The potential effect of salvianolic acid B against rat ischemic brain injury in combination with mesenchymal stem cells

IF 2.7 4区 医学 Q3 BIOCHEMISTRY & MOLECULAR BIOLOGY Journal of chemical neuroanatomy Pub Date : 2023-09-12 DOI:10.1016/j.jchemneu.2023.102338
Minli Yan , Zheming Li , Shijie Dai , Shouye Li , Pingping Yu
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Abstract

Background

Mesenchymal stem cells (MSCs) and Salvianolic acid B (SAB) are known to exert potent anti-inflammatory and anti-oxidative properties. But the effect of SAB and MSCs combination treatment on the cerebral ischemia/reperfusion injury (CI/RI) is not clear.

Methods

After the CI/RI animal model established, rats were administered with MSCs and SAB individually or combination treatment. To evaluate the therapeutic potential, behavioral tests, TTC staining, Hematoxylin-eosin (HE) staining, and immunofluorescence assays were performed to evaluate the neuroprotection and endogenous neurogenesis. Terminal deoxynucleotidyl transferase dUTP nick end labeling (TUNEL) staining and enzyme linked immunosorbent assay (ELISA) were performed to evaluate the anti-apoptosis and anti-inflammatory effect. Meanwhile, the expression of the TLR4/NF-ĸB/MYD88 signal pathway-related proteins was evaluated by Western blot.

Results

MSCs and SAB individually or combination treatment have protective effect in CI/RI rats. More importantly, the rats with the combination treatment showed a better behavioral recovery, neurogenesis and smaller infarct size compared with the rats administered with MSCs or SAB individually. Further research showed that the combination treatment decreased CI/RI induced inflammatory cytokines and oxidative stress, including inhibiting the production of IL-1β, IL-6, TNF-α, decreasing the levels of malondialdehyde (MDA), and increased the activity of superoxide dismutase (SOD). In addition, the neuroprotection effect of SAB and MSCs combination was achieved through the regulation of TLR4/NF-κB/MyD88 signaling pathway related proteins, including inhibition the protein levels of TLR4, MYD88, p-NF-κB p65, TRAF6-and action of SIRT1 in brain tissues.

Conclusion

The present study indicated that the MSCs and SAB combination treatment had better protective effect against rat ischemic brain injury. The combination of SAB and MSCs may provide a potent and promising strategy for the treatment of ischemic stroke and is worthy for further development.

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丹酚酸B与间充质干细胞联合应用对大鼠缺血性脑损伤的潜在作用。
背景:众所周知,间充质干细胞(MSC)和丹酚酸B(SAB)具有强大的抗炎和抗氧化特性。但SAB和MSCs联合治疗对脑缺血再灌注损伤(CI/RI)的影响尚不清楚。方法:建立大鼠CI/RI动物模型后,分别给予MSCs和SAB或联合用药。为了评估治疗潜力,进行了行为测试、TTC染色、苏木精-伊红(HE)染色和免疫荧光测定,以评估神经保护和内源性神经发生。采用末端脱氧核苷酸转移酶dUTP缺口末端标记(TUNEL)染色和酶联免疫吸附试验(ELISA)评价其抗细胞凋亡和抗炎作用。同时,通过蛋白质印迹法评估TLR4/NF-ĸB/MYD88信号通路相关蛋白的表达。结果:MSCs和SAB单独或联合治疗对CI/RI大鼠均有保护作用。更重要的是,与单独给予MSCs或SAB的大鼠相比,联合治疗的大鼠表现出更好的行为恢复、神经发生和更小的梗死面积。进一步研究表明,联合治疗降低了CI/RI诱导的炎性细胞因子和氧化应激,包括抑制IL-1β、IL-6、TNF-α的产生,降低了丙二醛(MDA)水平,提高了超氧化物歧化酶(SOD)活性。此外,SAB和MSCs组合的神经保护作用是通过调节TLR4/NF-κB/MyD88信号通路相关蛋白实现的,包括抑制脑组织中TLR4、MyD88、p-NF-κB p65、TRAF6的蛋白水平和SIRT1的作用。结论:MSCs和SAB联合治疗对大鼠缺血性脑损伤有较好的保护作用。SAB和MSCs的组合可能为缺血性中风的治疗提供一种有效且有前景的策略,值得进一步发展。
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阿拉丁
sodium β-glycerophosphate
¥47.00~¥50000.00
阿拉丁
ascorbic acid
¥15.00~¥20675.84
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dexamethasone
¥36.00~¥9880.00
上海源叶
Salvianolic acid B |≥98%
¥71.90~¥5614.00
阿拉丁
sodium β-glycerophosphate
来源期刊
Journal of chemical neuroanatomy
Journal of chemical neuroanatomy 医学-神经科学
CiteScore
4.50
自引率
3.60%
发文量
87
审稿时长
62 days
期刊介绍: The Journal of Chemical Neuroanatomy publishes scientific reports relating the functional and biochemical aspects of the nervous system with its microanatomical organization. The scope of the journal concentrates on reports which combine microanatomical, biochemical, pharmacological and behavioural approaches. Papers should offer original data correlating the morphology of the nervous system (the brain and spinal cord in particular) with its biochemistry. The Journal of Chemical Neuroanatomy is particularly interested in publishing important studies performed with up-to-date methodology utilizing sensitive chemical microassays, hybridoma technology, immunocytochemistry, in situ hybridization and receptor radioautography, to name a few examples. The Journal of Chemical Neuroanatomy is the natural vehicle for integrated studies utilizing these approaches. The articles will be selected by the editorial board and invited reviewers on the basis of their excellence and potential contribution to this field of neurosciences. Both in vivo and in vitro integrated studies in chemical neuroanatomy are appropriate subjects of interest to the journal. These studies should relate only to vertebrate species with particular emphasis on the mammalian and primate nervous systems.
期刊最新文献
Editorial Board Brain Mechanisms – An evolving perspective on the future of neuroscience Editorial Board Retraction notice to “Astrocyte response to melatonin treatment in rats under high-carbohydrate high-fat diet” [J. Chem. Neuroanat. 136 (2024) 102389] Retraction notice to “Coenzyme Q10 attenuates neurodegeneration in the cerebellum induced by chronic exposure to tramadol” [J. Chem. Neuroanat. 135 (2024) 102367]
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