Revealing the expression characteristics and potential regulatory mechanisms of hub oxidative stress related genes of spinal cord injury DOI Creative Commons
Jianfeng Li, Kuileung Tong,

Jiaxiang Zhou

et al.

Research Square (Research Square), Journal Year: 2023, Volume and Issue: unknown

Published: Oct. 13, 2023

Abstract Spinal cord injury (SCI) induces oxidative stress reactions, exacerbating secondary damage. Moderating after SCI holds paramount significance for alleviating injury. At the same time, comprehensive investigations into pathogenesis of in remain limited. In this study, we analyzed public datasets to identify differentially expressed stress-related genes (DEOSRGs) at various post-injury time points, identifying 25 hub (OSRGs). We also conducted tests and validations ascertain temporal expression patterns some both tissue single-cell levels. Subsequently, unveiled association between these immune cell infiltration. Functional pathway enrichment analyses were on DEOSRGs distinct revealing alterations enriched functions signaling pathways. Additionally, summarized potential communication characteristics related among different cells points level, along with associated ligand-receptor pairs. As a subsequent step, constructed mRNA-miRNA/mRNA-miRNA-lncRNA regulatory networks transcription factors OSRGs. Finally, leveraging DSigDB database, predicted compounds capable inhibiting eight genes, offering drugs or molecules targeted interventions following SCI. Consequently, study gaining deeper insights mechanisms timely

Language: Английский

The acute spinal cord injury microenvironment and its impact on the homing of mesenchymal stem cells DOI
Jinyi Liu,

Longju Qi,

Shengzhe Bao

et al.

Experimental Neurology, Journal Year: 2024, Volume and Issue: 373, P. 114682 - 114682

Published: Jan. 9, 2024

Language: Английский

Citations

5

Neuroprotective effect and possible mechanisms of the extract of ginkgo biloba for spinal cord injury in experimental animal: a meta-analysis and systematic review DOI
Ziming Wu, Wei Wu, Xing Ding

et al.

Nutritional Neuroscience, Journal Year: 2025, Volume and Issue: unknown, P. 1 - 14

Published: Feb. 28, 2025

Spinal cord injury (SCI) is a major challenge in the medical community because of its difficulty treatment and poor prognosis. Extract ginkgo biloba (EGb) has been widely used prevention age-related neurosensory disease, which considered to have effect neuroprotection. We performed systematic review evaluate neurobiological roles EGb for treating SCI rats. Pubmed, Embase, Sinomed China National knowledge Infrastructure were searched from their inception dates April 2024, 30 articles included. The quality score included studies ranged 4 7 out 10 points, all them randomization. It was shown that after SCI, administration could significantly improve motor function (WMD = 2.09 [1.59, 2.59], p < 0.00001). Subgroup analysis concluded at doses 10-50 mg/kg improved greatest extent. In comparison with control group, reduce lipid peroxidation inhibit inflammation (MDA: SMD -1.43 [-5.05,2.20], 0.00001; iNOS: WMD -22.17 [-35.45, -8.90], addition, this suggested can antagonize inflammation, oxidative stress resistance apoptosis, promote nerve growth myelin loss on SCI. Preclinical grade suggests that, collectively, may be promising natural neuroprotective agent unique advantages mechanisms action. More clinical randomized, blind controlled trials are also needed confirm

Language: Английский

Citations

0

Cutting-Edge Technologies Illuminate the Neural Landscape of Cancer: Insights into Tumor Development DOI
Yajing Wang, Zhao‐Jun Wang,

Xinyuan Mao

et al.

Cancer Letters, Journal Year: 2025, Volume and Issue: unknown, P. 217667 - 217667

Published: March 1, 2025

Language: Английский

Citations

0

NIR responsive microneedles patch used for promoting spinal cord injury repair by modulating mitochondrial ROS microenvironment DOI

Shuangshuang Chen,

Zelin Sang,

Yumei Li

et al.

Chemical Engineering Journal, Journal Year: 2025, Volume and Issue: unknown, P. 162247 - 162247

Published: April 1, 2025

Language: Английский

Citations

0

Synergistic Antioxidant and Anti-Ferroptosis Therapy via BPNS-Encapsulated Thermoresponsive Chitosan Hydrogel for Spinal Cord Injury Regeneration DOI Creative Commons
Yang Liu,

Yingkai Wang,

Xiangzi Wang

et al.

Pharmaceutics, Journal Year: 2025, Volume and Issue: 17(5), P. 573 - 573

Published: April 26, 2025

Background: Spinal cord injury (SCI) is a devastating neurological condition with limited therapeutic options. Current clinical interventions predominantly rely on prolonged or high-dose pharmacological regimens, often causing systemic toxicity and adverse events. Although black phosphorus nanosheets (BPNSs) exhibit remarkable reactive oxygen species (ROS)-scavenging capacity to mitigate oxidative damage, their rapid degradation severely compromises efficacy. Methods: This study presents thermosensitive hydrogel gelation properties by incorporating different proportions concentrations of sodium alginate (SA) into chitosan/β-glycerophosphate (CS/β-GP) loading it BPNS for the treatment SCI in rats. In vitro, physical composite were characterized cytotoxicity ROS scavenging abilities assessed using PC12 cells; vivo, behavioral tests, histopathological analysis, transcriptomics, immunohistochemistry, Western blotting performed explore effects mechanisms. Results: The results demonstrate that this effectively slows degradation, exhibits high capacity, reduces lipid peroxidation, thereby inhibits ferroptosis apoptosis, offering neuroprotective promoting motor function recovery. Conclusions: Our findings establish CS/β-GP/SA-BPNS as multifunctional platform SCI, synergizing sustained drug release ROS–ferroptosis–apoptosis axis modulation achieve neuroprotection functional restoration. strategy provides translatable paradigm combining nanotechnology biomaterial engineering neural repair.

Language: Английский

Citations

0

Ferroptosis: a new target for depression prevention and treatment DOI
Liang Wei,

Haowei Guo,

Luyao Li

et al.

Journal of Neural Transmission, Journal Year: 2025, Volume and Issue: unknown

Published: May 3, 2025

Language: Английский

Citations

0

Macrophage membrane-modified reactive oxygen species-responsive prodrug self-assembled nanoparticles for the targeted treatment of traumatic spinal cord injury DOI

Jinyu An,

Zhanshan Gao,

Yingqiao Li

et al.

Chemical Engineering Journal, Journal Year: 2024, Volume and Issue: 487, P. 150453 - 150453

Published: March 15, 2024

Language: Английский

Citations

3

Biomaterials targeting the microenvironment for spinal cord injury repair: progression and perspectives DOI

Yating Gao,

Yu Wang, Yaqi Wu

et al.

Frontiers in Cellular Neuroscience, Journal Year: 2024, Volume and Issue: 18

Published: May 9, 2024

Spinal cord injury (SCI) disrupts nerve pathways and affects sensory, motor, autonomic function. There is currently no effective treatment for SCI. SCI occurs within three temporal periods: acute, subacute, chronic. In each period there are different alterations in the cells, inflammatory factors, signaling spinal cord. Many biomaterials have been investigated of SCI, including hydrogels fiber scaffolds, some progress has made using multiple materials. However, limitations when individual treatment, these can be significantly improved by combining treatments with stem cells. order to better understand investigate new strategies its several combination therapies that include materials combined drugs, cytokines, etc. summarized current review.

Language: Английский

Citations

3

Pharmacologic activation of activating transcription factor 6 contributes to neuronal survival after spinal cord injury in mice DOI Open Access
Yong Chang, Lü Chen, Mingzhe Zhang

et al.

Journal of Neurochemistry, Journal Year: 2024, Volume and Issue: unknown

Published: Aug. 8, 2024

The impact of primary and secondary injuries spinal cord injury (SCI) results in the demise numerous neurons, there is still no efficacious pharmacological intervention for it. Recently, studies have shown that endoplasmic reticulum stress (ERS) plays a pivotal role recovery neurological function after injury. As process to cope with intracellular accumulation misfolded unfolded proteins which triggers ERS, protein response (UPR) an important maintaining homeostasis. And, recently disclosed small molecule AA147, selectively activates activating transcription factor 6 (ATF6), has promising effects several disease models. Thus, it seems feasible protect neurons by modulating UPR. In this study, were isolated from E17-19 C57BL/6J mouse embryos we observed AA147 effectively promoted survival alleviated neuronal apoptosis oxygen-glucose deprivation/reoxygenation (OGD/R) vitro. This was evident through decrease proportion PI-positive TUNEL-positive cells, increase BCL-2 expression, expression BAX C-caspase3. in-vivo experiments, these findings corroborated TUNEL staining immunohistochemistry. It also found enhanced three arms reduced CHOP expression. Besides, mitigated ROS probably upregulating catalase Furthermore, models mice established behavioral experiments revealed facilitated motor following SCI. pharmacologic activation ATF6 represents promise therapeutic approach ameliorate prognosis

Language: Английский

Citations

2

Oral Curcumin through Mesoporous Silica Nanomaterials with Distinct Morphologies: Synthesis, Characterization, Biosafety Evaluation, and Antioxidant Activity In Vivo DOI
Xue Yang, Lu Li,

Guoshuo Shang

et al.

Langmuir, Journal Year: 2024, Volume and Issue: unknown

Published: Dec. 18, 2024

Antioxidant play a crucial role in the prevention and treatment of diseases associated with oxidative stress. Curcumin (CUR), as natural antioxidant, exhibits numerous therapeutic properties, including anti-inflammatory, antibacterial, antitumor activities. However, its limited bioavailability poor water solubility hinder application an effective antioxidant. In this study, series mesoporous silica nanomaterials distinct morphologies, i.e., nanoparticles (MSN) nanorods (MSR) were synthesized by template–sediment–etching method. CUR was selected model drug encapsulated into these to improve vivo. The morphology size distribution MSN MSR determined through transmission electron microscopy (TEM) imaging Zetasizer analysis. Fourier transform infrared spectroscopy (FTIR) spectra confirmed successful encapsulation within nanomaterials. Furthermore, CUR-loaded nanomaterials, denoted CUR@MSN CUR@MSR, exhibited excellent DPPH ABTS free radical scavenging activity vitro. CUR@MSR also obvious vivo antioxidant activity. This study opens up new avenues for development enhanced antioxidants utilization

Language: Английский

Citations

1