Kulkarni P S, Srinivasan B D
Arch Ophthalmol. 1985 Jan;103(1):103-6. doi: 10.1001/archopht.1985.01050010109031.
We have compared the effects of nonsteroidal anti-inflammatory agents (NSAIDs) indomethacin, flurbiprofen, and aspirin administered either intraperitoneally (IP) or topically on rabbit conjunctival and anterior uveal prostaglandin (PG) synthesis. Doses of IP flurbiprofen and aspirin at or above 50 mg/kg almost completely inhibited PG synthesis in the conjunctiva and anterior uvea. Indomethacin at doses up to 100 mg/kg only partially inhibited PG synthesis in rabbit anterior uvea. Although IP flurbiprofen and aspirin were better than IP indomethacin in inhibiting PG synthesis in anterior uvea, 0.5% topical aspirin almost completely inhibited PG synthesis in the conjunctiva and anterior uvea, but 0.5% flurbiprofen and 0.5% indomethacin did not. A lower topical dose (0.01%) of aspirin prevented the production of PGs in the anterior uvea.
我们比较了非甾体抗炎药(NSAIDs)吲哚美辛、氟比洛芬和阿司匹林经腹腔注射(IP)或局部给药对兔结膜和前葡萄膜前列腺素(PG)合成的影响。腹腔注射氟比洛芬和阿司匹林剂量达到或高于50mg/kg时,几乎完全抑制结膜和前葡萄膜中的PG合成。剂量高达100mg/kg的吲哚美辛仅部分抑制兔前葡萄膜中的PG合成。虽然腹腔注射氟比洛芬和阿司匹林在抑制前葡萄膜中PG合成方面优于腹腔注射吲哚美辛,但0.5%的局部用阿司匹林几乎完全抑制结膜和前葡萄膜中的PG合成,而0.5%的氟比洛芬和0.5%的吲哚美辛则不能。较低局部剂量(0.01%)的阿司匹林可防止前葡萄膜中PG的产生。