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奈必洛尔的一氧化氮介导的静脉舒张作用。

Nitric oxide mediated venodilator effects of nebivolol.

作者信息

Bowman A J, Chen C P, Ford G A

机构信息

Department of Medicine, The University, Newcastle upon Tyne.

出版信息

Br J Clin Pharmacol. 1994 Sep;38(3):199-204. doi: 10.1111/j.1365-2125.1994.tb04342.x.

Abstract
  1. Nebivolol, a selective beta 1-adrenoceptor antagonist with antihypertensive effects, has haemodynamic effects suggestive of a direct vasodilator action. 2. The dorsal hand vein technique was used to determine whether nebivolol has venodilator action in vivo in man. 3. Nebivolol and atenolol were infused into the phenylephrine preconstricted superficial hand veins of 11 healthy male volunteers. In separate studies L-NMMA (0.1 microgram min-1) was pre- and co-infused with nebivolol to determine whether nitric oxide (NO) mediated mechanisms were present. Further studies with prostaglandin F2 alpha (PGF2 alpha) preconstriction were performed to exclude an alpha-adrenergic antagonistic effect of nebivolol. Effects of L-NMMA infusion on nitroglycerin venodilation were also determined. 4. Nebivolol produced a dose dependent venodilation, (72 +/- 18% maximum), whereas atenolol produced no significant venodilation. At doses of nebivolol producing plasma concentrations comparable with plasma levels achieved after standard oral dosing (10(-13)-10(-12) mol min-1) small (14 +/- 6% and 23 +/- 8%) but significant (P < 0.05) venodilation was observed. 5. The venodilator response to nebivolol was significantly reduced by infusion of L-NMMA (maximum dilation 18% vs 72%, P < 0.01). Venodilator responses to nitroglycerin were unaffected by L-NMMA infusion. A venodilator effect to nebivolol was also seen following preconstriction with PgF2 alpha (40 +/- 20% maximum). 6. Nebivolol has nitric oxide mediated, venodilator effects in man.
摘要
  1. 奈必洛尔是一种具有降压作用的选择性β1肾上腺素能受体拮抗剂,其血流动力学效应提示有直接血管舒张作用。2. 采用手背静脉技术来确定奈必洛尔在人体体内是否具有静脉舒张作用。3. 将奈必洛尔和阿替洛尔注入11名健康男性志愿者经去氧肾上腺素预收缩的手部浅表静脉。在单独的研究中,L - N - 甲基精氨酸(L - NMMA,0.1微克/分钟)在奈必洛尔之前和同时注入,以确定是否存在一氧化氮(NO)介导的机制。还进行了用前列腺素F2α(PGF2α)预收缩的进一步研究,以排除奈必洛尔的α肾上腺素能拮抗作用。也测定了L - NMMA注入对硝酸甘油静脉舒张的影响。4. 奈必洛尔产生剂量依赖性静脉舒张(最大舒张72±18%),而阿替洛尔未产生明显的静脉舒张。在奈必洛尔剂量产生的血浆浓度与标准口服给药后达到的血浆水平相当(10⁻¹³ - 10⁻¹²摩尔/分钟)时,观察到小幅度(14±6%和23±8%)但显著(P < 0.05)的静脉舒张。5. 注入L - NMMA后,奈必洛尔的静脉舒张反应显著降低(最大舒张18%对72%,P < 0.01)。L - NMMA注入对硝酸甘油的静脉舒张反应无影响。在用PGF2α预收缩后,也观察到奈必洛尔的静脉舒张作用(最大舒张40±20%)。6. 奈必洛尔在人体中具有一氧化氮介导的静脉舒张作用。

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