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首页> 外文期刊>Investigative ophthalmology & visual science >In vivo ocular efficacy profile of mapracorat, a novel selective glucocorticoid receptor agonist, in rabbit models of ocular disease.
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In vivo ocular efficacy profile of mapracorat, a novel selective glucocorticoid receptor agonist, in rabbit models of ocular disease.

机译:新型的选择性糖皮质激素受体激动剂马普拉考拉在眼部疾病兔模型中的体内眼部疗效概况。

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PURPOSE: To compare the efficacy of mapracorat (formerly ZK-245186, and subsequently BOL-303242-X), a novel selective glucocorticoid receptor agonist (SEGRA), with that of dexamethasone (DEX) in rabbit models of ocular disease. The effects of topical BOL-303242-X and DEX on intraocular pressure (IOP) and body weight changes were also evaluated. METHODS: Dry eye was induced by atropine sulfate administration and was treated with saline, BOL-303242-X (0.1%-1.0%), DEX (0.1%), Restasis 0.05% (Allergan, Inc., Irvine, CA), or Refresh Endura (Allergan, Inc.) three times per day for 7 to 8 days. For paracentesis studies, vehicle, BOL-303242-X (0.1%, 0.5%, and 1.0%), or DEX (0.1%) were repeatedly administered topically 3 hours before paracentesis and continued for 90 minutes afterward. For IOP and body weight measurements, right eyes of rabbits were topically treated with vehicle, BOL-303242-X (1.0% or 0.1%), or DEX (0.1%) four times per day for 6 weeks. RESULTS: In the dry eye model, BOL-303242-X and DEX were fully efficacious, maintaining tear volume and tear breakup time (TBUT) at baseline levels. Although Restasis improved tear volume compared with vehicle, no changes were observed in TBUT. In the paracentesis study, BOL-303242-X and DEX improved ocular inflammation. BOL-303242-X reduced protein and PGE(2) levels. Finally, BOL-303242-X showed no effects on integrated IOP or body weight, whereas DEX significantly increased integrated IOP and prevented the increase of body weight observed in the vehicle-treated animals. CONCLUSIONS: BOL-303242-X shows full anti-inflammatory efficacy (similar to DEX) in experimental models of dry eye and postoperative inflammation while demonstrating reduced effects in IOP and body weight. These data indicate that mapracorat, a SEGRA, shows efficacy similar to that of traditional steroids while exhibiting an improved side effect profile in IOP and muscle wasting.
机译:目的:为了比较一种新型的选择性糖皮质激素受体激动剂(SEGRA)马普考拉特(以前的ZK-245186,然后是BOL-303242-X)与地塞米松(DEX)在眼部疾病模型中的功效。还评估了局部BOL-303242-X和DEX对眼内压(IOP)和体重变化的影响。方法:硫酸阿托品引起干眼症,并用生理盐水,BOL-303242-X(0.1%-1.0%),DEX(0.1%),Restasis 0.05%(Allergan,Inc.,Irvine,CA)或每天刷新Endura(Allergan,Inc.)3次,持续7至8天。对于穿刺研究,在穿刺前3小时局部重复施用媒介物,BOL-303242-X(0.1%,0.5%和1.0%)或DEX(0.1%),此后持续90分钟。为了测量眼压和体重,兔的右眼每天用媒介物,BOL-303242-X(1.0%或0.1%)或DEX(0.1%)局部治疗,每周四次,共6周。结果:在干眼模型中,BOL-303242-X和DEX完全有效,可将泪液量和泪液破裂时间(TBUT)维持在基线水平。尽管与车辆相比,Restasis改善了泪液体积,但在TBUT中未观察到变化。在穿刺术研究中,BOL-303242-X和DEX改善了眼部炎症。 BOL-303242-X降低蛋白质和PGE(2)的水平。最后,BOL-303242-X对综合IOP或体重无影响,而DEX显着增加了综合IOP并阻止了在媒介物治疗动物中观察到的体重增加。结论:BOL-303242-X在干眼症和术后炎症实验模型中显示出完全的抗炎功效(类似于DEX),同时证明IOP和体重的减轻作用。这些数据表明,SEGRA的mapracorat表现出与传统类固醇相似的功效,同时在IOP和肌肉消瘦方面表现出改善的副作用。

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