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Management of acute scrotum in children: a 25-year single center experience on 558 pediatric patients.儿童急性阴囊的管理:25年单中心558例儿科患者的经验
Can J Urol. 2016 Dec;23(6):8594-8601.
4
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Arch Med Sci. 2016 Oct 1;12(5):928-934. doi: 10.5114/aoms.2015.47697. Epub 2015 Jan 14.
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Magnesium protects against bile duct ligation-induced liver injury in male Wistar rats.镁可保护雄性Wistar大鼠免受胆管结扎诱导的肝损伤。
Magnes Res. 2015 Jan-Mar;28(1):32-45. doi: 10.1684/mrh.2015.0380.
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Magnesium isoglycyrrhizinate protects hepatic L02 cells from ischemia/reperfusion induced injury.异甘草酸镁可保护肝L02细胞免受缺血/再灌注诱导的损伤。
Int J Clin Exp Pathol. 2014 Jul 15;7(8):4755-64. eCollection 2014.
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Proteomics, oxidative stress and male infertility.蛋白质组学、氧化应激与男性不育
Reprod Biomed Online. 2014 Jul;29(1):32-58. doi: 10.1016/j.rbmo.2014.02.013. Epub 2014 Mar 13.
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Split ejaculation study: semen parameters and calcium and magnesium in seminal plasma.分段射精研究:精液参数及精浆中的钙和镁
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The biochemical effects of ischemia-reperfusion injury in the ipsilateral and contralateral testes of rats and the protective role of melatonin.大鼠同侧和对侧睾丸缺血再灌注损伤的生化效应及褪黑素的保护作用。
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硫酸镁给药对大鼠睾丸缺血/再灌注损伤的影响

Effects of Magnesium Sulfate Administration on Testicular Ischemia/Reperfusion Injury in Rats.

作者信息

Moshkelani S, Asghari A, Abedi G, Jahandideh A, Mortazavi P

机构信息

Department of Clinical Sciences, Science and Research Branch, Islamic Azad University, Tehran, Iran.

Department of Pathobiology, Science and Research Branch, Islamic Azad University, Tehran, Iran.

出版信息

Arch Razi Inst. 2020 Mar;75(1):83-91. doi: 10.22092/ari.2018.123458.1251. Epub 2020 Mar 1.

DOI:10.22092/ari.2018.123458.1251
PMID:32292006
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8410161/
Abstract

This study aimed at investigating the effects of intraperitoneal (IP) administration of magnesium sulfate (MgSO4) on testicular ischemia-reperfusion (IR) injury in rats. In total, 50 adult Wistar rats were randomly divided into 5 groups. Group 1 received no injection (control); however, group 2 was subjected to 2 h of I and 24 h of R. Subsequently, group 3 was subjected to 2 h of 1, and after 1 h of I, 125 mg/kg MgSO4 was injected intraperitoneally followed by 24 h of R. Groups 4 and 5 were subjected to the same process as group 3, whereas the rats were injected with 250 and 500 mg/kg of MgSO4, respectively. After 24 h, the left testes of all rats were removed for histological analysis and antioxidant activities. According to the results, there was a significant increase in tissue malondialdehyde (MDA) among I/R rats (P<0.05), whereas MgSO4 decreased I/R-induced MDA (P<0.05). Furthermore, experimental I/R diminished glutathione peroxidase (GPx) and superoxide dismutase (SOD) levels significantly (P<0.05). Moreover, MgSO4 (250 and 500 mg/kg) increased GPx and SOD activity significantly in I/R rats (P<0.05). Furthermore, seminiferous tubules degenerated, and few spermatocytes were observed in the testis tubules of the I/R rats. Regarding pathological parameters, seminiferous tubules and spermatocyte were normal in the testes of MgSO4 (250 and 500 mg/kg)-treated experimental I/R-induced rats. In conclusion, this study demonstrated the beneficial effects of MgSO4 on testicular IR injury in rats.

摘要

本研究旨在探讨腹腔注射硫酸镁(MgSO4)对大鼠睾丸缺血再灌注(IR)损伤的影响。总共50只成年Wistar大鼠被随机分为5组。第1组不进行注射(对照组);然而,第2组经历2小时的缺血和24小时的再灌注。随后,第3组经历2小时的缺血,在缺血1小时后,腹腔注射125mg/kg硫酸镁,随后再灌注24小时。第4组和第5组经历与第3组相同的过程,而大鼠分别注射250mg/kg和500mg/kg的硫酸镁。24小时后,取出所有大鼠的左侧睾丸进行组织学分析和抗氧化活性检测。根据结果,缺血/再灌注大鼠的组织丙二醛(MDA)显著增加(P<0.05),而硫酸镁降低了缺血/再灌注诱导的MDA(P<0.05)。此外,实验性缺血/再灌注显著降低了谷胱甘肽过氧化物酶(GPx)和超氧化物歧化酶(SOD)水平(P<0.05)。而且,硫酸镁(250mg/kg和500mg/kg)显著增加了缺血/再灌注大鼠的GPx和SOD活性(P<0.05)。此外,缺血/再灌注大鼠的睾丸小管中生精小管退化,观察到的精母细胞很少。关于病理参数,在硫酸镁(250mg/kg和500mg/kg)处理的实验性缺血/再灌注诱导大鼠的睾丸中,生精小管和精母细胞正常。总之,本研究证明了硫酸镁对大鼠睾丸缺血再灌注损伤具有有益作用。