, or temperature on day of breeding can affect conception rates

  20. Sexed semen and embryo sexing • Biological mechanism • Sexed semen uses flow cytometry to sort genetically male and female sperm • Female (XY) sperm have 4% more DNA than male sperm • Embryo sexing entails obtaining a biopsy of the inner cellular mass (ICM) of the embryo to determine male or female status • Used in livestock industry (dairy cattle) • Ethical considerations in humans

  21. Sexed semen and embryo sexing • Challenges • Sexed semen • Reduced fertility • Higher concentration of sperm needed to ensure pregnancy • Embryo sexing • Reduced viability of embryo • Multiple pregnancies can occur

  22. Sexed semen and embryo sexing Management approaches • Sexed semen is preferred method, less risk to developing embryo • Less invasive • Sexed semen is used in combination with IVF technologies or AI • Embryo sexing require embryo transfer technique

  23. In vitro fertilization (IVF) • Commonly used practice in humans and livestock (cattle) • Biological mechanisms • Dam is administered a series of reproductive hormone (GnRH) to stimulate the development of Graafian follicles, a.k.a., superovulation • Oocytes are collected via aspiration and are incubated in an artificial lab environment, mimicking the environment of the uterus • Sperm is introduced to the oocytes and fertilization occurs • Embryos are developed to the blastocyst stage prior to transfer to the mother or dam

  24. In vitro fertilization (IVF) • Challenges • Patients or recipients using IVF technology usually face moderate to severe infertility problems • Poor quality ovum or sperm • Uterine rejection • May be used as a ‘last ditch effort’ for pregnancy • Incidence of multiple births are high • Ectopic pregnancies

  25. In vitro fertilization (IVF) • Management approaches • Age of the patient • Inversely related to the probability of multiple pregnancies and overall pregnancy success • Implantation rate • Attributed to many factors including quality of embryo • Selecting embryos with the greatest potential for survival • Matching synchrony of uterus to embryo stage of development • Number of embryos transferred • Directly related to risk of multiple pregnancies • Most controllable of the variables

  26. Embryo transfer (ET) • Biological mechanisms (in livestock) • A donor animal is super ovulated, bred by a sire (AI or live cover) • Fertilization occurs in vivo and embryos are collected prior to the implantation stage • Collected embryos can be then be transferred to a recipient (surrogate) animal with the same estrus synchrony as the donor or can be cryopreserved for a later implantation date

  27. Embryo transfer (ET) • Challenges • Reduced rate of pregnancy as compared to natural conception • Fresh embryos have better conception rate as compared to cryopreserved embryos • Synchronizing recipient animals with the donor animal • Retained embryos in donor animal resulting in pregnancy

  28. Embryo transfer (ET) • Management approaches • Optimizing synchrony for maximum pregnancy rates • Selecting appropriate recipients for breed and birth weight of offspring • Use of prostaglandin in donor animals to eliminate pregnancy due to retained embryo

  29. Intracytoplasmic sperm injection (ICSI) • Biological Mechanism • A single sperm is injected into unfertilized oocyte and is transferred to a recipient • Treatment for male factor infertility • Challenges • Potentially abnormal sperm can fertilize ova • Long term health affects, including genetic abnormalities • Lower birth weight • Abnormalities on the Y chromosome • Greater potential for developmental delays

  30. Intracytoplasmic sperm injection (ICSI) Management approaches • Men and women should have genetic screening for potential chromosomal abnormalities prior to fertility treatment • Men lacking a vas deferens can carry mutations increasing the risk of offspring with cystic fibrosis

  31. Gamete Intrafallopian transfer (GIFT) • Biological mechanisms • An unfertilized oocyte and sperm are combined outside of the uterus and are surgically transferred to the site of normal fertilization in the fallopian tube via laparoscopic technique • Fertilization occurs in vivo • Implantation occurs naturally

  32. Gamete Intrafallopian transfer (GIFT) • Challenges • Surgical intervention causes trauma and scarring • More invasive technique • Multiple pregnancies • Management approaches • Other techniques are more widely used (IVF) due to higher success rates

  33. Zygote intrafallopian transfer (ZIFT) • Biological mechanisms • Similar to GIFT however, oocyte and sperm are combined outside of the uterus and are not transferred until an embryo is produced • Management approaches • Other techniques are more widely used (IVF) due to higher success rates

  34. Donor ova, sperm or embryo • Donor oocyte, sperm or embryos can be used to generate offspring if poor quality ova or sperm exist or if there is a lack of a female or male counterpart • Challenges • Social implications • Lack of genetic history • Predisposition to risk of disease • Children may never know their parents

  35. Cloning (SCNT) • Producing genetically identical copies of a biological entity • Different types of methods: • Reproductive • Natural identical twinning • Somatic cell nuclear transfer (SCNT) • Non-reproductive • Recombinant DNA Technology • Therapeutic cloning

  36. Cloning (SCNT) • Challenges • Low conception rates • Increased birth weights • Increased incidence of genetic abnormalities • Decreased neonatal survival • Increased placentation abnormalities • Decreased life span of animal?? • Increased dystocia and prolonged gestation • Decreased genetic variation

  37. Cloning (SCNT) • Biological mechanisms • Low conception rates • Research is being done to explore this reality • Current methods of cloning are very artificial and vastly differ from normal in vivo embryo development • Methods to promote a more similar environment to what the embryo experiences in vivo • Increased birth weights • Possible link to media used in incubating cloned embryos • Fetal calf serum (FCS) promotes excessive growth of embryo

  38. Cloning (SCNT) • Biological mechanisms, cont… • Increased incidence of genetic abnormalities • Possible link to problems in cell reprogramming with SCNT • Electric charge fuses cells to promote cell proliferation • Decreased neonatal survival • Offspring can be less vigorous initially after birth • Anemia, enlarged organs, metabolic disturbances, problems thermoregulating, hypoxia can all contribute

  39. Cloning (SCNT) • Biological mechanisms, cont… • Increased placentation abnormalities • Mechanisms unknown • Hydrops amnion is a condition that is seen during gestation in cattle and sheep • Less frequent attachment sites but increased size of codyledons as compared to normal pregnancies in cattle • Intrauterine Growth Restriction (IUGR) • Decreased life span of animal ?? • “Dolly” the sheep only lived to 6 years of age • Controversial studies that cloning affects life span of offspring • Decreased telomere length has been associated with a decreased life span • Age of animal being cloned may affect life span of offspring (increased age shortens telomere length)

  40. Cloning (SCNT) • Biological mechanisms, cont… • Increased dystocia and prolonged gestation • Recipient animals carrying cloned animals fail to recognize the onset of parturition near term or the cloned fetus fails to induce parturition • Increased birth weights contribute to dystocia • Decreased genetic variation • Selection of cloned animal can potentially promote a genetically inferior or superior animal • Breeding pool can be narrowed • Long term effects?

  41. Cloning (SCNT) • Management approaches • Low conception rates • Matching synchrony of recipient animal with stage of embryo • Increased birth weights • Selecting larger framed, multi-parous recipient animals • Awareness of breed of embryo and potential birth weight • Caesarian section deliveries

  42. Cloning (SCNT) • Management approaches, cont… • Increased incidence of genetic abnormalities • Humane euthanasia or abortion in severe cases • Preventing the perpetuation of genetically inferior animals through selection • Decreased neonatal survival • Intensive care and monitoring of animal first week of life • Ensuring colostrum uptake • Temperature regulation

  43. Cloning (SCNT) • Management approaches, cont… • Increased placentation abnormalities • Close monitoring of recipient animals for hydrops amnion • Abort early in gestation if necessary • Pregnancy palpations/ultrasound to determine fetal well being • Decreased life span of animal ?? • Age of animal being cloned may affect life span of offspring (increased age shortens telomere length)

  44. Cloning (SCNT) • Management approaches, cont… • Increased dystocia and prolonged gestation • Know expected parturition dates • Induce parturition if necessary • Caesarian sections • Decreased genetic variation • Criteria for animal selection • Promoting healthy animals – not just based on phenotype

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