| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 4326517 | Brain Research | 2010 | 8 Pages |
Sympathetic postganglionic neurons play an important role in pathological pain. This study was designed to investigate the role of sympathetic postganglionic neurons in inflammatory pain induced by bee venom (BV). The effects of chemical (with guanethidine or 6-hydroxydopamine) or surgical sympathectomy on BV-induced spontaneous foot lifting, mechanical hyperalgesia, and edema were observed. The results showed that surgical or chemical sympathectomy significantly attenuated an increase in paw volume (PV) and a decrease in paw withdrawal mechanical threshold (PWMT) induced by BV; however, these interventions had no effect on BV-evoked spontaneous foot lifting. Furthermore, pharmacological blockade of adrenergic receptors via systemic delivery of phentolamine, an α-adrenergic receptor antagonist, or prazosin, an α1-adrenergic receptor antagonist, produced similar inhibitory effects on BV-induced changes in PV and PWMT, however, yohimbine, an α2-adrenergic receptor antagonist, had no such effects. These results suggest that the interaction between sympathetic postganglionic neurons and primary afferent neurons via α1-adrenergic receptor play key roles in BV-induced mechanical hyperalgesia and inflammatory swelling but not in spontaneous foot lifting.
Research Highlights►Sympathectomy attenuated bee venom-induced hyperalgesia and inflammation. ►Sympathectomy had no effect on bee venom-evoked spontaneous foot lifting. ►Phentolamine or prazosin inhibited bee venom-induced hyperalgesia and inflammation. ►Yohimbine had no such effects bee venom-induced hyperalgesia and inflammation.
