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10.1097/00024382-200115010-00008

http://scihub22266oqcxt.onion/10.1097/00024382-200115010-00008
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11198357!ä!11198357

suck abstract from ncbi


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pmid11198357      Shock 2001 ; 15 (1): 49-55
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  • Calcium uptake by sarcoplasmic reticulum is impaired during the hypodynamic phase of sepsis in the rat heart #MMPMID11198357
  • Wu LL; Ji Y; Dong LW; Liu MS
  • Shock 2001[Jan]; 15 (1): 49-55 PMID11198357show ga
  • Alterations of the ATP-dependent Ca2+ uptake in the cardiac sarcoplasmic reticulum (SR) during the 2 hemodynamically distinct phases of sepsis were investigated. Sepsis was induced by cecal ligation and puncture (CLP). Control rats were sham-operated. The SR vesicles were isolated by sucrose gradient centrifugation. The results show that the rates of ATP-dependent Ca2+ uptake in the cardiac SR were unaffected during the early hyperdynamic phase, whereas they were decreased by 41-46% (P < 0.01) during the late hypodynamic phase of sepsis. Analysis of the kinetics of Ca2+ transport indicates that during the late phase of sepsis, the Vmax values of Ca2+ pump for ATP and Ca2+ were decreased, whereas the affinities of Ca2+ pump for ATP and Ca2+ were unaffected. Magnesium stimulated, whereas vanadate inhibited the ATP-dependent Ca2+ uptake, but the Mg2+-stimulated and the vanadate-inhibited Ca2+ uptake activities were significantly lower during the late sepsis. Phosphorylation of SR by the cAMP-dependent and the calmodulin-dependent protein kinases stimulated the ATP-dependent Ca2+ uptake in the control and the early septic experiments, whereas it failed to stimulate Ca2+ uptake in the late sepsis. The extent of the phosphorylation-stimulated Ca2+ uptake activities was reduced by 65-69% (P < 0.01) during the early sepsis, and they were completely abolished during the late sepsis. These data indicate that the ATP-dependent Ca2+ uptake in cardiac SR was impaired during the late hypodynamic phase of sepsis. The impaired Ca2+ uptake during late sepsis was associated with a defective phosphorylation of SR proteins. Because the ATP-dependent Ca2+ uptake by cardiac SR plays an important role in the regulation of contraction-relaxation coupling, our findings may contribute to the understanding of the pathogenesis of altered cardiac function during the progression of sepsis.
  • |Adenosine Triphosphate/metabolism[MESH]
  • |Animals[MESH]
  • |Biological Transport/drug effects[MESH]
  • |Calcium-Transporting ATPases/metabolism[MESH]
  • |Calcium/*pharmacokinetics[MESH]
  • |Magnesium/pharmacology[MESH]
  • |Male[MESH]
  • |Myocardium/*metabolism[MESH]
  • |Phosphorylation[MESH]
  • |Proteins/metabolism[MESH]
  • |Rats[MESH]
  • |Rats, Sprague-Dawley[MESH]
  • |Sarcoplasmic Reticulum/drug effects/*metabolism[MESH]
  • |Sepsis/metabolism/*physiopathology[MESH]


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