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生长激素释放肽2可逆转荷结肠癌细胞小鼠因5-氟尿嘧啶化疗所致的厌食。

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

作者信息

Perboni Simona, Bowers Cyril, Kojima Shinya, Asakawa Akihiro, Inui Akio

机构信息

Unità Operativa Day Hospital Area Medicia, Azienda Ospedaliera di Desenzano sul Garda, Ospedale di Manerbio, Brescia, Italy.

出版信息

World J Gastroenterol. 2008 Nov 7;14(41):6303-5. doi: 10.3748/wjg.14.6303.

Abstract

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-fluoruracil (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.

摘要

80%的晚期癌症患者会出现癌症相关性厌食-恶病质综合征,这是化疗的主要障碍之一。胃饥饿素是一种促食欲激素,有人提出它可预防厌食。本研究的目的是确定在使用5-氟尿嘧啶(5-FU)进行细胞毒性治疗时添加胃饥饿素激动剂生长激素释放肽2(GHRP-2)是否能预防癌症恶病质小鼠化疗相关的厌食。33只荷瘤雌性BALB/c小鼠被随机分为四组,分别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。10只无瘤BALB/c小鼠接受安慰剂溶液。检查食物摄入量和生存率。药物注射6小时后,5-FU + GHRP-2联合治疗的小鼠累积食物摄入量比单独使用5-FU的小鼠显著增加(P = 0.0096)。第3天,与未处理组和溶剂对照组相比,接受GHRP-2、5-FU和5-FU + GHRP-2治疗的小鼠累积食物摄入量显著增加(分别为P = 0.0007、P = 0.0038和P = 0.0166)。5-FU + GHRP-2治疗的小鼠中位生存时间比5-FU治疗的小鼠长,尽管差异不显著(18天对15.5天,P = 0.7)。我们首次证明,在使用5-FU进行细胞毒性治疗时添加GHRP-2可改善早期厌食/恶病质综合征荷瘤小鼠的食欲。这些数据表明,GHRP-2可能通过改善癌症患者的营养状态来提高治疗效果和生活质量。

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