Lima Victor V, Giachini Fernanda R, Matsumoto Takayuki, Li Weiguo, Bressan Alecsander F M, Chawla Dhruv, Webb R Clinton, Ergul Adviye, Tostes Rita C
Institute of Biological and Health Sciences, Federal University of Mato Grosso, Barra do Garças, MT, Brazil
Institute of Biological and Health Sciences, Federal University of Mato Grosso, Barra do Garças, MT, Brazil.
Clin Sci (Lond). 2016 Jun 1;130(11):871-80. doi: 10.1042/CS20150777. Epub 2016 Feb 29.
Obesity and high fat intake induce alterations in vascular function and structure. Aberrant O-GlcNAcylation (O-GlcNAc) of vascular proteins has been implicated in vascular dysfunction associated with cardiovascular and metabolic diseases. In the present study, we tested the hypothesis that high-fat diet (HFD)-mediated increases in O-GlcNAc-modified proteins contribute to cerebrovascular dysfunction. O-GlcNAc-protein content was increased in arteries from male Wistar rats treated with a HFD (45% fat) for 12 weeks compared with arteries from rats on control diet (CD). HFD augmented body weight [(g) 550±10 compared with 502±10 CD], increased plasma triacylglycerols [(mg/dl) 160±20 compared with 95±15 CD] and increased contractile responses of basilar arteries to serotonin [5-hydroxytryptamine (5-HT)] [(pD2) 7.0±0.1 compared with 6.7±0.09 CD] and the thromboxane analogue 9,11-dideoxy-9α,11α-methanoepoxy prostaglandin F2α (U-46619) [(pD2) 7.2±0.1 compared with 6.8±0.09 CD]. Of importance, increased levels of O-GlcNAc [induced by 24 h-incubation of vessels with a potent inhibitor of O-GlcNAcase (OGA), O-(2-acetamido-2-deoxy-D-glucopyranosylidene)amino-N-phenylcarbamate (PugNAc)] increased basilar artery contractions in response to U-46619 [(pD2) 7.4±0.07 compared with 6.8±0.08 CD] and 5-HT [(pD2) 7.5±0.06 compared with 7.1±0.1 CD]. Vessels from rats on the HFD for 12 weeks and vessels treated with PugNAc displayed increased phosphorylation of p38 (Thr(180/182)) and extracellular signal-regulated kinase 1/2 (Erk1/2) (Ser(180/221)). Increased 5HT-induced contractions in arteries from rats on the HFD or in arteries incubated with PugNAc were abrogated by mitogen-activated protein kinase (MAPK) inhibitors. Our data show that HFD augments cerebrovascular O-GlcNAc and this modification contributes to increased contractile responses and to the activation of the MAPK pathway in the rat basilar artery.
肥胖和高脂肪摄入会导致血管功能和结构发生改变。血管蛋白异常的O-连接N-乙酰葡糖胺化(O-GlcNAc)与心血管和代谢疾病相关的血管功能障碍有关。在本研究中,我们检验了以下假设:高脂饮食(HFD)介导的O-GlcNAc修饰蛋白增加会导致脑血管功能障碍。与对照饮食(CD)大鼠的动脉相比,用HFD(45%脂肪)处理12周的雄性Wistar大鼠的动脉中O-GlcNAc蛋白含量增加。HFD增加了体重[(克)550±10,而CD组为502±10],增加了血浆三酰甘油[(毫克/分升)160±20,而CD组为95±15],并增加了基底动脉对血清素[5-羟色胺(5-HT)]的收缩反应[(pD2)7.0±0.1,而CD组为6.7±0.09]以及血栓素类似物9,11-二脱氧-9α,11α-甲环氧前列腺素F2α(U-46619)的收缩反应[(pD2)7.2±0.1,而CD组为6.8±0.09]。重要的是,O-GlcNAc水平升高[通过用O-GlcNAcase(OGA)的强效抑制剂O-(2-乙酰氨基-2-脱氧-D-吡喃葡萄糖亚基)氨基-N-苯基氨基甲酸酯(PugNAc)对血管进行24小时孵育诱导]增加了基底动脉对U-46619的收缩反应[(pD2)7.4±0.07,而CD组为6.8±0.08]和5-HT的收缩反应[(pD2)7.5±0.06,而CD组为7.1±0.1]。来自HFD喂养12周大鼠的血管和用PugNAc处理的血管显示p38(Thr(180/182))和细胞外信号调节激酶1/2(Erk1/2)(Ser(180/221))的磷酸化增加。丝裂原活化蛋白激酶(MAPK)抑制剂消除了HFD大鼠动脉或用PugNAc孵育的动脉中5HT诱导的收缩增加。我们的数据表明,HFD增加了脑血管中的O-GlcNAc,这种修饰导致大鼠基底动脉收缩反应增加以及MAPK途径的激活。