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  • 1995-1999  (2)
  • 1980-1984  (1)
  • 1995  (2)
  • 1981  (1)
  • Double-blind  (1)
  • Perfused heart  (1)
  • clonidine  (1)
  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Psychopharmacology 73 (1981), S. 77-80 
    ISSN: 1432-2072
    Keywords: Double-blind ; Sulpiride ; Haloperidol ; Chronic schizophrenia ; Drug concentration ; Prolactin level ; Clinical effects
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract In a double-blind study the therapeutic efficacy of sulpiride was compared to that of haloperidol — an established neuroleptic agent. A total of 30 female patients with a diagnosis of chronic schizophrenia were initially stabilised on the dosage of haloperidol which produced optimum therapeutic response when given once or twice daily. The patients were then randomly allocated to receive either sulpiride or haloperidol over a period of 12 weeks. Plasma drug concentrations and prolactin levels were determined. Clinical effects were evaluated by Brief Psychiatric Rating Scale (BPRS), Wing Rating Scale, and Extrapyramidal Symptoms Rating Scale (EPS). A standardised side-effects checklist was used. Treatment with sulpiride was associated with a significant rise in plasma prolactin level, but paradoxically these patients had significantly reduced extrapyramidal symptoms. No significant correlation was found between plasma sulpiride concentration and prolactin level or any of the clinical variables. The study confirms the antipsychotic activity of sulpiride.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Clinical autonomic research 5 (1995), S. 171-177 
    ISSN: 1619-1560
    Keywords: clonidine ; sympathetic nervous system ; blood pressure monitoring ; hypotension
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract This study assessed the effects of clonidine on blood pressure (BP) and heart rate responses to active standing, recorded continuously using a Finapres monitor. Ten subjects were given a placebo infusion over 1 h, followed by clonidine hydrochloride 1.5 µg/kg over 2 h. During placebo and at 1, 3 and 19 h following the clonidine infusion, heart rate and blood pressure were recorded during the second half of supine rest for 10 min, active standing and quiet standing for 7 min. Clonidine did not alter the size of immediate drop in BP on standing, although the nadir was lower. BP recovery was impaired, with a loss of the usual BP overshoot in most subjects and with delays in reaching supine levels of diastolic BP (6.1 versus 9.6 s; p 〈 0.01) and systolic BP (8.1 versus 12.3 s; p 〈 0.05). The compensatory initial heart rate rise was significantly increased from 47 to 53 beats/min (p 〈 0.05), athough the peak rate reached was reduced from 114 to 104 beats/min (p 〈 0.05). These results demonstrate that impairment of central sympathetic vasomotor drive leads to a delay in BP recovery and loss of initial BP overshoot immediately after standing, together with impaired maintenance of early steady-state BP.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Journal of comparative physiology 164 (1995), S. 622-628 
    ISSN: 1432-136X
    Keywords: Protein turnover ; Normoxia ; Anoxia ; Perfused heart ; Turtle, Trachemys sp
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Abstract Protein turnover was studied under conditions of normoxia and anoxia in isolated perfused turtle (Trachemys (=Pseudemys) scripta elegans) hearts at 15 °C. Protein synthesis was measured by 3H-labelled phenylalanine incorporation into the protein pool. Protein degradation was studied using the protein synthesis inhibitor cycloheximide and measuring phenylalanine release from the heart. Heart rate, cardiac output and ventricle pressure development were unaffected by 2 h of anoxia. Protein synthesis rate was tenfold lower in turtle heart than in rat heart at their respective body temperatures. However, 1 h of anoxia did not affect the rate of protein synthesis in turle heat. RNA content of both ventricle and atria decreased after anoxic perfusion. Protein synthesis rates in atria were higher than those of ventricle under conditions of either anoxia or normoxia. Protein degradation rate did not change in cycloheximide-treated turtle hearts after 2 h of anoxia. These findings indicate that lack of oxygen per se does not affect protein turnover in the isolated perfused turtle heart. This feature presumably allows protein turnover to proceed in vivo during routine dives at elevated temperatures. Also, the turtle heart is a good model system to study the effects of anoxia on protein turnover without the potentially confounding factor of contractile failure. These hearts are very resistant to anoxia and well able to maintain contractility for extended periods of time.
    Type of Medium: Electronic Resource
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