Researchers at Monash University in Melbourne, Australia, have observed atypical neurophysiological activity in amputees who experience synesthetic pain (pain synesthetes) when observing pain in another.
The researchers found that reduced alpha and theta brainwaves in pain synesthetes may reflect inhibition of normal inhibitory mechanisms (neurotransmitters involved in the processing of observed pain) as well as increased synesthetic pain.
The researchers used EEG to record brain activity in eight amputees who experienced both phantom and synesthetic pain, 10 amputees who experienced just phantom pain, and 10 healthy people with no amputations while they looked at images of hands or feet in potentially painful and non-painful situations.
When viewing the images, the researchers found that the pain synesthetes exhibited decreased theta and alpha brainwaves compared with the other volunteers. The researchers said that such a decrease reflects an increase in neural activity, suggesting that their mirror systems (neurons that fire when an animal observes the same action performed by another) are activated more strongly.
They said the traumatic experience associated with losing a limb may heighten the sensitivity of pain synesthetes to others’ pain. When threatened, our body naturally becomes hypervigilant to pain: our pain threshold lowers, which can make even small triggers painful. Pain synesthesia may be a symptom of an abnormal, ongoing hypervigilance, the researchers said.
Showing posts with label Human Brain. Show all posts
Showing posts with label Human Brain. Show all posts
Wednesday, June 1, 2011
Monday, May 16, 2011
Tiny variation in one gene may have led to crucial changes in human brain
A tiny variation within a single gene may determine the formation of brain convolutions, the deep fissures and convolutions that increase its surface area and allow for rational and abstract thoughts, researchers at Yale University have discovered.
A genetic analysis of a Turkish patient whose brain lacks the characteristic convolutions in part of his cerebral cortex revealed that the deformity was caused by the deletion of two genetic letters from 3 billion in the human genetic alphabet. Similar variations of the same gene, called laminin gamma3 (LAMC3), were discovered in two other patients with similar abnormalities.
An analysis of the gene shows that it is expressed during the embryonic period. This period is vital to the formation of dendrites, which form synapses or connections between brain cells, the researchers said.
They said that although the same gene is present in lower organisms with smooth brains, such as mice, somehow over time it has evolved to gain novel functions that are fundamental for human occipital cortex formation. Its mutation leads to the loss of surface convolutions, a hallmark of the human brain, the researchers said.
A genetic analysis of a Turkish patient whose brain lacks the characteristic convolutions in part of his cerebral cortex revealed that the deformity was caused by the deletion of two genetic letters from 3 billion in the human genetic alphabet. Similar variations of the same gene, called laminin gamma3 (LAMC3), were discovered in two other patients with similar abnormalities.
An analysis of the gene shows that it is expressed during the embryonic period. This period is vital to the formation of dendrites, which form synapses or connections between brain cells, the researchers said.
They said that although the same gene is present in lower organisms with smooth brains, such as mice, somehow over time it has evolved to gain novel functions that are fundamental for human occipital cortex formation. Its mutation leads to the loss of surface convolutions, a hallmark of the human brain, the researchers said.
Tiny variation in one gene may have led to crucial changes in human brain
A tiny variation within a single gene may determine the formation of brain convolutions, the deep fissures and convolutions that increase its surface area and allow for rational and abstract thoughts, researchers at Yale University have discovered.
A genetic analysis of a Turkish patient whose brain lacks the characteristic convolutions in part of his cerebral cortex revealed that the deformity was caused by the deletion of two genetic letters from 3 billion in the human genetic alphabet. Similar variations of the same gene, called laminin gamma3 (LAMC3), were discovered in two other patients with similar abnormalities.
An analysis of the gene shows that it is expressed during the embryonic period. This period is vital to the formation of dendrites, which form synapses or connections between brain cells, the researchers said.
They said that although the same gene is present in lower organisms with smooth brains, such as mice, somehow over time it has evolved to gain novel functions that are fundamental for human occipital cortex formation. Its mutation leads to the loss of surface convolutions, a hallmark of the human brain, the researchers said.
A genetic analysis of a Turkish patient whose brain lacks the characteristic convolutions in part of his cerebral cortex revealed that the deformity was caused by the deletion of two genetic letters from 3 billion in the human genetic alphabet. Similar variations of the same gene, called laminin gamma3 (LAMC3), were discovered in two other patients with similar abnormalities.
An analysis of the gene shows that it is expressed during the embryonic period. This period is vital to the formation of dendrites, which form synapses or connections between brain cells, the researchers said.
They said that although the same gene is present in lower organisms with smooth brains, such as mice, somehow over time it has evolved to gain novel functions that are fundamental for human occipital cortex formation. Its mutation leads to the loss of surface convolutions, a hallmark of the human brain, the researchers said.
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