ET-1 induced alterations of hepatic microcirculation: sinusoidal and extrasinusoidal sites of action

M Bauer, JX Zhang, I Bauer… - American Journal of …, 1994 - journals.physiology.org
M Bauer, JX Zhang, I Bauer, MG Clemens
American Journal of Physiology-Gastrointestinal and Liver …, 1994journals.physiology.org
Using epifluorescence microscopy, we investigated the dynamic changes in hepatic
sinusoidal hemodynamics in vivo during continuous infusion of endothelin-1 (ET-1) in
pentobarbital-anesthetized rats. ET-1 was infused for 20 min at rates of 2 or 10 pmol/min
either systemically or into the portal vein, followed by a 90-min recovery period. In contrast to
systemic application of ET-1 that did not cause a consistent hepatic microvascular effect, we
observed two different patterns of microcirculatory alterations during portal application …
Using epifluorescence microscopy, we investigated the dynamic changes in hepatic sinusoidal hemodynamics in vivo during continuous infusion of endothelin-1 (ET-1) in pentobarbital-anesthetized rats. ET-1 was infused for 20 min at rates of 2 or 10 pmol/min either systemically or into the portal vein, followed by a 90-min recovery period. In contrast to systemic application of ET-1 that did not cause a consistent hepatic microvascular effect, we observed two different patterns of microcirculatory alterations during portal application. Infusion of 2 pmol/min elicited a rapid, reversible decrease in sinusoidal diameter that was paralleled by a slight increase in red cell velocity, resulting in conservation of volumetric flow and sinusoid density. Infusion of 10 pmol/min resulted in a biphasic narrowing followed by transient increase in sinusoidal diameter and a profound and lasting decrease in red cell velocity, leading to an almost complete cessation of hepatic microvascular blood flow. These results indicate that ET-1 is a potent constrictor in the liver microcirculation in vivo and acts at both extrasinusoidal and sinusoidal sites, although the sinusoidal sites appear to be more sensitive to lower concentrations.
American Physiological Society
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