Lymphangions, the segments of lymphatic vessels between valves, exhibit structural characteristics in common with both ventricles and arteries. Although once viewed as passive conduits like arteries, it has become well established that lymphangions can actively pump lymph against an axial pressure gradient from low-pressure tissues to the great veins of the neck. A recently reported mathematical model, based on fundamental principles, predicted that lymphangions can transition from pump to conduit behavior when outlet pressure falls below inlet pressure. In this case, the axial pressure gradient becomes the major source of energy for the propulsion of lymph, despite the presence of cyclical contraction. In fact, flow is augmented when cyclical contractions are abolished. We therefore used an in vitro preparation to confirm these findings and to test the hypothesis that lymphangion contraction inhibits flow when outlet pressure falls below inlet pressure. Bovine postnodal mesenteric lymphatic vessels harvested from an abattoir were subjected to an inlet pressure of 5.0 cmH(2)O and an outlet pressure that decreased from 6.5 to 3.5 cmH(2)O under control conditions, stimulated with U-46619 (a thromboxane analog) and relaxed with calcium-free solution. Under control conditions, lymphatic flow markedly increased as outlet pressure fell below inlet pressure. In this case, the slopes of the flow versus axial pressure gradient increased with calcium-free conditions (61%, n = 8, P = 0.016) and decreased with U-46619 stimulation (21%, n = 5, P = 0.033). Our findings indicate that the stimulation of lymphatic contractility does indeed inhibit lymphatic flow when vessels act like conduits.
We developed a bovine model of mesenteric venous hypertension (MVH)by surgically occluding mesenteric veins for 3 days to investigate the functional and molecular adaptations of the mesenteric lymphatic vessels. The MVH model was characterized by an increase in mesenteric vein pressure from 10 to 30 mm Hg, a decrease in lymph protein concentration from 6 to 5 g/dL and an increase in intestinal water content from 72 to 78%. After 3‐days of MVH, isolated mesenteric lymphatic vessels demonstrated decreased contraction frequency, decreased ejection fraction and decreased stroke volume at each transmural pressure tested. Microarray analysis revealed that 117 genes were upregulated and 79 genes were down regulated in MVH lymphatics. A large number of the regulated genes are muscle contractile proteins, consistent with the changes in function. We further characterized changes in the mRNA of actin isoforms expressed in lymphatic muscle in response to venous hypertension. The smooth muscle actins (alpha and gamma) and skeletal actin were increased and cardiac actin decreased in lymphatics from the MHV model. Actin protein levels were analyzed by western blot analysis and revealed similar directional changes in response to MHV. These data suggest that lymphatic vessels undergo functional and molecular adaptation in response to changes in lymphdynamics in a time frame that may be important in resolution of edema. This work was supported by a LSI grant from Texas A&M University and CDC grant 623086.
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.
hi@scite.ai
10624 S. Eastern Ave., Ste. A-614
Henderson, NV 89052, USA
Copyright © 2024 scite LLC. All rights reserved.
Made with 💙 for researchers
Part of the Research Solutions Family.