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蛇床子素可改善高脂肪/高糖饮食诱导的肾损伤和代谢综合征。

Osthol Ameliorates Kidney Damage and Metabolic Syndrome Induced by a High-Fat/High-Sugar Diet.

机构信息

Department of Cardio-Renal Physiopathology, INC Ignacio Chávez, Mexico City 14080, Mexico.

Department of Biology, Faculty of Chemistry, National Autonomous University of Mexico (UNAM), Mexico City 04510, Mexico.

出版信息

Int J Mol Sci. 2021 Feb 28;22(5):2431. doi: 10.3390/ijms22052431.

Abstract

Excessive intake of fructose results in metabolic syndrome (MS) and kidney damage, partly mediated by its metabolism by fructokinase-C or ketohexokinase-C (KHK-C). Osthol has antioxidant properties, is capable of regulating adipogenesis, and inhibits KHK-C activity. Here, we examined the potential protective role of osthol in the development of kidney disease induced by a Western (high-fat/high-sugar) diet. Control rats fed with a high-fat/high-sugar diet were compared with two groups that also received two different doses of osthol (30 mg/kg/d or 40 mg/kg/d body weight BW). A fourth group served as a normal control and received regular chow. At the end of the follow-up, kidney function, metabolic markers, oxidative stress, and lipogenic enzymes were evaluated. The Western diet induced MS (hypertension, hyperglycemia, hypertriglyceridemia, obesity, hyperuricemia), a fall in the glomerular filtration rate, renal tubular damage, and increased oxidative stress in the kidney cortex, with increased expression of lipogenic enzymes and increased kidney KHK expression. Osthol treatment prevented the development of MS and ameliorated kidney damage by inhibiting KHK activity, preventing oxidative stress via nuclear factor erythroid 2-related factor (Nrf2) activation, and reducing renal lipotoxicity. These data suggest that the nutraceutical osthol might be an ancillary therapy to slow the progression of MS and kidney damage induced by a Western diet.

摘要

过量摄入果糖会导致代谢综合征(MS)和肾脏损伤,部分原因是果糖激酶-C 或酮己糖激酶-C(KHK-C)代谢所致。蛇床子素具有抗氧化特性,能够调节脂肪生成,并抑制 KHK-C 活性。在这里,我们研究了蛇床子素在由西方(高脂肪/高糖)饮食引起的肾脏疾病发展中的潜在保护作用。与对照组相比,给予高脂肪/高糖饮食的对照组大鼠与另外两组也接受了两种不同剂量的蛇床子素(30mg/kg/d 或 40mg/kg/d 体重 BW)。第四组作为正常对照组,给予常规饮食。在随访结束时,评估了肾功能、代谢标志物、氧化应激和脂肪生成酶。西方饮食诱导 MS(高血压、高血糖、高三酰甘油血症、肥胖、高尿酸血症)、肾小球滤过率下降、肾小管损伤以及肾脏皮质氧化应激增加,脂肪生成酶表达增加,肾 KHK 表达增加。蛇床子素治疗通过抑制 KHK 活性、通过核因子红细胞 2 相关因子(Nrf2)激活预防氧化应激以及减少肾脏脂肪毒性,预防了 MS 的发展并改善了肾脏损伤。这些数据表明,营养保健品蛇床子素可能是一种辅助治疗方法,可减缓由西方饮食引起的 MS 和肾脏损伤的进展。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8b2e/7957708/46fc56c57375/ijms-22-02431-g001.jpg

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