Dysfunction in brain structure may cause Huntington's disease
Dysfunction of a group of brain structures critical for movement and
impulse control may be behind Huntington's disease, according to a new
study that could lead to a therapy for the currently incurable disorder.
Scientists at Northwestern University in the US identified a link between Huntington's disease and dysfunction of the sub-thalamic nucleus, a component of the basal ganglia, a group of brain structures critical for movement and impulse control. Huntington's disease is characterised by the progressive loss of nerve cells in the brain and affects about one in 10,000 people. This fatal disorder is caused by a hereditary defect in a single gene.
"Although the genetic basis of the disease is well established, why the mutation leads to the expression of symptoms and loss of brain tissue remains poorly understood," said Mark Bevan, professor of physiology at Northwestern University Feinberg School of Medicine. The debilitating symptoms of Huntington's disease typically manifest in adulthood and involve loss of motor and cognitive function, depression and personality changes.
From the point of onset, symptoms develop and intensify over the following 10 to 25 years until death, typically due to complications associated with the disease.
"While research into Huntington's disease has focused on other parts of the basal ganglia, the sub-thalamic nucleus has been largely overlooked," said Bevan.
"This is surprising because patients with Huntington's disease have fewer nerve cells in the sub-thalamic nucleus. People who have suffered damage to the sub-thalamic nucleus exhibit excessive movement and impulsive behaviour, similar to patients with Huntington's disease," he said.
Using mice genetically engineered to carry the Huntington's disease gene, scientists discovered the electrical activity of the subthalamic nucleus was lost.
Impaired subthalamic activity was caused by anomalous receptor signalling, leading to defective energy metabolism and accumulation of damaging oxidants.
The researchers also found abnormalities in the sub-thalamic nucleus occur earlier than in other brain regions, and that sub-thalamic nucleus nerve cells progressively degenerate as the mice age, mirroring the human pathology of
Huntington's disease. "Our findings suggest early problems in the sub-thalamic
nucleus not only contribute to the symptoms of Huntington's disease, but are also likely to impair the processing capacity and health of other brain structures, more traditionally associated with the disease," Bevan said.
Currently, there is no cure for Huntington's disease; treatment can only alleviate some of the symptoms. A better understanding of aberrant brain receptor signalling that leads to nerve cell dysfunction could reveal a target for therapy, researchers said.
The study was published in the journal eLife.
this is only for your information, kindly take the advice of your doctor for medicines, exercises and so on.
Scientists at Northwestern University in the US identified a link between Huntington's disease and dysfunction of the sub-thalamic nucleus, a component of the basal ganglia, a group of brain structures critical for movement and impulse control. Huntington's disease is characterised by the progressive loss of nerve cells in the brain and affects about one in 10,000 people. This fatal disorder is caused by a hereditary defect in a single gene.
"Although the genetic basis of the disease is well established, why the mutation leads to the expression of symptoms and loss of brain tissue remains poorly understood," said Mark Bevan, professor of physiology at Northwestern University Feinberg School of Medicine. The debilitating symptoms of Huntington's disease typically manifest in adulthood and involve loss of motor and cognitive function, depression and personality changes.
From the point of onset, symptoms develop and intensify over the following 10 to 25 years until death, typically due to complications associated with the disease.
"While research into Huntington's disease has focused on other parts of the basal ganglia, the sub-thalamic nucleus has been largely overlooked," said Bevan.
"This is surprising because patients with Huntington's disease have fewer nerve cells in the sub-thalamic nucleus. People who have suffered damage to the sub-thalamic nucleus exhibit excessive movement and impulsive behaviour, similar to patients with Huntington's disease," he said.
Using mice genetically engineered to carry the Huntington's disease gene, scientists discovered the electrical activity of the subthalamic nucleus was lost.
Impaired subthalamic activity was caused by anomalous receptor signalling, leading to defective energy metabolism and accumulation of damaging oxidants.
The researchers also found abnormalities in the sub-thalamic nucleus occur earlier than in other brain regions, and that sub-thalamic nucleus nerve cells progressively degenerate as the mice age, mirroring the human pathology of
Huntington's disease. "Our findings suggest early problems in the sub-thalamic
nucleus not only contribute to the symptoms of Huntington's disease, but are also likely to impair the processing capacity and health of other brain structures, more traditionally associated with the disease," Bevan said.
Currently, there is no cure for Huntington's disease; treatment can only alleviate some of the symptoms. A better understanding of aberrant brain receptor signalling that leads to nerve cell dysfunction could reveal a target for therapy, researchers said.
The study was published in the journal eLife.
this is only for your information, kindly take the advice of your doctor for medicines, exercises and so on.
https://gscrochetdesigns.
https://gseasyrecipes.
https://kneereplacement-Labels: basal ganglia, brain structures, dysfunction, gene defect, hereditary, Huntington's, impulse control, incurable disorder, loss of nerve cells, motor and cognitive functions, mutations, sub-thalamic nucleus
posted by G S Iyer at 9:39 AM
0 Comments:
Post a Comment
<< Home