Coppi G, Falcone A
Department of Pharmacology, Research Centre, Poli Industria Chimica, Rozzano, Milan, Italy.
Eur J Pharmacol. 1990 Jun 21;182(1):185-8. doi: 10.1016/0014-2999(90)90511-4.
Hypovolemic shock was produced in rats by withdrawing about 50% of the estimated total blood volume. Following mean arterial pressure stabilization in the range of 22-23 mm Hg, the rats were given an i.v. bolus injection of L-6-ketopiperidine-2-carbonyl-L-leucyl-L-proline amide (RGH-2202) to be compared with thyrotropin-releasing hormone (TRH). RGH-2202, administered within 5 min following shock induction, dose dependently improved the mean arterial pressure and survival of the rats. The activity of RGH-2202 was superior to that of TRH after i.v. administration; both drugs showed a lower activity after i.m. administration.
通过抽取约50%估计的总血容量在大鼠中制造低血容量性休克。在平均动脉压稳定在22 - 23 mmHg范围内后,给大鼠静脉推注L - 6 - 酮哌啶 - 2 - 羰基 - L - 亮氨酰 - L - 脯氨酸酰胺(RGH - 2202),并与促甲状腺激素释放激素(TRH)进行比较。在休克诱导后5分钟内给予RGH - 2202,剂量依赖性地改善了大鼠的平均动脉压和存活率。静脉给药后,RGH - 2202的活性优于TRH;两种药物肌肉注射后活性均较低。