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J Neurophysiol 95: 2293-2303, 2006. First published October 26, 2005; doi:10.1152/jn.00114.2005
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Effect of Benzodiazepine Hypnotic Triazolam on Relationship of Blood Pressure and PaCO2 to Cerebral Blood Flow During Human Non-Rapid Eye Movement Sleep

Masahiko Hiroki1, Naofumi Kajimura2, Takeshi Uema5, Kenichi Ogawa3, Masami Nishikawa2, Masaaki Kato2, Tsuyoshi Watanabe2, Toru Nakajima6, Harumasa Takano2, Etsuko Imabayashi4, Takashi Ohnishi4, Yutaka Takayama2, Hiroshi Matsuda4, Makoto Uchiyama7, Masako Okawa8, Kiyohisa Takahashi2 and Hidenao Fukuyama1

1Human Brain Research Center, Kyoto University Graduate School of Medicine, Kyoto; 2Departments of Psychiatry, 3Anesthesiology, and 4Radiology, National Center Hospital for Mental, Nervous, and Muscular Disorders, National Center of Neurology and Psychiatry (NCNP), Tokyo; 5Department of Psychiatry, Osaka Prefectural General Hospital, Osaka,; 6Department of Psychiatry, Teikyo University School of Medicine, Kanagawa; 7Department of Psychiatry, National Institute of Mental Health, NCNP, Chiba; and 8Department of Psychiatry, Shiga University of Medical Science, Shiga, Japan

Submitted 1 February 2005; accepted in final form 3 October 2005

We sought to clarify the effect of short-acting benzodiazepine hypnotic on the relationship of arterial blood pressure and arterial partial pressure of carbon dioxide (PaCO2) to regional cerebral blood flow (rCBF) during human non-rapid-eye-movement (non-REM) sleep. Nine young normal volunteers were treated in a randomized, crossover design with triazolam or placebo and underwent positron emission tomography at night. During wakefulness and stage 2 and slow wave (stages 3 and 4) sleep, we measured mean arterial blood pressure (MAP), PaCO2, and absolute CBF. With triazolam compared to placebo, MAP reduced gradually. During stage 2 sleep, PaCO2 increased and whole-brain mean CBF decreased. With triazolam, relative rCBF of the left orbital basal forebrain decreased more during stage 2 than slow wave sleep, whereas absolute CBF of the occipital cortex and cerebral white matter remained constant. During triazolam-induced stage 2 sleep, absolute CBF of the cerebral white matter correlated more strongly to both MAP and PaCO2 than during placebo sleep and also correlated more strongly to both MAP and PaCO2 than absolute CBF of the occipital cortex. In the frontal white matter, during triazolam-induced stage 2 sleep compared to wakefulness, absolute CBF was significantly better correlated to MAP, but not to PaCO2. During triazolam-induced stage 2, the cerebral white matter may receive a modulated CBF regulation having the strengthened relationship of PaCO2 to CBF and, more locally, the frontal white matter may depend precariously on CBF regulation.


Address for reprint requests and other correspondence: M. Hiroki, Department of Radiology, Massachusetts General Hospital, Martinos/NMR Center, Building 149, 13th Street, Mailcode 149-2301, Charlestown, MA 02129-2060 (E-mail: CYI01752{at}nifty.com)







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