Demir Selim, Kazaz Ilke Onur, Kerimoglu Gokcen, Ayazoglu Demir Elif, Colak Fatih, Yilmaz Sedanur, Mentese Ahmet
Faculty of Health Sciences, Department of Nutrition and Dietetics, Karadeniz Technical University, Trabzon, Turkey.
Faculty of Medicine, Department of Urology, Karadeniz Technical University, Trabzon, Turkey.
J Invest Surg. 2022 May;35(5):1044-1049. doi: 10.1080/08941939.2021.1995540. Epub 2021 Nov 10.
The aim of this study was to investigate the effects of astaxanthin (ASX) on testicular torsion/detorsion (T/D) damage in rats in terms of oxidative stress and endoplasmic reticulum (ER) stress.
Eighteen male Sprague-Dawley rats were divided into three groups with six rats in each group: control, T/D and T/D + 20 mg/kg ASX. Torsion and detorsion times were applied as 4 h and 2 h, respectively. ASX application was performed 30 minutes before detorsion. At the end of the period, testicular tissues were removed and biochemical and histological analyzes were performed. To evaluate the degree of oxidative stress, tissue malondialdehyde (MDA), total oxidant status (TOS) and total antioxidant status (TAS) were determined using colorimetric methods, while tissue superoxide dismutase (SOD) levels were determined using ELISA kit. To evaluate the degree of ER stress, tissue glucose regulatory protein 78 (GRP78), activating transcription factor 6 (ATF6) and C/EBP homologous protein (CHOP) levels were determined using ELISA kits. Johnsen's testicle scoring system was used for histological evaluation.
In the T/D group, it is determined that statistically significant decreasing in TAS, SOD levels and Johnsen score, and increasing in TOS, OSI, MDA, GRP78, ATF6 and CHOP levels (p < 0.001) compared with control group. ASX administration statistically significantly restored this T/D-induced damage (p < 0.01).
This is the first study to show that ASX prevent T/D-induced testicular damage through its antioxidant activity. More comprehensive studies are needed to see the underlying mechanisms.
本研究旨在从氧化应激和内质网(ER)应激方面探讨虾青素(ASX)对大鼠睾丸扭转/去扭转(T/D)损伤的影响。
将18只雄性Sprague-Dawley大鼠分为三组,每组6只:对照组、T/D组和T/D + 20 mg/kg ASX组。扭转和去扭转时间分别为4小时和2小时。在去扭转前30分钟给予ASX。在实验期末,取出睾丸组织并进行生化和组织学分析。为评估氧化应激程度,采用比色法测定组织丙二醛(MDA)、总氧化剂状态(TOS)和总抗氧化剂状态(TAS),同时使用ELISA试剂盒测定组织超氧化物歧化酶(SOD)水平。为评估ER应激程度,使用ELISA试剂盒测定组织葡萄糖调节蛋白78(GRP78)、活化转录因子6(ATF6)和C/EBP同源蛋白(CHOP)水平。采用约翰森睾丸评分系统进行组织学评估。
与对照组相比,T/D组中TAS、SOD水平和约翰森评分在统计学上显著降低,而TOS、氧化应激指数(OSI)、MDA、GRP78、ATF6和CHOP水平升高(p < 0.001)。ASX给药在统计学上显著恢复了这种T/D诱导的损伤(p < 0.01)。
这是第一项表明ASX通过其抗氧化活性预防T/D诱导的睾丸损伤的研究。需要更全面的研究来了解潜在机制。