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Nitric oxide-dependent neutrophil recruitment: role in nasal secretion

Authors

  • L.-O. Cardell,

    1. Cardiovascular Research Institute and Departments of Medicine and Physiology, University of California San Francisco, San Francisco, CA, USA
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  • C. Agustí,

    1. Cardiovascular Research Institute and Departments of Medicine and Physiology, University of California San Francisco, San Francisco, CA, USA
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  • J. A. Nadel

    1. Cardiovascular Research Institute and Departments of Medicine and Physiology, University of California San Francisco, San Francisco, CA, USA
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L.-O. Cardell, Department of Otorhinolaryngology, Malmö University Hospital, S-205 02 Malmö, Sweden.

Abstract

Leukotriene B4 (LTB4), an inflammatory mediator, is a potent chemoattractant for neutrophils that plays an important role in nasal secretion via release of elastase. Nitric oxide (NO) is an important modulator of leucocyte–endothelial cell interactions, endogenously produced in large quantities in the paranasal sinuses.

To examine the role of NO in LTB4-stimulated nasal secretion.

A newly-developed method for isolating and superfusing a nasal segment in dogs was used.

Instillation of LTB4 into the nasal segment caused a time-dependent increase in the volume of airway fluid and in the recruitment of neutrophils. N(G)-nitro-l-arginine-methylester (L-NAME), an inhibitor of NO synthase, prevented LTB4-induced neutrophil recruitment and nasal secretion.

These studies show that NO modulates LTB4-induced neutrophil recruitment and subsequent fluid secretion in the nose, and they suggest a therapeutic role for NO inhibitors in modulating neutrophil-dependent nasal secretion.

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