Your browser doesn't support javascript.
loading
Functional and Morphological Differences of Muscle Mitochondria in Chronic Fatigue Syndrome and Post-COVID Syndrome.
Bizjak, Daniel Alexander; Ohmayer, Birgit; Buhl, Jasmine Leonike; Schneider, Elisabeth Marion; Walther, Paul; Calzia, Enrico; Jerg, Achim; Matits, Lynn; Steinacker, Jürgen Michael.
Afiliación
  • Bizjak DA; Division of Sports and Rehabilitation Medicine, University Hospital Ulm, 89075 Ulm, Germany.
  • Ohmayer B; Division of Sports and Rehabilitation Medicine, University Hospital Ulm, 89075 Ulm, Germany.
  • Buhl JL; Division of Sports and Rehabilitation Medicine, University Hospital Ulm, 89075 Ulm, Germany.
  • Schneider EM; Clinic of Anaesthesiology and Intensive Care Medicine, University Hospital Ulm, 89081 Ulm, Germany.
  • Walther P; Central Facility for Electron Microscopy, Ulm University, 89081 Ulm, Germany.
  • Calzia E; Institute for Anaesthesiologic Pathophysiology and Process Engineering, Ulm University, 89081 Ulm, Germany.
  • Jerg A; Division of Sports and Rehabilitation Medicine, University Hospital Ulm, 89075 Ulm, Germany.
  • Matits L; Division of Sports and Rehabilitation Medicine, University Hospital Ulm, 89075 Ulm, Germany.
  • Steinacker JM; Clinical & Biological Psychology, Institute of Psychology and Education, Ulm University, 89081 Ulm, Germany.
Int J Mol Sci ; 25(3)2024 Jan 30.
Article en En | MEDLINE | ID: mdl-38338957
ABSTRACT
Patients suffering from chronic fatigue syndrome (CFS) or post-COVID syndrome (PCS) exhibit a reduced physiological performance capability. Impaired mitochondrial function and morphology may play a pivotal role. Thus, we aimed to measure the muscle mitochondrial oxidative phosphorylation (OXPHOS) capacity and assess mitochondrial morphology in CFS and PCS patients in comparison to healthy controls (HCs). Mitochondrial OXPHOS capacity was measured in permeabilized muscle fibers using high-resolution respirometry. Mitochondrial morphology (subsarcolemmal/intermyofibrillar mitochondrial form/cristae/diameter/circumference/area) and content (number and proportion/cell) were assessed via electron microscopy. Analyses included differences in OXPHOS between HC, CFS, and PCS, whereas comparisons in morphology/content were made for CFS vs. PCS. OXPHOS capacity of complex I, which was reduced in PCS compared to HC. While the subsarcolemmal area, volume/cell, diameter, and perimeter were higher in PCS vs. CFS, no difference was observed for these variables in intermyofibrillar mitochondria. Both the intermyofibrillar and subsarcolemmal cristae integrity was higher in PCS compared to CFS. Both CFS and PCS exhibit increased fatigue and impaired mitochondrial function, but the progressed pathological morphological changes in CFS suggest structural changes due to prolonged inactivity or unknown molecular causes. Instead, the significantly lower complex I activity in PCS suggests probably direct virus-induced alterations.
Asunto(s)
Palabras clave

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Síndrome de Fatiga Crónica / COVID-19 Límite: Humans Idioma: En Revista: Int J Mol Sci Año: 2024 Tipo del documento: Article País de afiliación: Alemania

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Síndrome de Fatiga Crónica / COVID-19 Límite: Humans Idioma: En Revista: Int J Mol Sci Año: 2024 Tipo del documento: Article País de afiliación: Alemania