Perinatal lead (Pb) exposure results in sex-specific effects on food intake, fat, weight, and insulin response across the murine life-course

PLoS ONE

Volumn 9, Issue 8, 2014, Pages

  Faulk, Christopher ^a   Barks, Amanda ^a   Sánchez, Brisa N ^a   Zhang, Zhenzhen ^a   Anderson, Olivia S ^a   Peterson, Karen E ^a,b,c   Dolinoy, Dana C ^a  

^a UNIVERSITY OF MICHIGAN SCHOOL OF PUBLIC HEALTH   (United States)

^b UNIVERSITY OF MICHIGAN   (United States)

^c HARVARD SCHOOL OF PUBLIC HEALTH   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

INSULIN; LEAD ACETATE; GLUCOSE BLOOD LEVEL; LEAD;

AGE DISTRIBUTION; ANIMAL EXPERIMENT; ARTICLE; BODY COMPOSITION; BODY FAT; BODY WEIGHT; CONTROLLED STUDY; ENERGY EXPENDITURE; ENVIRONMENTAL EXPOSURE; FEMALE; FOOD INTAKE; GLUCOSE TOLERANCE; INSULIN RESPONSE; LEAD BLOOD LEVEL; MALE; MOUSE; NONHUMAN; PERINATAL PERIOD; PHYSICAL ACTIVITY; SEX DIFFERENCE; WEIGHT GAIN; ADVERSE EFFECTS; AGE; ANIMAL; AREA UNDER THE CURVE; CHEMISTRY; DOSE RESPONSE; DRUG EFFECTS; EATING; ENERGY METABOLISM; GLUCOSE BLOOD LEVEL; GLUCOSE TOLERANCE TEST; MILK; PATHOPHYSIOLOGY; PHENOTYPE; PREGNANCY; PRENATAL EXPOSURE; STATISTICAL MODEL;

AGE FACTORS; ANIMALS; AREA UNDER CURVE; BLOOD GLUCOSE; BODY COMPOSITION; BODY WEIGHT; DOSE-RESPONSE RELATIONSHIP, DRUG; EATING; ENERGY METABOLISM; FEMALE; GLUCOSE TOLERANCE TEST; LEAD; LINEAR MODELS; MALE; MATERNAL EXPOSURE; MICE; MILK; PHENOTYPE; PREGNANCY; PRENATAL EXPOSURE DELAYED EFFECTS; SEX FACTORS;

EID: 84905659626     PISSN: None     EISSN: 19326203     Source Type: Journal    
DOI: 10.1371/journal.pone.0104273     Document Type: Article

References (44)

1. Barker DJP (2004) The developmental origins of adult disease. Journal of the American College of Nutrition 23: 588S-595S.
2. Bateson P, Barker D, Clutton-Brock T, Deb D, D'Udine B, et al. (2004) Developmental plasticity and human health. Nature 430: 419-421. (Pubitemid 38987896)
3. Little BB, Spalding S, Walsh B, Keyes DC, Wainer J, et al. (2009) Blood lead levels and growth status among African-American and Hispanic children in Dallas, Texas-1980 and 2002: Dallas Lead Project II. Ann Hum Biol 36: 331-341.
4. Gonzalez-Cossio T, Peterson KE, Sanin LH, Fishbein E, Palazuelos E, et al. (1997) Decrease in birth weight in relation to maternal bone-lead burden. Pediatrics 100: 856-862. (Pubitemid 27463323)
5. Hernandez-Avila M, Peterson KE, Gonzalez-Cossio T, Sanin LH, Aro A, et al. (2002) Effect of maternal bone lead on length and head circumference of newborns and 1-month-old infants. Archives of environmental health 57: 482-488. (Pubitemid 36278192)
6. Afeiche M, Peterson KE, Sánchez BN, Cantonwine D, Lamadrid-Figueroa H, et al. (2011) Prenatal lead exposure and weight of 0- to 5-year-old children in Mexico city. Environ Health Perspect 119: 1436-1441.
7. Gollenberg AL, Hediger ML, Lee PA, Himes JH, Louis GM (2010) Association between lead and cadmium and reproductive hormones in peripubertal U.S. girls. Environ Health Perspect 118: 1782-1787.
8. Iavicoli I, Carelli G, Stanek EJ, Castellino N, Calabrese EJ (2004) Effects of low doses of dietary lead on puberty onset in female mice. Reprod Toxicol 19: 35-41. (Pubitemid 39164875)
9. Leasure JL, Giddabasappa A, Chaney S, Johnson JE, Jr., Pothakos K, et al. (2008) Low-level human equivalent gestational lead exposure produces sex-specific motor and coordination abnormalities and late-onset obesity in year-old mice. Environ Health Perspect 116: 355-361. (Pubitemid 351395604)
10. Kim R, Hu H, Rotnitzky A, Bellinger D, Needleman H (1995) A longitudinal study of chronic lead exposure and physical growth in Boston children. Environ Health Perspect 103: 952-957.
11. Padilla MA, Elobeid M, Ruden DM, Allison DB (2010) An examination of the association of selected toxic metals with total and central obesity indices: NHANES 99-02. International journal of environmental research and public health 7: 3332-3347.
12. Snyder JE, Filipov NM, Parsons PJ, Lawrence DA (2000) The efficiency of maternal transfer of lead and its influence on plasma IgE and splenic cellularity of mice. Tox Sci 57: 87-94.
13. Gulson BL, Mizon KJ, Korsch MJ, Palmer JM, Donnelly JB (2003) Mobilization of lead from human bone tissue during pregnancy and lactation - a summary of long-term research. Sci Total Enivron 303: 79-104. (Pubitemid 36144009)
14. Stewart PW, Delbagno V, Ng J, Burright R, Donovick P (1998) Subacute Pb exposure during development and unbaited tunnel maze performance in mice. Pharmacol Biochem Behav 59: 183-189. (Pubitemid 28053697)
15. Afeiche M, Peterson KE, Sánchez BN, Schnaas L, Cantonwine D, et al. (2012) Windows of lead exposure sensitivity, attained height, and body mass index at 48 months. J Pediatr 160: 1044-1049.
16. Meyer PA, Brown MJ, Falk H (2008) Global approach to reducing lead exposure and poisoning. Mutat Res 659: 166-175.
17. Jacobs DE, Clickner RP, Zhou JY, Viet SM, Marker DA, et al. (2002) The prevalence of lead-based paint hazards in U.S. housing. Environ Health Perspect 110: A599-606. (Pubitemid 35175051)
18. Muntner P, Menke A, DeSalvo KB, Rabito FA, Batuman V (2005) Continued decline in blood lead levels among adults in the United States: the National Health and Nutrition Examination Surveys. Arch Intern Med 165: 2155-2161. (Pubitemid 41434593)
19. Bridbord K, Hanson D (2009) A personal perspective on the initial federal health-based regulation to remove lead from gasoline. Environ Health Perspect 117: 1195-1201.
20. Gilbert SG, Weiss B (2006) A rationale for lowering the blood lead action level from 10 to 2 microg/dL. Neurotoxicology 27: 693-701. (Pubitemid 44232997)
21. Betts KS (2012) CDC updates guidelines for children's lead exposure. Environ Health Perspect 120: a268.
22. Waterland RA, Jirtle RL (2003) Transposable elements: targets for early nutritional effects on epigenetic gene regulation. Molecular and cellular biology 23: 5293-5300. (Pubitemid 36950884)
23. Weinhouse C, Anderson OS, Bergin IL, Vandenbergh DJ, Gyekis JP, et al. (2014) Dose-Dependent Incidence of Hepatic Tumors in Adult Mice following Perinatal Exposure to Bisphenol A. Environ Health Perspect.
24. Research IfLA (1966) Guide for the Care and Use of Laboratory Animals. Washington, DC: National Academy Press.
25. Morgan HD, Sutherland HG, Martin DI, Whitelaw E (1999) Epigenetic inheritance at the agouti locus in the mouse. Nat Genet 23: 314-318. (Pubitemid 29526429)
26. Anderson OS, Peterson KE, Sanchez BN, Zhang Z, Mancuso P, et al. (2013) Perinatal bisphenol A exposure promotes hyperactivity, lean body composition, and hormonal responses across the murine life course. FASEB journal 27: 1784-1792.
27. Pinn VW, Clayton JA, Begg L, Sass SE (2010) Public partnerships for a vision for women's health research in 2020. J Womens Health (Larchmt) 19: 1603-1607.
28. Turner RC, Holman RR, Matthews D, Hockaday TD, Peto J (1979) Insulin deficiency and insulin resistance interaction in diabetes: estimation of their relative contribution by feedback analysis from basal plasma insulin and glucose concentrations. Metabolism 28: 1086-1096. (Pubitemid 10191950)
29. Faulk C, Barks A, Liu K, Goodrich JM, Dolinoy DC (2013) Early-life lead exposure results in dose- and sex-specific effects on weight and epigenetic gene regulation in weanling mice. Epigenomics 5: 487-500.
30. Cederroth CR, Vinciguerra M, Kühne F, Madani R, Doerge DR, et al. (2007) A phytoestrogen-rich diet increases energy expenditure and decreases adiposity in mice. Environ Health Perspect 115: 1467-1473. (Pubitemid 47618089)
31. Li G, Kohorst JJ, Zhang W, Laritsky E, Kunde-Ramamoorthy G, et al. (2013) Early Postnatal Nutrition Determines Adult Physical Activity and Energy Expenditure in Female Mice. Diabetes.
32. Goodell S, Cortopassi G (1998) Analysis of oxygen consumption and mitochondrial permeability with age in mice. Mechanisms of ageing and development 101: 245-256. (Pubitemid 28209729)
33. Iavicoli I, Carelli G, Stanek EJ, Castellino N, Li Z, et al. (2006) Low doses of dietary lead are associated with a profound reduction in the time to the onset of puberty in female mice. Reprod Toxicol 22: 586-590. (Pubitemid 44548313)
34. Zhang A, Hu H, Sanchez BN, Ettinger AS, Park SK, et al. (2012) Association between prenatal lead exposure and blood pressure in children. Environ Health Perspect 120: 445-450.
35. Struzynska L, Dabrowska-Bouta B, Rafalowska U (1997) Acute lead toxicity and energy metabolism in rat brain synaptosomes. Acta neurobiologiae experimentalis 57: 275-281. (Pubitemid 28046679)
36. Flora G, Gupta D, Tiwari A (2012) Toxicity of lead: A review with recent updates. Interdisciplinary toxicology 5: 47-58.
37. Haider S, Saleem S, Tabassum S, Khaliq S, Shamim S, et al. (2013) Alteration in plasma corticosterone levels following long term oral administration of lead produces depression like symptoms in rats. Metabolic brain disease 28: 85-92.
38. Hu H, Rabinowitz M, Smith D (1998) Bone lead as a biological marker in epidemiologic studies of chronic toxicity: conceptual paradigms. Environ Health Perspect 106: 1-8. (Pubitemid 28122010)
39. Huzior-Balajewicz A, Pietrzyk JJ, Schlegel-Zawadzka M, Piatkowska E, Zachwieja Z (2001) The influence of lead and cadmium environmental pollution on anthropometric health factors in children. Przeglad lekarski 58: 315-324.
40. Ronco AM, Gutierrez Y, Gras N, Munoz L, Salazar G, et al. (2010) Lead and arsenic levels in women with different body mass composition. Biological trace element research 136: 269-278.
41. Guo J, Jou W, Gavrilova O, Hall KD (2009) Persistent diet-induced obesity in male C57BL/6 mice resulting from temporary obesigenic diets. PLoS ONE 4: e5370.
42. Bostrom P, Wu J, Jedrychowski MP, Korde A, Ye L, et al. (2012) A PGC1-alpha-dependent myokine that drives brown-fat-like development of white fat and thermogenesis. Nature 481: 463-468.
43. Bihaqi SW, Huang H, Wu J, Zawia NH (2011) Infant exposure to lead (Pb) and epigenetic modifications in the aging primate brain: implications for Alzheimer's disease. Journal of Alzheimer's disease: JAD 27: 819-833.
44. Schneider JS, Kidd SK, Anderson DW (2013) Influence of developmental lead exposure on expression of DNA methyltransferases and methyl cytosine-binding proteins in hippocampus. Toxicology letters 217: 75-81.