Abstract
Oxidative stress and mitochondrial disturbances are the common and important causative factors of aging, and play an important role in the late onset of sporadic neurodegenerative diseases, including Alzheimer disease (AD). Furthermore, emerging evidence from in vitro and in vivo disease models suggests that oxidative stress and increased vulnerability to induction of mitochondrial permeability transition leads to the pathogenesis of the neurological disorders. Towards the goals of developing effective neuroprotectors, this article describes the synthesis and neuroprotective studies of various derivatives of the naturally occurring alkaloid securinine, based on which a lead compound, allomargaritarine (a diastereomer of margaritarine), was identified as an effective therapeutic for neuroprotection. Allomargaritarine exhibits high antioxidant activity, and has significant mitoprotective effect on cellular models of neurodegeneration.
| Original language | American English |
|---|---|
| Journal | CNS and Neurological Disorders - Drug Targets |
| Volume | 15 |
| DOIs | |
| State | Published - Feb 1 2016 |
Keywords
- Aging
- Alkaloid Derivative
- Allomargaritarine
- Alzheimer Disease
- Animal Cell
- Animal Tissue
- Antioxidant Activity
- Cell Survival
- Controlled Study
- Disorders of Mitochondrial Functions
- Drug Synthesis
- Lipid Peroxidation
- MTT Assay
- Male
- Mitochondrial Membrane Potential
- Mitochondrial Permeability
- Nerve Degeneration
- Neuroprotection
- Newborn
- Nonhuman
- Oxidative Stress
- Plant Medicinal Product
- Rat
- Securinine
- Securinine Derivative
- Ultraviolet Spectroscopy
- Unclassified Drug
Disciplines
- Chemistry
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