富马酸二甲酯对大鼠睾丸缺血再灌注损伤的保护作用

IF 2.1 4区 医学 Q3 ANDROLOGY
Andrologia Pub Date : 2023-06-15 DOI:10.1155/2023/7086044
Atsushi Onishi, Koji Chiba, Shun Kawamura, Katsuya Sato, Yasuhiro Kaku, Keisuke Okada, Masato Fujisawa
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引用次数: 0

摘要

睾丸扭转后的缺血再灌注损伤(IRI)与睾丸组织的显著损伤有关。富马酸二甲酯(DMF)激活核因子红系2相关因子2(Nrf2)信号通路,从而诱导抗氧化和抗炎作用。我们分析了DMF在Sprague-Dawley大鼠(n=32)睾丸扭转/扭转后预防IRI的作用。将动物分为对照(假手术)、DMF(200 mg/kg/天)、IRI和IRI+DMF(IRI与200 mg/kg/天DMF)组。睾丸IRI是在1.5后通过解毒诱导的 h的扭转。DMF通过灌胃给药,每天从1 h,直到第7天进行睾丸切除术。计算睾丸与体重的比值。使用Johnsen和Cosentino评分对曲精管进行组织病理学评估。测定睾丸组织中丙二醛、超氧化物歧化酶和总谷胱甘肽水平。此外,通过定量聚合酶链反应测定Nrf2、血红素加氧酶1(HO-1)、NAD(P)H-醌脱氢酶1(NQO1)、核因子κB(NF-κB)和炎症细胞因子(白细胞介素1b(IL1b)、IL6和肿瘤坏死因子α(TNF-α))的水平。还评估了核Nrf2和细胞质HO-1和NQO1蛋白水平。DMF显著改善了睾丸与体重的比例,并减少了睾丸的组织病理学损伤。此外,它还显著提高了丙二醛、超氧化物歧化酶和总谷胱甘肽的浓度。此外,与未经治疗的IRI大鼠相比,它抑制了NF-κB和炎症细胞因子mRNA的表达(均p<0.05)。在IRI大鼠中,DMF处理后Nrf2、HO-1和NQO1的表达(mRNA和蛋白)显著升高(均p<0.05)。DMF给药激活Nrf2信号通路并诱导抗氧化和抗炎作用,从而改善IRI诱导的睾丸损伤。因此,DMF可以预防睾丸扭转后的IRI。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Dimethyl Fumarate Protects Rats against Testicular Ischemia–Reperfusion Injury

Dimethyl Fumarate Protects Rats against Testicular Ischemia–Reperfusion Injury

Ischemia–reperfusion injury (IRI) after testicular torsion is linked to significant damage in testicular tissue. Dimethyl fumarate (DMF) activates the nuclear factor erythroid 2-related factor 2 (Nrf2) signaling pathway, thereby inducing antioxidant and anti-inflammatory effects. We analyzed the usefulness of DMF in preventing IRI following testicular torsion/detorsion in Sprague-Dawley rats (n = 32). The animals were classified into control (sham), DMF (200 mg/kg/day), IRI, and IRI+DMF (IRI with 200 mg/kg/day DMF) groups. Testicular IRI was induced by detorsion after 1.5 h of torsion. DMF was administered via oral gavage daily from 1 h before testicular detorsion until day 7, when orchiectomy was performed. The testis-to-body weight ratio was calculated. Histopathological evaluation was performed using the Johnsen and Cosentino scores for seminiferous tubules. Malondialdehyde, superoxide dismutase, and total glutathione levels were determined in testicular tissues. Moreover, Nrf2, heme oxygenase 1 (HO-1), NAD(P)H quinone dehydrogenase 1 (NQO1), nuclear factor kappa B (NF-κB), and inflammatory cytokine (interleukin 1b (IL1b), IL6, and tumor necrosis factor alpha (TNF-α)) levels were determined through quantitative polymerase chain reaction. Nuclear Nrf2 and cytoplasmic HO-1 and NQO1 protein levels were also evaluated. DMF significantly improved the testis-to-body weight ratio and reduced histopathological damage in the testes. Moreover, it significantly improved the concentration of malondialdehyde, superoxide dismutase, and total glutathione. Furthermore, it inhibited NF-κB and inflammatory cytokine mRNA expression compared with the findings obtained in untreated rats with IRI (all p < 0.05). Nrf2, HO-1, and NQO1 expressions (mRNA and protein) were markedly elevated following DMF treatment in rats with IRI (all p < 0.05). DMF administration activated the Nrf2 signaling pathway and induced antioxidant and anti-inflammatory effects, thereby improving IRI-induced testicular damage. Thus, DMF may prevent IRI following testicular torsion.

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来源期刊
Andrologia
Andrologia 医学-男科学
CiteScore
5.60
自引率
8.30%
发文量
292
审稿时长
6 months
期刊介绍: Andrologia provides an international forum for original papers on the current clinical, morphological, biochemical, and experimental status of organic male infertility and sexual disorders in men. The articles inform on the whole process of advances in andrology (including the aging male), from fundamental research to therapeutic developments worldwide. First published in 1969 and the first international journal of andrology, it is a well established journal in this expanding area of reproductive medicine.
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