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Equisetum debile extract, especially the ethyl acetate type, may be a promising natural ingredient for anti-hair loss products.

Finasteride and dutasteride effectively treat hair loss in men and women, but may cause side effects like low libido and depression.

Taking 5α-reductase inhibitors with prednisolone can worsen its negative effects on metabolism.

DHT affects testicular development and regulates spermatogenesis in some fish.

Steroid hormones are crucial for body functions and have various medical uses, but their misuse can lead to dependence.

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

Testosterone's muscle-building effects do not require its conversion to DHT.

Men over 66 taking medication for prostate enlargement have a higher risk of depression and self-harm, especially in the first 18 months of treatment.

Finasteride slowly binds to 5-alpha-reductase, affecting enzyme stability and inhibitor potency.

Selective non-steroidal inhibitors of 5α-reductase type 1 can help treat DHT-related disorders.

New compounds show promise for treating hair loss, enlarged prostate, and prostate cancer, with some being more effective and having different side effects than current treatments.

5α-reductase inhibitors like finasteride may not be effective or safe for transgender individuals, and more research is needed.

New compounds were made that effectively block a specific enzyme related to androgen conditions.

Finasteride doesn't affect sleep spindles in men.

Finasteride effectively inhibits 5α reductase, while plant extracts like Permixon and Bazoton don't show significant results.

Finasteride affects male rat genitalia development, causing abnormalities during specific pregnancy days.

Finasteride effectively reduces hair growth in women with idiopathic hirsutism, but requires careful contraception during treatment.

Finasteride works better than Permixon in reducing dihydrotestosterone levels.

5α-reductase inhibitors and alpha-1 adrenergic antagonists together effectively treat benign prostatic hyperplasia, with long-term benefits.

New treatments for enlarged prostate are being developed to be more effective and have fewer side effects.

Testosterone therapy can modestly improve sexual function in menopausal women but should be used cautiously and is not recommended for routine measurement in sexual dysfunction or hirsutism.

The new compounds moderately block a specific enzyme and strongly counteract a male hormone, suggesting potential for treating certain male-related health conditions.

Certain natural compounds can block an enzyme linked to prostate enlargement and hair loss, showing potential for new treatments.

AGA is a genetic, hormonal hair loss treated with finasteride, minoxidil, and supplements, but new compounds are being developed.

The chapter explains the causes of excessive hair growth and masculinization in women and how to measure hormone levels related to these conditions.

Ageratum conyzoides L. extract may effectively and safely treat hair loss.

Hormone treatments in transsexual individuals reduce hair growth and oil production in male-to-females and increase them in female-to-males.

5α-reductase inhibitors can cause sexual problems, higher risk of aggressive prostate cancer, and depression.

Antidepressants, 5α-reductase inhibitors, and isotretinoin can cause long-lasting sexual dysfunction.

Certain drugs that block specific enzymes can help treat prostate diseases.