Horiguchi S, Ueno R, Hyodo M, Hayaishi O
Eur J Pharmacol. 1986 Mar 18;122(2):173-9. doi: 10.1016/0014-2999(86)90100-7.
The effect of intracisternal administration of three major prostaglandins on nociceptive responses was evaluated in mice. Prostaglandin D2 had biphasic effects on pain thresholds (hot plate and acetic acid writhing tests) when given in a dosage range of 5 ng to 5 micrograms per mouse. Lower doses of prostaglandin D2 (less than or equal to 15 ng) increased the sensitivity to pain stimulation. Higher doses (greater than or equal to 50 ng) caused hypoalgesia, which was completely blocked by intracisternal injection of 500 pg of naloxone. Prostaglandin E2 (5 ng-5 micrograms) also had a biphasic effect on pain thresholds, similar to the effect of prostaglandin D2. However, the hypoalgesia caused by a higher dose of prostaglandin E2 (5 micrograms) was not blocked at all by naloxone doses of up to 500 ng. Prostaglandin F2 alpha had little effect on pain thresholds. These results indicate that each prostaglandin has a specific effect on the modulation of nociception.
在小鼠中评估了脑池内注射三种主要前列腺素对伤害性反应的影响。当以每只小鼠5纳克至5微克的剂量范围给予前列腺素D2时,其对疼痛阈值(热板法和醋酸扭体试验)具有双相作用。较低剂量的前列腺素D2(小于或等于15纳克)会增加对疼痛刺激的敏感性。较高剂量(大于或等于50纳克)会导致痛觉减退,脑池内注射500皮克纳洛酮可完全阻断这种作用。前列腺素E2(5纳克 - 5微克)对疼痛阈值也有双相作用,类似于前列腺素D2的作用。然而,高达500纳克的纳洛酮剂量对较高剂量前列腺素E2(5微克)引起的痛觉减退完全没有阻断作用。前列腺素F2α对疼痛阈值几乎没有影响。这些结果表明,每种前列腺素对伤害感受的调节都有特定作用。