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依那西普可预防 cafeteria 饮食喂养大鼠的血管内皮功能障碍。

Etanercept Prevents Endothelial Dysfunction in Cafeteria Diet-Fed Rats.

机构信息

Department of General Surgery, Faculty of General Medicine, "Coltea" Hospital, Carol Davila University, 020021 Bucharest, Romania.

Department of General Surgery, Medical Faculty, Kocaeli University, Kocaeli 41380, Turkey.

出版信息

Int J Environ Res Public Health. 2022 Feb 14;19(4):2138. doi: 10.3390/ijerph19042138.

DOI:10.3390/ijerph19042138
PMID:35206342
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8872388/
Abstract

Obesity is associated with endothelial dysfunction and this relationship is probably mediated in part by inflammation. The current study evaluated the effects of etanercept, a tumor necrosis factor-alpha (TNF-α) inhibitor, on endothelial and vascular reactivity, endothelial nitric oxide synthase (eNOS) immunoreactivity, and serum and aortic concentrations of TNF-α in a diet-induced rat model. Male weanling Wistar rats were exposed to a standard diet and cafeteria diet (CD) for 12 weeks and etanercept was administered during CD treatment. Isolated aortas of the rats were used for isometric tension recording. Carbachol-induced relaxant responses were impaired in CD-fed rats, while etanercept treatment improved these endothelium-dependent relaxations. No significant change was observed in papaverine- and sodium nitroprusside (SNP)-induced relaxant responses. eNOS expression decreased in CD-fed rats, but no change was observed between etanercept-treated CD-fed rats and control rats. CD significantly increased both the serum and the aortic levels of TNF-α, while etanercept treatment suppressed these elevated levels. CD resulted in a significant increase in the body weight of the rats. Etanercept-treated (ETA) CD-fed rats gained less weight than both CD-fed and control rats.

摘要

肥胖与血管内皮功能障碍有关,这种关系可能部分通过炎症介导。本研究评估了肿瘤坏死因子-α(TNF-α)抑制剂依那西普对饮食诱导的大鼠模型内皮和血管反应性、内皮型一氧化氮合酶(eNOS)免疫反应性以及血清和主动脉 TNF-α浓度的影响。雄性断乳 Wistar 大鼠暴露于标准饮食和自助餐厅饮食(CD)12 周,并在 CD 治疗期间给予依那西普。大鼠的离体主动脉用于等长张力记录。在 CD 喂养的大鼠中,卡巴胆碱诱导的舒张反应受损,而依那西普治疗改善了这些内皮依赖性舒张反应。罂粟碱和硝普钠(SNP)诱导的舒张反应没有观察到显著变化。CD 喂养的大鼠中 eNOS 表达减少,但依那西普治疗的 CD 喂养大鼠与对照组大鼠之间没有观察到变化。CD 显著增加了血清和主动脉 TNF-α 的水平,而依那西普治疗抑制了这些升高的水平。CD 导致大鼠体重显著增加。依那西普治疗(ETA)CD 喂养的大鼠比 CD 喂养的大鼠和对照组大鼠体重增加更少。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9c90/8872388/6ac04cfc6cce/ijerph-19-02138-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9c90/8872388/830d334cb2cc/ijerph-19-02138-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9c90/8872388/cd2f74d21f1e/ijerph-19-02138-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9c90/8872388/9874246a59fd/ijerph-19-02138-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9c90/8872388/8234e5ab795a/ijerph-19-02138-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9c90/8872388/aa7cb2dfa9bb/ijerph-19-02138-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9c90/8872388/be66980b2b08/ijerph-19-02138-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9c90/8872388/95cef6450a3b/ijerph-19-02138-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9c90/8872388/6ac04cfc6cce/ijerph-19-02138-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9c90/8872388/830d334cb2cc/ijerph-19-02138-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9c90/8872388/cd2f74d21f1e/ijerph-19-02138-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9c90/8872388/9874246a59fd/ijerph-19-02138-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9c90/8872388/8234e5ab795a/ijerph-19-02138-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9c90/8872388/aa7cb2dfa9bb/ijerph-19-02138-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9c90/8872388/be66980b2b08/ijerph-19-02138-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9c90/8872388/95cef6450a3b/ijerph-19-02138-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9c90/8872388/6ac04cfc6cce/ijerph-19-02138-g008.jpg

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Pharmacological characterization of mechanisms involved in the vasorelaxation produced by rosuvastatin in aortic rings from rats with a cafeteria-style diet.瑞舒伐他汀对高脂饮食大鼠主动脉环血管舒张作用机制的药理学特性研究
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