Pulmonary Thromboxane Release Following Intestinal Reperfusion

• Published in: The Journal of surgical research Vol. 58; no. 6; pp. 552 - 557
• Main Authors: Turnage, Richard H., Kadesky, Kevin M., Bartula, Lori, Myers, Stuart I.
• Format: Journal Article Conference Proceeding
• Language: English
• Published: New York, NY Elsevier Inc 01.06.1995; Elsevier
• Subjects: Animals; Biological and medical sciences; Blood Pressure; Digestive system; Dinoprostone - secretion; Intestines - blood supply; Investigative techniques, diagnostic techniques (general aspects); Lung - blood supply; Lung - metabolism; Male; Medical sciences; Microcirculation - physiopathology; Pathology. Cytology. Biochemistry. Spectrometry. Miscellaneous investigative techniques; Rats; Rats, Sprague-Dawley; Reperfusion Injury - metabolism; Thromboxane A2 - secretion; Vertebrata; Mammalia; Reperfusion; Rat; Animal; Arachidonic acid derivatives; Lung; Rodentia; Gut; Exploration; Thromboxane
• ISSN: 0022-4804; 1095-8673
• DOI: 10.1006/jsre.1995.1087

Microvascular dysfunction is a prominent feature of the lung injury associated with intestinal reperfusion (IR). This study examines the hypothesis that IR induces pulmonary thromboxane A 2 (TxA 2) release, which contributes to pulmonary microvascular dysfunction. Sprague-Dawley rats underwent 120 min of intestinal ischemia and 60 min of reperfusion (IR). Sham-operated animals served as controls (SHAM). Following IR or SHAM, the lungs were perfused in vitro with a modified Krebs buffer and ventilated with room air. Eicosanoid levels within the pulmonary venous effluent and bronchoalveolar lavage (BAL) fluid were determined (TxB 2, 6-keto-PGF 1a, and PGE 2). Pulmonary artery pressure (PAP) was measured continuously and expressed as change from baseline in mm Hg. The dominant eicosanoid generated by the lungs in response to IR was TxB 2. TxB 2 levels in the pulmonary venous effluent of IR lungs were 75% greater than controls ( P = 0.005). Similarly, TxB 2 levels in the BAL were more than 2.5 times controls ( P = 0.001). The change in PAP of lungs from IR animals was significantly greater than that of controls (4.1 ± 1.5 vs 0.3 ± 0.54 mm Hg, IR vs SHAM, P = 0.01). The increased PAP associated with IR lungs was prevented by cyclooxygenase inhibition with indomethacin (-1.28 ± 0.29 mm Hg, P < 0.05) and thromboxane synthetase inhibition with imidazole (-1.75 ± 0.95 mm Hg, P < 0.05). These experiments support the hypothesis that IR up-regulates endogenous pulmonary TxA 2 release. Furthermore, the local release of TxA 2 by the lung may contribute to the microvascular dysfunction characteristic of IR-induced lung injury.