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δ-GABAA receptors affect alcohol consumption based on the estrous cycle and influence movement regardless of the cycle.

Valproic acid is a more effective treatment for vomiting in Alexander disease than other medications, with few side effects.

Mild exercise reduces pain in older rats through a brain chemical, while intense exercise reduces pain in all rats through a different pain-blocking process.

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

GTx-024 and Danazol affect the uterus like DHT, while GTx-007 has little impact.

Androgen self-administration might be controlled by membrane receptors, not nuclear ones.

Neuroactive steroids affect cocaine's rewarding effects through the sigma1 receptor.

Dobutamine does not mimic dopamine at therapeutic doses but may at very high concentrations; microfilaments, not microtubules, are important for wound healing in Xenopus embryos.

Smaller substituents at C-17 enhance the inhibitory activity of progesterone derivatives on 5alpha-reductase.

Selective androgen receptor modulators (SARMs) are a promising type of drug for various health conditions due to their targeted actions.

Combining dutasteride or finasteride with an α1 blocker is more effective for managing BPH than using either alone.

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

Two new compounds were found to build bone and muscle without affecting reproductive organs and skin oil glands.

New A-homo-B, 19-dinor steroids showed strong antiandrogenic activity without affecting the enzyme 5α-reductase or androgen receptor binding.

Using GnRHa agonists helps diagnose and treat ovarian hyperthecosis when surgery isn't possible.

Dienogest is safer and has fewer side effects than GnRH analogues for treating endometriosis.

A new treatment for hair loss shows promise with fewer side effects.

Removing certain brain receptors in mice worsens seizure severity and response to treatment during hormone withdrawal.

Potassium channel openers show promise for treating heart disease and other conditions, but more research is needed to fully understand their effects and safety.

Different botulinum toxin products and concentrations can effectively reduce sweating, itching, bladder pressure, hair loss, and muscle spasms.

New pregnane derivatives were more effective than finasteride at inhibiting a key enzyme for male pattern baldness.

Cromakalim relaxes various blood vessels, while minoxidil sulphate is more selective; they likely act on different potassium channels.

Certain progesterone derivatives can inhibit enzymes and reduce androgenic activity, potentially affecting prostate growth.

SLVs help maintain muscle stretch sensitivity and could aid in treating hypertension and muscle spasticity.

Scientists found new nonsteroidal compounds that can act like natural male hormones and might help treat male fertility and hormone issues.

Three specific 4-azasteroid-2-oximes showed strong enzyme inhibition, but less than finasteride.

GnRH analogues are effective for diagnosing and treating female androgen excess, offering a non-surgical option.

A new topical treatment for hair loss shows strong hair growth effects with low toxicity.

Dopamine agonists like pramipexole and ropinirole can cause reversible hair loss.

Epirubicin is as effective as doxorubicin for cancer treatment with less heart damage, but doesn't work on doxorubicin-resistant cancers.