Resultative Compound Verb in Modern Chinese : A Comment on Imai(1985) and Lu(1986)

<p>A. API and DMO suppresses NF-κB DNA binding ability in HCT116 cells. HCT116 cells were treated with DMO and API at indicated doses, nuclear extracts were prepared, and 20 μg of the nuclear extract protein was used for the ELISA-based DNA-binding assay *p<0.05; **p<0.005). B & C. NF-κB responsive elements linked to a luciferase reporter gene were transfected with wild-type or dominant-negative IκB and transfected cancer cells were treated at indicated doses for 6 h and luciferase activity was measured as described in Materials and Methods section. All luciferase experiments were done in triplicate and repeated twice (*p<0.05; **p<0.005). D. API abrogates constitutive IκBα phosphorylation in dose-dependent manner in HCT116 cells. HCT116 cells were treated with different concentrations of API (0, 5, 10 and 20 μM) for 6 h and cytoplasmic extract was prepared. Lysates were resolved on SDS gel and electrotransferred to a nitrocellulose membrane and probed with anti-phospho-IκBα/IκBα. The blot was washed, exposed to HRP-conjugated secondary antibodies for 1 h, and finally examined by chemiluminescence. GAPDH was used as loading control.</p

UV-VIS spectral studies of compound 5d in presence of CaCl₂ and ZnCl₂.

<p>The mixture of compound 5d (1 mM) and different concentrations of (A) CaCl₂ and (B) ZnCl₂ (0–2.0 mM) in a final volume of 1 mL PBS. The samples were monitored by spectroscopic scanning with the wavelength range of 200 to 300 nm.</p

Stereo view of 3D structure of the SVMP (Bothropasin) showing molecular interaction with the compound 5d.

<p>The interaction between the compound and active site residues are shown using a line representation colored by parent atoms except for carbon (green color). The ligand is presented in the ball and stick form with their parent color except for carbon (white color). Hydrogen bonds are presented as white dotted lines.</p

Effect of compound 5d on EC venom-induced fibrino(geno)lytic activity.

<p>EC venom (0.2 µg) was pre-incubated separately with different doses of compound 5d (1∶0; 1∶1; 1∶5; 1∶10; 1∶25 and 1∶50; venom: compound; w/w; Lane 2–7 respectively, Lane-1 represents substrate alone and Lane-8 represents substrate with 10 µg of compound 5d alone) for 10 min at 37°C. The reaction was initiated by adding respective substrates (A) fibrin and (B) fibrinogen and incubated for 30 min. Samples were electrophoresed on 10% SDS-PAGE and the gels were processed as described in <a href="http://www.plosone.org/article/info:doi/10.1371/journal.pone.0106364#s2" target="_blank">materials and methods</a> section.</p

Effect of compound 5d on procoagulant activity of EC venom.

<p>EC venom (0.6 µg) was pre-incubated with compound 5d at various doses and the procoagulant assay was performed as described in <a href="http://www.plosone.org/article/info:doi/10.1371/journal.pone.0106364#s2" target="_blank">materials and methods</a> section. Data are presented as the mean ± SEM, <b>***</b><i>p</i><0.001, a - significant compared to saline control group and ‡ - non-significant compared to venom alone group.</p><p>Effect of compound 5d on procoagulant activity of EC venom.</p

Effect of compound 5d on EC venom-induced edema activity.

<p>EC venom (0.6 µg) was pre-incubated with compound 5d at various doses and injected to the right food pad to groups of mice (n = 5) and then the respective assay was performed as described in the <a href="http://www.plosone.org/article/info:doi/10.1371/journal.pone.0106364#s2" target="_blank">materials and methods</a> section. Data are presented as the mean ± SEM, <b>***</b><i>p</i><0.001, a - significant compared to saline control group and ‡ - non-significant compared to venom alone group. The hemorrhage score is as follows: - nil; +++ High; ++ low.</p><p>Effect of compound 5d on EC venom-induced edema activity.</p

Light microphotograph of mice skeletal muscle sections.

<p>EC venom (5 µg) was pre-incubated separately with various doses of compound 5d (1∶0; 1∶5; 1∶10 and 1∶25; venom: compound; w/w) for 10 min at 37°C. The samples were injected intramuscularly into groups of mice (n = 5) in a total volume of 50 µL saline. Mice were anaesthetized and sacrificed after 3 h, the muscle tissue from the injected site was removed and processed for histopathological studies as described in <a href="http://www.plosone.org/article/info:doi/10.1371/journal.pone.0106364#s2" target="_blank">materials and methods</a> section. (A) Saline injected control section- note the intact basement membrane with striated myofibrils (B) EC venom-injected section shows the extensive disorganized myofibroblasts with infiltration of inflammatory leucocytes. (C)–(E) EC venom pre-incubated with the compound 5d injected section shows the inhibition and restoration of normal histology of muscle tissue (with respective doses of 1∶5; 1∶10 and 1∶25; venom: compound; w/w). (F) 150 µg Compound 5d alone injected section similar to saline control. Original magnification 40x.</p

Effect of compound 5d on EC venom-induced serum LDH and CPK levels in experimental animals in an independent injection experiment.

<p>EC venom (5 µg) was intramuscularly injected to the group of mice (n = 5) followed by compound 5d (250 µg) injection at various time intervals (0, 2.5, 5, 7.5 and 10 min) to the same site where venom had been injected, and then the respective assay was performed as described in the <a href="http://www.plosone.org/article/info:doi/10.1371/journal.pone.0106364#s2" target="_blank">materials and methods</a> section. Data are presented as the mean ± SEM, <b>***</b><i>p</i><0.001, <b>*</b><i>p</i><0.05, a - significant compared to saline control group and b - significant compared to venom alone group.</p><p>Effect of compound 5d on EC venom-induced serum LDH and CPK levels in experimental animals in an independent injection experiment.</p

Schematic representation for the synthesis of apigenin structural analogues.

<p>Schematic representation for the synthesis of apigenin structural analogues.</p

Effect of compound 5d on EC venom induced myotoxicity.

<p>EC venom (5 µg) was pre-incubated separately with varied doses of compound 5d (1∶0; 1∶5; 1∶10 and 1∶25; venom: compound; w/w) for 10 min at 37°C. The samples were injected intramuscularly into group of mice (n = 5) in a total volume of 50 µL saline. Mice were anaesthetized and sacrificed after 3 h and the assay was performed as described in <a href="http://www.plosone.org/article/info:doi/10.1371/journal.pone.0106364#s2" target="_blank">materials and methods</a> section. <a href="http://www.plosone.org/article/info:doi/10.1371/journal.pone.0106364#s3" target="_blank">Results</a> are expressed as mean ± SEM of three independent experiments. <b>***</b><i>p</i><0.001, <b>**</b><i>p</i><0.01, a - significant compared to saline control group and b - significant compared to venom alone group.</p