Female rats display higher methamphetamine-primed reinstatement and c-Fos immunoreactivity than male rats.
Female rats display higher methamphetamine-primed reinstatement and c-Fos immunoreactivity than male rats.
复制标题
雌性大鼠表现出较高的甲基苯丙胺引发的恢复和c-Fos免疫反应性比雄性大鼠。
DOI:
10.1016/j.pbb.2020.173089
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发表时间:
2021-03
影响因子:
3.6
通讯作者:
Bevins, Rick A.
中科院分区:
文献类型:
--
作者:
Pittenger, Steven T.;Chou, Shinnyi;Murawski, Nathen J.;Barrett, Scott T.;Loh, Olivia;Duque, Juan F.;Li, Ming;Bevins, Rick A.
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.
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影响因子:
6
作者:
Baicy, Kate;London, Edythe D.
通讯作者:
London, Edythe D.
影响因子:
4.2
作者:
Charntikov, Sergios;Pittenger, Steven T.;Pendyala, Gurudutt
通讯作者:
Pendyala, Gurudutt
影响因子:
6
作者:
Carter, BL;Tiffany, ST
通讯作者:
Tiffany, ST
影响因子:
3.4
作者:
COMER, SD;LAC, ST;CARROLL, ME
通讯作者:
CARROLL, ME
DOI:
10.1523/jneurosci.0005-12.2012
发表时间:
2012-04-04
期刊:
The Journal of neuroscience : the official journal of the Society for Neuroscience
影响因子:
--
作者:
Bossert JM;Stern AL;Theberge FR;Marchant NJ;Wang HL;Morales M;Shaham Y
通讯作者:
Shaham Y