加压素
氧气
氧气张力
精氨酸
化学
解剖
生物
内分泌学
生物化学
氨基酸
有机化学
作者
Hans Knotzer,Werner Pajk,Stephan Maier,Ruth Ladurner,Axel Kleinsasser,Volker Wenzel,Martina Dünser,Hanno Ulmer,Walter Hasibeder
出处
期刊:American Journal of Physiology-heart and Circulatory Physiology
[American Physical Society]
日期:2005-07-01
卷期号:289 (1): H168-H173
被引量:42
标识
DOI:10.1152/ajpheart.01235.2004
摘要
We investigated intestinal oxygen supply and mucosal tissue Po 2 during administration of increasing dosages of continuously infused arginine vasopressin (AVP) in an autoperfused, innervated jejunal segments in anesthetized pigs. Mucosal tissue Po 2 was measured by employing two Clark-type surface oxygen electrodes. Oxygen saturation of jejunal microvascular hemoglobin was determined by tissue reflectance spectrophotometry. Microvascular blood flow was assessed by laser-Doppler velocimetry. Systemic hemodynamic variables, mesenteric venous and systemic acid-base and blood gas variables, and lactate measurements were recorded. Measurements were performed at baseline and at 20-min intervals during incremental AVP infusion ( n = 8; 0.007, 0.014, 0.029, 0.057, 0.114, and 0.229 IU·kg −1 ·h −1 , respectively) or infusion of saline ( n = 8). AVP infusion led to a significant ( P < .05), dose-dependent decrease in cardiac index (from 121 ± 31 to 77 ± 27 ml·kg −1 ·min −1 at 0.229 IU·kg −1 ·h −1 ) and systemic oxygen delivery (from 14 ± 3 to 9 ± 3 ml·kg −1 ·min −1 at 0.229 IU·kg −1 ·h −1 ) concomitant with an increase in systemic oxygen extraction ratio (from 31 ± 4 to 48 ± 10%). AVP decreased microvascular blood flow (from 133 ± 47 to 82 ± 35 perfusion units at 0.114 IU·kg −1 ·h −1 ), mucosal tissue Po 2 (from 26 ± 7 to 7 ± 2 mmHg at 0.229 IU·kg −1 ·h −1 ), and microvascular hemoglobin oxygen saturation (from 51 ± 9 to 26 ± 12% at 0.229 IU·kg −1 ·h −1 ) without a significant increase in mesenteric venous lactate concentration (2.3 ± 0.8 vs. 3.4 ± 0.7 mmol/l). We conclude that continuously infused AVP decreases intestinal oxygen supply and mucosal tissue Po 2 due to a reduction in microvascular blood flow and due to the special vascular supply in the jejunal mucosa in a dose-dependent manner in pigs.
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