EFFECTS OF FLOW AND CONTRACTION ON LACTATE TRANSPORT IN THE PERFUSED RAT HINDLIMB

Citation
Pw. Watt et al., EFFECTS OF FLOW AND CONTRACTION ON LACTATE TRANSPORT IN THE PERFUSED RAT HINDLIMB, The American journal of physiology, 267(1), 1994, pp. 50000007-50000013
Citations number
28
Categorie Soggetti
Physiology
ISSN journal
00029513
Volume
267
Issue
1
Year of publication
1994
Part
1
Pages
50000007 - 50000013
Database
ISI
SICI code
0002-9513(1994)267:1<50000007:EOFACO>2.0.ZU;2-S
Abstract
A perfused rat hindlimb preparation was used to assess the effects of perfusate flow and electrical stimulation to mimic exercise on the rat es of lactate influx (measured by a dual tracer technique with [H-3]ma nnitol as the extracellular marker) and net lactate production. The sa me perfused muscle system was also used for assessing the effects of a lpha-cyano-4-hydroxycinnamate (CIN, 15 mM), phloretin (0.6 mM), and py ruvate on tracer lactate influx. Unidirectional lactate influx, oxygen uptake (VO2), and net lactate flux were all significantly dependent o n perfusate flow rate (all P < 0.05). The hindlimb was in net lactate production at all flow rates studied. Electrical stimulation (60 Hz, 1 00 ms, 20 V trains at 0.6 min(-1)) at perfusate lactate concentration of 1 mM significantly increased the hindlimb riot from 8.0 +/- 1.1 to 16.0 +/- 2.2 ml.kg(-1).min(-1) and production of lactate from -69 +/- 31 to -823 +/- 77 nmol.min(-1).g(-1) (both P < 0.001) but did not affe ct tracer-measured unidirectional lactate influx (nonstimulated: 235.4 +/- 78.1; stimulated: 235.0 +/- 31.0 nmol.min(-1).g(-1)). At a perfus ate flow of 0.55 ml.g(-1).min(-1) the unidirectional influx of 1 mM la ctate was markedly inhibited (90 +/- 5%) by 15 mM CIN. CIN also signif icantly reduced VO2 from 6.2 +/- 0.16 to 4.45 +/- 0.57 ml.kg(-1).min(- 1) (P < 0.05, n = 5). Phloretin (0.6 mM, n = 3) had no significant eff ect on lactate influx. Varying perfusate pyruvate concentration from 5 to 50 mM inhibited tracer lactate influx equally effectively as simil ar concentrations of lactate; the affinity of the process seemed to be similar for both molecules. These results add further experimental ev idence to suggest the presence of a lactate transporter in skeletal mu scle membrane and provide additional information concerning the physio logical characteristics of lactate transport in and out of muscle.