Effect of pentobarbital on visual processing in man
To investigate the effect of sedative agents on visual processing in humans, we analysed the BOLD contrast signal response to a visual stimulation paradigm in 15 healthy, adult volunteers using functional magnetic resonance imaging. The subjects were tested during alert state and under sedation foll...
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Published in | Human brain mapping Vol. 10; no. 3; pp. 132 - 139 |
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Main Authors | , , , , , , , |
Format | Journal Article |
Language | English |
Published |
New York
John Wiley & Sons, Inc
01.07.2000
Wiley-Liss |
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Online Access | Get full text |
ISSN | 1065-9471 1097-0193 |
DOI | 10.1002/1097-0193(200007)10:3<132::AID-HBM40>3.0.CO;2-2 |
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Abstract | To investigate the effect of sedative agents on visual processing in humans, we analysed the BOLD contrast signal response to a visual stimulation paradigm in 15 healthy, adult volunteers using functional magnetic resonance imaging. The subjects were tested during alert state and under sedation following intravenous administration of pentobarbital. The injection of pentobarbital not only significantly reduced the response signal strength but the reduction in BOLD contrast signal was related to the ratio of amount of sedative administered and the subject's body weight. The three subjects with the highest relative sedative dosage even displayed an inverted (negative) BOLD contrast signal. A significant reduction in the number of positively correlating pixels was found 15 min after administration of pentobarbital. All measured parameters returned to near pre‐sedative levels by the end of the experimental session. The relative dosage dependence of the strength of the BOLD signal the negative BOLD signal in the three subjects with the highest relative sedative dosage indicates that pentobarbital had a more pronounced effect on cerebral blood flow than on cerebral oxidative metabolism. Hum. Brain Mapping 10:132–139, 2000. © 2000 Wiley‐Liss, Inc. |
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AbstractList | To investigate the effect of sedative agents on visual processing in humans, we analysed the BOLD contrast signal response to a visual stimulation paradigm in 15 healthy, adult volunteers using functional magnetic resonance imaging. The subjects were tested during alert state and under sedation following intravenous administration of pentobarbital. The injection of pentobarbital not only significantly reduced the response signal strength but the reduction in BOLD contrast signal was related to the ratio of amount of sedative administered and the subject's body weight. The three subjects with the highest relative sedative dosage even displayed an inverted (negative) BOLD contrast signal. A significant reduction in the number of positively correlating pixels was found 15 min after administration of pentobarbital. All measured parameters returned to near pre-sedative levels by the end of the experimental session. The relative dosage dependence of the strength of the BOLD signal the negative BOLD signal in the three subjects with the highest relative sedative dosage indicates that pentobarbital had a more pronounced effect on cerebral blood flow than on cerebral oxidative metabolism. To investigate the effect of sedative agents on visual processing in humans, we analysed the BOLD contrast signal response to a visual stimulation paradigm in 15 healthy, adult volunteers using functional magnetic resonance imaging. The subjects were tested during alert state and under sedation following intravenous administration of pentobarbital. The injection of pentobarbital not only significantly reduced the response signal strength but the reduction in BOLD contrast signal was related to the ratio of amount of sedative administered and the subject's body weight. The three subjects with the highest relative sedative dosage even displayed an inverted (negative) BOLD contrast signal. A significant reduction in the number of positively correlating pixels was found 15 min after administration of pentobarbital. All measured parameters returned to near pre‐sedative levels by the end of the experimental session. The relative dosage dependence of the strength of the BOLD signal the negative BOLD signal in the three subjects with the highest relative sedative dosage indicates that pentobarbital had a more pronounced effect on cerebral blood flow than on cerebral oxidative metabolism. Hum. Brain Mapping 10:132–139, 2000. © 2000 Wiley‐Liss, Inc. To investigate the effect of sedative agents on visual processing in humans, we analysed the BOLD contrast signal response to a visual stimulation paradigm in 15 healthy, adult volunteers using functional magnetic resonance imaging. The subjects were tested during alert state and under sedation following intravenous administration of pentobarbital. The injection of pentobarbital not only significantly reduced the response signal strength but the reduction in BOLD contrast signal was related to the ratio of amount of sedative administered and the subject's body weight. The three subjects with the highest relative sedative dosage even displayed an inverted (negative) BOLD contrast signal. A significant reduction in the number of positively correlating pixels was found 15 min after administration of pentobarbital. All measured parameters returned to near pre-sedative levels by the end of the experimental session. The relative dosage dependence of the strength of the BOLD signal the negative BOLD signal in the three subjects with the highest relative sedative dosage indicates that pentobarbital had a more pronounced effect on cerebral blood flow than on cerebral oxidative metabolism.To investigate the effect of sedative agents on visual processing in humans, we analysed the BOLD contrast signal response to a visual stimulation paradigm in 15 healthy, adult volunteers using functional magnetic resonance imaging. The subjects were tested during alert state and under sedation following intravenous administration of pentobarbital. The injection of pentobarbital not only significantly reduced the response signal strength but the reduction in BOLD contrast signal was related to the ratio of amount of sedative administered and the subject's body weight. The three subjects with the highest relative sedative dosage even displayed an inverted (negative) BOLD contrast signal. A significant reduction in the number of positively correlating pixels was found 15 min after administration of pentobarbital. All measured parameters returned to near pre-sedative levels by the end of the experimental session. The relative dosage dependence of the strength of the BOLD signal the negative BOLD signal in the three subjects with the highest relative sedative dosage indicates that pentobarbital had a more pronounced effect on cerebral blood flow than on cerebral oxidative metabolism. To investigate the effect of sedative agents on visual processing in humans, we analysed the BOLD contrast signal response to a visual stimulation paradigm in 15 healthy, adult volunteers using functional magnetic resonance imaging. The subjects were tested during alert state and under sedation following intravenous administration of pentobarbital. The injection of pentobarbital not only significantly reduced the response signal strength but the reduction in BOLD contrast signal was related to the ratio of amount of sedative administered and the subject's body weight. The three subjects with the highest relative sedative dosage even displayed an inverted (negative) BOLD contrast signal. A significant reduction in the number of positively correlating pixels was found 15 min after administration of pentobarbital. All measured parameters returned to near pre‐sedative levels by the end of the experimental session. The relative dosage dependence of the strength of the BOLD signal the negative BOLD signal in the three subjects with the highest relative sedative dosage indicates that pentobarbital had a more pronounced effect on cerebral blood flow than on cerebral oxidative metabolism. Hum. Brain Mapping 10:132–139, 2000. © 2000 Wiley‐Liss, Inc. |
Author | Joeri, Philipp Thiel, Thorsten Martin, Ernst Loenneker, Thomas Hennig, Juergen Marcar, Valentine L. Ekatodramis, Dimitri Huisman, Thierry |
AuthorAffiliation | 1 University Children's Hospital Zurich Steinwiesstrasse, Zürich, Switzerland 2 University of Freiburg, Department of Radiology, Freiburg, Germany |
AuthorAffiliation_xml | – name: 1 University Children's Hospital Zurich Steinwiesstrasse, Zürich, Switzerland – name: 2 University of Freiburg, Department of Radiology, Freiburg, Germany |
Author_xml | – sequence: 1 givenname: Ernst surname: Martin fullname: Martin, Ernst email: Ernst.Martin@kispi.unizh.ch organization: University Children's Hospital Zurich Steinwiesstrasse, Zürich, Switzerland – sequence: 2 givenname: Thorsten surname: Thiel fullname: Thiel, Thorsten organization: University of Freiburg, Department of Radiology, Freiburg, Germany – sequence: 3 givenname: Philipp surname: Joeri fullname: Joeri, Philipp organization: University Children's Hospital Zurich Steinwiesstrasse, Zürich, Switzerland – sequence: 4 givenname: Thomas surname: Loenneker fullname: Loenneker, Thomas organization: University of Freiburg, Department of Radiology, Freiburg, Germany – sequence: 5 givenname: Dimitri surname: Ekatodramis fullname: Ekatodramis, Dimitri organization: University Children's Hospital Zurich Steinwiesstrasse, Zürich, Switzerland – sequence: 6 givenname: Thierry surname: Huisman fullname: Huisman, Thierry organization: University Children's Hospital Zurich Steinwiesstrasse, Zürich, Switzerland – sequence: 7 givenname: Juergen surname: Hennig fullname: Hennig, Juergen organization: University of Freiburg, Department of Radiology, Freiburg, Germany – sequence: 8 givenname: Valentine L. surname: Marcar fullname: Marcar, Valentine L. organization: University Children's Hospital Zurich Steinwiesstrasse, Zürich, Switzerland |
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Cites_doi | 10.1038/323806a0 10.1097/00004647-199701000-00009 10.1001/archneur.1976.00500080001001 10.1111/j.1399-6576.1975.tb05408.x 10.1002/mrm.1910300204 10.1176/ajp.104.12.765 10.1007/BF03005414 10.1002/mrm.1910350613 10.1002/ana.410220302 10.1113/jphysiol.1890.sp000321 10.1073/pnas.87.24.9868 10.1002/ana.410030502 10.1073/pnas.88.13.5829 10.1515/JBCPP.1990.1.1-4.191 10.1073/pnas.95.3.763 10.1073/pnas.83.4.1140 10.1152/physrev.1978.58.3.656 10.1073/pnas.89.12.5675 |
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Keywords | Human Regional blood flow Information integration Central nervous system Functional analysis Metabolism Visual system Chemotherapy Treatment Pentobarbital Vision Medical imagery Sedative Barbiturates Brain (vertebrata) |
Language | English |
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Notes | ArticleID:HBM40 Swiss National Foundation - No. 31-39706.93 istex:A8B3987612F24E62B2772FF49564359CAE6C3B2B ark:/67375/WNG-WHS07SS9-G The authors doloriously inform the reader that P. Joeri died unexpectedly on September 10, 1996. ObjectType-Article-2 SourceType-Scholarly Journals-1 ObjectType-Feature-1 content type line 23 ObjectType-Article-1 ObjectType-Feature-2 |
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References | Kuschinsky W (1990): Coupling of blood flow and metabolism in the brain. Basic Clin Physiol Pharmacol 1: 191-201. Lindauer U, Villringer A, Dirnagl U (1993): Characterization of CBF response to somatosensory stimulation: model and influence of anesthetics. Am J Physiol 264: H1223-H1228. Roy C, Sherrington C (1890): On the regulation of blood supply of the brain. J Physiol 11: 85-108. Nilsson L, Siesjö BK (1975): The effect of pentobarbitone anaesthesia on blood flow and oxygen consumption in the rat brain. Acta Anaesth Scand Suppl. 57: 18-24. Raichle ME, Grubb RL, Jr., Gado MH, Eichling JO, Ter-Pogossian MM (1976): Correlation between regional cerebral blood flow and oxidative metabolism. In vivo studies in man. Arch Neurol 33: 523-526. Buxton RB, Frank LR (1997): A model for the coupling between cerebral blood flow and oxygen metabolism during neural stimulation. J Cereb Blood Flow Metab 17: 64-72. Kuschinsky W, Wahl M (1978): Local chemical and neurogenic regulation of cerebral vascular resistance. Physiol Rev 58: 656-689. Chi OZ, Ryterband S, Field C (1989): Visual evoked potentials during thiopentone-fentanyl-nitrous oxide anaesthesia in humans. Can J Anaesth 36: 637-640. Purves MJ (1978): Control of cerebral blood vessels: present state of the art. Ann Neurol 3: 377-383. Bandettini PA, Jesmanowicz A, Wong EC, Hyde JS (1993): Processing strategies for time-course data sets in functional MRI of the human brain. Magn Reson Med 30: 161-173. Fox PT, Mintun MA, Raichle ME, Miezin FM, Allman JM, Van Essen DC (1986): Mapping human visual cortex with positron emission tomography. Nature 323: 806-809. Martin E, Joeri P, Loenneker T, Ekatodramis D, Vitacco D, Hennig J, Marcar V (1999): Visual processing in infants and children, using functional magnetic resonance imaging. Ped Res (in press). Sokoloff L (1981): Relationships among local functional activity, energy metabolism, and blood flow in the central nervous system. Fed Proc 40: 2311-2316. Fox P, Raichle ME (1986): Focal physiological uncoupling of cerebral blood flow and oxidative metabolism during somatosensory stimulation in human subjects. Proc Natl Acad Sci USA 83: 1140-1144. Kety S, Woodford R, Harmel M, Freyhan F, Appel K, Schmidt C (1947): -48): Cerebral blood flow and metabolism in schizophrenia. The effect of barbituratie semi-narcosis, insulin coma and electroshock. Am J Psychiat 104: 765-770. Kuschinsky W (1991): Physiology of cerebral blood flow and metabolism. Arzneimittel-Forschung 41: 284-288. Ogawa S, Lee TM, Kay AR, Tank DW (1990): Brain magnetic resonance imaging with contrast dependent on blood oxygenation. Proc Nat Acad Sci USA 87: 9868-9872. Lou HC, Edvinsson L, MacKenzie ET (1987): The concept of coupling blood flow to brain function: revision required? Ann Neurol 22: 289-297. Posner MI, Raichle ME (1998): The neuroimaging of human brain function. Proc Natl Acad Sci USA 95: 763-764. Prichard J, Rothman D, Novotny E, Petroff O, Kuwabara T, Avison M, Howseman A, Hanstock C, Shulman R (1991): Lactate rise detected by H-1 NMR in human visual cortex during physiologic stimulation. Proc Natl Acad Sci USA 88: 5829-5831. Kwong K, Belliveau J, Chesler D, Goldberg I, Weisskoff R, Poncelet B, Kennedy D, Hoppel B, Cohen M, Turner R, Cheng H, Brady T, Rosen B (1992): Dynamic magnetic resonance imaging of human brain activity during primary sensory stimulation. Proc Natl Acad Sci USA 89: 5675-5679. Loenneker T, Hennel F, Hennig J (1996): Multislice interleaved excitation cycles (MUSIC): an efficient gradient-echo technique for functional MRI. Magn Reson Med 35: 870-874. 1990; 1 1987; 22 1990; 87 1986; 323 1986; 83 1976; 33 1991; 88 1947; 104 1991; 41 1993; 30 1975; 57 1997; 17 1978; 3 1978; 58 1996; 35 1998; 95 1890; 11 1989; 36 1992; 89 1981; 40 1993; 264 1999 Raichle (10.1002/1097-0193(200007)10:3<132::AID-HBM40>3.0.CO;2-2-BIB20) 1976; 33 Roy (10.1002/1097-0193(200007)10:3<132::AID-HBM40>3.0.CO;2-2-BIB21) 1890; 11 Fox (10.1002/1097-0193(200007)10:3<132::AID-HBM40>3.0.CO;2-2-BIB4) 1986; 83 Posner (10.1002/1097-0193(200007)10:3<132::AID-HBM40>3.0.CO;2-2-BIB17) 1998; 95 Lindauer (10.1002/1097-0193(200007)10:3<132::AID-HBM40>3.0.CO;2-2-BIB11) 1993; 264 Buxton (10.1002/1097-0193(200007)10:3<132::AID-HBM40>3.0.CO;2-2-BIB2) 1997; 17 Kuschinsky (10.1002/1097-0193(200007)10:3<132::AID-HBM40>3.0.CO;2-2-BIB8) 1991; 41 Prichard (10.1002/1097-0193(200007)10:3<132::AID-HBM40>3.0.CO;2-2-BIB18) 1991; 88 Purves (10.1002/1097-0193(200007)10:3<132::AID-HBM40>3.0.CO;2-2-BIB19) 1978; 3 Bandettini (10.1002/1097-0193(200007)10:3<132::AID-HBM40>3.0.CO;2-2-BIB1) 1993; 30 Martin (10.1002/1097-0193(200007)10:3<132::AID-HBM40>3.0.CO;2-2-BIB14) 1999 Chi (10.1002/1097-0193(200007)10:3<132::AID-HBM40>3.0.CO;2-2-BIB3) 1989; 36 Nilsson (10.1002/1097-0193(200007)10:3<132::AID-HBM40>3.0.CO;2-2-BIB15) 1975; 57 Lou (10.1002/1097-0193(200007)10:3<132::AID-HBM40>3.0.CO;2-2-BIB13) 1987; 22 Kuschinsky (10.1002/1097-0193(200007)10:3<132::AID-HBM40>3.0.CO;2-2-BIB7) 1990; 1 Kwong (10.1002/1097-0193(200007)10:3<132::AID-HBM40>3.0.CO;2-2-BIB10) 1992; 89 Sokoloff (10.1002/1097-0193(200007)10:3<132::AID-HBM40>3.0.CO;2-2-BIB22) 1981; 40 Kuschinsky (10.1002/1097-0193(200007)10:3<132::AID-HBM40>3.0.CO;2-2-BIB9) 1978; 58 Loenneker (10.1002/1097-0193(200007)10:3<132::AID-HBM40>3.0.CO;2-2-BIB12) 1996; 35 Ogawa (10.1002/1097-0193(200007)10:3<132::AID-HBM40>3.0.CO;2-2-BIB16) 1990; 87 Kety (10.1002/1097-0193(200007)10:3<132::AID-HBM40>3.0.CO;2-2-BIB6) 1947; 104 Fox (10.1002/1097-0193(200007)10:3<132::AID-HBM40>3.0.CO;2-2-BIB5) 1986; 323 |
References_xml | – reference: Nilsson L, Siesjö BK (1975): The effect of pentobarbitone anaesthesia on blood flow and oxygen consumption in the rat brain. Acta Anaesth Scand Suppl. 57: 18-24. – reference: Bandettini PA, Jesmanowicz A, Wong EC, Hyde JS (1993): Processing strategies for time-course data sets in functional MRI of the human brain. Magn Reson Med 30: 161-173. – reference: Kwong K, Belliveau J, Chesler D, Goldberg I, Weisskoff R, Poncelet B, Kennedy D, Hoppel B, Cohen M, Turner R, Cheng H, Brady T, Rosen B (1992): Dynamic magnetic resonance imaging of human brain activity during primary sensory stimulation. Proc Natl Acad Sci USA 89: 5675-5679. – reference: Loenneker T, Hennel F, Hennig J (1996): Multislice interleaved excitation cycles (MUSIC): an efficient gradient-echo technique for functional MRI. Magn Reson Med 35: 870-874. – reference: Kuschinsky W, Wahl M (1978): Local chemical and neurogenic regulation of cerebral vascular resistance. Physiol Rev 58: 656-689. – reference: Raichle ME, Grubb RL, Jr., Gado MH, Eichling JO, Ter-Pogossian MM (1976): Correlation between regional cerebral blood flow and oxidative metabolism. In vivo studies in man. Arch Neurol 33: 523-526. – reference: Martin E, Joeri P, Loenneker T, Ekatodramis D, Vitacco D, Hennig J, Marcar V (1999): Visual processing in infants and children, using functional magnetic resonance imaging. Ped Res (in press). – reference: Lou HC, Edvinsson L, MacKenzie ET (1987): The concept of coupling blood flow to brain function: revision required? Ann Neurol 22: 289-297. – reference: Posner MI, Raichle ME (1998): The neuroimaging of human brain function. Proc Natl Acad Sci USA 95: 763-764. – reference: Sokoloff L (1981): Relationships among local functional activity, energy metabolism, and blood flow in the central nervous system. 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Can J Anaesth 36: 637-640. – reference: Kuschinsky W (1991): Physiology of cerebral blood flow and metabolism. Arzneimittel-Forschung 41: 284-288. – reference: Fox PT, Mintun MA, Raichle ME, Miezin FM, Allman JM, Van Essen DC (1986): Mapping human visual cortex with positron emission tomography. Nature 323: 806-809. – reference: Kuschinsky W (1990): Coupling of blood flow and metabolism in the brain. Basic Clin Physiol Pharmacol 1: 191-201. – reference: Fox P, Raichle ME (1986): Focal physiological uncoupling of cerebral blood flow and oxidative metabolism during somatosensory stimulation in human subjects. Proc Natl Acad Sci USA 83: 1140-1144. – reference: Kety S, Woodford R, Harmel M, Freyhan F, Appel K, Schmidt C (1947): -48): Cerebral blood flow and metabolism in schizophrenia. The effect of barbituratie semi-narcosis, insulin coma and electroshock. Am J Psychiat 104: 765-770. – reference: Roy C, Sherrington C (1890): On the regulation of blood supply of the brain. 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SubjectTerms | Adult Biological and medical sciences Brain Mapping Cerebrovascular Circulation - drug effects Cerebrovascular Circulation - physiology Energy Metabolism - drug effects Energy Metabolism - physiology Female Humans Investigative techniques, diagnostic techniques (general aspects) Magnetic Resonance Imaging Male Medical sciences Middle Aged Nervous system Pentobarbital - administration & dosage Pentobarbital - adverse effects Photic Stimulation Radiodiagnosis. Nmr imagery. Nmr spectrometry Visual Cortex - anatomy & histology Visual Cortex - drug effects Visual Cortex - physiology Visual Perception - drug effects Visual Perception - physiology |
Title | Effect of pentobarbital on visual processing in man |
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