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一种新型前列环素类似物贝拉普罗斯对假性内膜增生的抑制作用

Suppression of pseudointimal hyperplasia by a novel prostacyclin analogue: beraprost.

作者信息

Kim D I, Kambayashi J, Shibuya T, Sakon M, Kawasaki T, Mori T

机构信息

Department of Surgery, Samsung Medical Center, Seoul, Korea.

出版信息

Surg Today. 1995;25(8):722-8. doi: 10.1007/BF00311489.

Abstract

The aim of this study was to evaluate the effect of a novel prostaglandin I2 analogue, beraprost (BPT), on the pseudointimal hyperplasia (PIH) of polytetrafluoroethylene (PTFE) prostheses. A total of 12 rabbits were equally divided into three groups. The control group was given a placebo daily, group 1 was given BPT orally 2 mg/kg per day, and group 2 was given BPT orally 4 mg/kg b.i.d. Exactly 1 cm of the inferior vena cava was resected and replaced by a 3-cm PTFE tube graft. All the grafts were patent when harvested 4 weeks after implantation, but the lumens were narrowed to various extents by PIH. PIH, determined by the dry weight of the intraluminal tissue deposit, was significantly (P < 0.01) suppressed in groups 1 and 2 compared with the control group. High-magnification light microscopy with various staining methods revealed the PIH to be composed mainly of smooth muscle cells (SMCs) and collagen fibrils in all three groups. Transmission electron microscopy revealed that the majority of SMCs in groups 1 and 2 were contractile in form, in contrast with the synthetic form seen in the control group. In conclusion, BPT attenuated the PIH of PTFE grafts by inhibiting the phenotype change in the SMCs.

摘要

本研究的目的是评估一种新型前列腺素I2类似物贝拉前列素(BPT)对聚四氟乙烯(PTFE)人工血管假内膜增生(PIH)的影响。总共12只兔子被平均分为三组。对照组每天给予安慰剂,第1组每天口服2 mg/kg的BPT,第2组每天口服4 mg/kg,每日两次。精确切除1 cm的下腔静脉,并用3 cm的PTFE管状移植物进行替换。所有移植物在植入后4周收获时均通畅,但管腔因PIH而不同程度地变窄。与对照组相比,第1组和第2组中,通过腔内组织沉积物干重测定的PIH受到显著抑制(P < 0.01)。采用各种染色方法的高倍光学显微镜检查显示,所有三组中的PIH主要由平滑肌细胞(SMC)和胶原纤维组成。透射电子显微镜显示,第1组和第2组中的大多数SMC呈收缩型,与对照组中所见的合成型相反。总之,BPT通过抑制SMC的表型变化减轻了PTFE移植物的PIH。

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