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In vivo online magnetic resonance quantification of absolute metabolite concentrations in microdialysate

Scientific Reports volume 6, Article number: 36080 (2016) | Download Citation

Abstract

In order to study metabolic processes in animal models of diseases and in patients, microdialysis probes have evolved as powerful tools that are minimally invasive. However, analyses of microdialysate, performed remotely, do not provide real-time monitoring of microdialysate composition. Microdialysate solutions can theoretically be analyzed online inside a preclicinal or clinical MRI scanner using MRS techniques. Due to low NMR sensitivity, acquisitions of real-time NMR spectra on very small solution volumes (μL) with low metabolite concentrations (mM range) represent a major issue. To address this challenge we introduce the approach of combining a microdialysis probe with a custom-built magnetic resonance microprobe that allows for online metabolic analysis (1H and 13C) with high sensitivity under continuous flow conditions. This system is mounted inside an MRI scanner and allows performing simultaneously MRI experiments and rapid MRS metabolic analysis of the microdialysate. The feasibility of this approach is demonstrated by analyzing extracellular brain cancer cells (glioma) in vitro and brain metabolites in an animal model in vivo. We expect that our approach is readily translatable into clinical settings and can be used for a better and precise understanding of diseases linked to metabolic dysfunction.

Introduction

Microdialysis is a valuable tool for in vivo investigations and can be placed in many tissues and organs including brain for neurological investigations of Alzheimer1,2, brain tumors3, traumatic brain injuries4, neuronal functionality5 and pharmacokinetics of drugs6. In combination with magnetic resonance imaging (MRI), dialysate composition can be directly correlated with anatomical structures or pathological changes seen on MRI7,8. However, metabolic investigations of the dialysate are currently performed remotely and off-line from the MRI scanner9,10,11,12 due to the limited online sampling possibilities13,14. Integrating analytical devices within MRI scanners poses challenges (related to limited space and to magnetic interference), limiting the applications of correlation experiments. Here, we introduce a novel approach of online sampling of tissue dialysate under continuous flow utilizing a high resolution nuclear magnetic resonance (NMR) microprobe, closely coupled to an in vivo microdialysis inside an MRI scanner. We present two microprobes that allow for the online metabolic investigation at physiological concentrations (1H: 1.8 mM lactate in 60 s; 13C: 10.0 mM 3-13C lactate in 100 s). The applicability of the approach is demonstrated by investigating extracellular metabolites, from in vitro brain cancer cells and from in vivo microdialysate of rat brain.

Results

Micro-structured NMR/MRS probes have been fabricated in a variety of different geometries15,16,17,18,19,20,21,22,23,24,25,26,27,28 and have partly been applied to continuous flow investigations29,30 with solenoidal coils being the most sensitive to date15,16. Utilizing this fact with the goal of online detection of metabolites at physiological concentrations for in vivo studies, we have constructed two different microprobes with solenoidal geometry: a 1H-optimized probe tuned at 300 MHz and a 13C-optimized probe with unprecedented sensitivity tuned at 50 MHz.

The proton and carbon-13 microcoils are respectively interfaced and positioned inside MRI scanners operating at B0 = 7.0 T and B0 = 4.7 T (Fig. 1A,B), respectively. For both probes, the detected sample volume is 1 μL (2.4 mm in length and 750 μm in diameter) with an optimal filling factor of 92.5% (the ratio of the sample volume to the coil detection volume). The limits of detection (LOD) for the probes, corresponding to a signal-to-noise ratio (SNR) of 3, are 1.8 nmol in 60 s for the methyl protons (which corresponds to 5.4 nmol for one proton) of lactate and 10 nmol in 100 s for the carbon atoms in an enriched 3-13C lactate sample. Characteristics of the coils are summarized in Table 1 whereby the detection sensitivity has been normalized according to an established procedure (see ref. [25], equation 5 and Table 1) to a field strength of B0 = 14.1 T. The sensitivities amount to 12.7 nmol·s½ for the proton-optimized probe and 14.6 nmol·s½ for the carbon-optimized coil. The spectral resolution is optimized by placing the microcoil into a container filled with fluorinated solvent for increasing the magnetic field homogeneity at the site of the sample. The linewidths for the 1H- (B0 = 7 T) and 13C-optimized (B0 = 4.7 T) probes were determined using NMR lines from natural abundance and 13C-enriched lactate, respectively leading to proton linewidth of 15.0 Hz (0.05 ppm) and carbon linewidth of 3.5 Hz (0.07 ppm) inside the MRI scanners. The broadened line width can be explained by the increased susceptibility mismatch due to the proximity of the sample to the windings of the copper coil as has been previously investigated by Webb and coworkers31. Since we optimized the filling factor to over 90% we achieve a near optimal SNR but compromise the line-resolution. For 13C NMR experiments, a double resonant circuit, based on a single 13C-1H micro-size solenoid is used in transmit-receive mode (Fig. 1A). The circuit is optimized for 13C detection while the 1H channel can be used for the shimming procedure (homogenizing the magnetic field in the sample region). In addition, the 1H channel can also be utilized for proton decoupling in 13C experiments to further enhance the sensitivity, this being particularly useful for a 13C-enriched dialysate solution. Unlike the 13C microprobe, the 1H probe consists of two independent resonance circuits (Fig. 1B): a micro-solenoid is used for 1H excitation, detection and B0 shimming; the second resonant circuit, composed of a 1.5-cm diameter loop, is used as a 13C decoupling channel.

Figure 1: Experimental setups.
Figure 1

(A) Left: Circuit of the 1H/13C double resonant 13C-optimized probe for carbon detection at 50 MHz, right: photo illustration of the microprobe (red circles indicate the position of the microcoil). (B) Left: Circuit of the 1H- optimized probe for proton detection at 300 MHz with a separate 13C decoupling channel (75 MHz), right: photo illustration of the microprobe. (C) In vitro experiment utilizing a microprobe/microdialysis setup to collect and analyze extracellular glioma metabolites under a continuous flow. (D) In vivo setup to collect brain metabolites from a rat including the possibility of acquiring images of the brain with a surface proton coil (arrows indicate the flow of the buffer solution/dialysate).

Table 1: Probe characteristics.

The experimental setup for online in vitro and in vivo MR analysis of microdialysate is depicted in Fig. 1C,D. Inside the MRI scanner, a microdialysis probe is inserted in an Eppendorf tube containing cells or positioned inside the target’s brain region. The outlet-tube from the microdialysis is immediately passed through the microprobe for a real-time online metabolic profiling of the dialysate. Outside the scanner, the inlet-tube is connected to a syringe pump that continuously flows a buffer solution through the sample i.e., cells or brain.

In the in vitro study, we attempt to monitor the metabolism activities of cancer cells (glioma) supplied with 3-13C pyruvate. As shown in Fig. 1C, the microdialysis is placed inside a buffer solution containing U87-MG glioma cells. The MRS (magnetic resonance spectroscopy) acquisition begins as the 3-13C pyruvate is added to the suspension of cells. The MRS results from the subsequent sampling with the 13C and 1H microprobes are depicted in Fig. 2. With the 13C-optimized microprobe (Fig. 2A), signals for 13C labeled alanine, glutamine and lactate are detected in less than 17 minutes (B0 = 4.7 T) whereby most of the pyruvate has already been metabolized as confirmed by high-field spectroscopy experiments (see Methods section). The LOD for a measurement of 13C-enriched metabolites on a 17-minute timescale is 3.2 mM (i.e. 3.2 nmol in 1 μL), with a measured linewidth of 5.5 Hz. The same experiment was performed at B0 = 7 T with the 1H probe (Fig. 2B) by averaging over less than 4 minutes, and resulted in a LOD of 0.9 mM (900 pmol in 1 μL) for three protons of the methyl group of the 13C-enriched metabolites lactate, alanine and pyruvate (linewidth of 20.0 Hz) and an LOD of 1.4 mM for the two glutamine protons. Based on these LODs, single proton species are expected to be detectable if the concentration exceeds 2.7 mM (2.7 nmol in 1 μL). We note that alanine and lactate signals could be better distinguishable from each other with an improved linewidth; the existence of both metabolites was however confirmed by high field NMR spectroscopy at B0 = 11.7 T (see Methods information).

Figure 2: In vitro experiments on glioma cells.
Figure 2

(A) 13C spectrum of extracellular glioma metabolites in the dialysate after the addition of enriched 3-13C-pyruvate; acquired under continuous flow in 1000 s at B0 = 4.7 T (50 MHz). (B) 1H spectrum of extracellular glioma metabolites acquired after the addition of 3-13C-pyruvate at B0 = 7 T (300 MHz). The 1H-13C J-splitting shown in the spectrum indicates that the MRS-detected metabolites are originated from the supplied 3-13C-labeled pyruvate. (C) 13C decoupled spectrum shows the isotropic chemical shift signals of the metabolites from the microdialysate (differences in chemical shift compared to (B) are due to the Bloch-Siegert shift upon a strong decoupling field).

Differentiation between extracellular metabolites originating from the 13C enriched pyruvate substrate and other endogenous substrates can be performed (1) by observing J-splitting in the presence of 1JH,C coupling, and (2) by performing a subsequent 13C decoupling experiment after which only one singlet becomes visible for the 13C-enriched metabolites. For example, the spectrum from a 1H single-pulse experiment, Fig. 2B, displays the J-splitting for 13C-enriched pyruvate, glutamine, lactate and alanine. For residual pyruvate a J-splitting of 1JH,C ≈ 123 Hz was observed and for glutamine 1JH,C ≈ 130.6 Hz. The splitting of the “combined” lactate and alanine species corresponds to 129.8 Hz. Conversely, only isotropic chemical shift signals are observed in the 13C-decoupled experiment in Fig. 2C. Moreover, the direct 13C detection from 13C experiment also exhibits three distinct metabolite signals. These 1H and 13C spectroscopic results clearly confirm the presence the 13C-enriched metabolites in the dialysate; and thus, they indicate that the infused 13C-pyruvate has been metabolized by the cells.

In the in vivo study on a rat model, the microdialysis was inserted into the cortex of the rats’ brain via a guide cannula and connected to the inlet of the 1H probe. Under continuous flow with buffer solution that included 3 mM of DOTAREM® (Gd-DOTA and meglumine), the dialysate brain metabolites were analyzed. The gadolinium contrast agent serves three purposes: (1) monitoring the activity of the microdialysis inside the rat brain using MRI (Fig. 3A); (2) shortening the 13C longitudinal relaxation time for faster NMR acquisition; and (3) serving as an internal reference (the line of the meglumine methyl 1H appears at 2.8 ppm) for the NMR chemical shift as well as for the concentration. Fig. 3B depicts the time course for the in vivo experiments. In the beginning, when the perfusate flow is started, only protons of water and protons from meglumine are detected by the microcoil. The dialysate reaches the microcoil after 35 minutes and the extracellular brain metabolites become detectable at 1.2 ppm in the 1H NMR spectrum (0.7 mM concentration). The 35 minutes delay is due to the approximately 18 μL volume of tubing placed between the rat and the RF coil. This delay can be significantly reduced using shorter tubing with a smaller inner diameter. We expect that with an optimized tubing the volume can be reduced down to 1 μL which will allow for acquiring the first spectrum within a few minutes, making it more practical for in vivo use with patients. After 43 minutes the equilibrium concentration of lactate from the rat brain can be detected, which stays constant over the course of the experiment (139 minutes). The comparison with the meglumine standard reveals that a concentration of 1.1 mM extracellular lactate from the brain is detected at equilibrium. The existence of the lactate metabolite was further proven by high-field NMR spectroscopy (see Methods section).

Figure 3: In vivo experiments.
Figure 3

(A) T1-weighted MR images in axial (top) and sagittal (bottom) planes of microdialysis probe positioning before (left images) and after (right images) flowing the perfusate. The bright area demonstrates the diffusion of Gd-DOTA through the microdialysis membrane into the rat brain. (B) Time course of the spectroscopy experiments with the 1H-optimized microprobe at B0 = 7 T. The bottom line is the starting spectrum at t = 0 in which only the meglumine standard (left peak at 2.7 ppm) is visible. After t = 35 min lactate becomes observable (right peak at 1.3 ppm), the equilibrium is reached after 43 minutes (i.e. no increase in lactate concentration is visible over the course of a 139-minute experiment) and 1.1 mM lactate is detected in the dialysate under continuous flow and 3 minutes and 50 seconds of NMR acquisition.

With respect to translatability to clinical patients, we see great potential in combination with ultrahighfield MRI systems for which wholebody scanners up to 7T exist32. Although we present in our article the study of the brain in animal models, we would like to note that the use of microdialysis in connection with clinical patients is possible in many different organs. For examples, microdialysis probes have been applied to breast cancer research, and to liver, adipose tissue or skeletal muscle in vivo studies of patients33,34,35. Furthermore, clinical studies to probe pharmacokinetics and visualization with gadolinium contrast agents have been performed previously. However with the approach present here, it is now possible to carry out the measurement inside the MRI scanner without the necessity of performing the analysis at a remote place36. An advantage with clinical patients is that larger microdialysis membranes are used for sampling37. Thus, higher amounts of sample can be analyzed in slightly larger NMR microprobes which will further increase the SNR. Lastly, we expect that the microprobes are not only combinable with surface coil but could also be used together with volume coils. In this case, care has to be taken that the microprobe is still mounted inside a homogeneous region of the MRI system but far enough away from the imaging region to prevent artifacts.

We expect that the online MR metabolic analysis of microdialysate presented in this study opens new perspectives for metabolite profiling. The particular strength of the approach lies in the possibility to perform metabolic analysis in rapid succession of imaging experiments on a timescale of 3 to 20 minutes in order to investigate the metabolic evolution under chemiotherapeutic treatment or neural activity. As proof-of-principle in vivo experiments, we have successfully detected highly concentrated lactate (1.1 mM in the dialysate) with the microcoil. Lower concentrated metabolites are expected to become detectable with lower flow rates allowing for an improved exchange of metabolites into the membrane and by improving the microprobe. Further increases in resolution and sensitivity can be expected by utilizing higher order shims, by increasing the microcoil volume or by building microcoils for MRI scanners operating at higher magnetic fields.

The application of this combined microprobe and microdialysis systems is not only limited to the brain study, but it can also be implemented in other organs or living tissues. As microdialysis probes are being used in vivo in humans4 and microcoil probes are being utilized for human exploration18, we further expect that the MR approach presented here could be applied in clinical settings.

Methods

Microcoil design

The double-parallel microcoils (length = 2.4 mm) were handwound with 30 μm (13C probe, 80 windings) or 62.5 μm (1H probe, 38 windings) copper wire around a polyimide tubing (inner diameter = 750 μm and outer diameter = 780 μm) that was supported during the winding process by a glass capillary and was removed afterwards. The lower and upper end of the coil are supported by a larger polyimide tubing (inner diameter = 800 μm and outer diameter = 858 μm), eliminating the necessity of using glue, which may compromise the probe’s quality, for coil fixation. The coils were placed inside a 2 ml Eppendorf tube which was filled with FC-70 fluid.

Chemicals

Sodium L-lactate-3-13C solution, Sodium pyruvate-3-13C, D2O and all the inorganic salts were purchased from Sigma-Aldrich (St Louis, MO, USA), and used without further purification. Dotarem® was provided by Guerbet Group (Villepinte, France). The culture medium DMEM, the biological buffers, foetal calf serum (FCS), penicillin-streptomycin mixture, and trypsin were purchased from Gibco Corp - Thermo Fisher Scientific (Waltham, MA, USA).

Cell culture

Human glioblastoma U87-MG cell line, purchased by ATCC (LGC standards, Middlesex, UK), were cultured as monolayer at 37 °C in a 5% CO2-containing humidified atmosphere. The culture medium was composed of Dulbecco’s modified eagle medium (DMEM low glucose content and contains L-glutamine, reference 31885) supplemented with 10% (v/v) heat-inactivated FCS, 100 IU/mL penicillin, and 100 IU/mL streptomycin.

Experimental cell setup

Cells were separated from DMEM by centrifugation and washing with PBS buffer prior to the experiment. 7 × 106 cells were suspended in 300 μL of PBS buffer within an Eppendorf tube. With the aim of keeping the cells in suspension, a plastic tubing connected to an infusion pump for air injection was inserted into the cells solution leading to continuous stirring. The cell suspension was heated to 37 °C in all experiments with external circulating warm water. The temperature was checked with a thermocouple. No temperature induced shift in the resonances was observed during the experiments. A microdialysis probe was placed into the cells suspension and infused with a buffer solution (PBS in D2O containing 3 mM Dotarem®) under a flux of 500 nL/min with the use of an infusion pump (Legato 110, Phymep, Paris, France). The outlet tube of the microdialysis probe was inserted into the microcoil tube to analyse the dialysate by MR spectroscopy. 3–13C sodium pyruvate solution was added to yield an overall concentration of 150 mM. The experiment was continuously performed for 2 hours.

Additionally, a control experiment without 13C-pyruvate was performed (Fig. 4).

Figure 4: 1H spectrum of an in vitro control experiment.
Figure 4

Upon the absence of 3-13C pyruvate no 13C enriched source is detected. Lactate in natural abundance from an internal source is detected which is identified in the high field spectrum as well during the 13C experiments (see Fig. 5). However no other metabolites are identifiable in this control experiment.

Animal model

Adult female Wistar rats of 250 g weights were purchased from Charles River Laboratories and kept in standard housing (12 h light-dark cycles) with a standard rodent chow and water available ad libitum. Before the beginning of the experiment, the animals were acclimatized in a temperature-controlled environment for one week. Experiments were performed according to the national regulations and were approved by the research ethics committee of the University of Bordeaux. The animals were anesthetized with 2.5% isofluorane in a mixture of N2/O2 (70:30) via a facial mask.

Microdialysis Implantation

Microdialysis CMA7 metal free catheters (CMA microdialysis AB, Solna, Sweden) with molecular weight cutoffs of 6 kDa were sterilized and inserted into the brain of healthy rats. Sterile surgical procedures were used during the implantation of the microdialysis probes. The rats were deeply anesthetized and positioned in a stereotaxic instrument. The head was shaved and the skull was incised coronally between the ears, along the interaural line. Three small holes were created in the skull using a micro drill. In two holes, plastic screws were inserted while in the third hole a cannula guide was placed. The screws and the guide were fixed on the skull with dental glue and then the muscles and the skin were sutured. Following the surgery, the animals were housed individually and received doses of buprenorphine 0.05 mg/kg every 12 hours for 48 hours. Typically, the MR experiments took place 24 hours after the surgery.

In vivo setup

The rat was positioned in prone position and the microdialysis was placed into the guide reaching the targeted region of the brain. A 8 mm surface dual channel-coil (Doty Scientific, Columbia, South Carolina) was placed over the microdialysis probe on the rat head. MRI T1 weighted scans (Flash sequence, Repetition Time 75.51 ms, Echo Time 2.6 ms, 6 averages, acquisitions time 1.25 min, matrix size 256 × 256, slice thickness 1 mm, Field of View 35 × 35 mm) were performed to assess the well-positioning of the microdialysis probe and the effective release of Dotarem® in the cortical region. The outlet tube of the microdialysis probe was inserted into the microcoil tube to analyse the dialysate by MR Spectroscopy. The microdialysis probe was infused with a buffer solution (PBS in D2O containing 3 mM Dotarem® 3 mM) under a flux of 500 nL/min.

MR Experiments

1H experiments, in vitro and in vivo, were performed on a Bruker Biospec 12-cm bore 7.0 T using Paravision 6.0 software. A series of spectra (Single-pulse sequence, Repetition Time 1145 ms, 200 averages, acquisition duration 511.2 ms, spectral resolution 1.00 Hz/points, excitation pulse length 7.5 μs, flip angle 35°, excitation pulse power 250 mW, acquisition time 3.82 minutes, water suppression pulse, decoupling pulse) was acquired to check the metabolic evolution of dialysate.

13C experiments on U-87 cells were performed on a Bruker Biospec 12-cm bore 4.7 T using ParaVision 6.0 software. A series of spectra (Single Pulse sequence, Repetition Time 501.3 ms, 2000 averages, acquisition duration 500.0 ms, spectral resolution 1.00 Hz/points, excitation pulse length 10 μs,flip angle 50°, excitation pulse power 125 mW, acquisition time 16.71 minutes, decoupling pulse) was acquired to check the metabolic evolution of the dialysate.

High-field analysis of dialysates

High spectral resolution NMR experiments were performed on a Bruker DPX 500 MHz equipped with a BBI probe to confirm metabolites detection in MRI scanner. 1H spectra were obtained at 500.13 MHz through single pulse sequences (zg sequence, 128 scans, TD 16k, D1 1s) and single pulse with water suppression sequences (zgpr, 128 scans, TD 16k, D1 3s). 13C spectra were obtained at 125 MHz through single pulse excitation with power gate decoupling sequences (zgpg sequence, 128 scans, TD 16k, D1 1s). 2D HSQC 1H/13C acquisition was performed to determine the metabolites originating from enriched 13C pyruvate. We would like to note, that the observed metabolites in the high- field spectra depicted in Figs 5, 6, 7, 8 may have a different concentration than in the microcoil experiments since the spectroscopy experiment was run with the complete dialysate instead of measuring small portions of it.

Figure 5: 13C spectrum of the in vitro dialysate (dialysis experiment performed at B0 = 4.7T) detected at B0 = 11.7 T.
Figure 5
Figure 6: 1H spectrum of the in vitro dialysate (dialysis experiment performed at B0 = 7T) detected at B0 = 11.7 T.
Figure 6
Figure 7: HSQC (Heteronuclear Single Quantum Correlation) spectrum of the in vitro dialysate (dialysis experiment performed at B0 = 7T) detected at B0 = 11.7 T to confirm the existence of 13C labeled metabolites.
Figure 7
Figure 8: 1H spectrum of the in vivo dialysate detected at B0 = 11.7 T.
Figure 8

Ethical approval.

Experiments were carried out following the INSERM (Institut National de la Santé et de la Recherche Médicale) guidelines regarding the fair treatment of animals with approval of the Comité d’Ethique en Expérimentation Animale de Bordeaux.

Additional Information

How to cite this article: Glöggler, S. et al. In vivo online magnetic resonance quantification of absolute metabolite concentrations in microdialysate. Sci. Rep. 6, 36080; doi: 10.1038/srep36080 (2016).

Publisher’s note: Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

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Acknowledgements

The authors acknowledge funding by the Laboratory of Excellence TRAIL ANR-10-LABX-57 (research program Oncoflux). Dr. Wong acknowledges the support of the Agence Nationale de la Recherche ANR-12-JSV5-0005.

Author information

Author notes

    • Stefan Glöggler
    •  & Silvia Rizzitelli

    These authors contributed equally to this work.

Affiliations

  1. ISM, UMR 5255, Université Bordeaux, 33076, Bordeaux, France

    • Stefan Glöggler
    • , Silvia Rizzitelli
    • , Noël Pinaud
    • , Vanessa Zhendre
    •  & Yannick Crémillieux
  2. RMSB, UMR 5536, Université Bordeaux, 33076, Bordeaux, France

    • Gérard Raffard
    • , Véronique Bouchaud
    •  & Stéphane Sanchez
  3. CEA I2BM NeuroSpin, 91191, Gif-sur-Yvette, France

    • Guillaume Radecki
    •  & Luisa Ciobanu
  4. NIMBE, CEA, CNRS, Université Paris-Saclay, CEA Saclay, 91191, Gif-sur-Yvette, France

    • Alan Wong

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Contributions

S.G., S.R., A.W. and Y.C. conceived and designed the experiments. S.G., S.R., N.P., G.R., V.Z., V.B., S.S. and Y.C. performed the experiments. G.R., L.C. and A.W. provided expertise. All authors reviewed the manuscript. S.G. and S.R. contributed equally to this work.

Competing interests

The authors declare no competing financial interests.

Corresponding author

Correspondence to Yannick Crémillieux.

About this article

Publication history

Received

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Published

DOI

https://doi.org/10.1038/srep36080

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