Caffeic Acid Phenethyl Ester (CAPE): Biosynthesis, Derivatives and Formulations with Neuroprotective Activities.
Rebeca PérezViviana BurgosVíctor MarínAntonio Camins EspunyJordi OlloquequiIván González-ChavarríaHenning UlrichUrsula WynekeAlejandro LuarteLeandro OrtizCristian PazPublished in: Antioxidants (Basel, Switzerland) (2023)
Neurodegenerative disorders are characterized by a progressive process of degeneration and neuronal death, where oxidative stress and neuroinflammation are key factors that contribute to the progression of these diseases. Therefore, two major pathways involved in these pathologies have been proposed as relevant therapeutic targets: The nuclear transcription factor erythroid 2 (Nrf2), which responds to oxidative stress with cytoprotecting activity; and the nuclear factor NF-κB pathway, which is highly related to the neuroinflammatory process by promoting cytokine expression. Caffeic acid phenethyl ester (CAPE) is a phenylpropanoid naturally found in propolis that shows important biological activities, including neuroprotective activity by modulating the Nrf2 and NF-κB pathways, promoting antioxidant enzyme expression and inhibition of proinflammatory cytokine expression. Its simple chemical structure has inspired the synthesis of many derivatives, with aliphatic and/or aromatic moieties, some of which have improved the biological properties. Moreover, new drug delivery systems increase the bioavailability of these compounds in vivo, allowing its transcytosis through the blood-brain barrier, thus protecting brain cells from the increased inflammatory status associated to neurodegenerative and psychiatric disorders. This review summarizes the biosynthesis and chemical synthesis of CAPE derivatives, their miscellaneous activities, and relevant studies (from 2010 to 2023), addressing their neuroprotective activity in vitro and in vivo.
Keyphrases
- oxidative stress
- nuclear factor
- cerebral ischemia
- south africa
- poor prognosis
- diabetic rats
- dna damage
- transcription factor
- ischemia reperfusion injury
- signaling pathway
- blood brain barrier
- induced apoptosis
- toll like receptor
- lps induced
- subarachnoid hemorrhage
- binding protein
- traumatic brain injury
- brain injury
- cell proliferation
- pi k akt
- cell wall
- inflammatory response
- drug induced