Inhibition of poly (ADP-ribose) polymerase attenuates acute lung injury in an ovine model of sepsis.

Kazunori Murakami, Perenlei Enkhbaatar, Katsumi Shimoda, Robert A. Cox, Ann S. Burke, Hal K. Hawkins, Lillian D. Traber, Frank C. Schmalstieg, Andrew L. Salzman, Jon G. Mabley, Katalin Komjáti, Pál Pacher, Zsuzsanna Zsengellér, Csaba Szabo, Daniel L. Traber

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Abstract

It is known that in various pathophysiological conditions, reactive oxidants cause DNA strand breakage and subsequent activation of the nuclear enzyme poly(ADP ribose) polymerase (PARP). Activation of PARP results in cellular dysfunction. We hypothesized that pharmacological inhibition of PARP reduces the damage in the ovine model of acute lung injury (ALI). After smoke inhalation, Pseudomonas aeruginosa (5 x 109 cfu/kg) was instilled into both lungs. All of the animals were mechanically ventilated with 100% O2. The infusion of the PARP inhibitor (INO-1001, n = 6) began 1 h after the injury and thereafter through 24 h (3 mg bolus + 0.3 mg/kg/h, i.v.). Control animals (n = 6) were treated with saline. Sham injury animals (n = 8) received sham smoke and were mechanically ventilated in the same fashion. One-half of those sham animals (n = 4) were given the same dose of INO-1001. PaO2/FiO2 ratio at 24 h in saline and in the INO-1001-treated groups were 95 +/- 22 and 181 +/- 22, respectively (P < 0.05). Peak airway pressure at 24 h in the saline- and INO-1001-treated groups was 32.6 +/- 3.0 and 24.4 +/- 2.2, respectively (P < 0.05). Pulmonary shunt fraction was also significantly attenuated. INO-1001 treatment reduced pulmonary histological injury and attenuated poly (ADP-ribose) accumulation in the lung. In conclusion, inhibition of PARP improved the ALI after smoke inhalation and pneumonia. The results suggest that the activation of PARP plays a role in the pathophysiology of ALI in sheep.

Original languageEnglish (US)
Pages (from-to)126-133
Number of pages8
JournalShock (Augusta, Ga.)
Volume21
Issue number2
StatePublished - Feb 2004

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Poly(ADP-ribose) Polymerases
Acute Lung Injury
Sheep
Sepsis
Smoke
Lung
Inhalation
Poly Adenosine Diphosphate Ribose
Enzyme Activation
Wounds and Injuries
Lung Injury
Oxidants
Pseudomonas aeruginosa
Pneumonia
INO 1001
Pharmacology
Pressure
DNA

ASJC Scopus subject areas

  • Critical Care and Intensive Care Medicine
  • Physiology

Cite this

Murakami, K., Enkhbaatar, P., Shimoda, K., Cox, R. A., Burke, A. S., Hawkins, H. K., ... Traber, D. L. (2004). Inhibition of poly (ADP-ribose) polymerase attenuates acute lung injury in an ovine model of sepsis. Shock (Augusta, Ga.), 21(2), 126-133.

Inhibition of poly (ADP-ribose) polymerase attenuates acute lung injury in an ovine model of sepsis. / Murakami, Kazunori; Enkhbaatar, Perenlei; Shimoda, Katsumi; Cox, Robert A.; Burke, Ann S.; Hawkins, Hal K.; Traber, Lillian D.; Schmalstieg, Frank C.; Salzman, Andrew L.; Mabley, Jon G.; Komjáti, Katalin; Pacher, Pál; Zsengellér, Zsuzsanna; Szabo, Csaba; Traber, Daniel L.

In: Shock (Augusta, Ga.), Vol. 21, No. 2, 02.2004, p. 126-133.

Research output: Contribution to journalArticle

Murakami, K, Enkhbaatar, P, Shimoda, K, Cox, RA, Burke, AS, Hawkins, HK, Traber, LD, Schmalstieg, FC, Salzman, AL, Mabley, JG, Komjáti, K, Pacher, P, Zsengellér, Z, Szabo, C & Traber, DL 2004, 'Inhibition of poly (ADP-ribose) polymerase attenuates acute lung injury in an ovine model of sepsis.', Shock (Augusta, Ga.), vol. 21, no. 2, pp. 126-133.
Murakami, Kazunori ; Enkhbaatar, Perenlei ; Shimoda, Katsumi ; Cox, Robert A. ; Burke, Ann S. ; Hawkins, Hal K. ; Traber, Lillian D. ; Schmalstieg, Frank C. ; Salzman, Andrew L. ; Mabley, Jon G. ; Komjáti, Katalin ; Pacher, Pál ; Zsengellér, Zsuzsanna ; Szabo, Csaba ; Traber, Daniel L. / Inhibition of poly (ADP-ribose) polymerase attenuates acute lung injury in an ovine model of sepsis. In: Shock (Augusta, Ga.). 2004 ; Vol. 21, No. 2. pp. 126-133.
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abstract = "It is known that in various pathophysiological conditions, reactive oxidants cause DNA strand breakage and subsequent activation of the nuclear enzyme poly(ADP ribose) polymerase (PARP). Activation of PARP results in cellular dysfunction. We hypothesized that pharmacological inhibition of PARP reduces the damage in the ovine model of acute lung injury (ALI). After smoke inhalation, Pseudomonas aeruginosa (5 x 109 cfu/kg) was instilled into both lungs. All of the animals were mechanically ventilated with 100{\%} O2. The infusion of the PARP inhibitor (INO-1001, n = 6) began 1 h after the injury and thereafter through 24 h (3 mg bolus + 0.3 mg/kg/h, i.v.). Control animals (n = 6) were treated with saline. Sham injury animals (n = 8) received sham smoke and were mechanically ventilated in the same fashion. One-half of those sham animals (n = 4) were given the same dose of INO-1001. PaO2/FiO2 ratio at 24 h in saline and in the INO-1001-treated groups were 95 +/- 22 and 181 +/- 22, respectively (P < 0.05). Peak airway pressure at 24 h in the saline- and INO-1001-treated groups was 32.6 +/- 3.0 and 24.4 +/- 2.2, respectively (P < 0.05). Pulmonary shunt fraction was also significantly attenuated. INO-1001 treatment reduced pulmonary histological injury and attenuated poly (ADP-ribose) accumulation in the lung. In conclusion, inhibition of PARP improved the ALI after smoke inhalation and pneumonia. The results suggest that the activation of PARP plays a role in the pathophysiology of ALI in sheep.",
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AU - Murakami, Kazunori

AU - Enkhbaatar, Perenlei

AU - Shimoda, Katsumi

AU - Cox, Robert A.

AU - Burke, Ann S.

AU - Hawkins, Hal K.

AU - Traber, Lillian D.

AU - Schmalstieg, Frank C.

AU - Salzman, Andrew L.

AU - Mabley, Jon G.

AU - Komjáti, Katalin

AU - Pacher, Pál

AU - Zsengellér, Zsuzsanna

AU - Szabo, Csaba

AU - Traber, Daniel L.

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N2 - It is known that in various pathophysiological conditions, reactive oxidants cause DNA strand breakage and subsequent activation of the nuclear enzyme poly(ADP ribose) polymerase (PARP). Activation of PARP results in cellular dysfunction. We hypothesized that pharmacological inhibition of PARP reduces the damage in the ovine model of acute lung injury (ALI). After smoke inhalation, Pseudomonas aeruginosa (5 x 109 cfu/kg) was instilled into both lungs. All of the animals were mechanically ventilated with 100% O2. The infusion of the PARP inhibitor (INO-1001, n = 6) began 1 h after the injury and thereafter through 24 h (3 mg bolus + 0.3 mg/kg/h, i.v.). Control animals (n = 6) were treated with saline. Sham injury animals (n = 8) received sham smoke and were mechanically ventilated in the same fashion. One-half of those sham animals (n = 4) were given the same dose of INO-1001. PaO2/FiO2 ratio at 24 h in saline and in the INO-1001-treated groups were 95 +/- 22 and 181 +/- 22, respectively (P < 0.05). Peak airway pressure at 24 h in the saline- and INO-1001-treated groups was 32.6 +/- 3.0 and 24.4 +/- 2.2, respectively (P < 0.05). Pulmonary shunt fraction was also significantly attenuated. INO-1001 treatment reduced pulmonary histological injury and attenuated poly (ADP-ribose) accumulation in the lung. In conclusion, inhibition of PARP improved the ALI after smoke inhalation and pneumonia. The results suggest that the activation of PARP plays a role in the pathophysiology of ALI in sheep.

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