Antinociceptive mechanisms associated with diluted bee venom acupuncture (apipuncture) in the rat formalin test: involvement of descending adrenergic and serotonergic pathways

• Published in: Pharmacological research 2005-02, Vol.51 (2), p.183-188
• Main Authors: Kim, Hyun Woo, Kwon, Young Bae, Han, Ho Jae, Yang, Il Suk, Beitz, Alvin J., Lee, Jang Hern
• Format: Article
• Language: English
• Subjects: Acupuncture; Acupuncture - methods; Adrenergic Fibers - drug effects; Adrenergic Fibers - physiology; Analgesics - pharmacology; Animals; Antinociception; Bee venom; Bee Venoms - pharmacology; Bees; Male; Neural Pathways - drug effects; Neural Pathways - physiology; Pain Measurement - drug effects; Pain Measurement - methods; Rats; Rats, Sprague-Dawley; Serotonergic; Serotonin - physiology; α 2 Adrenergic
• ISSN: 1043-6618; 1096-1186
• DOI: 10.1016/j.phrs.2004.07.011

In a previous report, subcutaneous injection of diluted bee venom (dBV) into a specific acupuncture point (Zusanli, ST36), a procedure termed apipuncture, was shown to produce an antinociceptive effect in the rat formalin pain model. However, the central antinociceptive mechanisms responsible for this effect have not been established. Traditional acupuncture-induced antinociception is considered to be mediated by activation of the descending pain inhibitory system (DPIS) including initiation of its opioidergic, adrenergic and serotonergic components. The purpose of the present study was to investigate whether the antinociceptive effect of apipuncture is also mediated by the DPIS. Behavioral experiments verified that apipuncture significantly reduces licking behavior in the late phase of formalin test in rats. This antinociceptive effect of apipuncture was not modified by intrathecal pretreatment with naltrexone (a non-selective opioid receptor antagonist), prazosin (a α 1 adrenoceptor antagonist) or propranolol (an β adrenoceptor antagonist). In contrast, intrathecally injected idazoxan (an α 2 adrenoceptor antagonist) or intrathecal methysergide (a serotonin receptor antagonist) significantly reversed apipuncture-induced antinociception. These results suggest that apipuncture-induced antinociception is produced by activation of α 2 adrenergic and serotonergic components of the DPIS.