Search

everythinglearnresearchcommunity

for

Search:↓

PEA boosts allopregnanolone production and reduces oxidative stress in brain cells.

A new method accurately measures nine neuroactive steroids in small blood samples, helping to study brain diseases.

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

In late pregnancy, allopregnanolone reduces stress responses in rats by affecting brain chemicals.

Neurosteroid withdrawal increases α4 subunit expression in the hippocampus, which may relate to catamenial epilepsy in women.

Midazolam's antiseizure effects are mainly due to synaptic GABA-A receptors, not neurosteroids or extrasynaptic receptors.

Flutamide and a new synthetic steroid affected brain and prostate chemicals and showed potential for treating androgen-related conditions and epilepsy.

Allopregnanolone may help prevent nicotine withdrawal symptoms.

Sex hormones affect brain cells differently in males and females.

Targeting neurosteroids may help prevent drug relapse.

Pregnancy increases certain GABA_A receptors in rat brains, influenced by steroid levels.

Pregnancy-related hormone changes affect Y1 receptor gene expression in mice.

EPI-NCSCs from hair follicles may help treat brain development issues in mice.

Pregnancy affects fear memory and brain activity in female rats.

Progesterone helps adult male mice grow more neurons and improves memory.

The steroids allopregnanolone and allotetrahydrodeoxycorticosteron worsened absence seizures in rats.

Progesterone and its metabolites affect myelin protein expression differently in male and female rat Schwann cells.

Inhibiting 5α-reductase during late pregnancy shortens gestation, reduces litter size, and harms memory in rat offspring.

5α-reduced neurosteroids may help regulate glial cell differentiation.

Neurosteroids are crucial for stress response, and targeting specific receptors may help treat certain disorders.

Treatment during development affects hormone balance and sexual behavior in male rats.

Progesterone increases alcohol tolerance and withdrawal anxiety, while DHEAS prevents them.

Progesterone-derived neurosteroids affect GABA-A receptor expression, influencing epilepsy during menstrual cycles.

Progesterone significantly reduces neuroblastoma tumor growth without harming healthy cells.

Progesterone and its metabolites can prevent seizures without major side effects.

Neurosteroids help reduce seizures, but their withdrawal increases seizure activity.

Allopregnanolone may enhance alcohol's effects on dopamine neurons, influencing addiction risk.

Finasteride treatment can decrease certain steroids and increase others, possibly leading to depression symptoms in some cases.

Progesterone reduces anxiety and depression in female mice by increasing BDNF in the brain, needing 5α-reduction and estradiol.