Increased mRNAs for procollagens and key regulating enzymes in rat skeletal muscle following downhill running

Citation
Xy. Han et al., Increased mRNAs for procollagens and key regulating enzymes in rat skeletal muscle following downhill running, PFLUG ARCH, 437(6), 1999, pp. 857-864
Citations number
44
Categorie Soggetti
Physiology
Journal title
PFLUGERS ARCHIV-EUROPEAN JOURNAL OF PHYSIOLOGY
ISSN journal
00316768 → ACNP
Volume
437
Issue
6
Year of publication
1999
Pages
857 - 864
Database
ISI
SICI code
0031-6768(199905)437:6<857:IMFPAK>2.0.ZU;2-H
Abstract
The purpose of the study was to investigate pre-translational regulation of collagen expression after a single bout of exercise. We analysed steady-st ate messenger ribonucleic acid (mRNA) levels for collagen types I, III and IV, alpha- and beta-subunits of prolyl 4-hydroxylase and lysyl oxidase (enz ymes modifying procollagen chains), and enzyme activity of prolyl il-hydrox ylase from rat soleus muscle (MS) and the red parts of quadriceps femoris m uscle (MQF) after 12 h and after 1, 2, 4, 7 and 14 days of downhill (-13.5 degrees) treadmill running at a speed of 17 m.min(-1) for 130 min. Histolog ical and biochemical assays revealed exercise-induced muscle damage in MQF but not MS. Steady-state mRNA levels for the alpha- and beta-subunits of pr olyl 4-hydroxylase in MQF, lysyl oxidase in MS and MQF were increased 12 h after running, whereas prolyl 4-hydroxylase activity did not increase until 2 days after exercise. The mRNA levels for the fibrillar collagens (I and III) and basement membrane type IV collagen significantly increased 1 day a nd 12 h after exertion, respectively. Peak mRNA levels were observed 2-4 da ys after running, the increases being more pronounced in MQF than in MS. No significant changes were observed in types I or III collagen at the protei n level. Strenuous downhill running thus causes an increase in gene express ion for collagen types I and III and their post-translational modifying enz ymes in skeletal muscle in a co-ordinated manner. These changes, together w ith the increased gene expression of type IV collagen, may represent the re generative response of muscle extracellular matrix to exercise-induced inju ry and an adaptive response to running exertion.