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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Diabetologia 12 (1976), S. 483-488 
    ISSN: 1432-0428
    Keywords: Radiolabelled streptozotocin ; metabolism ; diabetes ; urinary and biliary excretion ; liver perfusion ; nicotinamide pretreatment
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary The excretion of radioisotope following the administration of three specifically14C-labelled forms of streptozotocin was investigated in the rat using ureter and bile duct cannulation techniques. The urine collected during the first hour following the administration of the drug contained the highest proportion of injected radioactivity (approximately 34% with (3′-methyl-14C)-streptozotocin and approximately 40% each with (1-14C)- and (2′-14C)-streptozotocin. Over the entire experimental period (6 hours), approximately 70% of the injected radioactivity of (1-14C)- and (2′-14C)-streptozotocin appeared in the urine. With (3′-methyl-14C)-streptozotocin, only 53% of the injected radioactivity appeared in the urine over the same period. In contrast to the high urinary excretion, less than 3 % of the injected radioactivity from all three radiolabelled streptozotocin samples appeared in the bile. The in vivo and in vitro metabolism of streptozotocin was also investigated. In addition to substantial amounts of unchanged drug, three radiolabelled metabolites (two major and one minor) were detected in the urine during the 6 hour collection period following the administration of (1-14C)- and (2′-14C)-streptozotocin. In contrast, only unchanged (3′-methyl-14C)-streptozotocin was detected in the urine collected over the same period following the administration of the methyl labelled drug. The two major metabolites were also produced when (1-14C)- and (2′-14C)-streptozotocin were incubated with a rat liver supernatant fraction (100,000 X g). The liver was further demonstrated to be the major site of metabolism in isolated liver perfusion studies in which both (1-14C)- and (2′-14C)-streptozotocin were quantitatively converted to the two major metabolites. The two major metabolites of (1-14C)-streptozotocin, whether produced in vivo or in vitro, were chromatographically homogeneous with the two major metabolites formed from (2′-14C)-streptozotocin. Nicotinamide pretreatment had no apparent effect on the urinary excretion of streptozotocin and its metabolites.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1432-0428
    Keywords: Streptozotocin-diabetes ; autoradiography ; radioactive ; pancreas ; liver ; kidney ; blood ; metabolism ; distribution
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary The distribution and cellular accumulation, in the rat, of three specifically 14C-labelled forms of streptozotocin were investigated. A significant pancreatic accumulation of radioactivity was observed with (3′-methyl-14C)-streptozotocin only. Autoradiographic studies revealed high levels of bound radioactivity in the islet tissue following the administration of (3′-methyl-14C)-streptozotocin whereas much lower levels of radioactivity were detected in the pancreatic tissue following the administration of either (1-14C)-streptozotocin or (2′-14C)-streptozotocin. In the pancreas, the amount of radioactivity bound to islet tissue was always significantly higher than that bound to acinar tissue. In addition to the islet tissue, the kidney cortex showed a very high level of bound radioactivity after the administration of (3′-methyl-14C)-streptozotocin. The results suggest that streptozotocin is rapidly metabolised by the rat. The apparent specificity for the accumulation of radiolabel from (3′-methyl-14C)-streptozotocin suggests that a metabolite derived from the methyl bearing ureido side chain of the drug may be specifically involved in the induction of tissue damage and the consequent development of diabetes.
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 1435-1803
    Keywords: nifedipine ; coronary embolized dog ; limitation of infarct size
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary We studied the ability of nifedipine, a calcium antagonist, to limit infarct size in the closed chest, coronary embolized dog. Immediately after embolization141Ce labelled microspheres were administered into the left ventricle. Myocardium not receiving microspheres was considered to be the region at risk. The nifedipine group (10 dogs) received a bolus (16 μg/kg i.v. over 8 minutes as a loading dose) followed by continuous infusion (1,000 μg/24 hours) 10 min after embolization. The control group (9 dogs) received an equal volume of saline. Twenty-four hours after embolization the dogs were sacrificed, the heart sectioned into 4-mm slices and the slices were stained with tetrazolium to reveal the infarct. The region at risk was determined by autoradiography of the microspheres in the heart slices. Infarct and risk zone volume were determined by planimetric methods. The nifedipine group had a significantly smaller infarct volume to risk zone voluem ratio than the control group (38.7±4.7% vs. 79.5±4.3%, p〈0.001). We conclude that nifedipine produces a sustained limitation of infarct size following permanent occlusion of a dog's coronary artery.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Springer
    Basic research in cardiology 83 (1988), S. 158-166 
    ISSN: 1435-1803
    Keywords: fluoro-oleic acid ; toxicity ; toxic effects oncardiac function
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Dichapetalum toxicarium seeds contain long chain fluoro-fatty acids, particularly fluorooleic acid, which in doses as low as 10 mg/kg can cause death. We have used the rat heart both in vivo and in vitro to assess the cardiovascular effects of various doses of the fluoro-oleic acid extract of the seeds ofDichapetalum toxicarium. Intraperitoneal administration of 0.25 ml of seed extract solution/kg body weight (estimated to be equivalent to 10 mg fluoro-oleic acid/kg body weight) or 0.5 ml/kg body weight (equivalent to 20 mg fluoro-oleic acid/kg body weight) resulted in death in all animals (n−6 in each group). The mean time from administration to death was 36.4±4 h and 21.0±2 h, respectively. Death was attributable to severe bradycardia which developed progressively throughout the experiment. Thus, during the first 6 h, heart rate fell by 32.2% from 450±7 beats/min to 305±36 beats/min (p〈0.01) in the 0.25 ml/kg group and by 66±10% to 150±20 beats/min (p〈0.001) in the 0.5 ml/kg group. Administration of the extract solution alone or oleic acid alone (equivalent to 0.5 ml/kg seed extract) to control rats had no effect. Investigating the effects of the seed extract in vitro, hearts (n=6 in each group) were perfused with buffer containing 0.5 ml/l seed extract (equivalent to 20 mg fluoro-oleic acid/l) or with buffer containing extract solution alone. In control hearts, there were no changes in heart rate or LVEDP over 150 min of aerobic perfusion; there were small declines in coronary flow, LVDP and LVdP/dtmax. Perfusion with seed extract resulted in a progressive decline in heart rate which, over the first 60 min of perfusion, fell by 53±7% from its control value of 323±11 beats/min to 153±20 beats/min (p〈0.001). Similarly, significant declines in coronaryflow (fell by 53±12% over 60 min), LVDP (fell by 61±12% over 60 min) and LVdP/dtmax (fell by 63±7% over 60 min) were observed. LVEDP began to increase after 30 min and by 60 min had increased to 2.8±0.4 kPa (control value=0 kPa). Perfusion with oleic acid (20 mg/l) alone had no adverse effect on cardiac contractile function. Metabolic studies showed that the administration of the seed extract resulted in a loss of myocardial high energy phosphates. Thus, ATP and creatine phosphate fell from their control values of 20.6±0.4 and 27.8±0.6 μmol/g dry weight to 3.9±0.4 and 2.4±0.4 μmol/g dry weight (p〈0.001 in each instance), respectively. Lactic acid content increased from 1.4±0.2 to 21.7±1.4 μmol/g dry weight (p〈0.001). In conclusion, our results indicate that the fluoro-oleic acid-containing extract ofDichapetalum toxicarium exerts its toxic effects by severely reducing cardiac function. In vivo this can lead to death of the animal.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Springer
    Basic research in cardiology 91 (1996), S. 12-15 
    ISSN: 1435-1803
    Keywords: Preconditioning ; ischemia ; infarct size ; adenosine ; angioplasty
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Type of Medium: Electronic Resource
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  • 6
    ISSN: 1435-1803
    Keywords: Adenosine triphosphate (ATP) ; creatine phosphate (CP) ; contractile recovery ; rat heart ; contractile failure
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary The adenosine triphosphate (ATP) content of isolated Langendorff-perfused rat hearts may be increased by more than 40% above the normal value by a 2-h perfusion with adenosine (15 μmol/l). This metabolic manipulation was used to investigate the hypothetical relationship between total tissue ATP content and ischaemia-induced contractile failure, ischaemic contracture and post-ischaemic functional recovery. Adenosine perfused hearts were submitted to 20 min of normothermic ischaemia and reperfused for 45 min with or without adenosine. Control experiments were performed with adenosine-free preischaemic perfusion. In identically designed experiments the tissue-protective effect of diltiazem (0.5 μmol/l) was determined and compared with the experiments with adenosine. At the end of 120 min of preischaemic perfusion, the ATP content of the adenosine treated hearts was 34.3±1.8 μmol/g dry weight (control=23.6±1.9 μmol/g, p〈0.01). After a period of 20 min of normothermic ischaemia, the ATP content of the adenosine hearts decreased to 13.3± .4 μmol/g, whereas ATP fell to 8.3±1.6 μmol/g in the control hearts. The creatine phosphate (CP) levels of adenosine hearts were significantly lower than those of the control group before ischaemia, but did not show major differences following ischaemia. During ischaemia, the contractile activity measured via an intraventricular balloon catheter, as well as ischaemic contracture did not differ between the adenosine and control hearts. The inclusion of diltiazem into the perfusate significantly delayed the onset of contracture. After 45 min of reperfusion, ATP contents of adenosine and control hearts reached similar values (8.4±2.3 and 8.3±2.9 μmol/g, respectively). Inclusion of adenosine (15 μmol/l in the reperfusion perfusate of the adenosine experiments prevented a further decrease, but did not increase tissue ATP content. CP values of all groups showed a partial recovery upon reperfusion, they did not differ significantly. Contractile recovery was equal in all experimental groups except for the diltiazem treated hearts, which showed during the first 10 min of reperfusion an improved mechanical performance. It is concluded that total tissue ATP is not necessarily a good indicator of functional capabilities under conditions of normothermic ischaemia and reperfusion in the isolated rat heart.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Springer
    Basic research in cardiology 83 (1988), S. 618-625 
    ISSN: 1435-1803
    Keywords: sex differences ; immatureheart ; cardiac function ; globalischemia ; reperfusion
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Currently there is considerable interest in the metabolism of the immature myocardium and in particular the mechanisms underlying its greater tolerance to ischemia than that of the adult heart. In order to investigate whether this tolerance is sex-related, we compared the recovery of function in isolated hearts from male and female neonatal rats (three to five days old) following 60 min of normothermic global ischemia and 30 min of reperfusion (n=8 per group). The female hearts exhibited significantly better (p〈0.05) recovery of rate (81±5% vs. 65±5%) and the rate-pressure product (73±9% vs. 37±8%), and a tendency towards better recovery of contractile function (left ventricular developed pressure, 89±9% vs. 59±12%; dP/dt, 84±12% vs. 54±13%). This evidence for greater resistance of female hearts to ischemic injury was supported by a delayed onset of contracture (mean time to onset, 29.4±2.7 min vs. 24.9±2.6 min). The loss in left ventricular compliance during ischemia and reperfusion was also smaller in the female hearts (increase in left ventricular end diastolic pressure, 6.5±1.2 mm Hg vs. 13.6±3.8 mm Hg). These results suggest that there may be sex-related differences in the tolerance of immature hearts to ischemia, a factor which should be taken into account in the design and interpretation of experimental studies.
    Type of Medium: Electronic Resource
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  • 8
    ISSN: 1435-1803
    Keywords: Allopurinol ; xanthinedehydrogenase/oxidase activity ; adeninenucleotides ; myocardialprotection ; normothermicglobalischemia ; cardioplegia ; freeradicals
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Isolated working rat hearts were subjected to aerobic perfusion (25 min), cardioplegic infusion (3 min), global ischemia (30 min at 37°C) and reperfusion (35 min). Measurements of myocardial xanthine oxidase and dehydrogenase activity, together with various adenine nucleotides and metabolites, were made at defined stages of the protocol (n=6/group). Allopurinol pretreatment (20 mg/kg body wt/day for 3 days) improved the postischemic recovery of cardiac function; thus, aortic flow (a representative index) recovered to 68.8±4.2% compared with 53.2±2.3% in untreated controls (p〈0.05). In fresh tissue, allopurinol pretreatment inhibited xanthine dehydrogenase activity by 73.1% (from 11.9±0.5 to 3.2±0.8 mIU/g wet wt: p〈0.05) and xanthine oxidase activity by 95.2% (from 8.3±1.2 to 0.4±0.2 mIU/g wet wt: p〈0.05); however, this inhibition was not maintained during perfusion. During reperfusion, myocardial xanthine dehydrogenase and oxidase activity was reduced by 40–60% (p〈0.05) in both allopurinol pretreated and control hearts. Tissue content of creatine phosphate, adenosine triphosphate and catabolites, NAD and inorganic phosphate were not different in allopurinol pretreated or control hearts during either ischemia or reperfusion. This study does not support the concept that allopurinol protects the rat heart during ischemia and reperfusion by inhibition of xanthine oxidase activity or by conservation of purines. It appears that allopurinol achieves its protective effects by some, as yet undefined, mechanism.
    Type of Medium: Electronic Resource
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