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腹腔内给予负载α-生育酚的纳米颗粒可改善大鼠卵巢扭转与复位模型中的缺血再灌注损伤。

Interaperitoneal Administration of Αlpha-Tocopherol Loaded Nanoparticles Improves Ischemia-Reperfusion Injury in Rat Ovaries Torsion and Detorsion Model.

作者信息

Najafpour Alireza, Azizizadeh Houman

机构信息

Department of Clinical Sciences, Faculty of Veterinary Medicine, Urmia Branch, Islamic Azad University, Urmia, Iran.

出版信息

Bull Emerg Trauma. 2018 Jul;6(3):207-216. doi: 10.29252/beat-060304.

Abstract

OBJECTIVE

To investigate effects of intraperitoneally administration of α-tocopherol loaded nanoparticles (TNP) on ischemia-reperfusion injury in ovaries.

METHODS

Thirty-five healthy female Wistar rats ~250g were randomized into seven experimental groups (n = 5): Group SHAM: The rats underwent only laparotomy. Group Ischemia: A 3- hour ischemia only. Group I/R: A 3-hour ischemia and a 3-hour reperfusion. Group I/T: A 3-hour ischemia only and 100 mg/kg intraperitoneal administration (IP) of α-tocopherol 2.5 hours after induction of ischemia. Group I/R/T: A 3-hour ischemia, a 3-hour reperfusion and 100 mg/kg IP of α-tocopherol 2.5 hours after induction of ischemia. Group I/TNP: A 3-hour ischemia only and 1 mg/kg IP of TNP 2.5 hours after induction of ischemia. Group I/R/TNP: A 3-hour ischemia, a 3-hour reperfusion and 1 mg/kg IP of TNP 2.5 hours after induction of ischemia.

RESULTS

Animals treated with αTNP showed significantly ameliorated development of ischemia and reperfusion tissue injury compared to those of other groups (=0.001). The significant higher values of SOD, tGSH, GPO, GSHRd and GST were observed in I/R/NC animals compared to those of other groups (=0.001). Damage indicators (NOS, MDA, MPO and DNA damage level) were significantly lower in I/R/NC animal compared to those of other groups (=0.001).

CONCLUSION

Intraperitoneal administration of TNP could be helpful in minimizing ischemia-reperfusion injury in ovarian tissue exposed to ischemia.

摘要

目的

研究腹腔注射α-生育酚负载纳米颗粒(TNP)对卵巢缺血再灌注损伤的影响。

方法

将35只体重约250g的健康雌性Wistar大鼠随机分为7个实验组(n = 5):假手术组(SHAM):大鼠仅接受剖腹手术。缺血组:仅进行3小时缺血。缺血/再灌注组(I/R):3小时缺血和3小时再灌注。缺血/T组(I/T):仅3小时缺血,缺血诱导后2.5小时腹腔注射(IP)100mg/kgα-生育酚。缺血/再灌注/T组(I/R/T):3小时缺血、3小时再灌注,缺血诱导后2.5小时腹腔注射100mg/kgα-生育酚。缺血/TNP组(I/TNP):仅3小时缺血,缺血诱导后2.5小时腹腔注射1mg/kg TNP。缺血/再灌注/TNP组(I/R/TNP):3小时缺血、3小时再灌注,缺血诱导后2.5小时腹腔注射1mg/kg TNP。

结果

与其他组相比,接受αTNP治疗的动物缺血和再灌注组织损伤的发展明显改善(P = 0.001)。与其他组相比,I/R/NC动物的超氧化物歧化酶(SOD)、总谷胱甘肽(tGSH)、谷胱甘肽过氧化物酶(GPO)、谷胱甘肽还原酶(GSHRd)和谷胱甘肽S-转移酶(GST)值显著更高(P = 0.001)。与其他组相比,I/R/NC动物的损伤指标(一氧化氮合酶(NOS)、丙二醛(MDA)、髓过氧化物酶(MPO)和DNA损伤水平)显著更低(P = 0.001)。

结论

腹腔注射TNP有助于将暴露于缺血的卵巢组织中的缺血再灌注损伤降至最低。

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