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咖啡酸苯乙酯对乙酰水杨酸诱导的大鼠肺损伤的保护作用

The Protective Effects of Caffeic Acid Phenethyl Ester on Acetylsalicylic Acid-induced Lung Injury in Rats.

作者信息

Taylan Mahşuk, Kaya Halide, Demir Melike, Evliyaoğlu Osman, Sen Hadice Selimoglu, Fırat Ugur, Keles Aysenur, Yilmaz Sureyya, Sezgi Cengizhan

机构信息

a Department of Pulmonary Diseases , Dicle University School of Medicine , Diyarbakir , Turkey.

b Department of Biochemistry , Dicle University School of Medicine , Diyarbakir , Turkey.

出版信息

J Invest Surg. 2016 Dec;29(6):328-334. doi: 10.3109/08941939.2016.1149641. Epub 2016 Mar 16.

Abstract

AIM

We aimed to investigate the protective effect of caffeic acid phenethyl ester (CAPE) on acetylsalicylic acid (ASA)-induced lung damage in rats in the present study.

METHODS

A total of 40 rats were randomly divided into five groups, with eight rats in each group-group 1: control, not receiving any medication; group 2: ASA (50 mg/kg/day); group 3: ASA (50 mg/kg/day) plus CAPE (20 μg/kg/day); group 4: ASA (100 mg/kg/day); and group 5: ASA (100 mg/kg/day) plus CAPE (20 μg/kg/day). ASA and CAPE were given via orogastric gavage for 5 days. The total oxidant status (TOS), total antioxidant capacity (TAC), oxidant stress index (OSI), and paraoxonase-1 (PON-1) activity of the blood samples and lung tissues were determined. Histopathological examinations of the lung tissues were performed by using light microscopic methods.

RESULTS

CAPE treatment significantly increased antioxidant PON-1 level both in the lung tissue and plasma (p < .05). Plasma antioxidant marker (TAC, PON-1) levels significantly increased and oxidant marker (TOS, OSI) levels significantly decreased in CAPE-treated rats (groups 3,5) compared to ASA given no-CAPE groups (group 2,4) (p < .05). Treatment with CAPE improved pulmonary interstitial inflammation and eosinophil accumulation due to ASA histopathologically.

CONCLUSION

Eosinophil-rich inflammation and oxidative stress play important roles in ASA-induced lung toxicity, and CAPE may protect against ASA-induced lung toxicity by reduction of oxidative damage and inflammation in rats.

摘要

目的

在本研究中,我们旨在探究咖啡酸苯乙酯(CAPE)对乙酰水杨酸(ASA)诱导的大鼠肺损伤的保护作用。

方法

总共40只大鼠被随机分为五组,每组8只。第一组:对照组,不接受任何药物治疗;第二组:ASA(50毫克/千克/天);第三组:ASA(50毫克/千克/天)加CAPE(20微克/千克/天);第四组:ASA(100毫克/千克/天);第五组:ASA(100毫克/千克/天)加CAPE(20微克/千克/天)。通过灌胃给予ASA和CAPE,持续5天。测定血液样本和肺组织的总氧化状态(TOS)、总抗氧化能力(TAC)、氧化应激指数(OSI)和对氧磷酶-1(PON-1)活性。使用光学显微镜方法对肺组织进行组织病理学检查。

结果

CAPE治疗显著提高了肺组织和血浆中抗氧化剂PON-1的水平(p < 0.05)。与未给予CAPE的ASA组(第二组、第四组)相比,CAPE治疗的大鼠(第三组、第五组)血浆抗氧化标志物(TAC、PON-1)水平显著升高,氧化标志物(TOS、OSI)水平显著降低(p < 0.05)。从组织病理学来看,CAPE治疗改善了由ASA引起的肺间质炎症和嗜酸性粒细胞积聚。

结论

富含嗜酸性粒细胞的炎症和氧化应激在ASA诱导的肺毒性中起重要作用,并且CAPE可能通过减少大鼠的氧化损伤和炎症来预防ASA诱导的肺毒性。

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