Source:http://linkedlifedata.com/resource/pubmed/id/10088174
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| Predicate | Object |
|---|---|
| rdf:type | |
| lifeskim:mentions | |
| pubmed:issue |
2
|
| pubmed:dateCreated |
1999-5-25
|
| pubmed:abstractText |
Ischemic preconditioning has been shown to ameliorate injury due to subsequent ischemia in several organs. However, relatively little is known about preconditioning and the kidney. To address this, rats were randomized to control (C, N = 14), 2 min of ischemic preconditioning (P2 N = 10), 3 periods of 2 min of ischemia separated by 5 min periods of reflow (P2,3 N = 7), or three 5 min periods of ischemia separated by 5 min of reflow (P5,3 N = 6) prior to 45 min of bilateral renal ischemia followed by 24 hours of reperfusion. We observed a lower serum creatinine after 24 hours of reflow in P2, P2, 3 but not P5, 3 rats compared with C. Histology was examined in the C and P2, 3 groups and demonstrated less severe injury in the P2, 3 group. To gain insight into the mechanism by which preconditioning ameliorated ischemic injury, we performed near IR spectroscopy and 31P NMR spectroscopy. Based on near IR spectroscopy, the P2, 3 group had closer coupling of cytochrome aa3 redox state with that of hemoglobin during reflow. In the 31P NMR studies, the changes in ATP and pHi were similar during ischemia, but the P2, 3 group recovered ATP and pHi faster than C. These data suggest that ischemic preconditioning may ameliorate ischemic renal injury as assessed by functional, metabolic and morphological methods. The mechanism(s) by which this occurs requires additional study.
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| pubmed:grant | |
| pubmed:language |
eng
|
| pubmed:journal | |
| pubmed:citationSubset |
IM
|
| pubmed:chemical | |
| pubmed:status |
MEDLINE
|
| pubmed:month |
Mar
|
| pubmed:issn |
0886-022X
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| pubmed:author | |
| pubmed:issnType |
Print
|
| pubmed:volume |
21
|
| pubmed:owner |
NLM
|
| pubmed:authorsComplete |
Y
|
| pubmed:pagination |
135-45
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| pubmed:dateRevised |
2010-11-18
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| pubmed:meshHeading |
pubmed-meshheading:10088174-Acute Kidney Injury,
pubmed-meshheading:10088174-Adenosine Triphosphate,
pubmed-meshheading:10088174-Animals,
pubmed-meshheading:10088174-Body Temperature,
pubmed-meshheading:10088174-Creatinine,
pubmed-meshheading:10088174-Disease Models, Animal,
pubmed-meshheading:10088174-Follow-Up Studies,
pubmed-meshheading:10088174-Hemoglobins,
pubmed-meshheading:10088174-Hydrogen-Ion Concentration,
pubmed-meshheading:10088174-Ischemia,
pubmed-meshheading:10088174-Ischemic Preconditioning,
pubmed-meshheading:10088174-Kidney,
pubmed-meshheading:10088174-Magnetic Resonance Spectroscopy,
pubmed-meshheading:10088174-Male,
pubmed-meshheading:10088174-Random Allocation,
pubmed-meshheading:10088174-Rats,
pubmed-meshheading:10088174-Rats, Sprague-Dawley,
pubmed-meshheading:10088174-Spectroscopy, Near-Infrared
|
| pubmed:year |
1999
|
| pubmed:articleTitle |
Ischemic preconditioning attenuates functional, metabolic, and morphologic injury from ischemic acute renal failure in the rat.
|
| pubmed:affiliation |
Department of Medicine, Medical College of Ohio, Toledo 43699-0008, USA.
|
| pubmed:publicationType |
Journal Article,
Comparative Study,
Research Support, U.S. Gov't, P.H.S.,
Research Support, Non-U.S. Gov't
|