Nakamura H, Mizushima Y, Seto Y, Motoyoshi S, Kadokawa T
Agents Actions. 1985 Sep;16(6):542-7. doi: 10.1007/BF01983660.
In order to explore the role of phospholipase A2 inhibition in the mechanisms of the action of glucocorticoids, it was investigated whether the steroid exhibits the analgesic and antipyretic actions as well as cyclo-oxygenase inhibitors such as indomethacin or not. Dexamethasone has been reported to produce the anti-inflammatory action with a lag time of at least 1 h at doses of up to 0.1 mg/kg in mice and rats. However, dexamethasone when given 4 h beforehand had no significant analgesic activity even at doses of 1 and 10 mg/kg i.v. in the acetic acid writhing test in rats. In mice, the significant reduction in writhes counts was seen when dexamethasone (1 and 10 mg/kg i.v.) was given 15 min or 4 h before phenylquinone injection; i.e. the activity had not the lag time. On the other hand, dexamethasone showed a strong antipyretic activity against both the fevers caused by LPS and yeast in rats. In the yeast-febrile rats, the antipyretic activity had a lag time of about 1 h, and was dose-related at doses as low as 0.03 to 0.3 mg/kg i.v.; the steroid markedly reduced the increased PGE2 content in the cerebrospinal fluid. The antipyretic activity after local injection into the cerebroventricle or the yeast pouch was stronger than that after systemic injection into the tail vein, although so large a difference in the activity between the dosage routes was not seen, suggesting that the site of the antipyretic action is in both the brain and periphery. The antipyretic activity of dexamethasone (10 mg/kg i.v.) was not seen in rabbits with fever caused by LPS.(ABSTRACT TRUNCATED AT 250 WORDS)
为了探究磷脂酶A2抑制在糖皮质激素作用机制中的作用,研究了该类固醇是否具有与吲哚美辛等环氧化酶抑制剂类似的镇痛和解热作用。据报道,地塞米松在小鼠和大鼠中以高达0.1mg/kg的剂量给药时,产生抗炎作用的滞后时间至少为1小时。然而,预先4小时给予地塞米松,即使在大鼠醋酸扭体试验中静脉注射1mg/kg和10mg/kg的剂量,也没有显著的镇痛活性。在小鼠中,在注射苯醌前15分钟或4小时给予地塞米松(静脉注射1mg/kg和10mg/kg)时,扭体次数显著减少;即该活性没有滞后时间。另一方面,地塞米松对大鼠内毒素和酵母引起的发热均显示出强烈的解热活性。在酵母致热大鼠中,解热活性的滞后时间约为1小时,在低至0.03至0.3mg/kg静脉注射剂量时与剂量相关;该类固醇显著降低了脑脊液中升高的前列腺素E2含量。尽管在给药途径之间未观察到如此大的活性差异,但脑室或酵母囊局部注射后的解热活性强于尾静脉全身注射后的解热活性,这表明解热作用部位在脑和外周。地塞米松(静脉注射10mg/kg)对由内毒素引起发热的兔子没有解热活性。(摘要截断于250字)