New Insights into D-Aspartate Signaling in Testicular Activity.
AKT
D-amino acids
D-aspartate
ERK1/2
MAMs
mitochondria
reproduction
spermatogenesis
steroidogenesis
testis
Journal
Cells
ISSN: 2073-4409
Titre abrégé: Cells
Pays: Switzerland
ID NLM: 101600052
Informations de publication
Date de publication:
22 Aug 2024
22 Aug 2024
Historique:
received:
20
07
2024
revised:
19
08
2024
accepted:
20
08
2024
medline:
28
8
2024
pubmed:
28
8
2024
entrez:
28
8
2024
Statut:
epublish
Résumé
D-aspartate (D-Asp) is an amino acid found in high concentrations in the testis and pituitary gland. Increasing evidence suggests that D-Asp promotes spermatogenesis by activating testosterone production in the Leydig cells via LH release from the pituitary gland. In vitro studies indicate that D-Asp may also influence steroidogenesis and spermatogenesis through autocrine and paracrine signals. D-Asp enhances StAR and steroidogenic enzyme expressions, facilitating testicular cell proliferation via the GluR/ERK1/2 pathway. Moreover, it supports spermatogenesis by enhancing the mitochondrial function in spermatocytes, aiding in the metabolic shift during meiosis. Enhanced mitochondrial function, along with improved MAM stability and reduced ER stress, has been observed in Leydig and Sertoli cells treated with D-Asp, indicating potential benefits in steroidogenesis and spermatogenesis efficiency. Conversely, D-Asp exerts a notable anti-apoptotic effect in the testis via the AMPAR/AKT pathway, potentially mediated by antioxidant enzyme modulation to mitigate testicular oxidative stress. This review lays the groundwork for future investigations into the molecules promoting spermatogenesis by stimulating endogenous testosterone biosynthesis, with D-amino acids emerging as promising candidates.
Identifiants
pubmed: 39195288
pii: cells13161400
doi: 10.3390/cells13161400
pii:
doi:
Substances chimiques
D-Aspartic Acid
4SR0Q8YD1X
Testosterone
3XMK78S47O
Aspartic Acid
30KYC7MIAI
Types de publication
Journal Article
Review
Langues
eng
Sous-ensembles de citation
IM