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heavy Metal toxicity
Heavy metals tend to accumulate in the body due to repeated exposure and poor metabolic processing and limited excretory pathways. Metals such as mercury, cadmium, and lead exhibit a high affinity for sulfur groups on proteins. Many of these bonds are stable, so the metals remain trapped in tissues, particularly the bones, brain, liver and kidneys.
The heavy metals most frequently associated with bioaccumulation in human tissues include:
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Cadmium
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Lead
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Mercury
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Arsenic
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Aluminium
Accumulation of these metals has wide-ranging and serious health implications, depending on the metal type, route and exposure level. Mercury as an example crosses the blood–brain barrier and accumulates in the brain. Once inside, these metals bind to neuronal proteins, disrupt cellular function, generate oxidative stress, and impair neurotransmission, contributing to neurodevelopmental disorders, mood disturbances and memory deficits.
Whereas a metal such as Cadmium accumulates in the liver and kidneys, with prolonged retention leading to renal dysfunction, bone demineralisation, hypertension, and increased risks for cancers and neurodegenerative conditions.
Lead in contrast is predominantly stored in bones and teeth, where it can be re-released into circulation during periods of bone turnover, leading to systemic re-exposure. It is particularly harmful to the developing brain, contributing to intellectual disability, ADHD, and behavioural disorders.
Therefore, detoxification of heavy metals is critical to prevent the risk and continued pathogenesis of wide-spread disorders. Supporting the body’s natural heavy metal detoxification means enhancing the systems responsible for binding, neutralizing, and eliminating toxic metals.
The liver plays a central role in the detoxification of the metals mentioned above, with the exception of aluminium, which is primarily eliminated via the kidneys, aided by proteins such as transferrin and substances like citrate. For most toxic metals, effective elimination depends on their conversion into more water-soluble or bile-compatible complexes, allowing safe excretion through urine or feces. This process relies on proper metal binding, transport to detox organs, and well functioning liver and kidney pathways.
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Glutathionation
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Methylation
The glutathionation pathway relies on the master antioxidant glutathione, once bound to glutathione, the metal is transported out of the liver and eliminated primarily through bile or urine.
The methylation pathway helps detoxify certain metals by attaching a small chemical group, called a methyl group, from a compound known as SAMe. This makes the metals easier to remove from the body. Methylation is especially important for clearing arsenic and mercury.
For the liver to carry this detoxification role, heavy metals must first be delivered to it in a bound form. This transport is mediated by various ‘chelators’, which are molecules that bind to metals and escort them through the bloodstream. Without proper binding, toxic metals such as cadmium, mercury, arsenic, and lead stay accumulated in tissues like the brain, liver, and kidneys where they cause significant damage.
One of the body’s primary natural chelators is metallothionein (MT), a protein produced in response to metal exposure and oxidative stress. MT securely binds metals and helps shuttle them into the liver, where they can be exchanged for essential minerals like zinc and directed into excretion pathways via bile or urine. In addition to MT, the body relies on other botanical agents that act as chelating compounds, supporting this process of metal mobilisation and clearance from the body.
The entire process of metal detoxification can be supported naturally, and it is an important focus of healing and health. Detoxifying these metals can help restore cellular energy production, improve immune resilience, allow repair of neurological, cardiovascular, and endocrine systems damaged from metal accumulation, and reduce symptoms such as fatigue, brain fog, hormonal imbalance, and immune dysregulation. [1][3][5]
signs + symptoms
Heavy metal toxicity is associated with a large variety of pathologies. The toxic effects depend on the type and form of metal and the route and duration of exposure. [5][19] Here we detail the most common metal toxicities separately and their associated health risks.
Mercury
Mercury exists in elemental, inorganic, and organic (methylmercury) forms, and each distributes differently. Methylmercury, the form most commonly absorbed from food, easily crosses the blood-brain barrier and accumulates in the brain, where it binds tightly to thiol groups on proteins and enzymes, disrupting nerve cell function.
Inorganic mercury tends to collect in the kidneys, where it binds to metallothionein and enzymes in the renal tubules, leading to long-term renal storage and potential toxicity.
Cognitive + Neurological
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Memory impairments
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Autism Spectrum Disorder - ASD
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Attention deficit Hyperactive Disorder - ADHD
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Scattered Mind
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Depression
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Anxiety
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Irritability
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Tremors
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Numbness or Tingling
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Sleep disturbances
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Headaches
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Visual and auditory changes
Cardiovascular
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High Blood Pressure
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Coronary artery disease
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Myocardial infarction
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Cardiac arrhythmias
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Generalised atherosclerosis
Systemic
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Autoimmunity
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Immune Suppression
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Kidney impairments
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Hair loss
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Hearing loss
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Visual disturbances (including peripheral vision loss or blurred vision)
[7] [19] [21 - 23] [58] [99]
Cadmium
Primarily accumulates in the kidneys and liver. It binds strongly to metallothionein and other cysteine-rich proteins, and because the cadmium–protein complexes are filtered and reabsorbed in the kidneys, cadmium can remain there for decades, damaging the kidneys over time.
Cognitive + Neurological
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Memory impairments
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Attention deficit Hyperactive Disorder - ADHD
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Scattered Mind
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Bipolar Disorder
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Neuropathy / Neuralgia
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Motor neuron disease
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Alzheimer’s Disease
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Parkinson’s Disease
Systemic
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Autoimmunity
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Hashimoto's Thyroiditis
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Immune Suppression
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Liver Damage and Impairment
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Kidney Damage and impairment
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Kidney Stones
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Bone demineralisation
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Type 2 diabetes
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GI inflammation
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Cardiovascular disease
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High Blood Pressure
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Cancer - Breast, prostate + kidney
Pregnancy
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Preeclampsia
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Decreased head circumference
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Decreased performance IQ in infants
[9] [24 - 30] [58] [88] [108]
Lead
Lead is absorbed through the gut or lungs and can distribute widely, but over 90% of the body’s burden in adults ends up stored in the bones and teeth. It replaces calcium in the hydroxyapatite crystals of bone, becoming an inert reservoir that can later leach into the blood during times of bone loss, such as pregnancy, menopause, or aging, leading to re-exposure.
Cognitive + Neurological
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Intellectual disability
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Autism Spectrum Disorder (ASD)
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Dyslexia
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Attention deficit Hyperactive Disorder - ADHD
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Scattered Mind
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Bipolar Disorder
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Psychosis
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Muscular weakness
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Peripheral neuropathy
Systemic
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Autoimmunity
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Hashimoto's Thyroiditis
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Immune Suppression
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Allergies
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Haemolytic anaemia: red blood cells are destroyed faster than they can be produced
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Reproductive hormonal dysruptions and infertility
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Vitamin D deficiency
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High Blood Pressure
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Cancer - lung, bladder
Pregnancy
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Miscarriage
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Preterm birth
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Small for gestational-age births
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Congenital heart defects
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Reduced cognitive development in the infant
[11] [12] [19] [29] [31 - 36] [108]
Arsenic
Arsenic is absorbed primarily through the gastrointestinal tract, lungs, and, to a lesser extent, the skin, depending on its chemical form and route of exposure. Once absorbed, arsenic is widely distributed throughout the body.
Cognitive + Neurological
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Memory impairments
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Poor mental performance
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Attention deficit Hyperactive Disorder - ADHD
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Scattered Mind
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Irritability
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Anxiety
Dermal + Nail
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Skin Pigmentation
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Skin lesions
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Mee’s Lines - opaque white semi-circular bands running horizontally across the fingernails
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Keratosis - Thickened, rough, or scaly skin patches
Systemic
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Autoimmunity
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Hashimoto's Thyroiditis
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Immune Suppression
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Cancer - lung, bladder, liver, kidney, skin
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Cardiovascular disease
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High Blood Pressure
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Pulmonary disease
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Diabetes
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Gastrointestinal complaints
Pregnancy
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Increased risk of congenital heart defects in infants
[13] [19] [29] [37 - 39] [99] [94][107]
Aluminium
Aluminium is primarily absorbed through the gastrointestinal tract. Once absorbed, aluminium binds to transferrin and distributes to the brain, bones, liver, and kidneys. In the brain, it accumulates in regions like the hippocampus and cortex, where it has been implicated in neurodegenerative diseases such as Alzheimer’s.
Cognitive + Neurological
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Memory impairments
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Autism Spectrum Disorder
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Alzheimer’s Disease
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Neurological degeneration
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Balance and Coordination issues
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Multiple sclerosis
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Parkinson’s Disease
Systemic
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Immune Suppression
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Breast cancer
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Poor glucose metabolism
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Mouth ulcers - Whitening toothpastes with aluminium
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Anemia
[16 - 18] [40 - 43] [58] [99]
Causes
Heavy metals are pervasive in many aspects of modern life including food, water, air, tobacco smoke, alcoholic beverages and many home products [1][2]. Below, details where exposure to each metal can occur.
Mercury + Methylmercury
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Fabric softeners
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Laxatives
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Vaccines
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Dental amalgams
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Tattooing
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Cosmetics
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Insecticides
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Fish - particularly shark, broadbill, marlin, and swordfish
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Mushrooms
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Rice consumption
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Industrial exposure
[3] [7]
Cadmium
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Iron or calcium deficiency increases oral cadmium absorption up to 10×
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Cigarette smoke - active and passive
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Air pollution
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Metal coatings
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Plastics
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Pigments
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Cosmetics
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Wine + Beer
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Contaminated soil and foods - rice, potato, wheat, romaine lettuce, spinach, soy + peanuts
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Cereal crops
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Shellfish - oysters, scallops
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Canned fish
[3] [6] [8] [9] [99]
Lead
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Lead-based paint used prior to 1977 chip, flake, and chalk with age or during renovations, these particles settle as fine dust on floors, and can be breathed in.
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Exposure to leaded gasoline and car exhaust - phased out in Australia in 2002
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Contaminated water from lead plumbing pipes, solder and old faucets.
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Contaminated soil, food, and water
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Occupational exposure
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Cigarette smoke
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Hair dyes - including Henna
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Cosmetics - lipstick and eyeshadow
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Occupational settings such as soldering, mining, machining, and surface preparation.
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Cooking with glazed ceramic cookware or pottery
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Antique Cutlery
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Wine
[1] [10 - 12]
Arsenic
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Pesticides, herbicides and fertilizers
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Wine
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Food - particularly grains, vegetables, legumes
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Rice - Particularly from Bangladesh, India, and Korea. Note: Australian grown rice is safe
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Livestock feed additives - Meat
[3] [6] [13 - 15] [57] [99]
Aluminium
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Food: tea, vegetables, baked goods
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Canned acidic food and beverages - Tomatoes, pickles, citrus drinks, sodas and beer
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Cooking utensils
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Drinking water
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Processed foods
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Soy-based infant formula
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Occupational exposure
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Airborne dust
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Cosmetics
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Antiperspirant deodorants
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Toothpastes - particularly whitening toothpastes
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Vaccines
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Antacids - Gaviscon and Mylanta
[1] [6] [16 - 18]
Hepatic Insufficiency - Nutritional Deficiency
The liver plays a central role in detoxifying heavy metals, primarily using two biochemical pathways: glutathionation and methylation.
Glutathionation involves the binding of heavy metals; mercury, cadmium, arsenic, and lead to glutathione which neutralizes the metal and makes it more water-soluble, allowing the body to safely excrete it via bile or urine.
Methylation is another detoxification route, especially important for certain forms of arsenic and mercury. It works by attaching a methyl group to the metal compound, changing the metal’s structure to enhance its excretion.
Each pathway relies on nutritional support in order to function efficiently and safely remove heavy metals from the body. The nutritional support is detailed below:
Glutathionation Pathway Support
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Glutamine
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Cysteine
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Glycine
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Vitamin C
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Zinc
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Magnesium
Methylation Pathway Support
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Trimethylglycine (TMG)
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Cysteine
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Magnesium
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B6
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B9
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B12
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Methionine
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Betaine
Glutathione Depletion
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Mercury
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Cadmium
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Lead
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Arsenic
Glutathione is a critical detoxifying agent defending against heavy metal toxicity as it directly binds to heavy metal ions through its sulfur group, forming stable glutathione-metal complexes that facilitate the detoxification and excretion of these toxicants. This complexation not only reduces the reactivity of metal ions but also prevents their participation in harmful reactions that generate oxidative stress.
As an example, copper increases glutathione activity, rapidly consuming available glutathione, while methylmercury inhibits the rate-limiting enzyme for GSH synthesis, γ-glutamylcysteine synthetase (GCS), thereby impairing GSH replenishment. As a result, sustained metal exposure leads to glutathione depletion, which compromises the cell’s capacity to neutralize and excrete metals.
This depletion not only reduces the overall efficiency of liver detoxification pathways but also allows for greater intracellular metal accumulation, heightening the risk of oxidative damage, enzyme dysfunction, and cellular injury. Thus, maintaining sufficient GSH levels is essential for effective heavy metal detoxification, and its depletion creates a vicious cycle that amplifies metal toxicity and cellular stress. [95]
Mothers Exposure + Breastfeeding
Breastfeeding can introduce heavy metals such as lead, cadmium, aluminium, and arsenic into an infant’s body, primarily as a result of the mother’s prior environmental or lifestyle exposures. These metals accumulate in maternal tissues over time from sources like contaminated air, water, food, or occupational contact. During lactation, especially in the early stages, the mother's body mobilizes stored nutrients and, unintentionally, stored toxicants. This process releases metals into the bloodstream, allowing them to transfer into breast milk. Research has identified metal concentrations are highest in colostrum, with levels gradually declining as lactation progresses. [63]
Iron Deficiency - Aluminium Only
Iron deficiency can contribute to increased aluminum accumulation and toxicity. Normally, aluminum binds to transferrin in the bloodstream, a protein primarily responsible for transporting iron. In cases of iron deficiency, the body compensates by increasing the expression of transferrin receptors, particularly in bone cells. This upregulation enhances the uptake of transferrin-bound metals, including aluminum. As a result, more aluminum enters bone tissue and is stored. [77]
References
[1] Andrade VM, Aschner M, Marreilha dos Santos AP. Neurotoxicity of Metal Mixtures. In: Aschner M, Costa LG, editors. Neurotoxicity of Metals [Internet]. Cham: Springer International Publishing; 2017. p. 227–65.
[2] Badr FM, El-Habit O. Heavy Metal Toxicity Affecting Fertility and Reproduction of Males. In: Bioenvironmental Issues Affecting Men’s Reproductive and Sexual Health [Internet]. Elsevier; 2018. p. 293–304.
[3] Chiocchetti G, Jadán-Piedra C, Vélez D, Devesa V. Metal(loid) contamination in seafood products. Critical Reviews in Food Science and Nutrition. 2017 Nov 22;57(17):3715–28.
[4] Aaseth J, Hilt B, Bjørklund G. Mercury exposure and health impacts in dental personnel. Environmental Research. 2018 Jul;164:65–9.
[5] Bjørklund G, Dadar M, Mutter J, Aaseth J. The toxicology of mercury: Current research and emerging trends. Environmental Research. 2017 Nov;159:545–54.
[6] Borowska S, Brzóska MM. Metals in cosmetics: implications for human health: Metals in cosmetics. Journal of Applied Toxicology. 2015 Jun;35(6):551–72.
[7] Ha E, Basu N, Bose-O’Reilly S, Dórea JG, McSorley E, Sakamoto M, et al. Current progress on understanding the impact of mercury on human health. Environmental Research. 2017 Jan;152:419–33.
[8] https://www.mdpi.com/2305-6304/13/4/313
[9] Jacobo-Estrada T, Santoyo-Sánchez M, Thévenod F, Barbier O. Cadmium Handling, Toxicity and Molecular Targets Involved during Pregnancy, Jul 22;18
[10] Kaličanin B, Velimirović D. A Study of the Possible Harmful Effects of Cosmetic Beauty Products on Human Health. Biological Trace Element Research. 2016 Apr;170(2):476–84.
[11] Pohl HR, Ingber SZ, Abadin HG. Historical View on Lead: Guidelines and Regulations. In: Sigel A, Sigel H, Sigel RKO, editors. Lead – Its Effects on Environment and Health [Internet]. Berlin, Boston: De Gruyter; 2017.
[12] Sachdeva C, Thakur K, Sharma A, Sharma KK. Lead: Tiny but Mighty Poison. Indian Journal of Clinical Biochemistry. 2018 Apr;33(2):132–46.
[13] Bolan S, Kunhikrishnan A, Chowdhury S, Seshadri B, Naidu R, Ok YS. Comparative analysis of speciation and bioaccessibility of arsenic in rice grains and complementary medicines. Chemosphere. 2017 Sep;182:433–40.
[14] Ettinger AS, Arbuckle TE, Fisher M, Liang CL, Davis K, Cirtiu C-M, et al. Arsenic levels among pregnant women and newborns in Canada: Results from the Maternal-Infant Research on Environmental Chemicals (MIREC) cohort. Environmental Research. 2017 Feb;153:8–16.
[15] Liu L, Zhang Y, Yun Z, He B, Zhang Q, Hu L, et al. Speciation and bioaccessibility of arsenic in traditional Chinese medicines and assessment of its potential health risk. Science of The Total Environment. 2018 Apr;619–620:1088–97.
[16] Bondy SC. Low levels of aluminum can lead to behavioral and morphological changes associated with Alzheimer’s disease and age-related neurodegeneration. NeuroToxicology. 2016 Jan;52:222–9.
[17] Colomina MT, Peris-Sampedro F. Aluminum and Alzheimer’s Disease. In: Aschner M, Costa LG, editors. Neurotoxicity of Metals [Internet]. Cham: Springer International Publishing; 2017. p. 183–97.
[18] Vignal C, Desreumaux P, Body-Malapel M. Gut: An underestimated target organ for Aluminum. Morphologie. 2016 Jun;100(329):75–84.
[19] Jan AT, Azam M, Siddiqui K, Ali A, Choi I, Haq QMR. Heavy Metals and Human Health: Mechanistic Insight into Toxicity and Counter Defense System of Antioxidants. Int J Mol Sci. 2015 Dec 10;16(12):29592–630.
[20] Saghazadeh A, Rezaei N. Systematic review and meta-analysis links autism and toxic metals and highlights the impact of country development status: Higher blood and erythrocyte levels for mercury and lead, and higher hair antimony, cadmium, lead, and mercury. Progress in Neuro-Psychopharmacology and Biological Psychiatry. 2017 Oct;79:340–68.
[21] Genchi G, Sinicropi MS, Carocci A, Lauria G, Catalano A. Mercury Exposure and Heart Diseases. Int J Environ Res Public Health [Internet]. 2017 Jan;14(1).
[22] Jafari T, Rostampour N, Fallah AA, Hesami A. The association between mercury levels and autism spectrum disorders: A systematic review and meta-analysis. Journal of Trace Elements in Medicine and Biology. 2017 Dec;44:289–97.
[23] Oulhote Y, Shamim Z, Kielsen K, Weihe P, Grandjean P, Ryder LP, et al. Children’s white blood cell counts in relation to developmental exposures to methylmercury and persistent organic pollutants. Reproductive Toxicology. 2017 68:207–14.
[24] Everson TM, Armstrong DA, Jackson BP, Green BB, Karagas MR, Marsit CJ. Maternal cadmium, placental PCDHAC1, and fetal development. Reproductive Toxicology. 2016 Oct;65:263–71.
[25] Guo Z-L, Wang J-Y, Gong L-L, Gan S, Gu C-M, Wang S-S. Association between cadmium exposure and urolithiasis risk. Medicine (Baltimore) [Internet]. 2018 Jan 5;97(1).
[26] Jablonska E, Socha K, Reszka E, Wieczorek E, Skokowski J, Kalinowski L, et al. Cadmium, arsenic, selenium and iron–Implications for tumor progression in breast cancer. Environmental Toxicology and Pharmacology. 2017 Jul;53:151–7.
[27] Jeong KS, Park H, Ha E, Hong Y-C, Ha M, Park H, et al. Performance IQ in children is associated with blood cadmium concentration in early pregnancy. Journal of Trace Elements in Medicine and Biology. 2015 Apr;30:107–11.
[28] https://www.mdpi.com/2571-8797/7/2/35
[29] Rehman K, Fatima F, Waheed I, Akash MSH. Prevalence of exposure of heavy metals and their impact on health consequences. Journal of Cellular Biochemistry. 2018 Jan;119(1):157–84.
[30] Shome S, Talukdar AD, Choudhury MD, Bhattacharya MK, Upadhyaya H. Curcumin as potential therapeutic natural product: a nanobiotechnological perspective. Journal of Pharmacy and Pharmacology. 2016 Dec;68(12):1481–500.
[31] Eberhart J, Lovely C, Rampersad M, Fernandes Y. Gene-environment interactions in development and disease. Wiley Interdiscip Rev Dev Biol [Internet]. 2017 Jan;6(1).
[32] Edwards M. Fetal Death and Reduced Birth Rates Associated with Exposure to Lead-Contaminated Drinking Water. Environmental Science & Technology. 2014 Jan 7;48(1):739–46.
[33] Liu Z, Yu Y, Li X, Wu A, Mu M, Li N, et al. Maternal lead exposure and risk of congenital heart defects occurrence in offspring. Reproductive Toxicology. 2015 Jan;51:1–6.
[34] Ou Y, Bloom MS, Nie Z, Han F, Mai J, Chen J, et al. Associations between toxic and essential trace elements in maternal blood and fetal congenital heart defects. Environment International. 2017 Sep;106:127–34.
[35] Rabito FA, Kocak M, Werthmann DW, Tylavsky FA, Palmer CD, Parsons PJ. Changes in low levels of lead over the course of pregnancy and the association with birth outcomes. Reproductive Toxicology. 2014 Dec;50:138–44.
[36] Wang H, Li J, Hao J-H, Chen Y-H, Liu L, Yu Z, et al. High serum lead concentration in the first trimester is associated with an elevated risk of small-for-gestational-age infants. Toxicology and Applied Pharmacology. 2017 Oct;332:75–80.
[37] Jin X, Tian X, Liu Z, Hu H, Li X, Deng Y, et al. Maternal exposure to arsenic and cadmium and the risk of congenital heart defects in offspring. Reproductive Toxicology. 2016 Jan;59:109–16.
[38] Minatel BC, Sage AP, Anderson C, Hubaux R, Marshall EA, Lam WL, et al. Environmental arsenic exposure: From genetic susceptibility to pathogenesis. Environment International. 2018 Mar;112:183–97.
[39] Saint-Jacques N, Brown P, Nauta L, Boxall J, Parker L, Dummer TJB. Estimating the risk of bladder and kidney cancer from exposure to low-levels of arsenic in drinking water, Nova Scotia, Canada. Environment International. 2018 Jan;110:95–104.
[40] Hosp C, Hamm H. Safety of available and emerging drug therapies for hyperhidrosis. Expert Opinion on Drug Safety. 2017 Sep 2;16(9):1039–49.
[41] https://pmc.ncbi.nlm.nih.gov/articles/PMC10707235/
[42] Mirza A, King A, Troakes C, Exley C. Aluminium in brain tissue in familial Alzheimer’s disease. Journal of Trace Elements in Medicine and Biology. 2017 Mar;40:30–6.
[43] Mold M, Umar D, King A, Exley C. Aluminium in brain tissue in autism. Journal of Trace Elements in Medicine and Biology. 2018 Mar;46:76–82.
[44] Flora SJS, Shrivastava R, Mittal M. Chemistry and pharmacological properties of some natural and synthetic antioxidants for heavy metal toxicity. Curr Med Chem. 2013;20(36):4540–74.
[45] Aaseth J, Skaug MA, Cao Y, Andersen O. Chelation in metal intoxication—Principles and paradigms. Journal of Trace Elements in Medicine and Biology. 2015 Jul;31:260–6.
[46] https://link.springer.com/article/10.1007/s10811-020-02052-0
[47] Yadav A, Mathur R, Samim M, Lomash V, Kushwaha P, Pathak U, et al. Nanoencapsulation of DMSA monoester for better therapeutic efficacy of the chelating agent against arsenic toxicity. Nanomedicine. 2014 Mar;9(4):465–81.
[48] Flora SJS, Pachauri V. Chelation in Metal Intoxication. International Journal of Environmental Research and Public Health. 2010 Jun 28;7(7):2745–88.
[49] Rafati-Rahimzadeh M, Rafati-Rahimzadeh M, Kazemi S, Moghadamnia AA. Current approaches of the management of mercury poisoning: need of the hour. Daru. 2014 Jun 2;22(1):46.
[50] Aranda N, Valls RM, Romeu M, Sánchez-Martos V, Albaladejo R, Fernández-Castillejo S, et al. Consumption of seafood and its estimated heavy metals are associated with lipid profile and oxidative lipid damage on healthy adults from a Spanish Mediterranean area: A cross-sectional study. Environmental Research. 2017 Jul;156:644–51.
[51].http://www.foodstandards.gov.au/consumer/chemicals/mercury/Pages/default.aspx
[52] Food Authority, NSW Government. Mercury and fish [Internet]. 2018 [cited 2018 Aug 9]. Available from: /foodsafetyandyou/life-events-and-food/pregnancy/mercury-and-fish
[53] Rendón-Ramírez A-L, Maldonado-Vega M, Quintanar-Escorza M-A, Hernández G, Arévalo-Rivas B-I, Zentella-Dehesa A, et al. Effect of vitamin E and C supplementation on oxidative damage and total antioxidant capacity in lead-exposed workers. Environmental Toxicology and Pharmacology. 2014 Jan;37(1):45–54.
[54] Colovic MB, Vasic VM, Djuric DM, Krstic DZ. Sulphur-containing Amino Acids: Protective Role Against Free Radicals and Heavy Metals. Curr Med Chem. 2018 Jan 30;25(3):324–35.
[55] Liu K, Zheng J, Chen F. Effects of washing, soaking and domestic cooking on cadmium, arsenic and lead bioaccessibilities in rice: Effects of cooking on Cd, As and Pb bioaccessibilities in rice. Journal of the Science of Food and Agriculture. 2018 Aug;98(10):3829–35.
[56] Pastorelli AA, Angeletti R, Binato G, Mariani MB, Cibin V, Morelli S, et al. Exposure to cadmium through Italian rice (Oryza sativa L.): Consumption and implications for human health. Journal of Food Composition and Analysis. 2018 Jun;69:115–21.
[57] Fransisca Y, Small DM, Morrison PD, Spencer MJS, Ball AS, Jones OAH. Assessment of arsenic in Australian grown and imported rice varieties on sale in Australia and potential links with irrigation practices and soil geochemistry. Chemosphere. 2015 Nov;138:1008–13.
[58] Xu L, Zhang W, Liu X, Zhang C, Wang P, Zhao X. Circulatory Levels of Toxic Metals (Aluminum, Cadmium, Mercury, Lead) in Patients with Alzheimer’s Disease: A Quantitative Meta-Analysis and Systematic Review. Journal of Alzheimer’s Disease. 2018 Feb 6;62(1):361–72.
[59] https://pubmed.ncbi.nlm.nih.gov/21455421/
[60] Rebelo FM, Caldas ED. Arsenic, lead, mercury and cadmium: Toxicity, levels in breast milk and the risks for breastfed infants. Environmental Research. 2016 Nov;151:671–88.
[61] Park Y, Lee A, Choi K, Kim H-J, Lee JJ, Choi G, et al. Exposure to lead and mercury through breastfeeding during the first month of life: A CHECK cohort study. Science of The Total Environment. 2018 Jan;612:876–83.
[62] Letinić G, Sarić M, Piasek M, Jurasović J, Varnai V, Grgec S, et al. Use of human milk in the assessment of toxic metal exposure and essential element status in breastfeeding women and their infants in coastal Croatia. J Trace Elem Med Biol. 2016 Dec;38:117–25.
[63] Chao H-H, Guo C-H, Huang C-B, Chen P-C, Li H-C, Hsiung D-Y, et al. Arsenic, Cadmium, Lead, and Aluminium Concentrations in Human Milk at Early Stages of Lactation. Pediatrics & Neonatology. 2014 Apr;55(2):127–34.
[64] Cherkani-Hassani A, Ghanname I, Mouane N. Assessment of cadmium levels in human breast milk and the affecting factors: A systematic review, 1971–2014. Critical Reviews in Food Science and Nutrition. 2017 Jul 24;57(11):2377–91.
[65] Al-Saleh I, Elkhatib R, Al-Rouqi R, Abduljabbar M, Eltabache C, Al-Rajudi T, et al. Alterations in biochemical markers due to mercury (Hg) exposure and its influence on infant’s neurodevelopment. International Journal of Hygiene and Environmental Health. 2016 Nov;219(8):898–914.
[66] Jadán-Piedra C, Vélez D, Devesa V. In vitro evaluation of dietary compounds to reduce mercury bioavailability. Food Chemistry. 2018 May;248:353–9.
[67] Jadán Piedra C, Sánchez V, Vélez D, Devesa V. Reduction of mercury bioaccessibility using dietary strategies. LWT - Food Science and Technology. 2016 Sep;71:10–6.
[68] Silva de Paula E, Carneiro MFH, Grotto D, Hernandes LC, Antunes LMG, Barbosa F. Protective effects of niacin against methylmercury-induced genotoxicity and alterations in antioxidant status in rats. Journal of Toxicology and Environmental Health, Part A. 2016 Feb 16;79(4):174–83.
[69] Li X, Jiang X, Sun J, Zhu C, Li X, Tian L, et al. Cytoprotective effects of dietary flavonoids against cadmium-induced toxicity: Mechanisms of dietary flavonoids against cadmium. Annals of the New York Academy of Sciences. 2017 Jun;1398(1):5–19.
[70] Brzóska MM, Rogalska J, Galazyn-Sidorczuk M, Jurczuk M, Roszczenko A, Tomczyk M. Protective effect of Aronia melanocarpa polyphenols against cadmium-induced disorders in bone metabolism: A study in a rat model of lifetime human exposure to this heavy metal. Chemico-Biological Interactions. 2015 Mar;229:132–46.
[71] Gong P, Chen F, Wang L, Wang J, Jin S, Ma Y. Protective effects of blueberries (Vaccinium corymbosum L.) extract against cadmium-induced hepatotoxicity in mice. Environmental Toxicology and Pharmacology. 2014 May;37(3):1015–27.
[72] Amamou F, Nemmiche S, Meziane R Kaouthar, Didi A, Yazit SM, Chabane-Sari D. Protective effect of olive oil and colocynth oil against cadmium-induced oxidative stress in the liver of Wistar rats. Food and Chemical Toxicology. 2015 Apr;78:177–84.
[73] Chaudhary S, Iram S, Raisuddin S, Parvez S. Manganese pre-treatment attenuates cadmium induced hepatotoxicity in Swiss albino mice. Journal of Trace Elements in Medicine and Biology. 2015 Jan;29:284–8.
[74] Abdelaziz I, Elhabiby M, Ashour A. Toxicity of cadmium and protective effect of bee honey, vitamins C and B complex. Human & Experimental Toxicology. 2013 Apr;32(4):362–70.
[75] https://pmc.ncbi.nlm.nih.gov/articles/PMC10222016/
[76] https://pmc.ncbi.nlm.nih.gov/articles/PMC9952547/
[77].https://www.sciencedirect.com/science/article/abs/pii/S0946672X22000219
[78] https://pubmed.ncbi.nlm.nih.gov/30783906/
[79] https://pmc.ncbi.nlm.nih.gov/articles/PMC8767391/
[80] Lee M, Cho S, Roh K, Chae J, Park J-H, Park J, et al. Glutathione alleviated peripheral neuropathy in oxaliplatin-treated mice by removing aluminum from dorsal root ganglia. Am J Transl Res. 2017 Mar 15;9(3):926–39.
[81] Wang X, Fan X, Yuan S, Jiao W, Liu B, Cao J, et al. Chlorogenic acid protects against aluminium-induced cytotoxicity through chelation and antioxidant actions in primary hippocampal neuronal cells. Food & Function. 2017;8(8):2924–34.
[82] Sharma DR, Wani WY, Sunkaria A, Kandimalla RJ, Sharma RK, Verma D, et al. Quercetin attenuates neuronal death against aluminum-induced neurodegeneration in the rat hippocampus. Neuroscience. 2016 Jun;324:163–76.
[83] Kinoshita H, Sohma Y, Ohtake F, Ishida M, Kawai Y, Kitazawa H, et al. Biosorption of heavy metals by lactic acid bacteria and identification of mercury binding protein. Research in Microbiology. 2013 Sep;164(7):701–9.
[84] Zhai Q, Yin R, Yu L, Wang G, Tian F, Yu R, et al. Screening of lactic acid bacteria with potential protective effects against cadmium toxicity. Food Control. 2015 Aug;54:23–30.
[85] Yi Y-J, Lim J-M, Gu S, Lee W-K, Oh E, Lee S-M, et al. Potential use of lactic acid bacteria Leuconostoc mesenteroides as a probiotic for the removal of Pb(II) toxicity. Journal of Microbiology. 2017 Apr;55(4):296–303.
[86] Ojekunle O, Banwo K, Sanni AI. In vitro and in vivo evaluation of Weissella cibaria and Lactobacillus plantarum for their protective effect against cadmium and lead toxicities. Letters in Applied Microbiology. 2017;64(5):379–85.
[87] Yu L, Zhai Q, Tian F, Liu X, Wang G, Zhao J, et al. Potential of Lactobacillus plantarum CCFM639 in Protecting against Aluminum Toxicity Mediated by Intestinal Barrier Function and Oxidative Stress. Nutrients [Internet]. 2016 Dec 2;8(12).
[88] Tinkov AA, Gritsenko VA, Skalnaya MG, Cherkasov SV, Aaseth J, Skalny AV. Gut as a target for cadmium toxicity. Environmental Pollution. 2018 Apr;235:429–34.
[89] Rennolds J, Malireddy S, Hassan F, Tridandapani S, Parinandi N, Boyaka PN, et al. Curcumin regulates airway epithelial cell cytokine responses to the pollutant cadmium. Biochemical and Biophysical Research Communications. 2012 Jan;417(1):256–61.
[90] https://iopscience.iop.org/article/10.1088/1742-6596/953/1/012237/pdf
[91] https://www.mdpi.com/2073-4441/15/22/3962
[92] https://pubmed.ncbi.nlm.nih.gov/28745369/
[93] https://europepmc.org/article/PMC/PMC10320409
[94] https://www.remedylane-co.com.au/hashimotos-thyroiditis
[95].https://www.sciencedirect.com/science/article/abs/pii/S0166445X98001167
[96] Winiarska-Mieczan A. The potential protective effect of green, black, red and white tea infusions against adverse effect of cadmium and lead during chronic exposure – A rat model study. Regulatory Toxicology and Pharmacology. 2015 Nov;73(2):521–9.
[97].Khalaf AA, Moselhy WA, Abdel-Hamed MI. The protective effect of green tea extract on lead induced oxidative and DNA damage on rat brain. NeuroToxicology. 2012 Jun;33(3):280–9.
[98].Chen L, Mo H, Zhao L, Gao W, Wang S, Cromie MM, et al. Therapeutic properties of green tea against environmental insults. J Nutr Biochem. 2017 Feb;40:1–13.
[99].https://pmc.ncbi.nlm.nih.gov/articles/PMC4427717/
[100].https://www.sciencedirect.com/science/article/pii/S0022316622141040
[101].https://pmc.ncbi.nlm.nih.gov/articles/PMC4488002/#B192
[102].https://bioconceptsengage.com.au/eresources/sulphur-containing-amino-acids-as-effective-at-chelating-as-conventional-methods
[103].https://bioconceptsengage.com.au/eresources/what-is-histidine
[104] https://onlinelibrary.wiley.com/doi/abs/10.1002/tox.23966
[105].https://www.sciencedirect.com/science/article/abs/pii/S0048969723003145
[106].https://www.sciencedirect.com/science/article/abs/pii/S0048969723003145
[107] https://pmc.ncbi.nlm.nih.gov/articles/PMC4986432/
[108] https://pmc.ncbi.nlm.nih.gov/articles/PMC4158644/
specific metal rIsks
Heavy metal toxicity signs and symptoms manifests in accordance to the type of metal, the route and duration of exposure. Although amongst the most prevalent metal toxicities there are cross over signs and symptoms that allow us to flag the need for testing and treatment. These common denominator symptoms include:
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Autoimmune Disorders
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Immune Suppression - Chronic Infections
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Anxiety
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Autism Spectrum Disorder - ASD
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Attention deficit Hyperactive Disorder - ADHD
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Scattered Mind
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Memory Impairments
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Neurological Diseases
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High Blood Pressure

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