Araújo C V, Lazzarotto C R, Aquino C C, Figueiredo I L, Costa T B, Alves L A de Oliveira, Ribeiro R A, Bertolini L R, Lima A A M, Brito G A C, Oriá R B
Laboratório da Biologia da Cicatrização, Ontogenia e Nutrição de Tecidos, INCT - Instituto de Biomedicina do Semiárido Brasileiro, Faculdade de Medicina, Universidade Federal do Ceará, Fortaleza, CE, Brasil.
Laboratório de Biologia Molecular e do Desenvolvimento, Universidade de Fortaleza, Fortaleza, CE, Brasil.
Braz J Med Biol Res. 2015 Jun;48(6):493-501. doi: 10.1590/1414-431X20144360. Epub 2015 Apr 28.
Apolipoprotein E (APOE=gene, apoE=protein) is a known factor regulating the inflammatory response that may have regenerative effects during tissue recovery from injury. We investigated whether apoE deficiency reduces the healing effect of alanyl-glutamine (Ala-Gln) treatment, a recognized gut-trophic nutrient, during tissue recovery after 5-FU-induced intestinal mucositis. APOE-knockout (APOE-/-) and wild-type (APOE+/+) C57BL6J male and female mice (N=86) were given either Ala-Gln (100 mM) or phosphate buffered saline (PBS) by gavage 3 days before and 5 days after a 5-fluorouracil (5-FU) challenge (450 mg/kg, via intraperitoneal injection). Mouse body weight was monitored daily. The 5-FU cytotoxic effect was evaluated by leukometry. Intestinal villus height, villus/crypt ratio, and villin expression were monitored to assess recovery of the intestinal absorptive surface area. Crypt length, mitotic, apoptotic, and necrotic crypt indexes, and quantitative real-time PCR for insulin-like growth factor-1 (IGF-1) and B-cell lymphoma 2 (Bcl-2) intestinal mRNA transcripts were used to evaluate intestinal epithelial cell turnover. 5-FU challenge caused significant weight loss and leukopenia (P<0.001) in both mouse strains, which was not improved by Ala-Gln. Villus blunting, crypt hyperplasia, and reduced villus/crypt ratio (P<0.05) were found in all 5-FU-challenged mice but not in PBS controls. Ala-Gln improved villus/crypt ratio, crypt length and mitotic index in all challenged mice, compared with PBS controls. Ala-Gln improved villus height only in APOE-/- mice. Crypt cell apoptosis and necrotic scores were increased in all mice challenged by 5-FU, compared with untreated controls. Those scores were significantly lower in Ala-Gln-treated APOE+/+ mice than in controls. Bcl-2 and IGF-1 mRNA transcripts were reduced only in the APOE-/- -challenged mice. Altogether our findings suggest APOE-independent Ala-Gln regenerative effects after 5-FU challenge.
载脂蛋白E(APOE=基因,apoE=蛋白质)是一种已知的调节炎症反应的因子,在组织从损伤中恢复的过程中可能具有再生作用。我们研究了在5-氟尿嘧啶(5-FU)诱导的肠道粘膜炎后的组织恢复过程中,apoE缺乏是否会降低丙氨酰谷氨酰胺(Ala-Gln)治疗的愈合效果,丙氨酰谷氨酰胺是一种公认的肠内营养物质。在5-氟尿嘧啶(5-FU)攻击(450mg/kg,腹腔注射)前3天和后5天,通过灌胃给予载脂蛋白E基因敲除(APOE-/-)和野生型(APOE+/+)的C57BL6J雄性和雌性小鼠(N=86)丙氨酰谷氨酰胺(100mM)或磷酸盐缓冲盐水(PBS)。每天监测小鼠体重。通过白细胞计数评估5-FU的细胞毒性作用。监测肠绒毛高度、绒毛/隐窝比值和绒毛蛋白表达,以评估肠道吸收表面积的恢复情况。隐窝长度、有丝分裂、凋亡和坏死隐窝指数,以及胰岛素样生长因子-1(IGF-1)和B细胞淋巴瘤2(Bcl-2)肠道mRNA转录本的定量实时PCR用于评估肠上皮细胞更新。5-FU攻击在两种小鼠品系中均导致显著体重减轻和白细胞减少(P<0.001),丙氨酰谷氨酰胺并未改善这一情况。在所有接受5-FU攻击的小鼠中均发现绒毛变钝、隐窝增生和绒毛/隐窝比值降低(P<0.05),而在PBS对照组中未发现。与PBS对照组相比,丙氨酰谷氨酰胺改善了所有受攻击小鼠的绒毛/隐窝比值、隐窝长度和有丝分裂指数。丙氨酰谷氨酰胺仅在APOE-/-小鼠中改善了绒毛高度。与未处理的对照组相比,所有接受5-FU攻击的小鼠隐窝细胞凋亡和坏死评分均增加。在丙氨酰谷氨酰胺处理的APOE+/+小鼠中,这些评分显著低于对照组。Bcl-2和IGF-1 mRNA转录本仅在接受APOE-/-攻击的小鼠中减少。总之,我们的研究结果表明,在5-FU攻击后,丙氨酰谷氨酰胺具有不依赖于APOE的再生作用。