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Conflicting evidence exists regarding the superiority of Polarized Training (POL) vs other training intensity distribution models. Compare POL vs threshold (THR) training on V̇Omax, endurance capacity (EC) and mitochondrial function. Fifteen male Wistar rats (336.1 ± 30.4 g) were divided in: POL (n = 5), THR (n = 5) or control (CON; n = 5) groups. V̇Omax (indirect calorimetry) and EC (treadmill exhaustion test) were determined at baseline four and eight-weeks of training. POL consisted of 80% running volume at 60%V̇Omax and 20% at 90%V̇Omax while THR trained only at 75%V̇Omax. Both protocols were isocaloric and performed 5d/week. All animals were housed in cages with access to running wheel to allow ad libitum activity. After training, animals were sacrificed and left ventricle (LV) myocardium, diaphragm, tibialis anterior and soleus muscles were collected for high-resolution respirometry, biochemical and histological analysis. There were no baseline differences between groups. After training V̇Omax and EC were similar between POL and THR even though THR V̇Omax was higher compared to CON. After training, there were also no significant differences in OXPHOS or any of the other major mitochondrial function markers assessed between POL and THR in any of the tissues analyzed. The expression of MFN1, MFN2, PGC-1α, TFAM, DRP1, OPA1 and TOM20 as well as the activity of citrate synthase were also similar between POL and THR in all tissues. There were no significant differences in endurance performance or markers of bioenergetic function between POL and THR after eight-weeks of training.
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http://dx.doi.org/10.1007/s13105-025-01079-6 | DOI Listing |
Acta Biochim Pol
June 2025
School of Pharmaceutical Sciences, Guizhou University, Guiyang, China.
Protein kinase C (PKC) is widely distributed in various tissues, organs, and cells. By catalyzing the phosphorylation of Ser/Thr residues on various proteins, PKC regulates the metabolism, growth, proliferation, and differentiation of multiple cells and plays a crucial role in transmembrane signal transmission. In dopamine receptor signal transduction, PKC regulates numerous physiological functions, such as dopamine release, internalization of the dopamine transporter, downregulation of dopamine receptors, etc.
View Article and Find Full Text PDFJ Physiol Biochem
May 2025
Faculty of Sport of University of Porto (FADE-UP), Research Centre in Physical Activity, Health and Leisure (CIAFEL), Porto, Portugal.
Conflicting evidence exists regarding the superiority of Polarized Training (POL) vs other training intensity distribution models. Compare POL vs threshold (THR) training on V̇Omax, endurance capacity (EC) and mitochondrial function. Fifteen male Wistar rats (336.
View Article and Find Full Text PDFMetabolites
January 2025
Sport Coaching College, Beijing Sport University, Beijing 100084, China.
Objective: This study aimed to explore the molecular response mechanisms of differential blood metabolites before and after 8 weeks of threshold and polarized training models using metabolomics technology combined with changes in athletic performance.
Methods: Twenty-four male rowers aged 14-16 were randomly divided into a THR group and a POL group (12 participants each). The THR group followed a threshold training model (72%, 24%, and 4% of training time in low-, moderate-, and high-intensity zones, respectively), while the POL group followed a polarized training model (78%, 8%, and 14% training-intensity distribution).
J Strength Cond Res
March 2025
Department of Physical Activity and Sports, Faculty of Education and Sports, University of Deusto, Bilbao, Spain.
Rivera-Köfler, T, Varela-Sanz, A, Padrón-Cabo, A, Giráldez-García, MA, and Muñoz-Pérez, I. Effects of polarized training vs. other training intensity distribution models on physiological variables and endurance performance in different-level endurance athletes: a scoping review.
View Article and Find Full Text PDFSci Adv
September 2024
Department of Molecular Biosciences, University of Texas, Austin, TX, USA.
RNA polymerase II relies on a repetitive sequence domain (YSPTSPS) within its largest subunit to orchestrate transcription. While phosphorylation on serine-2/serine-5 of the carboxyl-terminal heptad repeats is well established, threonine-4's role remains enigmatic. Paradoxically, threonine-4 phosphorylation was only detected after transcription end sites despite functionally implicated in pausing, elongation, termination, and messenger RNA processing.
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