枸杞子籽油对d -半乳糖诱导的大鼠睾丸Janus激酶1/信号转导和转录激活因子1/核因子-κB的影响。

Yang Zhangjie, Wang Yuxin, Chen Dongmei, Zhao Shuai, H U Na, M A Lianghong, M A Huiming
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引用次数: 0

摘要

目的:观察枸杞子籽油(FLSO)对d -半乳糖(d -半乳糖)诱导的衰老支持细胞(TM4细胞)中衰老相关蛋白的表达上调,探讨其对d -半乳糖诱导的大鼠睾丸炎症的影响。细胞计数试剂盒(CCK)-8法计数细胞数显示,与衰老模型相比,50、100和150 μg/mL浓度的FLSO处理的细胞数量较多。选取雄性Sprague-Dawley大鼠50只,8周龄,230 ~ 255 g,随机分为对照组、衰老模型组和FLSO(低、中、高剂量)组。Western blot和免疫荧光法检测核因子-κB (NF-κB)及其上游因子[Janus kinase 1 (JAK1)和信号转导及转录激活因子1 (STAT1)]的表达,酶联免疫吸附法定量相关炎症因子。采用约翰森评分法评价睾丸组织,探讨其生精功能。结果:100 μg/mL氟索处理后,白细胞介素-1β (IL-1β)(< 0.05)、IL-6(< 0.001)、肿瘤坏死因子α (TNF-α)(< 0.05)表达明显降低,血红素加氧酶-1 (HO-1)(< 0.001)、IL-10(< 0.05)表达升高。Western blotting检测,FLSO抑制NF-B表达,降低p-p65/p65(< 0.01)。实验组大鼠血清IL-1β(< 0.001)、IL-6(< 0.05)、TNF-(< 0.01)水平下降,IL-10(< 0.05)水平升高。免疫荧光检测结果显示,与大鼠衰老模型相比,FLSO组大鼠睾丸组织中JAK-1、STAT1表达明显升高(< 0.001),而FLSO组大鼠睾丸组织中NF-κB表达明显下降(< 0.001)。血清中抑制素B和睾酮水平均升高(< 0.05)。结论:本研究确定了FLSO对睾丸耐受炎症损伤的保护作用,表明FLSO可通过JAK-1/STAT1/NF-κB通路缓解炎症。
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Gouqizi () seed oil reduces D-galactose induced inflammation in testis of rats Janus kinase 1/signal transducerand activator of transcription 1/nuclear factor-κB and.

Objective: To investigate the efficacy of Gouqizi () seed oil (FLSO) on D-gal induced inflammation in testis of rats and .

Methods: In aging Sertoli cells (TM4 cells) induced by D-galactose (D-gal), the expression of upregulated aging-related proteins. The number of cells counted by cell counting kit (CCK)-8 assay showed a high number of cells disposed with FLSO at 50, 100 and 150 μg/mL compared to that for the aging model. , male Sprague-Dawley rats ( = 50, 8-week-old, 230-255 g) were randomly categorized into control, aging model, and FLSO (low-, medium-, and high-dose) groups. The expression of nuclear factor-κB (NF-κB) and its upstream factors [Janus kinase 1 (JAK1) and signal transducerand activator of transcription 1 (STAT1)] was detected by Western blot and immunofluorescence, related inflammatory factors quantified by enzyme-linked immunosorbent assay. Evaluation of testicular tissue by Johnsen score, the spermatogenic function was explored.

Results: The expression of interleukin-1β (IL-1β) ( < 0.05), IL-6 ( < 0.001), and tumor necrosis factor α (TNF-α) ( < 0.05) was decreased significantly, while that of heme oxygenase-1 (HO-1) ( < 0.001) and IL-10 ( < 0.05) was increased in cells disposed with FLSO 100 μg/mL. FLSO inhibited the expression of NF-B and declined p-p65/p65 ( < 0.01), as detected by Western blotting. In, the levels in serum of IL-1β ( < 0.001), IL-6 ( < 0.05), and TNF-( < 0.01) declined while IL-10 ( < 0.05) was upregulated post-FLSO treatment. In addition, the expression of JAK-1 and STAT1 increased significantly in testicular tissue of rats treated with FLSO as compared to the aging model of rats ( < 0.001), while the expression of NF-κB ( < 0.001) declined in the testis in the FLSO group, as assessed by immunofluorescence. The levels of inhibor B and testosterone in serum both increased (< 0.05).

Conclusions: In conclusion, this study determined the protective effects of FLSO to tolerate inflammatory injury in the testis, indicating that FLSO alleviates inflammation JAK-1/STAT1/NF-κB pathway.

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