Tissue conductivity is a biophysical marker of tissue structure and physiology. Present methods of measuring tissue conductivity are limited. Electrical impedance tomography, and magnetic resonance electrical impedance tomography rely on passing external current through the object being imaged, which prevents its use in most human imaging. Recently, the RF field used for MR excitation has been used to non-invasively measure tissue conductivity. This technique is promising, but conductivity at higher frequencies is less sensitive to tissue structure. Measuring tissue conductivity non-invasively at low frequencies remains elusive. It has been proposed that eddy currents generated during the rise and decay of gradient pulses could act as a current source to map low-frequency conductivity. This work centers on a gradient echo pulse sequence that uses large gradients prior to excitation to create eddy currents. The electric and magnetic fields during a gradient pulse are simulated by a finite-difference time-domain simulation. The sequence is also tested with a phantom and an animal MRI scanner equipped with gradients of high gradient strengths and slew rate. The simulation demonstrates that eddy currents in materials with conductivity similar to biological tissue decay with a half-life on the order of nanoseconds and any eddy currents generated prior to excitation decay completely before influencing the RF signal. Gradient-induced eddy currents can influence phase accumulation after excitation but the effect is too small to image. The animal scanner images show no measurable phase accumulation. Measuring low-frequency conductivity by gradient-induced eddy currents is presently unfeasible.

Tissue conductivity is a biophysical marker of tissue structure and physiology. Present methods of measuring tissue conductivity are limited. Electrical impedance tomography, and magnetic resonance electrical impedance tomography rely on passing external current through the object being imaged, which prevents its use in most human imaging. Recently, the RF field used for MR excitation has been used to non-invasively measure tissue conductivity. This technique is promising, but conductivity at higher frequencies is less sensitive to tissue structure. Measuring tissue conductivity non-invasively at low frequencies remains elusive. It has been proposed that eddy currents generated during the rise and decay of gradient pulses could act as a current source to map low-frequency conductivity. This work centers on a gradient echo pulse sequence that uses large gradients prior to excitation to create eddy currents. The electric and magnetic fields during a gradient pulse are simulated by a finite-difference time-domain simulation. The sequence is also tested with a phantom and an animal MRI scanner equipped with gradients of high gradient strengths and slew rate. The simulation demonstrates that eddy currents in materials with conductivity similar to biological tissue decay with a half-life on the order of nanoseconds and any eddy currents generated prior to excitation decay completely before influencing the RF signal. Gradient-induced eddy currents can influence phase accumulation after excitation but the effect is too small to image. The animal scanner images show no measurable phase accumulation. Measuring low-frequency conductivity by gradient-induced eddy currents is presently unfeasible.

Purpose

To investigate the B₀ orientation-dependent magnetic susceptibility of collagen fibrils within the articular cartilage and to determine whether susceptibility tensor imaging (STI) can detect the 3D collagen network within cartilage.

Methods

Multiecho gradient echo datasets (100-μm isotropic resolution) were acquired from fixed porcine articular cartilage specimens at 9.4 T. The susceptibility tensor was calculated using phase images acquired at 12 or 15 different orientations relative to B₀ . The susceptibility anisotropy of the collagen fibril was quantified and diffusion tensor imaging (DTI) was compared against STI. 3D tractography was performed to visualize and track the collagen fibrils with DTI and STI.

Results

STI experiments showed the distinct and significant anisotropic magnetic susceptibility of collagen fibrils within the articular cartilage. STI can be used to measure and quantify susceptibility anisotropy maps. Furthermore, STI provides orientation information of the underlying collagen network via 3D tractography.

Conclusion

The findings of this study demonstrate that STI can characterize the orientation variation of collagen fibrils where diffusion anisotropy fails. We believe that STI could serve as a sensitive and noninvasive marker to study the collagen fibrils microstructure. Magn Reson Med 78:1683-1690, 2017. © 2017 International Society for Magnetic Resonance in Medicine.

Birth defects of the heart and face are common, and most have no known genetic cause, suggesting a role for environmental factors. Maternal fever during the first trimester is an environmental risk factor linked to these defects. Neural crest cells are precursor populations essential to the development of both at-risk tissues. We report that two heat-activated transient receptor potential (TRP) ion channels, TRPV1 and TRPV4, were present in neural crest cells during critical windows of heart and face development. TRPV1 antagonists protected against the development of hyperthermia-induced defects in chick embryos. Treatment with chemical agonists of TRPV1 or TRPV4 replicated hyperthermia-induced birth defects in chick and zebrafish embryos. To test whether transient TRPV channel permeability in neural crest cells was sufficient to induce these defects, we engineered iron-binding modifications to TRPV1 and TRPV4 that enabled remote and noninvasive activation of these channels in specific cellular locations and at specific developmental times in chick embryos with radio-frequency electromagnetic fields. Transient stimulation of radio frequency-controlled TRP channels in neural crest cells replicated fever-associated defects in developing chick embryos. Our data provide a previously undescribed mechanism for congenital defects, whereby hyperthermia activates ion channels that negatively affect fetal development.