Objective: To study the influence of intra cerebroventricular injection of cholecystokinin octapeptide (CCK 8) on the effect of electroacupuncture (EA) i n antagonizing the electrical activity of pain related neurons ...
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Objective: To study the influence of intra cerebroventricular injection of cholecystokinin octapeptide (CCK 8) on the effect of electroacupuncture (EA) i n antagonizing the electrical activity of pain related neurons in caudate nucle us (Cd) and raising pain ***: 30 male Wistar rats were used. Operations were performed under general anesthesia with 20% urethane (1.0 g/kg of body weight). The radiant heat irradiation (nociceptive stimulus) induce d rat tail flick reaction was used as the pain index. Extracellular discharges o f pain related neurons pain excitatory neurons (PEN) and pain inhibitory ne urons (PIN) in Cd and tail flick latency (TFL) before and after cerebroventri cular microinjection of CCK 8 (15 ng) were recorded. Electroacupuncture (EA) wa s applied to bilateral "Zusanli" (ST 36).Results: ① The radiant heat focused on the tail of rats caused increase of the pain evoked discharging frequency and shortening of the evoked discharging latency of PEN or reduction of the pain evoked discharging frequency and prolongation of the inhibitory du ration of the evoked discharges of PIN and generated tail flick reflex simultaneously. ② EA of bilateral "Zusanli" (ST 36) for 15 min resulted in inh ibition of the electric activity of PEN as well as potentiation of the electrica l activity of PIN and a prolongation of tail flick latency (TFL), i.e. exhibitin g the analgesic effect of EA. The effects peaked immediately after EA, the net i ncrease value (NIV) of the pain evoked discharges of 19 PENs was reduced from 1 6.17±2.30 Hz to 5.45±2.96 Hz and TFL was prolonged from 5.03±0.31 sec to 8.89 ±0.58 sec simultaneously, the inhibitory duration of the pain evoked discharge s of 12 PINs was shortened from 5.19±0.24 sec to 2.52±0.33 sec and TFL was pro longed from 4.57±0.23 sec to 8.12±0.29 sec simultaneously. These changes recov ered gradually 10 min after EA. ③ The inhibitory effect of EA on the pain evok ed discharges of PEN and the potentiated effect of E
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