Lecture 42: Final Review. Martin Wessendorf, Ph.D.

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Transcription:

Lecture 42: Final Review Martin Wessendorf, Ph.D.

Lecture 33 cortex Heilbronner

5 lobes of the cortex Lateral view (left side) Mid-saggital view (right side)

Cellular organization of cortex

White matter

Lecture 34 Cortex 2 Heilbronner

Structural imaging

Functional imaging PET Radiotracer Can show glucose use or receptor binding sites Get a single time-point fmri Signal shows changes in blood flow (bloodoxygenation level dependent: BOLD) Can observe changes during tasks

Cortical regions & modularity Association cortex: not directly connected to sensory or motor pathways Modularity: brain areas are specialized Fusiform cortex: face recognition R parietal cortex only activated by L visual field Frontal cortex: character? DAMAGE DEFICITS

Lecture 35: Language & cortex Heilbronner

Diseases of cerebral cortex Vascular Stroke: ischemic vs. hemorrhagic Arteries supplying cerebral cortex Anterior, middle and posterior cerebral arteries Treatment for ischemic stroke: tissue plasminogen activator (TPA) ~3 hr time window Contraindicated for hemorrhagic stroke

Cerebral cortex is involved in all mental illnesses OCD: increased activity in anterior cingulate gyrus Depression: reduced activity in dorsolateral prefrontal cortex

Cortex & language Language is generally localized to Broca s and Wernicke s areas in the left hemisphere Loss of Broca s area: Broca s aphasia Able to produce words but not fluently Comprehension not affected Loss of Wernicke s area: Wernicke s aphasia Able to produce fluent but meaningless speech Comprehension poor

Lecture 36: Walking Rhythmic motor patterns created by central pattern generators These patterns can be chosen or modified by ascending & descending input

Initiating walking: mesencephalic locomotor area Stimulation can initiate walking (via glutamate) Higher intensity faster Cerebellum: Ventral spinocerebellar tract: info from CPGs Dorsal SCT: info from proprioceptors

Lecture 37: Addiction Brain-stimulation reward enhanced by dopamine

Brain changes with addiction Increased gene expression (cfos, etc) Increased spines on medium spiny neurons in n. accumbens

Types of neurodegenerative diseases (Lecture 38) Cognitive ( cerebral cortex) Alzheimer s, frontotemporal dementia, Pick s disease Motor Affecting motoneurons: ALS, spinal muscular atrophy Affecting cerebellum: Friedreich ataxia, ataxia-telangiectasia Affecting basal ganglia rigidity: Parkinson s disease, Progressive supranuclear palsy Affecting basal ganglia hyperkinesis: Huntingdon s disease Sensory Affecting vision: retinitis pigmentosa Mostly sporadic, increase with age, involve protein inclusions

Neurodegenerative diseases AD: memory loss that interferes with everyday life. Amyloidβ plaques & tau tangles seen FTD: atrophy of frontal & temporal lobes usually prior to age 65. Extreme behavioral/ personality (language) changes. 25% familial. Parkinson s: Loss of substantia nigra; presence of Lewy bodies; tremor/rigidity/bradykinesia/ instability. Treatment: DOPA/DA agonists; DBS ALS: 10% familial (early-onset). Loss of both upper and lower motoneurons. Muscle atrophy, difficulty speaking, swallowing, & breathing.

Neurodegenerative diseases caused by nucleotide repeats Genetic: due to repeated nucleotide sequences (often encoding glutamine) Increase # repeats sooner onset Huntingdon s disease: loss of medium spiny neurons in striatum, progressing to cortex, thalamus, cerebellum 35 repeats: normal; 40 repeats H. disease

Degeneration/ regeneration (lecture 39)

Degeneration/ regeneration

Neurogenesis (Lecture 40) Subventricular zone (SVZ) olfactory bulb No net growth: many cells die Needed for odor discrimination Subgranular zone (SGZ) 700 cells/day produced; most die ~2% of granule cells replaced/year. 4-8 weeks to mature and be incorporated Needed for memory Fluoxetine (Prozac) increases cell division antidepressant effect

Neural stem cells NSCs neurons, astrocytes and oligodendrocytes. Astrocytes & glia produced constantly @ low levels NSCs found in other areas but only generate neurons in SVZ & SGZ SVZ neurons can migrate into stroke infarct Olfactory receptor neurons reproduce and replace dying receptor neurons

Neurogenesis/gliogenesis Oligodendrocyte generation needed for learning motor task, but not for recall

Stem cells Embryonic stem cells, fetal stem cells, inducible pluripotent stem cells Fetal SCs work best but require much tissue Embryonic stem cells may teratomas

Lecture 41: memory & decision-making Long-term potentiation = LTP