Isoform-specific regulation of the lactate transporters MCT1 and MCT4 by contractile activity

Am J Physiol Endocrinol Metab. 2000 Nov;279(5):E1131-8. doi: 10.1152/ajpendo.2000.279.5.E1131.

Abstract

We examined the isoform-specific regulation of monocarboxylate transporter (MCT)1 and MCT4 expression by contractile activity in red and white tibialis anterior muscles. After 1 and 3 wk of chronic muscle stimulation (24 h/day), MCT1 protein expression was increased in the red muscles (+78%, P < 0.05). In the white muscles, MCT1 was increased after 1 wk (+191%) and then was decreased after 3 wk. In the red muscle, MCT1 mRNA accumulation was increased only after 3 wk (+21%; P < 0.05). In the white muscle, MCT1 mRNA was increased after 1 wk (+30%; P < 0.05) and 3 wk (+15%; P < 0.05). MCT4 protein was not altered in either the red or white muscles after 1 or 3 wk. MCT4 mRNA was transiently lowered (approximately 15%) in both muscles in the 1st wk, but MCT4 mRNA levels were back to control levels after 3 wk. In conclusion, chronic contractile activity induces the expression of MCT1 but not MCT4. This increase in MCT1 alone was sufficient to increase lactate uptake from the circulation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Carrier Proteins / genetics*
  • Carrier Proteins / metabolism
  • Electric Stimulation
  • Gene Expression Regulation*
  • Glycolysis
  • Male
  • Monocarboxylic Acid Transporters
  • Muscle Contraction / physiology*
  • Muscle Fibers, Fast-Twitch / metabolism
  • Muscle Proteins*
  • Oxidation-Reduction
  • RNA, Messenger / metabolism
  • Rats
  • Rats, Sprague-Dawley

Substances

  • Carrier Proteins
  • Monocarboxylic Acid Transporters
  • Muscle Proteins
  • RNA, Messenger
  • Slc16a3 protein, rat