Salvianolic acid A as a multifunctional agent ameliorates doxorubicin-induced nephropathy in rats

被引:48
作者
Fan, Hua-Ying [1 ]
Yang, Ming-Yan [1 ]
Qi, Dong [2 ]
Zhang, Zuo-Kai [1 ]
Zhu, Lin [1 ]
Shang-Guan, Xiu-Xin [1 ]
Liu, Ke [3 ]
Xu, Hui [1 ]
Che, Xin [1 ]
机构
[1] Yantai Univ, Sch Pharm, Yantai 264005, Shandong, Peoples R China
[2] Yantai Yu Huang Ding Hosp, Yantai 264000, Shandong, Peoples R China
[3] Shandong Target Drug Res Co Ltd, Yantai 264005, Shandong, Peoples R China
基金
中国国家自然科学基金;
关键词
NF-KAPPA-B; OXIDATIVE STRESS; NEPHROTIC SYNDROME; RENAL-DISEASE; ANGIOTENSIN-II; ACTIVATION; INJURY; MECHANISM; PODOCIN; KIDNEY;
D O I
10.1038/srep12273
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Nephrotic syndrome (NS) is still a therapeutic challenge. To date there is no ideal treatment. Evidence suggest that multidrug therapy has more effect than monotherapy in amelioration of renal injury. Salvianolic acid A (SAA) is the major active component of Salviae Miltiorrhizae Bunge. Previous studies have demonstrated that SAA is a multi-target agent and has various pharmacological activities. The pleiotropic properties of SAA predict its potential in the treatment of NS. The study investigated the effect of SAA on doxorubicin-induced nephropathy. The kidney function related-biochemical changes, hemorheological parameters and oxidative stress status were determined, and histological examination using light and transmission electron microcopies and western blot analysis were also performed. Results revealed that treatment with SAA alleviated histological damages, relieved proteinuria, hypoalbuminemia and hyperlipidemia, reduced oxidative stress, as well as improving hemorheology. Furthermore, SAA restored podocin expression, down-regulated the expression of NF-kappa B p65 and p-I kappa B alpha while up-regulating I kappa B alpha protein expression. Overall, as a multifunctional agent, SAA has a favorable renoprotection in doxorubicin-induced nephropathy. The anti-inflammation, antioxidant, amelioration of podocyte injury, improvement of hemorheology and hypolipidemic properties may constituent an important part of its therapeutic effects. All these indicate that SAA is likely to be a promising agent for NS.
引用
收藏
页码:1 / 11
页数:11
相关论文
共 43 条
[1]   Novel multidrug therapy for children with cyclosporine-resistant or -intolerant nephrotic syndrome [J].
Aizawa-Yashiro, Tomomi ;
Tsuruga, Kazushi ;
Watanabe, Shojiro ;
Oki, Eishin ;
Ito, Etsuro ;
Tanaka, Hiroshi .
PEDIATRIC NEPHROLOGY, 2011, 26 (08) :1255-1261
[2]   NF-κB in Renal Inflammation [J].
Belen Sanz, Ana ;
Dolores Sanchez-Nino, Maria ;
Mario Ramos, Adrian ;
Antonio Moreno, Juan ;
Santamaria, Beatriz ;
Ruiz-Ortega, Marta ;
Egido, Jesus ;
Ortiz, Alberto .
JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY, 2010, 21 (08) :1254-1262
[3]  
BERTANI T, 1982, LAB INVEST, V46, P16
[4]  
Bulucu F, 2000, CLIN NEPHROL, V53, P169
[5]   The nephrotic syndrome is an immunoinflammatory disorder [J].
Camici, Marcello .
MEDICAL HYPOTHESES, 2007, 68 (04) :900-905
[6]  
陈孟华, 2012, [肾脏病与透析肾移植杂志, Chinese Journal of Nephrology, Dialysis & Transplantation], V21, P450
[7]   Nephrotic plasma alters slit diaphragm-dependent signaling and translocates nephrin, podocin, and CD2 associated protein in cultured human podocytes [J].
Coward, RJM ;
Foster, RR ;
Patton, D ;
Ni, L ;
Lennon, R ;
Bates, DO ;
Harper, SJ ;
Mathieson, PW ;
Saleem, MA .
JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY, 2005, 16 (03) :629-637
[8]  
Dai SC, 2005, GUO JI MI NIAO XI TO, V25, P226
[9]  
Dong Y., 2005, CHINA J MODERN MED, V15, P2842
[10]   Nephrotic syndrome in childhood [J].
Eddy, AA ;
Symons, JM .
LANCET, 2003, 362 (9384) :629-639