Publications by authors named "Anne-Kristine Meinild Lundby"

The impact of training status and sex on intrinsic skeletal muscle mitochondrial respiratory capacity remains unclear. We examined this by analysing human skeletal muscle mitochondrial respiration relative to mitochondrial volume and cristae density across training statuses and sexes. Mitochondrial cristae density was estimated in skeletal muscle biopsies originating from previous independent studies.

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Article Synopsis
  • Heat acclimation leads to an increase in plasma volume (PV) within a week, but its long-term effects on hemoglobin mass (Hb) are less clear due to previous study durations not allowing sufficient blood cell production time.
  • A study with 21 male cyclists compared exercise-heat acclimation (HEAT) in 40°C and regular cold training (CON), revealing significant increases in PV and Hb in both groups, with HEAT showing a larger increase in Hb.
  • The results suggest that while Hb slightly increased with prolonged heat training, this change may be a compensatory response linked to the initial expansion of plasma volume, although the exact mechanisms are still not fully understood.
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Elite endurance athletes possess a high capacity for whole-body maximal fat oxidation (MFO). The aim was to investigate the determinants of a high MFO in endurance athletes. The hypotheses were that augmented MFO in endurance athletes is related to concomitantly increments of skeletal muscle mitochondrial volume density (Mito ) and mitochondrial fatty acid oxidation (FAO ), that is, quantitative mitochondrial adaptations as well as intrinsic FAO per mitochondria, that is, qualitative adaptations.

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  • Carbohydrate (CHO) restricted training enhances acute training responses, but the effects of repeated CHO restriction are less understood.
  • Two studies involving endurance athletes showed that extended CHO restriction led to different metabolic responses, including increased plasma insulin and cholesterol levels in high CHO recovery groups.
  • Despite changes in blood markers and fat oxidation during the workouts, the expected improvements in cellular signaling from CHO restriction did not materialize after athletes became accustomed to this training regimen.
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Physical inactivity alters glucose homeostasis in skeletal muscle, potentially developing into overt metabolic disease. The present study sought to investigate the role of skeletal muscle capillarization in glucose tolerance and insulin sensitivity (IS) using a classic human model of physical inactivity. Thirteen healthy males (age = 23 ± 2 years) underwent 4 days of full-time supervised and diet-controlled bed rest.

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New Findings: What is the central question of this study? Females rely to a greater extent than males on fat oxidation during exercise. Whether any difference in skeletal muscle mitochondrial phenotype and oxidative capacity contributes to this sexual dimorphism remains incompletely explored. What is the main finding and its importance? Female prioritization of fat during exercise occurs in parallel to augmented mitochondrial volume density and intrinsic fatty acid and lactate oxidation in skeletal muscle fibres compared with males, independently of aerobic exercise capacity.

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Arterial distensibility, an independent predictor of cardiovascular events, is transiently increased with acute hyperglycemia (AHG) in healthy individuals. Whether this response interacts with physical inactivity remains unknown. We examined the effects of short-term bed rest (BR) on the response of carotid artery distensibility (CD) to AHG, and the influence of underlying changes in insulin resistance and blood volume.

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The purpose of the present study was to characterize the progression of red blood cell volume (RBCV) expansion and potential volumetric and endocrine regulators of erythropoiesis during endurance training (ET). Nine healthy, untrained volunteers (age = 27 ± 4 yr) underwent supervised ET consisting of 3-4 × 60 min cycle ergometry sessions per week for 8 wk. Plasma volume (PV), RBCV, and overnight fasting hematological markers were determined before and at , , and of ET.

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Article Synopsis
  • - The study aimed to evaluate how differences in estimating blood volume compartments (like plasma or red cell volume) can occur when using methods based on blood measurements, like venous haematocrit, which might introduce errors due to higher whole body haematocrit levels.
  • - Four methods were tested: carbon monoxide (CO) re-breathing for hemoglobin mass, indocyanine green (ICG) for plasma volume, and sodium fluorescein (SoF) for red blood cell volume. Results showed no significant difference between ICG and CO re-breathing estimates when a correction factor was applied, while SoF provided lower RBC volume values than CO re-breathing.
  • - Although CO re-b
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Introduction: The carbon monoxide (CO) rebreathing method used for the determination of haemoglobin mass (Hb ) is associated with blood sample analysis (in this study: Radiometer ABL800). As an alternative hereto the aim of the present study was to evaluate the use of a portable and non-invasive CO pulse oximeter (Rad-57).

Method: With simultaneous determination of CO in the circulation by ABL800 (%HbCO) and Rad-57 (SpCO), Hb and blood volume (BV) were determined in duplicates in 24 volunteers.

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Anemia of CKD seems to be related to impaired production of renal erythropoietin (Epo). The glycosylation pattern of Epo depends on the synthesizing cell and thus, can indicate its origin. We hypothesized that synthesis of Epo from nonkidney cells increases to compensate for insufficient renal Epo production during CKD.

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The role of hypoxia on skeletal muscle mitochondria is controversial. Studies superimposing exercise training on hypoxic exposure demonstrate an increase in skeletal muscle mitochondrial volume density (Mito(VD)) over equivalent normoxic training. In contrast, reductions in both skeletal muscle mass and Mito(VD) have been reported following mountaineering expeditions.

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The membrane-assisted isoform immunoassay (MAIIA) quantitates erythropoietin (EPO) isoforms as percentages of migrated isoforms (PMI). We evaluated the effect of recombinant human EPO (rhEPO) on the distribution of EPO isoforms in plasma in a randomized, placebo-controlled, double-blinded, cross-over study. 16 healthy subjects received either low-dose Epoetin beta (5000 IU on days 1, 3, 5, 7, 9, 11 and 13); high-dose Epoetin beta (30.

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Purpose: Erythropoietin (EPO) is mainly synthesized within renal peritubular fibroblasts, and also other tissues such as the liver possess the ability. However, to what extent non-kidney produced EPO contributes to the hypoxia-induced increase in circulating EPO in adult humans remains unclear.

Methods: We aimed to quantify this by assessing the distribution of EPO glycoforms which are characterized by posttranslational glycosylation patterns specific to the synthesizing cell.

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