Background; Chronic pain is characterized by abnormal sensitivity to normal stimulation coupled with a feeling of unpleasantness. This condition afflicts people worldwide and severely impacts their QOL and has become an escalating health problem. Two major models are used to study chronic pain in animals, including nerve injury and the injection of a complete Freund's adjuvant (CFA) into the hind paw. However, how these models induce glutamatergic synaptic plasticity in the spinal cord is not fully understood. Methods; Using in vitro and in vivo whole-cell patch clamp recording, we analyzed spontaneous excitatory postsynaptic currents (sEPSCs).
Results; These models increased both the frequency and amplitude of sEPSCs in spinal dorsal horn (SDH) neurons. Next, we analyzed the active electrophysiological properties of neurons, which included; resting membrane potentials (RMPs) and the generation of action potentials (APs) in vitro. Interestingly, about 20% of recorded SDH neurons in this group elicited spontaneous APs (sAPs) without changing the RMPs. Furthermore, we performed in vivo whole-cell patch clamp recording in SDH neurons to analyze active electrophysiological properties under physiological conditions. Importantly, in vivo SDH neurons generated sAPs without affecting RMP in the nerve injury and the CFA group.
Conclusions; Our study describes how animal models of chronic pain influence both passive and active electrophysiological properties of SDH neurons.