Patients treated for male pattern hair with finasteride show, after discontinuation of the drug, altered levels of neuroactive steroids in cerebrospinal fluid and plasma
Caruso, Donatella; Abbiati, Federico; Giatti, Silvia; Romano, S.; Fusco, L.; Cavaletti, Guido; Melcangi, Roberto Cosimo
Journal of Steroid Biochemistry and Molecular Biology · 146:74-792015
Summary (paraphrased)
Extending the 2013 CSF findings, the Milan group profiled neuroactive steroids by LC-MS/MS in paired plasma and CSF from post-finasteride patients versus healthy controls. In CSF, progesterone and its 5α-reduced metabolites dihydroprogesterone and tetrahydroprogesterone were reduced while the precursor pregnenolone rose; dihydrotestosterone fell as testosterone and 3α-diol rose. Plasma showed the same directional pattern: higher pregnenolone, testosterone, 3α-diol, 3β-diol and 17β-estradiol with lower dihydroprogesterone and tetrahydroprogesterone. The pattern reads as a persistent 5α-reductase-blockade signature — precursor buildup upstream, downstream metabolite depletion — still present after the drug was stopped. A 2023 corrigendum (DOI 10.1016/j.jsbmb.2023.106405) is attached to the record.
Plain-language summary (paraphrased)
A larger follow-up confirmed and extended the 2013 findings: finasteride's effects ripple across the whole steroid-making pathway, not just the single step it blocks. Precursors pile up while downstream calming neurosteroids stay depleted — evidence of a broad, lasting rewiring of brain steroid chemistry.
Why it’s in the corpus
Maps the full precursor-buildup/downstream-depletion signature of persistent 5α-reductase blockade in human CSF and plasma — the biochemical fingerprint Powers' intracellular-trapping model and the glucuronidation thread build on.
Some fields on this page come from the release’s Markdown edition, which carries text the JSON edition omits.
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