Basal Ganglia. Steven McLoon Department of Neuroscience University of Minnesota
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1 Basal Ganglia Steven McLoon Department of Neuroscience University of Minnesota 1
2 Course News Graduate School Discussion Wednesday, Nov 1, 11:00am MoosT with Paul Mermelstein (invite your friends) 2
3 Course News Coffee Hour Thursday, Nov 2, 9:30-10:30am Monday, Nov 6, 9:00-10:00am Surdyk s Café in Northrop Auditorium Stop by for a minute or an hour! 3
4 Is the nervous system really this simple? 4
5 Basal Ganglia Anatomy The basal ganglia consist of a number of nuclei in the basal region of the telencephalon, diencephalon and midbrain. The largest nuclei are: Striatum Caudate nucleus Putamen Nucleus accumbens Globus pallidus Subthalamic nucleus Substantia nigra 5
6 Basal Ganglia Anatomy The striatum is part of the telencephalon. The striatum is composed of three nuclei: caudate nucleus putamen nucleus accumbens Anatomically, the striatum is more like one nucleus divided by the internal capsule, which comes together in front of the internal capsule. 6
7 Striatum: caudate nucleus putamen nucleus accumbens 7
8 Basal Ganglia Anatomy The caudate nucleus follows the lateral ventricle. 8
9 caudate nucleus putamen 9
10 caudate nucleus putamen 10
11 caudate nucleus putamen 11
12 caudate nucleus putamen 12
13 caudate nucleus 13
14 Basal Ganglia Anatomy Globus pallidus is part of the telencephalon. Globus pallidus is positioned just medial to the putamen. Globus pallidus has two divisions: external (GPe) part of the internal basal ganglia circuitry internal (GPi) part of the basal ganglia output system 14
15 GPe GPi 15
16 Basal Ganglia Anatomy The subthalamic nucleus is part of the diencephalon. The subthalamic nucleus is positioned just below the thalamus and above the substantia nigra in the midbrain. 16
17 subthalamic nucleus 17
18 Basal Ganglia Anatomy The substantia nigra is part of the midbrain (mesencephalon). The substantia nigra is positioned just below the subthalamic nucleus, between the cerebral peduncle (anterior) and red nucleus (posterior). The substantia nigra has two parts: Pars compacta (SNc) part of the internal basal ganglia circuitry (pigmented & dopamenergic) Pars reticulata (SNr) part of the basal ganglia output system 18
19 subthalamic nucleus substantia nigra 19
20 SNc SNr 20
21 Basal Ganglia Circuitry The main input to the basal ganglia is from cortex and is to the striatum. The input from cortex uses glutamate as the transmitter and is excitatory. 21
22 Basal Ganglia Circuitry Different parts of the striatum serve different functions: caudate eye movements & cognition putamen limb, trunk & facial movement nuc. accumbens emotion, drive & desire 22
23 Basal Ganglia Circuitry Medium spiny neurons in the striatum send axons to most basal ganglia nuclei. Medium spiny neurons use GABA as the transmitter, which is inhibitory. 23
24 Basal Ganglia Circuitry Intrinsic circuits process the information. Almost every known neurotransmitter is used in intrinsic basal ganglia circuitry. 24
25 Basal Ganglia Circuitry The main basal ganglia output is from globus pallidus internal (Gpi) and substantia nigra pars reticulata (SNr). Basal ganglia connects to the ventral anterior and ventral lateral nuclei of thalamus. The output uses GABA and is inhibitory. 25
26 Basal Ganglia Pathology Degeneration of neurons in the basal ganglia can cause: reduced body movements (hypokinesia) increased body movement (hyperkinesia) Hypokinesia: akinesia impaired initiation of movements bradykinesia slower and reduced movements rigidity resistance when someone moves a resting limb Hyperkinesia include involuntary movements: chorea rapid movements athetosis slow writhing movements ballisim flailing limb movements 26
27 Basal Ganglia Pathology Basal ganglia pathologies also cause cognitive deficits and other neurological problems. 27
28 Parkinson s Disease Degeneration of the dopaminergic neurons in substantia nigra pars compacta (SNc) causes Parkinson s disease. 28
29 Parkinson s Disease Degeneration of the dopaminergic neurons in substantia nigra pars compacta (SNc) causes Parkinson s disease. 29
30 Parkinson s Disease Degeneration of the dopaminergic neurons in substantia nigra pars compacta (SNc) causes Parkinson s disease. 30
31 Parkinson s Disease Symptoms (hypokinesia): resting tremor, pronounced in the hands all muscles resist being moved by another person (rigidity) difficulty initiating movements (akinesia) and slower movements (bradykinesia) 31
32 Parkinson s Disease The onset is typically after 50 years of age. ~1% of those 60 and older have Parkinson s. Consumption of caffeine reduces the risk of Parkinson s 32
33 Parkinson s Disease Treatment is oral administration of L-DOPA; L-DOPA is a dopamine precursor that can cross the blood-brain barrier and is converted into dopamine within the striatum. 33
34 Parkinson s Disease Transplantation of embryonic midbrain tissue to the striatum is effective in eliminating Parkinson s in animals, and has been used in over 400 patients over the past 20 years. Current research is focused on turning stem cells into dopaminergic neurons for therapeutic cell replacement. 34
35 Parkinson s Disease MPTP was originally synthesized by a chemistry graduate student. He was synthesizing a synthetic morphine for recreational purposes, and MPTP was a major impurity in his chemical reaction. He self administered his drug, and within a few days he had Parkinson s disease. He was successfully treated with L-DOPA but died a few months later from a cocaine overdose. Autopsy showed that his SNc dopaminergic neurons were lost. Unfortunately, this experiment was repeated later in the San Francisco drug community. MPTP is now used in the laboratory to induce Parkinson s disease in animals for research purposes. 35
36 Huntington s Disease Degeneration of medium spiny neurons in the striatum causes Huntington s disease or Huntington s chorea. The main symptom is hyperkinesia: involuntary rapid, random movements of the trunk and limbs; writhing of the hands is common. Symptoms typically appear midlife, years of age. Huntington s disease is due to an inherited, dominant mutation. 36
37 Genes & Protein Synthesis Protein synthesis: The sequence of nucleotides in DNA (a gene) is used as a template for synthesis of messenger RNA (mrna) in the nucleus mrna is used as a template for synthesis of a protein in the cytoplasm. DNA (gene) > mrna > protein 37
38 Genes & Protein Synthesis DNA is a chain of four nucleotides. mrna is a chain of four slightly different nucleotides. Protein is a chain of amino acids. The sequence of three nucleotides in the mrna, a codon, specifies the amino acid to assemble into the protein being synthesized. Thus, the sequence of nucleotides in a gene (DNA) ultimately determines the sequence of amino acids in a protein. 38
39 Huntington s Disease Huntington s disease is due to an inherited, dominant mutation: Due to an abnormal repeat of the CAG nucleotides in the huntington gene. CAG encodes for the amino acid glutamine. The CAG repeats in the gene result in a polyglutamine sequence in the huntington protein. The huntington protein is expressed by medium spiny neurons in the striatum. The mutant protein kills medium spiny neurons over time. 39
40 40
41 Huntington s Disease 41
42 Deep Brain Stimulation (DBS) DBS is used to treat numerous motor diseases. Electrodes are implanted in the globus pallidus internis or subthalamic nucleus. The frequency and strength of the stimulus is determined empirically. The effect can be dramatic, particularly with Parkinson disease. 42
43 Deep Brain Stimulation (DBS) 43
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