Literature DB >> 16400204

Observation of the fast response of a magnetic resonance signal to neuronal activity: a snail ganglia study.

Tae Seok Park1, Sang Yeon Lee, Ji-Ho Park, Min Hyoung Cho, Soo Yeol Lee.   

Abstract

We observed the response of a magnetic resonance signal to neuronal activity in dissected snail ganglia to investigate faster responding components than the blood oxygenation level dependent (BOLD) component. To eliminate the BOLD component completely from the magnetic resonance signal, we used dissected snail ganglia which have non-magnetic hemocyanin, other than hemoglobin, as an oxygen carrying protein. To activate the snail ganglia in synchronization with the magnetic resonance signal measurement, we applied 30 Hz electrical stimulation with a pulse width of 2 s to the ganglia just before the 90 degrees RF pulse. The increase of neuronal activity in the snail ganglia after the electrical stimulation was confirmed with extracellular potential recording. The magnetic resonance signal intensity, measured with the volume selection pulse sequence in a 3.0 T MRI, decreased by about 2.97 +/- 1.10% when the ganglia were activated by the electrical stimulation. We think that the MRI signal decrease is partly due to the magnetic field produced by the neuronal current and partly due to the Lorentz force exerted on the neurons when they were firing.

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Year:  2006        PMID: 16400204     DOI: 10.1088/0967-3334/27/2/008

Source DB:  PubMed          Journal:  Physiol Meas        ISSN: 0967-3334            Impact factor:   2.833


  12 in total

1.  Magnetic resonance imaging of oscillating electrical currents.

Authors:  Nicholas W Halpern-Manners; Vikram S Bajaj; Thomas Z Teisseyre; Alexander Pines
Journal:  Proc Natl Acad Sci U S A       Date:  2010-04-26       Impact factor: 11.205

2.  Direct magnetic resonance detection of neuronal electrical activity.

Authors:  Natalia Petridou; Dietmar Plenz; Afonso C Silva; Murray Loew; Jerzy Bodurka; Peter A Bandettini
Journal:  Proc Natl Acad Sci U S A       Date:  2006-10-12       Impact factor: 11.205

3.  Modeling direct effects of neural current on MRI.

Authors:  Leon Heller; Benjamin E Barrowes; John S George
Journal:  Hum Brain Mapp       Date:  2009-01       Impact factor: 5.038

4.  Direct detection of a single evoked action potential with MRS in Lumbricus terrestris.

Authors:  Alexander J Poplawsky; Raymond Dingledine; Xiaoping P Hu
Journal:  NMR Biomed       Date:  2011-07-05       Impact factor: 4.044

5.  Can high-field MREIT be used to directly detect neural activity? Theoretical considerations.

Authors:  R J Sadleir; S C Grant; E J Woo
Journal:  Neuroimage       Date:  2010-04-09       Impact factor: 6.556

6.  Direct detection of neural activity in vitro using magnetic resonance electrical impedance tomography (MREIT).

Authors:  Rosalind J Sadleir; Fanrui Fu; Corey Falgas; Stephen Holland; May Boggess; Samuel C Grant; Eung Je Woo
Journal:  Neuroimage       Date:  2017-08-14       Impact factor: 6.556

7.  Toward direct MRI of neuro-electro-magnetic oscillations in the human brain.

Authors:  Trong-Kha Truong; Kenneth C Roberts; Marty G Woldorff; Allen W Song
Journal:  Magn Reson Med       Date:  2019-01-16       Impact factor: 4.668

8.  Direct neural current imaging in an intact cerebellum with magnetic resonance imaging.

Authors:  Padmavathi Sundaram; Aapo Nummenmaa; William Wells; Darren Orbach; Daniel Orringer; Robert Mulkern; Yoshio Okada
Journal:  Neuroimage       Date:  2016-02-17       Impact factor: 6.556

9.  Modeling neuronal current MRI signal with human neuron.

Authors:  Qingfei Luo; Xia Jiang; Bin Chen; Yi Zhu; Jia-Hong Gao
Journal:  Magn Reson Med       Date:  2011-01-19       Impact factor: 4.668

10.  Physiologically evoked neuronal current MRI in a bloodless turtle brain: detectable or not?

Authors:  Qingfei Luo; Huo Lu; Hanbing Lu; David Senseman; Keith Worsley; Yihong Yang; Jia-Hong Gao
Journal:  Neuroimage       Date:  2009-06-16       Impact factor: 6.556

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