2018
DOI: 10.1016/j.nutres.2018.04.022
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Stigmasterol activates Cdc42-Arp2 and Erk1/2-Creb pathways to enrich glutamatergic synapses in cultures of brain neurons

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Cited by 24 publications
(10 citation statements)
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“…Lipophilic profiles could show the presence of steroid derivatives, but those works are not included in this review because herein are just referred the isolated and fully characterized metabolites. Nevertheless, the presence of β-sitosterol derivatives seems to be important due to their recognised biological properties and potential use in treatment of various illnesses [42], but also stigmasterol seems to be a potential therapeutic agent for neurodegenerative diseases [43]. Therefore, S. stellata can be a source of these important secondary metabolites.…”
Section: Structural Pattern Of the Secondary Metabolites Isolated mentioning
confidence: 99%
“…Lipophilic profiles could show the presence of steroid derivatives, but those works are not included in this review because herein are just referred the isolated and fully characterized metabolites. Nevertheless, the presence of β-sitosterol derivatives seems to be important due to their recognised biological properties and potential use in treatment of various illnesses [42], but also stigmasterol seems to be a potential therapeutic agent for neurodegenerative diseases [43]. Therefore, S. stellata can be a source of these important secondary metabolites.…”
Section: Structural Pattern Of the Secondary Metabolites Isolated mentioning
confidence: 99%
“…It also inhibited NMDA receptor-mediated excitotoxicity related to ischemic stroke [ 54 ]. Stigmasterol was reported to participate in axon and dendrite development, the modulation of synaptic transmission [ 55 ], reduction of amyloidogenic amyloid precursor protein (APP) processing, inhibition of acetylcholine esterase, and amelioration of memory impairment [ 56 ]. Ursolic acid protected the ischemic brain in mice by activating Nrf2 pathway, inhibiting the TLR4/NF- κ B pathway, and regulating metalloprotease/anti-metalloprotease imbalance [ 57 59 ].…”
Section: Discussionmentioning
confidence: 99%
“…Wu et al found that Hederagenin could be used as novel autophagic enhancer to play a role in neuroprotection by improving motor deficits in Parkinson's disease mice model 34 . Stigmasterol could ameliorate memory impairment and promotes neuritogenesis and synaptogenesis 35,36 . Ginsenosides from ginseng showed the great therapeutic potential in AD 37,38 .…”
Section: Discussionmentioning
confidence: 99%