Heeckt P F, Halfter W M, Schraut W H, Lee K K, Bauer A J
Department of Surgery, University of Pittsburgh, School of Medicine, Pa.
Surgery. 1993 Aug;114(2):449-56; discussion 456-7.
The purpose of this study was to determine whether morphologic and functional changes in intestinal smooth muscle occur after small bowel transplantation (SBTx) and during chronic rejection.
Orthotopic SBTx was performed in syngeneic (ACI-ACI, n = 6) and allogeneic (ACI-Lewis, n = 6) rat strain combinations. The latter received temporary immunosuppression (cyclosporine 15 mg/kg/body weight on postoperative days 0 to 6 once a day, postoperative days 7 to 28 every other day), which led to clinically quiescent chronic rejection of the graft by 90 days after SBTx. At that time structure and function of the jejunal muscularis externa were evaluated with histochemistry, mechanical organ bath, and intracellular electrical recording techniques.
Histochemistry showed a 1.5-fold thickening of the intestinal muscularis externa of syngeneic grafts, although contractile properties and intracellular electrical activity were not significantly different from controls. Allogeneic, chronically rejecting grafts showed a threefold increase in the thickness of the muscularis externa as a result of both smooth muscle hyperplasia and hypertrophy. Muscle strips from chronically rejecting grafts generated only 23% of the maximal contractile force generated by controls (bethanechol 300 mumol/L). Median effective concentration and threshold values were not significantly different. Intracellular electrical activity of circular smooth muscle cells revealed a significantly more depolarized resting membrane potential and a reduction in slow wave amplitude compared with controls.
Syngeneic SBTx resulted in a significant thickening of the muscularis externa with an apparent adaptation to control in vitro physiologic function. Allogeneic SBTx subject to chronic rejection leads to profound morphologic changes and functional impairments. Changes in muscle structure and function evolve before the clinical signs of graft rejection.
本研究旨在确定小肠移植(SBTx)后及慢性排斥反应期间肠道平滑肌是否发生形态学和功能变化。
在同基因(ACI-ACI,n = 6)和异基因(ACI-Lewis,n = 6)大鼠品系组合中进行原位SBTx。后者接受临时免疫抑制(术后第0至6天每天给予环孢素15 mg/kg体重,术后第7至28天隔天给药),这导致SBTx后90天移植物出现临床静止的慢性排斥反应。此时,采用组织化学、机械器官浴和细胞内电记录技术评估空肠外肌层的结构和功能。
组织化学显示同基因移植物的肠道外肌层增厚1.5倍,尽管收缩特性和细胞内电活动与对照组无显著差异。异基因慢性排斥移植物由于平滑肌增生和肥大,外肌层厚度增加了两倍。慢性排斥移植物的肌条产生的最大收缩力仅为对照组(氨甲酰甲胆碱300 μmol/L)的23%。半数有效浓度和阈值无显著差异。与对照组相比,环形平滑肌细胞的细胞内电活动显示静息膜电位明显去极化,慢波幅度降低。
同基因SBTx导致外肌层显著增厚,并明显适应体外生理功能的控制。遭受慢性排斥反应的异基因SBTx会导致深刻的形态学变化和功能损害。肌肉结构和功能的变化在移植物排斥的临床体征出现之前就已发生。