ENDOGENOUS HEME OXYGENASE/CARBON MONOXIDE SYSTEM MEDIATES LIPOPOLYSACCHARIDE-INDUCED INTUSSUSCEPTION IN RATS
Chinese Medical Sciences JournalVol. 0, Issue 2, Pages: 89-92(2000)
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ENDOGENOUS HEME OXYGENASE/CARBON MONOXIDE SYSTEM MEDIATES LIPOPOLYSACCHARIDE-INDUCED INTUSSUSCEPTION IN RATS
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CLC:R574.3
Published:2000
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ENDOGENOUS HEME OXYGENASE/CARBON MONOXIDE SYSTEM MEDIATES LIPOPOLYSACCHARIDE-INDUCED INTUSSUSCEPTION IN RATS[J]. Chinese medical sciences journal, 2000, 0(2): 89-92.
DOI:
ENDOGENOUS HEME OXYGENASE/CARBON MONOXIDE SYSTEM MEDIATES LIPOPOLYSACCHARIDE-INDUCED INTUSSUSCEPTION IN RATS[J]. Chinese medical sciences journal, 2000, 0(2): 89-92.DOI:
ENDOGENOUS HEME OXYGENASE/CARBON MONOXIDE SYSTEM MEDIATES LIPOPOLYSACCHARIDE-INDUCED INTUSSUSCEPTION IN RATS
摘要
Abstract
bjectives. To investigate the role of endogenous heme oxygenase (HO)/carbon monoxide (CO) system in regulating the process of intussusception (IN) induced by administration of lipopolysaccharide (LPS) in rats. Methods. IN model of rats were induced by lipopolysaccharide. HO activity was determined by the amount of bilirubin formation which was measured with a doublebeam spectrophotometer
and HbCO formation was measured by COoximeter. Results. The results showed that LPS (10mg/kg) caused IN in up to 40% of the rats at 6h after treatment of LPS. The incidence of IN were significantly increased by 50% (P<005) and by 832%(P<001) in HO substrate(hemeLlysinate)treated rats and in exogenous COtreated rats
respectively; but it was significantly decreased by 418%(P<005) after administration of ZnDPBG
an inhibitor of heme oxygenase (HO) activity. Furthermore
LPS increased HO activity
HbCO formation cGMP content within colic smooth muscle and the plasma level of cGMP
and these parameters were significantly elevated by 626%(P<001)
400%(P<001)
493%(P<005) and 38%(P<005)
respectively
compared with LPSnonIN rats. Conclusion. It is suggested that endogenous HO/CO system plays an important role in the process of IN induced by LPS
and inhibition of HO activity may decrease the formation of IN.