Abstract

BackgroundCisplatin (CDDP) is a highly effective chemotherapeutic agent used for therapy of many tumors and has been limited by its toxicity. Zengmian Yiliu granule (ZMYL), a compound preparation of traditional Chinese medicines, has been used in clinic as a complementary and alternative medicine for attenuating CDDP-induced toxicities and enhancing the tumor therapeutic effect of CDDP. The aim of the present study is to investigate hepaprotective effect of ZMYL against CDDP-induced hepatotoxicity. Further, the pharmacokinetic characteristics of CDDP in SKOV-3-bearing nude mice were observed.MethodsThe ICR mice were dosed orally with ZMYL for 7 days and then CDDP was injected intraperitoneally at a dose of 45 mg/kg body weight. The serum alanine aminotransferase (ALT) and aspartate aminotransferase (AST) levels were measured to evaluate the liver function. The total glutathione (T-GSH), reduced glutathione (GSH) and glutathione S-transferase (GST) levels were determined to evaluate the oxidant damage in liver homogenates. Tissue pathological change in liver was conducted by light microscopy analysis. The pharmacokinetic and tissue distribution of free and total platinum (Pt) after dosing of CDDP alone and combination with ZMYL were determined in SKOV-3-bearing nude mice by ICP-MS.ResultsOral administration of ZMYL prior to the CDDP treatment could prevent the CDDP-induced in lifting of ALT and AST, reduction of T-GSH, R-GSH and GST, and some histopathological alterations in ICR mice. Some differences in pharmacokinetic parameters between the two groups have been observed in higher CL and decreased MRT of free platinum (Pt) in plasma and total Pt in spleen in CDDP co-administration with ZMYL group. It indicated CDDP was cleared more quickly from blood and spleen, and could reduce the accumulation and toxic possibility of CDDP in combination with ZMYL.ConclusionsZMYL could be used as a beneficial supplement, which could attenuate CDDP-induced hepatotoxicity during CDDP chemotherapy and did not disturb the pharmacokinetics fate of CDDP significantly.Electronic supplementary materialThe online version of this article (doi:10.1186/s12906-015-0799-9) contains supplementary material, which is available to authorized users.

Highlights

  • Cisplatin (CDDP) is a highly effective chemotherapeutic agent used for therapy of many tumors and has been limited by its toxicity

  • Some previous pharmacodynamics studies revealed that Zengmian Yiliu granule (ZMYL) could regulate the immune function and improve the bone marrow suppression in tumor bearing mice destroyed by CDDP [15], inhibit neoangiogenesis of tumor vessels [16] and reverse the CDDP-resistance of resistant ovarian cancer in nude mice [17]. These results indicated that ZMYL could be as a potential complementary and alternative medicine for CDDP chemotherapy, the protective effect of ZMYL in CDDP-induced hepatotoxicity is needed to be investigated further

  • Light microscopy analysis revealed that in liver sections from mice treated with CDDP, CDDP treatment alone induced some alterations of the liver parenchyma when compared to both control and ZMYL-treated mice

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Summary

Introduction

Cisplatin (CDDP) is a highly effective chemotherapeutic agent used for therapy of many tumors and has been limited by its toxicity. The aim of the present study is to investigate hepaprotective effect of ZMYL against CDDP-induced hepatotoxicity. As a first-generation platinum (Pt) antitumor agent, cisplatin (cis-diaminedichloroplatinum, CDDP) has been widely used in chemotherapy either alone or in combination with other chemotherapeutic agents or with radiotherapy for treatment of a variety of different malignancies, including testicular cancer, ovarian cancer, (non-) small cell lung cancer, head and neck cancer and bladder cancer [1]. Despite its excellent anticancer activity, the clinical use of CDDP is often limited by its undesirable side effects, such as severe hepatotoxicity and nephrotoxicity [2, 3]. The elevated GSH and GST play an important role in protecting CDDP-induced hepatotoxicity

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