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四氢生物蝶呤联合奈必洛尔对 SHR 心脏舒张功能的影响。

Effects of Tetrahydrobiopterin Combined with Nebivolol on Cardiac Diastolic Function in SHRs.

机构信息

Cardiac Hospital, Lanzhou University Second Hospital.

出版信息

Biol Pharm Bull. 2019 Jul 1;42(7):1102-1111. doi: 10.1248/bpb.b18-00691. Epub 2019 Mar 14.

Abstract

This study aimed to evaluate the effects of combined use of tetrahydrobiopterin (BH4) and nebivolol on cardiac diastolic dysfunction in spontaneously hypertensive rats (SHRs). Twelve-week-old male SHRs were treated with BH4, nebivolol, or a combination of both. Left ventricle function was evaluated, and reactive oxygen species (ROS) production (including dihydroethidium (DHE) and 3-nitrotyrosine (3-NT)), nitric oxide synthase (NOS) activity and the level of NO in myocardial tissue were determined. The expression levels of endothelial NOS (eNOS), phospholamban (PLN), sarcoplasmic reticulum Ca ATPase (SERCA2a), β-adrenoceptor, cyclic guanosine monophosphate (cGMP), and protein kinase G (PKG) were assayed. Treatment with BH4, nebivolol, or both reversed the noninvasive indexes of diastolic function, including E/E' and E'/A', and the invasive indexes, including time constant of isovolumic left ventricle (LV) relaxation (tau), -dP/dt, -dP/dt/LV systolic pressure (LVSP), and LV end-diastolic pressure (LVEDP) in SHRs. mRNA and protein expression levels of eNOS dimer, phosphorylated PLN, SERCA2a, cGMP, and PKG in the myocardium of treated SHRs were significantly up-regulated compared with those in control rats (p < 0.05 or p < 0.01). The expression levels of 3-NT and DHE were reduced in all treated groups (p < 0.05 or p < 0.01). Notably, combined use of BH4 and nebivolol had better cardioprotective effects than monotherapies. BH4 or nebivolol has a protective effect on diastolic dysfunction in SHRs, and BH4 combined with nebivolol may exert a synergistically cardioprotective effect through activation of β-adrenoceptor and the NO/cGMP/PKG signaling pathway.

摘要

本研究旨在评估四氢生物蝶呤(BH4)和奈必洛尔联合使用对自发性高血压大鼠(SHR)心脏舒张功能障碍的影响。将 12 周龄雄性 SHR 用 BH4、奈必洛尔或两者联合治疗。评估左心室功能,并测定活性氧(ROS)产生(包括二氢乙啶(DHE)和 3-硝基酪氨酸(3-NT))、一氧化氮合酶(NOS)活性和心肌组织中的一氧化氮(NO)水平。测定内皮型一氧化氮合酶(eNOS)、磷蛋白(PLN)、肌浆网 Ca2+-ATP 酶(SERCA2a)、β-肾上腺素能受体、环鸟苷单磷酸(cGMP)和蛋白激酶 G(PKG)的表达水平。BH4、奈必洛尔或两者联合治疗逆转了 SHR 的非侵入性舒张功能指标,包括 E/E'和 E'/A',以及侵入性指标,包括等容左心室(LV)松弛时间常数(tau)、-dP/dt、-dP/dt/LV 收缩压(LVSP)和 LV 舒张末期压(LVEDP)。与对照组大鼠相比,治疗 SHR 心肌中 eNOS 二聚体、磷酸化 PLN、SERCA2a、cGMP 和 PKG 的 mRNA 和蛋白表达水平均显著上调(p<0.05 或 p<0.01)。所有治疗组的 3-NT 和 DHE 表达水平均降低(p<0.05 或 p<0.01)。值得注意的是,BH4 和奈必洛尔联合使用的心脏保护作用优于单药治疗。BH4 或奈必洛尔对 SHR 的舒张功能障碍具有保护作用,BH4 联合奈必洛尔可能通过激活β-肾上腺素能受体和 NO/cGMP/PKG 信号通路发挥协同的心脏保护作用。

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