Many links have been found between Parkinson’s disease and high levels of iron in the brain. The iron controlling protein, ferritin, can only monitor iron concentrations of a healthy human brain. Ferritin alters the iron, creating a non-toxic molecule that can be stored and is readily available if needed. Since a Parkinson’s diseased brain has an excess of iron, ferritin cannot control the surplus. As a result, the extra iron kills cells, creating toxins that poison and deteriorate the brain. Exploring the relationship between iron and Parkinson’s disease can guide research to help slow down or cure the disease.
Normally copper aids in the neuron functions in the brain and is an essential trace element that is active in the mitochondria of the liver. When the enzyme, cytochrome oxidase, of the mitochondrial cell is deactivated, the autosomal recessive disorder known as Wilson's Disease results. The resulting build-up of copper in the metabolic pathways of the nervous system causes muscular rigidity, spastic muscle contractions, and eventually mental deterioration. The copper, because of its redox reactivity, accumulates in the cells causing damage through oxidative modifications of proteins, lipids, and nucleic acids. Neuronally active substances that control basic human function, are affected by the inhibition of the enzymes dependent on copper. Wilson's Disease, because of the severity of the cause, is being experimentally treated with gene therapy, which injects the healthy gene controlling the enzyme expression into the organism's genome.
Because of its excellent biocompatibility, as well as ideal strength-to-weight ratio, titanium is the material of choice for bone-contacting implants in restorative medical procedures and dentistry. Titanium oxidizes spontaneously and forms a protective TiO2 layer on the surface of the implant. This allows for interfacial interactions with the bone and promotes cell adhesion and bone regrowth. Currently, studies are being done to develop ways to make this interaction even more favorable. A number of groups have completed experiments using different surface grades of titanium and after analysis with SEM, it was determined that a grooved titanium surface produces the best bone-implant interaction, allowing for the most cell adhesion and spreading.
Strontium can replace Calcium in the transmission of neurotransmitters in the brain. Peak efficiency of neurotransmitter transport is lower for strontium than for calcium, but last much longer. When strontium controls neurotransmitter release, the release is more asynchronous than it is when regulated by calcium as a result of the cell membrane's affinity for calcium. Strontium also acts as an effective antagonist of Calcium's neurotransmitter release by binding to the external cell membranre where divalent cation entry is regulated.