Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
5
pubmed:dateCreated
2005-4-18
pubmed:abstractText
We examined the modifying effects of a Kunitz trypsin inhibitor (KTI) and a Bowman-Birk trypsin inhibitor (BBI), purified from soybean, as intraperitoneal (i.p.) injection and dietary supplements on bacterial lipopolysaccharide (LPS)-induced lethality in mice. We initially examined the suppressing effects of i.p. injection of KTI (50 mg/kg) and BBI (50 mg/kg) on LPS-induced lethality after i.p. injection of LPS. Furthermore, groups of female C57BL/6 were fed a basal diet (control group) or the basal diet supplemented with KTI (50 g/kg) or BBI (50 g/kg). Here, we show that i.p. and daily oral administration of KTI, but not BBI, caused a significant reduction of the LPS-induced lethality; that LPS significantly induced plasma TNF-alpha, IL-1beta, and IL-6 levels in mice after LPS challenge; that concomitant administration of KTI, but not BBI, inhibits the LPS-induced plasma levels of these cytokines; and that KTI, but not BBI, suppressed LPS-induced upregulation of cytokine expression through suppression of phosphorylation of three mitogen-activated protein (MAP) kinase pathways, ERK1/2, JNK, and p38, in peritoneal macrophages. These data allow us to speculate that i.p. injection and dietary supplementation of a soybean KTI may play a role as a potent anti-inflammatory agent by inhibiting activation of MAP kinases, leading to the suppression of cytokine expression.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
May
pubmed:issn
1073-2322
pubmed:author
pubmed:issnType
Print
pubmed:volume
23
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
441-7
pubmed:dateRevised
2006-11-15
pubmed:meshHeading
pubmed-meshheading:15834310-Administration, Oral, pubmed-meshheading:15834310-Animals, pubmed-meshheading:15834310-Anti-Inflammatory Agents, pubmed-meshheading:15834310-Blotting, Western, pubmed-meshheading:15834310-Cytokines, pubmed-meshheading:15834310-Dietary Supplements, pubmed-meshheading:15834310-Dose-Response Relationship, Drug, pubmed-meshheading:15834310-Enzyme Activation, pubmed-meshheading:15834310-Female, pubmed-meshheading:15834310-Inflammation, pubmed-meshheading:15834310-Interleukin-1, pubmed-meshheading:15834310-Interleukin-6, pubmed-meshheading:15834310-Lipopolysaccharides, pubmed-meshheading:15834310-MAP Kinase Signaling System, pubmed-meshheading:15834310-Macrophages, pubmed-meshheading:15834310-Mice, pubmed-meshheading:15834310-Mice, Inbred C57BL, pubmed-meshheading:15834310-Phosphorylation, pubmed-meshheading:15834310-Signal Transduction, pubmed-meshheading:15834310-Soybeans, pubmed-meshheading:15834310-Time Factors, pubmed-meshheading:15834310-Trypsin Inhibitor, Kunitz Soybean, pubmed-meshheading:15834310-Tumor Necrosis Factor-alpha, pubmed-meshheading:15834310-Up-Regulation
pubmed:year
2005
pubmed:articleTitle
Dietary supplementation of soybean kunitz trypsin inhibitor reduces lipopolysaccharide-induced lethality in mouse model.
pubmed:affiliation
Department of Obstetrics and Gynecology, Hamamatsu University School of Medicine, Hamamatsu, Shizuoka, 431-3192, Japan. hirokoba@hama-med.ac.jp
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't