Medical College of Georgia, Department of Physiology, 1120 Fifteenth St, CA-3141, Augusta, GA 30912-3000, USA.
Hypertension. 2010 Jan;55(1):180-8. doi: 10.1161/HYPERTENSIONAHA.109.143818. Epub 2009 Nov 30.
O-GlcNAcylation augments vascular contractile responses, and O-GlcNAc-proteins are increased in the vasculature of deoxycorticosterone-acetate salt rats. Because endothelin 1 (ET-1) plays a major role in vascular dysfunction associated with salt-sensitive forms of hypertension, we hypothesized that ET-1-induced changes in vascular contractile responses are mediated by O-GlcNAc modification of proteins. Incubation of rat aortas with ET-1 (0.1 mumol/L) produced a time-dependent increase in O-GlcNAc levels and decreased expression of O-GlcNAc transferase and beta-N-acetylglucosaminidase, key enzymes in the O-GlcNAcylation process. Overnight treatment of aortas with ET-1 increased phenylephrine vasoconstriction (maximal effect [in moles]: 19+/-5 versus 11+/-2 vehicle). ET-1 effects were not observed when vessels were previously instilled with anti-O-GlcNAc transferase antibody or after incubation with an O-GlcNAc transferase inhibitor (3-[2-adamantanylethyl]-2-[{4-chlorophenyl}azamethylene]-4-oxo-1,3-thiazaperhyd roine-6-carboxylic acid; 100 mumol/L). Aortas from deoxycorticosterone-acetate salt rats, which exhibit increased prepro-ET-1, displayed increased contractions to phenylephrine and augmented levels of O-GlcNAc proteins. Treatment of deoxycorticosterone-acetate salt rats with an endothelin A antagonist abrogated augmented vascular levels of O-GlcNAc and prevented increased phenylephrine vasoconstriction. Aortas from rats chronically infused with low doses of ET-1 (2 pmol/kg per minute) exhibited increased O-GlcNAc proteins and enhanced phenylephrine responses (maximal effect [in moles]: 18+/-2 versus 10+/-3 control). These changes are similar to those induced by O-(2-acetamido-2-deoxy-d-glucopyranosylidene) amino-N-phenylcarbamate, an inhibitor of beta-N-acetylglucosaminidase. Systolic blood pressure (in millimeters of mercury) was similar between control and ET-1-infused rats (117+/-3 versus 123+/-4 mm Hg; respectively). We conclude that ET-1 indeed augments O-GlcNAc levels and that this modification contributes to the vascular changes induced by this peptide. Increased vascular O-GlcNAcylation by ET-1 may represent a mechanism for hypertension-associated vascular dysfunction or other pathological conditions associated with increased levels of ET-1.
O-GlcNAc 酰化增强血管收缩反应,脱氧皮质酮醋酸盐盐大鼠的血管中 O-GlcNAc 蛋白增加。因为内皮素 1(ET-1)在与盐敏感型高血压相关的血管功能障碍中起主要作用,我们假设 ET-1 诱导的血管收缩反应变化是通过 O-GlcNAc 修饰蛋白介导的。用 ET-1(0.1μmol/L)孵育大鼠主动脉会导致 O-GlcNAc 水平的时间依赖性增加,并降低 O-GlcNAc 转移酶和β-N-乙酰氨基葡萄糖苷酶的表达,这是 O-GlcNAc 酰化过程中的关键酶。ET-1 处理主动脉过夜可增加去甲肾上腺素的血管收缩(最大效应[摩尔]:19+/-5 与 11+/-2 载体)。当血管先前注入抗 O-GlcNAc 转移酶抗体或用 O-GlcNAc 转移酶抑制剂(3-[2-金刚烷乙基]-2-[{4-氯苯基}亚氨基亚甲基]-4-氧代-1,3-噻嗪烷-6-羧酸;100μmol/L)孵育时,未观察到 ET-1 作用。脱氧皮质酮醋酸盐盐大鼠的前脑啡肽原 ET-1 水平升高,表现为去甲肾上腺素的收缩增加,并增加 O-GlcNAc 蛋白水平。用内皮素 A 拮抗剂治疗脱氧皮质酮醋酸盐盐大鼠可消除血管中 O-GlcNAc 的增加,并防止去甲肾上腺素的血管收缩增加。用低剂量 ET-1(2pmol/kg/min)慢性输注的大鼠主动脉表现出 O-GlcNAc 蛋白增加和增强的去甲肾上腺素反应(最大效应[摩尔]:18+/-2 与 10+/-3 对照)。这些变化类似于 O-(2-乙酰氨基-2-脱氧-D-葡萄糖基亚氨基-N-苯基氨基甲酰基)氨基-N-苯基氨基甲酰胺(β-N-乙酰氨基葡萄糖苷酶抑制剂)诱导的变化。对照组和 ET-1 输注组大鼠的收缩压(毫米汞柱)相似(117+/-3 与 123+/-4mmHg;分别)。我们得出结论,ET-1 确实会增加 O-GlcNAc 水平,并且这种修饰有助于该肽诱导的血管变化。ET-1 引起的血管 O-GlcNAc 酰化增加可能是与高血压相关的血管功能障碍或其他与 ET-1 水平升高相关的病理状况的机制。