Search

everythinglearnresearchcommunity

for

Search:↓

The medications 5α-reductase inhibitors and spironolactone are generally safe for breast cancer patients on endocrine therapies and do not significantly increase breast cancer risk.

The enzymes 5α-reductase and 3α/β-hydroxysteroid oxidoreductase help create brain-active substances from progesterone and testosterone, which could be used for treatment, but more research is needed to ensure their safety and effectiveness.

Researchers developed a new method to find substances in herbs that can block a specific enzyme linked to hair loss.

Inhibiting 5α-reductase increases progesterone levels in late pregnant mares.

Two types of 5α-reductase are in dog skin, which might make dutasteride better than finasteride for treating dog hair loss.

Finasteride doesn't affect sleep spindles in men.

Finasteride effectively treats hair loss and enlarged prostate in men, with mild side effects.

Jute leaves may help reduce DHT levels, potentially aiding in conditions like hair loss and prostate issues.

Dutasteride and finasteride do not significantly affect bone density, blood fats, or blood production, but slightly lower PSA levels and minimally impact sexual function in healthy young men.

PNU157706 reduced rat sperm movement and fertility without affecting offspring health.

5α reductase inhibitors treat hair loss but may cause sexual side effects and risks.

Finasteride raises suicide-linked aggression and stops clozapine's positive effects in schizophrenia animals.

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

Finasteride negatively affects fish reproduction and gonadal development.

5α-Reductase inhibitors do not consistently increase testosterone levels in the blood.

The procedure accurately measures 5-alpha-dihydrotestosterone in blood, useful for standard tests.

S5αR inhibitors might help treat schizophrenia and other mental disorders but need more research.

Young girls whose mothers have PCOS may have higher activity of a specific enzyme that could lead to developing PCOS later.

Finasteride irreversibly affects human steroid 5α-reductase 2, providing insight into its catalytic mechanism and disease-related mutations.

Dutasteride protects dopamine neurons in Parkinson's mice, but Finasteride doesn't.

Finasteride treats enlarged prostate and baldness, but may cause limited urinary improvement and sex-related side effects.

New treatments for enlarged prostate are being developed, some of which may be more effective than current medications.

Dutasteride reduces DHT more effectively than finasteride.

Stiripentol shows promise as a potential treatment for androgen-related diseases but needs more testing.

Finasteride helps protect brain in old male rats.

Progesterone byproduct 5αP stimulates mammary tumor growth, but finasteride can suppress it.

Finasteride and dutasteride effectively treat hair loss, but may cause side effects like sexual dysfunction and depression.

Four new compounds were more effective than finasteride in treating prostate issues and hair loss, with one being 100 times more active and safe for use.

5-α-reductase inhibitors reduce prostate cancer risk but may cause sexual dysfunction and don't affect high-grade tumor or death rates.

Finasteride exposure harms tadpole reproduction and hormone balance.