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Thalamus and connections An anatomical journey Sam Terman January 30, 2017 • I have no disclosures. • “You are a masochist and a true American.” Objectives • Describe the development, structure, and function of the thalamus and its connections • Recognize disease processes affecting the thalamus Outline • Significance • Development • Gross anatomy • Nuclei organization • Vascular supply • Disease states Significance • “Inner chamber” or “bedroom” • Multimodal processing station (i.e….it does more than you think) • Sensory • Motor • Cerebellum • Basal ganglia • • • • Limbic and motivation Arousal, alertness, and sleep-wake cycles Cognition Language • Thalamus <-----------> Cortex Development Development Development • The prosencephalon divides into the diencephalon and the telencephalon. The diencephalon gives rise to, among other structures, the thalamus, globus pallidus, and hypothalamus. The telencephalon gives rise to the striatum and cerebral cortex. Gross Anatomy Gross anatomy Gross anatomy • Connected by the massa intermedia Nuclei organization • Relay (most of the thalamus) • • • • Lateral Medial Midline Anterior • Intralaminar • Reticular What goes in… …must come out • Fill in the blank: Most thalamocortical fibers project to layer __ of neocortex. “Layer IV contains a dense horizontal band of fibers--the external band of Baillarger. This band contains the terminal ramifications of the thalamocortical projections from specific thalamic relay nuclei. It is particularly prominent in the striated or primary visual cortex and known as the line of Gennari.” Most thalmocortical fibers project to layer IV Nuclei organization - Lateral • • • • • • • • • • • VPL (somatosensory spinal = body) VPM (somatosensory cranial nerve = face, taste) LGN (vision, “lateral light”) MGN (hearing, “medial music”) VL (from basal ganglia/cerebellum, RITE prefers cerebellum) VA (from basal ganglia) Pulvinar (behavioral orientation towards stimuli (i.e. visual), to diffuse association cortex) Lateral dorsal (like an anterior nucleus, multimodal) Lateral posterior (like pulvinar) Ventral medial (alertness) VIM (DBS target for ET) Nuclei organization - Lateral VPM VPL Nuclei organization - Lateral • Facial pain, thermal sensibility, fine touch and position sense all converge for the first time in the ventroposterior medial nucleus of the contralateral thalamus. The chief sensory nucleus of cranial nerve V serves fine touch, the spinal nucleus of cranial nerve V serves pain and thermal sensibility and the mesencephalic nucleus of cranial nerve V serves position sense. These sensory modalities converge in the contralateral thalamus in the ventroposterior medial nucleus of the thalamus while sensory information from the contralateral trunk and extremities converges on the ventroposterior lateral nucleus of the thalamus. • The ventral posterolateral nucleus projects to areas three, one, and two-the primary somesthetic area of the parietal lobe. The ventroposteromedial nucleus, that conveys facial sensation, also projects to the postcentral gyrus. What structure? LGN • LGN: convex shape (Napoleon's hat) • L = “Light” (vision) • Tract -> LGN -> Radiations > cortex LGN • Extra credit: How is the LGN organized? LGN • Each thalamus contains information from the contralateral hemifield • Layers alternate visual information • Layers 1 and 2 = magnocellular (rods, movement) • Layers 3 to 6 = parvocellular (cones, color) • In between = koniocellular (color, movement, integration, ?) • Layers alternate eyes • Layers 2, 3, 5 = ipsilateral thalamus • Layers 1, 4, 6 = contralateral thalamus LGN LGN Extrageniculate visual pathways • Pretectal area -> parasympathetics (pupillary light reflex) • SCN (circadian rhythms) • Superior colliculus (orient eyes and head to stimuli, saccades) -> pulvinar and lateral posterior nucleus -> association cortex (FEF, parietal) for visual attention and orientation • Superior colliculus -> tectospinal tract (reflex postural movements in response to visual stimuli) -> C1-C4 MGN • Medial = “music” MGN • What is the input to MGN? MGN • What is the input to MGN? • Inferior colliculus MGN Don’t get confused • Olives • Superior olive = hearing • Inferior olive = cerebellum • Colliculi • Inferior colliculus = hearing • Superior colliculus = vision • Lemniscus • Lateral lemniscus = hearing • Medial lemniscus = somatosensation Pulvinar • The pulvinar is an association nucleus in the thalamus involved in visual processing. The pulvinar receives fibers from the superior colliculus (extrageniculate) and projects to areas 17, 18 and 19. Both the inferior and lateral pulvinar have reciprocal connections with the occipital cortex. • Very close to LGN Insula • Insular cortex receives inputs from the ventromedial nucleus of the thalamus, relaying taste and visceral sensation. In addition, it receives nociceptive and thermal inputs from the posterior ventromedial nucleus, which is the site of termination of spinothalamic pathways arising from lamina I of the dorsal horn. Exception • What sensory modality doesn’t project to thalamus en route to primary cortex (hint: what haven’t we talked about?) • • • • • A) Somatosensation B) Taste C) Sight D) Sound E ) Smell Exception • Olfactory neurons project directly to (allo)cortex without synapsing in thalamus • That said, thalamus still processes olfaction (i.e. olfactory cortex -> MD) VA/VL • Inputs are basal ganglia and cerebellum VA/VL • Output to frontal/motor cortex Basal ganglia output to thalamus • Basal ganglia has 4 parallel channels • • • • Motor -> VA/VLo Oculomotor -> VA/MD Prefrontal -> VA/MD Limbic -> VA/MD • Also output to intralaminar (centromedian, parafascicular) nuclei -> back to striatum Basal ganglia outputs to thalamus • SNr/GPi -> thalamic fasciculus (AL + LF) -> thalamus (VA/VL) -> frontal lobe • Nomenclature 1: AL+LF = TF • Ansa lenticularis (loop around IC) • Lenticular fasciculus (plow through IC) • Nomenclature 2: • H fields of Forel (white dead guy, H=‘hood’) • H1 field of Forel = thalamic fasciculus Unrelated, but testable and in the neighborhood • What is the only excitatory connection in the basal ganglia classic model? Cerebellum output to thalamus • Cerebellum -> VLc -> premotor cortex Nuclei organization - Medial Nuclei organization - Medial Nuclei organization - Medial • MD • Limbic, executive function, behavior, motivation • Amygdala/olfactory cortex/limbic/prefrontal cortex/basal ganglia -> MD -> frontal cortex • The medial dorsal nucleus of the thalamus has rich connections with the amygdala, orbitofrontal region, and the temporal lobe. Lesions involving this nucleus typically involve disinhibition, utilization behavior, mania, and memory loss. • Motivation pathway: cingulate gyrus -> limbic striatum (ventral caudate, nucleus accumbens, olfactory tubercle) -> MD -> cortex Nuclei organization - Anterior Nuclei organization - Anterior Nuclei organization - Anterior • Anterior nucleus • Limbic • Mammillary body/hippocampal formation (mammillothalamic tract, Papez circuit) -> anterior n. -> cingulate gyrus • Lesions -> amnesia, confabulation, anomia. • The lateral dorsal nucleus has connections similar to those of the anterior nucleus to which it is adjacent though it may also have posterior parietal connections as well. Nuclei organization - Midline • Midline thalamic nuclei • Limbic, diffuse • Hyopthalamus/basal forebrain/amygdala/hippocampus -> midline nuclei amygdala/hipoccampus/limbic cortex Nuclei organization - Intralaminar • Intralaminar nuclei • Alertness/consciousness, motor relay for basal ganglia and cerebellum • Deep cerebellar nuclei, globus pallidus, ARAS, sensory pathways -> intralaminar nuclei -> cortex and striatum • I.e. inputs and outputs are to/from basal ganglia • Caudal: (including large centromedian nucleus): basal ganglia circuitry • Rostal: Basal ganglia circuitry, but also relay inputs from ARAS to cortex to maintain alertness • The intralaminar nuclei are cell groups within the internal medullary lamina, which separates the medial and lateral subdivisions of the thalamus. Its afferents are from nuclei in the brainstem reticular formation and somatosensory input, and has diffuse cortical projections Nuclei organization - Reticular Nuclei organization - Reticular • Reticular nucleus • Thin sheet just lateral to the rest of the thalamus, separated by the external medullary lamina • NOT synonymous with the brainstem reticular formation, but connected to ARAS so involved in alertness • Regulates state of other thalamic nuclei by inhibitory neurons and alertness • Only nucleus which doesn’t project to cortex • Cortex, ARAS, intralaminar nucleus -> reticular nuclei -> intralaminar nuclei, ARAS Nuclei organization - Reticular • Generates sleep spindles Nuclei Review • VPM v VPL (face versus body?) • MGN (input?) v LGN (Waterloo?) • VA v VL • MD v anterior (which one relays info hippocampus/Papez -> cingulate?) • What modality doesn’t pass through thalamus en route to cortex? • What’s interesting about reticular (2 things)? • What sensory modality comes up most with the pulvinar? Vascular supply 4 1 4 3 2 Vascular supply • Mostly posterior circulation • Four major arteries • Tuberothalamic (polar) • From Pcomm • Anterior thalamus, especially VA • Thalamoperforating (paramedian) • From P1 • Medial thalamus, especially DM • Thalamogeniculate • From P2 • Lateral thalamus, including VL • Posterior choroidal • From P2 • Posterior thalamus such as pulvinar • Tiny anterior circulation supply (not pictured) • Anterior choroidal artery • From ICA • Posterior limb of internal capsule and lateral thalamus Vascular supply • The thalamoperforating branches of the posterior cerebral arteries perfuse the medial and anterior regions of the thalamus. The thalamogeniculate branches of the posterior cerebral arteries perfuse the pulvinar and lateral nuclei. The inferior thalamic arteries arise from the posterior communicating arteries and perfuse the inferior portions of the thalamus. The medial posterior choroidal artery supplies the superior and medial portions of the thalamus. Disease states • Vascular • Drug mechanism • Prion • Metabolic • Movement Vascular: Lacunar syndrome • Pure sensory lacunar syndrome • Dejerine Roussy syndrome Vascular: Artery of percheron • Unilateral proximal PCA feeds bilateral paramedian thalami and rostral midbrain ….. zzzzzzzzz Vascular: Aphasia • “Paramedian infarcts of the thalamus can result in language disorders that resemble transcortical motor however there are more paraphasic errors and patients are slightly more fluent than a typical transcortical motor aphasia. Other common symptoms include behavioral changes and amnesia.” An 83-year-old right-handed woman presented with sudden right-sided hemiparesis, somnolence, and loss of normal speech. Speech was nonfluent with semantic paraphasias and wordfinding difficulties. Word repetition and comprehension were normal. MRI brain showed an area of restricted diffusion in the left thalamus consistent with acute infarction (figure 1). Speech fluency returned to normal after 2 days with occasional dysnomia and paraphasias. Left thalamic infarcts can result in aphasia that is characterized by lexical-semantic deficits and intact word repetition; fluency and comprehension are variably affected.1 Thalamic aphasia has been hypothesized to result from disconnection between cortical language centers and thalamic nuclei (figure 2).1,2. –Teaching NeuroImages Thalamic aphasia syndrome. Afzal U and Farooq MU, Neurology 2013;81;e177. http://www.neurology.org/content/81/23/e177.full.pdf Vascular: Anterior choroidal • Branch of ICA • Posterior limb of IC and lateral thalamus • Hemiparesis and quadruple sectoranopia Vascular: infarct-related dementia • Apparently a lesion of 0.5 cm in the MD is capable of producing a dementia since it is capable of disrupting the encoding circuit (producing an amnesia) and also the frontal-subcortical circuits (producing profound executive and behavioral dysfunction). Vascular: Susac • Susac syndrome is a clinical triad of retinal branch occlusion, hearing impairment, and MRI changes that resembles multiple sclerosis. In multiple sclerosis the lesions tend to be in the forceps and more peripheral margins of the corpus callosum. Susac syndrome tends to involve the midline of the corpus callosum. Other MR abnormalities seen in Susac syndrome include hyperintense scattered subcortical T2 lesions, leptomeningeal enhancement, and focal lesions in the basal ganglia and the thalamus. Vascular: Venous infarct • Sagittal T1 and axial proton density images show abnormal hyperintensity filling the vein of Galen and straight sinus, instead of the normal flow void expected. This is secondary to thrombus in these structures and has resulted in hemorrhagic venous infarction in the thalami. Mass effect from the infarctions has compressed the third ventricle, resulting in obstructive hydrocephalus of the lateral ventricles. The axial image shows prominent basal veins of Rosenthal (seen on either side of the vein of Galen as flow void), likely providing collateral venous drainage. The pineal gland is normal in appearance, but inferiorly displaced by the thrombus and mass effect. AVM Vascular: AVM • There is a large draining vein and nidus of smaller vascular structures within the right thalamus, with adjacent hemorrhage and mass effect on the third ventricle. The appearance is that of an arterial venous malformation. The vein of Galen malformation would extend in the posterior midline. A venous malformation would have a linear, radial or caput medusa pattern. A hemangioblastoma may be a cystic or solid highly vascular tumor however a large vein and vascular nidus as shown are not associated features. Vascular: hypoxia Drug mechanism • _____ blocks calcium channels in the thalamus. Drug mechanism • Ethosuxamide blocks calcium channels in the thalamus. • “Corticothalamic rhythms are believed to be involved in the generation of spike-and-wave discharges that are the characteristic electroencephalographic signs of absence seizures. The spontaneous pacemaker oscillatory activity of thalamocortical circuitry involves low threshold T-type Ca2+ currents in the thalamus, and ethosuximide is presumed to reduce these low threshold T-type Ca2+ currents in thalamic neurons.” – Ethosuxamide: from bench to bedside, Goren MZ and Onat F, CNS Drug Rev, 2007 Summer; 13(2):224-39. What is this? • Variant CJD • Rare prion disease typically seen in younger patients who present with rapidly progressive cognitive decline (but less rapid than sporadic CJD), cerebellar dysfunction, visual disturbance and may have increased signal intensity lesions on FLAIR views in the bilateral posterior thalami ("pulvinar sign"). • Florid amyloid plaque surrounded by rim of spongiform changes. Tonsillar biopsy particularly diagnostic. CJD • DWI: cortical gyri, caudate, and thalamus. Diagnosis? • A 50 year old begins experiencing insomnia followed by several months of panic attacks and hallucinations. This is followed by complete inability to sleep, rapid weight loss, unresponsiveness, and death six months later. His father perished similarly. Fatal familial insomnia • Autosomal dominant prion disease • Involves some atrophy of the thalamus Wernicke’s encephalopathy • The location of the T2 hyperintensity in the dorsal midbrain and the symmetrical abnormal enhancement in the mammillary bodies, periaqueductal tissue and dorsal midbrain and the FLAIR hyperintensity in the medial thalami are highly indicative of ________________________ in this clinical setting. • Question had a negative MRV and MRA (not vascular) Wilson’s • There is symmetric high signal intensity involvement of the putamen and thalami bilaterally. The globus pallidus is also involved but not exclusively as it is in many patients with carbon monoxide poisoning. The heads of the caudate and nuclei appear normal, and there is no significant overall atrophy of the brain. These are findings that tend to exclude Huntington disease while the high signal intensity within the globus pallidus and putamen is atypical for Parkinson disease. Gliomatosis cerebri, an infiltrating astrocytoma of the white matter, is excluded by the fact that the disease process spares the white matter where the tumor occurs. The correct response is Wilson disease. Movement • Essential tremor • Lesion part or all of the thalamus to suppress contralateral tremor • DBS of VIM • Thalamotomy • Side effect of bilateral thalamotomy? Speech Movement • Ballism • Associated with discrete lesions in the subthalamic nucleus. The dyskinesia occurs contralateral to the lesion and is associated with hypotonia. As the hemiballismus improves, the movements are more like chorea. The subthalamic nucleus modulates (suppresses) ispilateral basal ganglionic activity, which in turn modulates cortical motor outflow to the contralateral effector muscles. Movement • STN excites SNr/GPi, which inhibits thalamus Movement • Ballism Movement • Ballism • Associated with discrete lesions in the subthalamic nucleus. The dyskinesia occurs contralateral to the lesion and is associated with hypotonia. As the hemiballismus improves, the movements are more like chorea. The subthalamic nucleus modulates (suppresses) ispilateral basal ganglionic activity, which in turn modulates cortical motor outflow to the contralateral effector muscles. Movement • Dopamine excites direct pathway, and direct pathway excites thalamus/cortex (excite 2 negatives) • Dopamine inhibits indirect pathway, and indirect pathway inhibits thalamus/cortex (inhibits 3 negatives) Movement • Q: What’s the lesion in PD? • A: SNc Movement • DBS: depolarization block of STN (or GPi) for PD Movement • Q: What’s the lesion in HD? • A: Caudate and putamen, initially indirect pathway more affected • Later, both pathways degenerate, and rigid/hypokinetic parkinsonism can develop (and parkinsonism predominates in the young) Hypothalamus • A few recurrent themes • Sarcoid and NMO enjoy the diencephalon • Hamartoma = gelastic seizures • Begin with laughter, precocious puberty may occur, disorganized hypocellular collection of mature neurons and glia, not cystic (unlike craniopharyngiomas) • Dopamine = prolactin inhibitory factor Thalamus and connections An anatomical journey Sam Terman January 30, 2017