ReviewMicrocirculation (New York, N.Y. : 1994)2025
Eugene M Renkin. His Many Contributions to Microvascular Research With Examples of How They Inform Current Investigations of Microvascular Dysfunction.
Review in Microcirculation (New York, N.Y. : 1994), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
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Who cites it
3 citing papers in PubMed.
- Inflammation induced by snake venoms optimizes envenomation.The Journal of physiology · 2026Article
- Classification system proposed to guide the design, development, regulatory approval, and scaling of long acting, small- and macro-molecule parenteral products (CS-BLAP).Journal of pharmaceutical sciences · 2026Review
- Endothelial Surface Glycocalyx in Vascular Functions and Diseases.Advances in experimental medicine and biology · 2026Review
Corrections and comments
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Authors and funding
2 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Eugene Renkin used simplified uniform models of microvascular exchange units to describe the fundamental functions of the microcirculation: a cylindrical pore to characterize the barriers to exchange of water and solutes; a uniformly perfused capillary to distinguish flow-limited exchange from diffusion-limited exchange; and a membrane with large and small pores to describe macromolecule exchange between blood and lymph. A key idea linking these concepts to microvascular dysfunction is that local blood flows, microvascular pressures, and the permeability of the vascular wall are not uniformly distributed within microvascular beds. Renkin's concept of microvascular clearance of small solute was extended to show how heterogeneity in blood transit times compromised exchange. It was also extended to evaluate the relative contribution of diffusion, convection, and vesicle exchange to microvascular exchange of macromolecules when there is heterogeneity in macromolecule permeability, measured by the presence of large pores. An extension of his analysis to smaller proteins (14-20 KDa) showed that convective transport may limit the diffusion of inflammatory peptides, therapeutic agents, and toxins from the tissue into circulating blood. We include recent examples of the growing understanding of microvascular dysfunction in chronic disease and approaches to modeling heterogeneity in normal and diseased states.
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Registered trials
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