Final answer:
The first signs of neurodegeneration in Huntington's disease involve the loss of GABAergic neurons in the putamen, due to a genetic mutation affecting the huntingtin protein, impacting calcium regulation and leading to symptoms like involuntary movements and cognitive decline.
Step-by-step explanation:
Huntington's Disease Neurodegeneration
The first signs of neurodegeneration in Huntington's disease involve the loss of GABAergic neurons of the putamen. These neurons are a specific type of neuron known as GABAergic medium-sized spiny neurons and play a crucial role in the motor and cognitive functions of the brain. As Huntington's disease progresses, the degeneration of these neurons leads to a range of physical, psychological, and cognitive symptoms such as involuntary movements, difficulties with voluntary movement control, and cognitive decline. The disease is caused by a genetic mutation resulting in a longer than normal sequence in the huntingtin protein, which is believed to disrupt normal cellular processes and lead to neuron cell death, particularly affecting calcium regulation and mitochondrial function.
While Huntington's disease pathology is primarily characterized by loss of GABAergic neurons in the striatum, the degeneration of dopaminergic neurons is a hallmark of Parkinson's disease, particularly in the substantia nigra region of the brain. Parkinson's disease also presents with motor symptoms, but these are due to different underlying mechanisms and involve issues with the dopamine neurotransmitter system.