Abnormal Development - Heavy Metals

From Embryology
Revision as of 15:30, 19 August 2011 by S8600021 (Talk | contribs) (Some Recent Findings)


Metal contamination.jpg

The industrialization of the modern world has led to the proliferation in our environment of many different metal compounds. Some metals, such as zinc and iron are required in trace amounts for many biological functions. Other metals such as lead and mercury have had significant toxic effects on development.

There are historic examples of large scale disasters, for example the mercury poisoning of waterways in Japan (More? Mercury) Mercury poisoning (by methyl mercury) or Minamata disease had substantial neurological effects similar to Hunter Russell syndrome.

In addition to their direct toxic effects, the potential reduction in fetal growth and long-term effects should also be considered. Much of the basic research relies on studies in various animal models of development and we should also consider the ongoing development of new industrial products in the environment with unknown or untested effects upon development.

The specific effects of some metals are detailed in Material Safety and Data Sheets (MSDS) available from an chemical index page that relate to developmental abnormalities. These sheets are now generally required to be supplied along with the chemical purchased from a supplier and give a standardised description of the chemical, its physical properties, handling and health effects/toxicity. There are also several internet sites that have searchable databases of MSDS information. Note that handling chemical saftey may vary from country to country.

Environmental Links: Introduction | Low Folic Acid | Iodine Deficiency | Nutrition | Drugs | Australian Drug Categories | USA Drug Categories | Thalidomide | Herbal Drugs | Illegal Drugs | Smoking | Fetal Alcohol Syndrome | TORCH Infections | Viral Infection | Bacterial Infection | Zoonotic Infection | Toxoplasmosis | Malaria | Maternal Diabetes | Maternal Hyperthermia | Maternal Inflammation | Maternal Obesity | Hypoxia | Biological Toxins | Chemicals | Heavy Metals | Radiation | Prenatal Diagnosis | Neonatal Diagnosis | International Classification of Diseases | Fetal Origins Hypothesis

Some Recent Findings

  • Mercury levels in an urban pregnant population in Durham County, North Carolina[1] "The adverse effects of prenatal mercury exposure, most commonly resulting from maternal fish consumption, have been detected at very low exposure levels. The omega-3 fatty acids found in fish, however, have been shown to support fetal brain and vision development. Using data from a prospective, cohort study of pregnant women from an inland area in the US South, we sought to understand the fish consumption habits and associated mercury levels across subpopulations. Over 30% of women had at least 1 μg/L of mercury in their blood, and about 2% had blood mercury levels above the level of concern during pregnancy (≥ 3.5 μg/L). Mercury levels were higher among Asian/Pacific Islander, older, higher educated, and married women."
  • Nickel toxicity in embryos and larvae of the South American toad: effects on cell differentiation, morphogenesis, and oxygen consumption[2] "Nickel, a widely distributed heavy metal in the biosphere, produces systemic, carcinogenic, and teratogenic effects. The objectives of the present study are to report the acute, short-term chronic, and chronic toxicity of Ni in Rhinella arenarum embryos as well as the stage-dependent susceptibility to this heavy metal, including oxygen consumption, teratogenesis, and adverse effects on cell differentiation processes. ...The main teratogenic effects were retarded growth and development, extremely severe axis incurvations, persistent yolk plug, asymmetry, microcephaly and mouth and gill agenesia, and limited neuromuscular activity. Ciliated cells were not functional."
  • Arsenite induces oxidative injury in rat brain: synergistic effect of iron[3] "Sodium arsenite (arsenite)-induced neurotoxicity and its interaction with ferrous citrate (iron) was investigated in rat brain. In vitro data showed that arsenite (1-10 micromol/L) concentration dependently increased lipid peroxidation and the potency of arsenite was less than that of iron. ...Taken together, our study demonstrates that arsenite was less potent than iron in inducing oxidative stress. Furthermore, concomitant arsenite and iron potentiated oxidative injury in the nigrostriatal dopaminergic system, indicating that interaction of metals plays a more clinically-relevant role in pathophysiology of central nervous system neurodegeneration."
  • Cadmium induces retinoic acid signaling by regulating retinoic acid metabolic gene expression[4] "The transition metal cadmium is an environmental teratogen. In addition, cadmium and retinoic acid can act synergistically to induce forelimb malformations. ... Examination of gene expression demonstrated that the induction of retinoic acid signaling by cadmium may be mediated by overexpression of Bcmo1. Furthermore, cadmium inhibited the expression of Cyp26a1 and Cyp26b1, which are involved in retinoic acid degradation. These results indicate that cadmium-induced teratogenicity may be due to the ability of the metal to increase the levels of retinoic acid by disrupting the expression of retinoic acid-metabolizing genes."

Metal Toxicity

Heavy metals toxicity.gif
Heavy Metals Toxicity (Table: U.S. GEOLOGICAL SURVEY CIRCULAR 1133, 1995)

In another recent study using the sea urchin embryo, Japanese researchers have identified a hierarchy of toxic effects from different heavy metals.

"Interactive toxic effects between heavy metals were investigated using a sea urchin (Anthocidaris crassispina) bioassay. An effluent from an abandoned mine showed significant inhibitory effects on embryo development as well as producing specific malformations. The effects on the embryos were reproduced by synthetic polluted seawater consisting of eight metals (manganese, lead, cadmium, nickel, zinc, chromium, iron, and copper) at the concentrations detected in the mine effluent. This indicated that the heavy metals were responsible for the effects observed. Five heavy metals were ranked in decreasing order of toxicity as follows: Cu > Zn > Pb > Fe > Mn. Among these, zinc and manganese could cause malformation of the embryos. From bioassay results using 27 combinations of heavy metals, 16 combinations including zinc could produce specific malformations, such as radialized, exo-gastrulal, and spaceship Apollo-like gastrulal embryos. Zinc was one of the elements responsible for causing malformations and its effects were intensified by the presence of the other metals, such as manganese, lead, iron, and copper." Naomasa Kobayashia and Hideo Okamurab.

Metal in Water

A major dilemma is the biological difficulty of clearing heavy metals and the subsequent accumulation of these metals in the food chain mainly from the hydrologic environment.

Heavy metals water.gif


Lead pipe
CDC - Screening young children for lead poisoning

Lead in the environment is postnatally toxic and prenatally teratogenic.[5] Lead exposure can occur in industrial and mining and can also be derived from leaded petrol, old lead piping, historic paints, and other environmental sources).

For children aged less than 6 years of age the CDC (USA) has defined an elevated blood lead level (BLL) as >10 µg/dL, but also indicated that evidence exists for subtle effects at lower levels. (Links: CDC - Lead Poisoning Prevention Program | Blood Lead Levels in Young Children - United States and Selected States 1996-1999)

  • Lead crosses the placental barrier readily.
  • Fetal blood levels are directly proportional to maternal levels.
  • Lead poisoning affects virtually every system in the body, and often occurs with no distinctive symptoms.
  • Lead in our diet is mainly found in osseous (bone) structures.
  • Lead can damage a child's central nervous system, kidneys, and reproductive system and, at higher levels, can cause coma, convulsions, and death.
  • Even low levels of lead are harmful and are associated with decreased intelligence, impaired neurobehavioral development, decreased stature and growth, and impaired hearing acuity.
  • CDC has established a national surveillance system for children with elevated blood lead levels.
  • CDC helped to initiate federal activities to reduce lead in gasoline, which brought about declines in average blood lead levels in the U.S. population. Data from the most recent National Health and Nutrition Examination Survey (NHANES) show that the percentage of U.S. children with elevated blood lead levels has dropped from 88.2% in the late 1970s to 4.4% in the early 1990s. (NHANES Chart)

Related References

  • Interrelations of lead levels in bone, venous blood, and umbilical cord blood with exogenous lead exposure through maternal plasma lead in peripartum women[6]
  • Effect of breast milk lead on infant blood lead levels at 1 month of age[7]

Links: Normal Development - Milk | CDC - Childhood Lead Poisoning Publications



Used traditionally in the felting of hats, hence "mad hatters", a more recent example of mercury's toxicity was shown in Japan.

Minamata disease map.gif
Japan Minamata disease map

Japan had industrial mercury poisoning of waterways by methyl mercury causing Minamata disease, which had substantial neurological effects similar to Hunter Russell syndrome. For more information on mercury the chemical, see Mercury MSDS. There has also been a movie available "Medical Study of Minamata Disease".

Australia - Food Standards Australia New Zealand (FSANZ)

"FSANZ’s Chief Scientist, Dr Marion Healy, said ‘Our investigations show that the level of mercury in most fish caught and sold in Australia is low."

"The Australian Dietary Guidelines advise eating one or two fish meals per week for good health. The good news is that FSANZ has found it is safe for all population groups to eat 2-3 serves per week of most types of fish. There are only a few types of fish, which FSANZ recommends limiting in the diet – these are billfish (swordfish / broadbill and marlin ), shark/flake, orange roughy and catfish." FSANZ updates advice on mercury in fish (Australia only) 18 March 2004 see also 2 June 2011.

Links: [Australia - food standards | NSW Food Authority | USA - federal register proposal 2011



Hexavalent chromium (CrVI) is used in more than 50 industries and is an important heavy metal pollutant. A recent study (2005) in monkeys (Macaca radiata) has demonstrated an effect on testicular spermatogenesis, possibly by inducing free radical toxicity. If these effects also occur in humans, then spermatazoa development could also be affected, the study further suggested a supplementation of antioxidant vitamins may be beneficial to the affected subjects.[8]

Links: Related References



Lithium (Li, atomic number 3) is a soft alkali metal found in the natural environment, in industrial products (lithium batteries, some glass and ceramic products) and also is used to treat people with bipolar disorder. Lithium used as a drug, in a salt form, acts on the central nervous system as an antimanic agent to treat episodes of mania (frenzied, abnormally excited mood) associated with bipolar disorders. Lithium has been associated with fetal cardiac teratogenicity possibly by affecting Wnt/beta-catenin signaling.[9]

Links: Abnormal Development - Drugs | MedlinePlus - Lithium | MedlinePlus - Lithium Toxicity | OTIS - Lithium and Pregnancy PDF



A therapeutic radioactive form of yttrium used in microspheres for the internal treatment of various liver cancers. As such it would be unlikely to be found in a human development situation.



A rare, malleable and easily fusible post-transition metal that is chemically similar to gallium and thallium, and also shows properties intermediate between these two elements. Currently used industrially in liquid crystal displays and touchscreens, and historically in thin-films to form lubricated layers. Medically used in a radioactive form (indium-111) in nuclear medicine tests and as a radio-tracker. Indium is not known to be used by any biological organism. There are some animal teratogenic studies that have looked at the effect of indium salts (indium chloride).

Embryotoxic and teratogenic effects of indium chloride in rats and rabbits[10]"Indium was found to cross the placenta and appeared in fetal blood in proportion to the metal concentration of the maternal blood. In the amniotic fluid, indium concentrations remained below the detection limit. ...In rats, the effects of indium chloride causing fetal retardation was found to be independent of exposure time. The teratogenic effects were the highest on d 11 and 12 of gestation, when indium chloride caused gross external malformations. Data suggest that the teratogenic effects of indium chloride can be attributed primarily to a direct cytotoxic action of indium resulting from placental transfer, but the effect is not a selective one, as it appears only in the presence of maternal toxic effects."


  1. PMID 21556174
  2. Abelardo Andrés Sztrum, José Luis D'Eramo, Jorge Herkovits Nickel toxicity in embryos and larvae of the South American toad: effects on cell differentiation, morphogenesis, and oxygen consumption. Environ. Toxicol. Chem.: 2011, 30(5);1146-52 PubMed 21312246
  3. Su-Feng Fan, Pei-Ling Chao, Anya Maan-Yuh Lin Arsenite induces oxidative injury in rat brain: synergistic effect of iron. Ann. N. Y. Acad. Sci.: 2010, 1199;27-35 PubMed 20633106
  4. Yuxia Cui, Jonathan H Freedman Cadmium induces retinoic acid signaling by regulating retinoic acid metabolic gene expression. J. Biol. Chem.: 2009, 284(37);24925-32 PubMed 19556237
  5. Greg Cunningham Lead--toxicology and assessment in general practice. Aust Fam Physician: 2007, 36(12);1011-3 PubMed 18075625 | AFP
  6. H Y Chuang, J Schwartz, T Gonzales-Cossio, M C Lugo, E Palazuelos, A Aro, H Hu, M Hernandez-Avila Interrelations of lead levels in bone, venous blood, and umbilical cord blood with exogenous lead exposure through maternal plasma lead in peripartum women. Environ. Health Perspect.: 2001, 109(5);527-32 PubMed 11401766
  7. Adrienne S Ettinger, Martha María Téllez-Rojo, Chitra Amarasiriwardena, David Bellinger, Karen Peterson, Joel Schwartz, Howard Hu, Mauricio Hernández-Avila Effect of breast milk lead on infant blood lead levels at 1 month of age. Environ. Health Perspect.: 2004, 112(14);1381-5 PubMed 15471729
  8. M Michael Aruldhas, S Subramanian, P Sekar, G Vengatesh, Gowri Chandrahasan, P Govindarajulu, M A Akbarsha Chronic chromium exposure-induced changes in testicular histoarchitecture are associated with oxidative stress: study in a non-human primate (Macaca radiata Geoffroy). Hum. Reprod.: 2005, 20(10);2801-13 PubMed 15980013
  9. Jizhen Chen, Mingda Han, Shyam M Manisastry, Patrizia Trotta, Maria C Serrano, James C Huhta, Kersti K Linask Molecular effects of lithium exposure during mouse and chick gastrulation and subsequent valve dysmorphogenesis. Birth Defects Res. Part A Clin. Mol. Teratol.: 2008, 82(7);508-18 PubMed 18418887
  10. G Ungváry, E Szakmáry, E Tátrai, A Hudák, M Náray, V Morvai Embryotoxic and teratogenic effects of indium chloride in rats and rabbits. J. Toxicol. Environ. Health Part A: 2000, 59(1);27-42 PubMed 10681097



E D Weinberg Can iron be teratogenic? Biometals: 2010, 23(2);181-4 PubMed 20024603

Haobin Chen, Qingdong Ke, Thomas Kluz, Yan Yan, Max Costa Nickel ions increase histone H3 lysine 9 dimethylation and induce transgene silencing. Mol. Cell. Biol.: 2006, 26(10);3728-37 PubMed 16648469

Rita Hindin, Doug Brugge, Bindu Panikkar Teratogenicity of depleted uranium aerosols: a review from an epidemiological perspective. Environ Health: 2005, 4;17 PubMed 16124873

B Gulbis, E Jauniaux, J Decuyper, P Thiry, D Jurkovic, S Campbell Distribution of iron and iron-binding proteins in first-trimester human pregnancies. Obstet Gynecol: 1994, 84(2);289-93 PubMed 8041549

Search Pubmed

June 2010 "Heavy Metal Teratogen" All (744) Review (72) Free Full Text (86)

Search Pubmed: Heavy Metal Teratogen

External Links

External Links Notice - The dynamic nature of the internet may mean that some of these listed links may no longer function. If the link no longer works search the web with the link text or name. Links to any external commercial sites are provided for information purposes only and should never be considered an endorsement. UNSW Embryology is provided as an educational resource with no clinical information or commercial affiliation.

Glossary Links

A | B | C | D | E | F | G | H | I | J | K | L | M | N | O | P | Q | R | S | T | U | V | W | X | Y | Z | Numbers | Symbols

Cite this page: Hill, M.A. (2016) Embryology Abnormal Development - Heavy Metals. Retrieved October 24, 2016, from https://embryology.med.unsw.edu.au/embryology/index.php/Abnormal_Development_-_Heavy_Metals

What Links Here?
© Dr Mark Hill 2016, UNSW Embryology ISBN: 978 0 7334 2609 4 - UNSW CRICOS Provider Code No. 00098G