首页> 美国卫生研究院文献>Biomolecules >Protective Effect of Palm Oil-Derived Tocotrienol-Rich Fraction Against Retinal Neurodegenerative Changes in Rats with Streptozotocin-Induced Diabetic Retinopathy
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Protective Effect of Palm Oil-Derived Tocotrienol-Rich Fraction Against Retinal Neurodegenerative Changes in Rats with Streptozotocin-Induced Diabetic Retinopathy

机译:棕榈油衍生的生育三烯酚丰富的级分对链脲佐菌素诱发的糖尿病性视网膜病大鼠视网膜神经退行性变化的保护作用。

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摘要

Oxidative stress plays an important role in retinal neurodegeneration and angiogenesis associated with diabetes. In this study, we investigated the effect of the tocotrienol-rich fraction (TRF), a potent antioxidant, against diabetes-induced changes in retinal layer thickness (RLT), retinal cell count (RCC), retinal cell apoptosis, and retinal expression of vascular endothelial growth factor (VEGF) in rats. Additionally, the efficacy of TRF after administration by two different routes was compared. The diabetes was induced in Sprague-Dawley rats by intraperitoneal injection of streptozotocin. Subsequently, diabetic rats received either oral or topical treatment with vehicle or TRF. Additionally, a group of non-diabetic rats was included with either oral or topical treatment with a vehicle. After 12 weeks of the treatment period, rats were euthanized, and retinas were collected for measurement of RLT, RCC, retinal cell apoptosis, and VEGF expression. RLT and RCC in the ganglion cell layer were reduced in all diabetic groups compared to control groups ( < 0.01). However, at the end of the experimental period, oral TRF-treated rats showed a significantly greater RLT compared to topical TRF-treated rats. A similar observation was made for retinal cell apoptosis and VEGF expression. In conclusion, oral TRF supplementation protects against retinal degenerative changes and an increase in VEGF expression in rats with streptozotocin-induced diabetic retinopathy. Similar effects were not observed after topical administration of TRF.
机译:氧化应激在与糖尿病有关的视网膜神经变性和血管生成中起重要作用。在这项研究中,我们研究了富含生育三烯酚的馏分(TRF)(一种有效的抗氧化剂)对糖尿病引起的视网膜层厚度(RLT),视网膜细胞计数(RCC),视网膜细胞凋亡和视网膜表达的影响。大鼠血管内皮生长因子(VEGF)。另外,比较了通过两种不同途径给药后TRF的功效。腹膜内注射链脲佐菌素可在Sprague-Dawley大鼠中诱发糖尿病。随后,糖尿病大鼠接受了媒介物或TRF的口服或局部治疗。另外,还包括一组非糖尿病大鼠,它们接受了载体的口服或局部治疗。治疗期12周后,对大鼠实施安乐死,并收集视网膜以测量RLT,RCC,视网膜细胞凋亡和VEGF表达。与对照组相比,所有糖尿病组神经节细胞层的RLT和RCC均降低(<0.01)。但是,在实验期结束时,口服TRF治疗的大鼠与局部TRF治疗的大鼠相比,其RLT明显更高。对于视网膜细胞凋亡和VEGF表达进行了类似的观察。总之,口服TRF补充剂可预防链脲佐菌素诱发的糖尿病性视网膜病大鼠的视网膜退行性变化和VEGF表达的增加。局部施用TRF后未观察到类似效果。

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