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Objective: To compare the use of methylene blue and blue tissue marker in achieving sciatic nerve staining in cadaveric rats after perineural or intramuscular injection.
Study Design: Experimental, randomized, blinded, crossover cadaveric study.
Animals: A group of 16 fresh-frozen adult Wistar rat cadavers.
Methods: Phase I: ultrasound-guided sciatic nerve injections were performed using either methylene blue (Group Methb, n = 8) or a blue tissue marker (Group Tmarker, n = 8).
Phase Ii: ultrasound-guided biceps femoris intramuscular injections were performed with the same dyes (Group Methb IM, n = 8; Group Tmarker IM, n = 8). Volume of each injection was 0.1 mL, followed by a 5 minute interval before anatomical dissection. Positive staining was measured along the sciatic nerve in millimeters. Data analysis included t tests for parametric data and Wilcoxon and Fisher's exact tests for nonparametric data, with significance set at p < 0.05.
Results: Phase I: both solutions consistently stained the sciatic nerve in all pelvic limbs. However, the length of staining was significantly greater in Group Methb (18 ± 1.9 mm) than in Group Tmarker (4.7 ± 1.3 mm) (p < 0.001).
Phase Ii: sciatic nerve staining was observed in the Group Methb IM (7/7, 100%), with a median spread of 12 mm (interquartile range 11-12 mm), whereas no staining was detected in the Group Tmarker IM (0/8) (p = 0.015).
Conclusions: and clinical relevance Methylene blue achieved greater staining along the sciatic nerve than blue tissue marker. Furthermore, methylene blue diffused through the biceps femoris, effectively staining the sciatic nerve and surrounding tissues. This difference highlights the potential for overestimation in studies that use methylene blue and underscores the importance of selecting appropriate dye solutions.
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http://dx.doi.org/10.1016/j.vaa.2025.05.002 | DOI Listing |
Neuropharmacology
September 2025
Metabolic Disorders and Neuroscience Research Laboratory, Department of Pharmacy, Birla Institute of Technology and Sciences Pilani, Hyderabad Campus, Hyderabad, India. Electronic address:
Neuroinflammation is vital in vincristine-induced peripheral neuropathy (VIPN). Locally infiltrated macrophages polarize to pro-inflammatory M1-type, release inflammatory cytokines, and contribute to neuropathic pain. Histone deacetylase 3 (HDAC3) regulates macrophage polarization.
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September 2025
Department of Orthopedics, The Second Affiliated Hospital and Yuying Children's Hospital of Wenzhou Medical University, Wenzhou 325000, China; Key Laboratory of Orthopedics of Zhejiang Province, Wenzhou 325000, China; The Second School of Medicine, Wenzhou Medical University, Wenzhou 325000, China.
Peripheral nerve injury (PNI) is notoriously difficult to repair due to impaired axonal regeneration and dysregulated inflammatory microenvironments. This study demonstrates that crocin facilitates peripheral nerve regeneration by modulating the STAT3/Bcl-2/Beclin-1 signaling axis, enhancing autophagy while suppressing NLRP3 inflammasome-mediated pyroptosis. In a rat model of sciatic nerve crush injury, crocin treatment improved axonal regrowth and ultrastructural remyelination, as evidenced by upregulated expression of β3-Tubulin, neurofilament-200 (NF200), and myelin basic protein (MBP), alongside significantly elevated sciatic functional index (SFI) scores, reduced muscle atrophy, and diminished collagen deposition.
View Article and Find Full Text PDFBMJ Open
September 2025
Salisbury NHS Foundation Trust, Salisbury, UK.
Introduction: Difficulty with walking can lead to reduced quality of life for people with Parkinson's disease (pwPD); improving walking is considered a treatment priority. Drug therapies can control PD symptoms; however, pwPD often still experience mobility problems.Functional electrical stimulation (FES) induces movement in weak muscles via external electrical stimulation.
View Article and Find Full Text PDFSpinal muscular atrophy with respiratory distress type 1 (SMARD1) and Charcot Marie Tooth type 2S (CMT2S) are due to mutations in immunoglobulin mu binding protein two (IGHMBP2). We generated the -R604X mouse (R605X-humans) to understand how alterations in IGHMBP2 function impact disease pathology. The IGHMBP2-R605X mutation is associated with patients with SMARD1 or CMT2S.
View Article and Find Full Text PDFNeural Regen Res
September 2025
Department of Human Anatomy, Naval Medical University, Shanghai, China.
Peripheral nerve defect repair is a complex process that involves multiple cell types; perineurial cells play a pivotal role. Hair follicle neural crest stem cells promote perineurial cell proliferation and migration via paracrine signaling; however, their clinical applications are limited by potential risks such as tumorigenesis and xenogeneic immune rejection, which are similar to the risks associated with other stem cell transplantations. The present study therefore focuses on small extracellular vesicles derived from hair follicle neural crest stem cells, which preserve the bioactive properties of the parent cells while avoiding the transplantation-associated risks.
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