Triptolide improves nerve regeneration and functional recovery following crush injury to rat sciatic nerve

2014 ◽  
Vol 561 ◽  
pp. 198-202 ◽  
Author(s):  
Yong-Guang Zhang ◽  
Qing-Song Sheng ◽  
Hong-Kun Wang ◽  
Li Lv ◽  
Jun Zhang ◽  
...  
2020 ◽  
Vol 209 (1) ◽  
pp. 43-53 ◽  
Author(s):  
Zohreh Jahromi ◽  
Fahimeh Mohammadghasemi ◽  
Farshad Moharrami Kasmaie ◽  
Arash Zaminy

Peripheral nerve injury is a common clinical issue induced by trauma, tumor, and damage caused by treatment. Such factors create chemical and inflammatory alterations at the injury site, which increase nerve deterioration. Thus, minimizing these modifications can lead to nerve protection after injury. The present study sought to evaluate the possible improvement in nerve regeneration and enhancement of functional outcomes by cinnamaldehyde (Cin) administration following sciatic nerve crush in a rat model. Rats (n = 48) were distributed into 6 groups, including sham, injury, DMSO (vehicle group), and Cin groups (10, 30, and 90 mg/kg/day). Using small hemostatic forceps, crush injury was induced in the left sciatic nerve. Thereafter, Cin was administered for 28 successive days. Weekly records were taken for sciatic functional index (SFI) measurements. Further assessments including electrophysiological and histomorphometric evaluations, gastrocnemius muscle wet weight measurements, and estimation of the serum total oxidant status were performed. According to the results, Cin could accelerate sciatic nerve recovery after crush injury, and the dose of 30 mg/kg/day of Cin had better impacts on SFI recovery, muscle mass ratio, and myelin content. The current research demonstrated that Cin positively affects peripheral nerve restoration. Therefore, Cin therapy could be considered as a potential treatment method for peripheral nerve regeneration and its functional recovery. However, more investigations are required to further validate the study results and evaluate the optimal dose of Cin.


Microsurgery ◽  
2002 ◽  
Vol 22 (6) ◽  
pp. 234-241 ◽  
Author(s):  
Eftal Gudemez ◽  
Kagan Ozer ◽  
Brian Cunningham ◽  
Krzysztof Siemionow ◽  
Earl Browne ◽  
...  

2018 ◽  
Vol 57 (5) ◽  
pp. 821-828 ◽  
Author(s):  
Tao Lin ◽  
Shuai Qiu ◽  
Liwei Yan ◽  
Shuang Zhu ◽  
Canbin Zheng ◽  
...  

2005 ◽  
Vol 63 (7) ◽  
pp. 973-977 ◽  
Author(s):  
Awwad Al-Bishri ◽  
Lars Dahlin ◽  
Bo Sunzel ◽  
Jan Rosenquist

Neurosurgery ◽  
2018 ◽  
Vol 85 (3) ◽  
pp. 423-431
Author(s):  
Sara Alicia González Porto ◽  
Nieves Domenech ◽  
Francisco J Blanco ◽  
Alberto Centeno Cortés ◽  
Casto Rivadulla Fernández ◽  
...  

Abstract BACKGROUND Insulin-like growth factor 1 (IGF-1) was found to stimulate Schwann cell mitosis. Exogenous IGF-1 may improve nerve regeneration after cryopreservation. OBJECTIVE To evaulate the effect of intraneural administration of IGF-1 in cryopreserved nerve isografts. METHODS Eighteen millimeter grafts were used for bridging an 18-mm defect in the rat sciatic nerve. A total of 57 rats were randomly divided into three groups: (1) autograft (Group 1); (2) cryopreserved isograft (Group 2); (3) cryopreserved isograft with intraneural IGF-1 administration (Group 3). 12 weeks after surgery, functional recovery (Sciatic functional index [SFI], Swing speed [SS], nerve conduction velocity [NCV], amplitude of compound motor action potentials [CMAP], and gastrocnemius muscle index [GMI]) and nerve regeneration (myelin sheath area, total fiber counts, fiber density, and fiber width) were all evaluated. RESULTS The intraneural injection of IGF-1 significantly improved SFI and SS at weeks 10 and 12. There were no statistical differences between Groups 1 and 3 in any of the SFI or SS evaluations. CMAP and NCV in Group 1 were significantly higher than in Groups 2 and 3, and Group 3 had significantly higher CMAP and NCV compared to Group 2. No significant differences were found in fiber width. The number of nerve fibers, percentage of myelinated fibers, fiber density, and GMI was significantly higher in Group 1 compared to Group 2, but no significant differences were found between Groups 1 and 3. CONCLUSION The results show that intraneural injection of IGF-1 in an 18 mm cryopreserved isograft improve axonal regeneration and functional recovery.


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