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KMID : 0352720000240030143
Journal of Ginseng Research
2000 Volume.24 No. 3 p.143 ~ p.147
Ginsenosides Attenuate Formalin-Induced Pains Through Spinal and Supraspinal Sites
Seung Yeol Nah/So Rah Yoon
Seok Choi/Se Yeon Jung/Seok Chang Kim/Sung Ryong Ko/Ki Yeul Nam/Seung Yeol Nah
Abstract
In previous studies we have demonstrated that several individual ginsenosides such as Rc, Rd, Re and Ri relieves formalin-induced pain following systemic treatment. But it is unknown where these single ginsenosides induce antinociception. We investigated the antinoiceptive effect of four individual ginsenosides on formalin-induced pain after intrathecal (i.t.), intracereventricular (i.c.v.), or subcutaneous (s.c.) administration using mice. We found that ginsenoside Rc, Rd, and Re except Rf attenuated both acute and tonic phase of pain. Ginsenoside Rf attenuated only tonic phase of pain after i.t. administration. The ED_50/ was 1.0 (0.55¡­l.75 mg/kg) for Rc, 1.15 (0.6¡­2.25 mg/kg) for Rd, and 8.9 (3.9¡­20.5 mg/kg) for Re in acute phase of pain. The ED_50/ was 0.3 (0.1¡­0.85 mg/kg) for Rc, 0.6 (0.35¡­l.1 mg/kg) for Rd, 2.45 (1.25¡­4.65 mg/kg) for Re, and 1.9 (1.5¡­4.25 mg/kg) for Rf in tonic phase of pain. We also found that ginsenoside Rc, Rd, Re, and Rf after i.c.v. administration attenuated both acute and tonic phase of pain. The ED5o for acute phase of pain was 0.9 (0.55¡­l.4mg/kg) for Rc, 0.9 (0.45¡­1.7 mg/kg) for Rd, 0.93 (0.5¡­l .75 mg/kg) for Re, and 1.85 (0.95¡­3.5 mg/kg) for Rf. The ED_50/ for tonic phase of pain was 0.7 (0.45¡­1.05 mg/kg) for Rc,1.25 (0.7¡­2.2 mg/kg) for Rd, 0.85 (0.45¡­1.6 mg/kg) for Re, and 0.8 (0.4¡­1.45 mg/kg) for Rf. Thus, the order of the analgesic potency was Rc¡ÃRd>Re>Rf in both i.t. and i.c.v. administration routes. However, s.c. pretreatment of four ginsenosides did not reduce formalin-induced pain. These results suggest that analgesic effect of ginsenosides is achieved through spinal or supraspinal site(s) in formalin test.
KEYWORD
Ginsenoside Rc, Rd, Re, and Rf, pain, spinal and supraspinal sites, analgesia,
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