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褪黑素在大鼠模型中对肠道缺血再灌注诱导的急性肺损伤的保护作用可能比N-乙酰半胱氨酸更有效。

Melatonin can be, more effective than N-acetylcysteine, protecting acute lung injury induced by intestinal ischemia-reperfusion in rat model.

作者信息

Leite Alberto Andrade, Reiter Russel Joseph, Brandão Julio Cezar Mendes, Sakae Thiago Mamoru, Marinho Marcia, Camargo Celia Regina, Oliveira-Junior Itamar Souza

机构信息

Programa de Pos-Graduacao em Medicina Translacional, Universidade Federal de Sao Paulo, Sao Paulo, SP, BR.

Department of Cell Systems and Anatomy, UT Health Science Center at San Antonio, San Antonio, Texas, USA.

出版信息

Clinics (Sao Paulo). 2021 May 5;76:e2513. doi: 10.6061/clinics/2021/e2513. eCollection 2021.

DOI:10.6061/clinics/2021/e2513
PMID:33978073
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8075110/
Abstract

OBJECTIVES

The current study compared the impact of pretreatment with melatonin and N-acetylcysteine (NAC) on the prevention of rat lung damage following intestinal ischemia-reperfusion (iIR).

METHODS

Twenty-eight Wistar rats were subjected to intestinal ischemia induced by a 60 min occlusion of the superior mesenteric artery, followed by reperfusion for 120 min. Animals were divided into the following groups (n=7 per group): sham, only abdominal incision; SS+iIR, pretreated with saline solution and iIR; NAC+iIR, pretreated with NAC (20 mg/kg) and iIR; MEL+iIR, pretreated with melatonin (20 mg/kg) and iIR. Oxidative stress and inflammatory mediators were measured and histological analyses were performed in the lung tissues.

RESULTS

Data showed a reduction in malondialdehyde (MDA), myeloperoxidase (MPO), and TNF-alpha in the animals pretreated with NAC or MEL when compared to those treated with SS+iIR (p<0.05). An increase in superoxide dismutase (SOD) levels in the NAC- and MEL-pretreated animals as compared to the SS+iIR group (34±8 U/g of tissue; p<0.05) was also observed. TNF-α levels were lower in the MEL+iIR group (91±5 pg/mL) than in the NAC+iIR group (101±6 pg/mL). Histological analysis demonstrated a higher lung lesion score in the SS+iIR group than in the pretreated groups.

CONCLUSION

Both agents individually provided tissue protective effect against intestinal IR-induced lung injury, but melatonin was more effective in ameliorating the parameters analyzed in this study.

摘要

目的

本研究比较了褪黑素和N-乙酰半胱氨酸(NAC)预处理对预防大鼠肠缺血再灌注(iIR)后肺损伤的影响。

方法

28只Wistar大鼠接受肠系膜上动脉60分钟闭塞诱导的肠缺血,随后再灌注120分钟。动物分为以下几组(每组n = 7):假手术组,仅做腹部切口;SS + iIR组,用生理盐水预处理后进行iIR;NAC + iIR组,用NAC(20mg/kg)预处理后进行iIR;MEL + iIR组,用褪黑素(20mg/kg)预处理后进行iIR。检测肺组织中的氧化应激和炎症介质,并进行组织学分析。

结果

数据显示,与SS + iIR组相比,NAC或MEL预处理的动物丙二醛(MDA)、髓过氧化物酶(MPO)和肿瘤坏死因子-α(TNF-α)减少(p < 0.05)。与SS + iIR组相比,NAC和MEL预处理的动物超氧化物歧化酶(SOD)水平也有所增加(34±8 U/g组织;p < 0.05)。MEL + iIR组的TNF-α水平(91±5 pg/mL)低于NAC + iIR组(101±6 pg/mL)。组织学分析表明,SS + iIR组的肺损伤评分高于预处理组。

结论

两种药物单独使用均对肠缺血再灌注诱导的肺损伤具有组织保护作用,但褪黑素在改善本研究分析的参数方面更有效。

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本文引用的文献

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Therapeutic Algorithm for Use of Melatonin in Patients With COVID-19.新型冠状病毒肺炎患者使用褪黑素的治疗算法
Front Med (Lausanne). 2020 May 15;7:226. doi: 10.3389/fmed.2020.00226. eCollection 2020.
2
Melatonin Alleviates Radiation-Induced Lung Injury via Regulation of miR-30e/NLRP3 Axis.褪黑素通过调节 miR-30e/NLRP3 轴缓解放射性肺损伤。
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Gut-origin sepsis in the critically ill patient: pathophysiology and treatment.危重症患者的肠道源性脓毒症:发病机制与治疗。
Infection. 2018 Dec;46(6):751-760. doi: 10.1007/s15010-018-1178-5. Epub 2018 Jul 12.
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Melatonin attenuates lung ischaemia-reperfusion injury via inhibition of oxidative stress and inflammation.褪黑素通过抑制氧化应激和炎症减轻肺缺血再灌注损伤。
Interact Cardiovasc Thorac Surg. 2018 May 1;26(5):761-767. doi: 10.1093/icvts/ivx440.
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Melatonin as an antioxidant: under promises but over delivers.褪黑素作为一种抗氧化剂:承诺过多,兑现不足。
J Pineal Res. 2016 Oct;61(3):253-78. doi: 10.1111/jpi.12360. Epub 2016 Sep 1.
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Melatonin attenuates lung injury in a hind limb ischemia-reperfusion rat model.褪黑素减轻后肢缺血再灌注大鼠模型中的肺损伤。
Rev Port Pneumol (2006). 2015 Jan-Feb;21(1):30-5. doi: 10.1016/j.rppnen.2014.01.010. Epub 2015 Jan 20.
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I-FABP as biomarker for the early diagnosis of acute mesenteric ischemia and resultant lung injury.I-FABP 作为急性肠系膜缺血及由此导致的肺损伤早期诊断的生物标志物。
PLoS One. 2014 Dec 26;9(12):e115242. doi: 10.1371/journal.pone.0115242. eCollection 2014.
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