Skip to main content
Log in

Preferential effect of lead exposure during lactation on non-essential fatty acids in maternal organs

  • Articles
  • Published:
Lipids

Abstract

This study determined the effects of lead exposure during the lactational period on maternal organ FA compositions in rat dams that were fed either an n−3 adequate (n−3 Adq) or deficient (n−3 Def) diet prior to conception. On giving birth, dams were subdivided into four groups in a 2×2 design with n−3 FA supply and Pb exposure as the dependent variables. Pb acetate (0.2 wt%) was administered in the drinking water from the time they gave birth to weaning 3 wk later. Following weaning, the dams were decapitated. and the liver, plasma, kidney, brain, and retina analyzed for FA composition. The n−3 deficient diets markedly decreased the percentages of total n−3 FA, including docosahexaenoic acid (DHA), and increased total n−6 FA including both arachidonic (AA) and n−6 docosapentaenoic acids in all tissues (P<0.05). The principal effects of Pb occurred in the liver and plasma, where 20–32% losses in total FA concentration concurrent with increased relative percentages of AA (P<0.05) were observed. In kidney, the percentages of AA and DHA also increased after Pb exposure (P<0.05) with lesser effects in the nervous system. There was a diet x Pb interaction for liver, plasma, and retinal 20-C n−6 PUFA (P<0.05). Generally, shorter-chain saturated and monounsaturated FA concentrations were decreased after Pb exposure. An analysis of the changes in the tissue concentrations induced by Pb indicated that the increases in the percentages of PUFA likely reflected a preferential loss of non-EFA. The mechanisms by which Pb affects saturated and monounsaturated FA concentration are unknown.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

Abbreviations

AA:

arachidonic acid, 20∶4n−6

DGLA:

dihomo-γ-linolenic acid, 20∶3n−6

DHA:

docosahexaenoic acid, 22∶6n−3

DMA:

dimethyl acetal derivative

DPAn−3:

n−3 docosapentaenoic acid, 22∶5n−3

DPAn−6:

n−6 docosapentaenoic acid, 22∶5n−6

DTA:

docosatetraenoic acid, 22∶4n−6

EFA:

essential fatty acid

EPA:

eicosapentaenoic acid, 20∶5n−3

FA:

fatty acid

GLA:

γ-linolenic acid, 18∶3n−6

LA:

linoleic acid, 18∶2n−6

LNA:

α-linolenic acid, 18∶3n−3

n−3 Adq-Na:

n−3 adequate and Na control group

n−3 Adq-Pb:

n−3 adequate and Pb exposure group

n−3 Def-Na:

n−3 deficient and Na control group

n−3 Def-Pb:

n−3 deficient and Pb exposure group

NIAAA:

National Institute on Alcohol Abuse and Alcoholism

NIH:

National Institutes of Health

References

  1. Lim, S.-Y., Doherty, J., McBride, K., Miller-Ihli, N., Carmona, G., Stark, K., and Salem, N., Jr. (2005) Lead Exposure and (n−3) Fatty Acid Deficiency During Neonatal Development Affect Subsequent Spatial Task Performance and Olfactory Discrimination, J. Nutr. 135, 1019–1026.

    PubMed  CAS  Google Scholar 

  2. Bernard, S.M., and McGeehin, M.A. (2003) Prevalence of Blood Lead Levels > or =5 μg/dL Among US Children 1 to 5 Years of Age and Socioeconomic and Demographic Factors Associated with Blood Levels 5 to 10 μg/dL, Third National Health and Nutrition Examination Survey, 1988–1994, Pediatrics 112, 1308–1313.

    Article  PubMed  Google Scholar 

  3. Lewis, N.M., Widga, A.C., Buck, J.S., and Frederick, A.M. (1995) Survey of Omega-3 Fatty Acids in Diets of Midwest Low-Income Pregnant Women, J. Agromed. 2, 49–57.

    Article  Google Scholar 

  4. Stark, K.D., Beblo, S., Murthy, M., Buda-Abela, M., Janisse, J., Rockett, H., Whitty, J.E., Martier, S.S., Sokol, R.J., Hannigan, J.H., and Salem, N., Jr. (2004) Comparison of Bloodstream Fatty Acid Composition from African-American Women at Gestation, Delivery and Postpartum, J. Lipid Res. 46, 516–525.

    Article  PubMed  CAS  Google Scholar 

  5. Okuyama, H., Kobayashi, T., and Watanabe, S. (1996) Dietary Fatty Acids—The n−6/n−3 Balance and Chronic Elderly Diseases. Excess Linoleic Acid and Relative n−3 Deficiency Syndrome Seen in Japan, Prog. Lipid Res. 35, 409–457.

    Article  PubMed  CAS  Google Scholar 

  6. Salem, N., Jr., Litman, B., Kim, H.Y., and Gawrisch, K. (2001) Mechanisms of Action of Docosahexaenoic Acid in the Nervous System, Lipids 36, 945–959.

    Article  PubMed  CAS  Google Scholar 

  7. Uauy, R., Hoffman, D.R., Mena, P., Llanos, A., and Birch, E.E. (2003) Term Infant Studies of DHA and ARA Supplementation on Neurodevelopment: Results of Randomized Controlled Trials, J. Pediatr. 143, S17–S25.

    PubMed  CAS  Google Scholar 

  8. Banks, E.C., Ferretti, L.E., and Shucard, D.W. (1997) Effects of Low Level Lead Exposure on Cognitive Function in Children: A Review of Behavioral, Neuropsychological and Biological Evidence, Neurotoxicology 18, 237–281.

    PubMed  CAS  Google Scholar 

  9. Goyer, R.A. (1996) Results of Lead Research: Prenatal Exposure and Neurological Consequences, Environ. Health Perspect. 104, 1050–1054.

    PubMed  CAS  Google Scholar 

  10. Rice, D.C. (1996) Behavioral Effects of Lead: Commonalities Between Experimental and Epidemiologic Data, Environ. Health Perspect 104 (Suppl. 2), 337–351.

    PubMed  CAS  Google Scholar 

  11. Lim, S.-Y., Doherty, J., and Salem, N., Jr. (2005) Lead Exposure and (n−3) Fatty Acid Deficiency During Rat Neonatal Development Alter Liver, Plasma and Brain Polyunsaturated Fatty Acid Composition, J. Nutr. 135, 1027–1033.

    PubMed  CAS  Google Scholar 

  12. Donaldson, W.E., and Leeming, T.K. (1984) Dietary Lead: Effects on Hepatic Fatty Acid Composition in Chicks, Toxicol. Appl. Pharmacol. 73, 119–123.

    Article  PubMed  CAS  Google Scholar 

  13. Lawton, L.J., and Donaldson, W.E. (1991) Lead-Induced Tissue Fatty Acid Alterations and Lipid Peroxidation, Biol. Trace Elem. Res. 28, 83–97.

    Article  PubMed  CAS  Google Scholar 

  14. Lasley, S.M., Green, M.C., and Gilbert, M.E. (1999) Influence of Exposure Period on in vivo Hippocampal Glutamate and GABA Release in Rats Chronically Exposed to Lead, Neurotoxicology 20, 619–629.

    PubMed  CAS  Google Scholar 

  15. Reeves, P.G., Nielsen, F.H., and Fahey, G.C., Jr. (1993) AIN-93 Purified Diets for Laboratory Rodents: Final Report of the American Institute of Nutrition ad hoc Writing Committee on the Reformulation of the AIN-76A Rodent Diet, J. Nutr. 123, 1939–1951.

    PubMed  CAS  Google Scholar 

  16. Folch, J., Lees, M., and Sloane Stanley, G.H. (1957) A Simple Method for the Isolation and Purification of Total Lipids from Animal Tissues, J. Biol. Chem. 226, 497–509.

    PubMed  CAS  Google Scholar 

  17. Morrison, W.R., and Smith, L.M. (1964) Preparation of Fatty Acid Methyl Esters and Dimethylacetals from Lipids with Boron Fluoride-Methanol, J. Lipid. Res. 53, 600–608.

    Google Scholar 

  18. Salem, N., Jr., Reyzer, M., and Karanian, J. (1996) Losses of Arachidonic Acid in Rat Liver After Alcohol Inhalation, Lipids 31 (Suppl.), S153–S156.

    Article  PubMed  CAS  Google Scholar 

  19. Zimmermann, L., Pages, N., Antebi, H., Hafi, A., Boudene, C., and Alcindor, L.G. (1993) Lead Effect on the Oxidation Resistance of Erythrocyte Membrane in Rat Triton-Induced Hyperlipidemia, Biol. Trace Elem. Res. 38, 311–318.

    PubMed  CAS  Google Scholar 

  20. Knowles, S.O., and Donaldson, W.E. (1996) Dietary Lead Alters Fatty Acid Composition and Membrane Peroxidation in Chick Liver Microsomes, Poult. Sci. 75, 1498–1500.

    PubMed  CAS  Google Scholar 

  21. Knowles, S.O., Donaldson, W.E., and Andrews, J.E. (1998) Changes in Fatty Acid Composition of Lipids from Birds, Rodents, and Preschool Children Exposed to Lead, Biol. Trace Elem. Res. 61, 113–125.

    PubMed  CAS  Google Scholar 

  22. Osterode, W., and Ulberth, F. (2000) Increased Concentration of Arachidonic Acid in Erythrocyte Membranes in Chronically Lead-Exposed Men, J. Toxicol. Environ. Health A 59, 87–95.

    Article  PubMed  CAS  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Norman Salem Jr..

About this article

Cite this article

Lim, SY., Loewke, J., Doherty, J.D. et al. Preferential effect of lead exposure during lactation on non-essential fatty acids in maternal organs. Lipids 40, 685–693 (2005). https://doi.org/10.1007/s11745-005-1431-z

Download citation

  • Received:

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s11745-005-1431-z

Keywords

Navigation