Niinikoski Harri, Stoll Barbara, Guan Xinfu, Kansagra Ketan, Lambert Barry D, Stephens John, Hartmann Bolette, Holst Jens J, Burrin Douglas G
U.S. Department of Agriculture/ARS Children's Nutrition Research Center, Department of Pediatrics, Baylor College of Medicine, Houston, TX 77030, USA.
J Nutr. 2004 Jun;134(6):1467-74. doi: 10.1093/jn/134.6.1467.
Our aim was to determine the speed of onset of total parenteral nutrition (TPN)-induced mucosal atrophy, and whether this is associated with changes in intestinal blood flow and tissue metabolism in neonatal piglets. Piglets were implanted with jugular venous and duodenal catheters and either a portal venous or superior mesenteric artery (SMA) blood flow probe. At 3 wk of age, piglets were randomly assigned to receive continuous enteral formula feeding (n = 8) or TPN (n = 17) for 24 or 48 h. Blood flow was recorded continuously and piglets were given an i.v. bolus of bromodeoxyuridine and (13)C-phenylalanine to measure crypt cell proliferation and protein synthesis, respectively. After 8 h of TPN, portal and SMA blood flow decreased 30% compared with enteral feeding (P < 0.01), and remained near levels of food-deprived piglets for the remaining 48 h of TPN. After 24 h, TPN reduced jejunal inducible nitric oxide synthase (iNOS) activity and protein abundance (P < 0.05), small intestinal weight, and villous height (P < 0.01) compared with enterally fed piglets. Cell proliferation and DNA mass were decreased (P < 0.05) and apoptosis increased (P < 0.05) after 48 h of TPN. Protein synthesis was lower (P < 0.05) after 24 h of TPN, and protein mass was lower (P < 0.05) after 48 h of TPN, compared with enteral feeding. These data indicate that the transition from enteral to parenteral nutrition induced a rapid (<8 h) decrease in intestinal blood flow, and this likely precedes villous atrophy and the suppression of protein synthesis at 24 h, and of cell proliferation and survival at 48 h.
我们的目的是确定全胃肠外营养(TPN)诱导的黏膜萎缩的发生速度,以及这是否与新生仔猪肠道血流和组织代谢的变化有关。给仔猪植入颈静脉和十二指肠导管以及门静脉或肠系膜上动脉(SMA)血流探头。3周龄时,将仔猪随机分为两组,分别接受持续肠内配方奶喂养(n = 8)或TPN(n = 17)24或48小时。连续记录血流情况,并分别给仔猪静脉注射大剂量溴脱氧尿苷和(13)C-苯丙氨酸,以测量隐窝细胞增殖和蛋白质合成。TPN治疗8小时后,门静脉和SMA血流与肠内喂养相比下降了30%(P < 0.01),在TPN治疗的剩余48小时内,血流水平一直接近禁食仔猪的水平。24小时后,与肠内喂养的仔猪相比,TPN降低了空肠诱导型一氧化氮合酶(iNOS)活性和蛋白丰度(P < 0.05)、小肠重量和绒毛高度(P < 0.01)。TPN治疗48小时后,细胞增殖和DNA量减少(P < 0.05),细胞凋亡增加(P < 0.05)。与肠内喂养相比,TPN治疗24小时后蛋白质合成较低(P < 0.05),TPN治疗48小时后蛋白质总量较低(P < 0.05)。这些数据表明,从肠内营养过渡到胃肠外营养会导致肠道血流迅速(<8小时)下降,这可能先于24小时时的绒毛萎缩和蛋白质合成抑制,以及48小时时的细胞增殖和存活抑制。