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PMID: 1309402 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, Non-P.H.S. Research Support, U.S. Gov't, P.H.S.

Synergism between leukotriene B4 and thromboxane A2 in mediating acid-aspiration injury.

Surgery ·Vol. 111 ·No. 1 ·1992-01-00 ·Pages 55-61

Goldman G, Welbourn R, Kobzik L, Valeri CR, Shepro D, Hechtman HB

Abstract

Acid aspiration leads to thromboxane-dependent lung neutrophil sequestration associated with microvascular permeability increase. Leukotriene B4 (LTB4) is postulated to be a cofactor in the thromboxane-induced inflammatory response. This study tests the interaction between LTB4 and thromboxane, focusing on LTB4 induction of thromboxane-dependent lung neutrophil sequestration after acid aspiration. Anesthetized rats underwent tracheostomy and insertion of a cannula in a left lung segment. This was followed by instillation of either 0.1 ml 0.1N hydrochloric acid (n = 18) or 0.1 ml saline in control rats (n = 18). When assayed at 3 hours, acid aspiration led to increased plasma levels of LTB4 and thromboxane B2 (TxB2), higher than control values (p less than 0.05). The rise in plasma LTB4 was correlated (p less than 0.05; r = 0.83) with sequestration of neutrophils in the nonaspirated lung. The entrapment of thromboxane-dependent lung neutrophil was associated with an increase in protein concentration in bronchoalveolar lavage of the aspirated and nonaspirated sides and an increase in lung wet to dry weight ratio. Pretreatment of other rats (n = 18) with the lipoxygenase inhibitor diethylcarbamazine IV prevented an aspiration-induced rise in plasma LTB4 and TxB2. Further, there was an attenuation of lung leukosequestration and protein leak in bronchoalveolar lavage and lung edema (all p less than 0.05). Pretreatment of other rats (n = 12) with the leukotriene receptor antagonist FPL 55712 IV did not prevent the aspiration-induced rise in LTB4 or TxB2, but otherwise was as effective as diethylcarbamazine in preventing injury. Finally, other hydrochloric acid-aspirated rats (n = 8) were pretreated intravenously with the thromboxane synthetase inhibitor OKY 046 or the thromboxane receptor antagonist SQ 29548. Both agents limited the aspiration-induced rise in plasma LTB4 (p less than 0.05). The data indicate that localized acid aspiration induces synthesis of LTB4 and thromboxane A2. Inhibition of either leukotriene or thromboxane will limit PMN adhesion and increased lung permeability.

MeSH Terms
Animals Leukotriene B4/biosynthesis,physiology Male Neutrophils/physiology Pneumonia, Aspiration/metabolism,physiopathology Pulmonary Edema/chemically induced,physiopathology Rats Rats, Inbred Strains Thromboxane A2/metabolism,physiology Thromboxane B2/blood
Chemicals
Leukotriene B4 Thromboxane B2 Thromboxane A2
Authors & Affiliations
6 authors, click to expand affiliations / ORCID
Goldman G
Department of Surgery, Brigham and Women's Hospital, Boston, MA 02115.
Welbourn R
Kobzik L
Valeri C R
Shepro D
Hechtman H B
Article Info
Journal
Surgery
Abbr.
Surgery
ISSN
0039-6060
Published
1992-01-00
Pages
55-61
Language
English
Region
United States
NLM ID
0417347
Subset
IM
Grants
NIGMS NIH HHS · GM 24891-11 · United States
NIGMS NIH HHS · GM 35141-03 · United States
NHLBI NIH HHS · HL 16714-13 · United States
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