Polyphenolic Compounds from Lespedeza bicolor Protect Neuronal Cells from Oxidative Stress.
Darya V TarbeevaEvgeniy A PislyaginEkaterina S MenchinskayaDmitrii V BerdyshevAnatoliy I KalinovskiyValeria P GrigorchukNatalia P MishchenkoDmitry L AmininSergey A FedoreyevPublished in: Antioxidants (Basel, Switzerland) (2022)
Pterocarpans and related polyphenolics are known as promising neuroprotective agents. We used models of rotenone-, paraquat-, and 6-hydroxydopamine-induced neurotoxicity to study the neuroprotective activity of polyphenolic compounds from Lespedeza bicolor and their effects on mitochondrial membrane potential. We isolated 11 polyphenolic compounds: a novel coumestan lespebicoumestan A ( 10 ) and a novel stilbenoid 5'-isoprenylbicoloketon ( 11 ) as well as three previously known pterocarpans, two pterocarpens, one coumestan, one stilbenoid, and a dimeric flavonoid. Pterocarpans 3 and 6 , stilbenoid 5 , and dimeric flavonoid 8 significantly increased the percentage of living cells after treatment with paraquat (PQ), but only pterocarpan 6 slightly decreased the ROS level in PQ-treated cells. Pterocarpan 3 and stilbenoid 5 were shown to effectively increase mitochondrial membrane potential in PQ-treated cells. We showed that pterocarpans 2 and 3 , containing a 3'-methyl-3'-isohexenylpyran ring; pterocarpens 4 and 9 , with a double bond between C-6a and C-11a; and coumestan 10 significantly increased the percentage of living cells by decreasing ROS levels in 6-OHDA-treated cells, which is in accordance with their rather high activity in DPPH • and FRAP tests. Compounds 9 and 10 effectively increased the percentage of living cells after treatment with rotenone but did not significantly decrease ROS levels.
Keyphrases
- living cells
- fluorescent probe
- induced apoptosis
- oxidative stress
- cell cycle arrest
- single molecule
- cell death
- dna damage
- endoplasmic reticulum stress
- reactive oxygen species
- diabetic rats
- signaling pathway
- cerebral ischemia
- human health
- newly diagnosed
- climate change
- risk assessment
- endothelial cells
- subarachnoid hemorrhage
- heat stress
- heat shock