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|a pubmed25n0738.xml
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|a (DE-627)NLM22140581X
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|a (NLM)23019727
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|a DE-627
|b ger
|c DE-627
|e rakwb
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|a chi
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100 |
1 |
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|a Chen, Chuan-xi
|e verfasserin
|4 aut
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1 |
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|a The protective effects of inhibition of c-Jun N-terminal kinase signal pathway on the intestinal barrier in rats with endotoxemia
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|c 2012
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336 |
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|a Text
|b txt
|2 rdacontent
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337 |
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|a ohne Hilfsmittel zu benutzen
|b n
|2 rdamedia
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338 |
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|a Band
|b nc
|2 rdacarrier
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500 |
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|a Date Completed 29.07.2013
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|a Date Revised 02.12.2018
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|a published: Print
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|a Citation Status MEDLINE
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|a OBJECTIVE: To examine the protective effects of inhibition of c-jun N-terminal kinase (JNK) stress signal pathway on the injured barrier in endotoxemic rats
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|a METHODS: Twenty-four male Sprague Dwaley (SD) rats were randomly divided into control group, endotoxemia model group and JNK inhibitor group (n=8 each) to receive administration of: 1 normal saline 2 ml/kg + PPCES 2.5 ml/kg [vehicle of JNK inhibitor (SP600125), control group]; 2 lipopolysaccharide (LPS) 10 mg/kg + PPCES 2.5 ml/kg (endotoxemia model group); 3 LPS 10 mg/kg + JNK inhibitor (SP600125) 10 mg/kg (JNK inhibitor group). The activity and survival rate of the rats were recorded. Ileum tissue samples were collected 12 hours after drug administration for pathological examination. Blood samples were collected at the same time for determination of concentration of D-lactate by enzyme linked immunosorbent assay (ELISA)
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|a RESULTS: Rats in control group were active normally, and there was no death. Pathological examination showed there was edema of ileal mucosa, and shortening of villus and inflammatory cell infiltration in model group as compared with control group. JNK inhibitor greatly ameliorated the lesions compared with model group. The concentration of D-lactate (µg/L) in model group was significantly higher than that in control group. (943.8 ± 439.6 vs 227.9 ± 130.0, P<.05). JNK inhibitor could decrease the plasma D-lactate concentration (637.4 ± 114.4 vs 943.8 ± 439.6, P<.05)
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|a CONCLUSION: Inhibition of the JNK stress signal pathway could attenuate the intestinal barrier injury in endotoxemic rats
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|a Journal Article
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|a Research Support, U.S. Gov't, Non-P.H.S.
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7 |
|a Anthracenes
|2 NLM
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7 |
|a pyrazolanthrone
|2 NLM
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|a 1TW30Y2766
|2 NLM
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|a Lactic Acid
|2 NLM
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|a 33X04XA5AT
|2 NLM
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|a JNK Mitogen-Activated Protein Kinases
|2 NLM
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650 |
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7 |
|a EC 2.7.11.24
|2 NLM
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700 |
1 |
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|a Ouyang, Bin
|e verfasserin
|4 aut
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700 |
1 |
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|a Lai, Jian-bo
|e verfasserin
|4 aut
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700 |
1 |
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|a Qiu, Chun-fang
|e verfasserin
|4 aut
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700 |
1 |
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|a Guan, Xiang-dong
|e verfasserin
|4 aut
|
773 |
0 |
8 |
|i Enthalten in
|t Zhongguo wei zhong bing ji jiu yi xue = Chinese critical care medicine = Zhongguo weizhongbing jijiuyixue
|d 1998
|g 24(2012), 6 vom: 07. Juni, Seite 327-9
|w (DE-627)NLM098227793
|x 1003-0603
|7 nnns
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773 |
1 |
8 |
|g volume:24
|g year:2012
|g number:6
|g day:07
|g month:06
|g pages:327-9
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|a AR
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|d 24
|j 2012
|e 6
|b 07
|c 06
|h 327-9
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