Wallenstein M C
Eur J Pharmacol. 1983 May 20;90(1):65-73. doi: 10.1016/0014-2999(83)90214-5.
The present study investigates the results of pretreatment with five prostaglandin (PG) synthetase inhibitors on effects of morphine on body temperature, pupillary diameter, body movement and production of exophthalmos in rat. Hyperthermia, induced by a low dose of morphine, was inhibited in animals pretreated with any of the PG synthetase inhibitors. However, PG synthetase inhibitors had no clear effect on hypothermia induced by higher doses of morphine. The duration of morphine-induced catalepsy was attenuated by pretreatment with the PG synthetase inhibitors in a dose-related manner. The exophthalmos induced by all doses of morphine was either shortened in duration or inhibited by sulindac, paracetamol or ibuprofen. Morphine-induced mydriasis was either attenuated or inhibited by paracetamol, ibuprofen or meclofenamic acid. The results suggest that endogenous PGs play a role in morphine-induced hyperthermia, catalepsy, exophthalmos and mydriasis whereas a physiological role for PGs in morphine-induced hypothermia was not indicated.
本研究调查了五种前列腺素(PG)合成酶抑制剂预处理对吗啡对大鼠体温、瞳孔直径、身体活动及眼球突出产生的影响。低剂量吗啡诱导的体温过高在经任何一种PG合成酶抑制剂预处理的动物中受到抑制。然而,PG合成酶抑制剂对高剂量吗啡诱导的体温过低没有明显影响。PG合成酶抑制剂预处理以剂量相关的方式减弱了吗啡诱导的僵住症持续时间。所有剂量吗啡诱导的眼球突出,其持续时间在舒林酸、对乙酰氨基酚或布洛芬作用下均缩短或受到抑制。对乙酰氨基酚、布洛芬或甲氯芬那酸减弱或抑制了吗啡诱导的瞳孔散大。结果表明,内源性PG在吗啡诱导的体温过高、僵住症、眼球突出及瞳孔散大过程中发挥作用,而未显示PG在吗啡诱导的体温过低中发挥生理作用。