Intravenous ethanol infusion decreases human cortical γ-aminobutyric acid and N-acetylaspartate as measured with proton magnetic resonance spectroscopy at 4 tesla.
Intravenous ethanol infusion decreases human cortical γ-aminobutyric acid and N-acetylaspartate as measured with proton magnetic resonance spectroscopy at 4 tesla.
复制标题
DOI:
10.1016/j.biopsych.2011.06.026
复制
发表时间:
2012-02-01
影响因子:
10.6
通讯作者:
Mason, Graeme F.
中科院分区:
文献类型:
--
作者:
Gomez, Rosane;Behar, Kevin L.;Watzl, June;Weinzimer, Stuart A.;Gulanski, Barbara;Sanacora, Gerard;Koretski, Julia;Guidone, Elizabeth;Jiang, Lihong;Petrakis, Ismene L.;Pittman, Brian;Krystal, John H.;Mason, Graeme F.
Ethanol modulates glutamate and GABA function. However, little is known about the acute pharmacologic effects of ethanol on levels of GABA, glutamate, and other metabolites measurable in the human cortex in vivo using 1H magnetic resonance spectroscopy (MRS). Eleven healthy social drinkers received two intravenous ethanol infusions that raised breath alcohol levels to a clamped plateau of 60 mg/dL over 60–70 minutes. The first infusion established tolerability of the procedure, and the second procedure, conducted 15±12 days later, was performed during 1H MRS of occipital GABA, glutamate, and other metabolites. The time course of brain ethanol approximated that of breath ethanol, but venous ethanol lagged by about 7 minutes. GABA fell 13±8% after 5 minutes of the ethanol infusion and remained reduced (p=0.003) throughout the measurement. The combination of N-acetylaspartate and N-acetylaspartyl glutamate (summed as NAA) fell steadily during the infusion by 8±3% (p=0.0036). Ethanol reduced cortical GABA and NAA levels in humans. Reductions in GABA levels are consistent with facilitation of GABAA receptor function by ethanol. The gradual decline in NAA levels suggests inhibition of neural or metabolic activity in the brain.
登录
查看更多内容
影响因子:
7.6
作者:
Adalsteinsson, Elfar;Sullivan, Edith V.;Pfefferbaum, Adolf
通讯作者:
Pfefferbaum, Adolf
影响因子:
6.3
作者:
Biller, Armin;Bartsch, Andreas J.;Bendszus, Martin
通讯作者:
Bendszus, Martin
DOI:
10.1111/j.1530-0277.1998.tb03611.x
发表时间:
1998-02-01
期刊:
ALCOHOL-CLINICAL AND EXPERIMENTAL RESEARCH
影响因子:
--
作者:
Koob, GF;Roberts, AJ;Weiss, F
通讯作者:
Weiss, F
影响因子:
5.7
作者:
Ende, Gabriele;Walter, Sigi;Mann, Karl
通讯作者:
Mann, Karl
DOI:
10.1097/01.alc.0000150010.72739.58
发表时间:
2005-01-01
影响因子:
3.2
作者:
Mason, GF;Bendszus, M;Krystal, JH
通讯作者:
Krystal, JH