Kowalski Michał, Walczak Anna, Majsterek Ireneusz
Niepubliczny Zakład Opieki Zdrowotnej "Sal-Med", Łódź.
Postepy Hig Med Dosw (Online). 2008 Oct 31;62:582-92.
Glaucoma is one of the most important civilization diseases and leads to irreversible blindness. Inspite of many years of research, the causes of this disorder remain unclear. This disease is extremely difficult to diagnose because its primary phase is asymptomatic. After laborious research it has been discovered that metalloproteinases, i.e. proteolytic enzymes involved in the pathogenesis of many kinds of glaucoma, are crucial in glaucoma diagnosis. The overexpression of matrixins leads to degradation of extracellular matrix components, which results in eye tissue injury and changes of tissue properties. Structural disorders occurring in this way are one of the many key reasons for progressive glaucomatous optic neuropathy. The presence of altered expressions of MMP-1, -2, -3, -7, -9, and -12 and their tissue inhibitors TIMP-1 and -2 in the glaucomatous eye paves new ways for the diagnosis and treatment of open-angle glaucoma. The detection of polymorphisms and mutations in genes encoding these enzymes will allow qualifying a patient to a risk group and people who are already ill may be treated by regulation of metalloproteinases activity. This review focuses on the presence and function of metalloproteinases in open-angle glaucoma and on treatment possibilities through MMP regulation.
青光眼是最重要的文明病之一,可导致不可逆转的失明。尽管经过多年研究,这种疾病的病因仍不清楚。这种疾病极难诊断,因为其初期无症状。经过艰苦研究发现,金属蛋白酶,即参与多种青光眼发病机制的蛋白水解酶,在青光眼诊断中至关重要。基质金属蛋白酶的过度表达导致细胞外基质成分降解,从而导致眼组织损伤和组织特性改变。以这种方式发生的结构紊乱是进行性青光眼性视神经病变的众多关键原因之一。青光眼眼中MMP-1、-2、-3、-7、-9和-12及其组织抑制剂TIMP-1和-2表达改变的存在为开角型青光眼的诊断和治疗开辟了新途径。检测编码这些酶的基因中的多态性和突变将有助于将患者归入风险组,而对于已经患病的人,可以通过调节金属蛋白酶活性进行治疗。本综述重点关注金属蛋白酶在开角型青光眼中的存在和功能以及通过MMP调节的治疗可能性。