TOXICOLOGICAL EVALUATION AND METAL BIOAVAILABILITY IN PREGNANT RATS FOLLOWING EXPOSURE TO CLAY MINERALS IN THE DIET

Silicate clays are frequently added to animal feeds to bind and reduce the bioavailability of mycotoxins in the gastrointestinal tract. However, the bioavailability of trace metals in these clay feed additives has not been thoroughly investigated. Clays that act nonselectively may interact with nutrients, minerals, and other feedborne chemicals to pose significant hidden risks. In this study, a calcium montmorillonite clay (Novasil Plus, NSP) commonly used as an enterosorbent for aflatoxins and a sodium montmorillonite clay (Swy-2) (Source Clay Minerals Repository, Columbia, MO) were examined. Clays were supplemented in the balanced diet of Sprague-Dawley rats during pregnancy at a level of 2% (w/w). Evaluations of toxicity were performed on gestation d 16 and included maternal body weights, maternal feed intakes, litter weights, and embryonic resorptions. Liver, kidneys, tibia, brain, uterus, pooled placentas, and pooled embryonic mass were collected and weighed. Tissues were lyophilized and neutron activation analysis (NAA) was performed. Elements considered by NAA included Al, Ba, Br, Ca, Ce, Co, Cr, Cs, Cu, Dy, Eu, Fe, Hf, K, La, Lu, Mg, Mn, Na, Nd, Ni, Rb, S, Sb, Sc, Se, Sm, Sr, Ta, Tb, Te, Th, Ti, Tl, U, V, Yb, Zn, and Zr. Inductively coupled plasma–mass spectroscopy further confirmed that Al was below detection limits (<0.5 ppm) in the brain. Animals supplemented with either NSP or Swy-2 were similar to controls with respect to toxicity evaluations and metal analysis, with the exception of decreased brain Rb following clay supplementation. Overall, the results of this study suggest that neither NSP nor Swy-2, at relatively high dietary concentrations, influences mineral uptake or utilization in the pregnant rat.

[1]  Luda Bernstam, Jerome Nriagu MOLECULAR ASPECTS OF ARSENIC STRESS , 2000, Journal of toxicology and environmental health. Part B, Critical reviews.

[2]  R. Harvey,et al.  Hydrated sodium calcium aluminosilicate: a high affinity sorbent for aflatoxin. , 1988, Poultry science.

[3]  P. Ungaro,et al.  Clay ingestion: a rare cause of hypokalemia. , 1982, Annals of internal medicine.

[4]  N. Roberts,et al.  Increased absorption of aluminium from a normal dietary intake in dementia. , 1998, Journal of inorganic biochemistry.

[5]  M. Carretero,et al.  Clay minerals and their beneficial effects upon human health. A review , 2002 .

[6]  J. G. Penland,et al.  Moderately High Zinc Intake Impairs Verbal Memory of Healthy Postmenopausal Women on a Low Copper Diet , 2002 .

[7]  R. Harvey,et al.  Dietary hydrated sodium calcium aluminosilicate reduction of aflatoxin M1 residue in dairy goat milk and effects on milk production and components. , 1994, Journal of animal science.

[8]  H. Meiri,et al.  Toxic effects of alumino-silicates on nerve cells , 1990, Neuroscience.

[9]  E. C. Patterson,et al.  Effects of geophagia (kaolin ingestion) on the maternal blood and embryonic development in the pregnant rat. , 1977, The Journal of nutrition.

[10]  T. Phillips,et al.  Dietary clay in the chemoprevention of aflatoxin-induced disease. , 1999, Toxicological sciences : an official journal of the Society of Toxicology.

[11]  T. Phillips,et al.  Prevention of maternal and developmental toxicity in rats via dietary inclusion of common aflatoxin sorbents: potential for hidden risks. , 1998, Toxicological sciences : an official journal of the Society of Toxicology.

[12]  H. Severance,et al.  Profound muscle weakness and hypokalemia due to clay ingestion. , 1988, Southern medical journal.

[13]  J. C. Smith,et al.  Clay ingestion (geophagia) as a source of zinc for rats. , 1970, The Journal of nutrition.

[14]  R. Harvey,et al.  Effects on aflatoxin M1 residues in milk by addition of hydrated sodium calcium aluminosilicate to aflatoxin-contaminated diets of dairy cows. , 1991, American journal of veterinary research.

[15]  R. Harvey,et al.  Diminution of aflatoxicosis in growing chickens by the dietary addition of a hydrated, sodium calcium aluminosilicate. , 1990, Poultry science.

[16]  J. Domingo,et al.  Prevention and treatment of aluminum toxicity including chelation therapy: status and research needs. , 1996, Journal of toxicology and environmental health.

[17]  B. Fowler,et al.  Arsenic: health effects, mechanisms of actions, and research issues. , 1999, Environmental health perspectives.

[18]  L. Horrocks,et al.  Aluminum silicate toxicity in cell cultures , 1993, Neuroscience.

[19]  Michael F Hughes,et al.  Arsenic toxicity and potential mechanisms of action. , 2002, Toxicology letters.

[20]  F. Nielsen Nutritional requirements for boron, silicon, vanadium, nickel, and arsenic: current knowledge and speculation , 1991, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.

[21]  D. Anderson,et al.  Cytotoxicity of aluminum silicates in primary neuronal cultures , 1993, Neuroscience.

[22]  F. Nielsen Possibly Essential Trace Elements , 2000 .

[23]  I. Ferrier,et al.  Effect of silicon on gastrointestinal absorption of aluminium , 1993, The Lancet.

[24]  C. S. Alexander Cobalt-beer cardiomyopathy. A clinical and pathologic study of twenty-eight cases. , 1972, The American journal of medicine.

[25]  Timothy D Phillips,et al.  Characterization of clay-based enterosorbents for the prevention of aflatoxicosis. , 2002, Advances in experimental medicine and biology.

[26]  S. Marklund,et al.  Chronic cobalt exposure affects antioxidants and ATP production in rat myocardium , 2001, Scandinavian journal of clinical and laboratory investigation.

[27]  G. Rottinghaus,et al.  Efficacy of a hydrated sodium calcium aluminosilicate to reduce the toxicity of aflatoxin and T-2 toxin. , 1990, Poultry science.

[28]  M. Golub,et al.  Developmental and reproductive toxicity of inorganic arsenic: animal studies and human concerns. , 1998, Journal of toxicology and environmental health. Part B, Critical reviews.

[29]  P. Geissler,et al.  Perceptions of soil-eating and anaemia among pregnant women on the Kenyan coast. , 1999, Social science & medicine.

[30]  W. A. Carter,et al.  GEOPHAGIA WITH IRON DEFICIENCY AND HYPOKALEMIA. CACHEXIA AFRICANA. , 1964, Archives of internal medicine.

[31]  T. Phillips,et al.  Selective chemisorption and detoxification of aflatoxins by phyllosilicate clay. , 1995, Natural toxins.