Peculiarities of the Acetylcholine Action on the Contractile Function of Cardiomyocytes from the Left and Right Atria in Rats.
Xenia ButovaTatiana MyachinaRaisa SimonovaAnastasia M KochurovaYakov BozhkoMichael ArkhipovOlga SolovyovaGalina V KopylovaDaniil ShchepkinAnastasia KhokhlovaPublished in: Cells (2022)
Acetylcholine (ACh) is the neurotransmitter of the parasympathetic nervous system that modulates cardiac function, and its high concentrations may induce atrial fibrillation. We compared the ACh action on the mechanical function of single cardiomyocytes from the left atria (LA) and the right atria (RA). We exposed single rat LA and RA cardiomyocytes to 1, 10, and 100 µM ACh for 10-15 min and measured the parameters of sarcomere shortening-relengthening and cytosolic calcium ([Ca 2+ ] i ) transients during cell contractions. We also studied the effects of ACh on cardiac myosin function using an in vitro motility assay and analyzed the phosphorylation level of sarcomeric proteins. In LA cardiomyocytes, ACh decreased the time to peak sarcomere shortening, time to 50% relengthening, and time to peak [Ca 2+ ] i transients. In RA cardiomyocytes, ACh affected the time of shortening and relengthening only at 10 µM. In the in vitro motility assay, ACh reduced to a greater extent the sliding velocity of F-actin over myosin from LA cardiomyocytes, which was accompanied by a more pronounced decrease in phosphorylation of the myosin regulatory light chain (RLC) in LA cardiomyocytes than in RA cardiomyocytes. Our findings indicate that ACh plays an important role in modulating the contractile function of LA and RA, provoking more pronounced changes in the time course of sarcomere shortening-relengthening and the kinetics of actin-myosin interaction in LA cardiomyocytes.
Keyphrases
- rheumatoid arthritis
- high glucose
- atrial fibrillation
- disease activity
- binding protein
- heart failure
- ankylosing spondylitis
- left ventricular
- endothelial cells
- interstitial lung disease
- mesenchymal stem cells
- blood pressure
- coronary artery disease
- biofilm formation
- single cell
- heart rate variability
- idiopathic pulmonary fibrosis
- cystic fibrosis
- venous thromboembolism
- systemic sclerosis
- pseudomonas aeruginosa
- cell therapy
- heart rate