The value of DTI and DTT in evaluating the protective effect of neuregulin-1 on spinal cord transection models of Sprague–Dawley rats.
Tao Gong1, Guangbin Wang2, and Weibo Chen3

1Shandong University, Jinan, China, People's Republic of, 2Jinan, China, People's Republic of, 3Shanghai, China, People's Republic of

Synopsis

DTI can noninvasive evaluate the injury and prognosis of spinal cord, and NRG-1 has the function of protecting and repairing of injury spinal cord in rats.

Objective

To investigate the value of DTI and DTT in evaluating the protective effect of neuregulin-1 on spinal cord transection models of Sprague–Dawley (SD) rats.

methods

30 SD rats were randomly divided into three groups: normal saline (NS) group (10 rats), NRG-1 group (10 rats), health control group (HC) group (10 rats). T9/10 level spinal cord transection model was performed on NS group and NRG-1 group, and NS and NRG-1 were injected respectively after operation, once a day for three days; nothing treated was on HC group. MRI and DTI examinations were performed in three groups using 3.0T Philips MR scanner a week later. The date was transferred to Philips workstation to calculate the DTI indices. ROIs were placed in the spinal cord within 1 centimeter of the level of T9/10. The parameters: ADC values, FA values, Fiber density coefficient (FDi) and Fiber Length were acquired, and then taking those averages of multiple measurements as the final results.

Conventional MRI and DTI scans were conducted on 3.0T MR scanner (Philips Achieva TX, Best, The Netherlands) with wrist coil. The SD rats were mounted in supine position within the scanner. Conventional MRI scan, including T1-weighted and T2-weighted sagittal images, was completed with the SE sequence. DTI images were acquired with the parameters as follows: single shot spin-echo planar imaging(EPI) sequence, TR 3034ms, TE 66ms, max b-factor 800s/mm2, EPI factor 25, slice thickness 0.8mm, slice gap 0, acquisition matrix 64×68, FOV 106mm×106mm×16mm, total scan duration was 4 minutes 8 seconds. I

After image acquisition, the date was transferred to Philips workstation to calculate the DTI indices. For accurate positioning, DTI images confused with the sagittal T2-weighted images, ROIs were placed in the spinal cord within 1 centimeter of the level of T9/10. The parameters: ADC values, FA values, Fiber density coefficient (FDi), Fiber Length, were acquired, and then taking those averages of multiple measurements as the final results. The DTT of the spinal cord was generated with the parameters: anisotropy 0.2, angular 25°. Fig.1 Confused DTI images with T2-weighted sagittal images, placing the ROI on the axial map (Purple region) within 1 centimeter of the level T9/10. The ADC, FA, FDi, Length values were acquired.

Data were expressed as mean± SD, and were analyzed using SPSS 19.0. Statistical analysis using Student’s t-test, P < 0.05 was regarded as statistically significant.

Results

The ADC values, FA values, FDi and Fiber Length of NS group were(0.86±0.14)×10-3cm2/s, 0.28±0.09, 4.8±1.0 and(13.3±1.3)mm;NRG-1 group were(0.87±0.15)×10-3cm2/s, 0.33±0.04, 7.8±1.1 and(29.7±3.5)mm; HC group were(0.71±0.08)×10-3cm2/s, 0.67±0.07, 14.3±2.5 and(38.3±5.8)mm respectively. The ADC values of NS and NRG-1group were significantly decreased compared with HC group; however, there was no difference between NS and NRG-1. The FA values, FDi and Fiber Length of NRG-1group were all decreased compared with HC group, and increased compared with NS group, and the differences were statistically significant.

Fig.2 The MR Images of HC group. a. sagittal T2-weighted images show the spinal cord was intact, there was no abnormal signal; b. DTT map, demonstrating the fiber bundle was continuous.Fig.3 The MR Images of NRG-1 group. a. sagittal T2-weighted image show abnormal mixed signal at the level of T9/10(arrow), the swelling of close soft tissue in the back of the rats was caused by surgery; b. DTT map, demonstrating a part of fiber bundle at the level of T9/10 (arrow)was fracture.

Conclusion

DTI can noninvasive evaluate the injury and prognosis of spinal cord, and NRG-1 has the function of protecting and repairing of injury spinal cord in rats.

Acknowledgements

No acknowledgement found.

References

1. Li Y, Lein PJ, Ford GD, Liu C, Stovall KC, White TE, Bruun DA, Tewolde T, Gates AS, Distel TJ et al: Neuregulin-1 inhibits neuroinflammatory responses in a rat model of organophosphate-nerve agent-induced delayed neuronal injury. Journal of neuroinflammation 2015, 12:64.

2. Li Y, Lein PJ, Liu C, Bruun DA, Giulivi C, Ford GD, Tewolde T, Ross-Inta C, Ford BD: Neuregulin-1 is neuroprotective in a rat model of organophosphate-induced delayed neuronal injury. Toxicology and applied pharmacology 2012, 262(2):194-204.

3. Liu Y, Ford BD, Mann MA, Fischbach GD: Neuregulin-1 increases the proliferation of neuronal progenitors from embryonic neural stem cells. Developmental biology 2005, 283(2):437-445.

4. Tan GH, Liu YY, Hu XL, Yin DM, Mei L, Xiong ZQ: Neuregulin 1 represses limbic epileptogenesis through ErbB4 in parvalbumin-expressing interneurons. Nature neuroscience 2012, 15(2):258-266.

5. Wang S, Li Y, Paudyal R, Ford BD, Zhang X: Spatio-temporal assessment of the neuroprotective effects of neuregulin-1 on ischemic stroke lesions using MRI. Journal of the neurological sciences 2015.

6. Yang W, Liu TT, Song XB, Zhang Y, Li ZH, Hao Q, Cui ZH, Liu HL, Lei CL, Liu J: Neuregulin-1 protects against acute optic nerve injury in rat model. Journal of the neurological sciences 2015.

7. Nickl-Jockschat T, Stocker T, Krug A, Markov V, Huang R, Schneider F, Habel U, Eickhoff SB, Zerres K, Nothen MM et al: A Neuregulin-1 schizophrenia susceptibility variant causes perihippocampal fiber tract anomalies in healthy young subjects. Brain and behavior 2014, 4(2):215-226.

8. Mondragon-Lozano R, Diaz-Ruiz A, Rios C, Olayo Gonzalez R, Favila R, Salgado-Ceballos H, Roldan-Valadez E: Feasibility of in vivo quantitative magnetic resonance imaging with diffusion weighted imaging, T2-weighted relaxometry, and diffusion tensor imaging in a clinical 3 tesla magnetic resonance scanner for the acute traumatic spinal cord injury of rats: technical note. Spine 2013, 38(20):E1242-1249.

9. Jirjis MB, Kurpad SN, Schmit BD: Ex vivo diffusion tensor imaging of spinal cord injury in rats of varying degrees of severity. Journal of neurotrauma 2013, 30(18):1577-1586.

10. Kelley BJ, Harel NY, Kim CY, Papademetris X, Coman D, Wang X, Hasan O, Kaufman A, Globinsky R, Staib LH et al: Diffusion tensor imaging as a predictor of locomotor function after experimental spinal cord injury and recovery. Journal of neurotrauma 2014, 31(15):1362-1373.

11. Li XH, Li JB, He XJ, Wang F, Huang SL, Bai ZL: Timing of diffusion tensor imaging in the acute spinal cord injury of rats. Scientific reports 2015, 5:12639.

12. Wang F, Huang SL, He XJ, Li XH: Determination of the ideal rat model for spinal cord injury by diffusion tensor imaging. Neuroreport 2014, 25(17):1386-1392.

Figures

Fig.1

Fig.2a

Fig.2b

Fig.3a

Fig.3b



Proc. Intl. Soc. Mag. Reson. Med. 24 (2016)
2060