Improvement of LXR-mediated lipid metabolism in nephrotic model kidney accompanied by suppression of inflammation and fibrosis

被引:3
|
作者
Yonezawa, Sei [1 ,2 ]
Kawasaki, Yasushi [2 ,3 ]
Natori, Yasuhiro [2 ]
Sugiyama, Akinori [2 ]
机构
[1] Univ Shizuoka, Sch Pharmaceut Sci, Dept Med Biochem, 52-1 Yada,Suruga Ward, Shizuoka 4228526, Japan
[2] Iwate Med Univ, Sch Pharm, Hlth Chem, 1-1-1 Idaiodori, Yahaba, Iwate 0283694, Japan
[3] Iryo Sosei Univ, Fac Pharm, 5-5-1 Chuodai Iino, Iwaki, Fukushima 9708551, Japan
关键词
Nuclear receptor; LXR; T0901317; Nephrosis; Lipid metabolism; LIVER X RECEPTORS; ALPHA; CD36;
D O I
10.1016/j.bbrc.2023.05.019
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Kidney disease affects millions of people worldwide. Chronic kidney diseases, such as diabetic ne-phropathy, are often accompanied by nephrotic syndrome, which causes a large amount of protein and lipid to leak out into the urine. Leaked lipids are well known to accumulate in the proximal tubules as lipid droplets. However, the role of lipid metabolism in the kidney has not been thoroughly studied, and the relationship between accumulated lipid and pathological progression is often unknown. In this study, we showed that reducing accumulated lipids by exerting an agonistic effect on Liver X receptor, one of the nuclear receptors known to play an important role in lipid metabolism, suppressed the development of pathological conditions, such as inflammation and fibrosis, in a nephrosis model. Until now, many renal disease treatments have focused on suppressing the inflammatory response. However, it is now clear that even if the direct anti-inflammatory response is weak, the spread of inflammation and fibrosis can be suppressed by reducing accumulated lipids. Our results suggest that reducing abnormal lipid accumulation in the kidney could lead to disease treatment. (c) 2023 Elsevier Inc. All rights reserved.
引用
收藏
页码:122 / 127
页数:6
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