Carbogen inhalation increases oxygen transport to hypoperfused brain tissue in patients with occlusive carotid artery disease: increased oxygen transport to hypoperfused brain

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Carbogen inhalation increases oxygen transport to hypoperfused brain tissue in patients with occlusive carotid artery disease: increased oxygen transport to hypoperfused brain. / Ashkanian, Mahmoud; Gjedde, Albert; Mouridsen, Kim; Vafaee, Manouchehr; Hansen, Kim Vang; Ostergaard, Leif; Andersen, Grethe.

In: Brain Research, Vol. 1304, 2009, p. 90-5.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Ashkanian, M, Gjedde, A, Mouridsen, K, Vafaee, M, Hansen, KV, Ostergaard, L & Andersen, G 2009, 'Carbogen inhalation increases oxygen transport to hypoperfused brain tissue in patients with occlusive carotid artery disease: increased oxygen transport to hypoperfused brain', Brain Research, vol. 1304, pp. 90-5. https://doi.org/10.1016/j.brainres.2009.09.076

APA

Ashkanian, M., Gjedde, A., Mouridsen, K., Vafaee, M., Hansen, K. V., Ostergaard, L., & Andersen, G. (2009). Carbogen inhalation increases oxygen transport to hypoperfused brain tissue in patients with occlusive carotid artery disease: increased oxygen transport to hypoperfused brain. Brain Research, 1304, 90-5. https://doi.org/10.1016/j.brainres.2009.09.076

Vancouver

Ashkanian M, Gjedde A, Mouridsen K, Vafaee M, Hansen KV, Ostergaard L et al. Carbogen inhalation increases oxygen transport to hypoperfused brain tissue in patients with occlusive carotid artery disease: increased oxygen transport to hypoperfused brain. Brain Research. 2009;1304:90-5. https://doi.org/10.1016/j.brainres.2009.09.076

Author

Ashkanian, Mahmoud ; Gjedde, Albert ; Mouridsen, Kim ; Vafaee, Manouchehr ; Hansen, Kim Vang ; Ostergaard, Leif ; Andersen, Grethe. / Carbogen inhalation increases oxygen transport to hypoperfused brain tissue in patients with occlusive carotid artery disease: increased oxygen transport to hypoperfused brain. In: Brain Research. 2009 ; Vol. 1304. pp. 90-5.

Bibtex

@article{694dff9089cb11df928f000ea68e967b,
title = "Carbogen inhalation increases oxygen transport to hypoperfused brain tissue in patients with occlusive carotid artery disease: increased oxygen transport to hypoperfused brain",
abstract = "Hyperoxic therapy for cerebral ischemia reduces cerebral blood flow (CBF) principally from the vasoconstrictive effect of oxygen on cerebral arterioles. Based on a recent study in normal volunteers, we now claim that the vasodilatory effect of carbon dioxide predominates when 5% CO(2) is added to inhaled oxygen (the mixture known as carbogen). In the present study, we measured CBF by positron emission tomography (PET) during inhalation of test gases (O(2), carbogen, and atmospheric air) in healthy volunteers (n = 10) and in patients with occlusive carotid artery disease (n = 6). Statistical comparisons by an additive ANOVA model showed that carbogen significantly increased CBF by 7.51 + or - 1.62 ml/100 g/min while oxygen tended to reduce it by -3.22 + or - 1.62 ml/100 g/min. A separate analysis of the hemisphere contralateral to the hypoperfused hemisphere showed that carbogen significantly increased CBF by 8.90 + or - 2.81 ml/100 g/min whereas oxygen inhalation produced no reliable change in CBF (-1.15 + or - 2.81 ml/100 g/min). In both patients and controls, carbogen was as efficient as oxygen in increasing Sa(O2) or PaO(2) values. The study demonstrates that concomitant increases of CBF and Sa(O2) are readily obtained with carbogen, while oxygen increases only Sa(O2). Thus, carbogen improves oxygen transport to brain tissue more efficiently than oxygen alone. Further studies with more subjects are, however, needed to investigate the applicability of carbogen for long-term inhalation and to assess its therapeutic benefits in acute stroke patients.",
author = "Mahmoud Ashkanian and Albert Gjedde and Kim Mouridsen and Manouchehr Vafaee and Hansen, {Kim Vang} and Leif Ostergaard and Grethe Andersen",
note = "Keywords: Adult; Aged; Aged, 80 and over; Air; Analysis of Variance; Brain; Carbon Dioxide; Carotid Artery Diseases; Cerebrovascular Circulation; Female; Humans; Male; Middle Aged; Oxygen; Positron-Emission Tomography; Vasoconstrictor Agents",
year = "2009",
doi = "10.1016/j.brainres.2009.09.076",
language = "English",
volume = "1304",
pages = "90--5",
journal = "Brain Research",
issn = "0006-8993",
publisher = "Elsevier",

}

RIS

TY - JOUR

T1 - Carbogen inhalation increases oxygen transport to hypoperfused brain tissue in patients with occlusive carotid artery disease: increased oxygen transport to hypoperfused brain

AU - Ashkanian, Mahmoud

AU - Gjedde, Albert

AU - Mouridsen, Kim

AU - Vafaee, Manouchehr

AU - Hansen, Kim Vang

AU - Ostergaard, Leif

AU - Andersen, Grethe

N1 - Keywords: Adult; Aged; Aged, 80 and over; Air; Analysis of Variance; Brain; Carbon Dioxide; Carotid Artery Diseases; Cerebrovascular Circulation; Female; Humans; Male; Middle Aged; Oxygen; Positron-Emission Tomography; Vasoconstrictor Agents

PY - 2009

Y1 - 2009

N2 - Hyperoxic therapy for cerebral ischemia reduces cerebral blood flow (CBF) principally from the vasoconstrictive effect of oxygen on cerebral arterioles. Based on a recent study in normal volunteers, we now claim that the vasodilatory effect of carbon dioxide predominates when 5% CO(2) is added to inhaled oxygen (the mixture known as carbogen). In the present study, we measured CBF by positron emission tomography (PET) during inhalation of test gases (O(2), carbogen, and atmospheric air) in healthy volunteers (n = 10) and in patients with occlusive carotid artery disease (n = 6). Statistical comparisons by an additive ANOVA model showed that carbogen significantly increased CBF by 7.51 + or - 1.62 ml/100 g/min while oxygen tended to reduce it by -3.22 + or - 1.62 ml/100 g/min. A separate analysis of the hemisphere contralateral to the hypoperfused hemisphere showed that carbogen significantly increased CBF by 8.90 + or - 2.81 ml/100 g/min whereas oxygen inhalation produced no reliable change in CBF (-1.15 + or - 2.81 ml/100 g/min). In both patients and controls, carbogen was as efficient as oxygen in increasing Sa(O2) or PaO(2) values. The study demonstrates that concomitant increases of CBF and Sa(O2) are readily obtained with carbogen, while oxygen increases only Sa(O2). Thus, carbogen improves oxygen transport to brain tissue more efficiently than oxygen alone. Further studies with more subjects are, however, needed to investigate the applicability of carbogen for long-term inhalation and to assess its therapeutic benefits in acute stroke patients.

AB - Hyperoxic therapy for cerebral ischemia reduces cerebral blood flow (CBF) principally from the vasoconstrictive effect of oxygen on cerebral arterioles. Based on a recent study in normal volunteers, we now claim that the vasodilatory effect of carbon dioxide predominates when 5% CO(2) is added to inhaled oxygen (the mixture known as carbogen). In the present study, we measured CBF by positron emission tomography (PET) during inhalation of test gases (O(2), carbogen, and atmospheric air) in healthy volunteers (n = 10) and in patients with occlusive carotid artery disease (n = 6). Statistical comparisons by an additive ANOVA model showed that carbogen significantly increased CBF by 7.51 + or - 1.62 ml/100 g/min while oxygen tended to reduce it by -3.22 + or - 1.62 ml/100 g/min. A separate analysis of the hemisphere contralateral to the hypoperfused hemisphere showed that carbogen significantly increased CBF by 8.90 + or - 2.81 ml/100 g/min whereas oxygen inhalation produced no reliable change in CBF (-1.15 + or - 2.81 ml/100 g/min). In both patients and controls, carbogen was as efficient as oxygen in increasing Sa(O2) or PaO(2) values. The study demonstrates that concomitant increases of CBF and Sa(O2) are readily obtained with carbogen, while oxygen increases only Sa(O2). Thus, carbogen improves oxygen transport to brain tissue more efficiently than oxygen alone. Further studies with more subjects are, however, needed to investigate the applicability of carbogen for long-term inhalation and to assess its therapeutic benefits in acute stroke patients.

U2 - 10.1016/j.brainres.2009.09.076

DO - 10.1016/j.brainres.2009.09.076

M3 - Journal article

C2 - 19782665

VL - 1304

SP - 90

EP - 95

JO - Brain Research

JF - Brain Research

SN - 0006-8993

ER -

ID: 20688868