Aloperine protects the testis against testicular ischemia/reperfusion injury in rats

IF 4.3 3区 材料科学 Q1 ENGINEERING, ELECTRICAL & ELECTRONIC ACS Applied Electronic Materials Pub Date : 2024-09-10 DOI:10.1111/andr.13750
Shichao Wei, Junshen Xiao, Feng Ju, Zhaoyang Hu
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Abstract

BackgroundTesticular torsion/detorsion can cause testis loss and infertility. Aloperine is a major active alkaloid extracted from Sophora alopecuroides Linn. It has been shown to have organ‐protective effects. However, the effects of aloperine on the testis and its underlying mechanisms remain unclear.ObjectivesThis study investigated the effect of aloperine on testicular torsion/detorsion injury in rats.Materials and MethodsMale Sprague‐Dawley rats were randomized to the sham‐operated (sham), testicular I/R (TI/R), or aloperine preconditioning (ALOPre) or postconditioning (ALOPost) groups. All rats except for the sham‐operated rats were subjected to 3 h of right spermatic cord torsion (720°, clockwise), followed by 3 h of detorsion. Aloperine (10 mg/kg) was intravenously administered before testicular torsion (ALOPre) or at the onset of testicular detorsion (ALOPost). The therapeutic efficacy of aloperine was evaluated by histological analysis, oxidative stress evaluation, inflammatory response examination, apoptosis analysis, protein analysis, and immunohistological assessment.ResultsCompared with TI/R, aloperine protected both the ipsilateral and contralateral testes against unilateral testicular I/R, as evidenced by a reduced testicular weight to body weight (TW/BW) ratio (ALOPre: p = 0.0037; ALOPost: p = 0.0021) and volume (ALOPre: p = 0.0020; ALOPost: p = 0.0009), less structural damage with better Johnsen (ALOPre: p = 0.0013; ALOPost: p = 0.0021), and Cosentino scores (ALOPre: p < 0.0001; ALOPost: p < 0.0001), increased mean seminiferous tubule diameter and mean seminiferous tubule epithelial height, decreased testicular apoptosis, and less oxidative stress and inflammatory response. In addition, aloperine significantly stimulated the phosphorylation of signal transducer and activator of transcription (STAT)‐3 in the ipsilateral testes following detorsion. Administration of Ag490 suppressed STAT‐3 phosphorylation, thereby abrogating the protective effects exerted by aloperine on the ipsilateral testis.Discussion and ConclusionAloperine has a strong testicular protective effect on the ipsilateral and contralateral testes after testicular torsion/detorsion. This aloperine‐induced ipsilateral testicular protection is mediated via the STAT‐3 signaling pathway.
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阿洛哌啶能保护大鼠睾丸免受睾丸缺血再灌注损伤的伤害
背景睾丸扭转/脱出可导致睾丸缺失和不育。阿洛哌啶是从槐属植物中提取的一种主要活性生物碱。它已被证明具有器官保护作用。材料和方法将雄性 Sprague-Dawley 大鼠随机分为假手术组(sham)、睾丸 I/R 组(TI/R)、阿洛哌林预处理组(ALOPre)或后处理组(ALOPost)。除假手术大鼠外,所有大鼠均接受 3 小时的右侧精索扭转(720°,顺时针方向),然后再进行 3 小时的扭转。在睾丸扭转前(ALOPre)或睾丸扭转开始时(ALOPost)静脉注射阿洛哌嗪(10 毫克/千克)。通过组织学分析、氧化应激评估、炎症反应检查、细胞凋亡分析、蛋白质分析和免疫组织学评估来评价阿洛哌啶的疗效。结果与 TI/R 相比,阿洛哌啶能保护同侧和对侧睾丸免受单侧睾丸 I/R 的损伤,这体现在睾丸重量与体重(TW/BW)比值降低(ALOPre:p = 0.0037;ALOPost:p = 0.0021)和体积(ALOPre:p = 0.0020;ALOPost:p = 0.0009),较少的结构性损伤,较好的约翰森(Johnsen)(ALOPre:p = 0.0013;ALOPost:p = 0.0021)和科森蒂诺(Cosentino)评分(ALOPre:p < 0.0001;ALOPost:p <;0.0001),曲细精管平均直径和曲细精管上皮平均高度增加,睾丸凋亡减少,氧化应激和炎症反应减轻。此外,阿洛哌嗪还能明显刺激离体后同侧睾丸中信号转导和转录激活因子(STAT)-3的磷酸化。讨论和结论 阿洛哌啶对睾丸扭转/脱落后的同侧和对侧睾丸有很强的保护作用。阿洛哌啶诱导的同侧睾丸保护作用是通过 STAT-3 信号通路介导的。
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CiteScore
7.20
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4.30%
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567
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