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991.
Toshikazu Suzuki Mayumi Nagata Natsuko Kagawa Shiori Takano Nahrowi Jun Nomura 《Molecules (Basel, Switzerland)》2021,26(21)
Fruit peels, pericarps, or rinds are rich in phenolic/polyphenolic compounds with antioxidant properties and potentially beneficial effects against obesity and obesity-related non-communicable diseases. This study investigated the anti-obesity effects of matoa (Pometia pinnata) and salak (Salacca zalacca) fruit peel. Neither matoa peel powder (MPP) nor salak peel powder (SPP) affected the body weight, visceral fat weight, or serum glucose or lipid levels of Sprague–Dawley rats when included as 1% (w/w) of a high-fat diet (HFD). However, MPP significantly decreased the hepatic lipid level. MPP at a dose of 3% (w/w) of the HFD decreased body weight, visceral fat, and serum triglyceride levels as well as the hepatic lipid content. The inhibitory effect of MPP on hepatic lipid accumulation was not enhanced when its concentration was increased from 1% to 3% of the HFD. The anti-obesity effect of matoa was partly explained by the inhibitory effect of the matoa peel extract on fatty acid-induced secretion of ApoB-48 protein, a marker of intestinal chylomicrons, in differentiated Caco-2 cell monolayers. We identified hederagenin saponins that are abundant in MPP as potential anti-obesity substances. These results will contribute towards the development of functional foods with anti-obesity effects using the matoa fruit peel. 相似文献
992.
A. Uedono R. Suzuki T. Ohdaira T. Mikado S. Tanigawa M. Ban M. Kyoto T. Uozumi 《Journal of Polymer Science.Polymer Physics》2000,38(1):101-107
Open spaces and relaxation processes in the subsurface region of isotactic polypropylene were investigated by monoenergetic positron beams. From measurements of the lifetime spectra of positrons, the size of the open spaces in the subsurface region (≤ 0.2 μm) was found to be larger than that in the bulk; their differences were estimated as 20% at 295 K and 10% at 395 K. From conventional positron annihilation experiments, the glass‐transition temperatures, Tg (upper)and Tg(lower) were determined as 306 K and 278 K, respectively. These transition temperatures were associated with the onset temperatures of the molecular motions under the constraint imposed by crystalline regions and those free from the constraint, respectively. In the subsurface region, although the onset temperatures of the molecular motions were close to those in the bulk, the molecular motions above Tg (lower) were found to be suppressed. The annihilation characteristics of positrons with different implantation energies were also discussed. © 2000 John Wiley & Sons, Inc. J Polym Sci B: Polym Phys 38: 101–107, 2000 相似文献
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Akihiro Suzuki Yoshinori Sato Toshio Kunugi 《Journal of Polymer Science.Polymer Physics》1998,36(3):473-481
A continuous zone-drawing/zone-annealing method was applied to poly(ethylene terephthalate) fibers in order to improve their mechanical properties. Apparatus used for this treatment was assembled in our laboratory. The continuous zone-drawing treatment was carried out at a drawing temperature of 103°C under an applied tension of 6.6 MPa to fully orient amorphous chains in the drawing direction without inducing thermal crystallization. The continuous zone-annealing treatment was carried out twice at an annealing temperature of 160°C under 102.2 MPa and at 183°C under 161.1 MPa to crystallize the highly oriented amorphous chains. The fiber was continuously drawn and annealed at a rate of 420 mm/min. The fiber obtained had a birefringence of 0.260, a degree of crystallinity of 55%, a tensile modulus of 18 GPa, and a storage modulus of 21 GPa at 25°C. Despite the large difference in the treating speed between the continuous zone-annealing and zone-annealing, their values are approximately equal to those of the zone-annealed PET fiber that was reported previously. © 1998 John Wiley & Sons, Inc. J Polym Sci B: Polym Phys 36: 473–481, 1998 相似文献
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Naofumi Nakamura Kimihiro Suzuki 《Journal of polymer science. Part A, Polymer chemistry》1997,35(9):1719-1731
A kinetic study was carried out on the acetalization reaction of 1,3-butanediol, as a model compound for poly(vinyl alcohol) (PVA), in water, under acidic conditions. Since these equilibrium constants of ketalization reaction of 1,3-butanediol and ethylene glycol are so small, the kinetic parameters were estimated from the hydrolysis reactions of the corresponding ketals. It was made clear that these reactions proceed in the reversible bimolecular reaction, and the heat of reaction and activation energy are nearly equal to that of PVA. The rate constants of hydrolysis reaction (k′s) of model compounds were calculated on the basis of value of acetone ketal, Hammett-Taft's equation log k′s/k′so – 0.54(n – 6) = ρ*σ* was established, and the value of ρ* was obtained (3.60), which coincided with the value of PVA. Therefore, it was made clear that the hydrolysis reactions of acetals and ketals are electrophilic reaction (SE II reaction) and the step of rate determination is the formation of hemiacetal and hemiketal. The rate constants of hydrolysis reaction of 1,3-butanediol acetals and ketals were approximately 10–20 larger, and those of ethylene glycol were approximetly 50–80 larger except for ketals, and those of ethanol were roughly 2000–10,000 larger compared with that of high-molecular weight compound (PVA). It can be well explained that these differences in the rate constant depend on their entropy and the mobility of molecules. © 1997 John Wiley & Sons, Inc. J Polym Sci A: Polym Chem 35 : 1719–1931, 1997 相似文献
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