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- W3119656272 endingPage "173089" @default.
- W3119656272 startingPage "173089" @default.
- W3119656272 abstract "Methamphetamine (meth) dependence is often characterized by persistent and chronic relapse (i.e., return to drug use). Previous work suggests females may be at greater risk to relapse. In this study, we extended this limited evidence and identified sex-dependent neural substrates related to meth-triggered reinstatement. Male and female Sprague-Dawley rats were implanted with indwelling jugular catheters. Half of the rats were then trained to self-administer meth (0.05 mg/kg/inf); the other half self-administered saline during 21 daily sessions (2 h). Rats were then given 12 extinction sessions. Twenty-four hours after the last extinction session, rats received reinstatement testing. Half of the rats received a meth-prime (0.3 mg/kg, IP) injection and the remaining rats received a saline injection. This design resulted in 4 separate groups for each sex, allowing for careful investigation of brain regions related to meth-triggered reinstatement. Brains were harvested following the reinstatement session and c-Fos immunoreactivity was measured in multiple brain regions. Meth triggered reinstatement in both sexes and this effect was more robust in females compared to males. Significant sex differences were detected. Females showed greater c-Fos immunoreactivity in the cingulate cortex area 1, lateral orbitofrontal cortex, prelimbic cortex, caudate-putamen, nucleus accumbens core and shell, and central nucleus of the amygdala following meth-primed reinstatement." @default.
- W3119656272 created "2021-01-18" @default.
- W3119656272 creator A5006808220 @default.
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- W3119656272 creator A5065449132 @default.
- W3119656272 creator A5079430315 @default.
- W3119656272 creator A5085908160 @default.
- W3119656272 date "2021-02-01" @default.
- W3119656272 modified "2023-09-26" @default.
- W3119656272 title "Female rats display higher methamphetamine-primed reinstatement and c-Fos immunoreactivity than male rats" @default.
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