Inhibition of neuronal nitric oxide synthase by 7-nitroindazole attenuates acute lung injury in an ovine model

Perenlei Enkhbaatar, Kazunori Murakami, Katsumi Shimoda, Akio Mizutani, Roy McGuire, Frank Schmalstieg, Robert Cox, Hal Hawkins, Jeffery Jodoin, Steve Lee, Lillian Traber, David Herndon, Daniel Traber

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Abstract

Nitric oxide (NO) has been'shown to play a major role in acute lung injury (ALI) after smoke inhalation. In the present study, we developed an ovine sepsis model, created by exposing sheep to smoke inhalation followed by instillation of bacteria into the airway, that mimics human sepsis and pneumonia. We hypothesized that the inhibition of neuronal NO synthase (nNOS) might be beneficial in treating ALI associated with this model. Female sheep (n = 26) were surgically prepared for the study and given a tracheostomy. This was followed by insufflation of 48 breaths of cotton smoke (40°C) into the airway of each animal and subsequent instillation of live Pseudomonas aeruginosa [5 × 1011 colony forming units (CFU)] into each sheep's lung. All sheep were mechanically ventilated using 100% O2. Continuous infusion of 7-nitroindazole (7-NI), an nNOS inhibitor, NG-monomethyl-L-arginine (L-NMMA), a nonspecific NOS inhibitor, or aminoguanidine (AG), an inducible NOS inhibitor, was started 1 h after insult. The administration of 7-NI improved pulmonary gas exchange (PaO2/FIO2; where PaO2 is arterial PO2 and FIO2 is fractional inspired oxygen concentration) and pulmonary shunt fraction and attenuated the increase in lung wet-to-dry weight ratio seen in the nontreated sheep. Histologically, 7-NI prevented airway obstruction. The increase in airway blood flow after injury in the nontreated group was significantly inhibited by 7-NI. The increase in plasma concentration of nitrate and nitrite (NOx) was inhibited by 7-NI as well. Posttreatment with L-NMMA improved the pulmonary gas exchange, but AG did not. The results of the present study show that nNOS may be involved in the pathogenesis of ALI after smoke inhalation injury followed by bacterial instillation in the airway.

Original languageEnglish (US)
JournalAmerican Journal of Physiology - Regulatory Integrative and Comparative Physiology
Volume285
Issue number2 54-2
StatePublished - Aug 1 2003

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Nitric Oxide Synthase Type I
Acute Lung Injury
Sheep
omega-N-Methylarginine
Smoke
Pulmonary Gas Exchange
Nitric Oxide Synthase
Inhalation
Sepsis
Smoke Inhalation Injury
Lung
Insufflation
Tracheostomy
Pulmonary Edema
Airway Obstruction
Nitrites
Nitrates
Pseudomonas aeruginosa
7-nitroindazole
Pneumonia

Keywords

  • Acute respiratory distress syndrome
  • Pneumonia
  • Smoke inhalation

ASJC Scopus subject areas

  • Physiology

Cite this

Inhibition of neuronal nitric oxide synthase by 7-nitroindazole attenuates acute lung injury in an ovine model. / Enkhbaatar, Perenlei; Murakami, Kazunori; Shimoda, Katsumi; Mizutani, Akio; McGuire, Roy; Schmalstieg, Frank; Cox, Robert; Hawkins, Hal; Jodoin, Jeffery; Lee, Steve; Traber, Lillian; Herndon, David; Traber, Daniel.

In: American Journal of Physiology - Regulatory Integrative and Comparative Physiology, Vol. 285, No. 2 54-2, 01.08.2003.

Research output: Contribution to journalArticle

Enkhbaatar, P, Murakami, K, Shimoda, K, Mizutani, A, McGuire, R, Schmalstieg, F, Cox, R, Hawkins, H, Jodoin, J, Lee, S, Traber, L, Herndon, D & Traber, D 2003, 'Inhibition of neuronal nitric oxide synthase by 7-nitroindazole attenuates acute lung injury in an ovine model', American Journal of Physiology - Regulatory Integrative and Comparative Physiology, vol. 285, no. 2 54-2.
Enkhbaatar, Perenlei ; Murakami, Kazunori ; Shimoda, Katsumi ; Mizutani, Akio ; McGuire, Roy ; Schmalstieg, Frank ; Cox, Robert ; Hawkins, Hal ; Jodoin, Jeffery ; Lee, Steve ; Traber, Lillian ; Herndon, David ; Traber, Daniel. / Inhibition of neuronal nitric oxide synthase by 7-nitroindazole attenuates acute lung injury in an ovine model. In: American Journal of Physiology - Regulatory Integrative and Comparative Physiology. 2003 ; Vol. 285, No. 2 54-2.
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