Physiologia
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2673-9488

Physiologia ◽  
2022 ◽  
Vol 2 (1) ◽  
pp. 1-19
Author(s):  
Dulce E. Alarcón-Yaquetto ◽  
Ramón Figueroa-Mujica ◽  
Valeria Valverde-Bruffau ◽  
Cinthya Vásquez-Velásquez ◽  
Juan José Sánchez-Huamán ◽  
...  

(1) Background: Current diagnosis of anemia in high altitude populations uses an adjustment of observed hemoglobin (Hb) values. Such an approach has been challenged by findings in different populations in Tibet, Ethiopia and the Andes as inappropriate, as it might incorrectly classify an individual with complete iron stores as anemic. We aimed to assess the suitability of this approach in adult men and women from Cusco, Peru (3400 m); (2) Methods: Complete blood count and iron status biomarkers were measured in 345 subjects (189 females and 156 males), iron status biomarkers were quantified with enzyme-linked immunoassays; (3) Results: Anemia prevalence was overestimated when the altitude-adjustment factor was applied. Hematological parameters were better correlated to iron status biomarkers in the non-adjusted anemia category. When stratified by sex, only women showed a significant association between Hb and other hematological parameters with iron storage and availability (Hepcidin and TFR-F); (4) Conclusion: The prevalence of anemia is overestimated with current guidelines. The rate of anemia using non-adjusted Hb values is more closely related to the rates of anemia or iron deficiency when used hematological parameters, markers of iron status, and measurements of hepcidin and erythropoietin. Sex differences related to iron status were observed, suggesting that men are at a higher risk of iron overload than women at high altitudes. It could be highlighted that a personalized approach is important when assessing a subject, taking in to account hematological parameters as well as origin (Southern Andean or other).


Physiologia ◽  
2021 ◽  
Vol 1 (1) ◽  
pp. 22-33
Author(s):  
Shelby C. Osburn ◽  
Christopher G. Vann ◽  
David D. Church ◽  
Arny A. Ferrando ◽  
Michael D. Roberts

Muscle protein synthesis and proteolysis are tightly coupled processes. Given that muscle growth is promoted by increases in net protein balance, it stands to reason that bolstering protein synthesis through amino acids while reducing or inhibiting proteolysis could be a synergistic strategy in enhancing anabolism. However, there is contradictory evidence suggesting that the proper functioning of proteolytic systems in muscle is required for homeostasis. To add clarity to this issue, we sought to determine if inhibiting different proteolytic systems in C2C12 myotubes in conjunction with acute and chronic leucine treatments affected markers of anabolism. In Experiment 1, myotubes underwent 1-h, 6-h, and 24-h treatments with serum and leucine-free DMEM containing the following compounds (n = 6 wells per treatment): (i) DMSO vehicle (CTL), (ii) 2 mM leucine + vehicle (Leu-only), (iii) 2 mM leucine + 40 μM MG132 (20S proteasome inhibitor) (Leu + MG132), (iv) 2 mM leucine + 50 μM calpeptin (calpain inhibitor) (Leu + CALP), and (v) 2 mM leucine + 1 μM 3-methyladenine (autophagy inhibitor) (Leu + 3MA). Protein synthesis levels significantly increased (p < 0.05) in the Leu-only and Leu + 3MA 6-h treatments compared to CTL, and levels were significantly lower in Leu + MG132 and Leu + CALP versus Leu-only and CTL. With 24-h treatments, total protein yield was significantly lower in Leu + MG132 cells versus other treatments. Additionally, the intracellular essential amino acid (EAA) pool was significantly greater in 24-h Leu + MG132 treatments versus other treatments. In a follow-up experiment, myotubes were treated for 48 h with CTL, Leu-only, and Leu + MG132 for morphological assessments. Results indicated Leu + MG132 yielded significantly smaller myotubes compared to CTL and Leu-only. Our data are limited in scope due to the utilization of select proteolysis inhibitors. However, this is the first evidence to suggest proteasome and calpain inhibition with MG132 and CALP, respectively, abrogate leucine-induced protein synthesis in myotubes. Additionally, longer-term Leu + MG132 treatments translated to an atrophy phenotype. Whether or not proteasome inhibition in vivo reduces leucine- or EAA-induced anabolism remains to be determined.


Physiologia ◽  
2021 ◽  
Vol 1 (1) ◽  
pp. 12-12
Author(s):  
Agata Kolomanska

One of the top four scholarly journal publishers in the world [...]


Physiologia ◽  
2021 ◽  
Vol 1 (1) ◽  
pp. 3-11
Author(s):  
Dimitris Karampelas ◽  
Konstantinos Antonopoulos ◽  
Yiannis Michailidis ◽  
Michalis Mitrotasios ◽  
Athanasios Mandroukas ◽  
...  

Caffeine and nitrates have both been reported to enhance performance in power efforts; however, it is not clear which supplement is most effective. The aim of this study was to compare the effects of caffeine and nitrates on the performance of semi-professional soccer players during different fitness tests. Ten male soccer players in a randomized crossover design were assigned to receive caffeine (5 mg/kg body mass) (CG), nitrate ((250 mL/150 mg of NO3−) (NG), or a placebo (PG) on three different occasions. In each treatment, the participants performed the following tests: 10 m and 30 m sprints, the Illinois agility test, a countermovement jump test, a squat jump test, and a repeated sprint test (6 × 40 m). Caffeine boosted performance in jumps (CMJ: CGvsPG, p = 0.018; SJ: CGvsPG, p = 0.045 and CGvsNG, p = 0.001) and limited the decrease in performance in the RSA test (CGvsPG, p = 0.012). Nitrates limited the decrease in performance in the RSA test (NGvsPG, p = 0.035). In conclusion, the two supplements limited the decrease in performance in the test of repeated sprints, with caffeine showing a greater effect. Among the other tests, only caffeine improved performance, and only in the jumps. Thus, we can conclude that supplementation with caffeine 1 h before these kinds of activities at a dosage of 5 mg/kg of body weight can enhance performance.


Physiologia ◽  
2021 ◽  
Vol 1 (1) ◽  
pp. 1-2
Author(s):  
Philip J. Atherton

Physiologia (the Latin origins of Physiology, ISSN 2673-9488), is a new journal aimed at publishing original and review articles demonstrating conceptual advances across the realms of physiology [...]


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