Neurosteroidogenesis and progesterone anti‐inflammatory/neuroprotective effects

• Published in: Journal of neuroendocrinology 2018-02, Vol.30 (2), p.n/a
• Main Authors: De Nicola, A. F., Garay, L. I., Meyer, M., Guennoun, R., Sitruk‐Ware, R., Schumacher, M., Gonzalez Deniselle, M. C.
• Format: Article
• Language: English
• Subjects: Androgens; Aromatase; Axons; Cholesterol; Cognitive science; Dehydrogenases; Enzymes; Estrogens; Experimental allergic encephalomyelitis; Fusion protein; Inflammation; Mitochondria; mRNA; Multiple sclerosis; neuroinflammation; Neuroprotection; Neuroscience; Neurosteroidogenesis; Neurosteroids; Paracrine signalling; Progesterone; Progestin; Proteins; Spinal cord; Steroid 5α-reductase; Steroidogenic acute regulatory protein; Ultrastructure
• ISSN: 0953-8194; 1365-2826
• DOI: 10.1111/jne.12502

Progesterone shows anti‐inflammatory and promyelinating effects in mice with experimental autoimmune encephalomyelitis (EAE), a commonly used model for multiple sclerosis (MS). Because neurosteroids have been implicated as protective factors for MS and EAE, we analysed the expression of neurosteroidogenic enzymes in the compromised spinal cord of EAE mice. EAE was induced in female C57Bl6 mice, which were then killed on day 16 after induction. Progesterone was given by pellet implantation 1 week before EAE induction. Untreated EAE mice showed decreased mRNAs for the steroidogenic acute regulatory protein (Star), voltage‐dependent anion channel (VDAC), cholesterol side‐chain cleavage (P450scc), 5α‐reductase, 3α‐hydroxysteroid dehydrogenase (3α‐HSOR) and aromatase, whereas changes of 3β‐hydroxysteroid dehydrogenase (3β‐HSD) were not significant. mRNA translocator protein (18 kDa) (TSPO) was elevated, concomitantly with a reactive microgliosis. EAE mice also showed abnormal mitochondrial ultrastructure in axons and neuronal bodies, as well as reduced expression of fission and fusion protein mRNAs. Progesterone pretreatment before EAE induction increased Star, VDAC, P450scc, 5α‐reductase type I, 3α‐HSOR and aromatase mRNAs and did not modify 3β‐HSD. TSPO mRNA was decreased, possibly as a result of reversal of microgliosis. Progesterone pretreatment also improved mitochondrial ultrastructure and increased fission/fusion protein mRNAs. These mitochondrial effects may be part of the progesterone recovery of neurosteroidogenesis. The enzymes 3β‐HSD, 3α‐HSOR and 5α‐reductase are also responsible for the formation of androgens. Because MS patients and EAE rodents show changes of central androgen levels, it is likely that, together with progestins and oestrogens, neuroandrogens afford neuroprotection for EAE and MS. The data reviewed suggest that enhanced synthesis of neurosteroids contributes in an auto/paracrine manner to reinforce the neuroprotective and anti‐inflammatory effects of exogenous progesterone given to EAE mice.