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An experimental study of intravoxel incoherent motion diffusion-weighted imaging for evaluating the therapeutic effects of bone marrow mesenchymal stem cell in a rat model of peripheral nerve injury
LI Junfeng  MENG Fanqi  HUANG Wensheng  CHEN Qiuyi  PAN Jintong  GAO Jinyun  HAO Liantao  QIN Jinhua  LIANG Yingying  YU Xuewen  QIN Haodong  CHEN Yueyao 

Cite this article as: LI J F, MENG F Q, HUANG W S, et al. An experimental study of intravoxel incoherent motion diffusion-weighted imaging for evaluating the therapeutic effects of bone marrow mesenchymal stem cell in a rat model of peripheral nerve injury[J]. Chin J Magn Reson Imaging, 2026, 17(3): 22-29. DOI:10.12015/issn.1674-8034.2026.03.004.


[Abstract] Objective To investigate the value of quantitative parameters derived from intravoxel incoherent motion (IVIM) imaging in evaluating the therapeutic effects of bone marrow mesenchymal stem cell (BMMSC) in a rat model of peripheral nerve injury.Materials and Methods Thirty-six Sprague-Dawley (SD) rats were randomly assigned to a BMMSC group or a phosphate-buffered saline (PBS) control group. Each group underwent magnetic resonance imaging, motor function assessment, and histological analysis at five time points: before the operation and 1, 2, 3, and 4 weeks after the operation. IVIM perfusion fraction (f) assessed nerve perfusion, while T2-weighted imaging (T2WI) and T2 mapping assessed edema. Toluidine blue staining and immunofluorescence were used to assess neural structural alterations. The sciatic function index (SFI) was employed to assess functional recovery. The expression of vascular endothelial cell-specific markers (CD31) and inflammatory factors (IL-1α, IL-10 and PPARγ) was evaluated by immunohistochemistry.Results IVIM-f recovery, myelin regeneration, and nerve fiber repair were all significantly better in the BMMSC group than in the control group (all P < 0.05). Immunohistochemical analysis showed lower IL-1α and higher IL-10 and PPARγ levels in the BMMSC group than in the control group (all P < 0.05). And the expression of CD31 was significantly increased in the BMMSC group (P < 0.05). Moreover, the IVIM-f was closely correlated with both histopathological and functional outcomes.Conclusions Quantitative IVIM parameters, particularly IVIM-f, can reflect perfusion recovery and nerve regeneration earlier than T2 values after stem cell therapy in rats with peripheral nerve injury, and may serve as a potential imaging biomarker for evaluating the therapeutic efficacy of stem cell treatment.
[Keywords] peripheral nerve injuries;nerve regeneration;mesenchymal stem cells;intravoxel incoherent motion;magnetic resonance imaging;perfusion;regenerative microenvironment;inflammation

LI Junfeng1   MENG Fanqi1   HUANG Wensheng2   CHEN Qiuyi1   PAN Jintong1, 3   GAO Jinyun1   HAO Liantao1   QIN Jinhua1   LIANG Yingying4   YU Xuewen4   QIN Haodong5   CHEN Yueyao1*  

1 Department of Radiology, the Fourth Clinical Medical College of Guangzhou University of Chinese Medicine (Shenzhen Traditional Chinese Medicine Hospital), Shenzhen 518033, China

2 Department of Radiology, the Seventh Affiliated Hospital, Sun Yat-sen University, Shenzhen, 518107, China

3 Department of Nephrology, Shenzhen Hengsheng Hospital, Shenzhen 518101, China

4 Department of Pathology, the Fourth Clinical Medical College of Guangzhou University of Chinese Medicine (Shenzhen Traditional Chinese Medicine Hospital), Shenzhen 518033, China

5 MR Research Collaboration, Siemens Healthineers, Shanghai 200120, China

Corresponding author: CHEN Y Y, E-mail: drchenyueyao@163.com

Conflicts of interest   None.

Received  2025-11-06
Accepted  2026-01-08
DOI: 10.12015/issn.1674-8034.2026.03.004
Cite this article as: LI J F, MENG F Q, HUANG W S, et al. An experimental study of intravoxel incoherent motion diffusion-weighted imaging for evaluating the therapeutic effects of bone marrow mesenchymal stem cell in a rat model of peripheral nerve injury[J]. Chin J Magn Reson Imaging, 2026, 17(3): 22-29. DOI:10.12015/issn.1674-8034.2026.03.004.

[1]
ZHAI X, WANG Y. Physical modulation and peripheral nerve regeneration: a literature review[J/OL]. Cell Regen, 2024, 13(1): 32 [2025-11-06]. https://doi.org/10.1186/s13619-024-00215-9. DOI: 10.1186/s13619-024-00215-9.
[2]
ZOU Y, ZHANG G, YANG Y, et al. Advanced techniques and innovations in peripheral nerve repair: a comprehensive review for clinical and experimental reference[J]. Rev Neurosci, 2025, 36(3): 243-265. DOI: 10.1515/revneuro-2024-0101.
[3]
SAFFARI T M, MATHOT F, THALER R, et al. Microcomputed analysis of nerve angioarchitecture after combined stem cell delivery and surgical angiogenesis to nerve allograft[J]. J Plast Reconstr Aesthet Surg, 2021, 74(8): 1919-1930. DOI: 10.1016/j.bjps.2020.12.039.
[4]
YADAV A, RAMASAMY T S, LIN S C, et al. Autologous Platelet-Rich Growth Factor Reduces M1 Macrophages and Modulates Inflammatory Microenvironments to Promote Sciatic Nerve Regeneration[J/OL]. Biomedicines, 2022, 10(8): 1991 [2025-11-06]. https://doi.org/10.3390/biomedicines10081991. DOI: 10.3390/biomedicines10081991.
[5]
BIN Z, ZHIHU Z, JIANXIONG M, et al. Repairing peripheral nerve defects with revascularized tissue-engineered nerve based on a vascular endothelial growth factor-heparin sustained release system[J]. J Tissue Eng Regen Med, 2020, 14(6): 819-828. DOI: 10.1002/term.3048.
[6]
ZOU X F, ZHANG B Z, QIAN W W, et al. Bone marrow mesenchymal stem cells in treatment of peripheral nerve injury[J]. World J Stem Cells, 2024, 16(8): 799-810. DOI: 10.4252/wjsc.v16.i8.799.
[7]
SAFFARI S, SAFFARI T M, ULRICH D J O, et al. The interaction of stem cells and vascularity in peripheral nerve regeneration[J]. Neural Regen Res, 2021, 16(8): 1510-1517. DOI: 10.4103/1673-5374.303009.
[8]
KHODIR S A, IMBABY S, ABDEL ALLEM AMER M S, et al. Effect of mesenchymal stem cells and melatonin on experimentally induced peripheral nerve injury in rats[J/OL]. Biomed Pharmacother, 2024, 177: 117015 [2026-01-07]. https://www.ncbi.nlm.nih.gov/pubmed/38936196. DOI: 10.1016/j.biopha.2024.117015.
[9]
CHEN Y, PAN Z, MENG F, et al. Magnetic resonance imaging assessment of the therapeutic effect of combined electroacupuncture and stem cells in acute peripheral nerve injury[J/OL]. Front Cell Neurosci, 2022, 16: 1065557 [2026-01-07]. https://www.ncbi.nlm.nih.gov/pubmed/36605615. DOI: 10.3389/fncel.2022.1065557.
[10]
LIU K H, DING C W. The basic principle of intravoxel incoherent motion imaging and its application progress in Sjogren's syndrome[J]. Chin J Magn Reson Imaging, 2022, 13(1): 161-163. DOI: 10.12015/issn.1674-8034.2022.01.038.
[11]
CAROCA S, VILLAGRAN D, CHABERT S. Four functional magnetic resonance imaging techniques for skeletal muscle exploration, a systematic review[J/OL]. Eur J Radiol, 2021, 144: 109995 [2026-01-07]. https://www.ncbi.nlm.nih.gov/pubmed/34628310. DOI: 10.1016/j.ejrad.2021.109995.
[12]
ENGLUND E K, REITER D A, SHAHIDI B, et al. Intravoxel Incoherent Motion Magnetic Resonance Imaging in Skeletal Muscle: Review and Future Directions[J]. J Magn Reson Imaging, 2022, 55(4): 988-1012. DOI: 10.1002/jmri.27875.
[13]
ZIMMERMANN J, REOLON B, MICHELS L, et al. Intravoxel incoherent motion imaging in stroke infarct core and penumbra is related to long-term clinical outcome[J/OL]. Sci Rep, 2024, 14(1): 29631 [2025-11-06]. https://doi.org/10.1038/s41598-024-81280-7. DOI: 10.1038/s41598-024-81280-7.
[14]
PAN J T, MENG F Q, PAN Z X, et al. Magnetic resonance diffusion tensor imaging evaluation of electroacupuncture and stem cell therapy for acute peripheral nerve injury in rats[J]. Chin J Magn Reson Imaging, 2024, 15(6): 107-114, 122. DOI: 10.12015/issn.1674-8034.2024.06.016.
[15]
CHEN Y Y, ZHANG X, LIN X F, et al. DTI metrics can be used as biomarkers to determine the therapeutic effect of stem cells in acute peripheral nerve injury[J]. J Magn Reson Imaging, 2017, 45(3): 855-862. DOI: 10.1002/jmri.25395.
[16]
XIANG X, LIN X, ZHANG B, et al. Microvascular Dysfunction Associates With Outcomes in Hypertrophic Cardiomyopathy: Insights From the Intravoxel Incoherent Motion MRI[J]. J Magn Reson Imaging, 2023, 57(6): 1766-1775. DOI: 10.1002/jmri.28450.
[17]
LIANG Q, LIN H, LI J, et al. Combining Multifrequency Magnetic Resonance Elastography With Automatic Segmentation to Assess Renal Function in Patients With Chronic Kidney Disease[J]. J Magn Reson Imaging, 2025, 61(6): 2543-2555. DOI: 10.1002/jmri.29719.
[18]
LIU B, XIN W, TAN J R, et al. Myelin sheath structure and regeneration in peripheral nerve injury repair[J]. Proc Natl Acad Sci U S A, 2019, 116(44): 22347-22352. DOI: 10.1073/pnas.1910292116.
[19]
ZHANG L, CHEN X, WU L, et al. Ameliorative effects of escin on neuropathic pain induced by chronic constriction injury of sciatic nerve[J/OL]. J Ethnopharmacol, 2021, 267: 113503 [2026-01-07]. https://www.ncbi.nlm.nih.gov/pubmed/33091488. DOI: 10.1016/j.jep.2020.113503.
[20]
LAVORATO A, RAIMONDO S, BOIDO M, et al. Mesenchymal Stem Cell Treatment Perspectives in Peripheral Nerve Regeneration: Systematic Review[J/OL]. Int J Mol Sci, 2021, 22(2): 572 [2025-11-06]. https://doi.org/10.3390/ijms22020572. DOI: 10.3390/ijms22020572.
[21]
FAN B, LI C, SZALAD A, et al. Mesenchymal stromal cell-derived exosomes ameliorate peripheral neuropathy in a mouse model of diabetes[J]. Diabetologia, 2020, 63(2): 431-443. DOI: 10.1007/s00125-019-05043-0.
[22]
CLARK K, ZHANG S, BARTHE S, et al. Placental Mesenchymal Stem Cell-Derived Extracellular Vesicles Promote Myelin Regeneration in an Animal Model of Multiple Sclerosis[J/OL]. Cells, 2019, 8(12): 1497 [2025-11-06]. https://doi.org/10.3390/cells8121497. DOI: 10.3390/cells8121497.
[23]
JIANG X, YANG J, LIU F, et al. Embryonic stem cell-derived mesenchymal stem cells alleviate skeletal muscle injury induced by acute compartment syndrome[J/OL]. Stem Cell Res Ther, 2022, 13(1): 313 [2025-11-06]. https://doi.org/10.1186/s13287-022-03000-0. DOI: 10.1186/s13287-022-03000-0.
[24]
IVANOVA E, MATYUSHKIN A, SOROKINA A, et al. Low-Affinity NMDA Receptor Antagonist Hemantane in a Topical Formulation Attenuates Arthritis Induced by Freund's Complete Adjuvant in Rats[J]. Adv Pharm Bull, 2024, 14(1): 241-252. DOI: 10.34172/apb.2024.002.
[25]
SUH H R, CHO H Y. Reduction of Edema and Pain in Transcutaneous Electrical Nerve Stimulation Treated-Arthritic Rat[J]. Tohoku J Exp Med, 2024, 262(4): 245-252. DOI: 10.1620/tjem.2024.J006.
[26]
ZHAO S, ZHANG Q, LIU M, et al. Application of stem cells in engineered vascular graft and vascularized organs[J]. Semin Cell Dev Biol, 2023, 144: 31-40. DOI: 10.1016/j.semcdb.2022.10.003.
[27]
YIN L, XIE Z Y, XU H Y, et al. T2 Mapping and Fat Quantification of Thigh Muscles in Children with Duchenne Muscular Dystrophy[J]. Curr Med Sci, 2019, 39(1): 138-145. DOI: 10.1007/s11596-019-2012-8.
[28]
SONG G, SONG X, WANG J, et al. Evaluation of skeletal muscle microcirculation via magnetic resonance intravoxel incoherent motion perfusion imaging in an acute ischemia rabbit model[J]. Quant Imaging Med Surg, 2025, 15(9): 8064-8078. DOI: 10.21037/qims-2025-711.
[29]
LARGEAU B, CRACOWSKI J L, LENGELLE C, et al. Drug-induced peripheral oedema: An aetiology-based review[J]. Br J Clin Pharmacol, 2021, 87(8): 3043-3055. DOI: 10.1111/bcp.14752.
[30]
MSHEIK Z, MASSRY M EL, ROVINI A, et al. The macrophage: a key player in the pathophysiology of peripheral neuropathies[J/OL]. J Neuroinflammation, 2022, 19(1): 97 [2025-11-06]. https://doi.org/10.1186/s12974-022-02454-6. DOI: 10.1186/s12974-022-02454-6.
[31]
MURILLO B, MENDES SOUSA M. Neuronal Intrinsic Regenerative Capacity: The Impact of Microtubule Organization and Axonal Transport[J]. Dev Neurobiol, 2018, 78(10): 952-959. DOI: 10.1002/dneu.22602.
[32]
HU C, WU Z, LI L. Mesenchymal stromal cells promote liver regeneration through regulation of immune cells[J]. Int J Biol Sci, 2020, 16(5): 893-903. DOI: 10.7150/ijbs.39725.
[33]
ARABPOUR M, SAGHAZADEH A, REZAEI N. Anti-inflammatory and M2 macrophage polarization-promoting effect of mesenchymal stem cell-derived exosomes[J/OL]. Int Immunopharmacol, 2021, 97: 107823 [2026-01-07]. https://www.ncbi.nlm.nih.gov/pubmed/34102486. DOI: 10.1016/j.intimp.2021.107823.
[34]
LIA A, ANNESE T, FORNARO M, et al. Perivascular and endomysial macrophages expressing VEGF and CXCL12 promote angiogenesis in anti-HMGCR immune-mediated necrotizing myopathy[J]. Rheumatology (Oxford), 2022, 61(8): 3448-3460. DOI: 10.1093/rheumatology/keab900.
[35]
WANG X, XIE S, QIU C, et al. Use of Intravoxel Incoherent Motion Diffusion-Weighted Imaging to Assess Mesenchymal Stromal Cells Promoting Liver Regeneration in a Rat Model[J]. Acad Radiol, 2024, 31(12): 4955-4964. DOI: 10.1016/j.acra.2024.05.018.
[36]
KLAUSS M, MAIER-HEIN K, TJADEN C, et al. IVIM DW-MRI of autoimmune pancreatitis: therapy monitoring and differentiation from pancreatic cancer[J]. Eur Radiol, 2016, 26(7): 2099-2106. DOI: 10.1007/s00330-015-4041-4.
[37]
LE BIHAN D. What can we see with IVIM MRI?[J]. Neuroimage, 2019, 187: 56-67. DOI: 10.1016/j.neuroimage.2017.12.062.
[38]
LIM H K, JEE W H, JUNG J Y, et al. Intravoxel incoherent motion diffusion-weighted MR imaging for differentiation of benign and malignant musculoskeletal tumours at 3 T[J/OL]. Br J Radiol, 2018, 91(1082): 20170636 [2025-11-06]. https://doi.org/10.1259/bjr.20170636. DOI: 10.1259/bjr.20170636.
[39]
SHOR N, SENE T, ZUBER K, et al. Discriminating between IgG4-related orbital disease and other causes of orbital inflammation with intra voxel incoherent motion (IVIM) MR imaging at 3T[J]. Diagn Interv Imaging, 2021, 102(12): 727-734. DOI: 10.1016/j.diii.2021.06.006.
[40]
SI L, LIU X, LI X, et al. Diffusion kurtosis imaging and intravoxel incoherent motion imaging parameters in breast lesions: Effect of radiologists' experience and region-of-interest selection[J/OL]. Eur J Radiol, 2023, 158: 110633 [2026-01-07]. https://www.ncbi.nlm.nih.gov/pubmed/36470051. DOI: 10.1016/j.ejrad.2022.110633.
[41]
SPINNER G R, FEDERAU C, KOZERKE S. Bayesian inference using hierarchical and spatial priors for intravoxel incoherent motion MR imaging in the brain: Analysis of cancer and acute stroke[J/OL]. Med Image Anal, 2021, 73: 102144 [2026-01-07]. https://www.ncbi.nlm.nih.gov/pubmed/34261009. DOI: 10.1016/j.media.2021.102144.
[42]
MERISAARI H, FEDERAU C. Signal to noise and b-value analysis for optimal intra-voxel incoherent motion imaging in the brain[J/OL]. PLoS One, 2021, 16(9): e0257545 [2026-01-07]. https://www.ncbi.nlm.nih.gov/pubmed/34555054. DOI: 10.1371/journal.pone.0257545.

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