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Modulation of pulmonary permeability in vivo with agents that affect the cytoskeleton

G Goldman1, R Welbourn, S Alexander

  • 1Department of Surgery, Brigham and Women's Hospital, Boston, Mass. 02115.

Surgery
|April 1, 1991
PubMed

Insights

The study found that agents affecting the cytoskeleton, like cytochalasin B and leukotriene B4, increase polymorphonuclear leukocyte (PMN) diapedesis and lung vascular permeability in rats. Phalloidin, however, stabilized the cytoskeleton and reduced these effects.

Area of Science:

  • Pulmonary medicine
  • Cell biology
  • Immunology

Background:

  • The cytoskeleton of the microvascular barrier influences polymorphonuclear leukocyte (PMN) diapedesis and macromolecule transport.
  • In vitro studies suggest that agents reorganizing the cytoskeleton can alter diapedesis and permeability.

Purpose of the Study:

  • To investigate in vivo whether the pulmonary microvasculature cytoskeleton responds to agents that alter diapedesis and permeability.
  • To assess the effects of cytochalasin B, leukotriene B4, and phalloidin on PMN accumulation and lung vascular permeability in rats.

Main Methods:

  • Anesthetized rats (n=152) received initial and secondary bronchus treatments with saline, cytochalasin B, leukotriene B4, or phalloidin.
  • PMN accumulations, protein concentration in bronchoalveolar lavage fluid, and lung wet/dry weight ratios were measured 3 hours post-treatment.

Main Results:

  • Cytochalasin B and leukotriene B4 significantly increased PMN accumulation and protein levels compared to saline controls.
  • Phalloidin treatment did not significantly alter PMN accumulation or protein levels when used as a secondary treatment.
  • Combined cytochalasin B and leukotriene B4 treatments led to the highest PMN diapedesis and lung wet/dry ratios; phalloidin attenuated these effects.

Conclusions:

  • The pulmonary microvasculature cytoskeleton responds in vivo to agents that modulate its structure, affecting PMN diapedesis and vascular permeability.
  • Cytochalasin B and leukotriene B4 disrupt the barrier, while phalloidin stabilizes it, offering potential therapeutic implications.

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