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Citation for the original published paper (version of record):

Andersson, G., Orädd, G., Sultan, F., Novikov, L N. (2018)

In vivo Diffusion Tensor Imaging, Diffusion Kurtosis Imaging, and Tractography of a
Sciatic Nerve Injury Model in Rat at 9.4T
Scientific Reports, 8: 12911
https://doi.org/10.1038/s41598-018-30961-1

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OPEN In vivo Diffusion Tensor Imaging,

Diffusion Kurtosis Imaging, and
Tractography of a Sciatic Nerve
Received: 25 April 2018
Accepted: 24 July 2018 Injury Model in Rat at 9.4T
Published: xx xx xxxx
Gustav Andersson1,2, Greger Orädd1,3, Fahad Sultan1 & Lev N. Novikov1

Peripheral nerve injuries result in severe loss of sensory and motor functions in the afflicted limb. There
is a lack of standardised models to non-invasively study degeneration, regeneration, and normalisation
of neuronal microstructure in peripheral nerves. This study aimed to develop a non-invasive evaluation
of peripheral nerve injuries, using diffusion tensor imaging (DTI), diffusion kurtosis imaging (DKI), and
tractography on a rat model of sciatic nerve injury. 10 female Sprague Dawley rats were exposed to
sciatic nerve neurotmesis and studied using a 9.4 T magnet, by performing DTI and DKI of the sciatic
nerve before and 4 weeks after injury. The distal nerve stump showed a decrease in fractional anisotropy
(FA), mean kurtosis (MK), axonal water fraction (AWF), and radial and axonal kurtosis (RK, AK) after
injury. The proximal stump showed a significant decrease in axial diffusivity (AD) and increase of MK
and AK as compared with the uninjured nerve. Both mean diffusivity (MD) and radial diffusivity (RD)
increased in the distal stump after injury. Tractography visualised the sciatic nerve and the site of injury,
as well as local variations of the diffusion parameters following injury. In summary, the described
method detects changes both proximal and distal to the nerve injury.

Peripheral nerve injuries are frequently caused by minor accidents, traumatic injuries, surgery or disease. They
often result in severe loss of both sensory and motor functions in the afflicted limb. Although surgical techniques
have improved over the last decades, there is still a lack of good clinical outcomes, and some permanent loss in
function is often expected following traumatic nerve injury. There is a lack of reliable imaging techniques to spec-
ify the type of nerve injury, and to follow regenerating nerves in the clinical setting, but also in preclinical animal
models to non-invasively study the regeneration and normalisation of neuronal microstructure in peripheral
nerves. These would provide the research community with reproducible models for assessment of novel nerve
treatment regimes.
Magnetic resonance imaging (MRI) has become the gold standard for visualisation of the central nervous sys-
tem, but ultrasound and computer tomography are also important diagnostic tools when it comes to the nervous
system as a whole1. Following experimental injury, peripheral nerve damage can be visualised on MRI already
after 24 hours with a hyperintense T2 signal due to intra- and perineural edema2, but diagnostics are primarily
based on clinical and electromyographic findings1. Development of diffusion-based imaging techniques have
been introduced in order to produce in vivo reconstruction of peripheral nerves and possibly improve the diag-
nostic capabilities of MRI3–5.
Diffusion tensor imaging (DTI) can be employed to elucidate tissue architecture through the use of direc-
tionally varying gradient fields and by processing the recorded signal into a diffusion tensor. The DTI technique
is based on signal attenuation derived from the degree of restriction that water molecules are subjected to when
diffusing along the axis of the applied gradient. By registering the signal decay from multiple directions, the dif-
fusion in a given tissue, its orientation, and quantitative anisotropy can be modelled6,7. Parameters derived from
the diffusion tensor include the Fractional Anisotropy (FA); molecular diffusion rate, i.e. the Mean Diffusivity
(MD) or Apparent Diffusion Coefficient (ADC); as well as the axial diffusion rate (AD, or λ//) and radial diffusion

1
Department of Integrative Medical Biology, Umeå University, Umeå, Sweden. 2Department of Surgical and
Perioperative Science, Section of Hand and Plastic Surgery, Umeå University, Umeå, Sweden. 3Umeå Center for
Comparative Biology (UCCB), Umeå University, Umeå, Sweden. Correspondence and requests for materials should
be addressed to G.A. (email: [email protected])

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rate (RD, or λ⊥). Due to its primarily axonal architecture, water diffusion is anisotropic in healthy nerve fibres7,
and a multitude of studies have used this fact to attempt to describe pathological changes in the central nervous
system, CNS8–10 but legitimate concerns have been raised that DTI is incapable of fully distinguishing one type of
pathology from another11,12 and overinterpretation of what the DTI data represents from a structural or patho-
logical point of view should be avoided13. It is thus important to be careful in interpreting the cause of changes to
the DTI parameters. A technique that has the potential to further delineate microstructural aspects of CNS white
matter is diffusion kurtosis imaging (DKI). DTI is based on the assumption that water diffusion is Gaussian and
is thus unable to completely characterise tissue microstructure12,14. DKI, on the other hand, calculates parameters
while taking into account non-Gaussian diffusion, and may provide more information about heterogeneity of
nerve structures15–19. DKI has been shown to detect pathological processes where DTI does not, such as increase
in mean kurtosis (MK) long after MD changes have normalised14. The most common DKI parameters used aside
from MK, which corresponds to the average of the diffusion kurtosis along all diffusion directions, is axial kurto-
sis (AK) and radial kurtosis (RK) which describe the kurtosis along the axial and radial direction of the diffusion
ellipsoid respectively12. Further DKI data set derived parameters include axonal water fraction (AWF), intra- and
extra-axonal diffusivities, and the tortuosity, which can provide detailed information about microstructure of
highly aligned fibre bundles20.
A further application of DTI and DKI is performing tractography. With this technique it is possible to gener-
ate 3D reconstructions of neuronal fibres by use of tracking algorithms based on the calculated diffusion tensors
or the kurtosis diffusion orientation distribution function (dODF)21–24. DTI tractography has primarily been
employed in the CNS in order to describe the neuronal pathways, but it has been shown possible also for periph-
eral nerves25 where it has been used to study different pathologies such as nerve entrapment3, traumatic injury26
and tumour growth5. Ex vivo studies have shown that tractography is possible on chemically fixed peripheral
nerves27,28, and the in vivo DTI findings of crush injury has been compared with histology26,29 but without trac-
tography. A nerve injury model typically involves the sacrifice of the research animal at each time point of interest
in order to study the neuronal regeneration microscopically or by biochemical examinations, but in order to
adhere to the principles of ethical animal research, also known as the 3 R’s (Reduce, Replace, Refine), one should
constantly strive towards reducing the number of animals and minimise the suffering they endure in all fields
of research even further30. A non-invasive imaging technique could decrease the number of animals needed to
follow degenerative and regenerative changes in peripheral nerves as the same animal can be studied at multiple
timepoints, instead of sacrificing animals for histological examination at each timepoint. Furthermore, an imag-
ing protocol minimising scan times would also lower the risk of adverse effects on said research animals as a result
of general anaesthesia.
The purpose of this study was to establish an animal model to non-invasively assess degeneration of the sciatic
nerves in rat by use of DTI and DKI following neurotmesis. We also wanted to examine the possibility to use
DTI-based tractography to visualise the sciatic nerve and the nerve defect following axotomy.

Results
At 4 weeks post-operatively, all experimental animals displayed visible atrophy of the calf muscles in the operated
leg. The DTI scans displayed a clearly discernible sciatic nerve that could be visualised in all three planes (sagittal,
coronal and transverse) both preoperatively and at the 4-week scan. No animals were lost during the experiment,
nor did they display any adverse effects such as autophagy of the hind limb or infection. The mean SNR was
67.4 ± 11 when positioning the ROI in the uninjured nerve. Positioning the ROI in the distal stump following
injury, the SNR was 107.6 ± 11.

B-value impact on diffusion tensor parameters at ROI.  Friedmans test showed that there was
no significant difference of the estimated FA between the different b-value scans and multi-shell data in the
pre-operative scan (p = 0.395), the proximal stump (p = 0.166), or the distal stump (p = 0.620) of the injured
sciatic nerve (Fig. 1a). For MD, AD, and RD, there was a trend of decreased parameters at higher b-values in the
distal stump which was statistically significant (MD, p = 0.003; AD, p = 0.006; RD, p = 0.043). AD and RD also
showed a decrease in the uninjured nerve/pre-operative scan (AD, p = 0.027; RD, p = 0.023) (Fig. 1b).

Effect of nerve transection on diffusion tensor parameters.  Following transection of the sciatic
nerve, a significant decrease was seen in the FA of the distal stump as compared to the uninjured nerve (p = 0.015)
and the proximal stump (p = 0.015). The median FA was 0.58 (IQR 0.57–0.59) in the uninjured nerves, 0.36 (IQR
0.35–0.38) in the distal stump, and 0.53 (IQR 0.49–0.55) in the proximal stump after nerve injury (Fig. 1a). There
was a trend of the FA of the proximal stump being increased compared to the uninjured nerve, but following
Bonferroni correction, it was not considered statistically significant (p = 0.063).
The median MD was significantly increased in the distal stump (1.41; IQR 1.33–1.44) following injury as
compared to the uninjured nerve (1.12; IQR 1.09–1.18) and the proximal stump (1.03; IQR 0.95–1.10) (Fig. 1b).
A trend of decreased MD in the proximal stump was seen, but it was not statistically significant (p = 0.063).
The median AD was significantly decreased in the proximal stump (1.70; IQR 1.55–1.85) after injury when
compared with the uninjured nerve (1.98; IQR 1.91–2.06) and the distal stump (2.00; IQR 1.96–2.04), respec-
tively. However, no significant differences were noted in the distal stump as compared to the uninjured nerve
(Fig. 1c).
The median RD was significantly increased in the distal stump (1.09; IQR 1.04–1.12) after injury when com-
pared with the uninjured nerve (0.69; IQR 0.68–0.73) and the proximal stump (0.70; IQR 0.62–0.73), respectively.
However, no significant differences were noted between the proximal stump and the uninjured nerve (Fig. 1d).
All these changes were also observed when the individual b-values were used instead of the multi-shell
approach, but with some notable differences. The slight FA-value decrease in the proximal stump (0.57; IQR

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Figure 1.  Results of ROI based analysis. Median FA (a), MD (b), AD (c), and RD (d) measured in ROI in the
uninjured nerve, the distal stump and the proximal stump, at different b-values and of the multi-shell approach.
Friedmans Test confirmed that MD, AD, and RD decreases with increasing b-value in the distal stump. The
same was seen for AD and RD concerning the uninjured nerve. Error bars indicate the interquartile range
of ROI measurements. P-values presented at the top represent Friedmans test of variations within the group.
Asterisks indicate a statistically significant difference compared to the uninjured nerve.

Figure 2.  Tractography results. FA (a), MD (b), AD (c), and RD (d) of the whole DTI tractography of the
uninjured nerve, the distal stump and the proximal stump, at different b-values and of the multi-shell approach.
Friedmans Test confirmed that MD, AD, and RD decreases with increasing b-value in all tracts except for the
AD in the distal stump. Error bars indicate the interquartile range of ROI measurements. P-values presented
at the top represent Friedmans test of variations within the group. Asterisks indicate a statistically significant
difference compared to the uninjured nerve.

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Figure 3.  Comparison of ROI analysis and tractography. Comparison of multi-shell FA (a), MD (b), AD (c)
and RD (d) between ROI measurement and tractography. A statistically significant decrease was seen in the
tractography compared to the ROI measurement in the uninjured nerve for FA, and AD whereas RD was higher
in the tractography. The MD and AD was lower in the distal stump in the tractography, and the same was seen
for FA in the proximal stump. Error bar indicate the interquartile range of ROI measurements.

0.54–0.58) after injury was statistically significant compared to the uninjured nerve (0.61; IQR 0.60–0.65) when
using a b-value of 1000 s/mm2 (p = 0.027). Further, the difference in AD-value between the distal (1.41; IQR
1.36–1.48) and proximal stump (1.08; IQR 0.99–1.10) following injury was only statistically significant at b-values
of 800 s/mm2 (p = 0.027) and 1000 s/mm2 (p = 0.050). Using a b-value of 600 s/mm2 allowed the detection of a
significant difference (p = 0.039) in RD between the proximal stump (0.62; IQR 0.55–0.66) and the uninjured
nerve (0.70; IQR 0.65–0.73), which was not seen in other b-values or when the multi-shell approach was used.

Tractography.  Tractography based on the DTI parameters defined in the Materials and Methods section showed
a significant difference of the averaged FA of the whole tract for the different b-values and multi-shell approach in the
preoperative scans (p = 0.004), the proximal stump (p = 0.006), and the distal stump following nerve injury (p = 0.032),
where the multi-shell displayed the lowest FA value. The MD, AD, and RD showed a trend of decreasing at higher
b-values compared to the lower b-values (Fig. 2), which was statistically significant for both preoperative scans, as well
as the proximal stump, with the exception of MD for the distal stump and RD for the proximal stump.
When comparing the tracts of the uninjured nerve, the proximal stump, and the distal stump, the same relative
changes of the diffusion parameters as seen in the voxel-based analysis were detected (Fig. 2), with the exception
of the multi-shell approach which showed a statistically significant decrease in the proximal stump as compared
to the uninjured nerve, while none of the individual b-values did.
The FA’s of the tracts were lower than that of the ROI-based analysis, except for in the distal stump where no
significant difference was seen (Fig. 3a). The MD values of the tracts were lower than in the ROI for the distal
stump (Fig. 3b), and AD was significantly higher in the voxel-based analysis, except for in the proximal stump
where the difference was not statistically significant (p = 0.051) (Fig. 3c). RD was significantly higher in the tracts
in the uninjured nerve, but not in the proximal or distal stump (Fig. 3d).
By rendering the tracts with a colour gradient based on the diffusion tensor parameters, the most proximal and
distal part of the tracts, which were close to the edge of the receptive field of the surface coil, displayed a drop in the
diffusion parameters (Fig. 4a). The tractography also showed a variation in the diffusion indices at different points
along the injured nerves, with marked changes at the distal end of the proximal stump (Fig. 4g). In the tract analysis
based on the multi-shell tractographies, the same trend could be seen with drop in diffusion parameters closer to the
edge of the receptive field (Fig. 5), and when approaching the nerve bifurcation into the tibial and peroneal nerves.
Variations in the proximal stump following injury was very evident between individuals (Fig. 5b,d,f,h).

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Figure 4.  Tractography rendered based on the DTI indices. Local variations in DTI indices along the nerve
following injury (e–h) in the sciatic nerve of one the experimental animals. The tractography displayed lower FA
(a,e), MD (b,f), RD (c,g), and (d,h) at the edge of the coil (a, solid arrow) in both injured and uninjured nerves.
Marked variations in DTI measurements could be detected locally compared to the rest of the nerve (hollow
arrow). Circles indicate positioning of ROIs. Bar = 10 mm.

Effect of nerve transection on kurtosis imaging parameters.  Following injury, the MK increased in
the proximal stump (1.33; IQR 1.16–1.61) and decreased in the distal stump (0.27; IQR 0.23–0.46) as compared
to the uninjured nerve (0.89; IQR 0.80-0.11) (Fig. 6a). The same was seen for axonal kurtosis (AK) where the
proximal stump (0.89; IQR 0.77–1.01) showed a statistically significant increase over the uninjured nerve (0.54;
IQR 0.38–0.61), as well as a significant decrease in the distal stump (0.21; IQR 0.17–0.37) (Fig. 6c).
AWF was significantly decreased in the distal stump (0.21; IQR 0.17–0.26) compared to the proximal stump
(0.46; IQR 0.43–0.57) and the uninjured nerve (0.46; IQR 0.43–0.48) (Fig. 6b). RK was significantly decreased in
the distal stump (0.50; IQR 0.26–0.72) compared to the proximal stump (2.05; IQR 1.46–2.22) and the uninjured
nerve (1.82; IQR 1.47–2.02) (Fig. 6d).

Discussion
In previous studies, peripheral nerves have been visualised using diffusion tensor imaging and tractography3,5,25,31.
Most DTI studies have used CNS as a model, and a standardised in vivo model of peripheral nerve injury is yet
to be established although some examples have been described26,29. In order to develop the foundation for clin-
ically applicable DTI techniques for peripheral nerve injury, and to follow the principles of the 3 R’s of animal
research, we used a protocol designed to minimize scan time but still produce reliable results for detection of
structural changes in the injured nerves. Furthermore, using this technique instead of histological studies at mul-
tiple time-points will drastically decrease the total number of animals needed in peripiheral nerve research as the
same animal can be scanned repeatedly.
Although DTI is considered less sensitive in detecting crossing fibres of neural tissue in the CNS compared
to other high-order diffusion methods such as high angular resolution diffusion imaging (HARDI)17,32–34, due to
the basic architecture of peripheral nerves with mainly longitudinally aligned fibres outside the branching points,
one would expect it to be sufficient for performing tractography. A combination of tractography and placement of
ROI’s to calculate FA, MD, AD, and RD, could provide information about not only the localisation of injury, but
also the directions and the extent of subsequent nerve regeneration. Whether DTI is sensitive enough to detect
certain characteristics of regenerating nerve tissue such as myelination and edema has been investigated35–37,
and it is becoming all the more evident that DTI parameters are not sensitive enough to detect specific biological

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Figure 5.  Tract Analysis Report of the preoperative and postoperative tractographies. The colored line represents
the median value of all research animals. The grey lines represent the individual research animals tractography
analysis report. Close to the edges of the coils receptive field the parameter estimates appear less precise, and the
same can be seen when approaching the nerve bifurcation. FA decreases when approaching the nerve injury (b).
MD increases distally of the nerve injury (d). AD is lower in the proximal stump than the uninjured nerve but is
higher in the distal stump (e & f). RD increase when approaching the nerve injury and is further increased in the
distal stump (h). Y-axis represents the individual DTI indices. X-axis represents length of tracts in mm.

processes (i.e. inflammation, demyelination etc)12. Here, DKI has proved more promising as it is less sensitive to
interference by local edema12 and has also shown increased sensitivity in detecting certain pathological condi-
tions in the central nervous system38 as compared to DTI. Our results suggest that information concerning FA

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Figure 6.  Diffusion Kurtosis Imaging results. MK shows a statistically significant decrease in the distal stump
and increase in the proximal stump following injury. AWF is decreased in the distal stump. AK is decreased in
distal stump and increased in the proximal stump. RK is decreased in the distal stump following injury.

of the structures of interest can be detected at the entire range of b-values (600–1200 s/mm2), but the minute
changes in the proximal stump were only statistically significant at 1000 s/mm2, whereas proximal stump changes
of MD, AD and RD where most readily detected at 600 s/mm2. These variations may be indicative of what b-value
range to study the proximal stump, and in clinical cases where the MRI scan does not visualise the site of periph-
eral nerve injury, a decrease in AD could be indicative of a more distal injury. AD decrease has previously been
seen in cases of axonal injury34 which would be expected in this injury model as well. This, however, needs to be
validated in future studies, and one major concern may be the result of the tensor model being misinterpreted due
to inflammatory reactions in the area of interest. It has been shown that AD will decrease as a result of increased
cellularity, and RD and AD both will be affected by vasogenic edema39. However, our DKI results also indicate
changes occurring in the proximal stump following the nerve injury as evident by the rise in MK which would
imply increase in tissue heterogeneity15. As MK is less prone to be affected by cellular infiltration and edema than
traditional DTI12 the extra scan time for obtaining the extra b-values needed for diffusion kurtosis estimation can
be motivated. The increase in AK of the proximal stump may be related to changes to the intra-cellular structures,
whereas changes to RK which was most marked in the distal stump is considered to be more influenced by cellular
membranes and myelin12, which are expected to be disrupted following Wallerian degeneration40 of the distal
nerve stump, and thus resulting in a lower RK.
For the purpose of this study, we chose to create a nerve lesion using sharp transection at the midpoint
between the sciatic notch and the distal nerve bifurcation into major branches to be able to clearly visualise it
using DTI based tractography as this would be on a relative “straight” course of the nerve in the thigh of the rat.
This type of injury is known to cause Wallerian degeneration of the distal stump, with demyelination41. This study

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Figure 7.  Surgically exposed sciatic nerve in left hind limb of rat.

did not aim to study the functional outcome of the denervation, nor the degree of regeneration, but rather the in
vivo application of DTI, DKI, and tractography on the peripheral nerve following injury.
Pilot studies showed that motion artefacts and ghosting was a complicating factor even though the animal
was sufficiently sedated. DTI is known for its susceptibility to motion artefacts and eddy current artefacts42.
Respiratory and/or cardiac gating may have alleviated some of these issues but would also increase the scan time
markedly. We therefore designed the setup in such a way that it helped to decrease any motion artefacts. The
sciatic nerve model was selected since it is localised far away from the respiratory tract and the heart, and there
are no directly neighbouring major vessels, which minimises the negative impact of these structures on the scans.
Parallel imaging (GRAPPA) and ghost correction was used when performing the scans, and post-processing with
motion correction and eddy current correction, was also employed to minimize any artefacts commonly seen in
DTI scans42.
The current study demonstrates that structural changes can be detected with DTI and DKI not only in the
distal nerve stump undergoing Wallerian degeneration, including demyelination, but also in the proximal stump
where one would expect axonal dieback, cellular infiltration and sprouting of nerve fibres41. Whether or not
the detected parameter changes relate to these specific processes cannot be answered by DTI alone, but of note
was the finding that AD decreased in the proximal stump after 4 weeks when compared with the uninjured
nerve, indicating that DTI can detect the reactive processes in this area and not only in the distal nerve stump41.
Looking at our results it is evident that tractography helps visualise the characteristics at different levels in the
nerve. Although there were statistically significant changes at the position of the ROI, the Tract Analysis Report
showed that these changes may be more evident closer to the injury site, and it is therefore important to look at
the diffusion-based parameters over the whole nerve in order to not misinterpret the results. It was also evident
that the diffusion imaging is affected closer to the edges of the coils receptive field, likely due to increased inho-
mogeneity of the magnetic field and/or lower signal42.
Although there were statistically significant differences between certain b-values for MD, AD, and RD, the
practical importance of these minute differences can be questioned. These changes were not large enough to lead
to misinterpretation of the integrity of the nerve.
However, the variability in results with different b-values in this study may be of importance when looking
for small changes in peripheral nerves, as certain b-values detected statistically significant changes in the diffu-
sion parameters that were not seen in others, but the added value of performing DKI is likely to outperform DTI
parameter analysis. Previous studies have suggested that an optimal b-value for visualising peripheral nerves
using traditional DTI is 800 s/mm23,26. DKI requires multiple b-values, but the minimum requirement suggested
is two b-values and 15 directions43, which should not result in unreasonably long scan times.
This study is limited in that we chose a narrow range of b-values, mainly because this range is most commonly
employed in clinical settings for DTI42, but it may be considered a weakness of this study to not include a higher
b-value for the DK estimation, as a combination of 1000 and 2000 s/mm2 has been suggested as an ideal setting
for DKI in clinical use43. Furthermore, the use of the FA-map when positioning the ROI could potentially be
problematic in case of nerve deterioration to the degree of showing a similar FA value as that of the surrounding
tissues. In this study it did not present any issues, as the nerve, including the distal stump, was clearly visible (see
“Supplementary Information Fig. 1”), but using an alternative type of scan may serve as a better map to position
the ROIs. Furthermore, the use of single ROIs in the analysis of proximal and distal stump after surgery does not
give a complete view of the varying diffusivities along the tract, nor does an average of the whole tract either, as
was evident by the tract analysis report.
In conclusion, with this study we set out to establish a diffusion-based model of peripheral nerve injury detec-
tion. We used a sciatic nerve injury model in rat and utilized a 9.4 T Bruker BioSpec 94/20 USR system to collect
diffusion-weighted images to calculate the diffusion tensors and kurtosis parameters in the region of interest. The
positioning of the experimental animal and scan parameters employed is described, and the effects upon diffusion
and kurtosis parameters of interest 4 weeks following nerve injury are presented.
Further improvements to the protocol can be made with adapting the number of directions and choice of
b-values, however changes in both the proximal and distal stump can be detected using the present setup. Further
studies are required to specify the gradual changes of degeneration and possible reinnervation of the distal stump

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Figure 8.  Greyscale FA map with ROI positioned in the sciatic nerve. Axial (a), sagittal (b) and frontal views (c)
were used to verify the placement of ROI. In vivo tractography of the uninjured sciatic nerve in rat is shown in
(d). Bar = 10 mm. For FA maps from additional subjects, see “Supplementary Information Fig. 1”.

following injury as seen by DTI and DKI, but this setup should provide a good tool for non-invasive evaluation
of these aspects.

Methods
Experimental animals and surgery.  The experiments were performed on adult (10–14 weeks old, n = 10)
female Sprague-Dawley rats (Charles River Laboratories). The animal care and experimental procedures were
carried out in accordance with Directive 2010/63/EU of the European Parliament and of the Council on the pro-
tection of animals used for scientific purposes and were also approved by the Northern Swedish Committee for
Ethics in Animal Experiments (No. A50-13). All surgical procedures were performed under general anaesthesia
using isoflurane (Attane vet, 1000 mg/g, Oiramal Healthcare, UK). After surgery, the rats were given the analgesic
Finadyne (Schering-Plough, Denmark; 2.5 mg/kg, s.c.).
Under sterile conditions the left sciatic nerve was exposed (Fig. 7) and cut with a pair of straight micro scissors
at a point 5 mm distal to the sciatic notch.
®
The proximal nerve stump was covered with a thin layer of Spongostan (Johnson & Johnson Medicals, UK)
to prevent spontaneous nerve regeneration into the distal nerve stump, and the muscles and skin were closed in
layers.

In vivo imaging.  MRI scans were performed at two time points; pre-operatively and 4 weeks post-operatively
on the same animals. The animals were scanned using a 9.4 T Bruker BioSpec 94/20 USR system connected to a
®
rat brain array coil combined with a 87 mm QUAD resonator coil and running ParaVison 6.1 software (Bruker
Biospin Group, Bruker Corporations, Germany) under isoflurane anaesthesia. Respiration was monitored using
a respiration pillow (SA Instruments Inc., Stony Brook, USA).
The animals were positioned in a right lateral decubitus position with the brain array coil positioned over
the left hip and thigh. A custom-made foam support was placed between the legs of the animal to minimize
unwanted motion during the scans, and to achieve stable contact between the coil and the animal. Markings
were made on the foam support in order to allow the animal and coil positioning to be recreated for all scans (see
Supplementary Information Fig. 2). In order to minimize motion from abdominal breathing, a 2 cm wide strap
was placed directly proximal of the surface coil to stabilise the distal abdomen and pelvis of the animal.
An initial scan was performed to establish the position of the animal and localise the area of interest. The B0
field map was calculated before running the DTI scan in order to perform shimming. The data was collected
using a DTI EPI Spin Echo diffusion scheme with a total of 32 diffusion-sampling directions acquired in 100 axial
slices. In total, 6 b = 0-images were collected. The in-plane resolution and slice thickness were 0.4 mm in order to
achieve isotropic voxels. TE = 22 ms, TR = 8000 ms, no averaging. FOV 38.4 mm, matrix size 96 × 96. A DTI scan
with the b-value set to 600, 800, 1000, and 1200 s/mm2 was collected. Segmented k-space acquisition of 3 readout
segments was utilized. Navigator, Automatic Ghost Correction and Grappa Multishot Adjustment was activated.
The diffusion time was 10.5 ms. The diffusion encoding duration was 4.5 ms. Saturation slabs were positioned
medial to the thigh to cover bladder, intestines, tail and any other air pockets, in order to minimise artefacts. Each
DTI scan took 15 min, 12 secs for a total of approximately 61 minutes for all four b-value scans.

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Post-processing, tensor calculation and analysis of data was performed in DSI-studio (Dec 7 2016 Build).
DSI-Studio employs the same tensor calculation as is described by Jiang et al.44. The diffusion weighted image
data was processed with Motion Correction by registering the b0 images to the first b0 image to create a transfor-
mation matrix which is then applied to each DWI, and Eddy Current correction which registers DWI to the b0
and applies the registration matrix to the DWI’s. The images were up-sampled with a factor of 2 through linear
interpolation in order to facilitate the placement of ROI’s45. A multi-shell diffusion scheme was employed were
the four b-values were combined to produce a fifth DTI data file for each scan. One scan in the preoperative group
was excluded from this as the Motion correction was not able to correct for severe translocation in the collected
DWI’s. This was the result of the scan having to be restarted to collect the last two b-values, and the animal repo-
sitioned due to scanner malfunction at the time of scanning.
A spherical ROI consisting of a total of 19 voxels was manually placed at 10 mm proximal to the sciatic nerve
bifurcation into tibial and fibular nerves in the pre-operative scans. In the post-operative scans, the ROIs were
placed at 5 mm proximal and at 5 mm distal to the transection site. The reconstructed fractional anisotropy map
was used to position the ROI. All three viewports (axial, sagittal, coronal) were checked to make sure the ROI
was placed in the centre of the nerve, and that it did not extend outside the nerve tissue (Fig. 8). The same
ROI-position (XYZ-coordinate) was used for all four different b-value scans and the multi-shell data. The posi-
tion was manually controlled to verify that the localisation was the same following post-processing, as one scan
had been performed with repositioning of the animal which was too large for the motion correction to correct for
and manual correction of the ROI placement was required. The ROI was analysed for fractional anisotropy (FA),
mean diffusivity (MD), axial diffusivity (AD), and radial diffusivity (RD), and the averaged value (i.e. the mean)
of all the voxels in the ROI was used to perform the subsequent statistical analysis.
Tractography was performed for all b-values (600, 800, 1000, and 1200 s/mm2) and the multi-shell data sep-
arately using a deterministic fibre tracking algorithm46 of all fibres passing through the ROI’s described in earlier
text. Angular threshold was set at 30 degrees as our pilot studies showed minimal changes in tracking results in
the range 30–60 degrees, but a clear decrease in track length with lower angular thresholds <30, and an increase
of anatomically incorrect tracts at higher thresholds. Step size was 0.4 mm and the anisotropy threshold was set
at 0.3. Tracts shorter than 2 mm were discarded. The visualised tracts were rendered to display each diffusion
parameter separately with a colour gradient. The averaged (mean) diffusion parameters of the entire tracts were
used for statistical analysis. A tract analysis report was also produced to plot any local variations in the diffusion
tensor parameters by recording the diffusion tensor indices along the rendered tracts of the multi-shell derived
FA maps. Kurtosis tensor estimation was performed using the protocol described by Veraart et al.47. The four
b-value scans described in earlier text (600, 800, 1000, 1200 s/mm2, 32 directions) were used. Further white mat-
ter metrics were determined using the method described by Fieremans et al.48. Mean kurtosis and axonal water
fraction was subsequently analysed in DSI-studio by the placement of ROIs in the same localisations as the DTI
analysis.
In order to determine the signal-to-noise ratio (SNR), a numerical value was computed using two sequential
observations of b0 images in both the preoperative and postoperative scans. An averaged image and a difference
image of the two observations were computed using ImageJ (version 1.52a), then the SNR was computed as the
mean value of a ROI positioned at the area of interest (the sciatic nerve) in the average image divided by the
standard deviation over the voxels in the same ROI within the difference image49.

Statistical analysis.  Non-parametric statistics was used. A p-value of < 0.05 was considered significant.
The diffusion tensor parameters (FA, MD, AD, RD) in the non-operated sciatic nerve, and the proximal and
distal stump in the transected nerve, were compared between the different b-values and the multi-shell data
using Friedmans Test. Wilcoxon Signed Ranks test was used to detect any differences in diffusion and kurtosis
parameters (FA, MD, AD, RD, MK, AWF) between the pre-operative scan, and the post-operative scans of the
proximal and distal stump by pairwise comparisons. Bonferroni correction was used to correct for the multiple
comparisons, and the presented p-values are given in their corrected form. The presented values of the statistical
analysis are medians and interquartile range. IBM SPSS Statistics 24 (9.6.0.0) was used to perform all statistical
calculations.

Data availability.  The data (DTI-scans) generated and analysed during the current study are available from
the corresponding author on reasonable request.

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Acknowledgements
This work was supported by the Swedish Research Council (grant 2014-2306, Medicine and Health), Umeå
University and through a regional agreement between Umeå University and Västerbotten County Council (ALF).

Author Contributions
G.A. performed all surgical procedures, data collection, data analysis, figure preparation and produced the
manuscript draft. G.O. set up the DTI sequence and edited/reviewed the manuscript. L.N.N. supervised the
animal model design and execution, as well as edited/reviewed the manuscript. F.S. performed the diffusion
kurtosis tensor estimates and reviewed the manuscript. G.A., G.O., and L.N.N. were involved in the study design.

Additional Information
Supplementary information accompanies this paper at https://doi.org/10.1038/s41598-018-30961-1.
Competing Interests: The authors declare no competing interests.
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