Sex-Specific Alterations in Dopamine Metabolism in the Brain after Methamphetamine Self-Administration.
Atul P DaiwilePatricia SullivanSubramaniam JayanthiDavid S GoldsteinJean-Lud CadetPublished in: International journal of molecular sciences (2022)
Methamphetamine (METH) use disorder affects both sexes, with sex differences occurring in behavioral, structural, and biochemical consequences. The molecular mechanisms underlying these differences are unclear. Herein, we used a rat model to identify potential sex differences in the effects of METH on brain dopaminergic systems. Rats were trained to self-administer METH for 20 days, and a cue-induced drug-seeking test was performed on withdrawal days 3 and 30. Dopamine and its metabolites were measured in the prefrontal cortex (PFC), nucleus accumbens (NAc), dorsal striatum (dSTR), and hippocampus (HIP). Irrespective of conditions, in comparison to females, male rats showed increased 3,4-dihydroxyphenylalanine (DOPA) in the PFC, dSTR, and HIP; increased cys-dopamine in NAc; and increased 3,4-dihydroxyphenylethanol (DOPET) and 3,4-dihydroxyphenylacetic acid (DOPAC) in dSTR. Males also showed METH-associated decreases in DA levels in the HIP but increases in the NAc. Female rats showed METH-associated decreases in DA, DOPAL, and DOPAC levels in the PFC but increases in DOPET and DOPAC levels in the HIP. Both sexes showed METH-associated decreases in NAc DA metabolites. Together, these data document sex differences in METH SA-induced changes in DA metabolism. These observations provide further support for using sex as an essential variable when discussing therapeutic approaches against METH use disorder in humans.
Keyphrases
- prefrontal cortex
- transcription factor
- total hip arthroplasty
- uric acid
- ms ms
- white matter
- drug induced
- resting state
- spinal cord
- mental health
- genome wide analysis
- emergency department
- metabolic syndrome
- electronic health record
- multiple sclerosis
- body composition
- blood brain barrier
- cognitive impairment
- high glucose
- endothelial cells
- subarachnoid hemorrhage
- adverse drug
- resistance training
- brain injury