» Articles » PMID: 33346023

Negative Pressure Increases Microvascular Perfusion During Severe Hemorrhagic Shock

Overview
Journal Microvasc Res
Date 2020 Dec 21
PMID 33346023
Citations 2
Authors
Affiliations
Soon will be listed here.
Abstract

Hemorrhagic shock (HS) is a severe life-threatening condition characterized by loss of blood volume and a lack of oxygen (O) delivery to tissues. The objective of this study was to examine the impact of manipulating Starling forces in the microcirculation during HS to increase microvascular perfusion without restoring blood volume or increasing O carrying capacity. To decrease interstitial tissue pressure, we developed a non-contact system to locally apply negative pressure and manipulate the pressure balance in capillaries, while allowing for visualization of the microcirculation. Golden Syrian hamsters were instrumented with dorsal window chambers and subjected to a controlled hemorrhaged of 50% of the animal's blood volume without any fluid resuscitation. A negative pressure chamber was attached to the dorsal window chamber and a constant negative pressure was applied. Hemodynamic parameters (including microvascular diameter, blood flow, and functional capillary density [FCD]) were measured before and during the four hours following the hemorrhage, with and without applied negative pressure. Blood flow significantly increased in arterioles during negative pressure. The increase in flow through arterioles also improved microvascular perfusion as reflected by increased FCD. These results indicate that negative pressure increases flow in the microcirculation when fluid resuscitation is not available, thus restoring blood flow, oxygen delivery, and preventing the accumulation of metabolic waste. Applying negative pressure might allow for control of microvascular blood flow and oxygen delivery to specific tissue areas.

Citing Articles

Conventional versus Instillation Negative-Pressure Wound Therapy for Severe Soft Tissue Injury in Open Pelvic Fractures: A Retrospective Review.

Choi D, Cho W, Song H, Kwon J, Kang B, Jung H Yonsei Med J. 2025; 66(2):94-102.

PMID: 39894042 PMC: 11790408. DOI: 10.3349/ymj.2023.0473.


Hemorrhagic shock and fluid dynamics.

Cohen M, Monaghan S Physiol Rep. 2021; 9(6):e14813.

PMID: 33769690 PMC: 7995542. DOI: 10.14814/phy2.14813.


Application of negative tissue interstitial pressure improves functional capillary density after hemorrhagic shock in the absence of volume resuscitation.

Jani V, Jani V, Munoz C, Govender K, Williams A, Cabrales P Physiol Rep. 2021; 9(5):e14783.

PMID: 33661575 PMC: 7931804. DOI: 10.14814/phy2.14783.

References
1.
Lipowsky H, ZWEIFACH B . Application of the "two-slit" photometric technique to the measurement of microvascular volumetric flow rates. Microvasc Res. 1978; 15(1):93-101. DOI: 10.1016/0026-2862(78)90009-2. View

2.
Intaglietta M, Tompkins W . System for the measurement of velocity of microscopic particles in liquids. IEEE Trans Biomed Eng. 1971; 18(5):376-9. DOI: 10.1109/tbme.1971.4502869. View

3.
Arfors K, Bergqvist D, Intaglietta M, Westergren B . Measurements of blood flow velocity in the microcirculation. Ups J Med Sci. 1975; 80(1):27-33. DOI: 10.3109/03009737509178987. View

4.
Nolte D, Menger M, Messmer K . Microcirculatory models of ischaemia-reperfusion in skin and striated muscle. Int J Microcirc Clin Exp. 1995; 15 Suppl 1:9-16. DOI: 10.1159/000179088. View

5.
Pelletier C, Edis A, SHEPHERD J . Circulatory reflex from vagal afferents in response to hemorrhage in the dog. Circ Res. 1971; 29(6):626-34. DOI: 10.1161/01.res.29.6.626. View