Maternal ethanol exposure is associated with decreased plasma zinc and increased fetal abnormalities in normal but not metallothionein-null mice
dc.contributor.author | Carey, L. | |
dc.contributor.author | Coyle, P. | |
dc.contributor.author | Philcox, J. | |
dc.contributor.author | Rofe, A. | |
dc.date.issued | 2000 | |
dc.description.abstract | <h4>Background</h4>Ethanol profoundly affects fetal development, and this is proposed to be due primarily to a transient fetal zinc (Zn) deficiency that arises from the binding of Zn by metallothionein (MT) in the maternal liver. Zn homeostasis and fetal outcome were investigated in normal (MT+/+) and metallothionein-null (MT-/-) mice in response to ethanol exposure.<h4>Methods/results</h4>Mice were treated with saline or ethanol (0.015 m/g intraperitoneally at 0 and 4 hr) on day 8 of gestation (Gd8), and the degree of fetal dysmorphology was assessed on Gd18. The incidence of external abnormalities was significantly increased in offspring from MT+/+ dams exposed to ethanol, where 27.4% of fetuses were affected. MT-/- ethanol-, MT+/+ saline-, and MT-/- saline-treated dams had fetuses in which the frequencies of abnormalities were 2.2, 6.4, and 6.9%, respectively. To investigate Zn homeostasis, nonpregnant mice were killed at intervals over 16 hr after ethanol injection. Liver MT concentrations in MT+/+ mice were increased 20-fold by 16 hr, with a significant elevation evident by 4 hr, whereas liver Zn levels were also significantly increased by 2 hr and maintained for 16 hr. In parallel with these changes, plasma Zn concentrations in MT+/+ mice decreased by 65%, with minimum levels of 4.5+/-0.3 micromol/liter at 8 hr. Conversely, MT-/- mice exhibited increased plasma Zn concentrations, with peak values of 20.8+/-0.3 observed at 4 hr.<h4>Conclusion</h4>These findings link the teratogenic effect of ethanol to the induction of maternal MT and the limitation of fetal Zn supply from the plasma. | |
dc.description.statementofresponsibility | Carey, Luke C. ; Coyle, Peter ; Philcox, Jeffrey C. ; Rofe, Allan M. | |
dc.identifier.citation | Alcoholism: Clinical and Experimental Research, 2000; 24(2):213-219 | |
dc.identifier.doi | 10.1111/j.1530-0277.2000.tb04593.x | |
dc.identifier.issn | 0145-6008 | |
dc.identifier.issn | 1530-0277 | |
dc.identifier.uri | http://hdl.handle.net/2440/11696 | |
dc.language.iso | en | |
dc.publisher | Lippincott Williams & Wilkins | |
dc.source.uri | https://doi.org/10.1111/j.1530-0277.2000.tb04593.x | |
dc.subject | Liver | |
dc.subject | Fetus | |
dc.subject | Animals | |
dc.subject | Mice, Inbred C57BL | |
dc.subject | Mice | |
dc.subject | Prenatal Exposure Delayed Effects | |
dc.subject | Zinc | |
dc.subject | Ethanol | |
dc.subject | Metallothionein | |
dc.subject | Central Nervous System Depressants | |
dc.subject | Pregnancy | |
dc.subject | Female | |
dc.subject | Male | |
dc.title | Maternal ethanol exposure is associated with decreased plasma zinc and increased fetal abnormalities in normal but not metallothionein-null mice | |
dc.type | Journal article | |
pubs.publication-status | Published |