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乌拉地尔对大鼠睾丸扭转-复位损伤的保护作用。

Protective effect of urapidil on testicular torsion-detorsion injury in rats.

作者信息

Meštrović Jakov, Pogorelić Zenon, Drmić-Hofman Irena, Vilović Katarina, Todorić Davor, Popović Marijana

机构信息

Department of Pediatric Surgery, Split University Hospital Centre and Split University School of Medicine, Spinčićeva 1, 21 000, Split, Croatia.

Department of Medical Chemistry and Biochemistry, University of Split School of Medicine, Spinčićeva 1, 21 000, Split, Croatia.

出版信息

Surg Today. 2017 Mar;47(3):393-398. doi: 10.1007/s00595-016-1388-3. Epub 2016 Jul 21.

Abstract

PURPOSE

The aim of this study was to investigate the effect of urapidil and low-molecular weight heparin (LMWH) on testicular torsion-detorsion injury in rats.

METHODS

Thirty-two male Sprague-Dawley rats were used. In the torsion-detorsion (T/D) group, the left testis was twisted at 720° for 3 h. After 3 h of reperfusion, the testis was removed. Urapidil or LMWH was administered intraperitoneally 30 min before detorsion in the treatment groups.

RESULTS

Unilateral testicular torsion-detorsion caused significant increases in the malondialdehyde level and apoptosis and significant decreases in the superoxide dismutase (SOD) and glutathione peroxidase (GPx) activities in ipsilateral testes (p < 0.001). The rats treated with urapidil had a significant decrease in the malondialdehyde level and apoptosis and significant increases in the SOD and GPx activities in ipsilateral testes compared to the T/D group (p < 0.001). Animals treated with LMWH showed non-significant reductions in malondialdehyde levels and apoptosis compared to the T/D group. In addition, no significant difference in the SOD activities (p = 0.52) between the groups was found. The increase in the GPx activities was significant in the LMWH group compared to the T/D group (p < 0.001).

CONCLUSION

The administration of urapidil before detorsion prevents ischemia/reperfusion cellular damage in testicular tissue. LMWH was not found to have a beneficial effect on testicular T/D injury in rats.

摘要

目的

本研究旨在探讨乌拉地尔和低分子量肝素(LMWH)对大鼠睾丸扭转-复位损伤的影响。

方法

使用32只雄性Sprague-Dawley大鼠。在扭转-复位(T/D)组中,将左侧睾丸扭转720°,持续3小时。再灌注3小时后,取出睾丸。治疗组在复位前30分钟腹腔注射乌拉地尔或LMWH。

结果

单侧睾丸扭转-复位导致同侧睾丸丙二醛水平和细胞凋亡显著增加,超氧化物歧化酶(SOD)和谷胱甘肽过氧化物酶(GPx)活性显著降低(p<0.001)。与T/D组相比,乌拉地尔治疗的大鼠同侧睾丸丙二醛水平和细胞凋亡显著降低,SOD和GPx活性显著增加(p<0.001)。与T/D组相比,LMWH治疗的动物丙二醛水平和细胞凋亡无显著降低。此外,各组间SOD活性无显著差异(p=0.52)。与T/D组相比,LMWH组GPx活性的增加显著(p<0.001)。

结论

复位前给予乌拉地尔可预防睾丸组织缺血/再灌注细胞损伤。未发现LMWH对大鼠睾丸T/D损伤有有益作用。

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