Combined mental task and metaboreflex impair cerebral oxygenation in patients with type 2 diabetes mellitus.
Adult
Autonomic Nervous System
/ physiopathology
Biomarkers
/ blood
Case-Control Studies
Cerebrovascular Circulation
Chemoreceptor Cells
/ metabolism
Diabetes Mellitus, Type 2
/ diagnosis
Exercise
Female
Homeostasis
Humans
Male
Mental Processes
Middle Aged
Muscle Contraction
Muscle, Skeletal
/ innervation
Oxygen
/ blood
Oxygen Consumption
Random Allocation
Reflex
Time Factors
blood pressure
cardiovascular regulation
cerebral blood flow
stroke volume
systemic vascular resistance
Journal
American journal of physiology. Regulatory, integrative and comparative physiology
ISSN: 1522-1490
Titre abrégé: Am J Physiol Regul Integr Comp Physiol
Pays: United States
ID NLM: 100901230
Informations de publication
Date de publication:
01 04 2021
01 04 2021
Historique:
pubmed:
4
2
2021
medline:
11
5
2021
entrez:
3
2
2021
Statut:
ppublish
Résumé
Cardiovascular regulation is altered by type 2 diabetes mellitus (DM2), producing an abnormal response to muscle metaboreflex. During physical exercise, cerebral blood flow is impaired in patients with DM2, and this phenomenon may reduce cerebral oxygenation (COX). We hypothesized that the simultaneous execution of a mental task (MT) and metaboreflex activation would reduce COX in patients with DM2. Thirteen individuals suffering from DM2 (6 women) and 13 normal age-matched controls (CTL, 6 women) participated in this study. They underwent five different tests, each lasting 12 min: postexercise muscle ischemia (PEMI) to activate the metaboreflex, control exercise recovery (CER), PEMI + MT, CER + MT, and MT alone. COX was evaluated using near-infrared spectroscopy with sensors applied to the forehead. Central hemodynamics was assessed using impedance cardiography. We found that when MT was superimposed on the PEMI-induced metaboreflex, patients with DM2 could not increase COX to the same extent reached by the CTL group (101.13% ± 1.08% vs. 104.23% ± 2.51%,
Identifiants
pubmed: 33533319
doi: 10.1152/ajpregu.00288.2020
doi:
Substances chimiques
Biomarkers
0
Oxygen
S88TT14065
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM