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慢性输注α-三肌醇对清醒大鼠局部和心脏血流动力学的影响。

Effects of chronic infusions of alpha-trinositol on regional and cardiac haemodynamics in conscious rats.

作者信息

Gardiner S M, Kemp P A, Fallgren B, Bennett T

机构信息

Department of Physiology & Pharmacology, University of Nottingham Medical School, Queen's Medical Centre, England.

出版信息

Br J Pharmacol. 1994 Sep;113(1):129-36. doi: 10.1111/j.1476-5381.1994.tb16184.x.

Abstract
  1. Male, Long Evans rats (350-450 g) were chronically instrumented for the measurement of renal, mesenteric and hindquarters haemodynamics, and were given three consecutive, 24 h infusions of vehicle (sterile saline at 0.3 ml h-1, n = 8) or alpha-trinositol (D-myo-inositol-1,2,6-triphosphate) at 5, 20 and 80 mg kg-1 h-1 (0.3 ml h-1; n = 9). During infusion of alpha-trinositol at 5 or 20 mg kg-1 h-1, cardiovascular changes were little different from those seen during saline infusion. However, during infusion of alpha-trinositol at 80 mg kg-1 h-1 there were increases in hindquarters vascular conductance, renal flow and vascular conductance, that were all significantly different from the changes seen in the saline group. Infusion of alpha-trinositol at the high dose in naive rats (n = 8) had even more marked vasodilator effects. 2. Two groups of rats (n = 8 in each), chronically instrumented for the measurement of cardiac haemodynamics, were given 48 h infusions of saline (0.3 ml h-1) or alpha-trinositol (2 mg kg-1 bolus, 80 mg kg-1 h-1 infusion at 0.3 ml h-1). During the infusion of saline, there were slight reductions in heart rate, cardiac index, peak aortic flow, dF/dtmax and central venous pressure. In the animals receiving alpha-trinositol, with the exception of central venous pressure, all the above variables, together with total peripheral conductance, increased. 3. These results, collectively, indicate that incremental infusions of alpha-trinositol do not reveal its full vasodilator potential, possibly due to concurrent activation of counter-regulatory vasoconstrictor mechanisms. However, infusion of alpha-trinositol at a high dose causes substantial increases in renal,mesenteric and hindquarters flows and vascular conductances, supported by significant increases in indices of cardiac inotropism. Such effects, in the absence of significant hypotension, tachycardia or signs of desensitization, give alpha-trinositol a unique cardiovascular profile.
摘要
  1. 雄性Long Evans大鼠(体重350 - 450克)被长期植入仪器以测量肾、肠系膜和后肢的血流动力学,并连续24小时输注三次载体(0.3毫升/小时的无菌生理盐水,n = 8)或α-三磷酸肌醇(D-肌醇-1,2,6-三磷酸),剂量分别为5、20和80毫克/千克/小时(0.3毫升/小时;n = 9)。在以5或20毫克/千克/小时的剂量输注α-三磷酸肌醇期间,心血管变化与输注生理盐水期间所见变化几乎没有差异。然而,在以80毫克/千克/小时的剂量输注α-三磷酸肌醇期间,后肢血管传导性、肾血流量和血管传导性均增加,且这些变化与生理盐水组所见变化均有显著差异。在未处理的大鼠(n = 8)中以高剂量输注α-三磷酸肌醇具有更明显的血管舒张作用。2. 两组大鼠(每组n = 8)被长期植入仪器以测量心脏血流动力学,分别接受48小时的生理盐水(0.3毫升/小时)或α-三磷酸肌醇(2毫克/千克推注,80毫克/千克/小时以0.3毫升/小时的速度输注)输注。在输注生理盐水期间,心率、心脏指数、主动脉峰值血流、dF/dtmax和中心静脉压略有降低。在接受α-三磷酸肌醇的动物中,除中心静脉压外,上述所有变量以及总外周传导性均增加。3. 总体而言,这些结果表明,递增输注α-三磷酸肌醇并未充分显示其血管舒张潜力,这可能是由于同时激活了反调节血管收缩机制。然而,高剂量输注α-三磷酸肌醇会导致肾、肠系膜和后肢血流量及血管传导性大幅增加,同时心脏收缩力指标也显著增加。在无明显低血压、心动过速或脱敏迹象的情况下,这些作用赋予了α-三磷酸肌醇独特的心血管特征。

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