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  • Meeting abstract
  • Open Access

Arginine vasopressin compromises gut mucosal microcirculation in septic rats

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  • 1,
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Critical Care20026(Suppl 1):P132

https://doi.org/10.1186/cc1588

Published: 1 March 2002

Keywords

  • Arginine Vasopressin
  • Mucosal Blood Flow
  • Blinded Investigator
  • Control Laboratory Experiment
  • Arteriolar Diameter

Background

Arginine vasopressin (AVP) is increasingly used in the therapy of septic patients with hypotension [1]. In a prospective, controlled laboratory experiment we studied AVP-associated changes in the villus microcirculation of the septic rat ileum.

Methods

Twenty-four hours after caecal ligation and perforation to create sepsis, moderately hypotensive rats (average decrease in mean arterial pressure [MAP] 20% from pre-septic values) were anaesthetized. Next, intravital video-microscopy was performed on 6-10 villi of ileum mucosa (M0). The treatment group then received a continuous infusion of AVP to increase MAP by 20 mmHg (M1) and 40 mmHg (M2) from M0, while the control group received only normal saline. Measurements were repeated at M1 and M2. Video recordings were analysed by a blinded investigator. Diameter of terminal arterioles (Artd) were determined and stopped flow across the villus microcirculation (total arrest of villus blood flow > 1 s) was quantified.

Statistics

ANOVA with post-hoc test (Student-Newman-Keuls). Data are mean ± SD.

Results

AVP infusion was associated with a clear increase in stopped flow time at M1 and M2, while no change was observed for Artd (Table).

Table

 

Control (n = 5)

AVP (n = 5)

 

M0

M1

M2

M0

M1

M2

MAP (mmHg)

114 ± 7

109 ± 14

104 ± 11

108 ± 4

128 ± 5*

149 ± 4*

Artd (µm)

8.04 ± 0.78

7.63 ± 1.15

8.1 ± 0.71

7.12 ± 0.38

7.29 ± 0.59

7.42 ± 0.71

Stopped-flow (s min-1)

8 ± 3.5

6 ± 5.8

7 ± 5.2

11 ± 4.3

36 ± 11.2*-

41 ± 9.4*-

*P < 0.001 vs M0, -P < 0.001 AVP vs control.

Conclusion

These preliminary data demonstrate severe abnormalities in gut mucosal blood flow following AVP infusion in septic rats. Because no change occurred in terminal arteriolar diameters, the observed flow abnormalities could be due to either activities of AVP on larger arterioles or to a concomitant reduction in cardiac output [1].

Authors’ Affiliations

(1)
Department of Anaesthesiology, Operative Intensive Care Medicine, University of Münster, Münster, Germany

References

  1. Holmes CL, et al.: Chest 2001, 120: 989-1002. 10.1378/chest.120.3.989View ArticlePubMedGoogle Scholar

Copyright

© Biomed central limited 2001

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