An e.s.r. study of the motion of peroxy radicals in isotactic and atactic polypropylenes

E.s.r. spectra of peroxy radicals trapped in isotactic and atactic polypropylenes have been observed at various temperatures. The spectrum observed at 77 K was shown to be composed of one component by comparing it with that at 4 K. The spectra observed at higher temperatures comprised of two spectra arising from the rigid peroxy radicals and the mobile peroxy radicals. All of the observed spectra have been reconstructed by means of computer simulation and the changes in anisotropic g-values with temperature were estimated. The motion of the mobile fraction was shown to be rotation or rotatory vibration of the radicals around the chain axis both in the isotactic polypropylene and in the atactic polypropylene as well as in polyethylene and poly(tetrafluoroethylene) although the structures of the polymers are different, that is helical (polypropylene) or planar zigzag (polyethylene, poly(tetrafluoroethylene)).     

A new p-channel MOSFET with large-tilt-angle implanted punchthroughstopper (LATIPS)

A buried-channel p-MOSFET with a large-tile-angle implanted punchthrough stopper (LATIPS) is described. In this device the n⁺ LATIPS region was successfully realized adjacent to the p⁺ source/drain, even without a sidewall spacer, by taking advantage of the n⁺ large-tilt-angle implant. In spite of the relatively deep p⁺ junction of 0.2-μm depth and the low n-well concentration of 1×10¹⁶ cm^-3, the 0.5-μm LATIPS device (with corresponding channel length of 0.3 μm) achieved high punchthrough resistance, e.g. a low subthreshold swing of 95 mV/decade with a high transconductance of 135 mS/mm     

Decreased baroreflex sensitivity in patients with stable coronary artery disease is correlated with the severity of coronary narrowing

Although studies have shown that arterial baroreflex sensitivity (BRS) is decreased in patients with acute myocardial infarction, BRS changes in patients with stable coronary artery disease (CAD) have not been studied extensively. We assessed BRS by the phenylephrine method in 55 normotensive and nondiabetic patients with chronic effort angina, old myocardial infarction, or both. The control group consisted of 24 age-matched patients without coronary lesions. To identify factors that determine BRS in stable CAD, we performed multivariate analysis using age, sex, left ventricular ejection fraction, pulmonary artery wedge pressure, resting systolic blood pressure, resting heart rate, the number of stenotic coronary arteries, history of myocardial infarction, and the presence or absence of angina pectoris as variables. BRS was significantly lower in patients with CAD than in control subjects (5.9 +/- 2.9 vs 6.9 +/- 2.4 ms/mm Hg, p < 0.05). In patients with CAD, BRS was inversely correlated with age, the resting heart rate, and the number of stenotic coronary vessels (p < 0.001, p < 0.005, and p < 0.005, respectively), but was independent of other clinical parameters, including the history of myocardial infarction. In control subjects, BRS was significantly correlated only with age. These results indicate that BRS is decreased in patients with stable CAD, and this decrease is correlated with the extent and severity of coronary narrowing.     

Alternation in the coronary blood flow velocity pattern in patients with no reflow and reperfused acute myocardial infarction

1. The effects of fluvastatin, a new 3-hydroxy-3-methylglutaryl coenzyme A (HMG-CoA) reductase inhibitor, on the vascular angiotensin converting enzyme (ACE) activity in hyperlipidaemic rabbits were compared with those of enalapril, an ACE inhibitor. 2. Rabbits were fed a 1.5% cholesterol containing diet or normal diet for 16 weeks and treated with either fluvastatin or enalapril in the diet at the respective doses of 2 and 10 mg kg-1 day-1. The total cholesterol, triglyceride and phospholipid levels in serum were significantly increased in rabbits fed the high cholesterol diet. Treatment with fluvastatin but not enalapril resulted in a decrease in serum lipids. 3. The vascular ACE activities assessed via the cleavage rate from synthetic substrate in the aortic arches and upper thoracic aortae were increased by 8 to 10 times when the rabbits were made hyperlipidaemic. Fluvastatin as well as enalapril significantly lowered the tissue ACE in the aortae. 4. The ACE activities in serum did not alter in hyperlipidaemic rabbits either in the presence or absence of fluvastatin. The serum ACE activity was lowered by enalapril. 5. The lipid peroxide in serum as well as the plaque area in the thoracic aorta was significantly increased in the cholesterol diet-fed rabbits. Treatment with fluvastatin or enalapril reduced both serum lipid peroxide and plaque formation. The relaxant responses to acetylcoholine (ACh) were significantly suppressed in the cholesterol-fed rabbits. Treatment with fluvastatin or enalapril significantly reversed the suppression of ACh-induced relaxation. 6. It seems that the reduction of vascular ACE is not coupled to lipids and ACE activity in serum, but rather to lipid peroxidation. Thus, the decrease in vascular ACE activity by fluvastatin as well as the lipid-lowering effect may reduce the risk of atherosclerosis progression in the vasculature.     

Depth resolution and recoil cross section for analyzing hydrogen in solids using elastic recoil detection with 4He beam

Two aspects of the elastic recoil detection technique for analyzing H and D are described; i) experimental factors which effectively limit the depth resolution in Al film, and ii) determination of the recoil cross section for H(⁴He, ⁴He)H and D(⁴He, ⁴He)D reactions in the range of 1.5–3.0 MeV energy of ⁴He. Both experimental and theoretical estimates of the depth resolution are presented and are in good agreement each other. The theoretical estimate therefore provides a reliable guide to find optimum resolution conditions. The recoil cross section for H is more than double the theoretical Rutherford scattering value and that for D becomes greater than 30 times Rutherford near the resonance energy of 2.1 MeV ⁴He.     

Inhibitory effect of forskolin on myosin phosphorylation-dependent and independent contractions in bovine tracheal smooth muscle

In bovine tracheal smooth muscle, carbachol (CCh, 1 microM) and high K+ (72.7 mM) induced sustained increases in cytosolic Ca2+ level ([Ca2+]i), myosin light chain (MLC) phosphorylation and force of contraction. Forskolin (FK, 1-10 microM) inhibited the CCh-induced increase in [Ca2+]i, MLC phosphorylation and force in parallel. In contrast, FK inhibited the high K(+)-induced contraction and MLC phosphorylation without changing [Ca2+]i. In the absence of extracellular Ca2+ (with 0.5 mM EGTA), CCh (10 microM) and caffeine (20 mM) induced transient increase in [Ca2+]i and contractile force by releasing Ca2+ from cellular store. FK strongly inhibited the CCh-induced Ca2+ transient, but failed to inhibit the caffeine-induced Ca2+ transient. In the absence of external Ca2+, 12-deoxyphorbol 13-isobutylate (DPB, 1 microM) induced sustained contraction without increase in [Ca2+]i and MLC phosphorylation. FK inhibited this contraction without changing [Ca2+]i. In permeabilized muscle, Ca2+ induced contraction in a concentration-dependent manner. FK (10 microM) and cAMP (1-100 microM) shifted the Ca(2+)-force curve to the higher Ca2+ levels. CCh with GTP, GTP gamma S or DPB enhanced contraction in the presence of constant level of Ca2+. Forskolin and cAMP also inhibited the enhanced contractions in the permeabilized muscle. In the permeabilized, thiophosphorylated muscle, ATP induced contraction in the absence of Ca2+. cAMP (300 microM) had no effect on this contraction. These results suggest that forskolin inhibits agonist-induced contraction in tracheal smooth muscle by multiple mechanisms of action; 1) inhibition of MLC phosphorylation by reducing Ca2+ influx and Ca2+ release, 2) inhibition of MLC phosphorylation by changing the MLC kinase/phosphatase balance, and 3) inhibition of regulatory mechanism which is not dependent on MLC phosphorylation.     

TX-1877: design, synthesis, and biological activities as a BRM-functional hypoxic cell radiosensitizer

PURPOSE: 2-Nitroimidazole acetamide TX-1877 and its derivatives (TX-1877 analogs) were designed, synthesized, and evaluated by their in vitro and in vivo radiosensitization, tumor growth control, suppression of lung metastasis, and immunopotentiation, as biological response modifier (BRM)-functional hypoxic cell radiosensitizers. MATERIALS AND METHODS: TX-1877 analogs were designed and synthesized in our laboratory. In vitro radiosensitizing ability was estimated using EMT6/KU cells under hypoxic conditions. In vivo radiosensitization, antimetastasis, and immunopotentiation were evaluated using female C3H/He mice bearing the SCCVII tumor. Days (15 or 10) after the inoculation of 10(5) SCCVII tumor cells into the hinder thigh, a drug (0.4 mg/g) was administered i.p. and local irradiation of 30 Gy was given at 30 min after its administration. Tumor growth was observed for 20 days and mice were euthanized to count the number of metastatic nodules on the surface of the lungs. Tumor tissues were extirpated and stained by the ABC method at 1, 2, and 3 weeks after treatment for immunological evaluation. RESULTS: Novel types of bifunctional radiosensitizers, TX-1877 and its analogs possessing BRM-functions (i.e., antimetastatic and immunopotentiation effects) were developed. In vitro radiosensitizing abilities of TX-1877 and its analogs, with their partition coefficient values of more than 0.050, were comparable to misonidazole (MISO) at their doses of 1 mM. Tumor regrowth was suppressed evidently 20 days after the treatment in the irradiated group with TX-1877 (TX-1877 plus R) and with KIN-806 (KIN-806 plus R). The former group reduced markedly the mean number of metastatic lung nodules regardless of radiation therapy. TX-1877 and KIN-806 plus R induced helper T lymphocytes. The TX-1877, TX-1877 plus R, KIN-806, and KIN-806 plus R enhanced macrophage infiltration for 3 weeks after treatment. CONCLUSION: TX-1877 is an excellent BRM-functional hypoxic cell radiosensitizer, expected to be useful for clinical use.     

Coupling-current loss in a multifilamentary superconducting wire with a normal-metal core

Coupling-current losses in a multifilamentary superconducting wire with a normal metal core were calculated for the case of transverse magnetic fields. The results showed that the dependence of the coupling-current loss of such a wire on the rate of field variation is markedly different from that of a wire without the core, the former being characterized by two time constants while the latter by one. The theoretical result was confirmed experimentally. It was pointed out that in the case when a wire with Cu/CuNi matrices is to be used in a rapidly changing magnet field, Cu for a stabilization should be arranged at the centre of the wire rather than at the surface of the wire in order to reduce the loss.     

E.s.r. studies of peroxy radicals in polyethylene: 2. Peroxy radicals in urea — polyethylene complexes

Temperature dependent e.s.r. spectra of peroxy radicals in urea—polyethylene complex materials (UPEC) were discussed. Peroxy radicals in UPEC were much more stable than in normal polyethylene. Change of anisotropic g-values of the radicals with temperature were investigated and it was found that the g₁-axis, which was assigned to be parallel to the chain axis, seemed to be almost unchanged throughout the temperature range in the present study, but the g₂- and g₃-axes changed drastically. Using these results, it was concluded that the main motion of the radical sites was rotation around the chain axis and this motion was found to be much faster than in normal polyethylene, which we have already studied and which we reported recently. This is a reflection of the properties of the materials studied, i.e. interaction between molecular chains in UPEC must be much weaker than in normal polyethylene because of the presence of the wall of urea molecules in the former.