The distribution of the 5 alpha-reductase, the enzyme which converts testosterone into its 'active' metabolite dihydrotestosterone (DHT), has been studied in neurons, astrocytes and oligodendrocytes isolated from the brain of male rats by density gradient ultracentrifugation and in neurons and glial cells grown in cultures. Purity of cellular preparations was examined by electron and light microscopy. Purified neurons, astrocytes and oligodendrocytes, obtained from the brain of adult male rats, are all able to form DHT from testosterone and consequently possess a 5 alpha-reductase activity. Among the 3 cell types studied, neurons appear to be more active than oligodendrocytes and astrocytes. Moreover, between the two population of glial cells, the oligodendrocytes seem to possess a slightly higher enzymatic activity than that present in the astrocytes. Neurons appeared more active in metabolizing testosterone than glial cells also in cell culture experiments. It is presently believed that the 5 alpha-reduction of testosterone to DHT provides one of the mechanisms through which the hormone becomes effective in the CNS. This is supported by the present findings, which indicate that neurons are the cell population in which the 5 alpha-reductase is more concentrated. However, the presence of a considerable 5 alpha-reductase activity in glial cells indicates that also non-neuronal cells might participate in androgen-mediated events occurring in the brain.

5α-Reductase activity in isolated and cultured neuronal and glial cells of the rat / R.C. Melcangi, F. Celotti, M. Ballabio, P. Castano, R. Massarelli, A. Poletti, L. Martini. - In: BRAIN RESEARCH. - ISSN 0006-8993. - 516:2(1990 May 21), pp. 229-236.

5α-Reductase activity in isolated and cultured neuronal and glial cells of the rat

R.C. Melcangi
Primo
;
F. Celotti
Secondo
;
M. Ballabio;P. Castano;A. Poletti
Penultimo
;
L. Martini
Ultimo
1990

Abstract

The distribution of the 5 alpha-reductase, the enzyme which converts testosterone into its 'active' metabolite dihydrotestosterone (DHT), has been studied in neurons, astrocytes and oligodendrocytes isolated from the brain of male rats by density gradient ultracentrifugation and in neurons and glial cells grown in cultures. Purity of cellular preparations was examined by electron and light microscopy. Purified neurons, astrocytes and oligodendrocytes, obtained from the brain of adult male rats, are all able to form DHT from testosterone and consequently possess a 5 alpha-reductase activity. Among the 3 cell types studied, neurons appear to be more active than oligodendrocytes and astrocytes. Moreover, between the two population of glial cells, the oligodendrocytes seem to possess a slightly higher enzymatic activity than that present in the astrocytes. Neurons appeared more active in metabolizing testosterone than glial cells also in cell culture experiments. It is presently believed that the 5 alpha-reduction of testosterone to DHT provides one of the mechanisms through which the hormone becomes effective in the CNS. This is supported by the present findings, which indicate that neurons are the cell population in which the 5 alpha-reductase is more concentrated. However, the presence of a considerable 5 alpha-reductase activity in glial cells indicates that also non-neuronal cells might participate in androgen-mediated events occurring in the brain.
Rats, Inbred Strains ; Rats ; Animals ; Cholestenone 5 alpha-Reductase; Astrocytes ; Oligodendroglia ; Cells, Cultured ; Brain ; Oxidoreductases ; Male
Settore BIO/13 - Biologia Applicata
Settore BIO/16 - Anatomia Umana
Settore MED/04 - Patologia Generale
Settore MED/13 - Endocrinologia
21-mag-1990
Article (author)
File in questo prodotto:
File Dimensione Formato  
Melcangi 1990 Brain Res.pdf

accesso riservato

Tipologia: Pre-print (manoscritto inviato all'editore)
Dimensione 1.97 MB
Formato Adobe PDF
1.97 MB Adobe PDF   Visualizza/Apri   Richiedi una copia
Pubblicazioni consigliate

I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.

Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2434/183190
Citazioni
  • ???jsp.display-item.citation.pmc??? 3
  • Scopus 70
  • ???jsp.display-item.citation.isi??? 68
social impact