Department of Ophthalmology, Mayo Clinic , Rochester, Minnesota.
J Ocul Pharmacol Ther. 2014 Mar-Apr;30(2-3):138-42. doi: 10.1089/jop.2013.0199. Epub 2013 Dec 9.
Abstract Glaucoma is a leading cause of blindness in the United States affecting as many as 2.2 million Americans. All current glaucoma treatment strategies aim to reduce intraocular pressure, even in patients with normal tension glaucoma. Typically, this is accomplished by reducing the rate of aqueous flow by limiting aqueous production or enhancing drainage using drugs and surgery. Whereas these strategies are effective in diminishing vision loss, some patients continue to lose vision and many discontinue use of their medications because of undesirable side effects. Drugs known to be effective in altering conventional outflow have for the most part been abandoned from modern clinical practice due to undesirable side effects. Identification of new drugs that could enhance conventional outflow, would offer additional options in the treatment of glaucoma and ocular hypertension. To this end, our laboratory has recently uncovered a novel pathway for regulation of conventional outflow by the ciliary body. This pathway is dependent on soluble adenylyl cyclase, an enzyme that catalyzes the generation of cyclic adenosine 3',5' monophosphate (cAMP) in response to bicarbonate.
摘要 青光眼是美国导致失明的主要原因,影响了多达 220 万美国人。所有目前的青光眼治疗策略都旨在降低眼内压,即使是在正常眼压性青光眼患者中也是如此。通常,这是通过减少房水的产生速度或通过使用药物和手术来增强排水来实现的。虽然这些策略在减少视力丧失方面非常有效,但有些患者仍然会失明,许多患者由于不良反应而停止使用他们的药物。由于不良反应,已知能有效改变传统流出的药物在很大程度上已被现代临床实践所摒弃。鉴定能增强传统流出的新药,将为青光眼和高眼压症的治疗提供更多选择。为此,我们实验室最近发现了一种通过睫状体调节传统流出的新途径。这条途径依赖于可溶性腺苷酸环化酶,这种酶能催化碳酸氢盐产生环磷酸腺苷 3',5' 一磷酸(cAMP)。