TY - JOUR
T1 - Gold ions bio-released from metallic gold particles reduce inflammation and apoptosis and increase the regenerative responses in focal brain injury
AU - Larsen, Agnete
AU - Kolind, Kristian
AU - Pedersen, Dan Sonne
AU - Doering, Peter
AU - Pedersen, Mie Ostergaard
AU - Danscher, Gorm
AU - Penkowa, Milena
AU - Stoltenberg, Meredin
PY - 2008/10
Y1 - 2008/10
N2 - Traumatic brain injury results in loss of neurons caused as much by the resulting neuroinflammation as by the injury. Gold salts are known to be immunosuppressive, but their use are limited by nephrotoxicity. However, as we have proven that implants of pure metallic gold release gold ions which do not spread in the body, but are taken up by cells near the implant, we hypothesize that metallic gold could reduce local neuroinflammation in a safe way. Bio-liberation, or dissolucytosis, of gold ions from metallic gold surfaces requires the presence of disolycytes i.e. macrophages and the process is limited by their number and activity. We injected 20-45 mum gold particles into the neocortex of mice before generating a cryo-injury. Comparing gold-treated and untreated cryolesions, the release of gold reduced microgliosis and neuronal apoptosis accompanied by a transient astrogliosis and an increased neural stem cell response. We conclude that bio-liberated gold ions possess pronounced anti-inflammatory and neuron-protective capacities in the brain and suggest that metallic gold has clinical potentials. Intra-cerebral application of metallic gold as a pharmaceutical source of gold ions represents a completely new medical concept that bypasses the blood-brain-barrier and allows direct drug delivery to inflamed brain tissue.
AB - Traumatic brain injury results in loss of neurons caused as much by the resulting neuroinflammation as by the injury. Gold salts are known to be immunosuppressive, but their use are limited by nephrotoxicity. However, as we have proven that implants of pure metallic gold release gold ions which do not spread in the body, but are taken up by cells near the implant, we hypothesize that metallic gold could reduce local neuroinflammation in a safe way. Bio-liberation, or dissolucytosis, of gold ions from metallic gold surfaces requires the presence of disolycytes i.e. macrophages and the process is limited by their number and activity. We injected 20-45 mum gold particles into the neocortex of mice before generating a cryo-injury. Comparing gold-treated and untreated cryolesions, the release of gold reduced microgliosis and neuronal apoptosis accompanied by a transient astrogliosis and an increased neural stem cell response. We conclude that bio-liberated gold ions possess pronounced anti-inflammatory and neuron-protective capacities in the brain and suggest that metallic gold has clinical potentials. Intra-cerebral application of metallic gold as a pharmaceutical source of gold ions represents a completely new medical concept that bypasses the blood-brain-barrier and allows direct drug delivery to inflamed brain tissue.
KW - Animals
KW - Anti-Inflammatory Agents/administration & dosage
KW - Apoptosis/drug effects
KW - Brain Injuries/drug therapy
KW - Female
KW - Gold/administration & dosage
KW - Inflammation/prevention & control
KW - Mice
KW - Mice, Inbred C57BL
KW - Nerve Regeneration/drug effects
KW - Neurons/drug effects
KW - Particle Size
KW - Surface Properties
U2 - 10.1007/s00418-008-0448-1
DO - 10.1007/s00418-008-0448-1
M3 - Journal article
C2 - 18542984
SN - 0948-6143
VL - 130
JO - Histochemistry and cell biology
JF - Histochemistry and cell biology
IS - 4
M1 - 681
ER -