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新型VCP调节剂KUS121对随机型皮瓣缺血性损伤的影响

The effect of KUS121, a novel VCP modulator, against ischemic injury in random pattern flaps.

作者信息

Yoshimoto Koichi, Ikeguchi Ryosuke, Noguchi Takashi, Ando Maki, Sakamoto Daichi, Iwai Terunobu, Nishitani Kohei, Ikeda Hanako Ohashi, Kakizuka Akira, Matsuda Shuichi

机构信息

Department of Orthopaedic Surgery, Graduate School of Medicine, Kyoto University, Kyoto, Japan.

Department of Ophthalmology and Visual Sciences, Graduate School of Medicine, Kyoto University, Kyoto, Japan.

出版信息

PLoS One. 2024 Dec 26;19(12):e0299882. doi: 10.1371/journal.pone.0299882. eCollection 2024.

Abstract

Surgery using skin flaps is essential for soft tissue reconstruction. However, postoperative ischemic injury of the skin flap is a major complication and a top concern after the surgery. Currently, evidence-based drugs to fully prevent ischemic injury are not available. The purpose of this study was to evaluate the effect of KUS121, a VCP modulator, on flap ischemia using a rodent model. 26 Sprague-Dawley rats were randomly divided into two groups. The experimental group was intraperitoneally administered with 100 mg/kg KUS121 dissolved in 5% glucose solution 1 hour before surgery and once per day after surgery. The control group received the same amount of glucose solution on the same schedule. On day 7, 33.6 ± 3.7% of skin flaps in the control group had developed black necrosis compared with 26.4 ± 3.6% in the KUS121 group (p < 0.01). Immunohistochemistry showed that the KUS121 treatment reduced the number of apoptotic cells in the distal third of the flap (p < 0.01); moreover, in the KUS121-treated rats, the number of cells expressing CHOP, an endoplasmic reticulum (ER) stress marker, in the middle third of the flap was significantly lower than in the controls (p < 0.01). We examined the mRNA expression of Ddit3 (CHOP) and Casp3 (caspase-3) on day one after the surgery; mRNA expression of both genes appeared to decrease in the KUS121 group, as compared with the control group, although differences between groups were not significant. Thus, in a random pattern flap, KUS121 reduces ER stress and the number of apoptotic cells, thereby reducing ischemic damage of the flap.

摘要

使用皮瓣进行手术对于软组织重建至关重要。然而,皮瓣术后缺血性损伤是主要并发症,也是术后最受关注的问题。目前,尚无充分预防缺血性损伤的循证药物。本研究的目的是使用啮齿动物模型评估VCP调节剂KUS121对皮瓣缺血的影响。26只Sprague-Dawley大鼠被随机分为两组。实验组在手术前1小时腹腔注射溶解于5%葡萄糖溶液中的100 mg/kg KUS121,术后每天注射一次。对照组按相同时间表接受等量葡萄糖溶液。在第7天,对照组33.6±3.7%的皮瓣出现黑色坏死,而KUS121组为26.4±3.6%(p<0.01)。免疫组织化学显示,KUS121治疗减少了皮瓣远端三分之一处的凋亡细胞数量(p<0.01);此外,在接受KUS121治疗的大鼠中,皮瓣中间三分之一处表达内质网(ER)应激标志物CHOP的细胞数量显著低于对照组(p<0.01)。我们在手术后第一天检测了Ddit3(CHOP)和Casp3(caspase-3)的mRNA表达;与对照组相比,KUS121组这两个基因的mRNA表达似乎均有所下降,尽管组间差异不显著。因此,在随机模式皮瓣中,KUS121可减轻内质网应激和凋亡细胞数量,从而减少皮瓣的缺血性损伤。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/289a/11671021/227154496509/pone.0299882.g001.jpg

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