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首页> 外文期刊>European Journal of Pharmacology: An International Journal >Effects of trans-resveratrol on type 1 diabetes-induced inhibition of retinoic acid metabolism pathway in retinal pigment epithelium of Dark Agouti rats
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Effects of trans-resveratrol on type 1 diabetes-induced inhibition of retinoic acid metabolism pathway in retinal pigment epithelium of Dark Agouti rats

机译:反霉素对1型糖尿病型糖尿病患者诱导的黑暗刺染大鼠视网膜色素上皮型视黄酸代谢途径的影响

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摘要

Genesis and progression of diabetic retinopathy are due to glucotoxicity-induced changes in intracellular milieu in the retina. This study investigated effects of trans-resveratrol on type 1 diabetes-induced changes in gene expressions and retinoic acid metabolism pathway in the RPE (retinal pigment epithelium) of Dark Agouti rats. Microarray analysis showed differential expressions of 833 genes in the RPE of 14 day-long diabetic rats, which increased to 1249 after they received 5 mg/kg trans-resveratrol. Diabetes inhibited the expression of retinoic acid metabolism pathway genes-Lpl, Lrat, RPE65, Rdh5, Rdh10, Rdh12, Rlbp1 and Rbp1 and increased Crabp1. Trans-resveratrol further downregulated the expression of these genes except Lpl, Rdh5, and Rdh12 but upregulated Cyp26b1. RT-PCR showed inhibition of Lrat, Rdh5, and Rdh10 in diabetic rats supplemented with or without trans-resveratrol on 14d. Trans-resveratrol normalized Rdh5 and increased Lrat and Rdh10 transcriptions compared to control and diabetic rats. Trans-resveratrol amplified diabetes-induced inhibition of RPE65, but it inhibited the induced increase in Crabp1 transcription on 30d. Trans-resveratrol reversed the diabetes-induced decrease in Cyp26b1 transcription on 14d and 30d and normalized Cyp3a9 transcription on 30d. Transresveratrol normalized the diabetes-induced increase in Rdh5, Rdh10, and Cyp3a9 protein levels, but it further increased Cyp26b1 protein level. In conclusion, diabetes differentially regulates numerous genes in the RPE, including that of retinoic acid metabolism pathway. Trans-resveratrol supplementation is beneficial to normalize long-term effects, but not short-term effects, of diabetes on retinoic acid metabolism pathway in the RPE.
机译:糖尿病视网膜病变的成因和进展是由于视网膜中细胞内Milieu的葡萄酸毒性诱导的变化。本研究研究了转霉醇对糖尿病大鼠RPE(视网膜颜料上皮型)基因表达和视黄酸代谢途径的1型糖尿病诱导的变化的影响。微阵列分析显示在14天长的糖尿病大鼠RPE中的833个基因的差异表达,在接受5mg / kg反式白藜芦醇后增加至1249。糖尿病抑制视黄酸代谢途径基因-LPL,LRAT,RPE65,RDH5,RDH10,RDH12,RLBP1和RBP1和RBP1增加的表达。反霉醇进一步下调除LPL,RDH5和RDH12外,但除了LPL,RDH5和RDH12之外的表达,但上调CYP26B1。 RT-PCR显示抑制LRAT,RDH5和RDH10在14D上补充有或不含转霉醇的糖尿病大鼠。与对照和糖尿病大鼠相比,转霉rDH5和增加的LRAT和RD10转录增加。转铁糖醇扩增糖尿病诱导的RPE65抑制,但它抑制了30D的Crabp1转录的诱导增加。 Trans-erveratrol在30D上逆转14D和30D和30D和标准化CYP3A9转录的CYP26B1转录的糖尿病诱导的降低。 Transresvertrol标准化糖尿病诱导的RDH5,RDH10和CYP3A9蛋白水平增加,但进一步增加了CYP26B1蛋白质水平。总之,糖尿病差异地调节RPE中的许多基因,包括视黄酸代谢途径。反式白藜芦醇补充有利于正常化糖尿病在RPE中视黄酸代谢途径的长期效应,但不是短期影响。

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