2000
DOI: 10.1111/j.1530-0277.2000.tb01976.x
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Anxiety and Sensitivity to Ethanol and Pentobarbital in Alcohol Withdrawal Seizure‐Prone and Withdrawal Seizure‐Resistant Mice

Abstract: These results support the hypothesis that WSP mice are more sensitive than WSR mice to the anxiety-reducing effects of ethanol and pentobarbital. Some genes that influence this difference are likely to be the same as those that influence ethanol withdrawal severity. Thus, higher basal anxiety and greater genetic sensitivity to anxiolytic drug effects may relate to a greater genetic predisposition to the development of severe alcohol withdrawal signs.

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Cited by 13 publications
(5 citation statements)
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“…While WSP and WSR mice showed behavioral differences in both the LDT and MBT, these were apparently in opposite directions, consistent with suggestions that the LDT and MBT may assay different phenotypic aspects of anxiety. In the present study, WSP mice displayed more anxiety‐like behavior than WSRs in the LDT, consistent with previous findings that WSP mice exhibit greater anxiety than WSRs in the elevated‐plus maze (Gorin et al., ) and canopy stretched‐attend‐posture (Atkins et al., ) tests. Conversely, however, WSRs (females) exhibited greater anxiety‐like behavior than WSPs on the MBT, possibly related to their slightly higher BECs relative to males.…”
Section: Discussionsupporting
confidence: 93%
“…While WSP and WSR mice showed behavioral differences in both the LDT and MBT, these were apparently in opposite directions, consistent with suggestions that the LDT and MBT may assay different phenotypic aspects of anxiety. In the present study, WSP mice displayed more anxiety‐like behavior than WSRs in the LDT, consistent with previous findings that WSP mice exhibit greater anxiety than WSRs in the elevated‐plus maze (Gorin et al., ) and canopy stretched‐attend‐posture (Atkins et al., ) tests. Conversely, however, WSRs (females) exhibited greater anxiety‐like behavior than WSPs on the MBT, possibly related to their slightly higher BECs relative to males.…”
Section: Discussionsupporting
confidence: 93%
“…1), consistent with its effects in humans and animals (Abruzzi, 1964;Atkins et al, 2000) and similar to effects of some other GABAenhancing drugs (e.g., chlordiazepoxide) on zebrafish (Table 1). Recently suggested as a good model for studying GABA-ergic sedative agents, zebrafish possess multiple high-affinity sites and robust genomic/ proteomic responses to these drugs (Renier et al, 2007).…”
Section: Gaba-ergic Systemsupporting
confidence: 75%
“…Withdrawal severity may also play a role in the development of alcoholism and drug abuse specifically by encouraging further drug use to relieve anxiety (Holter et al ). Work in mice selectively bred for high and low handling‐induced convulsions after chronic ethanol treatment appears to support this idea (Atkins et al ). Thus, convulsion‐prone mice showed higher levels of baseline anxiety and were more sensitive to the anxiolytic effects of alcohol than convulsion‐resistant mice, suggesting that convulsion‐prone animals may be genetically predisposed to severe alcohol withdrawal symptoms.…”
Section: Vulnerability Traitsmentioning
confidence: 99%