Bioassay-guided isolation of neuroprotective compounds from Loranthus parasiticus against H₂O₂-induced oxidative damage in NG108-15 cells.
A parasite plant, Loranthus parasiticus (Loranthaceae), which is generally known as benalu teh (in Malay), Sang Ji Sheng (in Chinese), and baso-kisei (in Japan) distributed in south and southwest part of China, has been used as a folk medicine for the treatment of schizophrenia in southwest China. Loranthus parasiticus has various uses in folk and traditional medicines for bone, brain, kidney, liver, expels wind-damp, and prevents miscarriage.
The current study was designed to evaluate the neuroprotective activity of Loranthus parasiticus against hydrogen peroxide (H(2)O(2))-induced oxidative damage in NG108-15 hybridoma cells, so as to present evidence for the traditional use of this parasite plant in the treatment of oxidative stress related neurodegenerative diseases.
Dried and ground leaves of Loranthus parasiticus were extracted and fractionated into Loranthus parasiticus ethanol extract (LPEE), Loranthus parasiticus ethyl acetate fraction (LPEAF), and Loranthus parasiticus aqueous fraction (LPAF), which were subjected to neuroprotective activity assessment by 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) cell viability assay. Bioassay-guided fractionation and isolation was performed subsequently to identify the most neuroactive compound. Mechanism studies underlying the present neuroprotection model of the isolated neuroactive compound was evaluated by employing 2,7-dichlorofluorescein diacetate (DCFH-DA) for intracellular reactive oxygen species (ROS) measurement, annexin V/propidium iodide (PI) for translocation of membrane phosphatidyleserine to identify cells undergo apoptosis, 5,5',6,6'-tetrachloro-1,1',3,3' tetraethylbenzimidazolylcarbocyanine iodide (JC-1) for mitochondrial membrane potential (MMP) detection, and PI for cell cycle events analysis.
Among those tested extract and fractions (LPEE, LPEAF, and LPAF) in our previous screening, LPAF significantly (P<0.01) yielded the highest neuroprotective activity with 78.00±1.85% cell viability in a dose dependent manner, supporting a neuroprotective role for LPAF in vitro. AC trimer and (+)-catechin have been isolated from LPAF successfully through bioassay-guided fractionation and isolation approach and (+)-catechin exhibited stronger neuroprotective activity as compared with AC trimer. (+)-Catechin increased cell viability and decreased the level of intracellular reactive oxygen species (ROS) in a dose-dependent manner against H(2)O(2)-induced oxidative stress in NG108-15 cells. Moreover, (+)-catechin reduced total annexin V positive cells (early and late apoptotic cells), attenuated the collapsed of MMP, and inhibited cell cycle arrested at sub-G(1) population following H(2)O(2) insult.
Collectively, the use of Loranthus parasiticus as folk medicine in the treatment of mental disorder was attributed to the presence of proanthocyanidins in this parasite plant. These findings support the traditional use of Loranthus parasiticus which is capable in managing neurological disorder where oxidative stress is implicated.
Wong DZ
，Kadir HA
，Ling SK
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Inhibitory activities on mammalian central nervous system receptors and computational studies of three sesquiterpene lactones from Coriaria ruscifolia subsp. ruscifolia.
The electrophysiological characterization of sesquiterpene lactones from Coriaria ruscifolia subsp. ruscifolia has been tested on hippocampal neurons. The results for glycinergic rat hippocampal transmission and native γ-aminobutyric acid (GABA)ergic transmission on neurons (13DIV) are remarkably different for tutin, coriamyrtin, and dihydrotutin, being tutin the most potent inhibitor and dihydrotutin the least potent one. To understand the applied mechanism of action, we discuss the structural and electronic requirements for inhibitory activity by these sesquiterpene lactones when modulating receptors of the central nervous system. The structural and electrostatic properties of these compounds were compared to those of more active metabolites like picrotoxins. The minimal energy level of these structures was calculated and then optimized at the ab initio B3LYP/DGDZVP level of theory using Gaussian 03W software. This allowed calculation of the corresponding vibrational circular dichroism spectrum of coriamyrtin which rendered the molecular absolute configuration after comparison with an experimental spectrum. These results are consistent with those from studies of other models that provide the basis for the activity on the presence of the lactone at carbons 3 and 5, the presence of the hydroxyl group at position 6, and the different electronic distributions observed in tutin and coriamyrtin. The latter has an isopropenyl moiety at carbon 4 in contrast to the dihydrotutin isopropyl group at the same position, which could explain the difference in activity between dihydrotutin and tutin or coriamyrtin. The presence of the hydroxyl group at carbon 2 is not decisive since this functionality is present in tutin, the most active compound, and in dihydrotutin, the less active one.
Pérez C
，Becerra J
，Manríquez-Navarro P
，Aguayo LG
，Fuentealba J
，Guzmán JL
，Joseph-Nathan P
，Jiménez V
，Muñoz MA
，Silva M
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