التفاصيل البيبلوغرافية
| العنوان: |
Effects of okadaic acid on rat colon. |
| المؤلفون: |
Hosokawa, Masaya, Tsukada, Hideaki, Saitou, Tatsuhiko, Kodama, Masanobu, Onomura, Masahisa, Nakamura, Hiroshi, Fukuda, Kazuhito, Seino, Yutaka, Hosokawa, M, Tsukada, H, Saitou, T, Kodama, M, Onomura, M, Nakamura, H, Fukuda, K, Seino, Y |
| المصدر: |
Digestive Diseases & Sciences; Nov1998, Vol. 43 Issue 11, p2526-2535, 10p |
| مصطلحات موضوعية: |
COLON physiology, INTESTINAL mucosa physiology, ANIMAL experimentation, ANIMALS, COLON (Anatomy), COLONOSCOPY, DIARRHEA, ELECTROPHYSIOLOGY, ENZYME inhibitors, ETHERS, INTESTINAL mucosa, LACTATE dehydrogenase, MICROSCOPY, RATS, THROMBOSIS, TIME, PHARMACODYNAMICS, ANATOMY |
| مستخلص: |
Effects of okadaic acid (OA) on mucosal damage were examined in rat colon. OA was sprinkled on rat colon mucosa under observation with an electronic-endoscopic system, and OA was also applied to the in vivo microscopic field. The OA-induced changes in transepithelial conductance (Gt) were measured by the Ussing voltage clamp technique. By endoscopic observation, the luminal sprinkling of OA (60 nmol/kg) evoked transient microthrombi in the submucosal venule, which was followed by mucosal edema. Histological study after endoscopic observation showed submucosal fluid retention, suggesting an increase of vascular permeability. The microthrombi were also detected by in vivo microscopy. By electrophysiological study after endoscopic observation with and without OA addition, the basal Gt values were 54+/-6.2 and 36.2+/-4.2 mS/cm2, respectively (P < 0.01). Furthermore in control rats, the serosal addition of OA evoked an increase in Gt in a concentration-dependent manner without increasing lactate dehydrogenase release. 2,4,6-Triaminopyrimidinium inhibited OA-induced Gt change by 60%. These results indicate that OA evokes an increase in paracellular permeability of epithelium. We conclude that the developed microthrombi are the first key event of OA-induced mucosal damage, followed by an increase in permeability in the submucosal venule and in the paracellular pathway of the epithelium. [ABSTRACT FROM AUTHOR] |
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| قاعدة البيانات: |
Complementary Index |
