allopurinol and Intestinal-Obstruction

allopurinol has been researched along with Intestinal-Obstruction* in 5 studies

Other Studies

5 other study(ies) available for allopurinol and Intestinal-Obstruction

ArticleYear
[Bacterial translocation under the conditions of acute bowel obstruction].
    Vestnik Rossiiskoi akademii meditsinskikh nauk, 2006, Issue:9-10

    The article is dedicated to bacterial translocation under the conditions of acute small and large bowel obstruction, studied in experiment using bacteriological methods. The degree of contamination of internal organs, blood, and peritoneal exudate in the dynamics of the pathological process was determined. The study found that the use of allopurinol, a xanthine oxidase inhibitor, reduced the intensity of bacterial translocation.

    Topics: Acute Disease; Allopurinol; Animals; Ascitic Fluid; Bacterial Translocation; Bacteriological Techniques; Blood; Enzyme Inhibitors; Female; Intestinal Mucosa; Intestinal Obstruction; Intestine, Large; Intestine, Small; Liver; Lung; Male; Rabbits; Spleen; Time Factors; Xanthine Oxidase

2006
The effect of allopurinol pretreatment on intestinal hypoperfusion encountered after correction of intestinal volvulus.
    Journal of pediatric surgery, 1996, Volume: 31, Issue:9

    After reversal of blood flow following a prolonged period of ischemia, blood flow returns for a few seconds and is reduced afterward. This is called "no-reflow phenomenon." Antioxidants such as allopurinol have been shown to prevent the occurrence of this phenomenon in organs other than the intestine. An experimental study was conducted to investigate the effect of allopurinol pretreatment on intestinal blood flow after correction of intestinal volvulus in rabbits. In group 1, baseline intestinal blood flow (IBF) was evaluated using radiolabeled red blood cells. In group 2, 720 degrees intestinal volvulus was created and IBF was evaluated 6 hours later. In group 3, intestinal volvulus was created and devolvulus was performed 6 hours later. Intraperitoneal isotonic saline was injected 60 minutes before correction of the volvulus. IBF was evaluated after correction of the volvulus. Group 4 had the same procedures as group 3, but allopurinol (200 mg/kg) was injected in place of the isotonic saline. IBF stopped 6 hours after volvulus. Compared with the baseline group, IBF was significantly lower in the group with volvulus + devolvulus (P < .01). The IBF of the allopurinol-treated group was significantly higher than that of the isotonic saline group (P < .01) and it did not differ significantly from that of the baseline group. Histopathological examination showed that intestinal volvulus leads to histological injury. The histological injury was more pronounced in the devolvulus group and was less severe in the allopurinol group in comparison to the isotonic saline pretreatment group (P < .01). It is concluded that allopurinol pretreatment prevents the intestinal hypoperfusion (no-reflow phenomenon) and histological injury encountered after correction of intestinal volvulus of 6 hours' duration.

    Topics: Allopurinol; Animals; Antioxidants; Intestinal Obstruction; Intestines; Rabbits

1996
Changes in body fluid markers in intestinal ischemia.
    Journal of pediatric surgery, 1995, Volume: 30, Issue:10

    New Zealand rabbits were assigned randomly to three groups: sham operation, intestinal simple obstruction, and strangulation obstruction. To relate possible changes in the body fluid content of biochemical markers to the strangulation process, subsequent samples of blood and peritoneal fluid, for the determination of levels of creatine kinase (CK), lactic acid (LA), xanthine oxidase (XO), and inorganic phosphate (IP), were obtained at 1-, 2-, 4-, and 6-hour intervals, and intestinal histological specimens were graded blindly. Significant increases in plasma LA (3.93 +/- 0.26 v 2.99 +/- 0.37; P < .05), peritoneal LA (5.03 +/- 1.14 V 3.33 +/- 0.86; P < .05), and CK (940 +/- 146 v 772 +/- 165, P < .05) occurred after 1 hour of ischemic injury. Except for serum CK, all parameters in the blood and peritoneal fluid in group 3 were markedly elevated within 4 hours. The serum CK remained almost unchanged throughout the 6-hour study period. The results suggest that plasma LA, peritoneal LA, and CK are sensitive indicators in the early diagnosis of bowel ischemia; the determination of both serum and peritoneal XO and IP was also helpful for early diagnosis; in contrast, serum CK was not a useful indicator. The value of any biochemical marker as an early diagnostic tool for intestinal ischemia depends not only on its quantity but also on its location and mechanism of release.

    Topics: Animals; Ascitic Fluid; Biomarkers; Creatine Kinase; Intestinal Obstruction; Intestines; Ischemia; Lactates; Lactic Acid; Phosphates; Rabbits; Xanthine Oxidase

1995
The influence of intestinal congestion on survival of preserved liver grafts in rat liver transplantation.
    Transplantation, 1994, Oct-27, Volume: 58, Issue:8

    Topics: Adenosine; Allopurinol; Animals; Glutathione; Graft Survival; Insulin; Intestinal Obstruction; Liver; Liver Transplantation; Male; Organ Preservation; Organ Preservation Solutions; Portasystemic Shunt, Surgical; Raffinose; Rats; Rats, Wistar; Shock, Septic

1994
Measurements of blood flow and xanthine oxidase activity during postischemic reperfusion of the large colon of ponies.
    American journal of veterinary research, 1994, Volume: 55, Issue:8

    To assess right colic artery blood flow and relevance of xanthine dehydrogenase/xanthine oxidase after experimentally induced strangulation obstruction and reperfusion of the colon, 5 ponies were subjected to 2.5 hours of complete ischemia of the left dorsal and ventral colons, allowed to recover from surgery, and monitored during a 48-hour reperfusion period. Five ponies were subjected to sham surgery and served as controls. All ponies had a Doppler ultrasound blood flow monitor implanted on the right colic artery near the pelvic flexure 10 to 14 days prior to the ischemic period. Colic artery blood flow was monitored prior to, during, and for 4 hours after surgery. Blood samples from the right colic artery and vein distal to the obstruction site were collected during surgery (prior to ischemia, after 1 and 2 hours of ischemia, and after 10 and 60 minutes of reperfusion) for determination of arterial and venous blood gas tensions and electrolytes. Prior to surgery, blood selenium and plasma vitamin E (alpha-tocopherol) concentrations and blood glutathione peroxidase (GPX) activity were determined to assess the status of endogenous antioxidants. Combined xanthine dehydrogenase (XDH) plus xanthine oxidase (XO) activity, and XO activity alone (nanomoles per minute per gram of tissue) were determined, using a dual-spectrophotometric technique. Xanthine dehydrogenase and oxidase activities were determined prior to ischemia, after 1 and 2 hours of ischemia, and at 1 and 48 hours after reperfusion. Median blood flow in the experimental and control groups (156 ml/min and 110 ml/min, respectively) was not statistically different before surgery, and was significantly (P < 0.02) lower in the experimental (4 ml/min) vs the control group (72.5 ml/min) during the ischemic period. Experimental ponies had significantly (P < 0.03) lower right colic artery blood flow during the 4 hours immediately after recovery from anesthesia. Significant difference was not observed in right colonic venous bicarbonate concentration between groups at any time. Median right colonic venous PCO2, pH, and standard base excess were different (P < 0.001) between groups during the ischemic period only. Median venous oxygen saturation and median venous PO2 were significantly (P < 0.001) lower in the experimental ponies at the end of 2 hours of ischemia, but were significantly (P < 0.05) increased during the reperfusion phase. Median venous potassium concentration was significantly (P < 0.01) hig

    Topics: Animals; Antioxidants; Blood Flow Velocity; Colic; Colon; Disease Models, Animal; Electrolytes; Free Radicals; Horse Diseases; Horses; Hydrogen-Ion Concentration; Intestinal Obstruction; Oxygen; Reperfusion Injury; Vascular Resistance; Xanthine Oxidase

1994