cortex ARTICLE (mini-quiz 2) Flashcards

Laminar imaging of positive and negative BOLD in human visual cortex at 7 T

1
Q

Define “Direction of Information Flow” in brain imaging.

A

The direction of information flow refers to the transmission pathway of neural signals between brain regions. It’s crucial for understanding brain connectivity and helps identify hierarchical connections, such as feed-forward (lower to higher) and feedback (higher to lower) pathways.

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2
Q

What are feed-forward and feedback connections in the visual cortex?

A

Feed-forward connections send signals from lower to higher brain areas (e.g., retina to V1), typically ending in the granular layers. Feedback connections go from higher to lower areas (e.g., V2 to V1), modulating sensory input by ending in supra- and infra-granular layers.

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3
Q

What does BOLD stand for in fMRI?

A

BOLD stands for Blood Oxygenation Level Dependent, a signal in fMRI that tracks brain activity by detecting changes in blood oxygen levels associated with neural activity.

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4
Q

Describe the main advantage of ultra-high field MRI scanners in brain research.

A

Ultra-high field MRI scanners (7 Tesla and above) provide sub-millimeter resolution, enabling visualization of fine-scale structures in the human cortex in vivo, bridging gaps between human and animal studies.

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5
Q

What is the stria of Gennari in the primary visual cortex (V1)?

A

The stria of Gennari is a dense band of myelinated fibers in V1, marking the input area from the retina and distinguishing V1 anatomically.

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6
Q

Define “excitatory” and “suppressive” processes in the context of BOLD signal response.

A

Excitatory processes increase neural activity and often correspond to positive BOLD signals, while suppressive processes decrease activity and may correspond to negative BOLD signals, both reflecting cortical layer functionality.

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7
Q

What is a “laminar profile” in brain imaging?

A

A laminar profile represents imaging data across different cortical depths, enabling analysis of activity within specific cortical layers from gray/white matter boundaries to the cortical surface.

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8
Q

Explain the significance of BOLD signals across cortical depths.

A

BOLD signals across cortical depths allow for analysis of layer-specific brain activity, aiding in the differentiation of excitatory and suppressive neural processes within the cortex.

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9
Q

Define “gradient echo BOLD fMRI” and one limitation in high-resolution imaging.

A

Gradient echo BOLD fMRI captures BOLD signals through magnetic field gradients. A limitation is susceptibility to artifacts from large pial veins, which may mask finer neural activity.

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10
Q

What methodological improvement did this study employ for fine-scale imaging in V1?

A

The study used 0.55 mm isotropic resolution with 3D gradient echo EPI and high-density surface coils, enabling detailed laminar BOLD profiles across V1.

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11
Q

Describe the significance of using a unilateral dartboard pattern in the study’s design.

A

The dartboard pattern produces distinct contra-lateral and ipsi-lateral BOLD responses, allowing separate examination of excitatory and suppressive processes across cortical depth.

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12
Q

Define “isotropic resolution” in fMRI.

A

Isotropic resolution means that voxel dimensions are equal in all directions, ensuring spatial consistency across cortical depths, crucial for detailed cortical mapping.

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13
Q

What is the “equi-volume model” and why is it used in cortical depth analysis?

A

The equi-volume model creates a coordinate system across cortical depths, accounting for cortical thickness variations, which enhances accuracy in depth measurement across convoluted cortex areas.

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14
Q

What challenges are associated with BOLD imaging at sub-millimeter resolution?

A

BOLD imaging at this scale faces challenges from cortical folding and variable thickness, complicating signal consistency and data interpretation.

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15
Q

How does the angle of cortical surface relative to B0 affect %BOLD signal changes?

A

The %BOLD signal changes depending on cortical surface orientation to B0 due to alignment with large pial veins, creating signal variability unrelated to neural activity.

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16
Q

What is “T1-weighted imaging” and its application in brain studies?

A

T1-weighted imaging highlights tissue contrast based on T1 relaxation times, improving visibility of myelin-rich areas and cortical structures in high-resolution studies.

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17
Q

What is the relationship between positive BOLD signal and synaptic activity?

A

Positive BOLD signals correlate with increased synaptic activity, reflecting metabolic demand and blood flow linked to local field potential increases.

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18
Q

How does a negative BOLD signal relate to neural suppression?

A

Negative BOLD signals indicate reduced neural activity, often reflecting inhibitory or suppressive processes in the imaged brain region.

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19
Q

How does cortical gyrification impact laminar profile imaging?

A

Cortical gyrification, or folding, affects imaging by creating cortical thickness and orientation variations, complicating uniform high-resolution data acquisition.

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20
Q

What was the primary objective of the visual cortex laminar profile study?

A

To map excitatory and suppressive BOLD responses across cortical depth in V1, using high-resolution imaging to understand layer-specific stimulus processing.

21
Q

What were the characteristics of the study participants?

A

Five males, ages 25-39, with normal or corrected vision and familiarity with MRI environments. Ethics were governed by the Declaration of Helsinki and UMC Utrecht’s ethics committee.

22
Q

Why is participant MRI familiarity significant?

A

Familiarity reduces anxiety and movement artifacts, which can interfere with data reliability.

23
Q

How were visual stimuli presented in this study?

A

Stimuli were back-projected on a screen inside the MRI bore, viewed by participants through prisms and mirrors without head movement, ensuring stable imaging.

24
Q

Why was inter-stimulus interval (ISI) variability important?

A

ISI variability enhances engagement and sustains attention, supporting dynamic visual stimulus response tracking in the brain.

25
Q

Define “BOLD” and its role in this experiment.

A

BOLD (Blood-Oxygen-Level Dependent) imaging measures brain activity through blood oxygen level changes, tracking responses to visual stimuli across brain regions.

26
Q

What is a β coefficient map in fMRI?

A

A β coefficient map represents the amplitude of brain response to stimuli, showing response strengths in different visual fields.

27
Q

What was the imaging setup used for high-resolution acquisition?

A

A 7T MRI with a high gradient strength and 32-channel coil, allowing 0.5 mm isotropic resolution for precise visual cortex mapping.

28
Q

What is the role of “coregistration” in MRI data analysis?

A

Coregistration aligns images across sessions or modalities, allowing precise anatomical-functional overlays.

29
Q

Explain “motion correction” in MRI.

A

Motion correction reduces participant movement artifacts, preserving image quality, essential for high-resolution studies.

30
Q

Why use a “general linear model” (GLM) to analyze fMRI data?

A

GLM models the relationship between stimuli and BOLD response, offering a robust statistical framework for brain activity analysis.

31
Q

What does fMRI stand for, and what is its primary purpose in neuroimaging?

A

fMRI (functional Magnetic Resonance Imaging) is used to measure brain activity by detecting changes associated with blood flow, specifically tracking changes in blood oxygenation levels as an indirect measure of neural activity.

32
Q

Define the BOLD signal in fMRI.

A

BOLD (Blood Oxygen Level Dependent) signal refers to the change in MRI signal intensity based on variations in blood oxygen levels, indicating areas of neural activity. Positive BOLD suggests increased activity, while negative BOLD suggests decreased activity.

33
Q

What is a General Linear Model (GLM), and why is it important in fMRI analysis?

A

A GLM is a statistical model that explains observed data by linear combinations of variables. In fMRI, it models signal changes to identify relationships between neural activity and experimental conditions.

34
Q

What is Temporal Signal-to-Noise Ratio (TSNR), and why is it essential in fMRI?

A

TSNR measures signal stability over time by comparing signal intensity to noise. High TSNR values indicate stable, reliable data, crucial for accurate interpretation of fMRI signals.

35
Q

What does ‘motion correction’ mean in fMRI, and why is it necessary?

A

Motion correction is a preprocessing step to reduce artifacts from participant movement during scanning, improving data accuracy by adjusting for any displacement over time.

36
Q

What role does AFNI’s 3dDeconvolve function play in fMRI analysis?

A

3dDeconvolve estimates percentage changes in the BOLD signal by modeling it with a GLM, which helps to distinguish neural responses under various experimental conditions.

37
Q

What is T1-weighted (T1-w) imaging, and how is it used in this study?

A

T1-weighted imaging produces high-contrast images of anatomical structures and was used to obtain detailed intensity profiles across cortical depth, which were then aligned with BOLD profiles.

38
Q

Define the term ‘gradient-echo’ in the context of BOLD fMRI.

A

Gradient-echo is an MRI sequence used in BOLD fMRI that captures high-resolution functional activity, especially sensitive to oxygenation changes in larger veins, and is commonly employed to detect activity near the cortical surface.

39
Q

What is the ‘stria of Gennari,’ and where is it located?

A

The stria of Gennari is a highly myelinated band in the middle depth of the primary visual cortex (V1), used to identify functional and structural layers within the cortex.

40
Q

What is laminar profiling in fMRI, and how does it contribute to our understanding of brain function?

A

Laminar profiling assesses brain activity at various cortical depths, allowing researchers to analyze layer-specific neural responses, such as in the primary visual cortex (V1), to understand functional differences across cortical layers.

41
Q

How is the Pearson correlation used in analyzing BOLD signal profiles?

A

Pearson correlation quantifies the relationship between BOLD signal intensity and cortical depth, helping categorize profiles by trend strength (e.g., weak, middle, strong) based on linear relationships.

42
Q

What is the significance of the cosine of angle phi (ϕ) in BOLD signal analysis?

A

The cosine of angle phi (ϕ) describes the alignment between the cortical surface and the MRI’s magnetic field (B0), influencing BOLD signal intensity due to vascular orientation and affecting signal interpretation across cortical layers.

43
Q

What is the difference between ipsilateral and contralateral signals in brain imaging?

A

Ipsilateral signals originate on the same side of the brain as the stimulus, while contralateral signals arise from the opposite side, aiding in understanding hemisphere-specific responses to stimuli.

44
Q

Explain the purpose of using CBS-tools in segmenting high-resolution T1-w images for fMRI analysis.

A

CBS-tools enable precise segmentation of cortical layers to create a cortical depth coordinate system, which is essential for accurately mapping activity profiles across brain layers independent of cortical curvature.

45
Q

What is bootstrapping in the context of fMRI, and why is it useful?

A

Bootstrapping is a statistical method that creates multiple resampled datasets to estimate a stable median response and confidence intervals, improving the reliability of laminar activation patterns observed in fMRI.

46
Q

What does an equi-volume model refer to in cortical imaging studies?

A

The equi-volume model is a method that standardizes measurements across cortical depth by accounting for curvature, allowing accurate comparisons of laminar structure and activity across cortical layers.

47
Q

Why was a resolution of 0.55 mm isotropic used in this fMRI study?

A

This high resolution enables detailed laminar profiling, allowing researchers to distinguish subtle variations in BOLD signals across cortical depth for a more precise analysis of layer-specific activity.

48
Q

How might participant motion impact the accuracy of 3D-EPI data?

A

Motion can cause data misalignment, leading to inaccuracies in mapping BOLD signals and cortical depth analysis, potentially blurring laminar profiles or reducing the reliability of observed neural responses.

49
Q

Why might vascular anatomical differences between participants affect BOLD signal profiles?

A

Variability in vascular structures influences BOLD signal location and intensity, as individual differences in veins and micro-vasculature impact the shape and strength of BOLD profiles across participants.