Effect of carperitide (alpha-human atrial natriuretic polypeptide) on the cardiovascular system in experimental animals

The cardiovascular and diuretic actions of carperitide were studied in experimental animals. Carperitide relaxed various canine arteries and veins that were contracted by high K+ or norepinephrine. Carperitide stimulated particulate guanylate cyclase from rat thoracic aortas. Carperitide had almost no effect on coronary perfusion pressure or heart rate, but caused a slight decrease in contractile force in isolated guinea pig hearts. Carperitide tended to decrease isoproterenol-induced renin release from isolated rat kidney slices and elicited decreases in angiotensin II-induced aldosterone release from bovine zona glomerulosa cells. Intravenous injection of carperitide elicited decreases in arterial blood pressure and total peripheral resistance in the anesthetized and conscious dogs. Carperitide also elicited transient increases in cardiac output and coronary blood flow followed by slight decreases in them. Intravenous infusion of carperitide elicited decreases in pulmonary capillary wedge pressure, pulmonary pressure and right atrial pressure in association with elevating plasma carperitide (ANP like immuno-reactivity) level in dogs with heart failure induced by coronary artery occlusion and saline loading. These results suggest that carperitide decreases both preload and afterload and can improve the untoward hemodynamic alterations in animals with acute experimental heart failure.     

Vapor-phase carbonylation of methanol over lead on active carbon catalyst

Lead supported on active carbon showed a catalytic activity for the vapor phase carbonylation of methanol under pressurized conditions in the presence of methyl iodide promoter.     

Immunoassay on a power-free microchip with laminar flow-assisted dendritic amplification

We demonstrate a rapid (<30 min) and ultrasensitive (sub-picomolar) immunoassay on a microchip which needs no external power sources for fluid transport. We previously reported a rapid immunoassay of human C-reactive protein (CRP) on the power-free microchip with moderate sensitivity, i.e., a limit of detection (LOD) in sub-nanomolar range, due to the lack of signal amplification. In the current work, we have improved the LOD by 3 orders of magnitude by employing dendritic amplification (DA) methods. Specifically, a sandwich immunocomplex with a biotinylated secondary antibody was constructed on the inner surface of the microchannel as described in the previous report. Onto the immunocomplex, solutions of FITC-labeled streptavidin (F-SA) and biotinylated anti-streptavidin (B-anti-SA) were supplied to grow a dendritic structure. First, we alternately supplied the two solutions for layer-by-layer growth up to three layers. As a result, we obtained an LOD of 0.21 pM with a CRP sample volume of 1.0 microL and assay time of approximately 30 min under an ordinary fluorescence microscope. Second, to reduce the number of incubation steps, we have devised a new DA method: laminar flow-assisted dendritic amplification (LFDA). In this method, F-SA and B-anti-SA were simultaneously and continuously supplied from two laminar streams formed by a Y-shaped microchannel. The immunoassay with the LFDA for 10 min (total assay time of approximately 23 min) with a CRP sample volume of 0.5 microL yielded an LOD of 0.15 pM, which is equivalent to 75 zmol. The combination of the power-free microchip and the LFDA will provide a new opportunity for ultrasensitive point-of-care testing.     

Generative adversarial network for road damage detection

Machine learning can produce promising results when sufficient training data are available; however, infrastructure inspections typically do not provide sufficient training data for road damage. Given the differences in the environment, the type of road damage and the degree of its progress can vary from structure to structure. The use of generative models, such as a generative adversarial network (GAN) or a variational autoencoder, makes it possible to generate a pseudoimage that cannot be distinguished from a real one. Combining a progressive growing GAN along with Poisson blending artificially generates road damage images that can be used as new training data to improve the accuracy of road damage detection. The addition of a synthesized road damage image to the training data improves the F‐measure by 5% and 2% when the number of original images is small and relatively large, respectively. All of the results and the new Road Damage Dataset 2019 are publicly available ( https://github.com/sekilab/RoadDamageDetector ).     

Development of transient stability controller system (TSC) based on on-line stability calculation

A new transient stability controller system (TSC) based on on-line transient stability calculation has been developed. The TSC system prevents the power system from wide-area blackout by shedding generators optimally when a serious fault occurs. This system consists of a central processing unit (TSC-P), and four local units for fault detection (TSC-C), and seventeen units for generator shedding (TSC-T). The TSC-P selects optimal generators to be shed for stabilization based on on-line transient stability calculation for contingencies at 500 kV lines and buses every five minutes. The results are transmitted to the TSC-Cs periodically. Should any fault occur, only one TSC-C will detect the fault occurrence and send control signals to the TSC-Ts which actually generate shedding signals. To realize the TSC system, essential are fast stability evaluation methods for a large number of contingencies and effective selection methods of optimal generators to be shed for stabilization. This paper presents total algorithms applied in the TSC-P, the results of algorithm verification tests using a prototype system combined with a large-scale analog simulator, and the characteristics of the actual system.     

Identification and partial characterization of a glycoprotein species with high affinity for methylmercury in peripheral nervous tissues of man and experimental animals

A small amount of a glycoprotein species (21-kDa glycoprotein) with high affinity for methylmercury (MeHg) was detected in the post-nuclear or post-mitochondrial supernatant fraction of the homogenate of rat sciatic nerve on electrophoresis and autoradiography after binding of Me203Hg to the fraction. The 21-kDa glycoprotein was also found in the subcellular fractions of mouse, hamster, guinea pig, rabbit and human peripheral nervous tissues. Experiments with the cellular fractions of the tissues revealed that the 21-kDa glycoprotein is localized mainly in the myelin fraction, whereas it was not found in the cellular fractions of brain, spinal cord and nonneural tissues, such as kidney and liver. The specific binding activity of the 21-kDa glycoprotein with MeHg was 12-15 fold that of the major myelin protein, Po. It was shown that the interaction of the 21-kDa glycoprotein with MeHg was mediated through sulfhydryl groups in experiments with iodoacetamide and dithiothreitol. The amino acid compositions of the rat and human 21-kDa glycoproteins were similar but very different from that of a typical metallothionein. The N-terminal amino acid sequences of the two components of the rat 21-kDa glycoprotein were identical to those of P0 and PMP-22, respectively. The in vitro binding of MeHg was also observed in the myelin fraction obtained from the sciatic nerves of MeHg-dosed rats.     

Methotrexate suppresses nitric oxide production ex vivo in macrophages from rats with adjuvant-induced arthritis

This review discusses the relation between by-products of drinking water chlorination and cancer in the light of present toxicological and epidemiologic evidence. During the chlorination of drinking water, a complex mixture of by-products forms from chlorine and the organic and inorganic compounds present in raw water. The quality and quantity of such compounds depend on the specific nature of the organic material in raw waters, the inorganic material in raw water, pH, temperature, other water treatment practices, and the chlorine timing and dose added. Chlorination by-products are important mainly when surface water is used for drinking water as more organic compounds are present in surface waters than in ground waters. The gastrointestinal and urinary tract are the cancer sites that are most often associated with the use of chlorinated surface water or with the quantity of chlorination by-products in the water-supply network. Yet the microbial quality of drinking water should not be compromised by excessive caution over the potential long-term effects of disinfection by-products because the risk of illness and death resulting from exposure to pathogens in untreated drinking water may be several orders of magnitude greater than the cancer risks from chlorination by-products.     

Quantum dot phosphors free from hazardous elements: Current status and prospects for established materials and new ZnTe‐based alloys

Television broadcasts are moving to a digital video format based on ultra‐high‐definition (UHD). In addition to high resolution, such UHD displays require a wide color gamut. Quantum dots (QDs) have narrow and color‐tunable emission making these unique light sources for achieving a wide color gamut. Most progress in QDs has been made based on cadmium‐containing materials, as represented by CdSe. These systems have excellent performance in terms of their narrow‐band emission and high emission quantum yield; however, the toxicity of cadmium represents a barrier to practical applications of QD displays. Over the last decade, considerable efforts have been made to develop QDs that do not contain cadmium. Some established alternative materials include InP, CuInS₂, and lead halide perovskites. In addition, ZnTe‐based alloy QDs have recently been proposed as promising green and red phosphors. Narrow‐band and green emission (30 nm of full‐width at half‐maximum at a wavelength of 535 nm) has also been reported for Zn (Te, Se) alloy QDs. In this review article, we give a brief overview of progress in established cadmium‐free QDs and describe the current status and future challenges of new cadmium‐free QDs, ZnTe‐based alloy QDs.