HOMEPRODUCTSCOMPANYCONTACTFAQResearchDictionaryPharmaSign Up FREE or Login

Induction mechanism of small intestinal lesions caused by intravenous injection of endotoxin in rats.

Abstract
The pathogenesis of intestinal damage caused by bolus intravenous injection of endotoxin (ETX; 3 mg/kg) was investigated. Administration of ETX to rats induced reddish discoloration suggestive of bleeding, increased hemoglobin amounts, and leakage of plasma protein in the intestine. However, light microscopic examination of the intestine demonstrated blood congestion of the microvessels. Plasma accumulation was partially inhibited by combined pretreatment with a histamine H1 antagonist and a serotonin (5-HT) antagonist. Neither a 5-lipoxygenase inhibitor, a soybean trypsin inhibitor, nor atropine was observed to inhibit plasma accumulation. Both the intestinal leakage of plasma and the accumulation of hemoglobin were completely inhibited by indomethacin, a selective thromboxane A synthetase inhibitor (OKY 1581), and a stable PGI2 analogue (beraprost). Intravital microscopic observation of the microvessels of the small intestinal villi demonstrated microthrombus formation within several minutes after the injection of ETX, and pretreatment with OKY 1581 attenuated the formation of microthrombus. Platelet counts decreased significantly 10 min after ETX administration, and the decrease was not inhibited by pretreatment with either OKY 1581 or beraprost. Prothrombin time (PT) and activated partial thromboplastin time (APTT) were not prolonged. These observations thus suggest that microcirculatory disturbances by platelet thrombus, which are mediated by thromboxane A2 at least in part, play an important role in ETX-induced intestinal damage.
AuthorsM Shindo, M Majima, T Ohno, K Sugimoto, T Ohwada
JournalSurgery today (Surg Today) Vol. 26 Issue 8 Pg. 610-7 ( 1996) ISSN: 0941-1291 [Print] Japan
PMID8855494 (Publication Type: Journal Article)
Chemical References
  • Cyclooxygenase Inhibitors
  • Endotoxins
  • Enzyme Inhibitors
  • Methacrylates
  • beraprost
  • Thromboxane A2
  • endotoxin, Escherichia coli
  • 2-methyl-3-(4-(3-pyridinylmethyl)phenyl)-2-propenoic acid
  • Epoprostenol
  • Thromboxane-A Synthase
  • Indomethacin
Topics
  • Animals
  • Capillary Leak Syndrome (etiology)
  • Cyclooxygenase Inhibitors (therapeutic use)
  • Endotoxins (adverse effects)
  • Enzyme Inhibitors (therapeutic use)
  • Epoprostenol (analogs & derivatives)
  • Escherichia coli
  • Gastrointestinal Hemorrhage (etiology)
  • Indomethacin (therapeutic use)
  • Intestine, Small (blood supply, drug effects)
  • Male
  • Methacrylates (therapeutic use)
  • Microcirculation
  • Platelet Activation
  • Rats
  • Rats, Sprague-Dawley
  • Shock, Septic (etiology)
  • Specific Pathogen-Free Organisms
  • Thrombosis (etiology)
  • Thromboxane A2 (physiology)
  • Thromboxane-A Synthase (antagonists & inhibitors)

Join CureHunter, for free Research Interface BASIC access!

Take advantage of free CureHunter research engine access to explore the best drug and treatment options for any disease. Find out why thousands of doctors, pharma researchers and patient activists around the world use CureHunter every day.
Realize the full power of the drug-disease research graph!


Choose Username:
Email:
Password:
Verify Password:
Enter Code Shown: