Yoo Kyung Y, Kim Hak S, Moon Jai-Dong, Lee JongUn
Department of Anesthesiology, Research Institute of Medical Sciences, Chonnam National University Medical School, 5 Hak-dong, Gwangju 501-746, South Korea.
Anesth Analg. 2002 Jun;94(6):1505-9, table of contents. doi: 10.1097/00000539-200206000-00024.
We investigated whether sildenafil citrate (Viagra) may reduce the dose of nitrovasodilators to induce deliberate hypotension. Ten mongrel dogs were acutely instrumented with a femoral artery catheter and a pulmonary artery catheter. Sodium nitroprusside (SNP; 1-16 microg. kg(-1). min(-1)) or nitroglycerin (NTG; 2-32 microg. kg(-1). min(-1)) was IV given to induce hypotension. The study consisted of two occasions, in a random order, in each animal: one with sildenafil pretreatment (1 mg/kg IV followed by 0.3 mg. kg(-1). h(-1)) and the other without to serve as a control. Hemodynamic variables were continuously monitored. Plasma cyclic guanosine monophosphate (cGMP) concentrations were measured by radioimmunoassay. Both SNP and NTG produced dose-dependent decreases in mean arterial blood pressure without affecting the heart rate in the presence as well as in the absence of sildenafil. Systemic vascular resistance index and mean pulmonary arterial pressure were also decreased. The magnitude of mean arterial blood pressure and systemic vascular resistance index reductions caused by SNP was augmented by sildenafil, whereas that caused by NTG was not affected. Neither SNP nor NTG alone altered the plasma cGMP concentrations. Sildenafil increased the plasma cGMP concentration, which was further increased by SNP but not affected by NTG. These results indicate that sildenafil may reduce the dose of SNP in producing deliberate hypotension in the dog. The potentiation of SNP-induced hypotension by sildenafil may be related to an augmented accumulation of cGMP.
Sildenafil may reduce the dose of sodium nitroprusside required to induce deliberate hypotension and hence the potential for cyanide toxicity.
我们研究了枸橼酸西地那非(万艾可)是否可以降低硝基血管扩张剂的剂量以诱导控制性低血压。十只杂种犬被急性植入股动脉导管和肺动脉导管。静脉给予硝普钠(SNP;1 - 16微克·千克⁻¹·分钟⁻¹)或硝酸甘油(NTG;2 - 32微克·千克⁻¹·分钟⁻¹)以诱导低血压。该研究在每只动物中随机分为两次进行:一次进行西地那非预处理(静脉注射1毫克/千克,随后以0.3毫克·千克⁻¹·小时⁻¹持续给药),另一次不进行预处理作为对照。连续监测血流动力学变量。通过放射免疫测定法测量血浆环磷酸鸟苷(cGMP)浓度。在有和没有西地那非的情况下,SNP和NTG均使平均动脉血压呈剂量依赖性下降,而不影响心率。全身血管阻力指数和平均肺动脉压也降低。西地那非增强了SNP引起的平均动脉血压和全身血管阻力指数降低的幅度,而NTG引起的降低幅度不受影响。单独使用SNP或NTG均未改变血浆cGMP浓度。西地那非增加了血浆cGMP浓度,SNP使其进一步升高,但NTG对其无影响。这些结果表明,西地那非可能降低犬在产生控制性低血压时SNP的剂量。西地那非对SNP诱导的低血压的增强作用可能与cGMP的积累增加有关。
西地那非可能降低诱导控制性低血压所需的硝普钠剂量,从而降低氰化物毒性的可能性。