Pathways of renal injury in systemic gram-negative sepsis
被引:49
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作者:
El-Achkar, T. M.
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机构:
St Louis Univ, Dept Med, St Louis, MO 63103 USA
St Louis VA Med Ctr, St Louis, MO 63103 USASt Louis Univ, Dept Med, St Louis, MO 63103 USA
El-Achkar, T. M.
[1
,2
]
Hosein, M.
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机构:
Indiana Univ, Dept Med, Div Renal, Bloomington, IN 47405 USA
Indiana Univ, Indiana Ctr Biol Microscopy, Bloomington, IN 47405 USASt Louis Univ, Dept Med, St Louis, MO 63103 USA
Hosein, M.
[3
,4
]
Dagher, P. C.
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机构:
Indiana Univ, Dept Med, Div Renal, Bloomington, IN 47405 USA
Indiana Univ, Indiana Ctr Biol Microscopy, Bloomington, IN 47405 USASt Louis Univ, Dept Med, St Louis, MO 63103 USA
Dagher, P. C.
[3
,4
]
机构:
[1] St Louis Univ, Dept Med, St Louis, MO 63103 USA
[2] St Louis VA Med Ctr, St Louis, MO 63103 USA
[3] Indiana Univ, Dept Med, Div Renal, Bloomington, IN 47405 USA
[4] Indiana Univ, Indiana Ctr Biol Microscopy, Bloomington, IN 47405 USA
Acute renal failure is a grave complication of systemic gram-negative sepsis. The pathophysiological mechanisms of sepsis leading to kidney injury result in part from systemic inflammatory and haemodynamic alterations. These are triggered by the interaction of endotoxin with Toll-like receptor 4 (TLR4) on cells of the immune system. Recently, TLR4 and other co-effector molecules were identified on renal tubular and vascular cells. Furthermore, it was demonstrated that systemic endotoxin has direct access to renal sites where these receptors are expressed. Therefore, we review data in support of this novel pathway of renal injury in sepsis, whereby systemic endotoxin causes direct injury through interactions with local epithelial and endothelial TLR4.