2011•Zhongguo bingli shengli zazhiRequires access

Propofol inhibits activation of p38 MAPK in rat brain tissues with LPS-induced brain injury

Deng Bi-gao

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Abstract

AIM: To investigate the effects of propofol on lipopolysaccharide(LPS)-induced activation of p38 mitogen-activated protein kinase(p38 MAPK) and inducible nitric oxide synthase(iNOS) in brain tissues of rats.METHODS: Sprague-Dawley rats of both sexes were randomly divided into 3 groups(n=24 each): control group,LPS group and LPS+propofol group.The models of LPS-induced brain injury were established by injecting LPS(1 mg/kg) via left internal carotid artery in LPS group.Propofol(100 mg/kg) was given intraperitoneally immediately after the LPS was given in LPS+propofol group.The same volume of normal saline was given to the rats in control group.The rats were decapitated 6 h,24 h,48 h and 72 h after administration.The brains were immediately isolated to detect the water content,activation of p38 MAPK and the exepression of iNOS protein.Meanwhile,the pathological changes were observed under light microscope.RESULTS: The water content of the brain was higher in LPS group than that in control group.The protein levels of phosphorylated p38 MAPK(p-p38 MAPK) and iNOS in LPS group increased 6 h after LPS administration,reached the peak at 24 h,and still higher than those in control group at 48 h and 72 h(P0.05).The levels of those indexes were all lower in LPS+propofol group at various time points than those in corresponding LPS group(P0.05).The pathological changes were slighter than those in LPS group.The water content of the brain was positively correlated with the levels of p-p38 MAPK and iNOS(r=0.603,r=0.727,P0.05).CONCLUSION: Propofol attenuates LPS-induced brain injury by inhibiting the activation of p38 MAPK and down-regulating iNOS expression.

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AIM: To investigate the effects of propofol on lipopolysaccharide(LPS)-induced activation of p38 mitogen-activated protein kinase(p38 MAPK) and inducible nitric oxide synthase(iNOS) in brain tissues of rats.METHODS: Sprague-Dawley rats of both sexes were randomly divided into 3 groups(n=24 each): control group,LPS group and LPS+propofol group.The models of LPS-induced brain injury were established by injecting LPS(1 mg/kg) via left internal carotid artery in LPS group.Propofol(100 mg/kg) was given intraperitoneally immediately after the LPS was given in LPS+propofol group.The same volume of normal saline was given to the rats in control group.The rats were decapitated 6 h,24 h,48 h and 72 h after administration.The brains were immediately isolated to detect the water content,activation of p38 MAPK and the exepression of iNOS protein.Meanwhile,the pathological changes were observed under light microscope.RESULTS: The water content of the brain was higher in LPS group than that in control group.The protein levels of phosphorylated p38 MAPK(p-p38 MAPK) and iNOS in LPS group increased 6 h after LPS administration,reached the peak at 24 h,and still higher than those in control group at 48 h and 72 h(P0.05).The levels of those indexes were all lower in LPS+propofol group at various time points than those in corresponding LPS group(P0.05).The pathological changes were slighter than those in LPS group.The water content of the brain was positively correlated with the levels of p-p38 MAPK and iNOS(r=0.603,r=0.727,P0.05).CONCLUSION: Propofol attenuates LPS-induced brain injury by inhibiting the activation of p38 MAPK and down-regulating iNOS expression.

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Available abstract

AIM: To investigate the effects of propofol on lipopolysaccharide(LPS)-induced activation of p38 mitogen-activated protein kinase(p38 MAPK) and inducible nitric oxide synthase(iNOS) in brain tissues of rats.METHODS: Sprague-Dawley rats of both sexes were randomly divided into 3 groups(n=24 each): control group,LPS group and LPS+propofol group.The models of LPS-induced brain injury were established by injecting LPS(1 mg/kg) via left internal carotid artery in LPS group.Propofol(100 mg/kg) was given intraperitoneally immediately after the LPS was given in LPS+propofol group.The same volume of normal saline was given to the rats in control group.The rats were decapitated 6 h,24 h,48 h and 72 h after administration.The brains were immediately isolated to detect the water content,activation of p38 MAPK and the exepression of iNOS protein.Meanwhile,the pathological changes were observed under light microscope.RESULTS: The water content of the brain was higher in LPS group than that in control group.The protein levels of phosphorylated p38 MAPK(p-p38 MAPK) and iNOS in LPS group increased 6 h after LPS administration,reached the peak at 24 h,and still higher than those in control group at 48 h and 72 h(P0.05).The levels of those indexes were all lower in LPS+propofol group at various time points than those in corresponding LPS group(P0.05).The pathological changes were slighter than those in LPS group.The water content of the brain was positively correlated with the levels of p-p38 MAPK and iNOS(r=0.603,r=0.727,P0.05).CONCLUSION: Propofol attenuates LPS-induced brain injury by inhibiting the activation of p38 MAPK and down-regulating iNOS expression.

Key concepts: Propofol, Lipopolysaccharide, p38 mitogen-activated protein kinases, MAPK/ERK pathway, Nitric oxide synthase, Endocrinology, Nitric oxide, Internal medicine

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