首页> 外文OA文献 >Growth hormone releasing peptide 2 reverses anorexia associated with chemotherapy with 5-fluorouracil in colon cancer cell-bearing mice
【2h】

Growth hormone releasing peptide 2 reverses anorexia associated with chemotherapy with 5-fluorouracil in colon cancer cell-bearing mice

机译:生长激素释放肽2逆转含5-氟尿嘧啶的结肠癌荷瘤小鼠化疗所致的厌食

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

The cancer-associated anorexia-cachexia syndrome is observed in 80% of patients with advanced-stage cancer, and is one of the major obstacles in chemotherapy. Ghrelin is a orexigenic hormone that has been proposed to prevent anorexia. Aim of the study was to determine whether the addition of the ghrelin agonist growth hormone releasing peptide 2 (GHRP-2) to cytotoxic therapy with 5-fluorouracil (5-FU) prevents the anorexia associated with chemotherapy in cancer cachectic mice. Thirty-three BALB/c female tumour-bearing mice were randomized to receive a solution containing: (a) placebo; (b) GHRP-2; (c) 5-FU; or (d) 5-FU + GHRP-2. Ten BALB/c no tumour-bearing mice received placebo solution. Food intake and survival were checked. Six hours after the drug injection the cumulative food intake was significantly increased in mice treated with the combination of 5-FU + GHRP-2 versus the 5-FU alone (P = 0.0096). On day 3, the cumulative food intake of mice treated with GHRP-2, 5-FU and 5-FU + GHRP-2 significantly increased compared with naive and vehicle groups (P = 0.0007, P = 0.0038 and P = 0.0166, respectively). The median survival time was longer in 5-FU + GHRP-2 treated mice than in those with 5-FU, although it was not significant (18 d versus 15.5 d, P = 0.7). For the first time, we demonstrated that the addition of GHRP-2 to cytotoxic therapy with 5-FU improved appetite in tumour-bearing mice with anorexia/cachexia syndrome in early stage. These data suggest that GHRP-2 may improve the efficacy of therapy and the quality of life of cancer patients thank to the amelioration of their nutritional state.
机译:在80%的晚期癌症患者中观察到与癌症相关的厌食-恶病质综合征,这是化学疗法的主要障碍之一。生长激素释放肽是一种致食激素,已被提议预防厌食症。该研究的目的是确定在使用5-氟尿嘧啶(5-FU)的细胞毒性治疗中添加生长素释放肽激动剂生长激素释放肽2(GHRP-2)是否可以预防癌症恶病质小鼠中与化疗相关的厌食症。将33只BALB / c雌性荷瘤小鼠随机分配以接受含有以下成分的溶液:(a)安慰剂; (b)GHRP-2; (c)5-FU;或(d)5-FU + GHRP-2。十只没有肿瘤的BALB / c小鼠接受安慰剂溶液。检查食物摄入和存活。注射药物后6小时,与单独使用5-FU相比,用5-FU + GHRP-2联合治疗的小鼠的累积食物摄入量显着增加(P = 0.0096)。在第3天,与单纯组和媒介组相比,用GHRP-2、5-FU和5-FU + GHRP-2处理的小鼠的累积食物摄入量显着增加(分别为P = 0.0007,P = 0.0038和P = 0.0166)。 。经5-FU + GHRP-2处理的小鼠的中位生存时间长于经5-FU处理的小鼠,但无统计学意义(18 d对15.5 d,P = 0.7)。首次,我们证明了在早期使用厌食症/恶病质综合征的荷瘤小鼠中,将GHRP-2加入5-FU的细胞毒性治疗可改善食欲。这些数据表明,GHRP-2可以改善癌症患者的营养状况,从而可以提高治疗效果和改善癌症患者的生活质量。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号