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

Cytochrome P-450 enzymes in the skin help break down various substances and could be targeted to treat skin conditions.

Reconstructed skin models are useful for studying how skin processes certain chemicals.

Finasteride doesn't affect antipyrine metabolism, so interactions with cytochrome P-450 enzyme drugs are unlikely.

Anti-acne medications may work by reducing the activity of a protein involved in acne development.

A gene in Sebekia benihana, CYP-sb21, is needed for a specific reaction on the drug Cyclosporine A, which could be important for hair growth without affecting the immune system.

Modulating Cytochrome P450 activity could help develop new skin disease treatments.

Different species and human skin models vary in their skin enzyme activities, with pig skin and some models closely matching human skin, useful for safety assessments and understanding the skin's protective roles.

Drug metabolism affects how long a drug works, its interactions, activation, and toxicity, and is influenced by genetics, diet, illness, and other drugs.

The treatment reduced hair growth and testosterone in women with excess hair and had some effects on stress responses.

Different factors affect where drugs are absorbed in the small intestine, which is important for effective medication use.

Red ginseng may improve immunity, fatigue, memory, blood circulation, and menopausal symptoms, and is generally safe to consume.

Finasteride effectively blocks rat enzymes, but with varying methods and strength.

Spironolactone effectively reduces hair growth in women with hirsutism and is generally well-tolerated.

Spironolactone reduces the enzyme activity that converts testosterone to DHT, helping treat excessive hair growth in women.

Finasteride inhibits enzyme activity in rhesus macaques, suggesting they're useful for evaluating similar drugs.

The document concludes that treating female hair loss should target reducing excess androgen and blocking its effects on hair follicles, with the best treatments being hormonal therapy, adrenal suppression, and topical minoxidil.

Fluconazole can cause hair loss, but the exact cause is unknown.

Use the least toxic, most specific treatments for skin diseases, considering side effects and individual patient needs.

New antifungal treatments for a children's scalp infection are effective and safe, but it's not decided if they will become the preferred option over the old treatment.

Patients with acne vulgaris have lower serum irisin levels.

Spironolactone is a safe and effective treatment for reducing excessive hair growth in women.

Spironolactone can reduce hair growth in women with hirsutism.

Arachidonic acid helps hair grow by increasing growth factors and improving follicle health.

The study aims to find the best treatment for central serous chorioretinopathy by comparing various options.

Aldactone was more effective in reducing hair growth in women with hirsutism than Diane, despite having less impact on hormone levels.

Parathyroid hormones are important for hair growth, but their use in treating hair loss from chemotherapy is still uncertain.

Skin reactions to drugs are common and can be deadly, usually requiring stopping the drug and may be better prevented with genetic testing in the future.

Scientists improved an enzyme to better produce a hair growth-promoting chemical from an immunosuppressant.

Any drug can cause skin reactions, but antibiotics, NSAIDs, and psychotropic drugs are more common, with some reactions being life-threatening.