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1.
Article in English | WPRIM (Western Pacific) | ID: wpr-929246

ABSTRACT

Three new ursane-type triterpenoids, 3-oxours-12-en-20, 28-olide (1), 3β-hydroxyurs-12-en-20, 28-olide (2) and 3β-hydroxyurs-11, 13(18)-dien-20, 28-olide (3), were isolated from a potent anti-inflammatory and antibacterial fraction of the ethanolic extract of Rosmarinus officinalis. Their structures were elucidated by a combination of extensive 1D- and 2D-NMR experiments, MS data and comparisons with literature reports. Compounds 1-3 exhibited significantly inhibitory effects on nitric oxide production in lipopolysaccharide-activated mouse RAW264.7 macrophages, but no antibacterial activity was found at a concentration of 128 μg·mL-1.


Subject(s)
Animals , Mice , Drugs, Chinese Herbal/chemistry , Molecular Structure , Rosmarinus , Triterpenes/chemistry
2.
Article in English | WPRIM (Western Pacific) | ID: wpr-776909

ABSTRACT

Guided by TNF-α secretion inhibitory activity assay, four taraxastane-type triterpenoids, including two new ones, 22-oxo-20-taraxasten-3β, 30-diol (1) and 22α-hydroxy-20-taraxasten-30β, 30-triol (2), have been obtained from an active fraction of the petroleum ether-soluble extract of the the medicinal and edible plant Cirsium setosum. Their structures were elucidated by spectroscopic data and CD data analysis. In the TNF-α secretion inhibitory activity assay, compounds 1 and 2 were active with the IC of 2.6 and 3.8 μmol·L, respectively. In addition, compounds 1 and 2 showed moderately selective cytotoxicity against the human ovarian cancer (A2780) and colon cancer (HCT-8) cell lines.


Subject(s)
Animals , Humans , Mice , Cell Line, Tumor , Cell Survival , Cirsium , Chemistry , Ether , Chemistry , Macrophages , Metabolism , Molecular Structure , Plant Extracts , Chemistry , Pharmacology , Plants, Edible , Chemistry , Plants, Medicinal , Chemistry , Triterpenes , Chemistry , Pharmacology , Tumor Necrosis Factor-alpha , Metabolism
3.
J Neurosci ; 25(26): 6167-74, 2005 Jun 29.
Article in English | MEDLINE | ID: mdl-15987946

ABSTRACT

The primate anterior hippocampus (which corresponds to the rodent ventral hippocampus) receives inputs from brain regions involved in reward processing, such as the amygdala and orbitofrontal cortex. To investigate how this affective input may be incorporated into primate hippocampal function, we recorded neuronal activity while rhesus macaques performed a reward-place association task in which each spatial scene shown on a video monitor had one location that, if touched, yielded a preferred fruit juice reward and a second location that yielded a less-preferred juice reward. Each scene had different locations for the different rewards. Of 312 neurons analyzed in the hippocampus, 18% responded more to the location of the preferred reward in different scenes, and 5% responded to the location of the less-preferred reward. When the locations of the preferred rewards in the scenes were reversed, 60% of 44 hippocampal neurons tested reversed the location to which they responded, showing that the reward-place associations could be altered by new learning in a few trials. The majority (82%) of these 44 hippocampal neurons tested did not respond to reward associations in a visual discrimination, object-reward association task. Thus, the primate hippocampus contains a representation of the reward associations of places "out there" being viewed. By associating places with the rewards available, the concept that the primate hippocampus is involved in object-place event memory is now extended to remembering goals available at different spatial locations. This is an important type of association memory.


Subject(s)
Hippocampus/physiology , Memory/physiology , Neurons/physiology , Reward , Space Perception/physiology , Animals , Brain Mapping , Electrophysiology , Haplorhini , Microelectrodes , Pyramidal Cells/physiology
4.
Neuron ; 42(5): 817-29, 2004 Jun 10.
Article in English | MEDLINE | ID: mdl-15182720

ABSTRACT

Much evidence indicates that prefrontal cortex plays an important role in long-term recognition memory processes. Here, we report primate prefrontal neuronal responses carrying information necessary for long-term visual recognition memory. The responses of many neurons signaled stimulus familiarity even when the period over which stimuli had to be remembered extended to 24 hr. Such responses occurred frequently in ventromedial, orbitofrontal, and anterior cingulate but not dorsolateral prefrontal cortex. Prefrontal information processing, as indicated by the response latencies, started after that in inferior temporal cortex and might be related to retrieval processes, as responses were typically larger for familiar than for novel stimuli.


Subject(s)
Memory/physiology , Neurons/physiology , Prefrontal Cortex/cytology , Recognition, Psychology/physiology , Visual Perception/physiology , Action Potentials/physiology , Action Potentials/radiation effects , Analysis of Variance , Animals , Behavior, Animal , Brain Mapping , Discrimination, Psychological/radiation effects , Electric Stimulation/methods , Electrophysiology/methods , Eye Movements/physiology , Macaca mulatta , Male , Neural Inhibition/physiology , Neurons/classification , Neurons/radiation effects , Photic Stimulation , Prefrontal Cortex/physiology , Prefrontal Cortex/radiation effects , Reaction Time , Time Factors
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