Microvascular Physiologic and Anatomic Responses of the Guinea Pig to Experimental Arenavirus Infection

Abstract

These studies complete control observations in Guinea Pig strain 13 in preparation to examine microcirculatory disturbances in Pichinde virus infection. Findings are: Using lymph flux analysis from intestinal mesenteric lymphatics, protein reflection coefficient is .728 + or - .018 SEM, and permeability-surface area product is 3.21 + or - .29 ul/min/100g. For future studies involving endothelial monolayer transport from infected GP, in vitro new methods demonstrate 1) confluent endothelial monolayers can be assessed functionally from fluorescence intensity patterns of solutes in diffusion chambers, 2) cell morphology is identical to in vivo structure, 3) restricted diffusion develops after three days, and 4) single pore fits to permeabilities are excellent. Using ethane production to mark free radical production, we see 1) it is independent of minute ventilation, 2) is nearly exclusively produced in lung, 3) is inhibited by superoxide dismutase and catalase, 4) is tightly coupled to dietary iron, and 5) and is closely joined to microvascular abnormalities including increased filtration coefficient and lung water. New intravital microscopic methods including infusion of latex beads, have demonstrated: 1) stable images are achieved, 2) mesenteric microvessels normally do not leak dextran, 3) kinetics of Kupffer cell phagocytosis are measurable, and 4) topical tumor necrosis factor results in dextran leaks and blot hemorrhages. This may be important in the splanchnic pathogenesis of hemorrhagic fever. Keywords: Pichinde virus, Protein transport, Microcirculation, Water transport, Arenaviruses, Microvascular, Hemorrhage, Shock pathology.

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Document Details

Document Type
Technical Report
Publication Date
Mar 25, 1989
Accession Number
ADA207813

Entities

People

  • Murray A. Katz

Organizations

  • Veterans Administration Medical Center

Tags

DTIC Thesaurus Topics

  • Arteries
  • Blood
  • Blood Cells
  • Blood Flow
  • Cardiovascular Diseases
  • Cardiovascular Physiological Phenomena
  • Cells
  • Chemistry
  • Hemorrhage
  • Infection
  • Intercellular Junctions
  • Macrophages
  • Microvessels
  • Proteins
  • Rodents
  • Steady State
  • Veins

Fields of Study

  • Biology
  • Medicine

Readers

  • Cardiovascular Physiology
  • Immunology and Pathology
  • Virology (or Medical Virology).

Technology Areas

  • Space