The DOI matches its Crossref record; 17 of the 17 references it cites were found in a registry or an index.
Mesenteric Lymph Flow in Endotoxemic Guinea Pigs
Abstract
Background: Lipopolysaccharide (LPS) is a structural component of the outer membrane of gram-negative bacteria. LPS activates the host cells, leading to the production and release of proinflammatory cytokines. Given the induction duration for the release of cytokines, the initial mechanisms that produce LPS action on a timescale of minutes are not fully understood. We studied the effect of initial LPS-induced action on the lymphatic system by measuring the time-dependent changes in mesenteric lymph flow in guinea pigs in vivo . In addition, we determined the leakage of plasma protein into the lymphatic system using Evans blue dye. Methods and Results: The mesenteric lymphatic vessel was cannulated with a polyethylene catheter. We administered drugs via a catheter in jugular vein. The control animals received vehicle intravenously (i.v.). The experimental group received 1 mg/kg or 10 mg/kg LPS i.v. Twenty minutes before injection of the vehicle or LPS, Evans blue dye (5 mg/kg i.v.) was administered. Lymph output was measured every 20 min. The amount of Evans blue in the lymph was determined by spectrophotometry. The mesenteric lymph showed a steady flow rate of approximately 290 μL/kg/20 min. The lymph flow immediately increased after the administration of LPS and reached 3.4-fold and 7.4-fold after 1 h of 1 mg/kg and 10 mg/kg LPS injection, respectively. The albumin content in lymph significantly increased in proportion to the increased lymph volume. Conclusions: These results suggest that the early increase in mesenteric lymph flow rate in guinea pigs produced by LPS is mediated by vascular hyperpermeability and plasma albumin leakage.
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“In the literature, expansion of interstitial space is generally linked to increased transcapillary escape of plasma constituents into the interstitium, despite findings in experimental endotoxin‐treated animals that lymphatic backflow from the interstitium is also increased.26”
From Hypoalbuminemia: Pathogenesis and Clinical Significance (2019) · cites this paper as [26]
Citations
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Self-citation
Research works printed but not linked: 3
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Hypoalbuminemia: Pathogenesis and Clinical Significance
Soeters, P. B., Wolfe, R. R., & Shenkin, A. (2019) · Journal of Parenteral and Enteral Nutrition · doi:10.1002/jpen.1451 · Cited by 1,448
Inflammation-induced lymphangiogenesis and lymphatic dysfunction
Liao, S., & von der Weid, P. (2014) · Angiogenesis · doi:10.1007/s10456-014-9416-7 · Cited by 107
Chakraborty, S., Zawieja, S. D., Wang, W., Lee, Y., Wang, Y. J., von der Weid, P., Zawieja, D. C., & Muthuchamy, M. (2015) · American Journal of Physiology-Heart and Circulatory Physiology · doi:10.1152/ajpheart.00467.2015 · Cited by 65
Tran, C. D., Grice, D. M., Wade, B., Kerr, C. A., Bauer, D. C., Li, D., & Hannan, G. N. (2015) · Future Microbiology · doi:10.2217/fmb.15.54 · Cited by 48
Kim, H., Kim, B. H., Huh, B. K., Yoo, Y. C., Heo, C. Y., Choy, Y. B., & Park, J. (2017) · Biomaterials Science · doi:10.1039/c7bm00345e · Cited by 46
Metadata
- Authors
- Nemoto, K., Sato, H., Tanuma, K., & Okamura, T.
- Affiliations
- Nippon Medical School Hospital (JP)
- Shinjuku Vocational College of Acupuncture and Judo Therapy
- Corresponding author
- Nemoto, Kayo
- Venue
- Lymphatic Research and Biology
- Publisher
- SAGE Publications
- Published
- 2011-09-01
- Volume
- 9
- Issue
- 3
- Pages
- 129-134
- ISSN
- 1539-6851 (ISSN-L)
- 1557-8585
- OpenAlex
- W1989769256
- Cited by
- 10
- References
- 17
- Citations by year
- 2023: 1 · 2022: 1 · 2018: 1 · 2017: 1 · 2016: 1 · 2015: 2 · 2014: 2 · 2013: 1
- FWCI
- 0.47
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Lymphatic Research and Biology (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Health Sciences › Medicine › Oncology › Lymphatic System and Diseases
- Life Sciences › Immunology and Microbiology › Immunology › Immune Response and Inflammation
- Health Sciences › Medicine › Surgery › Lymphatic Disorders and Treatments
- Keywords
- lipopolysaccharide, endotoxemia, plasma protein leakage, albumin, Evans blue, lymphatic vessels, inflammatory cytokines, gram-negative bacterial endotoxin
- MeSH terms
- Animals, Blood Pressure, Capillary Permeability, Disease Models, Animal, Evans Blue, Guinea Pigs, Lipopolysaccharides, Lymph, Male, Mesentery, Endotoxemia, Lymphatic Vessels
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