“…and neuron–body fluids pathways. Moreover, in previous studies, the distribution and change in the expression of substance P (Lu et al, 2011), acid-sensing ion channel 3 (ASIC 3 ) (Wang et al, 2014), transient receptor potential vanniloid-1 (TRPV 1 ) (Xu et al, 2011), Wnt 5a (Wang J. et al, 2015), extracellular signal-regulated kinase-5 (ERK 5 ) (Wang C. G. et al, 2015), mechanistic target of rapamycin (mTOR) and ERK 1/2 (Li et al, 2015), neurokinin-1 receptor (NK 1 R) (Zhang et al, 2017), and adrenomedullin (Wu et al, 2015), as well as dozens of neuroactive substances (including neurotransmitters, receptors, and ion channel proteins) in the CSF-contacting nucleus in morphine physical dependence (Lu et al, 2011), inflammatory pain (Wang et al, 2014), neuropathic pain (Xu et al, 2011; Li et al, 2015; Wang C. G. et al, 2015; Wang J. et al, 2015), visceral pain (Zhang et al, 2017) and stress (Wu et al, 2015). Studying the characteristics of the CSF-contacting nucleus and understanding the changes in the substances distributed in the nucleus will help elucidate the function of the nucleus and its relationship to physiological processes.…”