Search

everythinglearnresearchcommunity

for

Search:↓

Finasteride given to baby rats reduces dopamine release and increases alcohol consumption in adult males.

Finasteride can have lasting negative effects on brain function and behavior by disrupting neurosteroid production.

Adrenal disorders can cause lasting brain and behavior issues in children.

Finasteride treatment changes brain steroid levels and receptors, affecting brain function even after stopping treatment.

Short-term finasteride use in male rats caused anxiety, depression, and memory problems.

Certain substances can decrease or increase exploratory behavior in rodents.

Neurosteroids can influence behavior by modulating brain inhibition, with potential for treating psychiatric disorders.

Neurosteroids in the brain can increase or decrease seizure risk in mice.

Finasteride affects young male rats' brain function and behavior negatively.

Changing allopregnanolone levels in baby rats affects their adult behavior and alcohol use.

Ethanol withdrawal reduces the brain's response to certain calming steroids, making seizures harder to control.

Finasteride may cause sexual and psychological side effects by affecting an enzyme related to epinephrine.

Long-term alcohol exposure alters brain receptor function differently in various brain regions.

Neurosteroids help protect fetal brains from asphyxia damage.

Ethanol boosts brain steroid production by activating NMDA receptors, affecting memory formation.

Neurosteroids may help treat disorders with too much dopamine activity.

Different rat and mouse strains respond differently to stress and alcohol, which may help us understand similar human mechanisms.

Seeing trauma causes fear in mice by lowering their natural fear-reducing hormones.

Stopping alcohol after long-term use causes anxiety and changes brain chemicals.

Finasteride treatment in rats changed the expression of genes related to psychiatric and neurological functions, and these changes persisted after stopping the drug.

Finasteride reduces certain behaviors caused by D1-like receptor agonists but not by D2-like receptor agonists in mice.

Finasteride may affect fetal brain development and increase arousal, but more research is needed for safety confirmation.

Stress and alcohol affect brain chemicals differently in rats, mice, and humans, influenced by genetic differences.

Pregnancy affects fear memory and brain activity in female rats.

Allopregnanolone likely doesn't influence ethanol's rewarding effects in these mice.

Finasteride withdrawal causes anxiety-like behavior in male rats.

Finasteride affects brain and blood steroids, causing lasting sexual and emotional side effects.

Finasteride may cause depression and affect brain and gut health in male rats.

Finasteride slows down motherly behavior in first-time pregnant rats.

Social isolation makes mice more sensitive to alcohol's effects on brain function.