Myogenic constriction and dilation of isolated lymphatic vessels
Open accessAbstract
We tested the hypothesis that lymphatics would exhibit myogenic constrictions and dilations to intraluminal pressure changes. Collecting lymphatic vessels were isolated from rat mesentery, cannulated, and pressurized for in vitro study. The lymphatic diameter responses to controlled intraluminal pressure steps of different magnitudes were tested in the absence and presence of the inflammatory mediator substance P, which is known to enhance lymphatic contractility. Myogenic constriction, defined as a time-dependent decrease in end-diastolic diameter over a 1- to 2-min period following pressure elevation (after initial distension), was observed in the majority of rat mesenteric lymphatic vessels in vitro and occurred over a relatively wide pressure range (1-15 cmH2O). Myogenic dilation, a time-dependent rise in end-diastolic diameter following pressure reduction, was observed in over half the vessels equilibrated at a low baseline pressure. Myogenic constrictions were independent of the cardiac-like and time-dependent compensatory decline in end-systolic diameter and increase in amplitude observed in almost all vessels following pressure elevation. Substance P increased the percentage of vessels exhibiting myogenic constriction, the magnitude and rate of constriction, and the pressure range over which constriction occurred. Our results demonstrate that myogenic responses occur in collecting lymphatic vessels and suggest that the response may aid in preventing vessel overdistens…
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Myogenic responses in lymphatic vessels are comparable to those in arteries, and lymphatic muscle exhibits rate-sensitive responses to pressure that are stronger than those in arteries.
“Myogenic responses in lymphatic vessels are comparable to those in arteries (65), and lymphatic muscle also exhibits rate-sensitive responses to pressure (66) that are stronger than those in arteries (67).”
From Transport and Immune Functions of the Lymphatic System. (2025) · cites this paper as [65]
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Scallan, J. P., Zawieja, S. D., Castorena‐Gonzalez, J. A., & Davis, M. J. (2016) · The Journal of Physiology · doi:10.1113/jp272088 · Cited by 424 · see citing works
Self-citationDavis, M. J., Earley, S., Li, Y.-S., & Chien, S. (2023) · Physiological Reviews · doi:10.1152/physrev.00053.2021 · Cited by 273 · see citing works
Self-citationTransport and Immune Functions of the Lymphatic System.
Davis, M. J., Zawieja, S. D., & King, P. D. (2025) · Annual Review of Physiology · doi:10.1146/annurev-physiol-022724-104908 · Cited by 42 · see citing works
Self-citation
- Authors
- Davis, M. J., Davis, A. M., Ku, C. W., & Gashev, A. A.
- Affiliations
- University of Missouri (US)
- Venue
- American Journal of Physiology-Heart and Circulatory Physiology
- Publisher
- American Physiological Society
- Published
- 2009-02
- Volume
- 296
- Issue
- 2
- Pages
- H293-H302
- ISSN
- 0363-6135 (ISSN-L)
- 1522-1539
- PMC
- PMC2643897
- OpenAlex
- W2106245989
- Cited by
- 78
- References
- 0
- Citations by year
- 2026: 3 · 2025: 4 · 2024: 3 · 2023: 4 · 2022: 2 · 2021: 5 · 2020: 2 · 2019: 9 · 2018: 7 · 2017: 2 · 2016: 4 · 2015: 5 · 2014: 4 · 2013: 5 · 2012: 7
- FWCI
- 2.11
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- American Journal of Physiology-Heart and Circulatory Physiology (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Funders
- National Heart, Lung, and Blood Institute (HL089784, R01HL089784)
- Topics
- Health Sciences › Medicine › Oncology › Lymphatic System and Diseases
- Health Sciences › Medicine › Surgery › Lymphatic Disorders and Treatments
- Health Sciences › Medicine › Infectious Diseases › Parasitic Diseases Research and Treatment
- Keywords
- lymphatic vessels, myogenic constriction, intraluminal pressure, substance P, lymphatic contractility, mesenteric lymphatics, end-diastolic diameter, inflammation, edema
- MeSH terms
- Animals, Constriction, Pathologic, Dilatation, Pathologic, Male, Mesentery, Muscle Contraction, Muscle Relaxation, Pressure, Substance P, Time Factors, Rats, Sprague-Dawley, Inflammation Mediators, Lymphatic Vessels, Rats, In Vitro Techniques
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