Matsugi T, Kageyama M, Nishimura K, Giles H, Shirasawa E
Developmental Research Laboratories, Santen Pharmaceutical Co., Ltd., Osaka, Japan.
Eur J Pharmacol. 1995 Mar 14;275(3):245-50. doi: 10.1016/0014-2999(94)00788-9.
The effects of the selective prostaglandin D2 (DP) receptor agonists, 572C85 ((+/-)-5-(3-carboxypropylthio)-1-(2-cyclohexyl-2-hydroxyethyl- amino)hexahydrocyclopenta(d)imidazol-2(1H)-one) and 192C86 ((+/-)-5-(3-carboxypropylthio)-1-(2-cyclohexyl-2-hydroxyethylidene - amino)-3-ethylhexahydrocyclopenta(d)imidazol-2(1H)-one), were determined on intraocular pressure regulation in rabbits and cats. 572C85 (50 micrograms) in rabbits maximally lowered intraocular pressure by 4.3 mm Hg, and significantly for 4 h compared to control. In cats 572C85 had a similar effect. 192C86 (50 micrograms) reduced intraocular pressure by 2.8 mm Hg for 2 h in rabbits. Following exposure to the specific DP receptor antagonist, BW A868C ((+/-)-3-benzyl-5-(6-carboxyhexyl)-1-(2-cyclohexyl-2-hydroxyethylamin o)- hydantoin; 50 micrograms), which had no effect on intraocular pressure by itself, 572C85 (50 micrograms) did not reduce intraocular pressure in rabbits and cats. The intraocular pressure lowering effect of the mixed DP and EP receptor agonist, BW245C (5-(6-carboxyhexyl)-1-(3-cyclohexyl-3-hydroxypropyl)-hydantoin; 50 micrograms), in cats was suppressed by only 64% by BW A868C (50 micrograms). These results clearly show that the DP receptors in rabbit and cat eyes are involved in intraocular pressure regulation. However, under baseline conditions DP receptor activity does not contribute to this regulation.
研究了选择性前列腺素D2(DP)受体激动剂572C85((±)-5-(3-羧丙基硫基)-1-(2-环己基-2-羟乙氨基)六氢环戊二烯并咪唑-2(1H)-酮)和192C86((±)-5-(3-羧丙基硫基)-1-(2-环己基-2-羟亚乙基氨基)-3-乙基六氢环戊二烯并咪唑-2(1H)-酮)对兔和猫眼压调节的影响。兔眼内注射572C85(50微克)可使眼压最大降低4.3毫米汞柱,与对照组相比,4小时内眼压显著降低。在猫眼中,572C85有类似作用。兔眼内注射192C86(50微克)可使眼压在2小时内降低2.8毫米汞柱。在给予特异性DP受体拮抗剂BW A868C((±)-3-苄基-5-(6-羧己基)-1-(2-环己基-2-羟乙氨基)乙内酰脲;50微克)后(其本身对眼压无影响),兔和猫眼内注射572C85(50微克)均未降低眼压。混合DP和EP受体激动剂BW245C(5-(6-羧己基)-1-(3-环己基-3-羟丙基)乙内酰脲;50微克)在猫眼中的降眼压作用仅被BW A868C(50微克)抑制64%。这些结果清楚地表明,兔和猫眼中的DP受体参与眼压调节。然而,在基线条件下,DP受体活性对这种调节无作用。