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Fetuses

Cortisol-Cortisone Conversion. Under normal conditions, this equilibrium slightly favors the oxidized compound. Similarly, the conversion of corticosterone to 11-deoxycorticosterone is also mediated by the liP-hydroxysteroid dehydrogenase enzyme system and requites NAD(P) /NAD(P)H. This conversion is especially important both in the protection of the human fetus from excessive glucocorticoid exposure, and in the protection of distal nephron mineral ocorticoid receptors from glucocorticoid exposure (14). The impairment of this conversion is thought to result in hypertension associated with renal insufficiency (15). [Pg.97]

Exposure to excessive amounts of lead over a long period of time (chronic exposure) increases the risk of developing certain diseases. The parts of the body which may be affected include the blood, nervous system, digestive system, reproductive system, and kidneys. These effects include anemia, muscular weakness, kidney damage, and reproductive effects, such as reduced fertiHty in both men and women, and damage to the fetus of exposed pregnant women. [Pg.52]

The alimentary symptoms may be overshadowed by neuromuscular dysfunction, accompanied by signs of motor weakness that may progress to paralysis of the exterior muscles or the wrist (wrist drop), and less often, of the ankles (foot drop). Encephalopathy, the most serious result of lead poisoning, frequendy occurs in children as a result of pica, ie, ingestion of inorganic lead compounds in paint chips this rarely occurs in adults. Nephropathy has also been associated with chronic lead poisoning (147). The toxic effects of lead may be most pronounced on the developing fetus. Consequendy, women must be particulady cautious of lead exposure (148). The U.S. Center for Disease Control recommends a blood level of less than 10 p.m per 100 mL for children. [Pg.73]

Lead is known to cause reproductive and developmental toxicity. Decreased sperm counts and abnormal sperm development have been reported in male workers heavily exposed to lead. Increased incidences of spontaneous abortion have been reported in female lead workers as well as in the wives of male lead workers (13). Lead crosses the placenta and has been found to cause irreversible neurologic impairment to the fetus at maternal blood levels as... [Pg.78]

Specific barriers may serve to limit dmg distribution. The placental barrier is of obvious importance to dmg action in the fetus. Dmg transfers across the placenta primarily by Hpid solubiHty. Hence, this barrier is not particularly restrictive. Similarly, the Hpid solubiHty of a dmg is a primary deterrninant in access to the brain and cerebrospinal fluid. Generally, hydrophilic or charged dmgs can also penetrate to these latter areas, but the result is slow and incomplete. The blood brain barrier is composed of cells having tight junctions which are much less permeable to solutes than are the endotheHal cells of other tissues. [Pg.269]

Myxedema and goiter are the main conditions for which thyroid preparations are indicated. The treatment of cretinism is difficult because it is recognized only at or after birth. Even if this disease could be diagnosed m utero, thyroid hormones do not readily cross the placental barrier. In addition, the fetus, as does a premature infant, rapidly deactivates the thyroid hormones. The halogen-free analogue DlMlT [26384-44-7] (3), which is resistant to fetal deiodinases, may prove useful for fetal hypothyroidism (cretinism). [Pg.47]

Recently, there has been increasing interest in the development of test methods to assess the possible adverse functional effects of exposing the fetus, both early and late in gestation (112,113). [Pg.237]

No teratogenic effects were observed in mice and rats exposed to vapor concentrations of 300 ppm. Exposure levels having no effect on the mother are not anticipated to affect the fetus (36). [Pg.30]

F. Reproductive toxins Chemicals which affect the reproductive capabilities including chromosomal damage (mutations) and effects on fetuses (teratogenesis) ... [Pg.182]

The effects of a teratogen on a fetus depend on the timing of the exposure, i.e., at which stage of organogenesis the exposure takes place. Exposure to a teratogen before implantation usually leads to death and abortion of the fetus. How-... [Pg.312]

In addition to direct effects of chemical compounds on the fetus, metabolic disturbances in the mother, such as diabetes or hyperthermia, or deficiencies of calories or specific nutrients such as vitamin A, zinc, and folic acid may lead to teratogenesis. Compounds that inhibit placental functions may also induce malformations, e.g., by inhibiting placental circulation. For example, hydroxyurea disrupts the placental circulation and induces malformations. In addition, it also induces DNA damage. [Pg.313]


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Androgenized fetuses

Anemia fetus

Caffeine fetus effects

Campylobacter fetus

Chemoreceptor Responses in the Fetus

Chlorambucil effects on fetus

Dead fetus

Developing fetus

Drugs effects on fetus

Embryos and fetuses

Embryos/fetuses

Fetus Blastocyst

Fetus Decidua

Fetus Oxygen consumption

Fetus Protein synthesis

Fetus Trophoblast

Fetus and

Fetus anomalies

Fetus biochemical measurements

Fetus control

Fetus death

Fetus deiodination

Fetus development

Fetus female

Fetus folic acid deficiency

Fetus functional

Fetus health assessment

Fetus hypothyroidism

Fetus iodine deficiency

Fetus lung development

Fetus lung maturation

Fetus maternal adaptation

Fetus maternal thyroid hormones

Fetus neural tube defects

Fetus protein requirements

Fetus reference data

Fetus restriction

Fetus synthase

Fetus teratogenesis

Fetus, effects

Fetus, steroid conjugation

Fetuses and newborns

Glucose Fetus

Hamster fetus

Harlequin fetus

Human fetus

Immunity Fetus

In fetus

Lactic Fetus

Male fetuses

Malnutrition Fetus

Methimazole effects on fetus

Methylmercury fetus

Passage of Potentially Noxious Substances into the Fetus and Infant

Penicillamine effects on fetus

Phantom fetus

Proteins Fetus

Reproductive toxic effects fetus

Research fetuses

Retained fetus syndrome

Stillborn fetuse

Teratogenic human fetus

Transport from mother to fetus

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