PT  - JOURNAL ARTICLE
AU  - Zurek, Nesia A.
AU  - Thiyagarajan, Sherwin
AU  - Ehsanian, Reza
AU  - Goins, Aleyah E.
AU  - Goyal, Sachin
AU  - Shilling, Mark
AU  - Lambert, Christophe G.
AU  - Westlund, Karin N.
AU  - Alles, Sascha R. A.
TI  - Machine Learning Elucidates Electrophysiological Properties Predictive of Multi- and Single-Firing Human and Mouse Dorsal Root Ganglia Neurons
AID  - 10.1523/ENEURO.0248-24.2024
DP  - 2024 Oct 01
TA  - eneuro
PG  - ENEURO.0248-24.2024
VI  - 11
IP  - 10
4099  - http://www.eneuro.org/content/11/10/ENEURO.0248-24.2024.short
4100  - http://www.eneuro.org/content/11/10/ENEURO.0248-24.2024.full
SO  - eNeuro2024 Oct 01; 11
AB  - Human and mouse dorsal root ganglia (hDRG and mDRG) neurons are important tools in understanding the molecular and electrophysiological mechanisms that underlie nociception and drive pain behaviors. One of the simplest differences in firing phenotypes is that neurons are single-firing (exhibit only one action potential) or multi-firing (exhibit 2 or more action potentials). To determine if single- and multi-firing hDRG neurons exhibit differences in intrinsic properties, firing phenotypes, and AP waveform properties, and if these properties could be used to predict multi-firing, we measured 22 electrophysiological properties by whole-cell patch-clamp electrophysiology of 94 hDRG neurons from six male and four female donors. We then analyzed the data using several machine learning models to determine if these properties could be used to predict multi-firing. We used 1,000 iterations of Monte Carlo cross-validation to split the data into different train and test sets and tested the logistic regression, k-nearest neighbors, random forest, support vector classifier, and XGBoost machine learning models. All models tested had a >80% accuracy on average, with support vector classifier, and XGBoost performing the best. We found that several properties correlated with multi-firing hDRG neurons and together could be used to predict multi-firing neurons in hDRG including a long decay time, a low rheobase, and long first spike latency. We also found that the hDRG models were able to predict multi-firing with 90% accuracy in mDRG neurons. Understanding these properties could be beneficial in the elucidation of targets on peripheral sensory neurons related to pain.