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  • 1985-1989  (3)
  • Biochemistry and Biotechnology  (1)
  • Catecholamine uptake inhibitors  (1)
  • Life and Medical Sciences  (1)
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Year
  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Naunyn-Schmiedeberg's archives of pharmacology 335 (1987), S. 269-273 
    ISSN: 1432-1912
    Keywords: Guinea-pig lung ; Noradrenaline ; Catecholamine uptake inhibitors ; α-Adrenoceptors ; Phentolamine ; Prazosin
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Contractile responses of guinea-pig peripheral lung strips to noradrenaline were determined in the presence of propranolol (2.5 × 10−6 mol/l). All strips (n = 44) contracted to noradrenaline and a geometric mean EC50 of 1.4 × 10−6 mol/l (1.1 × 10−6 mol/l, 1.8 x 10−6 mol/l 95% confidence limits) was obtained. Contractions were antagonised by phentolamine (5 × 10−7−10−5 mol/l) and by prazosin (10∞−10−7 mol/l). Dose-ratios (DR) were calculated and log (DR-1) was plotted against log concentration of antagonist to yield slopes (± SE) of 0.84 ± 0.14 and 0.73 ± 0.22 respectively which were not significantly different from unity. A pA2 value (± SE) of 6.7 ± 0.2 was obtained for phentolamine and 7.5 ± 0.1 for prazosin. Yohimbine (10−7−10−5 mol/l) did not significantly affect the maximal tension generated or the EC50 values for noradrenaline. These results suggest that α1 adrenoceptors are mediating the contractile responses to noradrenaline. In the presence of cocaine (10−5 mol/l, n=18), normetanephrine (2 × 10−5 mol/l, n = 15), hydrocortisone (2.5 × 10−5 mol/l, n = 15) and normetanephrine (2 × 10−5-5 mol/l) plus cocaine (10−6 5 mol/l, n=15) pA2 values for phentolamine of 6.9, 6.7, 6.6, and 6.3 respectively were obtained. Since these pA2 values are not significantly different from 6.7, it is unlikely that this original pA2 value, which is lower than values obtained with phentolamine at α-adrenoceptors in other tissues, may be explained by neuronal or extraneuronal uptake of noradrenaline. A possible explanation may be that more than one population of α-adrenoceptors contribute to changes in tension in peripheral lung strips.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Biotechnology and Bioengineering 31 (1988), S. 628-633 
    ISSN: 0006-3592
    Keywords: Chemistry ; Biochemistry and Biotechnology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Process Engineering, Biotechnology, Nutrition Technology
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 0148-7280
    Keywords: propanediol ; dimethylsulfoxide ; ethanol ; hyaluronidase ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology
    Notes: Cumulus-intact and -denuded unfertilized oocytes from two mouse strains were exposed to 1.5 m ethanol (EtOH) or two cryoproteclant solutions, 1.5 M propanediol (PROH) or 1.5 M dimethylsulfoxide (DMSO), for 4.5 min at 27°C, and the proportion of activating or degenerating oocytes studied. Exposure to DMSO did not significantly increase activation above that of oocytes not exposed to DMSO. Treatment of oocytes in PROH resulted in the activation of up to 87% of viable oocytes. This was significantly higher (P 〈01) than in control oocytes and comparable to the rate of activation after treatment with EtOH (59-96% activation). In solutions at 1°C, 47% of control oocytes were activated, which was not significantly different from the rate of activation in EtOH (36%) or PROH (50%) at 1°C. Following treatment with PROH, up to 87% of oocytes degenerated within a period of 6 h in vitro. The age of the oocytes (h post hCG) and the time of cumulus removal with the enzyme hyaluronidase, relative to the time of exposure to the chemicals, influenced the level of degeneration in most groups. Significantly fewer oocytes degenerated when cumulus cells were removed before treatment (0-31%) than when the cumulus was left intact throughout the treatment and 6 h culture period (10-87%). Exposure to PROH at 1°C reduced oocyte degeneration to 5%. We conclude that PROH causes significantly greater losses of oocytes as a result of parthenogenetic activation and degeneration than of exposure to DMSO.
    Additional Material: 5 Tab.
    Type of Medium: Electronic Resource
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