Ferulic acid induces mammalian target of rapamycin inactivation in cultured mammalian cells.

Ferulic acid (FA), a naturally occurring polyphenol abundant in vegetables and rice bran, is known to possess a potent antioxidant activity, thereby protecting cells from oxidative stress. In the present study, we show that in addition to its known anti-oxidant activity, ferulic acid exerts substantial inhibitory activity on cellular mammalian target of rapamycin (mTor)-signaling pathways. In HeLa cells and mouse primary hepatocytes cultured with conventional nutrient-rich media, ferulic acid (1 mM) elicited dephosphorylation of S6 kinase and its substrate ribosomal S6. The dephosphorylating activity of ferulic acid was almost comparable to that of rapamycin, an established mTor inhibitor (TORC1). We next investigated the effect of ferulic acid on autophagy, a major cellular degradative process, which significantly contributes to the maintenance of cell homeostasis. Using a conventional green fluorescent protein-microtubule-associated protein IA/IB light chain 3 (GFP-LC3) dot assay to evaluate autophagy flux, we showed that ferulic acid caused a significant increase in GFP-LC3 dots under serum-rich conditions in HeLa cells. The enhancement of autophagic flux by ferulic acid was almost equivalent to that of rapamycin. Furthermore, ferulic acid significantly enhanced autophagic degradation of (14)C-leucine-labeled long-lived proteins of cultured mouse hepatocytes under nutrient-rich conditions, but not nutrient-deprived conditions. These results indicate that ferulic acid is almost the equivalent of rapamycin in the ability to inhibit mTor (TORC1), which makes it a potent activator of basal autophagy.

Interleukin-11 links oxidative stress and compensatory proliferation.

Apoptotic cells can stimulate the compensatory proliferation of surrounding cells to maintain tissue homeostasis. Although oxidative stress is associated with apoptosis and necrosis, whether it contributes to compensatory proliferation is unknown. Here, we showed that interleukin-11 (IL-11), a member of the IL-6 family of proinflammatory cytokines, was produced by cells in an oxidative stress-dependent manner. IL-11 production depended on the activation in dying cells of extracellular signal-regulated kinase 2, which in turn caused the phosphorylation and accumulation of the transcription factor Fra-1 by preventing its proteasome-dependent degradation. Fra-1 was subsequently recruited to the Il11 promoter and activated gene transcription. Upon acute liver injury in mice, IL-11 was mainly produced by hepatocytes in response to reactive oxygen species that were presumably released from dying hepatocytes. IL-11 that was secreted by the dying cells then induced the phosphorylation of the transcription factor STAT3 in adjacent healthy hepatocytes, which resulted in their compensatory proliferation. Furthermore, an IL-11 receptor (IL-11R) agonist enhanced the proliferation of hepatocytes and ameliorated oxidative stress upon acetaminophen-induced liver injury. Conversely, the effects of acetaminophen were exacerbated in mice deficient in the IL-11R α subunit. Together, these results suggest that IL-11 provides a functional link between oxidative stress and compensatory proliferation.

[Heavy metal contents in insects collected from the Huludao City suffering pollution by zinc smelting and cholor-alkai production].

14 insect species, which were classified to three groups: the herbivorous, the polyphagous and the carnivorous, and earthworms were collected from the grasslands in Huludao City, Liaoning Province, China. Mercury, cadmium and lead contents in biota were determined to discuss the heavy metal pollution in organisms. Mercury, cadmium and lead contents were 0.168, 9.19 and 12.58 mg x kg(-1) in the herbivorous insects, respectively; 0.375, 24.43 and 17.71 mg x kg(-1) in the polyphagous insects, respectively; 0.928, 29.78 and 18.39 mg x kg(-1) in the carnivorous insects, respectively. It showed that heavy metal pollution in biota in Huludao City was heavy. Bioaccumulation abilities to heavy metals significantly differed with insect species. Snails and dragonflies could accumulate more mercury than the other insects and spiders could accumulate the most cadmium and lead in all insect species. These three metals investigated in insects were all sorted as the herbivorous < the polyphagous < the carnivorous. Cadmium and lead contents between the polyphagous and the carnivorous varied slightly. Correlation analysis showed that cadmium and lead contents were significantly related, but mercury and cadmium or mercury and lead were not. It indicated that cadmium and lead in insects were from the same pollution sources while mercury was more complex.

Mercury, cadmium and lead biogeochemistry in the soil-plant-insect system in Huludao City.

Mercury, cadmium, and lead concentrations of ashed plants and insects samples were investigated and compared with those of soil to reveal their biogeochemical processes along food chains in Huludao City, Liaoning Province, China. Concentration factors of each fragments of the soil-plant-the herbivorous insect-the carnivorous insect food chain were 0.18, 6.57, and 7.88 for mercury; 6.82, 2.01, and 0.48 for cadmium; 1.47, 2.24, and 0.57 for lead, respectively. On the whole, mercury was the most largely biomagnified, but cadmium and lead were not greatly accumulated in the carnivorous insects as expected when the food chain extended to the secondary consumers. Results indicated that concentration factors depended on metals and insects species of food chains.

[Transfer characteristics of mercury, lead, cadmium, zinc and cuprum from soil to vegetable around zinc smelting plant].

The transfer characteristics of Hg, Pb, Cd, Zn and Cu from soil to vegetables near zinc smelting plant in Huludao City, China were investigated, and the sources of heavy metals in the soil and vegetable were also analyzed. The results indicate that the Hg, Pb, Cd, Zn and Cu contents of vegetables are 0.013, 5.476, 2.852, 41.16 and 1.515 mg/kg (fresh weight), respectively, and the environment around Huludao Zinc Plant are contaminated seriously. The transfer factors (TF) of heavy metals decrease in the order of Cd > Zn > Cu > Pb > Hg. The transfer factors of heavy metals from soil to leaves are higher than from soil to other tissues. The heavy metals in soil derive from atmosphere, and the parts of Pb in the leaves of vegetable derive from atmosphere. Uptake of gaseous mercury is the predominant pathway by which mercury accumulates in the vegetable.

Sphingosine 1-phosphate protects rat liver sinusoidal endothelial cells from ethanol-induced apoptosis: Role of intracellular calcium and nitric oxide.

In alcoholic liver disease, ethanol-induced damage to sinusoidal endothelial cells (SECs) appears to be important in the progression of liver damage. However, little is known about the mechanisms responsible for protection of SECs against ethanol-induced injury. To elucidate the role of sphingosine 1-phosphate (S1P), which is stored in platelets and may be released from them on their activation, we investigated the effect of S1P on rat liver SECs in primary culture. Pretreatment of cells with 1 mumol/L S1P attenuated ethanol-induced apoptosis. Electron microscopy confirmed this protective effect of S1P on damaged SECs in liver tissues after perfusion of ethanol. In the absence of ethanol, S1P increased DNA synthesis as determined via incorporation of bromodeoxyuridine. S1P also ameliorated the decreased DNA synthesis of cells induced by ethanol. Addition of S1P to cells induced an increase in intracellular calcium concentrations and NO production in cells. Western blotting revealed that S1P significantly induced the activation of endothelial NO synthase (eNOS), but not Akt, and that S1P-induced activation of eNOS was blocked by trifluoperazine, a calmodulin inhibitor. Furthermore, N(G)-nitro-L-arginine methyl ester, a NO synthase inhibitor, cancelled the effect of S1P on DNA synthesis, apoptosis, and NO production in vitro as well as the protective effect of S1P on cell damage in situ. In conclusion, the biological effect of S1P is at least partially mediated by Ca(2+)-sensitive eNOS activation and subsequent NO formation; extracellular S1P could contribute to sinusoidal protection and remodeling in alcoholic liver injury.