Effects of Nogo-A and its receptor on the repair of sciatic nerve injury in rats

Jiang, Junjie; Yu, Yuanchen; Zhang, Zhiwu; Ji, Yuan; Guo, Hong; Wang, Xiaohua; Yu, Shengjun

doi:10.1590/1414-431x2020e10842

Cited by 3 publications

(2 citation statements)

References 33 publications

(33 reference statements)

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“… 19 This further causes growth cone collapse and inhibits CNS axons. 20 NgR is a receptor for Nogo protein inhibition, and the family includes NgR1, NgR2, and NgR3, among which NgR1 needs to bind to the low-affinity neurotrophic factor receptor p75 or TROY or the nervous system-specific transmembrane protein LINGO-1 to co-mediate the myelin inhibitory response because it cannot mediate transmembrane or intracellular signaling. 21 22 After a successful SCI model was established, Nogo-A, NgR, LINGO-1, RhoA, and ROCK II protein and mRNA expression increased in rat spinal cord tissue.…”

Section: Discussionmentioning

confidence: 99%

Effects of exercise training on neurological recovery, TGF-β1, HIF-1α, and Nogo-NgR signaling pathways after spinal cord injury in rats

Liu

et al. 2023

Clinics

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Section: Discussionmentioning

confidence: 99%

Effects of exercise training on neurological recovery, TGF-β1, HIF-1α, and Nogo-NgR signaling pathways after spinal cord injury in rats

Liu

et al. 2023

Clinics

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“…It has been reported in previous study that Shenfu injection might show anti-inflammatory or anti-oxidative effects on myocardial ischemia-reperfusion injury, sepsis, and acute lung injury in rats [20][21][22][23]. Nogo-NgR was associated with axonal regeneration, and inhibition of Nogo-NgR could attenuate nerve injury in previous studies [24][25][26]. Results of our study indicated that Shenfu injection may suppress CA-induced Nogo-NgR up-expression in the hippocampus of rats and improve neurological function, which suggested that Shenfu injection might protect brain in rats with CA and be helpful for axonal regeneration through Nogo/NgR pathway.…”

Section: Discussionmentioning

confidence: 99%

Shenfu Injection Protects Brain Injury in Rats with Cardiac Arrest through Nogo/NgR Pathway

Deng

Tang

Tuo

et al. 2022

Analytical Cellular Pathology

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The effect of Shenfu injection on brain injury after cardiac arrest (CA) and cardiopulmonary resuscitation (CPR) along with the underlying mechanism of axonal regeneration was explored. CA/CPR model in rats was established for subsequent experiments. A total of 160 rats were randomly divided into sham group, model group, conventional western medicine (CWM) group, Shenfu group, and antagonist group ( n = 32 per group). After 3 hours, 24 hours, 3 days, and 7 days of drug administration, the modified Neurological Severity Score tests were performed. The ultrastructure of the brain and hippocampus was observed by electron microscopy. Real-time quantitative polymerase chain reaction (PCR), western blotting, and immunohistochemistry were used to detect Nogo receptor (NgR) expression in the hippocampus and cerebral cortex, and Nogo–NgR expression in CA/CPR model. Neurological deficits in the model group were severe at 3 hours, 24 hours, 3 days, and 7 days after the recovery of natural circulation, whereas the neurological deficits in CWM, antagonist, and Shenfu group were relatively mild. The ultrastructure of neuronal cells in Shenfu group had relatively complete cell membranes and more vesicles than those in the model group. The results of PCR and western blotting showed lower messenger ribonucleic acid and protein expression of NgR in Shenfu group than the model group and CWM group. Immunohistochemical examination indicated a reduction of Nogo–NgR expression in Shenfu group and antagonist group. Our results suggested that Shenfu injection reduced brain injury by attenuating Nogo–NgR signaling pathway and promoting axonal regeneration.

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Human Umbilical Cord Mesenchymal Stem Cells Improve the Status of Hypoxic/Ischemic Cerebral Palsy Rats by Downregulating NogoA/NgR/Rho Pathway

Luo,

Qu,

et al. 2023

Cell Transplant

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Human umbilical cord mesenchymal stem cells (hUCMSC) have shown promising potential in ameliorating brain injury, but the mechanism is unclear. We explore the role of NogoA/NgR/Rho pathway in mediating hUCMSC to improve neurobehavioral status and alleviate brain injury in hypoxia/ischemia-induced CP (cerebral palsy) rat model in order to promote the clinical application of stem cell therapy in CP. The injury model of HT22 cells was established after 3 h hypoxia, and then co-cultured with hUCMSC. The rat model of CP was established by ligation of the left common carotid artery for 2.5 h. Subsequently, hUCMSC was administered via the tail vein once a week for a total of four times. The neurobehavioral status of CP rats was determined by behavioral experiment, and the pathological brain injury was determined by pathological staining method. The mRNA and protein expressions of NogoA, NgR, RhoA, Rac1, and CDC42 in brain tissues of rats in all groups and cell groups were detected by real-time quantitative polymerase chain reaction (RT-qPCR), Western blot, and immunofluorescence. The CP rats exhibited obvious motor function abnormalities and pathological damage. Compared with the control group, hUCMSC transplantation could significantly improve the neurobehavioral situation and attenuate brain pathological injury in CP rats. The relative expression of NogoA, NgR, RhoA mRNA, and protein in brain tissues of rats in the CP group was significantly higher than the rats in the sham and CP+hUCMSC group. The relative expression of Rac1, CDC42 mRNA, and protein in brain tissues of rats in the CP group was significantly lower than the rats in the sham and CP+hUCMSC group. The animal experiment results were consistent with the experimental trend of hypoxic injury of HT22 cells. This study confirmed that hUCMSC can efficiently improve neurobehavioral status and alleviate brain injury in hypoxia/ischemia-induced CP rat model and HT22 cell model through downregulating the NogoA/NgR/Rho pathway.

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Effects of Nogo-A and its receptor on the repair of sciatic nerve injury in rats

Cited by 3 publications

References 33 publications

Effects of exercise training on neurological recovery, TGF-β1, HIF-1α, and Nogo-NgR signaling pathways after spinal cord injury in rats

Effects of exercise training on neurological recovery, TGF-β1, HIF-1α, and Nogo-NgR signaling pathways after spinal cord injury in rats

Shenfu Injection Protects Brain Injury in Rats with Cardiac Arrest through Nogo/NgR Pathway

Human Umbilical Cord Mesenchymal Stem Cells Improve the Status of Hypoxic/Ischemic Cerebral Palsy Rats by Downregulating NogoA/NgR/Rho Pathway

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