Abstract
Amethystic agents represent only one class of substances or conditions that can antagonize the actions of alcohol (ethanol). To gain a proper perspective, we should recognize several situations in which many of the acute and long-term effects of ethanol can be blocked:
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1.
Prevention or reversal of ethanol-induced euphoria or stimulation (e.g., by alpha methyl-p-tyrosine in man; Ahlenius et al., 1973)
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2.
Antagonism of ethanol-induced sedation or hypnosis (e.g., by calcium chelators such as ED TA and EGTA in mice; Erickson et al., 1978)
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3.
Antagonism of ethanol preference (e.g., by acetaldehyde in mice; Sanders et al. vn1977)
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4.
Reduction of ethanol intake (e.g., by disulfiram in man; Kitson, 1977)
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5.
Blockade of the production of tolerance to ethanol (e.g., by cortexolone, a glucocorticoid receptor blocker in mice; Tabak-off and Yanai, 1979)
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6.
Prevention of the development of physical dependence to ethanol (e.g., by naloxone in mice; Blum et al., 1977)
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7.
Suppression of ethanol withdrawal reactions, once they have begun (e.g., by sodium bromide in mice; Goldstein, 1979)
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8.
Amelioration of the acute withdrawal phase of alcoholism (e.g., by chlormethiazole, a sedative-hypnotic drug, in man; McGrath, 1975)
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9.
Improvement in alcohol-induced hepatic dysfunction (e.g., by propylthiouracil in man; Orrego et al., 1979)
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10.
Treatment of the alcohol-induced “tiorganic brain syndrome” (e.g., by EMD 21657, an experimental drug, in man; Saletu et al., 1978)
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Erickson, C.K. (1983). Amethystic Agents in the Treatment of Alcohol Intoxication. In: Kissin, B., Begleiter, H. (eds) The Biology of Alcoholism. Springer, Boston, MA. https://doi.org/10.1007/978-1-4613-3518-4_14
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