Identification of peripheral nerve functional fascicles in Sprague-Dawley rats by the carbon quantum dot-Annexin V antibody complex.


Journal

Scientific reports
ISSN: 2045-2322
Titre abrégé: Sci Rep
Pays: England
ID NLM: 101563288

Informations de publication

Date de publication:
28 Oct 2024
Historique:
received: 11 06 2024
accepted: 21 10 2024
medline: 28 10 2024
pubmed: 28 10 2024
entrez: 28 10 2024
Statut: epublish

Résumé

To explore a method to identify the sensory and motor fascicles of the peripheral nerve to achieve accurate peripheral nerve functional fascicle suture. The peripheral nerve Sunderland V injury model, muscle branch of the femoral nerve and saphenous nerve were established in the bilateral femoral nerves of Sprague-Dawley (SD) rats. The specific samples were grouped as follows: the main trunk of the femoral nerve was exposed bilaterally and cut with microscopic scissors in the main trunk of the femoral nerve to prepare a model of Sunderland V injury in the mixed fascicle of peripheral nerves; the muscle branch of the femoral nerve was exposed bilaterally and cut in the middle section of the muscle branch of the femoral nerve to prepare a model of Sunderland V injury in the motor fascicle of peripheral nerves; the saphenous nerve was exposed bilaterally and cut at 1 cm below the patella to prepare a model of Sunderland V injury to the sensory fascicle of the peripheral nerves. A carbon quantum dot (CD)-annexin V antibody complex was prepared and applied to the distal and proximal nerve stumps of the peripheral nerve Sunderland V injury model groups of SD rats. Under the excitation light source of a 380 nm uv lamp, fluorescence color development was observed under a fluorescence microscope after 5, 10, 15, and 20 min. At 5 min, sections of the bilateral femoral nerve trunk, muscular branches of the femoral nerve, and Sunderland V lesion of the saphenous nerve in SD rats were only dark in color under the microscope, and there was no difference in fluorescence. The intensity of the staining increased significantly for 10-20 min. The sensory fascicles and saphenous nerves of the femoral nerve trunk showed blue fluorescence under the CD-Annexin V antibody complex staining, while the motor fascicles and muscle branches of the femoral nerve trunk showed no fluorescence. Fluorescence intensity gradually decreased after 20 min of staining. There was no significant difference in the staining intensity at 5, 10, 15, and 20 min in each group. Our results suggest that the CD-Annexin antibody complex can be used to identify functional fascicles of peripheral nerves in SD rats.

Identifiants

pubmed: 39463438
doi: 10.1038/s41598-024-77276-y
pii: 10.1038/s41598-024-77276-y
doi:

Substances chimiques

Annexin A5 0
Carbon 7440-44-0
Antibodies 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

25691

Informations de copyright

© 2024. The Author(s).

Références

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Auteurs

Xianyu Meng (X)

Department of Orthopedics, The First Affiliated Hospital of Heilongjiang University of Chinese Medicine, Harbin, 150040, P. R. China. mengxianyu1973@yeah.net.

Changqing Li (C)

Heilongjiang University of Chinese Medicine, Harbin, 150006, China.

Aoyun Cui (A)

Heilongjiang University of Chinese Medicine, Harbin, 150006, China.

Xu Zhang (X)

Department of Orthopedics, The First Affiliated Hospital of Heilongjiang University of Chinese Medicine, Harbin, 150040, P. R. China.

Lina Zhao (L)

Department of Orthopedics, The First Affiliated Hospital of Heilongjiang University of Chinese Medicine, Harbin, 150040, P. R. China.

Binbin Zhao (B)

Department of Orthopedics, The First Affiliated Hospital of Heilongjiang University of Chinese Medicine, Harbin, 150040, P. R. China.

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