The cholinergic and non-cholinergic effects of organophosphates and oximes in cultured human myoblasts
Related Experiment Video
Updated: May 17, 2026

Cholinergic Ligand–dependent Modulation of Oxidative Phosphorylation Coupling in Digitonin-permeabilized BE(2)-C Neuroblastoma Cells
Published on: April 28, 2026
Maja Katalinić1, Katarina Miš, Sergej Pirkmajer
1Institute for Medical Research and Occupational Health, Zagreb, Croatia.
Abstract:
Organophosphorus compounds (OPs) and oximes may interfere with other molecules than AChE in the living systems, affecting in this way various cellular processes and underlying mechanisms. These non-cholinergic effects may contribute to the clinical status in OP poisoning and therefore deserve equal scientific attention. Here, we investigated the effects of tabun and oxime K048 on the processes known to be involved in muscle response to the environmental factors, like IL-6 release and the regulation of the heat shock proteins (HSPs). While IL-6 stimulates muscle regeneration, which follows well known OP-induced myopathy, HSPs have cytoprotective effect against various stress factors including xenobiotics. All our experiments were carried out on cultured human myoblasts, as the precursors of muscle regeneration. We found unchanged AChE mRNA level after tabun/K048 treatment meaning that tabun and K048 did not interfere with the transcription or stability of this mRNA in the time period tested, even if AChE catalytic activity was significantly affected. On the other hand, after myoblast exposure to tabun, we observed significant changes in the protein levels of HSP 27 and in the secretion of IL-6. Namely, secretion of IL-6 decreased to 53% and the level of HSP 27 increased by 34% compared to the control level. Both effects were attenuated if myoblasts were pretreated with oxime K048, but not if they were treated with K048 after exposure to tabun. The molecular mechanism underlying these effects remains to be elucidated. However, it seems that these effects could be associated with OPs and oximes as a specific group of compounds rather than as a specific compound itself. Overall, the effects of OPs and oximes demonstrated here might play an important role in muscle regeneration which importantly determines the final outcome of OP myotoxicity.
Insights
Organophosphorus compounds and oximes impact muscle cells beyond AChE, affecting IL-6 and HSP 27. Pretreatment with oxime K048 mitigates these non-cholinergic effects in muscle regeneration.
Area of Science:
- Biochemistry
- Toxicology
- Cell Biology
Background:
- Organophosphorus compounds (OPs) and oximes can exert non-cholinergic effects in biological systems.
- These effects may influence cellular processes and contribute to clinical outcomes in OP poisoning.
- Interactions with molecules other than acetylcholinesterase (AChE) warrant investigation.
Purpose of the Study:
- To investigate the non-cholinergic effects of tabun (an OP) and oxime K048 on human myoblasts.
- To examine the impact on interleukin-6 (IL-6) secretion and heat shock protein (HSP) 27 levels.
- To understand the role of these effects in muscle regeneration and myotoxicity.
Main Methods:
- Experiments conducted on cultured human myoblasts.
- Treatment with tabun and oxime K048.
- Analysis of AChE mRNA levels, AChE catalytic activity, IL-6 secretion, and HSP 27 protein levels.
Main Results:
- Tabun and K048 did not alter AChE mRNA levels but affected AChE activity.
- Tabun exposure decreased IL-6 secretion by 53% and increased HSP 27 levels by 34%.
- Oxime K048 pretreatment attenuated these effects; post-treatment did not.
Conclusions:
- OPs and oximes exhibit non-cholinergic effects on myoblasts, influencing IL-6 and HSP 27.
- These effects are compound-group specific rather than compound-specific.
- Understanding these mechanisms is crucial for addressing OP-induced myotoxicity and muscle regeneration.
More Related Videos
Related Concept Videos
Anticholinesterase Agents: Poisoning and Treatment
Irreversible agents form a strong bond with the cholinesterase enzyme, making it inactive. The breakdown of the phosphorylated enzyme is slower than the...
Indirect-Acting Cholinergic Agonists: Mechanism of Action
Reversible inhibitors like edrophonium bind to a specific part of the enzyme called the anionic catalytic site. They form noncovalent bonds, which means they are not strongly attached to the enzyme. This creates a temporary and less stable enzyme–inhibitor complex, leading to...
Indirect-Acting Cholinergic Agonists: Pharmacokinetics
Reversible agents containing quaternary amines, such as neostigmine and edrophonium, are not easily absorbed orally because they are...
Indirect-Acting Cholinergic Agonists: Chemistry and Structure-Activity Relationship
Reversible inhibitors display short to medium durations of action. Short-acting agents include simple alcohols with...
Direct-Acting Cholinergic Agonists: Chemistry and Structure-Activity Relationship
The direct-acting...
Indirect-Acting Cholinergic Agonists: Pharmacological Actions
At the neuromuscular junction, these agents work by inhibiting the breakdown of acetylcholine, allowing it to remain bound to the receptor and bind to nearby receptors. This process leads to repetitive firing of the endplate, causing muscle...

