Translational Pain Research: Electrophysiological Evaluation of Cynomolgus Monkey DRG Neurons

Translational Pain Research: Electrophysiological Evaluation of Cynomolgus Monkey DRG Neurons

ICE Bioscience ICE Bioscience

ICE Bioscience

Your Trusted Partner in Drug Discovery Services

发布日期: 2025年3月6日
+ 关注

Background

Voltage-gated sodium channel Nav1.8 plays a key role in peripheral pain signal transmission and is a proven target in the development of non-opioid analgesics. Tetrodotoxin-resistant (TTX-R) sodium currents in dorsal root ganglion (DRG) neurons are primarily mediated by Nav1.8 and represent a critical readout for assessing analgesic compounds.

While high-throughput screening using human Nav1.8-expressing cell lines provides valuable potency data at the target level, these systems lack the complex physiological environment of native sensory neurons. Cynomolgus monkey DRG neurons, as a non-human primate model with high genetic similarity to humans, offer a critical bridge for validating analgesic candidates in a more biologically relevant context, particularly when human primary DRG neurons are not available.

Methods

We evaluated the Nav1.8 inhibitor VX-548 across multiple species using whole-cell patch-clamp recordings to assess inhibition of TTX-R currents under both resting (TP1) and half-inactivated (TP2) channel states.

Tested models included:

  • Human Nav1.8-CHO stable cell line
  • Rat DRG neurons
  • Mouse DRG neurons
  • Cynomolgus monkey DRG neurons

Results

Cross-Species Comparison of VX-548 Potency

TP1: Resting state; TP2: Half-inactivated state

These results demonstrate that Cynomolgus monkey DRG neurons demonstrated sub-nanomolar Nav1.8 inhibition potency similar to that observed in human Nav1.8-expressing cell lines, supporting their use as a translational model to confirm compound activity in native neuronal systems.

Figure 1. Concentration-dependent effect of VX-548 on human Nav1.8-CHO stable cell line, rat and mouse DRG neurons TTX-R currents ?in resting state.
Figure 2. Concentration-dependent effect of VX-548 on human Nav1.8-CHO stable cell line, rat and mouse DRG neurons TTX-R currents in half-inactivated state.
Figure 3. Representative currents of human Nav1.8-CHO stable line, before and after VX-548 application at different concentrations in resting and half-inactivated state.
Figure 4. Representative currents of cyno DRG neurons TTX-R channel, before and after VX-548 application at different concentrations in resting and half-inactivated state.
Figure 5. Representative currents of rat DRG neurons TTX-R channel, before and after VX-548 application at different concentrations in resting and half-inactivated state.
Figure 6. Representative currents of mouse DRG neurons TTX-R channel, before and after VX-548 application at different concentrations in resting and half-inactivated state.

Case Example: Inhibitory Effect of Compound X on Cynomolgus Monkey DRG

To further demonstrate the value of cynomolgus monkey DRG assays, Compound X was tested for its ability to inhibit TTX-R sodium currents.

Figure 7: Concentration-dependent inhibition of TTX-R currents by Compound X in cynomolgus monkey DRG neurons.
Figure 8. Representative image of cultured DRG neurons from cynomolgus monkey. The arrow indicates a typical DRG neuron.

This study highlights the high sensitivity of cynomolgus monkey DRG neurons, making them ideal for:

  • Identifying potent Nav1.8 inhibitors
  • Bridging preclinical and clinical pharmacology
  • Supporting dose selection and risk assessment

Conclusion

Cynomolgus monkey DRG neurons provide a translational model for validating Nav1.8-targeted analgesics beyond recombinant systems. While human Nav1.8-expressing cell lines are essential for early-stage screening, cyno DRG assays allow confirmation of compound activity in native sensory neurons, offering greater physiological relevance.

By integrating cyno DRG electrophysiology into the screening workflow, researchers can enhance the predictability of preclinical data and better support the transition to clinical development in pain therapeutics.


要查看或添加评论，请登录

ICE Bioscience的更多文章