Parkhouse W S, Dobson G P, Hochachka P W
Department of Zoology, University of British Columbia, Vancouver, Canada.
Am J Physiol. 1988 Feb;254(2 Pt 2):R302-9. doi: 10.1152/ajpregu.1988.254.2.R302.
The purpose of this investigation was to examine the fuels supporting high-intensity progressive exercise and their regulation within rainbow trout. During the sustained swim, red muscle (RM) used 97% (17.5 mumol/g) of its glycogen, whereas white muscle (WM) glycogen only declined 31% (7.3 mumol/g). During the burst swim, WM glycogen content decreased 10.4 mumol/g at a rate that exceeded the sustained swim rate by 6.2-fold. Lactate content increased 11-fold at a rate 25 times its sustained swim rate. The exhaustive swim resulted in a decrease of 36.6 mumol/g in liver glycogen, whereas WM glycogen content declined to very low values and lactate reached 43 mumol/g. RM glycogen levels remained low during these exercise bouts. Phosphocreatine (PCr)-buffered ATP declines (WM 7.3-2.7 mumol/g, RM 3.4-1.6 mumol/g) with the time course of the large ATP decreases being related to near depletion of PCr. Decreases in the total adenylate pool were compensated for by the accumulation of inosine 5'-monophosphate in both tissue types. Free ADP (ADPf) contents increased in both tissues by three- to fivefold. ATP/ADPf and cytosolic phosphorylation potentials decreased from 7- to 20-fold. Cytosolic redox potential remained relatively constant at approximately 145 within both fiber types. The changes in adenine nucleotide parameters are associated with the respective activation of the different fiber types and glycolytic flux.
本研究的目的是研究支持虹鳟高强度渐进性运动的燃料及其在虹鳟体内的调节。在持续游泳期间,红肌(RM)消耗了其糖原的97%(17.5微摩尔/克),而白肌(WM)糖原仅下降了31%(7.3微摩尔/克)。在爆发性游泳期间,WM糖原含量下降了10.4微摩尔/克,下降速率超过持续游泳速率6.2倍。乳酸含量增加了11倍,速率是持续游泳速率的25倍。力竭性游泳导致肝糖原减少36.6微摩尔/克,而WM糖原含量降至极低水平,乳酸含量达到43微摩尔/克。在这些运动过程中,RM糖原水平一直很低。磷酸肌酸(PCr)缓冲的ATP下降(WM从7.3微摩尔/克降至2.7微摩尔/克,RM从3.4微摩尔/克降至1.6微摩尔/克),且大量ATP下降的时间进程与PCr的近乎耗尽有关。两种组织类型中,总腺苷酸池的减少都通过5'-单磷酸肌苷的积累得到了补偿。两种组织中的游离ADP(ADPf)含量均增加了三到五倍。ATP/ADPf和胞质磷酸化电位下降了7到20倍。两种纤维类型中的胞质氧化还原电位在大约145时保持相对恒定。腺嘌呤核苷酸参数变化与不同纤维类型的各自激活以及糖酵解通量有关。