A Pilot Study of Inhaled CO Therapy in Neonatal Hypoxia-Ischemia: Carboxyhemoglobin Concentrations and Brain Volumes

Objective: The objective of this pilot study was to start evaluating the efficacy and the safety (i.e., carboxyhemoglobin concentration of carbon monoxide (CO)) as a putative neuroprotective therapy in neonates.Study Design: Neonatal C57BL/6 mice were exposed to CO at a concentration of either 200 o...

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Main Authors: Martha Douglas-Escobar, Monique Mendes, Candace Rossignol, Nikolay Bliznyuk, Ariana Faraji, Abdullah S. Ahmad, Sylvain Doré, Michael D. Weiss
Format: Article
Language:English
Published: Frontiers Media S.A. 2018-05-01
Series:Frontiers in Pediatrics
Subjects:
Online Access:http://journal.frontiersin.org/article/10.3389/fped.2018.00120/full
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spelling doaj-a2131cce15994f6d9de67fd9644fd6b82020-11-24T20:59:59ZengFrontiers Media S.A.Frontiers in Pediatrics2296-23602018-05-01610.3389/fped.2018.00120352951A Pilot Study of Inhaled CO Therapy in Neonatal Hypoxia-Ischemia: Carboxyhemoglobin Concentrations and Brain VolumesMartha Douglas-Escobar0Monique Mendes1Candace Rossignol2Nikolay Bliznyuk3Ariana Faraji4Abdullah S. Ahmad5Sylvain Doré6Sylvain Doré7Sylvain Doré8Sylvain Doré9Michael D. Weiss10Department of Pediatrics, University of California, San Francisco, San Francisco, CA, United StatesDepartment of Anesthesiology, Center for Translational Research in Neurodegenerative, McKnight Brain Institutive, University of Florida, Gainesville, FL, United StatesDepartment of Pediatrics, University of Florida, Gainesville, FL, United StatesDepartment of Agricultural and Biological Egineering, University of Florida, Gainesville, FL, United StatesDepartment of Pediatrics, University of Florida, Gainesville, FL, United StatesDepartment of Anesthesiology, Center for Translational Research in Neurodegenerative, McKnight Brain Institutive, University of Florida, Gainesville, FL, United StatesDepartment of Anesthesiology, Center for Translational Research in Neurodegenerative, McKnight Brain Institutive, University of Florida, Gainesville, FL, United StatesDepartment of Neurology, Center for Translational Research in Neurodegenerative, McKnight Brain Institutive, University of Florida, Gainesville, FL, United StatesDepartment of Psychiatry, Center for Translational Research in Neurodegenerative, McKnight Brain Institutive, University of Florida, Gainesville, FL, United StatesDepartment of Neuroscience, Center for Translational Research in Neurodegenerative, McKnight Brain Institutive, University of Florida, Gainesville, FL, United StatesDepartment of Pediatrics, University of Florida, Gainesville, FL, United StatesObjective: The objective of this pilot study was to start evaluating the efficacy and the safety (i.e., carboxyhemoglobin concentration of carbon monoxide (CO)) as a putative neuroprotective therapy in neonates.Study Design: Neonatal C57BL/6 mice were exposed to CO at a concentration of either 200 or 250 ppm for a period of 1 h. The pups were then sacrificed at 0, 10, 20, 60, 120, 180, and 240 min after exposure to either concentration of CO, and blood was collected for analysis of carboxyhemoglobin. Following the safety study, 7-day-old pups underwent a unilateral carotid ligation. After recovery, the pups were exposed to a humidified gas mixture of 8% oxygen and 92% nitrogen for 20 min in a hypoxia chamber. One hour after the hypoxia exposure, the pups were randomized to one of two groups: air (HI+A) or carbon monoxide (HI+CO). An inhaled dose of 250 ppm of CO was administered to the pups for 1 h per day for a period of 3 days. At 7 days post-injury, the pups were sacrificed and the brains analyzed for cortical and hippocampal volumes.Results: CO exposure at 200 and 250 ppm produced a peak carboxyhemoglobin concentration of 21.52 ± 1.18% and 27.55 ± 3.58%, respectively. The carboxyhemoglobin concentrations decreased rapidly, reaching control concentrations by 60 min post exposure. At 14 days of age (7 days post injury), the HI+CO (treated with 1 h per day of 250 ppm of CO for 3 days post injury) had significant preservation of the ratio of ipsilateral to contralateral cortex (median 1.07, 25% 0.97, 75% 1.23, n = 10) compared the HI+A group (p < 0.05).Conclusion: CO exposure of 250 ppm did not reach carboxyhemoglobin concentrations which would induce acute neurologic abnormalities and was effective in preserving cortical volumes following hypoxic-ischemic injury.http://journal.frontiersin.org/article/10.3389/fped.2018.00120/fullbabiesischemic strokepreclinicaltherapeutic gas
collection DOAJ
language English
format Article
sources DOAJ
author Martha Douglas-Escobar
Monique Mendes
Candace Rossignol
Nikolay Bliznyuk
Ariana Faraji
Abdullah S. Ahmad
Sylvain Doré
Sylvain Doré
Sylvain Doré
Sylvain Doré
Michael D. Weiss
spellingShingle Martha Douglas-Escobar
Monique Mendes
Candace Rossignol
Nikolay Bliznyuk
Ariana Faraji
Abdullah S. Ahmad
Sylvain Doré
Sylvain Doré
Sylvain Doré
Sylvain Doré
Michael D. Weiss
A Pilot Study of Inhaled CO Therapy in Neonatal Hypoxia-Ischemia: Carboxyhemoglobin Concentrations and Brain Volumes
Frontiers in Pediatrics
babies
ischemic stroke
preclinical
therapeutic gas
author_facet Martha Douglas-Escobar
Monique Mendes
Candace Rossignol
Nikolay Bliznyuk
Ariana Faraji
Abdullah S. Ahmad
Sylvain Doré
Sylvain Doré
Sylvain Doré
Sylvain Doré
Michael D. Weiss
author_sort Martha Douglas-Escobar
title A Pilot Study of Inhaled CO Therapy in Neonatal Hypoxia-Ischemia: Carboxyhemoglobin Concentrations and Brain Volumes
title_short A Pilot Study of Inhaled CO Therapy in Neonatal Hypoxia-Ischemia: Carboxyhemoglobin Concentrations and Brain Volumes
title_full A Pilot Study of Inhaled CO Therapy in Neonatal Hypoxia-Ischemia: Carboxyhemoglobin Concentrations and Brain Volumes
title_fullStr A Pilot Study of Inhaled CO Therapy in Neonatal Hypoxia-Ischemia: Carboxyhemoglobin Concentrations and Brain Volumes
title_full_unstemmed A Pilot Study of Inhaled CO Therapy in Neonatal Hypoxia-Ischemia: Carboxyhemoglobin Concentrations and Brain Volumes
title_sort pilot study of inhaled co therapy in neonatal hypoxia-ischemia: carboxyhemoglobin concentrations and brain volumes
publisher Frontiers Media S.A.
series Frontiers in Pediatrics
issn 2296-2360
publishDate 2018-05-01
description Objective: The objective of this pilot study was to start evaluating the efficacy and the safety (i.e., carboxyhemoglobin concentration of carbon monoxide (CO)) as a putative neuroprotective therapy in neonates.Study Design: Neonatal C57BL/6 mice were exposed to CO at a concentration of either 200 or 250 ppm for a period of 1 h. The pups were then sacrificed at 0, 10, 20, 60, 120, 180, and 240 min after exposure to either concentration of CO, and blood was collected for analysis of carboxyhemoglobin. Following the safety study, 7-day-old pups underwent a unilateral carotid ligation. After recovery, the pups were exposed to a humidified gas mixture of 8% oxygen and 92% nitrogen for 20 min in a hypoxia chamber. One hour after the hypoxia exposure, the pups were randomized to one of two groups: air (HI+A) or carbon monoxide (HI+CO). An inhaled dose of 250 ppm of CO was administered to the pups for 1 h per day for a period of 3 days. At 7 days post-injury, the pups were sacrificed and the brains analyzed for cortical and hippocampal volumes.Results: CO exposure at 200 and 250 ppm produced a peak carboxyhemoglobin concentration of 21.52 ± 1.18% and 27.55 ± 3.58%, respectively. The carboxyhemoglobin concentrations decreased rapidly, reaching control concentrations by 60 min post exposure. At 14 days of age (7 days post injury), the HI+CO (treated with 1 h per day of 250 ppm of CO for 3 days post injury) had significant preservation of the ratio of ipsilateral to contralateral cortex (median 1.07, 25% 0.97, 75% 1.23, n = 10) compared the HI+A group (p < 0.05).Conclusion: CO exposure of 250 ppm did not reach carboxyhemoglobin concentrations which would induce acute neurologic abnormalities and was effective in preserving cortical volumes following hypoxic-ischemic injury.
topic babies
ischemic stroke
preclinical
therapeutic gas
url http://journal.frontiersin.org/article/10.3389/fped.2018.00120/full
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