Protective Effects of Dendropanax morbifera against Cisplatin-Induced Nephrotoxicity without Altering Chemotherapeutic Efficacy

被引:15
作者
Kim, Ji Su [1 ]
Kim, Kyeong Seok [1 ]
Son, Ji Yeon [1 ]
Kim, Hae Ri [1 ]
Park, Jae Hyeon [1 ]
Lee, Su Hyun [1 ]
Lee, Da Eun [1 ]
Kim, In Su [1 ]
Lee, Kwang Youl [2 ,3 ]
Lee, Byung Mu [1 ]
Kwak, Jong Hwan [1 ]
Kim, Hyung Sik [1 ]
机构
[1] Sungkyunkwan Univ, Sch Pharm, Div Toxicol, Suwon 16419, South Korea
[2] Chonnam Natl Univ, Coll Pharm, Div Mol Biol, Gwangju 61186, South Korea
[3] Chonnam Natl Univ, Res Inst Drug Dev, Gwangju 61186, South Korea
基金
新加坡国家研究基金会;
关键词
cisplatin; Dendropanax morbifera; renoprotective effect; antioxidants; chemotherapy; xenograft model; ACUTE KIDNEY INJURY; OXIDATIVE STRESS; RENAL INJURY; BIOMARKER; MECHANISMS; APOPTOSIS;
D O I
10.3390/antiox8080256
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
Use of the chemotherapeutic agent cisplatin (CDDP) in cancer patients is limited by the occurrence of acute kidney injury (AKI); however, no protective therapy is available. We aimed to investigate the renoprotective effects of Dendropanax morbifera water extract (DM) on CDDP-induced AKI. Male Sprague-Dawley rats (six animals/group) received: Vehicle (control); CDDP (6 mg/kg, intraperitoneally (i.p.); DM (25 mg/kg, oral); or DM + CDDP injection. CDDP treatment significantly increased blood urea nitrogen (BUN), serum creatinine (sCr), and pro-inflammatory cytokines (IL-6 and TNF-alpha), and severely damaged the kidney architecture. Urinary excretion of protein-based AKI biomarkers also increased in the CDDP-treated group. In contrast, DM ameliorated CDDP-induced AKI biomarkers. It markedly protected against CDDP-induced oxidative stress by increasing the activity of endogenous antioxidants and reducing the levels of pro-inflammatory cytokines (IL-6 and TNF-alpha). The protective effect of DM in the proximal tubules was evident upon histopathological examination. In a tumor xenograft model, administration of DM enhanced the chemotherapeutic activity of CDDP and exhibited renoprotective effects against CDDP-induced nephrotoxicity without altering chemotherapeutic efficacy. Our data demonstrate that DM may be an adjuvant therapy with CDDP in solid tumor patients to preserve renal function.
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页数:16
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