2012•Unpublished venueRequires access

The effects and mechanism of lipopolysaccharide pretreatment on endotoxemia in rats

Kunpeng Wang

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Abstract

Objective To investigate the effects and mechanism of lipopolysaccharide(LPS) pretreatment on endotoxemia in rats.Methods Male Wistar rats were randomly divided into three groups: saline group(N,n=24),LPS-treated group(L,n=24),and LPS-pretreated group(P,n=24).Intrapreitoneal injection of LPS was given to rats in Group P at baseline and 24th hour,while NS were given to rats in Group N and Group L instead.Intravenous injections of LPS were given to rats in Group L and P for construction of endotoxemia,while NS was given to Group N.The hemodynamics was observed constantly.TNF-α and NO levels were analyzed 2,4 and 6 hours after modeling.The lung,heart,liver,kidney and small intestine tissues were stained with hemotoxylin and eosin for observation.Results The pretreatment of LPS significantly reversed the endotoxemia-induced hemodynamic change(P0.05).Significantly elevation of TNF-α and NO were revealed in Group L,when comparing with those in Group N,which were significantly attenuated by pretreatment of LPS in Group P(P0.05).Moreover,significant alleviation in LPS-induced pathological impairment in heart,lung,liver,kidney and intestine were also observed in Group P.Conclusion Pretreatment of small dose of LPS protects rats from endotoxemia via reduction of TNF-α and NO.

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Objective To investigate the effects and mechanism of lipopolysaccharide(LPS) pretreatment on endotoxemia in rats.Methods Male Wistar rats were randomly divided into three groups: saline group(N,n=24),LPS-treated group(L,n=24),and LPS-pretreated group(P,n=24).Intrapreitoneal injection of LPS was given to rats in Group P at baseline and 24th hour,while NS were given to rats in Group N and Group L instead.Intravenous injections of LPS were given to rats in Group L and P for construction of endotoxemia,while NS was given to Group N.The hemodynamics was observed constantly.TNF-α and NO levels were analyzed 2,4 and 6 hours after modeling.The lung,heart,liver,kidney and small intestine tissues were stained with hemotoxylin and eosin for observation.Results The pretreatment of LPS significantly reversed the endotoxemia-induced hemodynamic change(P0.05).Significantly elevation of TNF-α and NO were revealed in Group L,when comparing with those in Group N,which were significantly attenuated by pretreatment of LPS in Group P(P0.05).Moreover,significant alleviation in LPS-induced pathological impairment in heart,lung,liver,kidney and intestine were also observed in Group P.Conclusion Pretreatment of small dose of LPS protects rats from endotoxemia via reduction of TNF-α and NO.

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Available abstract

Objective To investigate the effects and mechanism of lipopolysaccharide(LPS) pretreatment on endotoxemia in rats.Methods Male Wistar rats were randomly divided into three groups: saline group(N,n=24),LPS-treated group(L,n=24),and LPS-pretreated group(P,n=24).Intrapreitoneal injection of LPS was given to rats in Group P at baseline and 24th hour,while NS were given to rats in Group N and Group L instead.Intravenous injections of LPS were given to rats in Group L and P for construction of endotoxemia,while NS was given to Group N.The hemodynamics was observed constantly.TNF-α and NO levels were analyzed 2,4 and 6 hours after modeling.The lung,heart,liver,kidney and small intestine tissues were stained with hemotoxylin and eosin for observation.Results The pretreatment of LPS significantly reversed the endotoxemia-induced hemodynamic change(P0.05).Significantly elevation of TNF-α and NO were revealed in Group L,when comparing with those in Group N,which were significantly attenuated by pretreatment of LPS in Group P(P0.05).Moreover,significant alleviation in LPS-induced pathological impairment in heart,lung,liver,kidney and intestine were also observed in Group P.Conclusion Pretreatment of small dose of LPS protects rats from endotoxemia via reduction of TNF-α and NO.

Key concepts: Lipopolysaccharide, Hemodynamics, Kidney, Saline, Medicine, Lung, Internal medicine, Endocrinology

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