Effect of Ozone Fumigation on Physiological Processes and Bioactive Compounds of Red-Veined Sorrel (Rumex sanguineus ssp. sanguineus)

The present study was designed to identify the effects of ozone fumigation of red-veined sorrel plants on the selected physiological parameters and contents of bioactive compounds in the plant leaves. Sorrel plants grown in a pot experiment were subjected, at the final stage of growth, to ozone fumigation at a concentration of 1 ppm (mg m−3) for one, three, five, seven, and 10 min. The ozone treatment was followed with measurements performed one, four, and eight days later. The relative chlorophyll content in the leaves and selected chlorophyll fluorescence parameters (maximum quantum yield of PSII photochemistry, the maximum quantum yield of primary photochemistry and the performance index) and gas exchange parameters were assessed (net photosynthetic rate, transpiration rate, stomatal conductance, and intercellular CO2 concentration). By using the same leaves, the plant material was also assessed for the contents of bioactive compounds (total polyphenols) and for antioxidant properties (ABTS and DPPH assays). The ozone treatment did not produce adverse changes in the physiological parameters of the sorrel plants. Furthermore, no visible damage to the leaves was observed. On the other hand, the ozone fumigation induced the phenomenon of elicitation as a result of which it was observed that the ozone-treated sorrel plants had higher total polyphenol contents and greater antioxidant potential, compared to the plants of the same species grown in a traditional way without the ozone fumigation. Application of ozone fumigation in the production of Rumex sanguineus is associated with increased bioactive potential of the raw material obtained

Monocyte chemoattractant protein-induced protein 1 impairs adipogenesis in 3T3-L1 cells

Monocyte chemoattractant protein-induced protein 1 (MCPIP1) encoded by the ZC3H12a gene (also known as Regnase-1) is involved in the regulation of degradation of mRNA of inflammatory modulators and for processing of pre-miRNA. These functions depend on the presence of the PIN domain. Moreover, MCPIP1 was described as a negative regulator of NF-?B and AP-1 signaling pathways although mechanisms underlying such activity remain unknown. We aimed at determining the role of MCPIP1 in adipogenesis. Here, we present evidence that Mcpip1 transcription is transiently activated during 3T3-L1 transition from pre- to adipocytes. However Mcpip1 protein expression is also strongly decreased at day one after induction of adipogenesis. Knockdown of Mcpip1 results in an upregulation of C/EBP? and PPAR? mRNAs, whereas overexpression of MCPIP1 reduces the level of both transcription factors and impairs adipogenesis. MCPIP1-dependend modulation of C/EBP? and PPAR? levels results in a modulation of the expression of downstream controlled genes. In addition, decreased C/EBP?, but not PPAR?, depends on the activity of the MCPIP1 PIN domain, which is responsible for RNase properties of this protein. Together, these data confirm that MCPIP1 is a key regulator of adipogenesi