García-Urkia N, Asensio A B, Cano A, Samprón N, García-Arenzana J M, Bachiller P, Aldazabal P, Eizaguirre I
Unidad Experimental, Hospital Donostia, San Sebastián.
Cir Pediatr. 2007 Jul;20(3):180-2.
Total parenteral nutrition (TPN) is not free of complications. One of the most serious is cholestasis; the cause of this complication is unclear but it may be due to a lack of an enteral stimulus for cholecystokinin (CCK) production. CCK is essential for contraction of the gallbladder and also stimulates intrahepatic bile flow. Its absence may contribute to cholestasis. After any hepatic aggression, the Kupffer cells respond and release proinflammatory cytokines, such as interleukin-1 (IL-1) and tumour necrosis factor alpha (TNF-alpha), which increase the hepatic damage. The objective of this experimental study has been to observe the effect that the exogenous administration of CCK could have on hepatic damage in experimental short bowel with and without TPN, determined using the serum levels of IL-1 and TNF-alpha.
A resection of 80% of the small bowel was performed on 53 Wistar rats and a continuous infusion of saline or TPN was initiated. The rats were divided into the following groups: SHAM (N = 14): normal saline infusion and free access to food and water. TPN (N = 15): Standard TPN. SHAM-CCK (N = 14): same as the SHAM group but with a daily dose of CCK. TPN-CCK (N = 10): same as the TPN group but with a daily dose of CCK. At the end of the experiment, the animals were sacrificed and blood samples were obtained to determine the IL-1 and TNF-alpha values by ELISA.
The IL-1 and TNF-alpha levels were higher in the TPN group (7.537 and 5.899 pg/mL, respectively) than in the SHAM group (6.509 and 4.989 pg/mL, respectively) (p > 0.05). The TNF-alpha values were higher in the SHAM group (4.989 pg/mL) than in the SHAM-CCK group (4.583 pg/mL) (p < 0.001). The IL-1 and TNF-alpha levels were higher in the TPN group than in the TPN-CCK group (6.709 and 4.794 pg/mL, respectively) (p < 0.001 for TNF-alpha).
全胃肠外营养(TPN)并非没有并发症。其中最严重的一种是胆汁淤积;这种并发症的病因尚不清楚,但可能是由于缺乏对胆囊收缩素(CCK)产生的肠内刺激。CCK对胆囊收缩至关重要,还能刺激肝内胆汁流动。其缺乏可能导致胆汁淤积。在任何肝脏受到侵害后,库普弗细胞会做出反应并释放促炎细胞因子,如白细胞介素-1(IL-1)和肿瘤坏死因子α(TNF-α),这会增加肝脏损伤。本实验研究的目的是观察外源性给予CCK对有或无TPN的实验性短肠模型中肝脏损伤的影响,通过检测IL-1和TNF-α的血清水平来确定。
对53只Wistar大鼠进行80%小肠切除术,并开始持续输注生理盐水或TPN。大鼠被分为以下几组:假手术组(N = 14):输注生理盐水,可自由进食和饮水。TPN组(N = 15):标准TPN。假手术-CCK组(N = 14):与假手术组相同,但每日给予一剂CCK。TPN-CCK组(N = 10):与TPN组相同,但每日给予一剂CCK。实验结束时,处死动物并采集血样,通过酶联免疫吸附测定法(ELISA)测定IL-1和TNF-α值。
TPN组的IL-1和TNF-α水平(分别为7.537和5.899 pg/mL)高于假手术组(分别为6.509和4.989 pg/mL)(p > 0.05)。假手术组的TNF-α值(4.989 pg/mL)高于假手术-CCK组(4.583 pg/mL)(p < 0.001)。TPN组的IL-1和TNF-α水平高于TPN-CCK组(分别为6.709和4.794 pg/mL)(TNF-α的p < 0.001)。