To identify the function of genes that regulate the processing of proglutelin, we performed an analysis of glup3 mutants, which accumulates excess amounts of proglutelin and lack the vacuolar processing enzyme (VPE). VPE activity in developing seeds from glup3 lines was reduced remarkably compared with the wild type. DNA sequencing of the VPE gene in glup3 mutants revealed either amino acid substitutions or the appearance of a stop codon within the coding region. Microscopic observations showed that alpha-globulin and proglutelin were distributed homogeneously within glup3 protein storage vacuoles (PSVs), and that glup3 PSVs lacked the crystalline lattice structure typical of wild-type PSVs. This suggests that the processing of proglutelin by VPE in rice is essential for proper PSV structure and compartmentalization of storage proteins. Growth retardation in glup3 seedlings was also observed, indicating that the processing of proglutelin influences early seedling development. These findings indicate that storage of glutelin in its mature form as a crystalline structure in PSVs is required for the rapid use of glutelin as a source of amino acids during early seedling development. In conclusion, VPE plays an important role in the formation of protein crystalline structures in PSVs.
Hugoniot measurements on the highly dense, pure B4C polycrystal were performed by the inclined-mirror method to study the elastoplastic transition and to search phase transition. In inclined-mirror streak photographs, the smoothly jagged structure was observed at the free-surface shape in the plastic region. The Hugoniot-elastic limit (HEL) has been determined to be approximately 19.5GPa. In the plastic region, a kink was observed at a particle velocity of around 1.26km∕s. The shock velocity (US)–particle velocity (UP) Hugoniot relations in the plastic region were given by US=3.7+5.4UPkm∕s in the Up range of 0.54–1.26km∕s and US=9.61+0.73UPkm∕s in the Up range of 1.26–4.3km∕s. The S value (0.73) in US=C0+SUP above UP=1.26km∕s is significantly small compared with the result of Vogler et al. [J. Appl. Phys. 95, 4173 (2004)], and was much smaller than those of many oxides and nitrides. This material behaved as an elastoisotropic solid above the HEL and showed a large and linear change in the pressure-density plot above 38GPa (UP=1.26km∕s), which indicated the onset of a phase transition.
Articles you may be interested inMechanical relaxation in a Zr-based bulk metallic glass: Analysis based on physical models J. Appl. Phys. 112, 033518 (2012); 10.1063/1.4745019 Shock compression response of a Zr-based bulk metallic glass up to 110 GPa
ABSTRACT-Potencyand duration of muscle relaxant activity of eperisone hydrochloride were examined after percutaneous administration in the intercollicular decerebrated rat rigidity model and compared to those of eperisone after intravenous injection. A continuous movement was loaded on the hindlimb of the rat model to maintain stable rigidity. The tonus of the hindlimb was recorded by EMG from the triceps surae and was quantified by using the public domain NIH Image program. Eperisone ointment administered percutaneously showed significant muscle relaxant activity at 8.4 cm2 (4.2 mg of eperisone)/rat. The effect was dose-dependent and lasted over 60 min. Intravenously injected eperisone showed significant activity at 1.25 mg/kg, but the decrease of tone was lost within 30 min after injection. Plasma eperisone levels were monitored in the same model, and they were well correlated to the dosage. These results suggest that per cutaneously administered eperisone is absorbed efficiently and shows potent and long-lasting muscle relax ant activity.
Pharmacokinetic parameters and bioavailability of a new cardiotonic agent, loprinone hydrochloride, in beagle dogs were determined by measuring plasma levels of loprinone after intravenous bolus and oral administration. The plasma half-life after intravenous administration of loprinone varied among individuals over the range 2.65-15.40 h. The bioavailability after oral administration of loprinone as a solution was 37.1%. Effects of enterohepatic circulation on the time-course of plasma levels after intravenous administration of the drug were also studied in bile-duct-cannulated beagle dogs. The amounts of loprinone and its glucuronide excreted in bile during 8 h after administration were 25.4 and 8.6% of the dose, respectively, indicating the possibility of enterohepatic circulation. The plasma half-life in bile-duct-cannulated beagle dogs was 1.98 h. These results indicate that the variation in the half-life in beagle dogs resulted from enterohepatic circulation and that the true half-life is about 2 h. The relative bioavailability after oral administration of the drug as a powder in a capsule compared with a solution was 95.7%. In addition, the amounts of loprinone and its glucuronide excreted in bile, and the AUC of plasma level after infusion for 30 min into the portal vein in bile-duct-cannulated beagle dogs were similar to those after bolus intravenous administration. These results show that the low bioavailability reflects incomplete absorption.
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