Effects Of DMA Research Articles

Effect of the macromolecular architecture on the thermoresponsive behavior of poly(N-isopropylacrylamide) in copolymers with poly(N,N-dimethylacrylamide) in aqueous solutions: Block vs random copolymers

Three samples from each type of poly(N-isopropylacrylamide)-block-poly(N,N-dimethylacrylamide) (PNIPAM-b-PDMA) block copolymers and poly(N-isopropylacrylamide-co-N,N-dimethylacrylamide) (P(NIPAM-co-DMA)) random copolymers with similar chemical composition were synthesized by RAFT polymerization. The effects of DMA on the thermoresponse of its two kinds of copolymers with NIPAM were comparatively investigated by turbidity analysis, variable-temperature 1H NMR and dynamic light scattering with PNIPAM homopolymer as a control. It was discovered that the phase transition temperature, the temperature response window and the hysteresis values of the PNIPAM-b-PDMA and P(NIPAM-co-DMA) counterpart were significantly different. In particular, the temperature response window, which represents the sensitivity of response, is smaller for random copolymers than that of block copolymers in aqueous solution, indicating that the temperature response of random copolymers is more sensitive than that of block copolymers. The possible reasons leading to different thermo-responsive phase transition characteristics between block copolymers and random copolymers are discussed, and the formation of different hydrophobic structures with the temperature increasing is ascribed.

The electronic structures and magnetic properties of mixed-valence Fe-based metal-organic VNU-15 frameworks: a theoretical study from linear response DFT+U calculations.

The crystal symmetries, electronic structures, and magnetic properties of metal–organic VNU-15 frameworks (VNU = Vietnam National University) were investigated using density functional calculations (DFT) with an on-site Coulomb repulsion approximation, Ueff, of 4.30 eV, determined via the linear response method. Two different orientations of dimethylammonium (DMA+) cations in VNU-15 were investigated. Antiferromagnetic configurations were predicted to be the ground states, with Fe ions in high-spin states for both phases. Furthermore, VNU-15 had intrinsic semiconductor electronic behavior with a small band gap of about 1.20 eV. The change in the orientation of DMA+ led to changes in the dispersion of the band structure, the band gap, and the Fe contributions to the valence band and conduction band. A fascinating feature was found involving exchange of oxidation numbers between two adjacent Fe atoms in the two phases. Our results revealed that VNU-15 has strong oxidation activity and predicted the important role of an anisotropic effect on the hole and electron effective masses. The findings presented that the electronic and magnetic properties could be controlled via hydrogen bonds and proved VNU-15 to be a prospective material for photocatalytic applications.

Suppressive effect of β,β-dimethylacryloyl alkannin on activated dendritic cells in psoriasis by the TLR7/8 pathway

β,β-dimethylacryloyl alkannin (DMA) is a key component of Lithospermum and possesses good efficacy for treating psoriasis. DMA inhibits activated dendritic cells (DCs), but the mechanism is unknown. Therefore, this study aimed to explore the modulation of the TLR7/8 pathway by DMA in psoriasis-activated DCs. Models of psoriasis-like skin lesions were established using BALB/c mice; 8 mice were treated with DMA (2.5mg/kg). Bone marrow cells were isolated and induced into DCs using R848, a TLR7/8 agonist. Splenic CD11c+ cells were detected by flow cytometry. Skin CD11c+ cells were detected by immunofluorescence. TLR7, TLR8, MYD88, and IRAKM proteins were detected by Western blot. The effects of DMA on surface molecules of DCs were observed by flow cytometry. mRNA expression of inflammatory factors was detected by qRT-PCR. Secreted cytokines were detected by cytometric bead array. Compared with the model group, psoriasis-like skin lesions were alleviated by DMA, the splenic CD11c+ cells were significantly decreased (P<0.01), and CD11c+ cell numbers in skin lesions were decreased (P<0.01). Expression levels of TLR7, MYD88, and IRAKM were significantly decreased (P<0.05). R848-stimulated DCs showed increased expression of I-A/I-E, CD80, and CD86 (P<0.01), increased IL-23 and IL-1β mRNA and secretion (P<0.05), and increased TLR7, TLR8, MYD88, and IRAKM expression (P<0.01); DMA inhibited all of these effects of the TLR7/8 pathway activation by R848 (P<0.05). In conclusion, DMA could inhibit psoriasis-activated DCs via the TLR7/8 pathway.

Role of the Alkali Labile Sites, Reactive Oxygen Species and Antioxidants in DNA Damage Induced by Methylated Trivalent Metabolites of Inorganic Arsenic

In the last decade arsenic metabolism has become an important matter of discussion. Methylation of inorganic arsenic (iAs) to monomethylarsonic acid (MMA(V)) and dimethylarsinic acid (DMA(V)) is considered to decrease arsenic toxicity. However, in addition to these pentavalent metabolites, the trivalent metabolites monomethylarsonous (MMA(III)) and dimethylarsinous acid (DMA(III)) have been identified recently as intermediates in the metabolic pathway of arsenic in cultured human cells. To examine the role of oxidative damage in the generation of DNA strand breaks by methylated trivalent arsenic metabolites, we treated human lymphocytes with both metabolites at non-cytotoxic concentrations. We further tested whether these effects are sensitive to modulation by the antioxidants ascorbate (Vitamin C) and selenomethionine (Se-Met). Both trivalent metabolites produced oxidative stress related DNA damage, consisting of single strand breaks and alkali-labile sites, with MMA(III) being more potent at low concentrations than DMA(III). Neither MMA(III) nor DMA(III) induced DNA-double strand breaks. The oxidative stress response profiles of the metabolites were parallel as determined by lipid peroxidation induction. MMA(III) induced peroxidation from the lowest concentration tested, while effects of DMA(III) were apparent only at concentrations above 10 muM. The antioxidant Se-Met exhibited a more pronounced inhibition of trivalent arsenic metabolite-induced oxidative-DNA damage than did vitamin C. The present findings suggest that DNA damage by methylated trivalent metabolites at non-cytotoxic concentrations may be mediated by a mix of reactive oxygen and nitrogen oxidized species.

Effects of μ-, δ-, and κ-opioid agonists and enkephalinase inhibitor RB101 in two inbred rat strains

Analgesic and suppressive effects of selective μ- (DAGO), δ- (DME), and κ- (DAKLI) opioid agonists are compared with those of aminopeptidase N and neutral endopeptidase RB101 in rats of WAG/G and Fischer-344 rats. Fischer-344 rats were more susceptible to suppressive effects of DAGO and analgesic effect of DME. It is concluded that in these rats peculiarities of the μ- and δ-opioid systems determine susceptibility to locomotor depression and analgesia, respectively. There is no correlation between effects of DAGO and RB101 in these strains. This implies that depressive effect of RB101 is not mediated though μ-opioid systems. In contrast, the effects of DMA on pain sensitivity in WAG/G and F-344 rats are opposite to those of RB101. This suggests that specific features in the activity of cerebral δ-OS can determine the sensitivity of RB101-induced analgesia.

S13-3 - Effects of DMA on cultured neuronal cells: Studies in PCΙ2 cells

S13-3 - Effects of DMA on cultured neuronal cells: Studies in PCΙ2 cells

Studies on cellular adhesion in tissue culture: XIV. Positively charged surface groups and the rate of cell adhesion

Attempts were made to identify positively charged groups at the surfaces of Ehrlich ascites tumour (EAT) cells, and particles of polystyrene polymer which had adsorbed proteins after incubation in serum-containing culture medium. The cells and particles were treated with 2,4,6-trinitrobenzene sulphonic acid (TNBS) or 2,3-dimethylmaleic anhydride (DMA), which react with amino and other cationic groups. The increases in cell and particle anodic electrophoretic mobility were consistent with approx. 5% of the total surface charge of each, being due to positively charged groups. The effects of DMA or TNBS treatment of the cells and/or polystyrene surfaces, on the rates of cell adhesion to these surfaces were then determined. The significantly slower rates of adhesion after some modes of treatment suggest that positively charged groups at the surfaces of EAT cells play a part in their initial contact with and adhesion to, protein-coated plastic surfaces. However, quantitatively the role of cationic groups is a minor one in this part of the adhesion process.