Wan-Jie Du1 • Shufen Hu1 • Xin Li1 • Ping-An Zhang1,2 • Xinghong Jiang1 • Shan-Ping Yu3 • Guang-Yin Xu1,2,*
1Laboratory for Translational Pain Medicine, Institute of Neuroscience, Soochow University, Suzhou 215123, China
2Center for Translational Medicine, The Zhangjiagang Affiliated Hospital of Soochow University, Zhangjiagang 215600, China
3Department of Anesthesiology, Emory University School of Medicine, Atlanta, GA 30307, USA
The pathophysiology of visceral pain in patients with irritable bowel syndrome remains largely unknown. Our previous study showed that neonatal maternal deprivation (NMD) does not induce visceral hypersensitivity at the age of 6 weeks in rats. The aim of this study was to determine whether NMD followed by adult stress at the age of 6 weeks induces visceral pain in rats and to investigate the roles of adrenergic signaling in visceral pain. Here we showed that NMD rats exhibited visceral hypersensitivity 6 h and 24 h after the termination of adult multiple stressors (AMSs). The plasma level of norepinephrine was significantly increased in NMD rats after AMSs. Whole-cell patch-clamp recording showed that the excitability of dorsal root ganglion (DRG) neurons from NMD rats with AMSs was remarkably increased. The expression of β2 adrenergic receptors at the protein and mRNA levels was markedly higher in NMD rats with AMSs than in rats with NMD alone. Inhibition of β2 adrenergic receptors with propranolol or butoxamine enhanced the colorectal distention threshold and application of butoxamine also reversed the enhanced hypersensitivity of DRG neurons. Overall, our data demonstrate that AMS induces visceral hypersensitivity in NMD rats, in part due to enhanced NE-β2 adrenergic signaling in DRGs.
Irritable bowel syndrome; Dorsal root ganglion; Norepinephrine; Visceral pain; Stress