Mercury Concentration In Milk Research Articles

Mercury concentration in the milk of mothers living near the southern coast of the Caspian Sea during different stages of lactation period

The aim of this study was to determine mercury levels and changes during lactation in colostrum, transitional milk, and mature milk (1 month and 2 months post partum). The mercury mean concentration in milk samples collected from 18 women was 90 ± 20 and 100 ± 30 ng L−1 for colostrum and transitional milk, respectively. Also, mean concentration of 160 ± 70 and 140 ± 50 ng L−1 for mature milk 1 month and up to 2 months post partum were found. The concentration of mercury did not decline during the lactation period. Mercury daily intake was estimated when the infants were fed human milk only. The intakes ranged from 0.0 to 80 and from 0.0 to 70 ng kg−1 body weight day−1 for colostrum and transitional milk, respectively. For mature milk at the first month and up to 2 months the intakes were estimated from 1 to 200 and from 0.0 to 270 ng kg−1 body weight day−1. Significant difference was found between mothers without amalgam-filled teeth and mothers with one to five amalgam-filled teeth. Fruit and vegetable consumption showed negative correlation with the mercury concentration in human milk.

Effect of teeth amalgam on mercury levels in the colostrums human milk in Lenjan

Human milk is usually the only source of food for infants during the first 4 to 5months of their life. Maternal environmental mercury exposure is directly related to fish consumption or amalgam filling. In this research, 38 human milk samples were collected from mothers of Lenjan area who were not occupationally exposed with mercury. Mercury concentration in human milk was determined by AMA254 Mercury Analyzer. A level of mercury was examined in relation to somatometric, demographic and dental amalgam parameters. Obtained results showed that only dental amalgam significantly increased the mercury level in human milk (p < 0.001). The mean mercury concentrations in milk of mothers without teeth fillings (n = 13), with one to three teeth fillings (n = 10), and four to eight teeth fillings (n = 15) were 2.87, 5.47, and 13.33μg/l, respectively. The result of this study also showed a positive correlation of mercury milk levels with the number of teeth fillings of the mother (p < 0.05, r = 0.755). The estimated weekly intake of mercury of a breastfed infant in this study was, in some cases, higher than provisional tolerance weekly intake recommended by FAO/WHO, which pose a threat to their health.

Lactational Exposure and Neonatal Kinetics of Methylmercury and Inorganic Mercury in Mice

The concentration of mercury in milk and the distribution pattern in the sucking pup was followed over time after administration of a single iv injection of 0.5 mg/kg body wt of203Hg-labeled methylmercuric chloride or mercuric chloride to lactating mice on Day 10 of lactation. Mercury concentrations in milk of the dams and in whole body, blood, plasma, GI-tract, liver, kidneys, and brain of the offspring were followed up to 11 days after dosing (until lactational Day 21). Following the inorganic mercury dose to the dams, most of the mercury in milk was delivered to the pups during the first 24 h, but the maximum mercury concentration in plasma and tissues of pups was not reached until 7 days after dosing, indicating a prolonged absorption of inorganic mercury in the sucking pup. Pups of dams given methylmercury were exposed to a much lower and constant mercury concentration in milk. The estimated accumulated mercury dose via milk per pup of dams given methylmercury was less than half of that estimated after the inorganic mercury dose. When the accumulated dose via milk from methylmercury-exposed dams was compared to the amount of mercury in pup's carcass (whole body minus GI-tract including content), it was revealed that almost all mercury delivered via milk was absorbed, and that the suckling pups had a very low elimination of mercury until lactational Day 17. Lactational exposure following a maternal methylmercury or inorganic mercury dose resulted in almost similar mercury concentrations in liver, kidneys, and plasma of the suckling, but higher concentrations in brain (as most 14 times) and also twice as high mercury body burden in the methylmercury group. Thus, differences in kinetics indicate that lactational exposure of methylmercury is a greater hazard for the breast-fed infant than inorganic mercury.

Indices of mercury contamination during breast feeding in the Amazon Basin

Mercury pollution, due to gold mining has spread through the Amazon ecosystem reaching the food chain and affecting the indigenous people of the region. We studied the mercury contamination of 47 mothers and infants and the role of breast feeding in indices of mercury body burden in both groups, by measuring hair and milk Hg levels. Total mercury concentration of breast milk ranged from 0.0 to 24.8 (5.85, 5.2 S.D.) ng/g. Calculated levels of mercury exposure of breast fed babies indicated that 53% were above tolerable daily intakes (0.5 μg/kg body weight) recommended for adults by WHO. Mercury concentration in maternal hair was higher than in hair from breast-fed babies. Correlation analysis showed that mercury hair concentration in infants was significantly affected by maternal mercury contamination during pregnancy, but not during the post-natal breast-feeding period. The mercury concentration in milk was not significantly correlated with maternal or infant’s hair Hg. A statistically significant correlation was found only between maternal and infant’s hair mercury concentration ( r=0.675; P=0.0001).

Kinetics of Methylmercury and Inorganic Mercury in Lactating and Nonlactating Mice

The elimination of mercury was followed for 9 days (Days 10–19 of lactation) in milk and/or 21 days in blood and plasma of lactating and nonlactating mice administered a single iv injection of either203Hg-labeled methylmercuric chloride or203Hg-labeled mercuric chloride (0.5 mg Hg/kg body wt). Demethylation of methylmercury to inorganic mercury was taken into consideration by analyzing the data with a combined pharmacokinetic model based on the assumption of constant blood plasma ratios for methylmercury and inorganic mercury. A three-compartment model fitted the blood and plasma concentrations vs time profiles for both compounds. Plasma clearance and volume of distribution at steady state for methylmercury were 95.3 ml/h/kg and 18,500 ml/kg, respectively, in lactating mice, and significantly higher than in nonlactating mice with values of 47.1 ml/h/kg and 9400 ml/kg, respectively. The terminal half-lives of methylmercury in plasma were similar, 170 h in lactating and 158 h in nonlactating mice. No differences were observed between the pharmacokinetic parameters in lactating and nonlactating mice administered inorganic mercury. The lactational transfer of mercury was more efficient following administration of inorganic mercury than after administration of methylmercury, with a five times higher peak concentration in milk, higher milk:plasma concentration ratios, and 8% of the administered dose excreted in milk compared with 4% for methylmercury. Mercury concentrations in milk following an iv dose of inorganic mercury decreased with a terminal half-life of 107 h, whereas after administration of methylmercury, the concentration of total mercury in milk remained at an almost constant level during the whole period of investigation. There was a nonlinear relationship between mercury in milk and plasma following inorganic mercury administration. It is suggested that inorganic mercury enters the mammary gland by a carrier-mediated transport system, which is saturated at high plasma levels of inorganic mercury. The present study shows that physiological changes during lactation alter the pharmacokinetics for methylmercury in mice but not for inorganic mercury.

Milk transfer of inorganic mercury to suckling rats

The transport of mercury into rat milk, and uptake in the suckling offspring was studied after peroral administration of inorganic mercury to lactating control rats, and to rats fed selenite in the diet. On day 8, 9, 10, or 11 of lactation, dams were administered a single oral dose of 0.1, 0.4, 0.7, 1.3, or 5.8 mg Hg/kg bw labeled with 203mercuric acetate. There was a linear relationship between mercury concentrations in dam's plasma and milk. The level of mercury in milk was approximately 25% of the level in plasma. After 3 d, milk levels were reduced to half the levels at 24 h. In the suckling offspring, exposed to mercury via milk during 3 d, the mercury level in blood was approximately 1% of the level in maternal blood. Mercury concentration in milk was linearly correlated to the levels in kidney, liver, and brain in the suckling offspring after 3 d exposure to mercury via milk. Selenite treatment of rats, 1.3 micrograms Se/g diet for 5 mo, resulted in increased transport of mercury to milk, probably because of increased plasma levels of mercury. However, selenite treatment of the dams did not cause any increased tissue levels of mercury in the suckling offspring.