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Neural Imaging II: Imaging Brain Function ANA 516: February 13, 2007 Jane E. Joseph, PhD

Neural Imaging II: Imaging Brain Function ANA 516: February 13, 2007 Jane E. Joseph, PhD

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Page 1: Neural Imaging II: Imaging Brain Function ANA 516: February 13, 2007 Jane E. Joseph, PhD

Neural Imaging II: Imaging Brain Function

ANA 516:

February 13, 2007

Jane E. Joseph, PhD

Page 2: Neural Imaging II: Imaging Brain Function ANA 516: February 13, 2007 Jane E. Joseph, PhD

Outline

• Physiological Basis of functional MRI (fMRI)

• Experimental Design and Data Analysis Issues

• Brief survey of fMRI studies in animals (mostly)

Page 3: Neural Imaging II: Imaging Brain Function ANA 516: February 13, 2007 Jane E. Joseph, PhD

What is fMRI?

One of a number of brain imaging techniques that reveal some dynamic, in vivo aspect of brain function.

Page 4: Neural Imaging II: Imaging Brain Function ANA 516: February 13, 2007 Jane E. Joseph, PhD

What is fMRI?S

patia

l res

olut

ion

Temporal resolution

Page 5: Neural Imaging II: Imaging Brain Function ANA 516: February 13, 2007 Jane E. Joseph, PhD

What is fMRI?

• An INDIRECT measure of neural activity

• Measures relative concentrations of de-oxygenated blood

• Don’t need any contrast agents or radiation

Page 6: Neural Imaging II: Imaging Brain Function ANA 516: February 13, 2007 Jane E. Joseph, PhD

Brief History of MRI / fMRI

• 1890 -- Roy and Sherrington postulated that changes in activity associated with brain function would lead to increases in blood flow in those regions

• 1945 – Bloch and Purcell share the Nobel prize for their work with magnetic resonance

Page 7: Neural Imaging II: Imaging Brain Function ANA 516: February 13, 2007 Jane E. Joseph, PhD

Brief History of fMRI

• 1990 – Ogawa, et al. showed that MR images could be used to detect changes in blood oxygenation in vivo (in mouse brain)

• 1991 – First human fMRI studies

Page 8: Neural Imaging II: Imaging Brain Function ANA 516: February 13, 2007 Jane E. Joseph, PhD

fMRI vs Other techniquesNon-invasive which makes it ideal for:

(1) developmental studies (kids can go in MRI scanner)

(2) longitudinal studies (kids / people can go in multiple

times)(3) aging studies

Widely available (c.f. PET, TMS)

No known health risks (c.f. PET)

Page 9: Neural Imaging II: Imaging Brain Function ANA 516: February 13, 2007 Jane E. Joseph, PhD

fMRI vs Other techniques

fMRI is NOT a good choice in certain situations:

• Many surgical implants cannot go in MRI scanner

• Presence of metal in body (or on body – tattoos, makeup)

• To measure neurotransmitters (use spectroscopy or PET)

Page 10: Neural Imaging II: Imaging Brain Function ANA 516: February 13, 2007 Jane E. Joseph, PhD

fMRI vs Other techniques

fMRI is NOT a good choice in certain situations:

• Claustrophobia• To study gross motor behavior• Certain patient populations with

movement disorders (e.g PD)

Page 11: Neural Imaging II: Imaging Brain Function ANA 516: February 13, 2007 Jane E. Joseph, PhD

Structural v. Functional MRI

POSTERIORPOSTERIOR

Page 12: Neural Imaging II: Imaging Brain Function ANA 516: February 13, 2007 Jane E. Joseph, PhD

What is the physiological process or event that contributes to contrast in a functional image? POSTERIOR

Page 13: Neural Imaging II: Imaging Brain Function ANA 516: February 13, 2007 Jane E. Joseph, PhD

Want to measure some aspect of neural activity, but fMRI does not do this directly

Instead, fMRI is based on changes in oxygen consumption and blood flow, which are indirectly related to neural activity

Page 14: Neural Imaging II: Imaging Brain Function ANA 516: February 13, 2007 Jane E. Joseph, PhD

Excitatory post-synaptic potentials (EPSPs), Inhibitory post-synaptic potentials (IPSPs), and Action potentials (APs) are not very metabolically demanding

But the return to resting state does require energy!

Page 15: Neural Imaging II: Imaging Brain Function ANA 516: February 13, 2007 Jane E. Joseph, PhD

How is blood flow related to neural activity?

Increased neural activity causes release of vasoactive substances, which cause vessels (arterioles) to dilate – these effects can occur locally and upstream from the activity

Page 16: Neural Imaging II: Imaging Brain Function ANA 516: February 13, 2007 Jane E. Joseph, PhD

How are these physiological changes measured with MRI?

Deoxygenated hemoglobin (dHb) is paramagnetic (e.g. has unpaired electrons) due to losing O2 molecules

dHb disrupts the magnetic field locally (dephasing spins shorten T2*)

Page 17: Neural Imaging II: Imaging Brain Function ANA 516: February 13, 2007 Jane E. Joseph, PhD

More dHb loss of MR signal

Pure O2 (100%)

20% O2

Page 18: Neural Imaging II: Imaging Brain Function ANA 516: February 13, 2007 Jane E. Joseph, PhD

oxygenated blood

de-oxygenated blood

Page 19: Neural Imaging II: Imaging Brain Function ANA 516: February 13, 2007 Jane E. Joseph, PhD

oxygenated blood

de-oxygenated blood

magnetic field gradient

De-oxy hemoglobin disrupts magnetic field and causes a signal loss

Page 20: Neural Imaging II: Imaging Brain Function ANA 516: February 13, 2007 Jane E. Joseph, PhD

oxygenated blood

de-oxygenated blood

magnetic field gradient

Surplus of oxy hemogolobin relatively lower concentration of deoxy hemoglobin in active regions

Page 21: Neural Imaging II: Imaging Brain Function ANA 516: February 13, 2007 Jane E. Joseph, PhD

oxygenated blood

de-oxygenated blood

magnetic field gradient

Less decrement in signal (OR small increments in signal) at activated sites

Page 22: Neural Imaging II: Imaging Brain Function ANA 516: February 13, 2007 Jane E. Joseph, PhD

Blood Oxygenation Level Dependent Contrast (BOLD):

1. dHb is paramagnetic

2. Surplus of oxygenated blood at sites of activation

Page 23: Neural Imaging II: Imaging Brain Function ANA 516: February 13, 2007 Jane E. Joseph, PhD

Early fMRI studies (Belliveau, et al. 1991)

Look at blank screen

Look at flashing checkerboard pattern

This study not based on BOLD but used contrast !!!!

Subtract Image A from Image B

Page 24: Neural Imaging II: Imaging Brain Function ANA 516: February 13, 2007 Jane E. Joseph, PhD

First BOLD fMRI studies (Kwong, et al. 1992)

Page 25: Neural Imaging II: Imaging Brain Function ANA 516: February 13, 2007 Jane E. Joseph, PhD

First BOLD fMRI studies (Kwong, et al. 1992)

Page 26: Neural Imaging II: Imaging Brain Function ANA 516: February 13, 2007 Jane E. Joseph, PhD

First BOLD fMRI studies (Blamire, et al. 1992)

Page 27: Neural Imaging II: Imaging Brain Function ANA 516: February 13, 2007 Jane E. Joseph, PhD

Blamire, et al. (1992) showed that the BOLD response is delayed relative to the neural events associated with stimulus presentation (hemodynamic lag)

we are not measuring neural processes directly

Page 28: Neural Imaging II: Imaging Brain Function ANA 516: February 13, 2007 Jane E. Joseph, PhD

BOLD response is related to neural activity (even though it is delayed)

Page 29: Neural Imaging II: Imaging Brain Function ANA 516: February 13, 2007 Jane E. Joseph, PhD

-1.5

-1.0

-0.5

0.0

0.5

1.0

1.5

2.0

2.5

-5 0 5 10 15 20 25 30 35 40

Time since stimulus onset (s)

BO

LD

sig

na

l ch

an

ge

(%

)

A typical hemodynamic response (HDR):

y-axis:

Usually express in % change from baseline

POSTERIOR

Page 30: Neural Imaging II: Imaging Brain Function ANA 516: February 13, 2007 Jane E. Joseph, PhD

A typical functional brain activation map

Page 31: Neural Imaging II: Imaging Brain Function ANA 516: February 13, 2007 Jane E. Joseph, PhD

Talairach Atlas (Talairach & Tournoux, 1988)

-y

anterior

posterior

superior

inferior

left

right

+y +x

-x

+z

-z Anterior commissure

Posterior commissure

Page 32: Neural Imaging II: Imaging Brain Function ANA 516: February 13, 2007 Jane E. Joseph, PhD

Brodmann’s Areas (Brodmann, 1909)Lateral Surface Primary Sensory:

- Visual (17)

- Auditory (41)

- Motor (4)

- Somatosensory (1,2,3)

Secondary:

- Visual (18)

- Auditory (42)

Association:

- Visual (19, 37)

- Auditory (22)

- Somatosensory (5)

Page 33: Neural Imaging II: Imaging Brain Function ANA 516: February 13, 2007 Jane E. Joseph, PhD

Brodmann’s Areas (Brodmann, 1909)Medial Surface

Primary Sensory:

- Olfactory (28, 38)

Association:

- Limbic (23, 24, 25, 26, 27, 29, 30, 31, 32, 33)

Page 34: Neural Imaging II: Imaging Brain Function ANA 516: February 13, 2007 Jane E. Joseph, PhD

Experimental Design and Data Analysis Issues

• Technique constraints

• Limitations on experimental designs

• Advantages of fMRI

Page 35: Neural Imaging II: Imaging Brain Function ANA 516: February 13, 2007 Jane E. Joseph, PhD

Technique Constraints

• BOLD signal ~= neuronal activity

• Poor temporal resolution

• No information about temporal order of events

• Spatial resolution

Page 36: Neural Imaging II: Imaging Brain Function ANA 516: February 13, 2007 Jane E. Joseph, PhD

Limitations on Experimental Design

• No ferrous magnetic materials in scanner• Use tasks that minimize amount of movement

(gross motor tasks, speaking?)• Auditory stimulus presentation may be

masked by scanner noise• Limits on length of experiments (hardware

limitations and subject comfort)• Subtraction Technique

Page 37: Neural Imaging II: Imaging Brain Function ANA 516: February 13, 2007 Jane E. Joseph, PhD

Limitations on Experimental Design

• Subtraction Technique:

– Must have a baseline condition with which to compare an experimental condition

– May also have a control condition (or several)

– What is a good baseline condition?

Page 38: Neural Imaging II: Imaging Brain Function ANA 516: February 13, 2007 Jane E. Joseph, PhD

Advantages of fMRI

• Can do repeated measures learning, practice, intervention, recovery of function

• Can test pediatric populations developmental, longitudinal and aging studies

• Can look at individual-subject activation patterns

Page 39: Neural Imaging II: Imaging Brain Function ANA 516: February 13, 2007 Jane E. Joseph, PhD

Some applications

• Imaging brain function in animals

Page 40: Neural Imaging II: Imaging Brain Function ANA 516: February 13, 2007 Jane E. Joseph, PhD

Zhang et al. (2006). NeuroImage, 33, 636-643

Pharmacological MRI (phMRI) in MPTP lesioned rhesus monkeys

Page 41: Neural Imaging II: Imaging Brain Function ANA 516: February 13, 2007 Jane E. Joseph, PhD

Functional MRI (fMRI) in alert, unanesthetized rhesus monkeys

Joseph et al. (2006). Journal of Neuroscience Methods, 157, 10-24

Page 42: Neural Imaging II: Imaging Brain Function ANA 516: February 13, 2007 Jane E. Joseph, PhD
Page 43: Neural Imaging II: Imaging Brain Function ANA 516: February 13, 2007 Jane E. Joseph, PhD

Both monkeys showed novelty detection effects in the amygdala (only 1 monkey shown here)

Page 44: Neural Imaging II: Imaging Brain Function ANA 516: February 13, 2007 Jane E. Joseph, PhD

BOLD imaging of spinal cord in rats

Lilja et al. (2006). The Journal of Neuroscience, 26, 6330-6336

Hindlimb electrical stimulation dorsal column activity on the ipsilateral side

Page 45: Neural Imaging II: Imaging Brain Function ANA 516: February 13, 2007 Jane E. Joseph, PhD

BOLD imaging of spinal cord in humans

Stracke et al. (2005). Neuroradiology, 47, 127-143

Stimulate different fingers dorsal column activity in different dermatomes

Page 46: Neural Imaging II: Imaging Brain Function ANA 516: February 13, 2007 Jane E. Joseph, PhD

MRI of insect brains!

Page 47: Neural Imaging II: Imaging Brain Function ANA 516: February 13, 2007 Jane E. Joseph, PhD