Literature DB >> 8342699

Anoxia-tolerant hepatocytes: model system for study of reversible metabolic suppression.

L T Buck1, S C Land, P W Hochachka.   

Abstract

Chrysemys picta bellii is well known for its ability to survive extended anoxic periods and has been widely used as a model system to study anoxic metabolism. Described here is a method for the isolation of anoxia-tolerant hepatocytes from this species. Freshly isolated hepatocytes were determined to be viable based on trypan blue exclusion, gluconeogenic capacity from [14C]lactate, responsiveness to epinephrine and glucagon, and maintenance of cellular adenylate concentrations. Under anoxic conditions for 10 h there was no significant increase in cell staining and no decrease in cellular ATP concentration. Furthermore, the addition of cyanide at the 5-h mark did not result in any significant differences in these parameters; however, iodoacetate added at this time caused trypan blue staining to increase and ATP concentrations to fall. The rate of glucose production from the cells was threefold greater under anoxic than normoxic conditions, underscoring the important role of the liver in supplying substrate during anoxia. From the rate of O2 consumption and rate of lactate production under anaerobic conditions, ATP turnover rates were calculated to be 68.4 +/- 7.2 and 6.5 +/- 0.43 mumol ATP.g-1.h-1, respectively; this corresponds to a 90% decrease in metabolic rate during anoxia. Within a cellular system such as this the more complex regulatory mechanisms involved in a large coordinated reduction in metabolism can be probed.

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Year:  1993        PMID: 8342699     DOI: 10.1152/ajpregu.1993.265.1.R49

Source DB:  PubMed          Journal:  Am J Physiol        ISSN: 0002-9513


  10 in total

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Authors:  Joseph Y Cheung; Salim Merali; JuFang Wang; Xue-Qian Zhang; Jianliang Song; Carmen Merali; Dhanendra Tomar; Hanning You; Annick Judenherc-Haouzi; Philippe Haouzi
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3.  Evolution of the oxygen sensitivity of cytochrome c oxidase subunit 4.

Authors:  K M Kocha; K Reilly; D S M Porplycia; J McDonald; T Snider; C D Moyes
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4.  Transformation to ischaemia tolerance of frog brain function corresponds to dynamic changes in mRNA co-expression across metabolic pathways.

Authors:  Min Hu; Joseph M Santin
Journal:  Proc Biol Sci       Date:  2022-07-27       Impact factor: 5.530

Review 5.  Hibernating without oxygen: physiological adaptations of the painted turtle.

Authors:  Donald C Jackson
Journal:  J Physiol       Date:  2002-09-15       Impact factor: 5.182

6.  A heme-protein-based oxygen-sensing mechanism controls the expression and suppression of multiple proteins in anoxia-tolerant turtle hepatocytes.

Authors:  S C Land; P W Hochachka
Journal:  Proc Natl Acad Sci U S A       Date:  1995-08-01       Impact factor: 11.205

7.  The role of DNA methylation during anoxia tolerance in a freshwater turtle (Trachemys scripta elegans).

Authors:  Sanoji Wijenayake; Kenneth B Storey
Journal:  J Comp Physiol B       Date:  2016-02-03       Impact factor: 2.200

8.  Endothelial cell tolerance to hypoxia. Potential role of purine nucleotide phosphates.

Authors:  A V Tretyakov; H W Farber
Journal:  J Clin Invest       Date:  1995-02       Impact factor: 14.808

9.  Mitochondrial matrix pH acidifies during anoxia and is maintained by the F1Fo-ATPase in anoxia-tolerant painted turtle cortical neurons.

Authors:  Peter John Hawrysh; Leslie Thomas Buck
Journal:  FEBS Open Bio       Date:  2019-03-14       Impact factor: 2.693

10.  Anoxia-induced changes in reactive oxygen species and cyclic nucleotides in the painted turtle.

Authors:  Matthew Edward Pamenter; Michael David Richards; Leslie Thomas Buck
Journal:  J Comp Physiol B       Date:  2007-03-09       Impact factor: 2.230

  10 in total

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