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  • 1
    ISSN: 1573-2614
    Keywords: Measurement techniques: electroencephalography ; Metabolism: hypoglycemia ; Brain: electroencephalography ; Hormones: concentrations ; Monitoring
    Source: Springer Online Journal Archives 1860-2000
    Topics: Computer Science , Medicine
    Notes: Abstract Acute insulin-induced hypoglycemia provokes changes in central nervous system activity and release of counterregulatory hormones. The clinical relationship between central nervous system activity, hormone secretion, and vital signs has not to our knowledge been previously reported. We used computerized electroencephalographic (CEEG) analysis to monitor 5 nondiabetic subjects during acute insulin-induced hypoglycemia (0.75 U/kg intravenous push). Their glucose nadir was 38±6 mg/dl (mean ± 1 SD). A three-phase pattern of change in CEEG power in response to hypoglycemia was observed: phase 1 was characterized by an increase in total CEEG power (natural log of activity = 9.1±1.3 µV2) over baseline (8.7±1.2 µV2) in the theta, delta, and beta frequency bands. This phase preceded and coincided with the glucose nadir. During phase 2, power in all frequency bands fell significantly below baseline. A nadir in CEEG power (8.0±1.6 µV2) occurred 40 to 55 minutes after insulin injection as glucose levels were rising. During phase 3 there was a return to baseline in CEEG power and frequency spectra. Heart rate increase just before phase 1; peak heart rate (91±8 beats/min) coincided with peak CEEG power and was significantly higher than basal rate (71±11,P〈0.05). A significant increase in respiratory rate occurred during phase 1 of the CEEG and persisted through phase 2. A significant decrease in mean blood pressure (nadir = 73±6 mm Hg) below preinsulin blood pressure (81±8 mm Hg,P〈0.05) coincided with the nadir of CEEG power in phase 2. Blood pressure returned to basal levels during phase 3. Peak plasma epinephrine (652±207 versus 46±30 pg/ml), norepinephrine (500±219 versus 273±107 pg/ml), and pancreatic polypeptide levels (1,023±689 versus 114±24 pg/ml) were all significantly elevated over respective basal concentrations (P〈0.05). Peak hormone levels occurred during CEEG phase 2. This study demonstrates a temporal association of changes in CEEG power, vital signs, and hormonal secretion. These techniques may be applicable for further investigation of the clinical neuroendocrinology of the response to acute hypoglycemia.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Colloid & polymer science 262 (1984), S. 788-792 
    ISSN: 1435-1536
    Keywords: Liquid crystal formation ; Poly(γ-benzyl L-glutamate) ; Aggregation ; Phase separation ; Solvent effect
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract Solvent effects on the phase separation of poly(γ-benzyl L-glutamate) to liquid crystal and isotropic solution have been observed in various helicogenic solvents. The temperature-composition phase diagrams have been determined for each solution. The critical concentrations,ν 2 * , at which the phase separation occours have been compared in various solvents. In dimethylformamide in which the polymer is molecularly dispersed, the observedν 2 * value has agreed with that calculated by Flory's theory. In some solvents in which the polymer aggregates in a head-to-tail mode such as chloroform, the observedν 2 * values have been considerably small. It is assumed that the polymer aggregates behave as longer particles than the original particles. In dioxane in which the polymer aggregates highly both in a head-to-tail and a side-by-side modes, theν 2 * value has been a little larger than that in chloroform. In this case the relationship between the aggregation and the liquid crystal formation is so complicated that further investigation is necessary. In aromatic solvents such asm-cresol that dissolves the polymer almost molecularly, theν 2 * is smaller than that in dimethylformamide. Therefore, the intermolecular interactions between the phenyl groups in the side groups of the polymer and those in solvent molecules must be considered.
    Type of Medium: Electronic Resource
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