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使用体外和体内糖尿病周围神经病变模型研究红海海洋海绵提取物的神经保护作用

Neuroprotective Effect of Red Sea Marine Sponge Extract Using In Vitro and In Vivo Diabetic Peripheral Neuropathy Models.

作者信息

Magadmi Rania, Borouk Kariman, Youssef Diaa T A, Shaala Lamiaa A, Alrafiah Aziza R, Shaik Rasheed A, Alharthi Sameer E

机构信息

Pharmacology Department, Faculty of Medicine, King Abdulaziz University, Jeddah 22254, Saudi Arabia.

Department of Natural Products, Faculty of Pharmacy, King Abdulaziz University, Jeddah 21589, Saudi Arabia.

出版信息

Pharmaceuticals (Basel). 2022 Oct 24;15(11):1309. doi: 10.3390/ph15111309.

Abstract

Diabetic peripheral neuropathy (DPN) is a common complication of diabetes. Oxidative stress plays an important role in the pathophysiology of DPN. Red Sea marine sponge extract has a promising neuroprotective effect, presumably owing to its antioxidant and anti-inflammatory properties. Thus, this study aimed to investigate the neuroprotective effect of the sponge extract on in vitro and in vivo models of DPN. Mice dorsal root ganglia (DRG) were cultured with high glucose (HG) media and used as an in vitro model of DPN. Some of the DRGs were pre-treated with 2 mg/mL of . The extract significantly improved the HG-induced decreased neuronal viability and the neurite length. It improved the oxidative stress biomarkers in DRG cultures. The DPN model was induced in vivo by an injection of streptozotocin at a dose of 150 mg/kg in mice. After 35 days, 0.75 mg/kg of the extract improved the hot hyperalgesia and the DRG histology. Although the sponge extract did not reduce hyperglycemia, it ameliorated the oxidative stress markers and pro-inflammatory markers in the DRG. In conclusion, the current study demonstrates the neuroprotective effect of Red Sea sponge extract against experimentally induced DPN through its antioxidant and anti-inflammatory mechanisms.

摘要

糖尿病周围神经病变(DPN)是糖尿病常见的并发症。氧化应激在DPN的病理生理学中起重要作用。红海海洋海绵提取物具有显著的神经保护作用,可能归因于其抗氧化和抗炎特性。因此,本研究旨在探讨海绵提取物对DPN体外和体内模型的神经保护作用。将小鼠背根神经节(DRG)用高糖(HG)培养基培养,用作DPN的体外模型。部分DRG用2mg/mL的[提取物名称未给出]进行预处理。该提取物显著改善了HG诱导的神经元活力降低和神经突长度缩短。它改善了DRG培养物中的氧化应激生物标志物。通过给小鼠注射剂量为150mg/kg的链脲佐菌素在体内诱导DPN模型。35天后,0.75mg/kg的提取物改善了热痛觉过敏和DRG组织学。尽管海绵提取物没有降低血糖,但它改善了DRG中的氧化应激标志物和促炎标志物。总之,本研究证明了红海海绵提取物通过其抗氧化和抗炎机制对实验性诱导的DPN具有神经保护作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7986/9693000/5156dc8be52b/pharmaceuticals-15-01309-g001.jpg

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