Inhaled Nitric Oxide Improves Outcomes After Successful Cardiopulmonary Resuscitation in Mice

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Inhaled Nitric Oxide Improves Outcomes After Successful Cardiopulmonary Resuscitation in Mice

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Title: Inhaled Nitric Oxide Improves Outcomes After Successful Cardiopulmonary Resuscitation in Mice
Author: Minamishima, Shizuka; Kida, Kotaro; Tokuda, Kentaro; Wang, Huifang; Sips, Patrick; Kosugi, Shizuko; Mandeville, Joseph B.; Buys, Emmanuel; Brouckaert, Peter; Liu, Philip K.; Liu, Christina; Bloch, Kenneth Daniel; Ichinose, Fumito

Note: Order does not necessarily reflect citation order of authors.

Citation: Minamishima, S., K. Kida, K. Tokuda, H. Wang, P. Y. Sips, S. Kosugi, J. B. Mandeville, et al. 2011. “Inhaled Nitric Oxide Improves Outcomes After Successful Cardiopulmonary Resuscitation in Mice.” Circulation 124 (15) (September 19): 1645–1653. doi:10.1161/circulationaha.111.025395. Open manuscript version available here: http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3199136/
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Abstract: Background—Sudden cardiac arrest (CA) is a leading cause of death worldwide. Breathing nitric oxide (NO) reduces ischemia/reperfusion injury in animal models and in patients. The objective of this study was to learn whether inhaled NO improves outcomes after CA and cardiopulmonary resuscitation (CPR).
Methods and Results—Adult male mice were subjected to potassium-induced CA for 7.5 minutes whereupon CPR was performed with chest compression and mechanical ventilation. One hour after CPR, mice were extubated and breathed air alone or air supplemented with 40 ppm NO for 23 hours. Mice that were subjected to CA/CPR and breathed air exhibited a poor 10-day survival rate (4 of 13), depressed neurological and left ventricular function, and increased caspase-3 activation and inflammatory cytokine induction in the brain. Magnetic resonance imaging revealed brain regions with marked water diffusion abnormality 24 hours after CA/CPR in mice that breathed air. Breathing air supplemented with NO for 23 hours starting 1 hour after CPR attenuated neurological and left ventricular dysfunction 4 days after CA/CPR and markedly improved 10-day survival rate (11 of 13; P=0.003 versus mice breathing air). The protective effects of inhaled NO on the outcome after CA/CPR were associated with reduced water diffusion abnormality, caspase-3 activation, and cytokine induction in the brain and increased serum nitrate/nitrite levels. Deficiency of the α1 subunit of soluble guanylate cyclase, a primary target of NO, abrogated the ability of inhaled NO to improve outcomes after CA/CPR.
Conclusions—These results suggest that NO inhalation after CA and successful CPR improves outcome via soluble guanylate cyclase–dependent mechanisms.
Published Version: doi:10.1161/CIRCULATIONAHA.111.025395
Other Sources: http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3199136/
Citable link to this page: http://nrs.harvard.edu/urn-3:HUL.InstRepos:14229248
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