1973
DOI: 10.3181/00379727-142-37102
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Mammary Transfer of 203Hg from Mothers to Brains of Nursing Rats

Abstract: The major routes of excretion of mercury by animals thus far studied are the kidney and gastrointestinal tract. However, lungs and mammary glands have also been known to excrete mercury (1). The mammary gland has been reported to contain radioactivity when mice were intravenously injected with 203HgC12 (2). Women (3, 4), guinea pigs2 and rats (5-7) have also been reported to secrete milk containing mercury. To our knowledge, studies to determine the quantitative transfer of mercury from lactating mothers to th… Show more

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Cited by 15 publications
(2 citation statements)
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“…The bioaccumulation of methylmercury (MeHg) in marine life, particularly tuna, presents a threat for developing fetuses whose mothers frequently eat this fish during their pregnancies, particularly because it is thought that mercury accumulates more readily in the fetal brain than in the maternal brain, interrupting patterns of cell fate, proliferation, migration, and neural outgrowth [36-38]. Because young children cannot metabolize mercury at the same rates as adults, exposure through either maternal or childhood consumption is of great concern.…”
Section: Discussionmentioning
confidence: 99%
“…The bioaccumulation of methylmercury (MeHg) in marine life, particularly tuna, presents a threat for developing fetuses whose mothers frequently eat this fish during their pregnancies, particularly because it is thought that mercury accumulates more readily in the fetal brain than in the maternal brain, interrupting patterns of cell fate, proliferation, migration, and neural outgrowth [36-38]. Because young children cannot metabolize mercury at the same rates as adults, exposure through either maternal or childhood consumption is of great concern.…”
Section: Discussionmentioning
confidence: 99%
“…In general, MeHg levels in the fetus exceed maternal levels, reflecting an incomplete blood–brain barrier and lack of MeHg excretion in the fetus [40]. The most significant difference in organ retention (neonates > adults) is associated with MeHg brain concentrations [41, 42]. The developing fetus is five to ten times more sensitive to MeHg than the adult [43] due, in part, to the high sensitivity of developmental processes (i.e., cellular division, differentiation, and migration) to disruption by MeHg [4445], as well as increased MeHg concentrations in fetal brains (referred to as a “sink” for MeHg).…”
Section: Methylmercury and Its Inhibitory Effects On Neurodevelopmentmentioning
confidence: 99%