Peter P, Martin U, Sharma A, Dunne F
University Hospital Birmingham NHS Trust, Selly Oak, Birmingham, UK.
J Clin Pharm Ther. 2006 Apr;31(2):153-9. doi: 10.1111/j.1365-2710.2006.00718.x.
The aim of this study was to examine the effect of the cadioselective B(1)-adrenoceptor blocker nebivolol on glycaemic control, lipid profile and markers of oxidative stress in patients with type 2 diabetes over a 6-month period.
Twenty-six patients with mild to moderate hypertension (140-160 mmHg systolic, 90-105 mmHg diastolic) confirmed on 24-h blood pressure monitoring, were treated with nebivolol 5 mg daily for 6 months. Total serum cholesterol, triglycerides, high-density lipoprotein (HDL) cholesterol and low-density lipoprotein (LDL) subfractions, lipid hydroperoxides (LHPs) and total antioxidant capacity (TAC) were measured before and after 6 months of treatment.
Nebivolol, as expected, reduced mean daytime systolic and diastolic pressures on ambulatory monitoring (149 +/- 9 to 140 +/- 13 mmHg, P = 0.02 and 84 +/- 7 to 77 +/- 9 mmHg, P < 0.001). There were no significant changes in serum cholesterol or triglycerides following treatment but a significant increase in HDL cholesterol was noted (1.12 +/- 0.19 to 1.25 +/- 0.36 mmol/L, P = 0.008). Patients showed a highly significant reduction in TAC from 501 +/- 57 to 422 +/- 29 trolox equivalent (P < 0.001). Baseline LHPs were very high and showed no significant change over the 6-month period (18.7 +/- 7.4 and 18.7 +/- 10.9 micromol/L). The LDL score increased significantly from 1.7 +/- 0.7 to 2.3 +/- 0.7 (P = 0.0002) at 6 months suggesting a change to a more atherogenic lipid profile. Neither weight nor glycaemic control changed during treatment.
Nebivolol appears to be lipid neutral and may even have a positive effect on HDL cholesterol. Despite this it may promote the formation of potentially atherogenic LDL subfractions possibly as a result of reduced antioxidant defences. Further studies are needed to clarify the changes observed in parameters of oxidative stress.
本研究旨在探讨心脏选择性β₁肾上腺素能受体阻滞剂奈必洛尔在6个月期间对2型糖尿病患者血糖控制、血脂谱及氧化应激标志物的影响。
26例经24小时血压监测确诊为轻度至中度高血压(收缩压140 - 160 mmHg,舒张压90 - 105 mmHg)的患者,每日服用5 mg奈必洛尔,治疗6个月。在治疗6个月前后测量血清总胆固醇、甘油三酯、高密度脂蛋白(HDL)胆固醇和低密度脂蛋白(LDL)亚组分、脂质过氧化氢(LHP)和总抗氧化能力(TAC)。
正如预期的那样,奈必洛尔在动态监测中降低了日间平均收缩压和舒张压(从149±9 mmHg降至140±13 mmHg,P = 0.02;从84±7 mmHg降至77±9 mmHg,P < 0.001)。治疗后血清胆固醇或甘油三酯无显著变化,但HDL胆固醇显著升高(从1.12±0.19 mmol/L升至1.25±0.36 mmol/L,P = 0.008)。患者的TAC从501±57降至422±29 Trolox当量,显著降低(P < 0.001)。基线LHP非常高,在6个月期间无显著变化(分别为18.7±7.4和18.7±10.9 μmol/L)。6个月时LDL评分从1.7±0.7显著升至2.3±0.7(P = 0.0002),表明脂质谱向更具动脉粥样硬化性转变。治疗期间体重和血糖控制均未改变。
奈必洛尔似乎对血脂无不良影响,甚至可能对HDL胆固醇有积极作用。尽管如此,它可能会促进潜在动脉粥样硬化性LDL亚组分的形成,这可能是由于抗氧化防御能力降低所致。需要进一步研究以阐明氧化应激参数中观察到的变化。