食品科学 ›› 2013, Vol. 34 ›› Issue (21): 325-328.doi: 10.7506/spkx1002-6630-201321065

• 营养卫生 • 上一篇    下一篇

葡萄籽原花青素对顺铂诱发小鼠肾毒性的保护作用

郭卓雨,高丽萍*,李 贞   

  1. 生物活性物质与功能食品北京市重点实验室,北京联合大学应用文理学院,北京 100191
  • 收稿日期:2013-06-26 修回日期:2013-10-09 出版日期:2013-11-15 发布日期:2013-10-28
  • 通讯作者: 高丽萍 E-mail:gaolip62@163.com
  • 基金资助:

    北京联合大学人才强校计划人才资助项目(BPHR2011A01)

Protective Effect of Grape Seed Proanthocyanidin Extract against Cisplatin-induced Nephrotoxicity in Mice

GUO Zhuo-yu,GAO Li-ping*,LI Zhen   

  1. Beijing Municipal Key Laboratory of Biological Active Substance and Functional Food, College of Applied Arts and Science,
    Beijing Union University, Beijing 100191, China
  • Received:2013-06-26 Revised:2013-10-09 Online:2013-11-15 Published:2013-10-28
  • Contact: GAO Li-ping E-mail:gaolip62@163.com

摘要:

目的:探讨葡萄籽原花青素(GSPE)对顺铂(CDDP)诱发小鼠肾毒性的作用影响,并探讨可能的作用机制。方法:选用60只成年雄性小鼠,随机分为正常组、CDDP模型组、GSPE+CDDP提前组和GSPE+CDDP同时组4组,正常组、CDDP模型组和GSPE+CDDP同时组每日喂饲常规饲料,灌胃蒸馏水,GSPE提前组小鼠灌胃GSPE200mg/(kg•d),持续12d。实验第10天,正常组小鼠腹腔注射生理盐水,其余组一次性腹腔注射CDDP 20mg/kg以建立CDDP肾损伤模型,同时组则同时进行GSPE 200mg/kg灌胃。腹腔注射后第3天处死动物,测定各组小鼠血清尿素氮(BUN)、肌酐(Scr)含量及肾组织超氧化物歧化酶(SOD)、谷胱甘肽过氧化物酶(GSH-Px)、一氧化氮合成酶(NOS)活性,同时测定丙二醛(MDA)、一氧化氮(NO)含量。结果:GSPE对CDDP所致小鼠肾组织抗氧化酶(SOD、GSH-Px)活力降低和血清尿素氮(BUN)、肌酐(Scr)及脂质过氧化物含量(MDA、NO、NOS)升高有明显抑制作用(P<0.01或P<0.05),且提前使用GSPE组其保护作用优于CDDP与GSPE同时使用组。结论:GSPE对CDDP诱发小鼠肾组织氧化损伤具有保护作用,其机制可能与GSPE降低脂质过氧化物,升高抗氧化酶活力有关。

关键词: 葡萄籽原花青素, 顺铂, 肾毒性, 保护作用

Abstract:

Objective: To investigate the protective effect and possible mechanisms of grape seed proanthocyanidin extract
(GSPE) against cisplatin (CDDP)-induced nephrotoxicity in mice. Methods: A total of 60 adult male mice were randomly
divided into control group, CDDP model group, GSPE + CDDP pretreatment group and GSPE + CDDP co-administration
group. The blank control, CDDP model and GSPE + CDDP co-administration groups were fed a normal diet and orally
administered with distilled water during the administration period, while the GSPE + CDDP pretreatment group with GSPE
at 200 mg/(kg•d) for 12 consecutive days. After administration for 10 days, the blank control group was given normal saline
by intraperitoneal injection while a single injection of CDDP (20 mg/kg) in the remaining groups was carried out to establish
mouse model of renal injury. At the end of the administration period (13th day), all mice were sacrificed to determine serum
blood urine nitrogen (BUN) and serum creatinine concentration (Scr) contents, superoxide dismutese (SOD), glutathione
peroxidase (GSH-Px) and nitric oxide synthase (NOS) activities, and malonaldehyde (MDA) and nitrogen oxide (NO)
contents. Results: The GSPE pretreatment group could significantly inhibit the CDDP-induced inactivation of antioxidant
enzymes (SOD and GSH-Px) and the increase in serum blood urine nitrogen (BUN) and serum creatinine concentration
(Scr) contents as well as the levels of lipid peroxide (MDA, NO and NOS) in renal tissues of mice (P < 0.05 or P < 0.01),
and these effects were better than those observed for the GSPE + CDDP co-administration group. Conclusion: GSPE has a
protective effect on CDDP-induced nephrotoxicity in mice. The possible mechanism is associated with the fact that GSPE
can decrease the contents of lipid peroxide, and can increase the antioxidant enzyme activities.

Key words: grape seed proanthocyanidin extract (GSPE), cisplatin, nephrotoxicity, protective effect

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