Nowicki Philip T, Dunaway David J, Nankervis Craig A, Giannone Peter J, Reber Kristina M, Hammond Susan B, Besner Gail E, Caniano Donna A
Center for Cell and Vascular Biology, Columbus Children's Research Institute, Department of Pediatrics, Division of Neonatology, Ohio State University, USA.
J Pediatr. 2005 Jun;146(6):805-10. doi: 10.1016/j.jpeds.2005.01.046.
We asked if the tissue concentration of the potent vasoconstrictor endothelin-1 (ET-1) is greater in areas of human preterm intestine that demonstrate histologic evidence of necrotizing enterocolitis (NEC) when compared with relatively healthy areas within the same resection specimen. We then evaluated if ET-1 participates in hemodynamic regulation within intestinal subserosal arterioles harvested from portions of human preterm intestine that demonstrate NEC.
Human preterm intestine resected for NEC was divided into three zones based on proximity to the perforation (zone 1 most proximal, zone 3 most distal). Histologic evidence of NEC was determined in each zone (normal = 0, advanced necrosis = 6). The tissue concentration of ET-1 was determined by enzyme-linked immunosorbent assay within intestinal homogenates prepared from each zone. Arteriolar hemodynamics were determined in vitro on subserosal arterioles harvested from different zones. Arteriolar flow rate, diameter, and resistance were determined at pressure gradients (DeltaP) of 20 and 40 mmHg under control conditions and again after blockade of endothelin ET A receptors with BQ610 (10 -9 mol/L).
The tissue concentration of ET-1 (pg/mg protein) and histologic score in the three zones were: zone 1: 84 +/- 14, 5.5 +/- 0.3; zone 2: 99 +/- 12, 4.7 +/- 0.4, and zone 3: 33 +/- 9, 0.8 +/- 0.6, respectively (M +/- SD, n = 10 resection specimens, P < .05, zone 3 vs zones 1 and 2). Zone 2 arterioles demonstrated significantly lower flow rate and diameter and increased resistance under control conditions than zone 3 arterioles when DeltaP was either 20 or 40 mmHg (n = 7, P < .05). Treatment with BQ610 had no effect on zone 3 arterioles but significantly vasodilated zone 2 arterioles, increasing flow rate and vessel diameter, and decreasing vascular resistance (n = 7, P < .05).
The tissue concentration of ET-1 is greater in human preterm intestine that demonstrates histologic evidence of NEC. Arterioles harvested from intestine exhibiting histologic evidence of NEC demonstrate vasoconstriction when compared with arterioles from relatively healthy intestine in the same resection specimen. This vasoconstriction was reversed by blockade of endothelin ET A receptors.
我们探讨与同一切除标本中相对健康的区域相比,在显示坏死性小肠结肠炎(NEC)组织学证据的人类早产肠区域中,强效血管收缩剂内皮素-1(ET-1)的组织浓度是否更高。然后我们评估ET-1是否参与从显示NEC的人类早产肠部分采集的肠浆膜下小动脉的血流动力学调节。
因NEC而切除的人类早产肠根据与穿孔的距离分为三个区域(区域1最靠近近端,区域3最靠近远端)。在每个区域确定NEC的组织学证据(正常=0,晚期坏死=6)。通过酶联免疫吸附测定法测定从每个区域制备的肠匀浆中ET-1的组织浓度。在体外对从不同区域采集的浆膜下小动脉进行小动脉血流动力学测定。在20和40 mmHg的压力梯度(ΔP)下,在对照条件下以及在用BQ610(10-9 mol/L)阻断内皮素ET A受体后再次测定小动脉流速、直径和阻力。
三个区域中ET-1的组织浓度(pg/mg蛋白质)和组织学评分分别为:区域1:84±14,5.5±0.3;区域2:99±12,4.7±0.4,区域3:33±9,0.8±0.6(均数±标准差,n = 10个切除标本,区域3与区域1和2相比,P < 0.05)。当ΔP为20或40 mmHg时,区域2小动脉在对照条件下的流速和直径明显低于区域3小动脉,阻力增加(n = 7,P < 0.05)。用BQ610处理对区域3小动脉无影响,但可使区域2小动脉明显血管舒张,增加流速和血管直径,并降低血管阻力(n = 7,P < 0.05)。
在显示NEC组织学证据的人类早产肠中,ET-1的组织浓度更高。与同一切除标本中相对健康肠段的小动脉相比,从显示NEC组织学证据的肠中采集的小动脉表现出血管收缩。这种血管收缩通过阻断内皮素ET A受体而逆转。