Library

feed icon rss

Your email was sent successfully. Check your inbox.

An error occurred while sending the email. Please try again.

Proceed reservation?

Export
  • 1
    ISSN: 1432-2013
    Keywords: Key words Dynorphins ; Kappa opioid receptor ; Nicotinic receptors ; Opioids ; Patch clamp ; PC12 cells
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract  The authors studied effects of opioid receptor agonists on neuronal nicotinic-receptor-mediated current in PC12 cells using whole-cell current recording. At 1 µM, [d-Ala, N-Me, Phe, Gly-ol]- enkephalin (DAMGO), a selective µ receptor agonist, or 10 µM methionine-enkephalin, a µ and δ receptor agonist, did not inhibit the current elicited by 30 µM nicotine significantly. Dynorphin A (1–17) (0.1–1 µM), an endogenous κ receptor agonist, and U50488 (0.1–10 µM), a non-peptide selective κ receptor agonist, depressed the nicotine-induced current reversibly in a dose-dependent manner. They accelerated the current decay, resulting in greater effects on the non-desensitized current than the peak current. These effects were not affected by nor-binaltrophimine, a selective κ receptor antagonist, or by inclusion of guanosine 5′-O-(2-thiobiphosphate) (GDP[β-S]), a GTP binding protein blocker, into the pipette solution. These results demonstrate that two κ opioid receptor agonists, dynorphin A (1–17) and U50488, inhibit neuronal nicotinic-receptor-mediated current without the involvement of opioid receptors or GTP binding proteins. The acceleration of the current decay suggests a direct action on nicotinic receptors such as open channel block, or augmentation of desensitization. Modulation of neuronal nicotinic receptors by dynorphins may play a role in some areas where dynorphin release sites and neuronal nicotinic receptors are colocalized.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 2
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 34 (1987), S. 1657-1665 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: A gravimetric method was applied to determine the solubility of CO2 in poly(vinyl cyclohexanecarboxylate) below 1 atm. The temperatures were varied from 5 to 85°C, above and below the glass transition temperature. The sorption isotherms were concave to the pressure axis below Tg and they were tentatively analyzed by the dual-mode sorption model. Above Tg, the isotherms were linear and described by the Henry's law. Below 75°C, the diffusion coefficients of CO2 were also obtained from the half-time of the sorption process.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 3
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 35 (1988), S. 517-528 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Low-pressure gas permeation measurements were performed on poly(vinyl cyclohexanecarboxylate) to evaluate its transport characteristics. The transport data of CO2, O2, N2, He, and Ar, were presented as a function of temperature ranging from 15 to 85°C. The apparent transport parameters were determined by the time lag method above and below the glass transition temperature and they were compared with other polymers of similar chemical structures. The side chain of the polymer has a bulky cyclohexyl group, which seemed to increase gas diffusivity. The activation energy for diffusion seemed to be related with the polarity of side chain. The relationships between gas diffusivity, physical properties, and chemical structure were qualitatively discussed in comparison with the data on poly(vinyl benzoate) and poly(vinyl acetate).
    Additional Material: 11 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 4
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 35 (1988), S. 1715-1724 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Sorption of CO2 in poly(vinyl benzoate) was gravimetrically measured at pressures up to 1 atm. Sorption isotherms were determined above and below the glass transition temperature Tg from 5 to 85°C. The isotherms were analyzed by the dual-mode sorption model assuming that the plasticizing effect of sorbed CO2 is negligible at this pressure range. The solubilities and Henry's law dissolution parameters were compared with those obtained by the high-pressure sorption and permeation measurements. Henry's law dissolution parameters were in good agreement with one another. However, the solubilities first determined here were smaller than those determined by the high-pressure sorption experiment at the same temperature. It was clear that the Langmuir capacity of the present specimen was smaller in spite of similar high-pressure CO2 exposure. Relaxation of the polymer was expected to be one of the reasons. This expectation was confirmed from the observation and analysis of sorption isotherms after two kinds of treatments. After annealing above Tg, the Langmuir capacity was shown to be decreased to 1/2 or even to 1/3 from the sorption isotherms below 45°C. This means that the conditioning to the high-pressure CO2 surely has a large effect on the nature of glassy polymer. Just after high-pressure CO2 exposure at 25°C, increased solubility was observed. Furthermore, the slow decrease of solubility, that is, the decrease of conditioning effect, was also followed from the continual measurements at 25°C. This result reflects not only the characteristic of sorption capacity after high-pressure CO2 exposure, but also the relaxation of polymer in glassy state.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 5
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 24 (1986), S. 1525-1539 
    ISSN: 0887-6266
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: A gravimetric method for determining precisely the solubility of gases in polymers at high pressure is described. The solubilities of N2 and CO2 in low-density polyethylene (LDPE); CO2 in polycarbonate (PC); and N2, CH4, C2H6, and CO2 in polysulfone (PSUL) have been measured as a function of pressure up to 50 atm. Most of the measured sorption isotherms agreed closely with published data, but reproducible and time-dependent hysteresis in the sorption of CO2, C2H6, and CH4 in glassy polymers, PC, and PSUL, was observed in this study for the first time. Like the well known conditioning effect of high-pressure CO2 on the sorption capacity of glassy polymers, these hysteresis phenomena are believed to be due to the plasticizing effect of sorbed gases. On the basis of the current data, the dual-mode sorption model including the plasticization by sorbed gas is discussed and a primitive equation for the concentration of sorbed gases in a quasiequilibrium state of sorption or desorption is proposed.
    Additional Material: 10 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 6
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 24 (1986), S. 2107-2115 
    ISSN: 0887-6266
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The dilation of low-density polyethylene accompanied by the sorption of CO2 was measured by microscopy under pressures up to 50 atm at temperatures from 25 to 55°C. The dilatometry measurement, which is also applied to the determination of the thermal expansion coefficient, is directly performed by a cathetometer. The dilation of LDPE by sorbed CO2 is linear with concentration. The buoyancy correction is described for the CO2 sorption isotherms in LDPE. The partial molar volume of CO2 in LDPE, calculated from the dilation and the sorption isotherms, is almost independent of temperature.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 7
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 24 (1986), S. 535-547 
    ISSN: 0887-6266
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: High-pressure sorption (up to 50 atm) for CO2, N2, and Ar in poly(vinyl benzoate) (PVB) was studied at temperatures from 25 to 70°C by a gravimetric method utilizing an electromicrobalance. The results are described by Henry's law above the glass transition temperature Tg for all gases. The dual-mode sorption model, Henry's law plus a Langmuir isotherm, applies to the sorption isotherms of N2 and Ar in the glassy state, and the dual-mode parameters are given. For CO2, a new type of sorption isotherm is observed below Tg. The isotherm is concave to the pressure axis in the low-pressure region and turns into a straight line with increasing CO2 pressure which can be extrapolated back to the coordinate origin. The linear part of the isotherm is characteristic of the rubbery state, while the nonlinear part stems from glassystate behavior. The “glass transition solubility” of CO2, at which PVB film changes from the glassy to the rubbery state, decrease as the temperature increases. The disappearance of microvoids, that is, the decrease of the Langmuir capacity, may be due to a large plasticizing effect of sorbed CO2. The difference between the N2 and Ar isotherms and the CO2 isotherm is discussed from this standpoint.
    Additional Material: 10 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 8
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 26 (1988), S. 1409-1424 
    ISSN: 0887-6266
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Dilation of poly(vinyl benzoate) and poly(vinyl butyral) accompanying sorption of carbon dioxide is measured with a cathetometer under pressures up to 50 atm at 25°C. Sorption isotherms for carbon dioxide in these polymers were also determined gravimetrically. Each dilation isotherm plotted versus pressure, as well as the sorption isotherm, showed an inflection point corresponding to the glass transition of the polymer-gas system. The dilation isotherms changed their form at that point from concave to convex to the pressure axis or to a straight line. Dilation and sorption isotherms exhibited time-dependent hysteresis below the inflection point but not above the point. Partial molar volumes of carbon dioxide in polymers, which were determined from dilation and sorption data above the point, were found to be independent of concentration and larger than those below the point. The latter volumes depended on concentration. Based upon the extended dual-mode sorption concept, which takes account of plasticization of polymer by sorbed gas, a dilation model was developed. Dilation data were described well by the model.
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 9
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 28 (1990), S. 1955-1964 
    ISSN: 0887-6266
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Plasticization of poly(ethyl methacrylate) (PEMA) by CO2 is investigated by dielectric relaxation spectroscopy. The dissipation factor of a dielectric cell containing the film and air gaps is measured as a function of frequency (1-10,000 kHz) and CO2 pressure (0-60 atm) over the temperature range 35-115°C. A maximum in the frequency dependence of the dissipation factor, which is attributed to the α relaxation of PEMA, shifts to higher frequency with increasing temperature, pressure, or concentration. The apparent activation energy of the isosteric relaxation decreases from 28 to 23 kcal/mol as the concentration is increased from 0 to 90 cm3 (STP)/cm3 (polym). The relaxation peak temperature at fixed frequency decreases with increasing concentration. The effect of hydrostatic pressure on the dielectric relaxation is estimated and compared with values for the PEMA-He and PEMA-Ar systems. The plasticizing effect of sorbed CO2 is discussed on the basis of the relaxation data.
    Additional Material: 9 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 10
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 29 (1991), S. 225-234 
    ISSN: 0887-6266
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Sorption and dilation isotherms for argon in poly(ethyl methacrylate) (PEMA) are reported for pressures up to 50 atm over the temperature range 5-85°C. At temperatures below the glass transition (Tg=61°C), sorption isotherms are well described by the dual-mode sorption model; and isotherms above Tg follow Henry's law. However, isotherms for dilation due to sorption are linear in pressure at all temperatures over the range investigated. Partial molar volumes of Ar in PEMA are obtained from these isotherms. The volumes are approximately constant above Tg (about 40 cm3/mol), whereas the volumes below Tg are smaller and dependent on both temperature and concentration (19-26 cm3/mol). By analyzing the experimental data according to the dual-mode sorption and dilation model, the volume occupied by a dissolved Ar molecule and the mean size of microvoid in the glass are estimated to be 67 129 Å3, respectively. The cohesive energy density of the polymer is also estimated as 61 cal/cm3 from the temperature dependence of the dual-mode parameters.
    Additional Material: 9 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
Close ⊗
This website uses cookies and the analysis tool Matomo. More information can be found here...