Permittivity of ex vivo healthy and diseased murine skeletal muscle from 10 kHz to 1 MHz

A better understanding of the permittivity property of skeletal muscle is essential for the development of new diagnostic tools and approaches for neuromuscular evaluation. However, there remain important knowledge gaps in our understanding of this property in healthy and diseased skeletal muscle, which hinder its translation into clinical application. Here, we report the permittivity of gastrocnemius muscle in healthy wild type mice and murine models of spinal muscular atrophy, muscular dystrophy, diabetes, amyotrophic lateral sclerosis and in a model of myofiber hypertrophy. Data were measured ex vivo from 10 kHz to 1 MHz using the four-electrode impedance technique. Additional quantitative histology information were obtained. Ultimately, the normative data reported will offer the scientific community the opportunity to develop more accurate models for the validation and prediction of experimental observations in both pre-clinical and clinical neuromuscular disease research.


Background & Summary
Electromagnetism constitutes a basic physical principle widely used in the field of biomedical engineering, designed to monitor and treat a broad spectrum of conditions including Parkinson's disease 1 and brain tumors 2,3 . Understanding how different biological tissues and fluids interact with electromagnetic fields is essential for improving the accuracy of existing analytical techniques as well as developing new diagnostic tools and therapies.
In electromagnetism, permittivity is one fundamental material parameter affecting the propagation of electromagnetic fields. When exposed to an electromagnetic field, the dipole moment of the material's molecules opposes the external electric field and so the net electric field is reduced within the material. In other words, the permittivity is a measure of the ability to store an electric charge in the polarization of the material.
Basic and applied scientific endeavors have reported the permittivity property for well over 100 years in a collective effort to understand the propagation of electromagnetic fields in the human body [4][5][6][7][8][9][10][11][12][13] . The birth of biomedical engineering and the field of electrophysiology arose from these pioneers' early multidisciplinary studies applying new theory, tools and methods. For example, voltage clamp and telegrapher's equations made it possible to understand how ionic currents give rise to the action potential 14 . Another prominent contribution that emerged from studying tissues' permittivity includes the development of the bidomain model to study cardiac muscle, which laid the foundation for the development of implantable cardiac pacemakers.
Previous studies have reported permittivity values of specific tissue as a function of the applied frequency. However, a recent meta-analysis revealed that major gaps in the knowledge of the frequency-dependence of the conductivity and relative permittivity in many tissues still exist 15 , especially for those tissues such as skeletal muscle, in which these properties are directionally dependent [16][17][18][19][20] . For example, prior authors acknowledged the technical limitations of their reported paravertebral muscle permittivity values nominally measured along and across the muscle fiber directions 21 .
In addition, some previous studies of the permittivity property of biological specimens did not specify the state of the tissue examined, even though it is known that the permittivity values change postmortem 22 and with temperature 23 , nor did they specify the extent of disease, if any, present, and some did not include healthy control www.nature.com/scientificdata www.nature.com/scientificdata/ tissue for comparison. Other noteworthy factors that have not been exhaustively evaluated include the variation of tissues' permittivity with age, gender, and disease progression. This missing information highlights critical gaps in our understanding of the factors that affect the permittivity property of biological tissues required to aid in identification of clinically abnormal results in pathological tissue.
The present study is motivated by the need to obtain permittivity values from both healthy and diseased skeletal muscle to aid in the diagnosis and monitoring of patients with neuromuscular disorders (NMDs). Analysis of muscle histology performed over the course of disease progression has shown that the composition and structure of skeletal muscle tissue changes as a function of the specific NMD. For example, in amyotrophic lateral sclerosis (ALS) muscle fibers tend to atrophy over time 24 , whereas in Duchenne muscular dystrophy, the lack of dystrophin protein 25 , causes a loss of muscle fibers and their progressive substitution by fat and fibrous tissue 26 .
Changes in the permittivity property in diseased muscle establishes the underlying scientific premise of electrical impedance myography (EIM) 27,28 , a relatively new electrodiagnostic technique that is gradually finding its niche for the assessment of NMD progression and the success of therapeutic intervention 29 . EIM is a non-destructive technique that is based on the measurement of the electrical impedance of individual muscles or groups of muscles. The permittivity property of the muscle can be extracted from the EIM values by accounting for the experimental setup. To date, however, EIM studies that have reported permittivity values of diseased muscle are scarce and often the data are incomplete, evaluating permittivity values at only a single frequency 30 . For www.nature.com/scientificdata www.nature.com/scientificdata/ EIM to achieve its full potential, it is paramount to first establish normative permittivity values in the frequency range where the histological alterations in disease would be expected to have an effect.
Here, using EIM technique, we report the conductivity and relative permittivity values of mouse muscle in healthy and four disease models (i.e., spinal muscular atrophy, muscular dystrophy, diabetes, amyotrophic lateral sclerosis) and in a drug-induced model of myofiber hypertrophy, which represents an all-encompassing effort by www.nature.com/scientificdata www.nature.com/scientificdata/ our group over the course of the last three years. The objective of this report is to equip the reader with a comprehensive database of the permittivity properties of healthy and diseased skeletal muscle from 10 kHz to 1 MHz, in both longitudinal and transverse directions. We also include additional quantitative histology data and periodic measurements obtained during disease progression. Providing the permittivity of healthy and diseased muscle

Methods
Terminology and definitions. The permittivity ε determines the dielectric behavior of materials when exposed to an applied electric field and it is defined as (dimensionless) www.nature.com/scientificdata www.nature.com/scientificdata/ r 0 ɛ ɛ ɛ where ε r is the relative permittivity (dimensionless), σ is the total conductivity of the material (S m −1 ), ω is the (angular) frequency of the field measured (rad s −1 ), ε 0 = 8.85 · 10 −12 is the permittivity of the vacuum (F m −1 ), and i is the imaginary unit (dimensionless). In skeletal muscle, due to its highly organized cellular and fascicular structure, the permittivity is different along and perpendicular to the direction determined by the myofibers orientation 31 . Here, we calculated the longitudinal and transverse conductivity and relative permittivity from longitudinal and transverse resistance R and reactance X muscle data measured using a dielectric cell with the four-electrode technique, obese/Diabetic mice. The DB/DB mouse (BKS.Cg-Dock7m +/+ Leprdb/J) was chosen as a model of diabetes type II and obesity [36][37][38][39] . Mice homozygous for the diabetes spontaneous mutation (Leprdb) become obese at approximately three to four weeks of age. Elevations of plasma insulin begin at 10 to 14 days and elevations of blood sugar at four to eight weeks. Homozygous mutant mice are polyphagic, polydipsic, and polyuric. These mice are well known for their obesity and for developing substantial intramuscular fat deposition by approximately 8 weeks of age. Ten male mice (5 weeks, JAX strain #000642) were studied at 6 and 20 weeks (5 mice per time point). Ten WT type C57BLKS/J (JAX strain #000662) served as controls (5 mice per time point).
Mice with myofiber hypertrophy. Twenty male wild type mice (C57BL/6J, 8 weeks of age, JAX strain #000664) were obtained. Starting at 9 weeks of age, mice were divided randomly into two groups of 10 mice per group. Mice were treated twice weekly with subcutaneous injections of either phosphate-buffered saline (PBS) or the myostatin ligand trap ActRIIB-mFc (Acceleron Pharma, Cambridge, MA, USA) at a dose of 3.3 mg/kg. ActRIIB-mFc (also termed RAP-031) 41 is a protein comprised of a form of the extracellular domain of ActRIIB fused to a mouse Fc that acts as a ligand trap to inhibit myostatin signaling. Animals were weighed weekly with an analytical balance (AS64, Adventurer SL, Ohaus Corporation, Pine Brook, NJ, USA) to ensure correct dosing www.nature.com/scientificdata www.nature.com/scientificdata/ throughout the course of the study. All procedures were performed after 5 weeks of treatment with ActRIIB-mFc. Dose-dependent impedance and functional data were published elsewhere 42 . Ex vivo analysis of excised gastrocnemius muscle. Following euthanasia via CO 2 inhalation, the gastrocnemius muscle was excised at its proximal extent just below the knee and distally by cutting the gastrocnemius tendon at its insertions, after removing the bicep femoris muscle. Each gastrocnemius muscle was trimmed with a scalpel to 5 mm (width) × 5 mm (length) centered at the belly of the muscle in order to fit into the dielectric measuring cell.
Dielectric cell. We used the dielectric cell described elsewhere 43 . Briefly, the dielectric cell was made of two flat plate stainless steel electrodes for applying electrical current side to side of the slab of muscle. The voltage electrodes were two monopolar EMG needles in contact the top surface of the muscle (Carefusion #902-DMG50-TP). The geometrical dimensions of the dielectric cell were 5 mm (width) × 5 mm (length), the muscle height measured with a caliper. The distance between the voltage electrodes was 4 mm. The slab of muscle was inserted into the cell first with the muscle fibers oriented parallel (longitudinal) and then perpendicular (transverse) to the current electrodes. The geometric factor K was determined from measurements of saline solution with the corresponding height of each tissue sample.

Statistical analysis.
Student's t-tests, two-tailed, significance p = 0.05 was used to statistically examine the myofiber cross sectional area difference between healthy and diseased muscle tissue as quantified through histological assessment of the muscle.

Histological analysis.
After ex vivo EIM measurements were completed, the left gastrocnemius was fixed in 10% formalin, embedded in paraffin and sectioned into 10 μm slices. Sections were stained with collagen VI antibodies (ab6588; Abcam, Cambridge, MA, USA) to identify the cell membrane and with 4′,6-diamidino-2-phenylindole to stain nuclei. Individual sections were viewed at 20X and photographed with an epifluorescence microscope (Axio Imager M1, Zeiss, Oberkochen, Germany). Myofiber area was identified and analyzed with FIJI (ImageJ, NIH) using the muscle morphometry plug-in (Anthony Sinadinos using Eclipse IDE) to calculate the cross sectional area of the myofibers. On average, ~250 fibers were counted per muscle. Careful attention was paid to measure all cells that appeared to be myofibers, with the goal of measuring representative fields that accurately reflected the overall status of the muscle.

Data Records
The dataset described is freely available in PhysioNet 44 . The format of the data files is the same for healthy and diseased muscle conditions. The anisotropic permittivity property measured in longitudinal and transverse directions is organized in columns while the frequency dependence is organized in rows. For each time point measured, which also is organized in columns, the permittivity average value and the standard error of the mean are reported.

technical Validation
Our murine data on SMA (Fig. 1), MDX (Fig. 2), DB/DB (Fig. 3), ALS (Fig. 4), and a model of myofiber hypertrophy (Fig. 5) fill the gap of previous studies published in the literature. A single-frequency summary of conductivity values is provided in Table 1 (multi-frequency data are available in PhysioNet). Regarding the relative permittivity (not shown), we found the longitudinal values were greater than in transverse direction in the low frequencies, an observation that had been previously attributed to the polarization of the t-tubule muscle system 20,31,45 .
In the absence of in vivo human muscle permittivity values, mouse muscle permittivity data reported here allow the user to approximate, through the use of analytic models, EIM values for the conditions studied. It also gives the user the ability to predict the temporal evolution with disease progression using the permittivity from different time points. For example, EIM phase angle θ can be computed in the longitudinal and transverse direction as follows where f is the frequency in Hz. The reader can also use the permittivity reported to perform more accurate numerical simulation studies using finite element models for example.

Code availability
The algorithm used in this work to convert impedance data to permittivity is described in Eq. 2.