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  • 5  (1)
  • 5-(p-hydroxyphenyl)-5-phenylhydantoin  (1)
  • 5-diphenylhydantoin  (1)
  • Keywords Hyperinsulinaemia  (1)
  • 1
    ISSN: 1432-0428
    Keywords: Keywords Hyperinsulinaemia ; pancreas ; transplantation ; atherosclerosis ; cholesterol.
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Hyperinsulinaemia may play a role in the development of atherosclerosis; however, the direct effect of endogenous insulin on the atherosclerotic process is not well understood. To clarify this situation we performed pancreas transplantation with systemic venous drainage in Wistar Shionogi (WS) and Spontaneous Hypertensive (SHR) rats. Both rats received syngeneic pancreaticoduodenal transplants from donor rats. SHR rats were used to observe the additive effects of both hypertension and hyperinsulinaemia on the atherosclerotic process. Peak blood insulin levels after a glucose load were approximately two times higher in transplanted rats than in non-transplanted WS and SHR rats. By contrast, there was no difference in plasma glucose responses between transplanted and non-transplanted rats. Hyperinsulinaemia was not related to dyslipidaemia and hypertension in transplanted rats. Nine months after transplantation, the cholesterol ester contents of the aortas of both WS and SHR transplanted rats were significantly higher than in the control rats (WS: 1.9 ± 1.0 vs 3.8 ± 2.1 mg/g dry tissue, p 〈 0.01; SHR: 1.7 ± 1.3 vs 3.7 ± 1.4 mg/g dry tissue, p 〈 0.05). No differences were demonstrated in the thickness of the intima or in the histology of the aortas of transplanted and control rats. To study the mechanism for cholesterol ester accumulation in the arterial wall, we measured neutral cholesterol ester hydrolase activities in vascular medial smooth muscle cells. Insulin significantly suppressed neutral cholesterol ester hydrolase activities in medial smooth muscle cells. Our results indicate that endogenous hyperinsulinaemia contributes to the development of atherosclerosis by accelerating cholesterol ester accumulation in the arterial wall. [Diabetologia (1996) 39: [1276–1283]
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    European journal of clinical pharmacology 9 (1975), S. 79-83 
    ISSN: 1432-1041
    Keywords: 5 ; 5-diphenylhydantoin ; 5-(p-hydroxyphenyl)-5-phenylhydantoin ; amobarbital ; drug elimination ; interindividual variation ; correlation studies
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Medicine
    Notes: Summary The concentration of 5,5-diphenylhydantoin (DPH) in serum was determined at selected time intervals in seven healthy male volunteers starting 10 h after an oral dose of 400 mg sodium DPH was given. The data were analyzed according to a one-compartment model assuming first-order kinetics. The mean serum half-life was 19.28 h±5.87 (SD). A positive correlation coefficient (r=0.84, p〈0.05) was found between the serum DPH half-life and the serum amobarbital half-life in the seven subjects. The urinary levels of free plus conjugated 5-(p-hydroxyphenyl)-5-phenylhydantoin were determined for 12 h periods over a minimum of two days following the 400 mg oral dose of sodium DPH. Subjects with a short DPH half-life tended to excrete in urine a greater amount ofp-HPPH as compared to subjects with a long DPH half-life. In the case of one subject, the urinary excretion ofp-HPPH plateaued five days after DPH administration and the apparent elimination half-life determined from thep-HPPH urinary excretion data was 19.16 h as compared to the value of 19.53 h calculated from the DPH serum levels.
    Type of Medium: Electronic Resource
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